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Diagnosis of Restless Legs Syndrome

Diagnostic Test list for Restless Legs Syndrome:

The list of medical tests mentioned in various sources as used in the diagnosis of Restless Legs Syndrome includes:

Restless Legs Syndrome Diagnosis: Book Excerpts

Tests and diagnosis discussion for Restless Legs Syndrome:

There is no laboratory test that can make a diagnosis of RLS and, when someone with RLS goes to see a doctor, there is usually nothing abnormal the doctor can see or detect on examination. Diagnosis therefore depends on what a person describes to the doctor. To help make a diagnosis, the doctor may ask about all current and past medical problems, family history, and current medications. A complete physical and neurological exam may help identify other conditions that may be associated with RLS, such as nerve damage (neuropathy or a pinched nerve) or abnormalities in the blood vessels. Basic laboratory tests may be done to assess general health and to rule out anemia. Further studies depend on initial findings. (Source: excerpt from Restless Legs Syndrome: NWHIC)

Diagnosis of Restless Legs Syndrome: medical news summaries:

The following medical news items are relevant to diagnosis and misdiagnosis issues for Restless Legs Syndrome:

Diagnostic Tests for Restless Legs Syndrome: Online Medical Books

16 MEDICAL BOOKS ONLINE! Review excerpts from medical books online, free, without registration, for more information about diagnostis of Restless Legs Syndrome.


RESTLESS LEG SYNDROME: Ask the Following Questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is there a history of drug use? Many drugs, including barbiturates and benzodiazepines, may cause a restless leg syndrome.
  2. Are there abnormalities on neurologic examination? Various forms of peripheral neuropathy and multiple sclerosis may be associated with restless leg syndrome. Parkinson's disease may also be associated with the restless leg syndrome.
  3. Is there pallor? Various types of anemia may be associated with restless leg syndrome also.

DIAGNOSTIC WORKUP

Routine tests include a CBC, sedimentation rate, urinalysis, urine drug screen, chemistry panel, glucose tolerance test, and nerve conduction velocity studies. SSEP studies may be useful in detecting multiple sclerosis. Doppler studies may detect peripheral vascular disease. A pregnancy test should be done on a woman of child-bearing age. A therapeutic trial of a combination of dopa and carbidopa may be useful.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

ABDOMINAL PAIN, CHRONIC RECURRENT: Ask the following questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is there a family history of migraine or epilepsy? Migraine and epilepsy both present with abdominal pain.
  2. Is the pain colicky or persistent? Chronic colicky abdominal pain may be due to chronic cholecystitis, cholelithiasis, renal calculus, or partial intestinal obstruction.
  3. What is the location of the pain? If the pain is located in the upper abdomen, then one should consider peptic ulcer disease, pancreatitis, cholecystitis, and cholelithiasis. If the pain is located in the flanks, one should consider renal calculus and pyelonephritis. If the pain is located in the lower abdomen, one should consider diverticulitis, salpingitis, endometritis, and chronic appendicitis. Regional ileitis also may be located in the lower abdomen, particularly in the right lower quadrant.
  4. What is the relationship to meals? Abdominal pain relieved by food may be due to a peptic ulcer. Abdominal pain brought on by food may be due to abdominal angina. If the pain comes on 2 to 3 hr after a meal, it may be due to a peptic ulcer. On the other hand, pain that comes on 1 to 2 hr after meals, especially if it's a fatty meal, may be related to cholecystitis and cholelithiasis.
  5. Is there fever associated with the abdominal pain? Fever and abdominal pain may be due to pyelonephritis, diverticulitis, or appendicitis.
  6. Is there a history of chronic alcoholism? The history of chronic alcoholism suggests acute and chronic pancreatitis.
  7. Is there blood in the stool? The presence of blood in the stool would, of course, suggest peptic ulcer disease and diverticulitis.
  8. Is there an abdominal mass? The presence of an abdominal mass, particularly in the midepigastrium, suggests a pancreatic cyst related to chronic pancreatitis. A mass in the right lower quadrant might be related to regional ileitis or salpingitis. A mass in the left lower quadrant may be related to diverticulitis and salpingitis.

DIAGNOSTIC WORKUP

Routine laboratory tests include a CBC, sedimentation rate, urinalysis, urine culture, sensitivity, colony count, chemistry panel, serum amylase and lipase, pregnancy test, stool for occult blood, and stools for ovum and parasites. A chest x-ray, EKG, and flat plate of the abdomen should also be done. A urine porphobilinogen will help exclude porphyria.

If these tests are negative, then an upper gastrointestinal (GI) series, esophagogram, and gallbladder ultrasound would be done for upper abdominal pain; an IVP would be done for flank pain; and a barium enema and sigmoidoscopy would be performed for lower abdominal pain.

If these studies are inconclusive, a gastroenterologist should be consulted for endoscopic procedures. If there is upper abdominal pain, esophagoscopy, gastroscopy, and duodenoscopy would be performed. Endoscopic retrograde cholangiopancreatography (ERCP) may be required to diagnose cholangitis or common duct stones. If there is lower abdominal pain, colonoscopy would be performed. A CT scan of the abdomen and pelvis is a useful diagnostic tool also. Gallium scans may detect a diverticular abscess or other localized area of chronic inflammation. Pelvic ultrasound may be useful in lower abdominal pain, especially in females. Aortography and angiography will be useful in abdominal angina. Lymphangiography can be helpful in discovering retroperitoneal tumors. Ultimately, exploratory laparotomy may still be necessary in some cases.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

ABDOMINAL PAIN, ACUTE: Ask the following questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Where is the pain located? If it is diffuse, one should consider pancreatitis, mesenteric artery occlusion, or ruptured peptic ulcer. In addition, another viscus may be perforated, such as a ruptured ectopic, and there may be peritonitis. If it is focal, we need to know what quadrant it is in. For example, acute cholecystitis is in the right upper quadrant, whereas diverticulitis is usually in the left lower quadrant.
  2. What is the nature of the pain? Colicky abdominal pain suggests intestinal obstruction, renal calculus, and cholelithiasis or common duct stone, whereas constant pain is typical of pancreatitis, a ruptured peptic ulcer, appendicitis, diverticulitis, and a ruptured ectopic pregnancy.
  3. Does the pain radiate? The pain of acute cholecystitis typically radiates to the right scapular or right shoulder. The pain of a ruptured peptic ulcer may also radiate to the shoulder. The pain of acute renal calculus may radiate to the testicle.
  4. What are the associated signs and symptoms? Shock with generalized tenderness and rebound and diminished or absent bowel sounds should suggest a ruptured peptic ulcer or acute pancreatitis. However, acute right upper quadrant pain with nausea and vomiting should suggest acute cholecystitis. On the other hand, appendicitis is more insidious in onset and is associated with anorexia and nausea, rarely vomiting, as well as constipation. Renal colic presents with hematuria.
  5. Could this patient's abdominal pain be due to an extra-abdominal condition? Remember, lobar pneumonia, myocardial infarction, diabetic acidosis, and porphyria may be responsible for acute abdominal pain. There are numerous other conditions that need to be considered.

DIAGNOSTIC WORKUP

It is wise to consult a general surgeon at the outset. All patients with acute abdominal pain should have a stat, flat, and upright plate of the abdomen, a chest x-ray to rule out pneumonia, an electrocardiogram (EKG) to rule out myocardial infarction, and a complete blood count (CBC), urinalysis, amylase, and chemistry panel. Sometimes lateral decubitus films of the abdomen are necessary to show the step ladder pattern of intestinal obstruction. A pregnancy test is ordered when age and sex dictate it!

When these tests fail to confirm the clinical diagnosis, x-ray contrast studies or ultrasound may be necessary. For example, an intravenous pyelogram (IVP) can be done for a suspected renal calculus. Serial cardiac enzymes may confirm a myocardial infarction. Gallbladder ultrasound can be done to confirm cholecystitis and cholelithiasis. A nuclear scan of the gallbladder with iminodiacetic acid derivatives is very accurate in detecting acute cholecystitis. Ultrasonography may also help diagnose impending rupture of an abdominal aneurysm or ectopic pregnancy. A peritoneal tap may diagnose a ruptured ectopic pregnancy. Laparoscopy should also be considered. A urine porphobilinogen helps exclude porphyria. A double enema may help diagnose intestinal obstruction. A computed tomography (CT) scan of the abdomen is the next logical step.

If the diagnosis remains in doubt, an exploratory laparotomy must be done before the patient's condition deteriorates. The only case where this might be risky is acute pancreatitis. If this is suspected and the serum amylase is repeatedly normal, a quantitative urine amylase or peritoneal tap may confirm the diagnosis. Endoscopy may need to be done to diagnose a peptic ulcer, gastritis, gastric tumor, or reflux esophagitis. In obscure cases of appendicitis and diverticulitis, a contrast barium enema may help confirm the diagnosis. Angiography can diagnose an aneurysm or mesenteric infarction.

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

BACK PAIN: Ask the following questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is the pain of acute onset or gradual onset? If it is acute onset, one must consider the possibility of epidural abscess, pyelonephritis, or other abdominal conditions as the cause of the back pain. If it is gradual onset, one should consider that it may be a tumor, particularly of the spinal cord or cauda equina, a pelvic tumor, or an aortic aneurysm that is compressing one of the nerve roots. In addition, chronic conditions such as lumbar spondylosis, rheumatoid spondylitis, and prostatitis must be considered.
  2. Is there a history of trauma? If there is a history of trauma, one should consider a compression fracture of the spine, a sprain or herniated disk, as well as spondylolisthesis. Without a history of trauma, one should consider a tumor, herpes zoster, or dissecting aneurysm. Lumbar spondylosis might be silent for a while only to cause pain after a significant traumatic event.
  3. Is there radiation of the pain around the trunk or into the extremities? Radiation of the pain would certainly be more likely to signify a space-occupying lesion of the spinal column such as a tumor, an epidural abscess, or a herniated disk. If there is no radiation, one would consider osteoarthritis or lumbar spondylosis and rheumatoid spondylitis.
  4. Finally, are there bladder symptoms associated with the pain? If there are, then one must consider the possibility of a spinal cord tumor, cauda equina tumor, or kidney disease.

DIAGNOSTIC WORKUP

All patients with back pain need to have a CBC, urinalysis, and probably a urine culture, as well as a chemistry panel. A sedimentation rate should be done if rheumatoid arthritis is suspected. All patients should also have plain x-rays of the thoracic and/or lumbar spine. It is very important to get anterior posterior views, as well as oblique and lateral views. At this point it is wise to observe the results of conservative therapy before ordering expensive diagnostic tests. If there is doubt about the diagnosis at this point, a neurologic or orthopedic specialist may be consulted. If there is radiation of the pain into the extremities or around the trunk and definite neurologic findings, one should proceed to a CT scan or MRI immediately. The CT scan costs about half as much as the MRI and usually will show any significant herniated disks, primary or metastatic tumor. Even without radiation of pain into the extremities or definite neurologic findings, a patient with persistent back pain should have a CT scan or MRI. EMG will be useful in identifying radiculopathy.

When all these studies are negative, it might be wise to get a bone scan because this will show the increased uptake of the sacroiliac joints in rheumatoid spondylitis. Also, one should test for the HLA B27 antigen. In the event that all of the above studies are negative, the possibility of a non-neurologic condition or nonorthopedic condition causing the back pain should be considered. Perhaps abdominal ultrasound should be done to rule out an aortic aneurysm. Perhaps a pelvic tumor or prostatic tumor should be reconsidered. Perhaps there is a pancreatic tumor that is causing the back pain. Occasionally, combined myelography and CT scan is the only way to identify a lesion. Exploratory surgery is rarely necessary. Older patients should have a serum protein electrophoresis (for multiple myeloma) and acid phosphatase or PSA to rule out prostatic carcinoma.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

BREAST PAIN: Ask the following questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is it unilateral or bilateral? Unilateral breast pain should make one think of an infectious process or advanced carcinoma. Bilateral breast pain should make one think of pregnancy. This may be a normal pregnancy or an ectopic pregnancy.
  2. Is there an associated mass? A tender breast mass is most likely a mastitis or abscess, but advanced carcinoma can also produce a tender breast mass. If there are tender masses in both breasts, chronic cystic mastitis should be considered.
  3. Is there a discharge? A bloody discharge associated with a tender breast should make one think of a carcinoma.
  4. Is there fever? Fever associated with a tender breast or tender breast mass is most likely acute mastitis or abscess.

DIAGNOSTIC WORKUP

If there is a fever and discharge, a culture and sensitivity of the discharge should be done before beginning antibiotics. When there is a localized tender mass, referral to a general surgeon should be made. Patients with bilateral breast pain without any masses identified should have a pregnancy test. If this is negative and the pain is associated with the menstrual cycle, they should be treated as having premenstrual tension. A gynecologist may need to be consulted. If there is persistent bilateral breast pain in a young unmarried female, perhaps a psychiatrist should be consulted.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

CHEST PAIN: Ask the following questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is the chest pain acute or chronic? If it is acute, one must consider acute myocardial infarction, pulmonary embolism, pneumothorax, pericarditis, and fractures. If the chest pain is chronic, one must consider chronic coronary insufficiency, esophagitis, hiatal hernia, and various chest wall conditions.
  2. Is the pain constant or intermittent? Constant pain suggests acute myocardial infarction, pulmonary infarction, dissecting aneurysm, and pneumonia. Intermittent pain would suggest coronary insufficiency, Tietze's disease, and DaCosta's syndrome.
  3. Is there associated significant hypertension? Significant hypertension would make one think of dissecting aneurysm, but it is also found occasionally in acute myocardial infarction.
  4. Is the pain relieved by antacids? Relief by antacids should prompt one to consider esophagitis and hiatal hernia.
  5. Is the pain precipitated or increased by breathing? The pain of pleurisy, costochondritis, rib fractures, and pneumothorax is precipitated or increased by breathing.
  6. Is there associated hemoptysis? Hemoptysis should make one consider a pulmonary embolism.
  7. Is there fever and purulent sputum? Fever and purulent sputum should make one consider pneumonia.
  8. Is there dyspnea? Dyspnea should make one consider pneumothorax, pulmonary embolism, and pneumonia, as well as congestive heart failure secondary to acute myocardial infarction.
  9. Is it aggravated by movement? Aggravation of the chest pain by movement should suggest pericarditis. Remember, myocardial infarctions may also have extension into the pericardium and must be considered at times.
  10. Is it relieved by nitroglycerin? Relief by nitroglycerin should suggest a coronary insufficiency, but esophagospasm may be relieved by nitroglycerin also.

DIAGNOSTIC WORKUP

All patients should have a CBC, sedimentation rate, chemistry panel, VDRL test, chest x-ray, and EKG. If there is sputum, a smear and culture should be done as soon as possible.

If a myocardial infarction is suspected, then serial EKGs and tests for the isoenzyme of creatine kinase (CK-MB) should be done if the initial EKG and enzymes do not show any significant changes. Serum cardiac troponin levels may also be diagnostic of a myocardial infarct. Thallium-201 scintigraphy is useful in diagnosing both myocardial infarction and coronary insufficiency. Exercise tolerance tests may help diagnose coronary insufficiency. Immediate coronary angiography should be undertaken if the condition deteriorates. This can be followed by immediate balloon angioplasty, reperfusion therapy, or bypass surgery.

If a pulmonary embolism is suspected, arterial blood gases and a ventilation-perfusion scan should be done. d -dimer testing of whole blood is a sensitive test of pulmonary embolus. Pulmonary angiography may need to be done if these are negative and pulmonary embolism is still strongly suspected.

If esophageal disease is suspected, an upper GI series with esophagogram should be done; this can be followed with esophagoscopy and gastroscopy if needed. A Bernstein test (acid perfusion of the esophagus) may reproduce the exact pain and distinguish esophageal reflux from a cardiac source of the pain. Ambulatory pH monitoring may also diagnose reflux esophagitis.

If pericarditis is suspected, echocardiography and possibly a CT scan of the chest and pericardium may be necessary. Coronary angiography may be necessary to diagnose coronary insufficiency. Echocardiography is also helpful in diagnosing mitral valve prolapse and the various myocardiopathies. Twenty-four-hr Holter monitoring is useful in diagnosing many causes of intermittent chest pain.

Referral to a cardiologist or pulmonologist may be appropriate at any point in this workup. Dissecting aneurysm may be confirmed by a CT scan or MRI of the chest.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

EXTREMITY PAIN, LOWER EXTREMITY: Ask the following questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is the extremity pain of acute or gradual onset? Acute onset would suggest arterial embolism, deep vein thrombophlebitis, and cellulitis. If there is a history of trauma, it would suggest a fracture, sprain, or torn ligament.
  2. Is there limitation of motion of the joints? A positive Patrick's test would indicate hip pathology, including greater trochanter bursitis. A positive McMurray test would indicate a torn meniscus.
  3. Are there positive neurologic findings? A positive femoral stretch test would suggest a herniated disk at L2-3 or L3-4, whereas a positive Lasègue's sign would indicate a herniated disk at L4-5 or L5 to S1. Combined motor and sensory deficits may indicate radiculopathy or neuropathy.
  4. Is there a positive Homans' sign? This is a very important examination, as one would not want to miss a deep vein thrombophlebitis.
  5. Is there diminished or absent peripheral pulses? Diminished or absent pulses would suggest arterial embolism, peripheral arteriosclerosis, or Leriche's syndrome (thrombosis of the terminal aorta).
  6. Is there focal tenderness, swelling, or erythema of the extremity? This would suggest cellulitis, superficial thrombophlebitis, osteomyelitis, lymphangitis, and other types of infections. Tenderness without significant swelling or erythema would be suggestive of bursitis or deep vein thrombophlebitis.

DIAGNOSTIC WORKUP

Often bursitis and myofascitis can be diagnosed by the dramatic relief obtained from a lidocaine injection. If there is clear-cut joint pathology, an x-ray of the joints, arthritis profile, and synovial fluid analysis will usually provide a diagnosis. MRI is useful in the diagnosis of a torn meniscus. If a deep-pain thrombophlebitis is suspected, venous Doppler ultrasound, impedance plethysmography, or a contrast venogram may be done. If an arterial embolism or chronic peripheral arterial disease is suspected, femoral angiography can be done. If a herniated disk or other pathology of the lumbar spine is suspected, plain films of the lumbar spine should be obtained. It might be wise at this point also to obtain a CBC, sedimentation rate, and chemistry panel to determine the alkaline phosphatase, calcium, and phosphorus. In older males, tests for acid phosphatase and PSA should be done.

If these tests are unrevealing, it is wise to refer the patient to a neurologic specialist before any more expensive tests are ordered. He will probably order a CT scan of the lumbar spine and may do nerve conduction velocity studies, EMG examinations, or dermatomal SSEP studies as indicated. In difficult neurologic problems, a combined myelography and CT scan is preferred over MRI. Bone scans will help diagnose obscure fractures and osteomyelitis, both of the lumbar spine and the lower extremities.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

EXTREMITY PAIN, UPPER EXTREMITY: Ask the following questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is there limitation of motion of the joints? Limitation of motion of a joint would suggest not only various types of arthritis, fracture, or torn ligaments, but also inflammation of surrounding structures such as the bursa or tendons. For example, limitation of motion of the shoulder would suggest impingement syndrome, frozen shoulder, rheumatoid or osteoarthritis, subacromial bursitis, and a torn rotator cuff.
  2. Is the limitation of motion both active and passive or active only? If the limitation of motion is only active, one should suspect tendinitis or bursitis. If the limitation of motion is both active and passive, one should suspect the various forms of arthritis, as well as bone tumors, osteomyelitis, and adhesive capsulitis.
  3. Is there weakness or paresthesia? Weakness and especially paresthesia suggest a neurologic origin for the pain, and one should be considering brachial plexus neuritis, carpal tunnel syndrome, ulnar entrapment, and radiculopathy.
  4. Are there vasomotor or trophic changes? Vasomotor changes would suggest Raynaud's phenomena and sympathetic dystrophy. Trophic changes along with vasomotor changes would suggest a peripheral neuropathy also.
  5. Are there positive neurologic signs in the lower extremities? Diffuse hypoactive reflexes with stocking deficits in the lower extremities would suggest a peripheral neuropathy, whereas hyperactive reflexes in the lower extremities would suggest a cervical cord tumor, cervical spondylosis, or multiple sclerosis.
  6. Is there a positive Tinel's sign at the wrist or elbow? Tinel's sign at the wrist would suggest carpal tunnel syndrome, whereas Tinel's sign at the elbow would suggest ulnar entrapment if it is over the ulnar nerve or pronator syndrome if it is over the median nerve.
  7. Are Adson's tests positive? Adson's tests are positive in thoracic outlet syndrome, whether it is due to a cervical rib, scalenus-anticus syndrome, Wright syndrome (pectoralis minor syndrome), or a costoclavicular compression.

DIAGNOSTIC WORKUP

X-rays of the affected joints need to be done if there is tenderness or limitation of motion. Further workup of joint pain can be found on page 279 . When there are abnormal neurologic findings, an x-ray of the cervical spine, nerve conduction velocity studies, and EMG examinations need to be done. Referral to a neurologist should be made for these tests. If there is a typical radicular pain and a herniated cervical disk is strongly suspected, MRI of the cervical spine should be done. This is an expensive test, but when there are obvious signs of radiculopathy, it is worthwhile. Perhaps dermatomal somatosensory studies should be done when there is confusion about whether a herniated disk is pathologic. If a vascular lesion is suspected, angiography and venography should be ordered. ANA and nail fold capillary loop dilation and dropout study may diagnose Raynaud's phenomena; a small injection of lidocaine and steroids locally may be diagnostic in cases of carpal tunnel syndrome.

When there is intermittent pain, an exercise tolerance test should be done to exclude coronary insufficiency. A stellate ganglion block may be helpful in diagnosing reflex sympathetic dystrophy. Remember that other nerve blocks may be done and one should not hesitate to call an anesthesiologist for help in this area. Various forms of bursitis may be diagnosed by a therapeutic trial of lidocaine and corticosteroid injections.

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

EYE PAIN: Ask the following questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is there redness of the eye? Redness of the eye suggests definite eye pathology. Without redness, one should suspect disease in the adjacent structures or retrobulbar neuritis.
  2. If there is redness, is there periorbital edema as well? Periorbital edema should suggest a cavernous sinus thrombosis or herpes zoster.
  3. If there is periorbital edema, is there a rash? A rash, particularly vesicular rash, would suggest herpes zoster.
  4. In cases without redness of the eye, is there any abnormality on examination both with the naked eye and with the ophthalmoscope? A dilated pupil would certainly suggest glaucoma; ophthalmoscopic examination may show optic neuritis or retinal detachment. A visual field examination may detect optic neuritis, retrobulbar neuritis, and retinal artery occlusion. A visual acuity check may pick up a refractive error.
  5. Finally, is there headache associated with the eye pain? This would be suggestive of migraine or cluster headache.

DIAGNOSTIC WORKUP

The primary care specialist may want to treat cases of obvious conjunctivitis without a culture and sensitivity. However, a smear and culture is useful especially if Neisseria is suspected. A smear may also reveal eosinophils suggesting allergic conjunctivitis. The primary care specialist may also use fluorescein dye to diagnose a foreign body. Most primary care physicians feel competent to use tonometry to diagnose glaucoma and may feel competent to use a slit lamp. However, when there is any doubt about the diagnosis, the most cost-effective approach is to refer the patient to an ophthalmologist.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

FACE PAIN: Ask the following questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is the pain constant or intermittent? Intermittent pain would suggest trigeminal neuralgia, cluster headaches, or atypical migraine. Constant pain would suggest any local abnormalities in the structures underlying the face such as an abscessed sinus, an abscessed tooth, or a neoplasm in these areas.
  2. Is the pain increased by chewing? Pain that is increased by chewing very often may be related to the temporomandibular joint syndrome, but it could be related to trigeminal neuralgia or dental caries.
  3. Is there an associated nasal discharge? An associated bloody nasal discharge would make one think of a nasopharyngeal carcinoma, but a purulent discharge would make one think of acute or chronic sinusitis. A watery nasal discharge often accompanies cluster headaches or atypical migraine.
  4. Are there abnormal neurologic findings? Face pain sometimes accompanies multiple sclerosis, acute Wallenberg's syndrome, and advanced acoustic neuromas. The pain in the trigeminal distribution associated with multiple sclerosis often is intermittent and suggests trigeminal neuralgia.

DIAGNOSTIC WORKUP

The first thing to determine is whether there is an infectious or neoplastic process in the structures underlying the face. X-rays of the sinuses and teeth and CT scans of the sinuses and brain may be necessary to further elucidate this. An x-ray of the temporomandibular joint may be helpful. An MRI of the temporomandibular joint is the procedure of choice to rule out pathology of this joint. Referral to a dentist to evaluate the patient's teeth or to an ear, nose, and throat specialist to evaluate sinusitis may be necessary.

To rule out cluster headaches or atypical migraine, a histamine test may be done. It may be wise to see the patient during an attack so that superficial temporal artery compression can be done to rule out migraine and/or a shot of sumatriptan succinate can be given, which should provide immediate results in cluster headache and atypical migraine.

A trial of carbamazepine (Tegretol®) can be given in cases of suspected trigeminal neuralgia, but referral to a neurosurgeon for an alcoholic injection of the maxillary or mandibular branches of trigeminal nerve will more likely make the diagnosis and solve the patient's problem.

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

FLANK PAIN: Ask the Following Questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is there associated fever? The presence of fever along with chest pain should make one think of a perinephric abscess or pyelonephritis. Occasionally, however, hypernephroma can cause fever and flank pain, as can bilateral hydronephrosis.
  2. Is there a flank mass? The presence of flank pain along with a flank mass should make one think of a hypernephroma, hydronephrosis, polycystic kidneys, or perinephric abscess.
  3. Is there hematuria? The presence of pain and hematuria should make one think of renal calculus first, but the possibility of a renal infarction, polycystic kidneys, and tuberculosis of the kidneys must be considered also. Hematuria is also found in a hypernephroma.

DIAGNOSTIC WORKUP

Routine tests include a CBC, sedimentation rate, chemistry panel, urinalysis, and urine culture. An intravenous pyelogram is the next logical step. If these fail to make a definitive diagnosis, one should consider ordering an abdominal ultrasound or a CT scan of the abdomen. If a renal infarction is suspected, aortography and renal angiography may be ordered. When the above tests are all negative, one should consider x-rays of the lumbosacral spine and MRI of the thoracic and lumbar spine. Consulting a urologist is prudent before ordering expensive diagnostic tests.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

HEEL PAIN: Ask the Following Questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Are there abnormalities on inspection of the heel? Inspection of the heel may disclose an ulcer, foreign body, cellulitis, plantar wart, and other disorders.
  2. Is the patient a child? Children often have Sever's disease (osteochondritis of the heel).
  3. Is there tenderness or deformity of the Achilles tendon? Tenderness or deformity of the Achilles tendon should suggest Achilles tendinitis, rupture, or bursitis.
  4. Are there abnormalities on x-ray examination? An x-ray may disclose a calcaneal fracture, osteomyelitis, a tumor, or calcaneal spur. If the x-ray is negative, plantar fasciitis is the most likely diagnosis, but one should also consider gout.

DIAGNOSTIC WORKUP

In addition to a plain x-ray of the foot, a CBC, sedimentation rate, chemistry panel, and arthritis panel should be done. A bone scan may disclose an occult fracture. Response to a trigger point injection should be evaluated. If the diagnosis is still in doubt, referral to an orthopedic surgeon or podiatrist should be made before ordering expensive diagnostic tests such as a CT scan or MRI.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

HIP PAIN: Ask the Following Questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is there a positive straight-leg raising test or other neurologic signs? The presence of positive straight-leg raising tests or other neurologic signs would suggest a herniated disk, a cauda equina tumor, or other neurologic disorders of the lumbar spine. Meralgia paresthetica will cause characteristic loss of sensation in the distribution of the lateral femoral cutaneous nerve.
  2. Is there a positive Patrick's test or limitation of the range of motion of the hip? These findings suggest a greater trochanter bursitis or hip joint pathology such as fracture, osteoarthritis, rheumatoid arthritis, metastasis, slipped femoral epiphysis, Legg-Perthes disease, rheumatic fever, or transient synovitis.
  3. Is there tenderness of the greater trochanter bursa? Tenderness of the greater trochanter bursa will help differentiate greater trochanter bursitis. It is also seen in hysteria.
  4. Is the patient a child or an adult? If the patient is a child, transient synovitis, slipped femoral epiphysis, Legg-Perthes disease, and rheumatic fever should be considered. If the patient is an adult, it is more likely that the problem is osteoarthritis, a fracture, rheumatoid arthritis, metastasis, or avascular necrosis.
  5. Is there a history of trauma? A history of trauma would suggest that there is a fracture or a sprain of the hip joint, but the clinician should remember that a fracture in the elderly often occurs with no history of trauma.

DIAGNOSTIC WORKUP

A CBC, sedimentation rate, chemistry panel, arthritis panel, tuberculin test, and x-rays of the lumbosacral spine and hip will diagnose 90% of the cases. These are relatively expensive in comparison to MRI. A bone scan may be necessary to diagnose occult fractures. A serum protein electrophoresis will help diagnose multiple myeloma. A trigger point injection of the greater trochanter bursa or ischiogluteal bursa will assist in the diagnosis of these conditions. An orthopedic surgeon should be consulted before ordering MRI of the lumbar spine or hip. However, MRI is especially important if the diagnosis of avascular necrosis is suspected.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

JAW PAIN: Ask the Following Questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Are there abnormalities on examination of the teeth or gums? A thorough examination of the teeth and gums may disclose dental caries, gingivitis, oral tumors, or alveolar abscess.
  2. Is the pain intermittent? Intermittent pain should suggest a trigeminal neuralgia or glossopharyngeal neuralgia.
  3. Is there a rash? The presence of a rash would suggest herpes zoster. Be sure to examine the eardrum for Ramsay Hunt's syndrome.

DIAGNOSTIC WORKUP

Routine diagnostic studies include a CBC, sedimentation rate, chemistry panel, arthritis panel, and an x-ray of the teeth and jaw. X-ray of the sinuses may be helpful. At this point referral to a dentist or oral surgeon should be made if there is still diagnostic difficulty. He may order an MRI of the temporomandibular joint, which is the procedure of choice in evaluating this joint. If all tests are negative or equivocal, perhaps a psychiatric referral is in order.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

JOINT PAIN: Ask the Following Questions:
(Algorithmic Diagnosis of Symptoms and Signs)

  1. Is the joint pain localized to a single joint? Localization to a single joint should suggest a septic arthritis, gout, tuberculosis, hemophilia, sickle cell disease, trauma, avascular necrosis, and pseudogout.
  2. Is there fever? The presence of fever should make one think of septic arthritis, rheumatic fever, gonococcal arthritis, Reiter's syndrome, lupus erythematosus, Lyme arthritis, polymyalgia rheumatica, Still's disease, and rheumatoid arthritis.
  3. Is there a urethral discharge? The presence of a urethral discharge should make one think of Reiter's syndrome or gonococcal arthritis.
  4. Is there low back pain? The presence of low back pain should suggest rheumatoid spondylitis, ochronosis, and gout.
  5. Is the arthritis migratory? The presence of migratory arthritis should make one think of rheumatic fever and rat-bite fever.
  6. What is the age of the patient? Younger patients may have sickle cell disease, hemophilia, trauma, rheumatic fever, Still's disease, and gonococcal arthritis. Older patients are more likely to have osteoarthritis, polymyalgia rheumatica, and gout. It should be noted that there is considerable overlap here.

DIAGNOSTIC WORKUP

Routine studies include a CBC, sedimentation rate, ASO titer, ANA, cross-reacting protein (CRP), urinalysis, chemistry panel, arthritis panel, and x-rays of the involved joints. It is also wise at times to order a bone survey. Synovial fluid analysis and culture should be done if there is sufficient joint effusion. A trial of therapy may be initiated at this point and will assist in the diagnosis. For example, a course of colchicine may be given to rule out gout.

If there is still doubt, a rheumatology consultation should be made. Other tests that may be done include a gonococcal antibody titer and a coagulation profile. If there is a urethral discharge, a smear and culture of the material should be made. If there is fever, febrile agglutinins, serologic tests for Lyme disease, brucellin antibody titer, blood cultures, and a Monospot test may be done. If collagen disease is suspected, antinuclear antibodies and anti-DNA antibodies may be sought. If sickle cell anemia is suspected, a sickle cell preparation should be done. A bone scan will help diagnose rheumatoid spondylitis and ochronosis. A urine for homogentisic acid will diagnose ochronosis also. An MRI may diagnose a torn meniscus and other condition.

 

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Source: Algorithmic Diagnosis of Symptoms and Signs, 2003

Restless Legs: Differential Diagnosis
(In a Page: Signs and Symptoms)

  • Normal snoring with periodic limb movements
  • Nocturnal leg cramps
    –Associated with painful, crampy calves
  • Chronic insomnia
  • Sleep disturbance due to medication/drugs
    –Commonly associated with decongestants, steroids, caffeine, and β-blockers
    –May be due to withdrawal from tobacco, alcohol, or illicit drugs
    –Akathisia (e.g., neuroleptics, dopamine antagonists, drug withdrawal)
    • Restless legs syndrome
      –Feelings of creeping, crawling, burning, pulling, itching, tugging, and discomfort in the legs are relieved by involuntary leg movement
      –Most patients are >50 years old
      –Often unilateral
      –Positive family history in 1/3 of cases
      –Symptoms are exacerbated by pregnancy, end-stage renal failure (dialysis increases restless legs activity; kidney transplant improves symptoms), and some medications (e.g., lithium antidepressants, dopamine antagonists)
    • Peripheral neuropathy
      –Associated with numbness, tingling, and pain
      –Leg pain not relieved by movement
      –Consider diabetes and deficiencies of vitamin B12 and folate
    • Peripheral vascular disease
    • Deep venous thrombosis, venous stasis
    • Delayed deep sleep syndrome
    • Hyperthyroidism
    • Sleep deprivation
    • Sleep anxiety
    • Spinal cord/vertebral disc disease
    • Extrapyramidal symptoms due to medications (e.g., dystonic reaction, pseudoparkinsonism, neuroleptic malignant syndrome from antipsychotics)

    Workup and Diagnosis

    • History and physical examination
      –Restless legs is one of the most common causes of insomnia
      –Inquire about sleep patterns and sleep history from patient and bed partner
      –Determine whether pain is relieved by movement
      –Include complete medication history (e.g., tricyclic antidepressants are often prescribed for insomnia, but tend to worsen restless legs)
    • Initial labs may include CBC, iron studies, fasting glucose, BUN/creatinine, electrolytes, calcium, magnesium, TSH, vitamin B12, and pregnancy test
      –If anemic, a workup for blood loss is indicated (e.g., colon and upper GI evaluation, urinalysis for hematuria, consider endometrial biopsy in older women)
  • Sleep study to define sleep pathology

» READ BOOK EXCERPT ONLINE »

Source: In a Page: Signs and Symptoms, 2004

Low Back Pain/Swelling: Differential Diagnosis
(In a Page: Signs and Symptoms)

  • Lumbosacral muscle strain
    –Most common etiology of low back pain
    –Most common cause of disability in adults <45 years old
    –Aggravated by movement, better with rest
  • Lumbar disc herniation
    –Especially of L4-L5 and L5-S1
    –Usually with unilateral radiation down the leg in a dermatomal pattern
    –Increased pain with sitting
    • Spinal stenosis
      –Back and bilateral buttock and thigh pain in older patients relieved by rest (pseudoclaudication)
      –Increased pain with standing
    • Sacral-iliac joint dysfunction
      –Especially in young, thin women or in pregnancy
      –Unilateral upper buttock pain, relieved with movement
    • Vertebral fracture
      –Often associated with trauma or osteoporosis
    • Spondylolisthesis
      –Especially in young athletes
    • Secondary gain (e.g., drug seeking, disability or liability issue)
    • Extraspinal causes (e.g., radiation from kidney stones)
    • Systemic causes (<1%)
      –Inflammation (e.g., ankylosing spondylitis): Morning stiffness, limited mobility
      –Infection: Osteomyelitis, abscess
      –Abdominal aortic aneurysm
      –Cancer (especially metastases from prostate, lung, colon, and breast or myeloma); constant, worsening pain, wakes up from sleep
      –Cauda equina syndrome
      –Paget's disease

    Workup and Diagnosis

    • History and physical are the most important diagnostic tools
      –Evaluate for range of motion, sensation, strength, straight leg raise test, reflexes, and neurovascular status
    • Imaging studies (e.g., X-ray, MRI, CT scan, myelogram, discogram) are indicated if “red flags” are present, if pain or limited function is refractory to treatment, or if trauma has occurred
    • Evaluate for “red flags” that may indicate serious conditions—if present, further workup is necessary (e.g., lumbosacral X-ray, CBC, ESR, calcium, electrolytes, alkaline phosphatase, bone scan, metastatic workup)
      –Red flags that suggest fracture: Major trauma, minor trauma, or strenuous lifting in an older or osteoporotic patient
      –Red flags that suggest tumor or infection: Age >50 or <20, history of cancer, constitutional symptoms (weight loss, fever), IV drug use, immunosuppression, pain worse at night
      –Red flags that suggest cauda equina syndrome: Saddle anesthesia, recent onset of incontinence, severe or progressive neurological deficit in leg
    • If red flags are absent, no imaging is necessary for 4–6 weeks; if pain persists, an MRI is the most useful study
    '>>'>

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Source: In a Page: Signs and Symptoms, 2004

Abdominal Pain in Lower Quadrants: Differential Diagnosis
(In a Page: Signs and Symptoms)

Right lower quadrant

  • Appendicitis
  • Diverticulitis
  • Salpingitis/Pelvic inflammatory disease
  • Endometritis
  • Endometriosis
  • Ectopic pregnancy
  • Hemorrhage or rupture of ovarian cyst
  • Renal calculus
  • Intussusception
    Pelvic/hypogastric region
  • Cystitis
  • Salpingitis/Pelvic inflammatory disease
  • Ectopic pregnancy
  • Diverticulitis
  • Strangulated hernia
  • Endometriosis
  • Appendicitis
  • Ovarian cyst
  • Ovarian torsion
  • Testicular torsion
  • Bladder distension
  • Nephrolithiasis
  • Prostatitis
  • Malignancy
  • Abdominal aortic aneurysm
    Left lower quadrant
  • Diverticulitis
  • Intestinal obstruction
  • Colitis
  • Strangulated hernia
  • Inflammatory bowel disease
  • Gastroenteritis
  • Pyelonephritis
  • Nephrolithiasis
  • Mesenteric lymphadenitis or thrombosis
  • Aortic aneurysm
  • Volvulus
  • Salpingitis/Pelvic inflammatory disease

Workup and Diagnosis

  • Complete history and examination
    –Note progression of symptoms (duration, rapidity of onset, intensity), associated complaints (e.g., anorexia, diarrhea, fever), urinary complaints, exposure to illness and medication, and past medical history including prior episodes
    –Note body positioning that tends to relieve pain; signs of dehydration or fever
    –Vitals and full pulmonary, cardiac, abdominal, back, pelvic, and rectal examinations
    –Abdominal examination should include bowel sounds, distension, tympany, tenderness, palpation for masses and organomegaly, rebound tenderness, and guarding
  • Initial evaluation includes CBC with differential cell counts, electrolytes, BUN/creatinine, glucose, calcium, urinalysis, urine culture, and β-hCG level
  • Abdominal/pelvic ultrasound and/or CT, obstructive series, and KUB may be indicated
  • Consider endocervical gonorrhea/chlamydia cultures in sexually active females, laparoscopy, barium enema, intravenous pyelogram, stool cultures, and/or fecal fat

» READ BOOK EXCERPT ONLINE »

Source: In a Page: Signs and Symptoms, 2004

Abdominal Pain in Upper Quadrants: Differential Diagnosis
(In a Page: Signs and Symptoms)

Right upper quadrant pain

  • Cholecystitis
  • Fatty liver or NASH
  • Congested liver (e.g., secondary to heart failure)
  • Cholangitis
  • Hepatitis
  • Gastritis or pancreatitis (see below)
  • Pneumonia
  • Fitz-Hugh-Curtis syndrome (gonococcal perihepatitis secondary to pelvic inflammatory disease)

  • Epigastric pain
  • Gastritis
  • PUD
  • Pancreatitis
  • Gastroenteritis
  • Intestinal obstruction
  • Myocardial infarction
  • Aortic aneurysm
    Left upper quadrant pain
  • Peptic ulcer disease
  • Gastritis
  • GERD
  • Splenic infarct
  • Pulmonary embolism
  • Pancreatitis
  • Acute splenomegaly (e.g., mononucleosis)
  • Left lower lobe pneumonia
    Nonfocal pain
  • Herpes
  • Sickle cell crisis
  • Irritable bowel
  • Mesenteric ischemia
  • Peritonitis
  • Pleurisy
  • Uremia
  • Lead poisoning
  • Porphyria
  • Toxin ingestion

Workup and Diagnosis

  • History of associated symptoms; relation of pain to eating; anorexia; alcohol use; and location, quality, and intensity of pain
  • Physical exam should focus on heart, lungs, abdomen, and back examinations
  • Initial laboratory tests may include CBC with differential, electrolytes, urinalysis, BUN/creatinine, liver function tests, LDH, amylase/lipase, magnesium, and PT/PTT/INR
  • Chest and abdominal X-rays
  • Abdominal ultrasound and/or CT scan
  • Hepatitis viral serology
  • Percutaneous transhepatic cholangiography (PTCA) and/or ERCP
  • Upper GI endoscopy (EGD) or upper GI series with barium swallow
  • Cultures of blood, urine, and trachea/gastric aspirates
  • Evaluation of possible cardiac and pulmonary etiologies may require ECG (pulmonary embolus may show S in I, Q in III, inverted T in III), cardiac isoenzymes, pleural tap, echocardiogram, and stress test

» READ BOOK EXCERPT ONLINE »

Source: In a Page: Signs and Symptoms, 2004

Abdominal Pain with Rebound Tenderness: Differential Diagnosis
(In a Page: Signs and Symptoms)

  • Appendicitis is the most common etiology
  • Cholecystitis
  • Diverticulitis
  • Gastroenteritis
  • Pancreatitis
  • Perforated duodenal ulcer
  • Gastritis
  • Biliary or renal colic
  • Mesenteric ischemia
  • Ruptured abdominal aortic aneurysm
  • Bowel obstruction
  • Bacterial peritonitis
  • Intra-abdominal or pelvic abscess
  • Colitis
  • Urinary tract infection or pyelonephritis
  • Perforated viscus
  • Sickle cell crisis
  • Gynecologic etiologies
    –Pelvic inflammatory disease
    –Tubo-ovarian abscess
    –Ruptured ectopic pregnancy
    –Ovarian cyst rupture or torsion
  • Intussusception
  • Nonabdominal causes of pain that mimic an acute abdomen are numerous and may include myocardial infarction, atypical angina, pericarditis, pneumonia, pulmonary embolus, and pelvic pathology (e.g., pelvic inflammatory disease, ovarian torsion)

Workup and Diagnosis

  • Distinguish etiologies requiring emergent or urgent surgical intervention (e.g., ruptured aortic aneurysm, perforated viscus, appendicitis, intestinal obstruction, ischemic bowel, ruptured ectopic pregnancy) from non-emergent causes
  • History and physical examination
    –Nature of pain, location, onset, duration, intensity, similarity to past episodes, aggravating and alleviating factors, guarding, bowel sounds, distension, presence of a mass, blood on rectal exam, and cervical or adnexal tenderness
    –In general, patients who present with extremely severe pain of immediate onset require surgical intervention
    –Crampy, colicky pain that occurs in waves implies distension of a hollow viscus (e.g., renal colic, intestinal obstruction)
    –Constant, localized pain implies inflammation (e.g., appendicitis, diverticulitis, cholecystitis)
    –Hypotension and shock may be present
  • Initial tests include CBC, electrolytes, BUN/creatinine, LFTs, amylase/lipase, urinalysis, and pregnancy test
  • Plain abdominal X-rays may reveal obstruction, perforation (free air), or other pathology
  • Ultrasound is a quick, inexpensive test for biliary tract disease, AAA, ectopic pregnancy, or peritoneal fluid
  • Abdominal CT will often establish the diagnosis for appendicitis, aortic aneurysm, and diverticulitis
  • Diagnostic peritoneal lavage may be indicated in cases of suspected trauma, bowel perforation, or peritonitis

» READ BOOK EXCERPT ONLINE »

Source: In a Page: Signs and Symptoms, 2004

Breast Pain & Discharge: Differential Diagnosis
(In a Page: Signs and Symptoms)

Breast pain

  • Fibrocystic change
    –Most common benign breast condition
    –Clinically present in 50% and histologically in 90% of women
  • Mastitis
    –Associated with lactation
  • Extramammary causes of pain (e.g., cervical radiculitis, costochondritis, herpes zoster, angina)
  • Breast cancer
    –Occurs in 1/9 women (lifetime risk)
  • Cyst
  • Breast abscess
  • Unilateral or bilateral gynecomastia
  • Phylloides tumor
  • Intraductal papilloma
  • Fat necrosis
  • Trauma
  • Fibroadenoma
  • Lipoma
  • Pregnancy
    Breast discharge
  • Duct ectasia
  • Galactorrhea
  • Mondor's disease
  • Chronic nipple stimulation
  • Pregnancy
  • Hypothyroidism
  • Sarcoidosis
  • Systemic lupus erythematosus
  • Cirrhosis or other hepatic disease
  • Breast cancer
    –Occurs in 1/9 women (lifetime risk)
  • Intraductal papilloma
  • Fibrocystic change
  • Medications (e.g., phenothiazines, metoclopramide, tricyclic antidepressants, reserpine, opiates, cimetidine, androgens)
  • Hypothalamic and pituitary abnormalities (e.g., prolactinoma, acromegaly, empty sella syndrome)
  • Pseudocyesis

Workup and Diagnosis

  • History includes past medical history, duration and pattern of pain and/or discharge, family history of breast or gynecologic cancer, and menstrual/pregnancy history
  • Breast exam 7–9 days after menstrual flow
    –Fibrocystic areas: Slightly irregular, mobile, bilateral, upper outer quadrant; compression causes tenderness
    –Breast cancer: Solitary, irregular, or stellate; hard, nontender, fixed; not clearly delineated from surrounding tissue, ± lymphadenopathy
    –Mastitis: Inflamed, edematous, erythematous, indurated, tender areas, axillary lymphadenopathy
    –Nipple discharge: Bloody or serosanguinous discharge is suspicious for cancer; oral contraceptives, estrogens, or elevated prolactin levels may result in clear, serous, or milky discharge
  • Diagnostic mammogram is indicated in patients >30 years old who present with solitary or dominant mass or asymmetric thickening
    –Compare with prior mammograms if possible
  • Ultrasound is used to distinguish solid versus cystic
  • Fine-needle aspiration, breast biopsy, cytologic exam of discharge, ductogram and/or galactogram may be indicated
  • Endocrine evaluation may include prolactin levels, TSH, FSH, and LH

» READ BOOK EXCERPT ONLINE »

Source: In a Page: Signs and Symptoms, 2004

Elbow Pain/Swelling: Differential Diagnosis
(In a Page: Signs and Symptoms)

  • Trauma
    • Fracture
      –Radial head fracture is most common: Usually due to a fall on an outstretched arm, resulting in pain with supination
      –Olecranon fracture: Pain with extension
      –Distal humerus fractures are less common
    • Dislocation
      –Nursemaid's elbow (subluxation of the radial head) occurs in young children who were pulled by an outstretched arm; children will refuse to move the arm
      –In adults, dislocations generally occur secondary to falling on an outstretched arm; 80% are associated with an olecranon fracture
    • Bursitis: Due to trauma, inflammation, infection
    • Epicondylitis
      –Degeneration of the tendinous insertion at the lateral or medial epicondyles
      –Lateral epicondylitis (“tennis elbow”): Due to extensor muscle overuse (results in pain with pronation and wrist dorsiflexion)
      –Medial epicondylitis (“golfer's elbow”): Due to flexor muscle overuse (results in decreased grip strength and pain with pronation or wrist flexion)
    • Ulnar nerve entrapment
      –Usually in the groove of the posterior aspect of the medial epicondyle
      –Occurs acutely after direct trauma or with prolonged pressure or overuse
      –Causes acute medial aching with numbness and tingling in fourth and fifth digits
  • Osteoarthritis
  • Rheumatoid arthritis
  • Gouty arthritis
  • Infection
  • Distal biceps tendon rupture
    • Pronator syndrome
      –Median nerve entrapment distal to elbow
      from racquet or throwing sports
      –Anterior pain and distal paresthesias
      –Pain with resisted pronation
    • Radial tunnel syndrome
      –Compression of the radial nerve as it crosses the head of the radius
  • Loose body (e.g., bone fragment)
  • Workup and Diagnosis

    • History and physical examination
      –Include careful exam of the hand, wrist, elbow, and shoulder of the affected side
      –Evaluate for pain, paresthesias, bony point tenderness, crepitus on palpation, swelling and ecchymosis, limited range of motion, and neurovascular compromise (e.g., coolness, pallor, loss of distal pulses)
  • Standard X-rays include A/P, lateral, and oblique views
  • Aspiration may be diagnostic as well as therapeutic for bursitis; send for cultures and crystals
  • Occasionally, nerve conduction tests are indicated to evaluate nerve entrapment and/or carpal tunnel syndrome
  • Rarely, an MRI is indicated; may be considered if the treatment is not progressing as planned
  • » READ BOOK EXCERPT ONLINE »

    Source: In a Page: Signs and Symptoms, 2004

    Flank Pain/CVA Tenderness: Differential Diagnosis
    (In a Page: Signs and Symptoms)

    • Degenerative disk disease and/or disk herniation is the most frequent cause of pain
    • Muscle spasm or cramping
    • Trauma
    • Nephrolithiasis/urolithiasis (renal or ureteral calculi or stones) is the most common urinary tract etiology
    • Pyelonephritis (acute or chronic)
      E. coli is the most common cause of upper and lower urinary infections, followed by Staphylococcus saprophyticus
      –Acute pyelonephritis is usually a complication of a lower UTI
      –Chronic pyelonephritis is usually associated with obstruction
      • Perirenal (kidney) abscess
      • Acute pancreatitis
      • Glomerulonephritis
      • Herpes zoster
      • Bacterial cystitis
      • Polycystic kidney disease
      • Renal infarction or trauma
      • Papillary necrosis
      • Duodenal ulcer
      • Cholecystitis or biliary colic
      • Pneumonia
      • Appendicitis
      • Obstructive uropathy
      • Ectopic pregnancy
      • Cervicitis
      • Renal or bladder cancer
      • Leaking or ruptured abdominal aortic aneurysm

      Workup and Diagnosis

      • History should include onset, duration, quality, intensity, and location of pain; radiation; associated symptoms (e.g., nausea/vomiting, fever, dysuria, hematuria, rash); history of recent trauma or illness; and family history of renal disease or cancer
      • Exam should include complete cardiovascular, pulmonary, abdominal, and genitourinary exam, and pelvic exam if suspect cervicitis or ectopic pregnancy
        –Turner's sign (bluish discoloration at flank) and/or Cullen's sign (bluish discoloration at the umbilicus) indicate retroperitoneal hemorrhage and may be present in cases of pancreatitis or ruptured AAA
        –Initial labs may include CBC, ESR, electrolytes, BUN/creatinine, calcium, amylase/lipase, liver function tests, pregnancy test, blood cultures, urinalysis, and urine culture
      • Urine cytology, cystoscopy, and biopsy may be indicated if renal or bladder cancer is suspected
      • Renal or abdominal ultrasound or abdominal CT scan
      • Spiral CT scan without contrast is the gold standard to diagnose stones and urinary tract obstruction
      • Intravenous pyelography has high sensitivity/specificity for stones, urinary tract obstruction, and renal cysts
      • Voiding cystourethrography
      • Lumbosacral X-ray may be indicated to evaluate for degenerative joint disease
      • Lumbosacral MRI may be indicated to evaluate for disk disease

    » READ BOOK EXCERPT ONLINE »

    Source: In a Page: Signs and Symptoms, 2004

    Jaw Pain/Swelling: Differential Diagnosis
    (In a Page: Signs and Symptoms)

  • Dental or periodontal pathology
    –Associated with temperature sensitivity and pain upon biting
    • TMJ disorders
      –Associated with unilateral or bilateral achy pain and diffuse tenderness of the masseter and temporalis muscles
      –Exaggerated by jaw use
      –Joint may be tender to palpation
      –“Clicking” sounds are often present
      –More common in females age <50
    • Giant cell (temporal) arteritis
      –Unilateral pain in older patients
      –Headache, jaw claudication, and vision loss
      • Mucosal lesions (buccal mucosa, hard and soft
        palate, floor of mouth, or oropharynx)
        –Aphthous ulcers
        –Herpes simplex or coxsackievirus B
        –Cancer
        –Tongue or lip lesions
      • Paranasal sinus pathology
        –Most common pathology is maxillary
        sinusitis secondary to viral URI
        –Pain is often referred to the upper molars
    • Salivary gland pathology, including inflammation (e.g., parotiditis), ductal stone, or neoplasm
    • Headache with radiation to the jaw
    • Referred pain from cardiac, cervical spine, pulmonary, or throat disease
    • Neuralgias (e.g., trigeminal, glossopharyngeal)
      • Neuropathies
        –Systemic neuropathies (e.g., HIV, diabetes)
        –Dental/alveolar neuropathies, usually
        subsequent to extrinsic trauma (e.g., blow to face, dental surgical intervention)
    • Behavioral disorders
    • Primary neoplasms of the maxilla, mandible, or major salivary gland
    • Metastases to mandible, maxilla, or TMJ
    • Herpes zoster or post-herpetic neuralgia
    • Fibromyalgia
    • Rheumatologic disease (e.g., Sjögren's syndrome)
    • Systemic arthritis (e.g., rheumatoid arthritis)

    Workup and Diagnosis

    • History and physical examination, with focus on the head and neck
      –Review onset, character, and pattern of pain; past medical and surgical history; associated symptoms (e.g., weight loss, sinus pain, skin complaints); and complete review of systems, including screening for local and systemic pathology and a cervical evaluation for muscle, neural, or skeletal referred pain
      –Perform a thorough oral exam of the buccal mucosa, lips, hard palate, soft palate, posterior pharynx, floor of mouth, and the top, sides, and undersurface of the tongue
      –Perform a head, neck, ear, nose, cardiac, pulmonary, and lymphatic exam
      –Suspect dental pathology until proven otherwise
    • Initial workup is aimed at assessing the mouth and jaw for dental, periodontal, or TMJ disorders
    • Appropriate laboratory studies are based upon the suspected diagnosis (e.g., CBC and ESR for temporal arteritis)
    • Imaging studies may include Panorex films, sinus X-ray, CT scan, and/or MRI
    • Therapeutic trial of medications (e.g., NSAIDs)
    • Temporal artery biopsy is indicated if ESR elevated
    • Biopsy any suspicious lesion
    • Referral to a dental or medical specialist may be necessary
    '>

    » READ BOOK EXCERPT ONLINE »

    Source: In a Page: Signs and Symptoms, 2004

    Knee Pain/Swelling: Differential Diagnosis
    (In a Page: Signs and Symptoms)

    • Degenerative joint disease (osteoarthritis)
    • Ligamentous injury
      –ACL: Positive Lachman (more sensitive) and anterior drawer test
      –PCL: Positive thumb sign (more sensitive) and posterior drawer test
      –MCL: Pain and/or increased laxity with valgus stress
      –LCL: Pain and/or increased laxity with varus stress
    • Meniscus tear
      –Patient may complain of pain and locking; positive McMurray circumduction test
    • Patellofemoral syndrome
    • Iliotibial band syndrome
      –Pain along the lateral aspect of the knee accompanied by a palpable or audible snapping
      –Occurs almost exclusively in runners
    • Pes anserine bursitis
      –Patients complain of pain along the medial aspect of the knee (at pes anserinus insertion)
      –Caused by repetitive movement that creates an inflammatory response
    • Joint effusion
      –May be secondary to osteoarthritis, inflammatory arthritis, ligament injury, gout, pseudogout, or infection
    • Joint infection (septic joint)
      Staphylococcus aureus is most common
      Neisseria gonorrhoeae is common in adolescents and young adults
      Salmonella is common in sickle cell patients
      Haemophilus influenzae is common in children
    • Osteochondritis dissecans (OCD)
      –Osteonecrosis of subchondral bone
      –Most commonly seen in the knee
      –Patient reports a gradual onset of pain
      –Exam reveals tenderness of the affected area with manipulation
    • In the pediatric population, consider Osgood-Schlatter disease, physeal injury, and discoid meniscus
    • Hip or foot/ankle disease with referred pain to the knee
    • Malignancy
    • Osteomyelitis

    Workup and Diagnosis

    • History and physical examination are often diagnostic
      –Inspect the patient's gait for limitations of motion or other abnormalities
      –Visually assess symmetry between the knees: Note swelling, deformity, erythema, and muscle atrophy
      –Palpate: Note tenderness, warmth, and crepitus
      –“Milk the joint” to elicit an effusion
      –Test for range of motion (active and passive)
      –Perform McMurray circumduction test and ligament testing (e.g., Lachman test, anterior/posterior drawer tests, thumb sign, varus/valgus stress tests)
    • X-rays are often indicated
      –AP, lateral, and merchant or sunrise films of both knees
      –When possible, also obtain weight-bearing A/P films
      –Merchant and sunrise X-rays of the patella are used to evaluate alignment and injury to the patella
      –On occasion, tunnel views of the knee are useful (e.g., for OCD)
    • Joint aspiration should be performed in patients with joint effusions; fluid analysis includes cell count with differential, crystals, Gram stain, and culture
    • MRI may not be necessary during initial evaluation, but may help with confirmation of specific injuries and surgical planning (e.g., PCL tear, meniscus tear, OCD)
    • Bone scan may be used to evaluate malignancy or infection
    • In some cases, blood work may include CBC, ESR, C-reactive protein, alkaline phosphatase, and uric acid

    » READ BOOK EXCERPT ONLINE »

    Source: In a Page: Signs and Symptoms, 2004

    Neck Stiffness/Pain: Differential Diagnosis
    (In a Page: Signs and Symptoms)

    • Trauma
      –Paraspinal neck stiffness: Commonly due to motor vehicle collisions (“whiplash”) or abnormal sleep posture
      –Cervical spine fracture with spasm of neck muscles
      –Subarachnoid hemorrhage: Most commonly due to ruptured cerebral aneurysm
      –Epidural hematoma
      –SCIWORCA: Spinal Cord Injury Without Radiographic Abnormality occurs in pediatric patients with ligamentous laxity and hypermobility of the cervical spine
      –Rotary atlantoaxial subluxation: Subluxation of the cervical spine at C1-C2 level, resulting in sternocleidomastoid spasm with tilting of the head toward the affected side and chin pointed toward the ipsilateral side
    • Infection
      –Meningitis: Often bacterial (e.g., Neisseria meningitidis, Streptococcus pneumoniae) or viral (e.g., HIV, Epstein-Barr virus, enterovirus, herpes simplex virus)
      –Cervical lymphadenitis
      –Tonsillopharyngitis
      –Epiglottitis
      –Retropharyngeal abscess
      –Epidural abscess
      –Discitis
    • Torticollis: Idiopathic sternocleidomastoid spasm, resulting in tilting of the head toward the affected side with the chin pointed to the contralateral side
    • Inflammatory
      –Rheumatoid arthritis
      –Ankylosing spondylitis
      –Degenerative joint disease
    • Tumors (especially leptomeningeal metastases)
    • Dystonic reaction: Idiosyncratic drug reaction, often to psychiatric medications (e.g., haloperidol, prochlorperazine)

    Workup and Diagnosis

    • History and physical examination focusing on evidence of trauma and infection
      –All patients with possible traumatic injury should be maintained in a cervical collar and backboard until diagnostic workup is complete
    • Initial labs may include CBC, electrolytes, BUN/creatinine, calcium, glucose, and ESR
    • Blood cultures are indicated if infectious etiologies are suspected
    • Lumbar puncture with CSF analysis is useful in cases of suspected infection or subarachnoid hemorrhage
    • Cervical spine radiographs are indicated in trauma or neck infection (may reveal prevertebral soft-tissue swelling)
    • Head CT scan without contrast may show bleeding in cases of subarachnoid hemorrhage (fails to reveal subarachnoid blood in 10% of cases)
    • Neck CT scan may be indicated in suspected soft tissue disease (e.g., retropharyngeal abscess) or occult vertebral fracture if not adequately visualized on plain films
    • MRI of the spine may be indicated in suspected epidural abscess or epidural hematoma

    » READ BOOK EXCERPT ONLINE »

    Source: In a Page: Signs and Symptoms, 2004

    Pelvic Pain - Female: Differential Diagnosis
    (In a Page: Signs and Symptoms)

    Acute pain (<6 months)

    • Pregnancy-related
      –Ectopic pregnancy
      –Threatened abortion
      –Incomplete abortion
      –Septic abortion
      –Ruptured corpus luteal cyst
    • Gynecologic (noncyclic)
      –Ovarian cyst
      –Pelvic inflammatory disease
      –Tubo-ovarian abscess
      –Vaginitis/cervicitis
      –Ovarian torsion
      –Uterine fibroids
      –Pelvic (ovarian, uterine, urinary) neoplasm
      –Pelvic floor prolapse (cystocele/rectocele)
    • Gynecologic (cyclic pain)
      –Primary dysmenorrhea
      –Endometriosis
      –IUD
      –Mittelschmerz (midcycle ovulation)
    • Nongynecologic
      –Irritable bowel syndrome
      –UTI/pyelonephritis
      –Nephrolithiasis
      –Appendicitis
      –Diverticulitis
      –Sexual abuse/trauma
      –Abdominal aortic aneurysm
      –Mesenteric ischemia/infarction

    • Chronic pain (>6 months)
    • Very difficult to diagnose; differential includes gynecologic and nongynecologic etiologies (above), as well as the following
      –Pelvic adhesions
      –Interstitial cystitis
      –Inflammatory bowel disease
      –Adenomyosis
      –Leiomyoma (fibroids)
      –Hernia (femoral or inguinal)
      –Depression
      –Irritable bowel syndrome
      –Diverticulosis or diverticular abscess
      –Lymphoma
    • Less common etiologies (“zebras”) include pelvic congestion syndrome, mesenteric adenitis, surgical adhesions, Asherman's syndrome, foreign body (e.g., tampon), abdominal wall nerve entrapment, and porphyria

    Workup and Diagnosis

    • History and physical examination
      –Note the nature, severity, onset, radiation, duration of pain; relation to menstrual cycle, intercourse, or other activities; chronic versus acute; chance of pregnancy
      –Note associated symptoms: Fever, nausea, vomiting, dysuria, frequency, vaginal bleeding/discharge, abdominal or back pain
      –Screen for domestic violence and sexual abuse
      –Full abdominal and pelvic exams, including speculum, bimanual, and rectal exam
    • Laboratory studies may include urine pregnancy test, urinalysis, urine Gram stain and culture, cervical cultures for Chlamydia and gonorrhea, and wet mount of vaginal smear
    • Consider ultrasound if ovarian cyst, torsion, or mass is suspected, or to evaluate for intrauterine versus ectopic pregnancy
    • Diagnostic laparoscopy for acute abdomen or endometriosis
    '>

    » READ BOOK EXCERPT ONLINE »

    Source: In a Page: Signs and Symptoms, 2004

    Shoulder Pain/Swelling: Differential Diagnosis
    (In a Page: Signs and Symptoms)

    • Trauma and sports related injuries
      –Acromioclavicular dislocation (“separated shoulder”)
      –Sternoclavicular dislocation
      –Glenohumeral dislocation
      –Proximal humeral fractures
    • “Impingement syndrome”
      –Progressive degeneration and inflammation of the subacromial contents (rotator cuff and subacromial bursa) in part due to compression between the acromion and the head of the humerus
      –May result in rotator cuff tear
    • Rotator cuff strain, tear, or rupture
      –May occur acutely (secondary to trauma) or, more commonly, due to a relatively mild (e.g., reaching overhead) insult to a chronically degenerative cuff
    • Degenerative joint disease
    • Tendonitis
    • Subacromion and/or subcapsular bursitis
    • AC joint inflammation
      • Calcific tendonitis
        –Deposition of calcium crystals in the rotator cuff with resulting inflammation and severe pain
      • Suprascapular nerve entrapment
      • Bicipital tendonitis
        • Adhesive capsulitis
          –Thickened, scarred joint capsule and “frozen shoulder” due to prolonged postinjury or postsurgery immobilization
        • Cervical disc disease and radiculopathy
        • Gout
        • Pseudogout
        • Connective tissue disease (e.g., rheumatoid arthritis, SLE)
        • Brachial plexus injury
        • Septic arthritis
        • Referred pain from MI, cholecystitis, splenic injury
        • Malignancy (e.g., apical lung)
        • Lyme disease
        • Fibromyalgia
        • Thoracic outlet syndrome
        • Reflex sympathetic dystrophy
        • Rib dislocation/rib pain
        • Acute axillary vein thrombosis

        Workup and Diagnosis

        • History and physical examination
          –Inspection for asymmetry, dislocation, or atrophy
          –Note range of motion, strength, sensory, crepitus, pain with passive and/or active motion
          –Perform a complete neurovascular exam
      • Plain X-rays of shoulder; cervical spine films and chest X-ray may also be useful
      • X-ray or CT scan may identify chronic, degenerative arthritis
      • Shoulder MRI evaluates the anatomy of the rotator cuff and associated soft tissue; may differentiate partial from complete tears
      • EMG can help discern nerve entrapments, cervical disc disease, or brachial plexus injury
      • Diffuse shoulder or acromioclavicular pain may require workup for medical etiologies, including ESR, ANA, rheumatoid factor, and TSH

    » READ BOOK EXCERPT ONLINE »

    Source: In a Page: Signs and Symptoms, 2004

    Wrist & Hand Pain/Swelling: Differential Diagnosis
    (In a Page: Signs and Symptoms)

    • Carpal tunnel syndrome
      –Most common cause of significant wrist discomfort and morbidity
      –Associated with repetitive use activities (e.g., typing)
      –Pain and numbness symptoms result from entrapment of the median nerve under the transverse ligament
    • Overuse injury
    • Osteoarthritis
    • Tenosynovitis (DeQuervain's) of the radial wrist
      –Results from inflammation of the tendon sheaths of the extensor pollicis brevis and abductor pollis longus
      • Ganglion cysts
        –Common growths of tendons and ligaments in the wrist area occurring on both the dorsal and ventral surface
        –They are compressible, round, often tender, and mobile
      • Trauma
        –The most common mechanism of injury is a fall on the outstretched hand
        –The most commonly fractured carpal bone is the scaphoid
        –Other mechanisms include direct blows, crush injuries, fall on an angulated wrist, and severe twisting motions
      • Fibromyalgia
      • Compartment syndrome
      • Chest or shoulder masses, resulting in compression of lymphatic or venous systems
      • Venous thrombosis of the subclavian or distal veins
      • Flaccid paralysis following a CVA
      • Angioedema secondary to hymenoptera sting
      • Rheumatologic disease
      • Peripheral neuropathy
      • Insect or animal bite/sting
      • Infection (e.g., staphylococcus aureus, streptococci)

      Workup and Diagnosis

      • History and physical examination of the hand, wrist, elbow, and shoulder
        –Tinel's sign is positive if pain is elicited by tapping the anterior wrist
        –Phalen's sign is positive if wrist flexion for >30 seconds elicits pain or numbness
      • Lab investigation is usually unnecessary, but may include rheumatoid factor, ANA, ESR, CBC, uric acid, TSH, β-hCG (pregnancy test)
    • Standard X-rays include PA, lateral, and oblique views
    • EMG and nerve conduction studies are indicated if carpal tunnel syndrome or other neuropathy is suspected
    • Arthrocentesis with crystal analysis may be indicated if warmth and redness are noted in the wrist and MCP joints
    • Bone scan may be necessary to evaluate for avascular necrosis, occult fracture, or bone infection
    • Rarely, CT or MRI is indicated
    • Shoulder/chest CT may be indicated to evaluate for masses resulting in nerve entrapment or vascular compromise

    » READ BOOK EXCERPT ONLINE »

    Source: In a Page: Signs and Symptoms, 2004

    Seizures/Convulsions: Differential Diagnosis
    (In a Page: Signs and Symptoms)

    • Partial seizure (involve only part of the brain)
      –Simple (no altered consciousness)
      –Complex (with altered consciousness)
    • Generalized seizure (involve both hemispheres)
      –Tonic-clonic
      –Atonic
      –Tonic
      –Myoclonic
      –Absence
    • Epilepsy
      –Recurrent unprovoked seizures of any or multiple types, which may be idiopathic or symptomatic
      • Secondary seizure
        –Metabolic abnormalities (e.g., electrolyte disturbances, hypoglycemia)
        –Drug effects, intoxication, or withdrawal
        –Head injury/trauma
        –Febrile seizures in children
        –Structural lesions (e.g., tumor, subdural hematoma)
        –Cerebrovascular etiologies (e.g., cerebral infarct, intracerebral hemorrhage, subarachnoid hemorrhage
        –Hypoxic-ischemic encephalopathy
        –Infection (e.g., meningitis, encephalitis)
        –Hypoxia
      • Nonepileptic seizure
        –Not associated with abnormal electrical activity in the brain
        –Patients with loss of consciousness secondary to cerebral hypoperfusion (fainting, syncope) may occasionally exhibit brief periods of twitching or convulsive movements resembling seizure activity
        –Psychological disturbances (pseudoseizure)
      • Inborn errors of metabolism
        –Disorders of amino acid metabolism
        –Organic acidemias
        –Urea cycle disorders
        –Mitochondrial disorders
        –Peroxisomal disorders
        –Glycogen storage disorders
        –Disorders of sugar metabolism
      • Rasmussen's encephalitis
        –Causes seizures and progressive hemispheric dysfunction in infants

      Workup and Diagnosis

      • History and physical examination
        –In many instances, the most useful history is obtained from a witness of the seizure rather than the patient him- or herself, because seizures commonly cause altered consciousness and may result in postictal confusion
        –Appropriate classification of seizure type may help to suggest etiology and treatment (e.g., a partial seizure resulting in isolated clonic jerking of the right arm is suggestive of pathology in the left frontal lobe)
        –Evidence of postictal paralysis on examination may also help to suggest the part of the brain involved
      • Initial labs should include CBC, electrolytes, glucose, O2 saturation, calcium, magnesium, glucose, and BUN/creatinine
      • CT is suitable for emergent evaluation, but MRI is more sensitive
      • CSF examination if CNS infection (e.g., meningitis) or subarachnoid hemorrhage is suspected
      • Drug screen and ethanol level
      • EEG
      • Video EEG monitoring may be useful in cases of refractory epilepsy as part of evaluation for epilepsy surgery or suspected nonepileptic seizures

    » READ BOOK EXCERPT ONLINE »

    Source: In a Page: Signs and Symptoms, 2004

    Otalgia (Ear Pain): Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

    External ear

      • Otitis externa
        –Pinnae and especially tragus, are exquisitely tender
    • Impacted cerumen
      –Hearing loss and aural fullness
      • Foreign body
        –Items such as beads, toys, and even extruded tympanostomy tubes
      • Trauma
        –Any object inserted into the ear canal may cause trauma, including Q-tips
      • Perichondritis
        –Inflammation or infection of the cartilage of the pinna and canal, sparing the lobule (since there is no cartilage there)
      • Myringitis
        –Tympanic membrane granulation or de-epithelialization

      Middle ear/mastoid
    • Acute otitis media
      –Otalgia may precede middle ear effusion
      • Otitis media with effusion
        –May occur in the absence or presence of an active infection
    • Eustachian tube dysfunction
      –Negative intratympanic pressure
      • Barotrauma
        –Pretreatment with topical nasal decongestants may be effective prophylaxis
      • Mastoiditis
        –Associated with postauricular pain and normal tympanic membrane/middle ear

      Non-otologic (secondary)
      • Cranial nerve referred pain
        –III: Dental infection, temporal-mandibular joint (TMJ) syndrome
        –VII: Herpes zoster oticus (Ramsay Hunt syndrome)
        –IX: Tonsillitis, pharyngitis
        –X: Laryngitis, GERD, thyroiditis
    • Cervical nerve referred pain
      –Neck infections, lymph nodes, cysts
      –Cervical spine disorders
    • Paranasal sinusitis
    • Migraines
    • Neuralgias

    Workup and Diagnosis

      • History
        –Onset, duration, and specific quality of pain
        –Ability to localize (may distinguish otologic from nonotologic)
        –Associated otologic symptoms: Otorrhea, hearing loss, imbalance, prior ear surgery, antecedent events
        –Pain associated with mastication, swallowing, voice change, purulent rhinorrhea
      • Otologic exam
        –Inspection and palpation of pinna, tragus, and preauricular area, and mastoid bone
        –Direct otoscopy for signs of external- or middle-ear infection or inflammation
        –Obstructing cerumen or foreign bodies must be removed to evaluate deeper structures
      • Complete head and neck exam
        –Nose and nasal cavities, oral cavity, and pharynx (particularly teeth and tonsils), TMJ
        –Examination of nasopharynx and larynx may require fiberoptic endoscopy
    • Tympanometry, if middle ear status (fluid, retraction, perforation) is not evident from otoscopy
    • CT or MRI
      –Useful to delineate extent of cholesteatoma, mastoiditis, petrous apicitis, tumor
      –May be necessary to evaluate either otologic disease or an ill child with nonotologic source (rule out abscess or tumor)

    » READ BOOK EXCERPT ONLINE »

    Source: In A Page: Pediatric Signs and Symptoms, 2007

    Seizures – Childhood: Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

    • Febrile seizure
    • Cerebral dysgenesis: Disorders of neuronal migration, heterotopias, lissencephaly
    • Epilepsy syndromes
      –Childhood absence
      –Juvenile absence
      –Juvenile myoclonic epilepsy (JME)
      –Benign rolandic epilepsy (BRE)
    • Meningitis/encephalitis (e.g., HSV)
    • Cerebral abscess
    • Postinfectious (e.g., ADEM)
    • Hyponatremia
    • Hypernatremia
    • Hypocalcemia
    • Hypoglycemia
    • Toxins: Ingestions or sedative withdrawal
    • Trauma
    • Pyridoxine deficiency
    • Neoplasm
    • Degenerative
      –Alpers disease
      –Rett syndrome
      –Unterricht-Lundborg disease
      –Lafora disease
      –Neuronal ceroid lipofuscinosis
    • Genetic
      –Angelman syndrome
      –Aicardi syndrome
      • Metabolic
        –Medium chain acyl-CoA dehydrogenase deficiency (MCAD)
        –Myoclonus epilepsy and ragged-red fibers syndrome (MERRF)
        –Sialidosis
        –Glucose transporter deficiency
        –Urea cycle defects
    • Vascular: Stroke, hemorrhage, vasculitis
    • Hashimoto encephalitis
    • Seizure mimics
      –Breath-holding spells
      –Syncope, convulsive syncope
      –Gastroesophageal reflux
      –Cardiac arrhythmia
      –Movement disorder
      –Migraine
      –Benign paroxysmal vertigo
      –Parasomnia
      –Pseudo-seizure
      –Rage attack

    Workup and Diagnosis

    • History: Detailed description of the spell, loss of consciousness, eye deviation, time of onset, other suspicious spells (jerking, staring, day-dreaming), birth and developmental history, previous history of head trauma, encephalitis, febrile seizures, medications at home, recent infections
    • Physical exam: Dysmorphic features, skin rash, retinal exam for cherry-red spot, macular degeneration, hepatosplenomegaly, meningismus
    • Full neurologic examination: Postictal weakness can provide clues to the focus of seizures (Todd paralysis)
    • Labs: Glucose, electrolytes, calcium, toxicology screen, ammonia, lactate, pyruvate, genetic testing for specific disorders (MECP2 mutation for Rett, FISH on chromosome 15 for Angelman)
    • Lumbar puncture to rule out infection (including HSV PCR), glucose transporter deficiency
      • EEG can help make the diagnosis of focal vs generalized epilepsy
        –Crucial for decisions of treatment choices
    • MRI can help determine any structural abnormalities, including cerebral dysgenesis, abscess, neoplasm, temporal lobe sclerosis
    • For other specific etiologies, one can follow up with skin biopsy, CSF amino acids, biotinidase level, TSH, anti-thyroglobulin antibodies, rheumatologic workup

    » READ BOOK EXCERPT ONLINE »

    Source: In A Page: Pediatric Signs and Symptoms, 2007

    Seizures – Neonatal: Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

    • Hypoxic ishemic encephalopathy
    • Bacterial meningitis/sepsis
    • Stroke
    • Cerebral dysgenesis
    • Electrolyte disturbances
      –Hypoglycemia
      –Hyponatremia
      –Hypomagnesemia
      –Hypocalcemia
    • Maternal drug use
      –Drug withdrawal after delivery
      –Direct effect of drugs, such as cocaine
    • Congenital infections (TORCH)
      –Toxoplasmosis
      –Syphilis
      –Rubella
      –CMV
      –HSV
    • HSV encephalitis
      • Intracranial hemorrhage
        –Subdural hemorrhage
        –Intraparenchymal hemorrhage
        –Intraventricular hemorrhage in the premature infant
        –Subarachnoid hemorrhage
    • Urea cycle disturbances
    • Smith-Lemli-Opitz syndrome
    • Nonketotic hyperglycinemia
    • Pyridoxine deficiency
    • Fructose dysmetabolism
    • Amino acidurias
      –Maple syrup urine disease
      –Proprionic acidemia
    • Molybdenum cofactor deficiency
    • Mitochondrial encephalopathy
    • Glucose transporter deficiency
      • Benign etiologies
        –Benign idiopathic neonatal seizures (fifth day fits)
        –Benign familial neonatal seizures
    • Movements commonly mistaken for seizures
      –Benign neonatal sleep myoclonus
      –Jitteriness (may be secondary to hypoglycemia, drug withdrawal, or idiopathic)
      –Gastroesophageal reflux (arching, writhing)
      –Breath-holding spell

    Workup and Diagnosis

    • History: Previous pregnancies, fetal movements, infections, blood pressure problems during pregnancy, maternal drug/medication use, family history, Apgar scores, nuchal cord, birth weight, feeding problems, association of the spells to feeding and sleep
    • Physical exam
      –Deformities, dermatoglyphics, skin lesions, hepatosplenomegaly, funduscopic exam, corneal opacities
      –Mental status: Spontaneous level of activity of the infant; responsiveness to light, sound, and touch
      –Muscle tone: Passive manipulation of limbs
      –Primary neonatal reflexes (Moro, palmar grasp, tonic neck response) and muscle stretch reflexes
    • Labs: Glucose, electrolytes, lactate, liver function tests, ammonia, TORCH titers, pyruvate, chromosomes, 17-hydroxycorticosteroid, serum amino acids, copper
    • Neuroimaging: CT or MRI
    • Lumbar puncture for meningitis and encephalitis, including HSV, glucose transporter deficiency, nonketotic hyperglycinemia
    • EEG: Critical in making the diagnosis of seizures in the newborn; monitoring of the child during one of the spells is the best way to make the diagnosis of seizures
    • If gastroesophageal reflux is suspected, pH/thermistor monitoring is helpful to document a temporal relation

    » READ BOOK EXCERPT ONLINE »

    Source: In A Page: Pediatric Signs and Symptoms, 2007

    Abdominal Pain: Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

    Epigastric pain

      • Peptic ulcer disease/GERD
        –May be due to Helicobacter pylori or NSAID use
    • Gallbladder disease
      –Most commonly with hemolytic disorders
      • Pancreatitis
        –Trauma and idiopathic are common causes

      Periumbilical pain
    • Functional abdominal pain/IBS
      –Most common cause of nonorganic pain
      –Occurs in children 3–15 years old
    • Appendicitis
      –Periumbilical pain moves to RLQ
    • Gastroenteritis (virus, bacteria, parasite)
    • Carbohydrate intolerance
      –Lactase, fructase, trehelase deficiency
    • Abdominal migraine
    • Drugs
      –Antibiotics, anticonvulsants, bronchodilators
    • Small bowel bacterial overgrowth
    • Streptococcal pharyngitis
      Suprapubic pain
    • Urinary tract infection
      –With dysuria, fever, foul-smelling urine
      –Pyelonephritis may have CVA tenderness
    • Constipation
      –Accounts for 3% of visits to pediatrician
      –May have a palpable fecal mass
    • Urinary retention
      • Hydrometrocolpos
        –Associated with imperforate hymen
        –Cyclic pain with onset of menstrual cycle

      Right lower quadrant pain
    • Appendicitis
    • Ovarian torsion
    • Pelvic inflammatory disease
    • Ectopic pregnancy
    • Mittelschmerz
      –Pain midcycle with ovulation
    • Inflammatory bowel disease
      –Classic for terminal ileal Crohn disease
    • Iliopsoas abscess
    • Inguinal hernia
    • Right lower lobe pneumonia

    Workup and Diagnosis

      • History
        –Type of pain, location, radiation, duration
        –Relieving and worsening factors including foods
        –Awakens from sleep, activity level, emesis, diarrhea
        –Nausea, hematochezia, melena, fever, dysuria, hematuria
        –Sexual activity, anorexia, headache, cough, rashes
        –Stool frequency, joint complaints
    • Surgical history: Previous abdominal surgery
    • Social history: Stressors, changes in school or family
    • Physical exam
      –Height, weight, temperature, pulse
      –General appearance, hydration status
      –Pharyngeal erythema/exudates, abdominal tenderness
      –Psoas sign, obturator sign, palpable masses
      –Rectal exam including hemoccult
      –Rashes, joint swelling, vaginal exam
    • Labs: Geared toward history and physical findings
      –Consider CBC with differential, urinalysis, and culture
      –stool for culture and O&P
      –Amylase and lipase, LFTs, H. pylori antibody (IgG)
      –Hydrogen breath test for sugar intolerance
      –Pregnancy test, vaginal cultures
      –Throat culture
    • Consider KUB or obstruction series
    • Abdominal CT scan with contrast versus ultrasound
    • Pelvic ultrasound for torsion, ectopic pregnancy, abscess, hydrometrocolpos

    » READ BOOK EXCERPT ONLINE »

    Source: In A Page: Pediatric Signs and Symptoms, 2007

    Back Pain: Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

      • Muscular strain, disk herniation
        –Most common in adolescents who are involved in competitive or contact sports; may be occupational
    • Spondyloarthropathy
      –Ankylosing spondylitis is found primarily in boys, characterized by sacroiliitis, LE oligoarthritis, and may be associated with IBD
      • Malalignment
        –Scoliosis: Idiopathic form is most common in girls, may be familial, may be secondary to neurologic disorder
        –Hyperlordosis
      • Infectious
        –Diskitis: Characterized by spine stiffness and muscular spasm, Staphylococcus aureus is the usual pathogen, blood culture may be positive
        –Vertebral osteomyelitis: Exquisite point tenderness, pathogen may be S. aureus, Streptococcus pneumoniae, or others such as tuberculosis or brucellosis
        –Acute transverse myelopathy: Generally follows an upper respiratory tract infection; characterized by back pain, distal weakness and paresthesias at the midthoracic level
      • Urinary tract
        –Urinary tract infection: Most common in postpubertal girls, occurrence in boys or prepubertal girls may require evaluation for urinary tract anomalies, especially if recurrent
        –Urolithiasis: Associated with hypercalcuria, cystinuria, Lesch-Nyhan; characterized by intense flank pain and hematuria
      • Malignancy
        –Primary spinal cord or column tumors (osteogenic sarcoma, neuroblastoma)
        –Metastatic tumors (neuroblastoma)
        –Bone marrow infiltration (leukemia, lymphoma)
      • Gynecologic
        –Menstrual cramps
        –PID
        –Endometriosis

      Workup and Diagnosis

        • History
          –Onset, duration, location of symptoms
          –History of trauma, heavy lifting, overuse, athletics
          –Systemic symptoms such as fever, irritability
          –Menstrual and sexual history
          –Past medical history of similar complaints, orthopedic conditions, general medical conditions
          –Family history of scoliosis, rheumatic disease
        • Physical exam
          –General appearance, fever, irritability
          –Spinal contour, symmetry
          –Gait, posture
          –Range of motion limitations
          –Point tenderness, SI tenderness
          –Associated neurologic findings (sensation, strength, DTRs)
      • Labs
        –If rheumatologic condition is suspected, consider CBC, ESR, ANA, RF, HLA typing
        –If infectious process is suspected, obtain CBC, ESR
        –Urine microscopy and culture
      • Studies
        –Plain films can reveal fractures such as spinal compression fractures, disk space abnormalities, and sacroiliac abnormalities associated with spondyloarthrosis
        –MRI may be required to discover disk herniation, disk space infection, tumors

    » READ BOOK EXCERPT ONLINE »

    Source: In A Page: Pediatric Signs and Symptoms, 2007

    Chest Pain: Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

    • Musculoskeletal
      –Sharp, stabbing pain that is usually very well localized, often worsened by deep breath or cough
      –Costochondritis: Tender parasternal pain at insertion of ribs into cartilage en route to sternum; increases with palpation or mild chest compression (possibly postviral)
      –Injury to chest wall
    • Pulmonary
      –Very common cause, usually associated with respiratory symptoms: Shortness of breath, cough, exercise intolerance
      –Asthma (most common), often only EIA; may have personal/family history of atopy (asthma, eczema, seasonal allergies); shortness of breath is usually primary complaint, with feeling of chest tightness/pain as a secondary symptom
      –Pleuritic chest pain: Sharp, stabbing pain with deep breaths, indicates pleural space inflammation, probably postinfectious (especially viral)
      –Pneumonia: Chest pain secondary to cough or pleural involvement
      –Pneumothorax can occur spontaneously, especially in tall, thin athletes
    • Gastrointestinal
      –GERD and PUD: Burning, substernal pain with eating, worse at night
      –Rarely pancreatitis (with back pain too), cholecystitis, hiatal hernia, hepatitis
    • Cardiac: Rare in children
      –Precordial catch syndrome: Sharp, brief (seconds) chest pain usually associated with rising from lying or sitting; unclear etiology, but of no significance
      –Pericarditis: Inflammation of the pericardium; often postviral, may represent connective tissue/autoimmune, cancer, bacterial infection (very ill appearing with fever), or post-cardiac surgery; patients often lean forward to decrease the pain
      –MI (rare): Congenital coronary anomaly, post-Kawasaki, cocaine use, hypertrophic cardiomyopathy
      –Aortic dissection: Consider if features or history of Marfan syndrome is present
    • Workup and Diagnosis

      • History
        –Activity at onset, (chest pain with exercise is a red flag!), precipitating/relieving factors, quality of pain (sharp vs dull)
        –Associated symptoms (shortness of breath, diaphoresis, cough/wheeze, nausea/vomiting), recent illness, response to eating, sleeping, different foods (caffeine, chocolate, spicy, or high-fat foods)
        –Personal/family history of asthma, allergies, eczema
        –Recent diagnosis of heart disease or death in a family member often generates fear in the patient or parent, prompting the evaluation of chest pain
        –Social history: Recent life stressors (school problems, family discord, etc.); drug use, especially cocaine
        • Physical exam
          –Reproducible with palpation likely musculoskeletal
          –Chest exam: Wheezing, rales, crepitus
          –Cardiac exam: Usually normal, even with cardiac causes; pericarditis is associated with rub
      • Chest X-ray for infiltrates, pneumonia, pneumothorax
      • ECG and cardiac enzymes are rarely required but relatively inexpensive and readily available, and can rule out MI and provide reassurance for families
      • Cardiac stress test
        –Continuous ECG monitoring while the patient exercises to evaluate for coronary insufficiency
        –Used for patients with exercise-induced chest pain and/or coronary abnormalities

    » READ BOOK EXCERPT ONLINE »

    Source: In A Page: Pediatric Signs and Symptoms, 2007

    Hip Pain: Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

      • Septic arthitis
        –Surgical emergency due to irreversible chondrolysis and epiphyseal injury
        –Acute process leading to decreased hip range of motion, severe pain with passive range of motion
      • Slipped capital femoral epiphysis (SCFE)
        –Typically in obese, adolescent males with aching groin, hip, or knee
        –May have externally rotated hip position and gait
      • Legg-Calvé-Perthes
        –Presents at younger age than SCFE (3–8 years old)
        –Five times greater incidence in boys than girls
        –Pain in hip or knee, decreased active and passive ROM, and Trendelenburg gait
      • Developmental dysplasia of the hip (DDH)
        –Early diagnosis with newborn exam finding of easily dislocatable hip
        –Older infants have limited hip abduction
      • Osteomyelitis
        –Vague symptoms may make this a difficult diagnosis
        –Limp, fever, pain in the proximal thigh or pseudoparalysis of an extremity in an infant may be the only sign
      • Fracture
        –Consider accidental and nonaccidental trauma
        –Pain, limited ambulation, limited active and passive ROM, or inability to bear weight
      • Transient monoarticular synovitis
        –Often preceded 1–2 weeks by upper respiratory infection
        –Antalgic gait, moderate pain in hip, groin, or knee, and uncomfortable range of motion
      • Neoplasia
        –Although primary bone disorders do not generally present with hip pain, other malignancies such as acute leukemia may initially present with bone or joint pain
    • Vertebral osteomyelitis/diskitis
      –Referred pain from lumbrosacral region may present as hip pain

    Workup and Diagnosis

      • Despite urgency of surgical emergencies, a thorough history is essential
        –Onset and duration of symptoms, location, and character of pain
        –Previous trauma, preceding illness, or associated symptoms
        –Past medical history/family history: Bone, hematologic, and metabolic disorders
    • Labs
      –CBC with differential, platelets, PT/INR, ESR, CRP
    • Radiographic evaluation
      –Plain X-ray: AP pelvis and frog-leg lateral of the pelvis, full length femur, and knee films
      –CT scan: Helps define bony anatomy especially with 3D reconstruction images
      –MRI may demonstate joint effusion in synovitis and infection, marrow edema in osteomyelitis, physeal widening in SCFE, or occult fracture such as femoral neck stress fracture
      –Ultrasound for newborn DDH
      • Nuclear medicine
        –Triple-phase bone scan may be helpful when the diagnosis is questionable, or if differentiating between bone and joint infections
      • Interventional radiology
        –Joint aspiration to evaluate for septic arthritis

    » READ BOOK EXCERPT ONLINE »

    Source: In A Page: Pediatric Signs and Symptoms, 2007

    Knee Pain: Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

    • Septic arthritis
      –Characterized by redness, swelling or effusion, warmth, pain with active and passive ROM, fever or chills
      –Requires urgent evaluation and diagnosis
    • Osgood-Schlatter disease (OSD)
      –Repetitive microtrauma to the bone-tendon junction where patellar tendon inserts into the secondary ossification center of the tibial tubercle
      –Onset at early adolescence, more often in athletes
    • Sinding-Larsen-Johansson disease
      –Similar to OSD, except localized to distal pole of the patella
    • Meniscal pathology
      –Meniscal tears are usually associated with acute trauma, and involve pain and swelling with mechanical symptoms such as popping, clicking, or locking
      –Discoid meniscus: Mechanical symptoms and plain X-rays show squaring, widening, and cupping
    • Ligamentous injury
      –Medial collateral ligament sprain via overuse injury or valgus force to knee
      –Anterior cruciate ligament tear associated with sport noncontact pivoting injury, associated with a “pop” and immediate swelling
      –Posterior cruciate tear associated with direct trauma to anterior tibia or hyperflexion with plantar flexed foot
      –Lateral collateral ligament injury is rare
      • Osteochondritis dissecans
        –Trauma resulting in separation of subchondral bone and cartilage at lateral aspect of medial femoral condyle
      • Patellar subluxation/dislocation
        –Lateral displacement of patella associated with increased Q angle, genu valgum, and femoral anteversion (more common in women)
      • Bursitis
        –Chronic friction over pes anserine, iliotibial band, or capsular bursa leads to inflammation and thickening of the bursa
    • Bipartite patella
      –Common variant of patellar ossification

    Workup and Diagnosis

      • History
        –Specific location, duration, onset, aggravating or alleviating factors, and pain characteristics
        –Previous trauma, preceding illness, or associated symptoms
        –Past medical history and family history including bone, hematologic, or metabolic disorders
      • Physical exam
        –Bilateral hip, knee, and ankle exam
        –Redness, warmth, effusion, active and passive ROM
        –Palpate joint line, patella, tibial tubercle, pes anserine, and medial/lateral ligaments
        –Patella tracking or apprehension, varus/valgus stress, Lachman, and anterior posterior drawer tests
        –Crepitus along the flexion arc and McMurray test
      • Labs
        –Often not needed unless concerned about infection
        –CBC with differential, platelets, PT/INR, ESR, CRP
        –Knee aspirate for cell count and differential with Gram stain, culture, and crystals
      • Radiography
        –Plain X-ray: Screening knee films include AP, lateral, Merchant views
        –AP pelvis and frog-leg lateral of the pelvis or femur films if indicated by exam findings
    • MRI to show soft tissues such as meniscus and ligaments
      –May demonstate joint effusion in synovitis/infection, marrow edema in osteomyelitis, ligament rupture

    » READ BOOK EXCERPT ONLINE »

    Source: In A Page: Pediatric Signs and Symptoms, 2007

    Toeing Out: Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

    • Femoral retroverson
      –Usually bilateral with excessive external and limited internal range of motion of both hips
    • External tibial torsion
      –More common than femoral retroversion
      –May be related to in utero positioning and is sometimes associated with calcaneovalgus foot
    • Slipped capital femoral epiphysis (SCFE)
      –Most common in obese adolescent boys
      –Unilateral out-toeing with painful hip
      –Pain and limited range of motion or antalgic externally rotated gait pattern
    • Talipes calcaneovalgus
      –Positional deformity in which the foot is extremely dorseflexed and everted
    • Everted flat feet
      –Children stand in a toe out position but toe in when walking
    • Triceps surae muscle contracture
      –Can be seen with cerebral palsy
    • Vertical talus (rocker-bottom foot)
    • Congenital absence of the fibula
      –Shortening of the peroneal and triceps surae muscles result in bowing of the tibia and equinovalgus
    • Maldirection of the acetabulum
      –If the acetabulum faces posteriorly, leg position is everted

    Workup and Diagnosis

    • History is generally limited
      –Development and milestones are generally normal
      –Hip pain and limp are red flags for SCFE
    • Physical examination consists of a rotational profile using four elements to help with diagnosis and monitoring
    • First element: Hip rotation
      –Measurement is performed in prone position, hips extended and knees flexed to 90°
      –Lateral rotation; external rotation with >70° indicates femoral retroversion
      –Medial rotation; internal rotation with <20° also indicates femoral retroversion
    • Second element: Thigh-foot angle
      –Measurement is performed in prone position, hips extended, and knee flexed at 90°, evaluating long axis of foot relative to axis of thigh
      –Neutral or foot pointed outward >40° (normal 0–30°) indicates external tibial torsion
    • Third element: Foot evaluation
      –Foot alignment is assessed in prone and standing position; heel bisector line should line up with second metatarsal
    • Fourth element: Foot progression angle (gait evaluation)
      –When the child walks, estimate the angle of the foot relative to the line of progression
      –If patella is outward, then the femur may be retroverted
      –If patella points straight, then the tibia or foot is causing the deviation
    >

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    Source: In A Page: Pediatric Signs and Symptoms, 2007

    Toeing In: Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

    • Femoral anteversion
      –Most common cause of intoeing in children between 2 and 6 years old
      –Incidence in females is twice that of males
      –Femoral shaft internal alignment leads to entire lower limb to be inwardly rotated
    • Internal tibial torsion
      –Most common cause of intoeing in children less than 2 years of age
      –Inward rotation of the tibia leads to intoeing
    • Metatarsus adductus
      –Forefoot is adducted, with a concave medial foot border with increased space between the first and second toes
      –May be due to in utero packaging problems; thus is associated with a higher incidence of hip dysplasia
      • Muscle force imbalance
        –Neuromuscular disorders such as cerebral palsy have a higher incidence of lower extremity rotational abnormalities due to increased muscular tone and dynamic imbalance
      • Pronated feet (flatfeet)
        –Children typically stand with feet in valgus position, because this is unstable for walking; children toe in to shift the center of gravity to the center of the foot
    • Knock knees
    • Maldirection of the acetabulum
      –If the acetabulum is directed anteriorly toeing in will stabilize the hip joint

    Workup and Diagnosis

      • History is generally limited
        –Often the family gives a history that the child tends to stumble or fall more than other children
        –Development and milestones are usually normal
    • Physical exam consists of a rotational profile using four elements to help with diagnosis and monitoring the progression of intoeing
      • First element: Hip rotation
        –Measured with the patient prone, hips extended, and knees flexed 90°
        –Lateral rotation; external rotation with <20° indicates femoral anteversion
        –Medial rotation; internal rotation with >70° also indicates femoral anteversion
      • Second element: Thigh-foot angle
        –Measurement in prone position of long axis of foot relative to axis of thigh with knee flexed at 90°
        –Neutral or foot pointed inward indicates internal tibial torsion
      • Third element: Foot evaluation
        –Foot alignment is assessed in prone position, and heel bisector line lines up with second metatarsal
    • Fourth element: Foot progression angle (gait evaluation)
      –When the child walks, estimate the angle of the foot relative to the line of progression
      –If patella is inward, then the femur may be anteverted
      –If patella points straight, then the tibia or foot is causing the deviation
    >

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    Source: In A Page: Pediatric Signs and Symptoms, 2007

    Scrotal Pain: Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

    • Testicular torsion
      –Twisting of the spermatic cord and vessels, resulting in testicular ischemia
      –Patients present with an excruciatingly painful swollen testicle with or without a history of previous milder episodes (intermittent torsion)
      –May occur at any age (including in utero)
    • Torsion of the appendix testis
      –May be difficult to distinguish clinically from testicular torsion
      –Typically, pain is less severe and the onset less acute (over several days as opposed to several hours)
      –Most common ages 7–12 years
    • Testicular trauma
      –Blunt trauma occurs as saddle injuries, in sports such as soccer and baseball, and during altercations
    • Epididymitis
      –Inflammation of the epididymis usually secondary to bacteria
      –Rare before puberty and often seen in sexually active young men with acutely swollen and painful testis
      –Pain is usually less acute in onset than torsion
      • Inguinal hernia
        –Incarcerated inguinal hernia may present as a painful, edematous scrotum
      • Orchitis
        –Inflammation of the testes due to viral infection; classically mumps
        –Patient presents with an acutely swollen, red testicle(s)
        –Uncommon since widespread vaccination
    • Henoch-Schönlein purpura
      –Vasculitis characterized by palpable purpura usually in the lower half of the body
      –Painful testicular swelling can be a sign of this disorder
      • Varicocele
        –A collection of dilated veins in the scrotum
        –Usually painless, but occasionally patients may complain of chronic nagging pain and discomfort (especially during physical activity)
        –Presents after puberty

      Workup and Diagnosis

      • History
        –History of trauma, viral symptoms, rash
        –Sexual history and history of STDs
        –Past medical history of similar episodes
      • Physical exam
        –With testicular torsion, the absence of the cremasteric reflex is one of the most characteristic features; the affected testis is also often higher and more horizontal than the contralateral testis
        –In epididymitis and orchitis, elevation of the testis improves the pain, and the cremasteric reflex is usually preserved
        –In torsion of the appendix testis, a bluish dot may be seen in the superior portion of the affected testis
        –A hernia often can be felt extending from the inguinal area into the scrotum
        –A varicocele is described as feeling like a “bag of worms,” and is best examined with the patient standing
      • Urinalysis
        –Normal in patients with torsion
        –Pyuria is a feature of epididymitis
      • Doppler ultrasound is indicated for patients in whom the physical exam is not diagnostic; it may be bypassed by the surgeon in the interest of time when the exam is very specific for testicular torsion

    » READ BOOK EXCERPT ONLINE »

    Source: In A Page: Pediatric Signs and Symptoms, 2007

    Asymmetric Limbs: Differential Diagnosis
    (In A Page: Pediatric Signs and Symptoms)

    • Physiologic: Left leg is often longer than right, and right arm is longer than left, though it is usually not noticeable
    • Disturbances of bone
      –Increased blood flow such as occurs in arthritis (infectious, inflammatory), neoplasms, or AVM
      –Premature closure of epiphysis occurs with infection, fracture, radiation therapy, JRA
      –Fracture may also result in malposition or malunion
      –Diaphyseal operations (bone grafts, osteotomy)
      –Developmental dysplasia of the hip
      –Coxa vara, tibia vara (Blount disease)
      –Hypoplastic bones (short femur)
      –Legg-Calvé-Perthes disease
      –SCFE
      –Syndromes such as Albright; Ollier disease; neurofibromatosis
      –Rickets
      • Hemihypertrophy
        –Idiopathic: May be associated with other anomalies involving GU tract, hemangiomas, mental retardation, and pigmented skin lesions
        –Associated with tumors: Wilms, adrenocortical, hepatoblastoma
        –Associated with dysmorphogenic syndromes: Beckwith-Wiedemann, Russell-Silver, Proteus
        –Associated with soft tissue abnormalities: Lymphedema, Klippel-Trenaunay-Weber syndrome
        • Neuromuscular disorders
          –Cerebral palsy
          –Poliomyelitis
          –Myelomeningocele
          –Peripheral neuropathy
          –Focal cerebral lesions (Sturge-Weber syndrome)
          –Stroke (due to coagulopathies, sickle cell disease)
      • Hemophilia (bleeding into a joint)
      • Reflex sympathetic dystrophy (RSD)
      • Congenital syphilis
      • Absence or hypoplasia of thumb and radius (Holt-Oram syndrome, TAR syndrome)

      Workup and Diagnosis

      • History
        –Past medical and surgical history
        –Constitutional symptoms (fever, fatigue, weight loss)
        –Family history of similar disorder
      • Physical exam
        –Joint exam should include erythema, warmth, swelling, hyperflexibility, decreased range of motion, tenderness including pain localized to bone
        –Leg-length discrepancy can be measured from symphysis pubis to lateral malleoli while patient is supine or by putting blocks of various thickness under the short leg until pelvis is leveled
        –Dysmorpic features, skin lesions
        –Neurologic exam for muscle weakness, decreased tone, reflexes, mental status
      • Labs
        –Infectious and inflammatory markers such as CBC, ESR, CRP, viral or bacterial titers and/or cultures; tumor markers; chromosomal analysis and genetic markers
        –Radiologic evaluation as indicated by history and physical exam to find abnormalities in any part of musculoskeletal system (lytic lesions, soft tissue and joint swelling)
        –Bone age
        –Leg lengths measured by teleoroentgenogram, orthoradiograph, scanogram, or CT

    » READ BOOK EXCERPT ONLINE »

    Source: In A Page: Pediatric Signs and Symptoms, 2007

    ABDOMINAL PAIN, GENERALIZED: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    If the onset is acute, a general surgeon should be consulted at the outset. Ominous signs include boardlike rigidity, rebound tenderness, and shock with nausea and vomiting. Hyperactive bowel sounds of a high-pitched tinkling character with distention and obstipation suggest intestinal obstruction. On the other hand, normal bowel sounds, little distention, good vital signs, and minimal tenderness suggest gastroenteritis or other diffuse irritation of the bowel.

    It is wise to pass a nasogastric tube and attach to suction and proceed with a CBC, urinalysis, an immediate flat plate and upright of the abdomen, chest x-ray, serum amylase and lipase levels, and chemistry panel. Sometimes, lateral decubitus films are necessary to reveal the stepladder pattern of intestinal obstruction. A pregnancy test should be ordered if age and gender dictates it.

    If these tests fail to confirm the clinical diagnosis and the patient’s condition is deteriorating, it is probably wise to proceed with an exploratory laparotomy immediately. If the patient’s condition is stable, one may order more diagnostic tests depending on the location of the pain and other symptoms and signs. For example, if the pain seems more localized to the RUQ, a gallbladder ultrasound or nuclear scan may be ordered. If it is still considered generalized, perhaps a CT scan of the abdomen and pelvis is indicated. Monitoring vital signs and doing repeated CBCs, serum amylase levels, and flat plates of the abdomen are useful in borderline cases.

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    Source: Differential Diagnosis in Primary Care, 2007

    LOW BACK PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    Our first priority in a patient who presents with low back pain is to rule out anything serious such as a herniated disc or cauda equina tumor. A pelvic and rectal examination must be performed to exclude a pelvic tumor or prostate carcinoma. A careful neurologic examination must be done. If one is too busy to do that, referral to an orthopedic surgeon or neurologist is indicated. The neurologic exam should include an SLR test, femoral stretch test, careful sensory examination, and an assessment for asymmetric reflexes. It is wise to carefully measure the thighs and calves to reveal muscular atrophy. Any findings to support a diagnosis of radiculopathy are a reasonable indication for a CT scan or MRI of the lumbar spine. However, it may be wise to have a neurologist or neurosurgeon examine the patient first because these tests are expensive.

    If the patient has normal neurologic, pelvic, and rectal examinations, it is perfectly legitimate to manage the patient conservatively for a while without any testing other than clinical. Close follow up is important in these cases, however. Should the pain persist despite rest and conservative treatment, a more thorough diagnostic workup is indicated regardless of the lack of objective findings. This will include plain films or CT scan and an arthritis panel.

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    Source: Differential Diagnosis in Primary Care, 2007

    ARM PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The association of other symptoms and signs found on a good history and physical examination is most important in pinpointing the diagnosis. Thus, arm pain with tenderness and limitation of motion at the elbow suggests tennis elbow, gout, or rheumatoid arthritis. Arm pain with loss of sensation in the distribution of the median nerve suggests carpal tunnel syndrome. Injection of lidocaine into bursa or trigger points may be diagnostic.

    The laboratory workup should include x-rays of the involved area and of the cervical spine, especially if there is a radicular distribution of the pain. If there are focal neurologic signs, a neurologist should be consulted before ordering an MRI: A cervical rib will not be missed in this way. An ECG and myocardial enzymes may be necessary to exclude a myocardial infarct, and an exercise tolerance test will help exclude coronary insufficiency. Arteriogram, phlebogram, lymphangiogram, electromyogram (EMG) with nerve conduction studies, myelogram, and nerve blocks will be necessary in specific cases.

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    Source: Differential Diagnosis in Primary Care, 2007

    BREAST PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The diagnosis of a painful breast is usually made by taking a careful history. What drugs are the patient taking? Associated symptoms and signs (see sections on bloody discharge, page 90 and swelling, page 92) are also important. A culture of the discharge, mammography, and serum, estrogen, and prolactin levels may be important, but referral to an endocrinologist is wise when the history does not provide a simple solution, especially when the pain is bilateral. Biopsy (frozen section) is necessary when tumor is suspected and mammography is equivocal, because faith in mammography has declined somewhat in recent years.

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    Source: Differential Diagnosis in Primary Care, 2007

    CHEST PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    A possible myocardial infarction must be the first consideration in all adults with acute chest pain especially if there are significant alterations of the vital signs. Consequently, serial ECGs, serial cardiac enzymes, and hospitalization will often be necessary. Once this condition has been excluded, we can turn our attention to the other possibilities. Arterial blood gases, chest x-ray, and a lung scan may be ordered to exclude a pulmonary embolism. Pulmonary angiography may be necessary in some cases. A chest x-ray may be ordered to rule out pneumonia. Acute chest pain related to esophagitis is often relieved by swallowing lidocaine viscus, an extremely useful tool in the differential diagnosis. Relief of the pain with nitroglycerin under the tongue or by spray will support the diagnosis of coronary insufficiency. Tenderness of the costochondral junctions with relief on lidocaine injection into the point of maximum tenderness suggests Tietze syndrome (costochondritis). In cases of chronic chest pain, an exercise tolerance test with thallium scan should be done to rule out coronary insufficiency or myocardial infarct. It may be wise to do immediate coronary angiography if the condition deteriorates so that balloon angiography, bypass surgery, or reperfusion therapy may be initiated. Dissecting aneurysm is revealed by CT scan or MRI of the chest.

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    Source: Differential Diagnosis in Primary Care, 2007

    ELBOW PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    In the approach to the diagnosis, the traumatic conditions and arthritic disorders will probably stand out. A diagnostic dilemma occurs when the elbow looks normal and has good movement. Nevertheless, most of these cases are caused by tennis elbow, myositis, and fasciitis. Thus, a simple injection at the trigger point will assist the diagnosis and give the patient immediate and sometimes lasting relief. If this is unsuccessful, referral to an orthopedic surgeon is wise.

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    Source: Differential Diagnosis in Primary Care, 2007

    EPIGASTRIC PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The approach to the diagnosis of midepigastric pain is identical to that for generalized abdominal pain (see page 22).

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    EYE PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The approach to the diagnosis of eye pain involves a careful search for inflammation of the various anatomic structures; then a drop or two of fluorescent dye is inserted and the cornea inspected for lacerations, herpes ulcers, and foreign bodies. Finally, tenometry may be done. Referral to an ophthalmologist is often necessary, but the astute clinician will want to x-ray the sinuses, ask about a history of migraine, do a visual field, and rule out systemic diseases beforehand.

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    Source: Differential Diagnosis in Primary Care, 2007

    FACIAL PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The approach to the diagnosis of face pain includes a careful history and physical with a good neurologic examination. The sinuses are transilluminated and x-rays may be performed. The teeth and occlusion are examined carefully and possibly x-rayed. A histamine test may be indicated. The busy physician may want to refer the patient to a neurologist immediately, but this will obviously take away the challenge.

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    Source: Differential Diagnosis in Primary Care, 2007

    FLANK PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The diagnosis of flank pain usually involves careful examination of the urine and a urine culture, an IVP, and plain films of the abdomen and spine. If these are negative, bone scans, arteriogram, and other tests listed below may be required. CT has eliminated the need for exploratory laparotomy in many cases.

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    Source: Differential Diagnosis in Primary Care, 2007

    GROIN PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    In the approach to the diagnosis of groin pain, a mass or tender structure is usually present in the groin. If the mass is a lymph node, careful examination of the genitalia and lower extremities will often show the cause, but a urethral or vaginal smear and culture may be necessary to show gonorrhea. Investigation of the genitourinary (GU) tract and the GI tract for causes of referred pain is then undertaken, if the mass is reducible a hernia is likely and referral to a surgeon is in order. Incarcerated hernias, of course, demand immediate referral.

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    Source: Differential Diagnosis in Primary Care, 2007

    HAND AND FINGER PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    In diagnosis, most of these conditions will be obvious on inspection. The difficulty arises when the hand looks normal. Then one must check for the following:

    1. Carpal tunnel syndrome by tapping the volar aspect of the wrist (Tinel sign)
    2. Brachial plexus neuralgia and scalenus anticus syndrome by Adson tests
    3. Causalgia by stellate ganglion block to see if pain is relieved
    4. Cervical spine disease by a roentgenogram, possibly a myelogram or MRI, and nerve blocks of the various roots. Referral to a neurologist is often necessary. In early rheumatoid arthritis, the joints may be normal on inspection but pain and stiffness of the hands and fingers in the morning is an excellent clue.

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    Source: Differential Diagnosis in Primary Care, 2007

    HIP PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The history and physical examination will allow differentiation of many of the conditions listed above. For example, the history of trauma suggests sprain, fracture, or contusion. Remember fractures of the hip can occur in the elderly without a history of trauma. A positive straight leg raising (SLR) test suggests a herniated disc or other cauda equina pathology. X-ray of hip and lumbosacral spine will help rule out fracture or osteoarthritis but CT scan, bone scan, or an MRI may be necessary. If x-rays and laboratory examinations are negative, a trial of lidocaine injections into the greater trochanter bursa or other trigger points may be diagnostic.

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    Source: Differential Diagnosis in Primary Care, 2007

    JOINT PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The approach to the diagnosis of joint pain includes a careful history and examination for other signs such as swelling, redness, and hyperthermia of the joints. If multiple joints are involved, look for rheumatoid arthritis, lupus, and osteoarthritis. Single joint involvement suggests gonorrhea, septic arthritis, tuberculosis, or gout, among other things. Small joints are involved more frequently in rheumatoid arthritis, Reiter syndrome, and lupus, although the large joints are more frequently involved in osteoarthritis, gonorrhea, tuberculosis, and other infections. Remember, however, that both osteoarthritis and gonorrhea may involve the small joints of the hands and feet. Rheumatic fever presents a migratory arthritis and this is a helpful differential point. When the knee joint is involved, the astute clinician will always examine for a torn or subluxated meniscus and loose cruciate or collateral ligaments. MRI or arthroscopy will pin down this diagnosis. Listed below are the most valuable diagnostic tests. Synovial fluid analysis for uric acid and calcium pyrophosphate, the character of the mucin clot, a white cell count, and culture can be done in the office and may make the diagnosis almost immediately. This may eliminate the need for hospitalization.

    A therapeutic trial of aspirin or colchicine is useful in diagnosing rheumatic fever and gout, respectively. If the joint fluid examination is nonspecific and no systemic signs of infection are evident, the injection of steroids into the joint is reasonable while the physician waits for the results of more sophisticated diagnostic tests.

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    Source: Differential Diagnosis in Primary Care, 2007

    Myoclonus: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    If the patient is stable, evaluate his level of consciousness (LOC) and mental status. Ask about the frequency, severity, location, and circumstances of myoclonus. Has he ever had a seizure? If so, did myoclonus precede it? Is myoclonus ever precipitated by a sensory stimulus? During the physical examination, check for muscle rigidity and wasting, and test deep tendon reflexes.

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Breast pain [Mastalgia]: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    Begin by asking the patient if breast pain is constant or intermittent. For either type, ask about onset and character. If it's intermittent, determine the relationship of pain to the phase of the menstrual cycle. Is the patient a nursing mother? If not, ask about any nipple discharge and have her describe it. Is she pregnant? Has she reached menopause? Has she recently experienced flulike symptoms or sustained injury to the breast? Has she noticed a change in breast shape or contour?

    Ask the patient to describe the pain. She may describe it as sticking, stinging, shooting, stabbing, throbbing, or burning. Determine if the pain affects one breast or both, and ask the patient to point to the painful area.

    Instruct the patient to place her arms at her sides, and inspect the breasts. Note their size, symmetry, and contour and the appearance of the skin. Remember that breast shape and size vary and that breasts normally change during menses, pregnancy, and lactation and with aging. Are the breasts red or edematous? Are the veins prominent?

    Note the size, shape, and symmetry of the nipples and areolae. Do you detect ecchymosis, a rash, ulceration, or a discharge? Do the nipples point in the same direction? Do you see signs of retraction, such as skin dimpling or nipple inversion or flattening? Repeat your inspection, first with the patient's arms raised above her head and then with her hands pressed against her hips.

    Palpate the breasts, first with the patient seated and then with her lying down and a pillow placed under her shoulder on the side being examined. Use the pads of your fingers to compress breast tissue against the chest wall. Proceed systematically from the sternum to the midline and from the axilla to the midline, noting any warmth, tenderness, nodules, masses, or irregularities. Palpate the nipple, noting tenderness and nodules, and check for discharge. Palpate axillary lymph nodes, noting any enlargement. (See Breast pain: Common causes and associated findings.)

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Seizures, absence: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    If you suspect a patient is having an absence seizure, evaluate its occurrence and duration by reciting a series of numbers and then asking him to repeat them after the attack ends. If the patient has had an absence seizure, he can’t do this. Alternatively, if the seizures are occurring within minutes of each other, ask the patient to count for about 5 minutes. He’ll stop counting during a seizure and resume when it’s over. Look for accompanying automatisms. Find out if the family has noticed a change in behavior or deteriorating schoolwork.

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Seizures, complex partial: History
    (Handbook of Signs & Symptoms (Third Edition))

    If you witness a complex partial seizure, never attempt to restrain the patient. Instead, lead him gently to a safe area. (Exception: Don’t approach him if he’s angry or violent.) Calmly encourage him to sit down, and remain with him until he’s fully alert. After the seizure, ask him if he experienced an aura. Record all observations and findings.

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Seizures, generalized tonic-clonic: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    If you didn’t witness the seizure, obtain a description from the patient’s companion. Ask when the seizure started and how long it lasted. Did the patient report unusual sensations before the seizure began? Did the seizure start in one area of the body and spread, or did it affect the entire body right away? Did the patient fall on a hard surface? Did his eyes or head turn? Did he turn blue? Did he lose bladder control? Did he have other seizures before recovering?

    If the patient may have sustained a head injury, observe him closely for loss of consciousness, unequal or nonreactive pupils, and focal neurologic signs. Does he complain of a headache and muscle soreness? Is he increasingly difficult to arouse when you check on him at 20-minute intervals? Examine his arms, legs, and face (including tongue) for injury, residual paralysis, or limb weakness.

    Next, obtain a history. Has the patient ever had generalized or focal seizures before? If so, do they occur frequently? Do other family members also have them? Is the patient receiving drug therapy? Is he compliant? Also, ask about sleep deprivation and emotional or physical stress at the time the seizure occurred.

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Seizures, simple partial: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    Make sure to record the patient’s seizure activity in detail; your data may be critical in locating the lesion in the brain. Does the patient turn his head and eyes? If so, to what side? Where does movement first start? Does it spread? Because a partial seizure may become generalized, you’ll need to watch closely for loss of consciousness, bilateral tonicity and clonicity, cyanosis, tongue biting, and urinary incontinence. (See “Seizures, generalized tonic-clonic,” page 554.)

    After the seizure, ask the patient to describe exactly what he remembers, if anything, about the seizure. Check the patient’s LOC, and test for residual deficits (such as weakness in the involved extremity) and sensory disturbances.

    Then obtain a history. Ask the patient what happened before the seizure. Can he describe an aura or did he recognize its onset? If so, how — by a smell, a visual disturbance, or a sound or visceral phenomenon such as an unusual sensation in his stomach? How does this seizure compare with others he has had?

    Also, explore fully any history — recent or remote — of head trauma. Check for a history of stroke or recent infection, especially with a fever, headache, or stiff neck.

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Abdominal pain: History and physical examination

    (Handbook of Signs & Symptoms (Third Edition))

    If the patient has no life-threatening signs or symptoms, take his history. Ask him if he has had this type of pain before. Have him describe the pain — for example dull, sharp, stabbing, or burning. Ask if anything relieves the pain or makes it worse. Ask the patient if the pain is constant or intermittent and when the pain began. Constant, steady abdominal pain suggests organ perforation, ischemia, or inflammation or blood in the peritoneal cavity. Intermittent, cramping abdominal pain suggests that the patient may have obstruction of a hollow organ.

    If pain is intermittent, find out the duration of a typical episode. In addition, ask the patient where the pain is located and if it radiates to other areas.

    Find out if movement, coughing, exertion, vomiting, eating, elimination, or walking worsens or relieves the pain. The patient may report abdominal pain as indigestion or gas pain, so have him describe it in detail.

    Ask the patient about substance abuse and any history of vascular, GI, GU, or reproductive disorders. Ask the female patient about the date of her last period, changes in her menstrual pattern, or dyspareunia.

    Ask the patient about appetite changes. Ask about the onset and frequency of nausea or vomiting. Find out about increased flatulence, constipation, diarrhea, and changes in stool consistency. When was the last bowel movement? Ask about urinary frequency, urgency, or pain. Is the urine cloudy or pink?

    Perform a physical examination. Take the patient’s vital signs, and assess skin turgor and mucous membranes. Inspect his abdomen for distention or visible peristaltic waves and, if indicated, measure his abdominal girth.

    Auscultate for bowel sounds and characterize their motility. Percuss all quadrants, noting the percussion sounds. Palpate the entire abdomen for masses, rigidity, and tenderness. Check for costovertebral angle (CVA) tenderness, abdominal tenderness with guarding, and rebound tenderness. (See Abdominal pain: Common causes and associated findings, pages 14 to 17.)

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Arm pain: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    If the patient reports arm pain after an injury, take a brief history of the injury from the patient. Then quickly assess him for severe injuries requiring immediate treatment. If you’ve ruled out severe injuries, check pulses, capillary refill time, sensation, and movement distal to the affected area because circulatory impairment or nerve injury may require immediate surgery. Inspect the arm for deformities, assess the level of pain, and immobilize the arm to prevent further injury.

    If the patient reports continuous or intermittent arm pain, ask him to describe it and to relate when it began. Is the pain associated with repetitive or specific movements or positions? Ask him to point out other painful areas because arm pain may be referred. For example, arm pain commonly accompanies the characteristic chest pain of myocardial infarction, and right shoulder pain may be referred from the right upper quadrant abdominal pain of cholecystitis. Ask the patient if the pain worsens in the morning or in the evening, if it prevents him from performing his job, and if it restricts movement. Also ask if heat, rest, or drugs relieve it. Finally, ask about preexisting illnesses, a family history of gout or arthritis, and current drug therapy.

    Next, perform a focused examination. Observe the way the patient walks, sits, and holds his arm. Inspect the entire arm, comparing it with the opposite arm for symmetry, movement, and muscle atrophy. (It’s important to know if the patient is right- or left-handed.) Palpate the entire arm for swelling, nodules, and tender areas. In both arms, compare active range of motion, muscle strength, and reflexes.

    If the patient reports numbness or tingling, check his sensation to vibration, temperature, and pinprick. Compare bilateral hand grasps and shoulder strength to detect weakness.

    If a patient has a cast, splint, or restrictive dressing, check for circulation, sensation, and mobility distal to the dressing. Ask the patient about edema and if the pain has worsened within the last 24 hours.

    Examine the neck for pain on motion, point tenderness, muscle spasms, or arm pain when the neck is extended with the head toward the involved side. (See Arm pain: Common causes and associated findings.)

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Back pain: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    If life-threatening causes of back pain are ruled out, continue with a complete history and physical examination. Be aware of the patient's expressions of pain as you do so. Obtain a medical history, including past injuries and illnesses, and a family history. Ask about diet and alcohol intake. Also, take a drug history, including past and present prescriptions and over-the-counter drugs.

    Next, perform a thorough physical examination. Observe skin color, especially in the patient's legs, and palpate skin temperature. Palpate femoral, popliteal, posterior tibial, and pedal pulses. Ask about unusual sensations in the legs, such as numbness and tingling. Observe the patient's posture if pain doesn't prohibit standing. Does he stand erect or tend to lean toward one side? Observe the level of the shoulders and pelvis and the curvature of the back. Ask the patient to bend forward, backward, and from side to side while you palpate for paravertebral muscle spasms. Note rotation of the spine on the trunk. Palpate the dorsolumbar spine for point tenderness. Then ask the patient to walk — first on his heels, then on his toes; protect him from falling as he does so. Weakness may reflect a muscular disorder or spinal nerve root irritation. Place the patient in a sitting position to evaluate and compare patellar tendon (knee), Achilles tendon, and Babinski's reflexes. Evaluate the strength of the extensor hallucis longus by asking the patient to hold up his big toe against resistance. Measure leg length and hamstring and quadriceps muscles bilaterally. Note a difference of more than ⅜" (1 cm) in muscle size, especially in the calf.

    To reproduce leg and back pain, position the patient in a supine position on the examining table. Grasp his heel and slowly lift his leg. If he feels pain, note its exact location and the angle between the table and his leg when it occurs. Repeat this maneuver with the opposite leg. Pain along the sciatic nerve may indicate disk herniation or sciatica. Also, note the range of motion of the hip and knee.

    Palpate the flanks and percuss with the fingertips or perform fist percussion to elicit costovertebral angle tenderness.

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Chest pain: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    If the chest pain isn't severe, proceed with the history. Ask if the patient feels diffuse pain or can point to the painful area. Sometimes a patient won't perceive the sensation he's feeling as pain, so ask whether he has any discomfort radiating to his neck, jaw, arms, or back. If he does, ask him to describe it. Is it a dull, aching, pressurelike sensation? A sharp, stabbing, knifelike pain? Does he feel it on the surface or deep inside? Find out whether it's constant or intermittent. If it's intermittent, how long does it last? Ask if movement, exertion, breathing, position changes, or eating certain foods worsens or helps relieve the pain. Does anything in particular seem to bring it on?

    Review the patient's history for cardiac or pulmonary disease, chest trauma, intestinal disease, or sickle cell anemia. Find out which medications he's taking, if any, and ask about recent dosage or schedule changes.

    Take the patient's vital signs, noting tachypnea, fever, tachycardia, oxygen saturation, paradoxical pulse, and hypertension or hypotension. Also, look for jugular vein distention and peripheral edema. Observe the patient's breathing pattern, and inspect his chest for asymmetrical expansion. Auscultate his lungs for pleural friction rub, crackles, rhonchi, wheezing, or diminished or absent breath sounds. Next, auscultate for murmurs, clicks, gallops, or pericardial friction rub. Palpate for lifts, heaves, thrills, gallops, tactile fremitus, and abdominal masses or tenderness. (See Chest pain: Common causes and associated findings, pages 136 and 137.)

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Eye pain: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    If the patient's eye pain doesn't result from a chemical burn, take a complete history. Have the patient describe the pain fully. Is it an ache or a sharp pain? How long does it last? Is it accompanied by burning, itching, or discharge? Find out when it began. Is it worse in the morning or late in the evening? Ask about recent trauma or surgery, especially if the patient complains of sudden, severe pain. Does he have headaches? If so, find out how often and at what time of day they occur.

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Flank pain: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    If the patient’s condition isn’t critical, take a thorough history. Ask about the pain’s onset and apparent precipitating events. Have him describe the pain’s location, intensity, pattern, and duration. Find out if anything aggravates or alleviates it.

    Ask the patient about changes in his normal pattern of fluid intake and urine output. Explore his history for a urinary tract infection (UTI) or obstruction, renal disease, or recent streptococcal infection.

    During the physical examination, palpate the patient’s flank area and percuss the CVA to determine the extent of pain.

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Jaw pain: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    Begin the patient history by asking him to describe the pain’s character, intensity, and frequency. When did he first notice the jaw pain? Where on the jaw does he feel pain? Does the pain radiate to other areas? Sharp or burning pain arises from the skin or subcutaneous tissues. Causalgia, an intense burning sensation, usually results from damage to the fifth cranial, or trigeminal, nerve. This type of superficial pain is easily localized, unlike dull, aching, boring, or throbbing pain, which originates in muscle, bone, or joints. Also ask about aggravating or alleviating factors.

    Ask about recent trauma, surgery, or procedures, especially dental work. Ask about associated signs and symptoms, such as joint or chest pain, dyspnea, palpitations, fatigue, a headache, malaise, anorexia, weight loss, intermittent claudication, diplopia, and hearing loss. (Keep in mind that jaw pain may accompany more characteristic signs and symptoms of life-threatening disorders such as chest pain in a patient with an MI.)

    Focus your physical examination on the jaw. Inspect the painful area for redness, and palpate for edema or warmth. Facing the patient directly, look for facial asymmetry indicating swelling. Check the TMJs by placing your fingertips just anterior to the external auditory meatus and asking the patient to open and close, and to thrust out and retract his jaw. Note the presence of crepitus, an abnormal scraping or grinding sensation in the joint. (Clicks heard when the jaw is widely spread apart are normal.) How wide can the patient open his mouth? Less than 1 ⅛" (3 cm) or more than 2⅜"  (6 cm) between the upper and lower teeth is abnormal. Next, palpate the parotid area for pain and swelling, and inspect and palpate the oral cavity for lesions, elevation of the tongue, or masses.

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Neck pain: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    If the patient hasn’t sustained trauma, find out the severity and onset of his neck pain. Where specifically in the neck does he feel pain? Does anything relieve or worsen the pain? Is there any particular event that precipitates the pain? Also, ask about the development of other symptoms such as headaches. Next, focus on the patient’s current and past illnesses and injuries, diet, drug history, and family health history.

    Thoroughly inspect the patient’s neck, shoulders, and cervical spine for swelling, masses, erythema, and ecchymoses. Assess active range of motion in his neck by having him perform flexion, extension, rotation, and lateral side bending. Note the degree of pain produced by these movements. Examine his posture, and test and compare bilateral muscle strength. Check the sensation in his arms, and assess his hand grasp and arm reflexes. Attempt to elicit Brudzinski’s and Kernig’s signs if there isn’t a history of neck trauma, and palpate the cervical lymph nodes for enlargement. (See Neck pain: Common causes and associated findings, pages 432 and 433.)

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Rectal pain: History and physical examination
    (Handbook of Signs & Symptoms (Third Edition))

    If the patient reports rectal pain, inspect the area for bleeding; abnormal drainage, such as pus; or protrusions, such as skin tags or thrombosed hemorrhoids. Also, check for inflammation and other lesions. A rectal examination may be necessary.

    After the examination, proceed with your evaluation by taking the patient’s history. Ask him to describe the pain. Is it sharp or dull, burning or knifelike? How often does it occur? Ask if the pain is worse during or immediately after defecation. Does the patient avoid having bowel movements because of anticipated pain? Find out what alleviates the pain.

    Make sure to ask appropriate questions about the development of associated signs and symptoms. For example, does the patient experience bleeding along with rectal pain? If so, find out how frequently this occurs and whether the blood appears on the toilet tissue, on the surface of the stool, or in the toilet bowl. Is the blood bright or dark red? Also, ask whether the patient has noticed other drainage, such as mucus or pus, and whether he’s experiencing constipation or diarrhea. Ask when he last had a bowel movement. Obtain a dietary history.

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    Source: Handbook of Signs & Symptoms (Third Edition), 2006

    Complex regional pain syndrome: Diagnosis
    (Professional Guide to Diseases (Eighth Edition))

    There’s no laboratory test for CRPS, so the diagnosis is based on the patient’s history and clinical findings. A history of injury to an extremity may point to CRPS. Bone X-rays may aid in ruling out other conditions, such as osteomyelitis and stress fractures, which cause similar signs and symptoms. Additional tests may include bone scans, nerve conduction studies, and thermography (a test to show temperature changes and lack of blood supply in the painful area of the affected limb). With early diagnosis, prognosis improves.

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    Source: Professional Guide to Diseases (Eighth Edition), 2005

    Pain disorder: Diagnosis
    (Professional Guide to Diseases (Eighth Edition))

    For characteristic findings in patients with this condition, see Diagnosing pain disorder, page 476.

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    Source: Professional Guide to Diseases (Eighth Edition), 2005

    Myoclonus: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    If the patient is stable, evaluate level of consciousness and mental status. Ask about the frequency, severity, location, and circumstances of the myoclonus. Has he ever had a seizure? If so, did myoclonus precede it? Is the myoclonus ever precipitated by a sensory stimulus? During the physical examination, check for muscle rigidity and wasting, and test deep tendon reflexes.

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Breast pain [Mastalgia]: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    Begin by asking the patient if breast pain is constant or intermittent. For either type, ask about onset and character. If it’s intermittent, determine the relationship of pain to the phase of the menstrual cycle. Is the patient a breast-feeding mother? If not, ask about any nipple discharge and have her describe it. Is she pregnant? Has she reached menopause? Has she recently experienced any flulike symptoms or sustained an injury to the breast? Has she noticed any change in breast shape or contour?

    Ask your patient to describe the pain. She may describe it as sticking, stinging, shooting, stabbing, throbbing, or burning. Determine if the pain affects one breast or both, and ask the patient to point to the painful area.

    Instruct the patient to place her arms at her sides, and inspect the breasts. Note their size, symmetry, and contour and the appearance of the skin. Remember that breast shape and size vary and that breasts normally change during menses, pregnancy, and lactation and with aging. Are the breasts red or edematous? Are the veins prominent?

    Note the size, shape, and symmetry of the nipples and areolae. Do you detect ecchymosis, a rash, ulceration, or a discharge? Do the nipples point in the same direction? Do you see signs of retraction, such as skin dimpling or nipple inversion or flattening? Repeat your inspection, first with the patient’s arms raised above her head and then with her hands pressed against her hips.

    Palpate the breasts, first with the patient seated and then with her lying down and a pillow placed under her shoulder on the side being examined. Use the pads of your fingers to compress breast tissue against the chest wall. Proceed systematically from the sternum to the midline and from the axilla to the midline, noting any warmth, tenderness, nodules, masses, or irregularities. Palpate the nipple, noting tenderness and nodules, and check for discharge. Palpate axillary lymph nodes, noting any enlargement. (See Breast pain: Causes and associated findings, page 134.)

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Eye pain [Ophthalmalgia]: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    If the patient’s eye pain doesn’t result from a chemical burn or from acute angle-closure glaucoma, take a complete history. Have the patient describe the pain fully. Is it an ache or a sharp pain? How long does it last? Is it accompanied by burning, itching, or a discharge? Find out when it began. Is it worse in the morning or late in the evening? Ask about recent trauma or surgery, especially if the patient complains of severe pain that developed suddenly. Does he have headaches? If so, find out how often and at what time of day they occur.

    During the physical examination, don’t manipulate the eye if you suspect trauma. Carefully assess the eyelids and conjunctivae for redness, inflammation, and swelling. Then examine the eyes for ptosis or exophthalmos. Finally, test visual acuity with and without correction, and assess extraocular movements. Characterize any discharge. (See Examining the external eye, page 322.)

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Seizures, absence: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    If you suspect a patient is having an absence seizure, evaluate its occurrence and duration by reciting a series of numbers and then asking him to repeat them after the attack ends. If the patient has had an absence seizure, he’ll be unable to do this. Alternatively, if the seizures are occurring within minutes of each other, ask the patient to count for about 5 minutes. He’ll stop counting during a seizure and resume when it’s over. Look for accompanying automatisms. Find out if the family has noticed a change in behavior or deteriorating schoolwork.

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Seizures, complex partial: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    If you witness a complex partial seizure, never attempt to restrain the patient. Instead, lead him gently to a safe area. (Exception: Don’t approach him if he’s angry or violent.) Calmly encourage him to sit down, and remain with him until he’s fully alert. After the seizure, ask him if he experienced an aura. Record all observations and findings.

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Seizures, generalized tonic-clonic: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    If you didn’t witness the seizure, obtain a description from the patient’s companion. Ask when the seizure started and how long it lasted. Did the patient report any unusual sensations before the seizure began? Did the seizure start in one area of the body and spread, or did it affect the entire body right away? Did the patient fall on a hard surface? Did his eyes or head turn? Did he turn blue? Did he lose bladder control? Did he have any other seizures before recovering?

    If the patient may have sustained a head injury, observe him closely for loss of consciousness, unequal or nonreactive pupils, and focal neurologic signs. Does he complain of headache and muscle soreness? Is he increasingly difficult to arouse when you check on him at 20-minute intervals? Examine his arms, legs, and face (including tongue) for injury, residual paralysis, or limb weakness.

    Next, obtain a history. Has the patient ever had generalized or focal seizures before? If so, do they occur frequently? Do other family members also have them? Is the patient receiving drug therapy? Is he compliant? Ask about sleep deprivation and emotional or physical stress at the time the seizure occurred.

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Seizures, simple partial: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    Be sure to record the patient’s seizure activity in detail; your data may be critical in locating the lesion in the brain. Does the patient turn his head and eyes? If so, to what side? Where does movement first start? Does it spread? Because a partial seizure may become generalized, you’ll need to watch closely for loss of consciousness, bilateral tonicity and clonicity, cyanosis, tongue biting, and urinary incontinence. (See “Seizures, generalized tonic-clonic,” page 708.)

    After the seizure, ask the patient to describe exactly what he remembers, if anything, about the seizure. Check the patient’s LOC, and test for residual deficits (such as weakness in the involved extremity) and sensory disturbances.

    Then obtain a history. Ask the patient what happened before the seizure. Can he describe an aura or did he recognize its onset? If so, how—by a smell, a visual disturbance, or a sound or visceral phenomenon, such as an unusual sensation in his stomach? How does this seizure compare with others he has had?

    Explore fully any history, recent or remote, of head trauma. Check for a history of stroke or recent infection, especially with fever, headache, or a stiff neck.

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Abdominal pain: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    If the patient has no life-threatening signs or symptoms, take his history. Ask him if he has had this type of pain before. Have him describe the pain—for example, is it dull, sharp, stabbing, or burning? Ask if anything relieves the pain or makes it worse. Ask the patient if the pain is constant or intermittent and when the pain began. Constant, steady abdominal pain suggests organ perforation, ischemia, or inflammation or blood in the peritoneal cavity. Intermittent, cramping abdominal pain suggests the patient may have an obstruction of a hollow organ.

    If pain is intermittent, find out the duration of a typical episode. In addition, ask the patient where the pain is located and if it radiates to other areas.

    Find out if movement, coughing, exertion, vomiting, eating, elimination, or walking worsens or relieves the pain. The patient may report abdominal pain as indigestion or gas pain, so have him describe it in detail.

    Ask the patient about substance abuse and any history of vascular, GI, GU, or reproductive disorders. Ask the female patient the date of her last menses and if she has had changes in her menstrual pattern or dyspareunia.

    Also ask about appetite changes and the onset and frequency of nausea or vomiting. Find out about increased flatulence, constipation, diarrhea, and changes in stool consistency. When was his last bowel movement? Ask about urinary frequency, urgency, or pain. Is the urine cloudy or pink?

    Perform a physical examination. Take the patient’s vital signs, and assess skin turgor and mucous membranes. Inspect his abdomen for distention or visible peristaltic waves and, if indicated, measure his abdominal girth.

    Auscultate for bowel sounds and characterize their motility. Percuss all quadrants, noting the percussion sounds. Palpate the entire abdomen for masses, rigidity, and tenderness. Check for costovertebral angle (CVA) tenderness, abdominal tenderness with guarding, and rebound tenderness. (See Abdominal pain: Causes and associated findings, pages 16 to 21.)

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Arm pain: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    If the patient reports arm pain after an injury, take a brief history of the injury from the patient. Then quickly assess him for severe injuries requiring immediate treatment. If you’ve ruled out severe injuries, check pulses, capillary refill time, sensation, and movement distal to the affected area because circulatory impairment or nerve injury may require immediate surgery. Inspect the arm for deformities, assess the level of pain, and immobilize the arm to prevent further injury.

    If the patient reports continuous or intermittent arm pain, ask him to describe it and to relate when it began. Is the pain associated with repetitive or specific movements or positions? Ask him to point out other painful areas because arm pain may be referred. For example, arm pain commonly accompanies the characteristic chest pain of myocardial infarction, and right shoulder pain may be referred from the right-upper-quadrant abdominal pain of cholecystitis. Ask the patient if the pain worsens in the morning or in the evening, if it prevents him from performing his job, and if it restricts any movements. Also ask if heat, rest, or drugs relieve it. Finally, ask about any preexisting illnesses, a family history of gout or arthritis, and current drug therapy.

    Next, perform a focused examination. Observe the way the patient walks, sits, and holds his arm. Inspect the entire arm, comparing it with the opposite arm for symmetry, movement, and muscle atrophy. (It’s important to know if the patient is right- or left-handed.) Palpate the entire arm for swelling, nodules, and tender areas. In both arms, compare active range of motion, muscle strength, and reflexes.

    If the patient reports numbness or tingling, check his sensation to vibration, temperature, and pinprick. Compare bilateral hand grasps and shoulder strength to detect weakness.

    If the patient has a cast, splint, or restrictive dressing, check for circulation, sensation, and mobility distal to the dressing. Ask the patient about edema and if the pain has worsened within the last 24 hours.

    Examine the neck for pain on motion, point tenderness, muscle spasms, or arm pain when the neck is extended with the head toward the involved side. (See Arm pain: Causes and associate findings.)

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Back pain: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    If life-threatening causes of back pain are ruled out, continue with a complete history and physical examination. Be aware of the patient’s expressions of pain as you do so. Obtain a medical history, including past injuries and illnesses, and a family history. Ask about diet and alcohol intake. Also, take a drug history, including past and present prescription and over-the-counter drugs.

    Next, perform a thorough physical examination. Observe skin color, especially in the patient’s legs, and palpate skin temperature. Palpate femoral, popliteal, posterior tibial, and pedal pulses. Ask about unusual sensations in the legs, such as numbness and tingling. Observe the patient’s posture if pain doesn’t prohibit standing. Does he stand erect or tend to lean toward one side? Observe the level of the shoulders and pelvis and the curvature of the back. Ask the patient to bend forward, backward, and from side to side while you palpate for paravertebral muscle spasms. Note rotation of the spine on the trunk. Palpate the dorsolumbar spine for point tenderness. Then ask the patient to walk—first on his heels, then on his toes; protect him from falling as he does so. Weakness may reflect a muscular disorder or spinal nerve root irritation. Place the patient in a sitting position to evaluate and compare patellar tendon (knee), Achilles tendon, and Babinski’s reflexes. Evaluate the strength of the extensor hallucis longus by asking the patient to hold up his big toe against resistance. Measure leg length and hamstring and quadriceps muscles bilaterally. Note a difference of more than ⅜” (1 cm) in muscle size, especially in the calf.

    To reproduce leg and back pain, place the patient in a supine position on the examining table. Grasp his heel and slowly lift his leg. If he feels pain, note its exact location and the angle between the table and his leg when it occurs. Repeat this maneuver with the opposite leg. Pain along the sciatic nerve may indicate disk herniation or sciatica. Also, note the range of motion of the hip and knee.

    Palpate the flanks and percuss with the fingertips or perform fist percussion to elicit costovertebral angle tenderness.

    » READ BOOK EXCERPT ONLINE »

    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Chest pain: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    If the chest pain isn’t severe, proceed with the history. Ask if the patient feels diffuse pain or can point to the painful area. Sometimes a patient won’t perceive the sensation he’s feeling as pain, so ask whether he has any discomfort radiating to his neck, jaw, arms, or back. If he does, ask him to describe it. Is it a dull, aching, pressurelike sensation? A sharp, stabbing, knifelike pain? Does he feel it on the surface or deep inside? Find out whether it’s constant or intermittent. If it’s intermittent, how long does it last? Ask if movement, exertion, breathing, position changes, or eating certain foods worsens or helps relieve the pain. Does anything in particular seem to bring it on?

    Review the patient’s history for cardiac or pulmonary disease, chest trauma, intestinal disease, or sickle cell anemia. Find out which medications he’s taking, if any, and ask about recent dosage or schedule changes.

    Take the patient’s vital signs, noting tachypnea, fever, tachycardia, oxygen saturation, paradoxical pulse, and hypertension or hypotension. Also, look for jugular vein distention and peripheral edema. Observe the patient’s breathing pattern, and inspect his chest for asymmetrical expansion. Auscultate his lungs for pleural friction rub, crackles, rhonchi, wheezing, and diminished or absent breath sounds. Next, auscultate for murmurs, clicks, gallops, and pericardial friction rub. Palpate for lifts, heaves, thrills, gallops, tactile fremitus, and abdominal masses or tenderness. (See Chest pain: Causes and associated findings, pages 164 to 167.)

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Facial pain: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    Begin by characterizing the patient’s facial pain. Is it stabbing, throbbing, or dull? When did it begin? How long has it lasted? What relieves or worsens it? Ask the patient to point to the painful area. If facial pain is recurrent, have him describe a typical episode. Review his medical and dental history, noting especially previous head trauma, dental disease, and infection.

    Carefully examine the face and head. Inspect the ear for vesicles and changes in the tympanic membrane to rule out referred ear pain. Inspect the nose for deformity or asymmetry. Evaluate the condition of the mucous membranes and septum as well as the size and shape of the turbinates. Characterize any secretions. Palpate the frontal, ethmoid, and maxillary sinuses for tenderness and swelling.

    Evaluate oral hygiene by inspecting the teeth for caries, percussing any diseased teeth for pain, and asking the patient about any sensitivity to hot, cold, or sweet liquids or foods. Have him open and close his mouth as you palpate the temporomandibular joint for tenderness, spasm, locking, and crepitus.

    Examine the function of cranial nerves V and VII. To evaluate cranial nerve V, instruct the patient to clench his teeth. Then palpate the temporal and masseter muscles and evaluate muscle contraction. Test pain and sensation on his forehead, cheeks, and jaw. Next, test the corneal reflex by lightly touching the cornea with a piece of cotton.

    To evaluate cranial nerve VII, inspect the face for symmetry and then have the patient perform facial movements that demonstrate facial muscle strength—raising his eyebrows, frowning, showing his teeth, closing his eyes tightly, and wrinkling his nose. (See Major nerve pathways of the face.)

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Flank pain: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    If the patient’s condition isn’t critical, take a thorough history. Ask about the pain’s onset and apparent precipitating events. Have him describe the pain’s location, intensity, pattern, and duration. Find out if anything aggravates or alleviates it.

    Ask the patient about any changes in his normal pattern of fluid intake and urine output. Explore his history for urinary tract infection (UTI) or obstruction, renal disease, or recent streptococcal infection.

    During the physical examination, palpate the patient’s flank area and percuss the CVA to determine the extent of pain.

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Jaw pain: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    Begin the patient history by asking the patient to describe the pain’s character, intensity, and frequency. When did he first notice the jaw pain? Where on the jaw does he feel pain? Does the pain radiate to other areas? Sharp or burning pain arises from the skin or subcutaneous tissues. Causalgia, an intense burning sensation, usually results from damage to the fifth cranial, or trigeminal, nerve. This type of superficial pain is easily localized, unlike dull, aching, boring, or throbbing pain, which originates in muscle, bone, or joints. Also ask about aggravating or alleviating factors.

    Ask about recent trauma, surgery, or procedures, especially dental work. Ask about associated signs and symptoms, such as joint or chest pain, dyspnea, palpitations, fatigue, headache, malaise, anorexia, weight loss, intermittent claudication, diplopia, and hearing loss. (Keep in mind that jaw pain may accompany more characteristic signs and symptoms of life-threatening disorders, such as chest pain in a patient with an MI.)

    Focus your physical examination on the jaw. Inspect the painful area for redness, and palpate for edema or warmth. Facing the patient directly, look for facial asymmetry indicating swelling. Check the TMJs by placing your fingertips just anterior to the external auditory meatus and asking the patient to open and close, and to thrust out and retract his jaw. Note the presence of crepitus, an abnormal scraping or grinding sensation in the joint. (Clicks heard when the jaw is widely spread apart are normal.) How wide can the patient open his mouth? Less than 1 ⅛” (3 cm) or more than 2⅜” (6 cm) between upper and lower teeth is abnormal. Next, palpate the parotid area for pain and swelling, and inspect and palpate the oral cavity for lesions, elevation of the tongue, or masses.

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Neck pain: History and physical examination
    (Professional Guide to Signs & Symptoms (Fifth Edition))

    If the patient hasn’t sustained trauma, find out the severity and onset of his neck pain. Where specifically in the neck does he feel pain? Does anything relieve or worsen the pain? Is there any particular event that precipitates the pain? Also, ask about the development of other symptoms such as headaches. Next, focus on the patient’s current and past illnesses and injuries, diet, drug history, and family health history.

    Thoroughly inspect the patient’s neck, shoulders, and cervical spine for swelling, masses, erythema, and ecchymoses. Assess active range of motion in his neck by having him perform flexion, extension, rotation, and lateral side bending. Note the degree of pain produced by these movements. Examine his posture, and test and compare bilateral muscle strength. Check the sensation in his arms, and assess his hand grasp and arm reflexes. Attempt to elicit Brudzinski’s and Kernig’s signs if there is not a history of neck trauma, and palpate the cervical lymph nodes for enlargement. (See Neck pain: Causes and associated findings, pages 548 to 551.)

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    Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

    Seizures: History.
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

    Seizures can be confused with migraines and syncope.

    A. Characteristics of the seizure

    1. What was witnessed? Does the patient fall? Is there urinary or fecal incontinence, tongue biting, or loss of consciousness? Is there a postictal period? Is there staring, lip smacking, or automatisms? Seizure activity in neonates may present with subtle activities such as apnea, tremors, grimacing, or spasms.

     2. What can the patient remember? Are there associated sensations (odors, lights, emotions, tactile input)? Is there an aura?

     3. At what age was seizure onset? What is the frequency of the spells?

    4. What is the setting? Is there evidence supporting anoxia or hypoxia? Was there a sudden rise in temperature (4)? Did the seizure follow flashing lights, exercise, sleeplessness, fasting, or menses?

    5. Red flags include adult age at onset, changing pattern, and regression of motor skills.

     B. Chronology of the seizure. Most seizures present a characteristic pattern. A pattern of change or worsening of seizures can indicate new causation.

     C. Family history. Febrile, myoclonic, primary idiopathic seizures, and genetic syndromes with seizures often present a familial pattern.

     D. Psychosocial aspects. Ask how the family, teachers, employers interact with the patient.

     E. Other information. Important data include use of alcohol or drugs, medications that lower seizure threshold, toxic occupational or recreational chemicals, and severe physical [previous head trauma, central nervous system (CNS) infection, chronic illness] or psychosocial stressors.

    Physical examination (PE)

    A. Focused neurologic examination. Examine level of consciousness, pupils, fundi, cranial nerves, reflexes, gait, muscle strength, general sensory, coordination, and Romberg’s sign (4). Look for abnormal motor activity and test for abnormal reflexes.

    B. Additional PE

     1. Look for signs of systemic illness: cardiac disease (cyanosis, pallor, irregular rhythm, cool extremities) and chronic alcoholism (ascites, jaundice, caput medusae, and bruising).

     2. Look for residual signs of trauma or limb asymmetry.

    3. Look for dysmorphic manifestations of heritable disease: vascular malformations (Sturge–Weber), adenoma sebaceum (tuberous sclerosis), or café au lait spots and subcutaneous nodules (neurofibromatosis).

    4. Gingival hypertrophy suggests phenytoin therapy.

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Chest Pain, Atypical: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

    A. Characteristics of the chest pain. Important questions to ask: What is the quality of pain? Where is it located? What is its duration and intensity? What symptoms accompany the pain? Does anything trigger the chest pain or make the pain better or worse? Is there any relationship between exertion and the pain?

     B. Determining the likelihood of ischemic heart disease. Four major features in the initial history and physical examination can be used to determine the likelihood of IHD. They are in order of importance:

     1. Angina description (definite angina, probable angina, probably not angina, and not angina).

     2. Prior myocardial infarction [by history, or electrocardiographic (EKG) findings].

    3. Age (risk of IHD increases with age).

    4. Number of risk factors (e.g., diabetes, smoking, hypercholesterolemia, and hypertension).

     C. Features suggesting nonanginal pain. Features suggesting nonanginal pain include pleuritic pain (sharp or knifelike pain brought on by respiratory movements or cough), pain localized with one finger, pain reproduced by movement or palpation of the chest wall or arms, constant pain lasting for days, and very brief episodes of pain lasting a few seconds (1).

     D. Other key considerations. Key considerations in the history include the following:

    1. All presentations of chest pain should be taken seriously until proven to be benign.

    2. The description of pain can be greatly influenced by socioeconomic status, education, culture, and personality.

    3. A review of cardiac risk factors is appropriate for all patients who present with chest pain.

    4. Red flags suggesting a noncardiac, life-threatening condition include tachypnea, dyspnea, and hypoxemia.

    5. Sharp, stabbing, or pleuritic qualities do not completely exclude an ischemic cause (Chapter 8.5). In the Multicenter Chest Pain Study, IHD was diagnosed in 22% of patients coming to the emergency room with a sharp quality pain (2).

    Physical examination

    No reliable physical signs can be used to determine whether a patient with atypical chest pain has ischemic heart disease. The main purpose of the examination is to assess the patient for evidence of complications from atherosclerotic disease (e.g., peripheral vascular disease, cerebrovascular disease, and congestive heart failure). Pay attention to findings on the vascular examination (e.g., peripheral artery bruits, retinal arteriolar changes, the presence of a cardiac gallop) and for signs of the consequences of diminished myocardial contractility (e.g., lower extremity edema or pulmonary crackles) (Chapter 7.5).

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Chest Pain, Substernal: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

    A. Characteristics of pain in stable angina

     1. Quality. The pain of angina pectoris is often not described as a pain at all. Instead, it is frequently referred to as a squeezing, heaviness, or pressure sensation lasting 5 to 10 minutes. Diaphoresis, dyspnea, nausea, and vomiting often accompany the discomfort. Pain that is sharp, stabbing (especially if exacerbated by deep inspiration), pain reproducible with chest wall palpation, and pain lasting seconds or days to weeks is less likely to be from CAD.

     2. Location. Generally, angina is poorly localized in the retrosternal area, anterior chest, or epigastrium and typically radiates to the left arm, neck, or jaw.

     3. Precipitating and alleviating factors. Angina is often precipitated by conditions that increase myocardial oxygen demand, most commonly physical exertion, emotional stress, or cold weather. It is relieved promptly with rest or sublingual nitroglycerin.

     B. Characteristics of pain in unstable angina. According to the clinical practice guidelines recently developed by the Agency for Health Care Policy (1), unstable angina is defined as:

    1. Angina at rest lasting greater than 20 minutes.

     2. New onset angina (< 2 months) precipitated by walking one to two blocks or by climbing one flight of stairs at a normal pace.

     3. Angina that is more frequent, longer in duration, or occurring at a lower threshold.

    C. Risk factors. The Framingham Heart Study along with numerous other large epidemiologic studies has established the following risk factors for   CAD (2):

    1. Sex and age: men aged 45 years or older; women aged 55 years or older; women with premature menopause without hormone replacement.

    2. Family history: MI or sudden death occurring in a first-degree male relative aged 55 years or younger or in a first-degree female relative aged 65 years or younger.

    3. Smoking: in men who smoke one pack per day, a three- to fivefold risk for CAD compared with nonsmokers. Those who quit smoking can reach the same risk level of nonsmokers within 2 years of stopping.

    4. Hypertension: blood pressure greater or equal to 140/90 (Chapter 7.8).

    5. Cholesterol: total cholesterol greater than 200; low-density lipoprotein (LDL) greater than 130; high-density lipoprotein (HDL) less than 35. An HDL level above 60 is protective.

    6. Diabetes mellitus: a twofold increase in CAD, compared with nondiabetics (Chapter 14.1).

    Physical examination

     A. Focused physical examination. This should include vital signs (notably blood pressure). During a symptomatic episode, the finding of a mitral regurgitation murmur, S3 or S4 gallop, bruits or precordial lift all suggest a high likelihood of CAD. Findings of xanthelasma, tendinous xanthomata, tobacco-stained teeth and fingernails, and decreased or asymmetrical peripheral pulses indicate the likely presence of cardiac risk factors. >

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Low Back Pain: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

     The history should include evaluation for “red flag” conditions.

    A. Pain characteristics. Assess the nature of the pain, along with the onset and duration of the symptom. Is there any radiating pain, leg weakness, or paresthesia? Pseudoclaudication is suggestive of spinal stenosis. Pain radiating below the knee is more likely to be a true radiculopathy (1). Nerve root compression is highly unlikely without sciatic pain (1). Was the onset after a traumatic event? A seemingly insignificant episode (e.g., a minor fall) may be a “red flag” for fracture in an elderly patient. Are there alleviating or exacerbating factors? Does the pain limit the patient physically or socially? Is there a history of previous back problems or back surgery?

    B. Review of systems. Look for associated symptoms that can indicate a “red flag” condition or an underlying medical cause. Gastrointestinal and genitourinary symptoms are particularly important, especially incontinence (Chapter 10.10).

     C. Psychosocial information. Has the patient initiated any new activities? If work-related, assess typical job tasks. Investigate whether the back pain could have any relationship, sexual, or mood implications. Sexual activity can be severely affected simply because of pain, but sexual dysfunction can also result from neurologic abnormalities associated with the cause of the back pain. Back pain is associated with depression and poor sleep patterns. Drug-seeking behavior may be exhibited along with a complaint of back pain. Addiction may have resulted from former or on-going treatment of the pain. Legal issues can complicate the diagnosis and treatment of back pain. Ask the patient whether litigation involving the back pain is under consideration.

    Physical examination

    Evaluation should be both general and specific. It is prudent to leave the potentially most painful parts of the examination to the end.

     A. General. Examination includes auscultation of the heart and assessment of peripheral pulses and blood pressure. Abdominal examination should focus on possible causes of back pain (Table 12.5). Assess gait.

     B. Neurologic. The lower extremity examination includes motor strength, deep tendon reflexes, sensation, proprioception, and certain functional maneuvers (Table 12.6). Romberg and Babinski reflexes should also be assessed. Rectal examination should assess sphincter tone, which can be compromised in sacral root dysfunction. In the primary care setting, most clinically significant disc herniations will be detected by the following limited examination: dorsiflexion of the great toe and ankle, Achilles reflex, light touch sensation of the medial (L 4), dorsal (L5), and lateral (S1) aspect of the foot, and the straight leg raise (SLR) test (1).

     C. Musculoskeletal. Assess range of motion of the spine and lower extremities. Perform the SLR test passively with the patient supine. Note the angle of leg elevation precipitating pain. A positive test for sciatica is buttock pain radiating to the posterior thigh, and perhaps to the lower leg and foot. Sciatica, with pain and resistance on internal rotation of the hip, can indicate piriformis muscle spasm or strain. The SLR test is usually negative in spinal stenosis (2). Percussion of the spine and upper pelvis helps to identify areas of localized tenderness, as in fracture, metastatic disease, and some rheumatologic conditions. Palpate standard trigger points looking for fibromyalgia. Check for paraspinal muscle spasm. Measure thigh and calf circumferences to look for muscular atrophy.

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Monarticular Joint Pain: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

    A. Timing of the pain. What is the onset and duration of the pain? Was there a specific inciting incident or trauma? When does the pain occur? Pain wakening the patient from sleep may suggest a malignancy. Is pain present at rest? Does movement or weightbearing exacerbate the symptom? Any associated joint stiffness?

    B. Location of the pain. Localization to the joint is typical in osteoarthritis (OA). Exceptions are hip OA, where pain can localize to the groin or thigh, and OA of the spine, where pain can localize to the buttocks. Radiation of the pain may suggest periarticular or neuropathic problems.

    C. Associated symptoms. Fever, night sweats, or weight loss may suggest an infectious cause or an underlying systemic illness. Rash can occur with infectious or inflammatory arthritides.

     D. Medical history. Many medical problems can be associated with an inflammatory or a degenerative arthritis (Table 12.7). Knowledge of prior joint surgery or prosthesis placement is important. A history of childhood joint disease (e.g., slipped capital epiphysis) or bone disease (e.g., osteochondritis dissecans) can predispose to early onset degenerative joint disease.

     E. Social history. The patient’s support system is especially important if severe functional impairment is present. The employment or recreational history may indicate a risk of repetitive joint trauma. Sexual risk factors and a history of alcohol or intravenous (IV) drug abuse are important.

    F. Medications. What medication or treatment has been used and what was the response? A history of systemic steroid use can lead to osteonecrosis of the femoral head.

    Physical examination

    Is discomfort apparent? Is fever present? Assess the patient’s gait and note if a mobility aide is used. Inspect the joint for surgical or traumatic scars, muscle atrophy, deformity, joint swelling, and erythema. Palpate for warmth, tenderness, and effusion. Evaluate joint range of motion (ROM). If active ROM is full and normal, evaluation of passive ROM is unnecessary. Pain with active, but not passive ROM suggests a periarticular process. Depending on the joint involved, palpate the relevant periarticular structures and perform the appropriate provocative maneuvers. Examine for rash.

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Abdominal Pain: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

    A. History of present illness. Medication use, alcohol and tobacco history, and menstrual history in women are vital. When did the pain begin and what are the characteristics of the pain? Use the “OPQRST” approach outlined below to question the patient about pain characteristics.

     1. O:Onset of pain. Pain of sudden onset or that awakens a patient from sleep can represent appendicitis, leaking abdominal aortic aneurysm, ectopic pregnancy, pancreatitis, or perforating ulcer. Gradual onset of pain can represent cholecystitis, diverticulitis, inflammatory bowel disorders, or pancreatitis. Longstanding pain without debility that is worsened by emotional stress is suggestive of irritable bowel syndrome.

     2. P:Palliative or Provocative factors (diet, exercise, sleep, bowel movement, and so on).

    3. Q:Quality of pain—pain descriptors are often associated with specific causes:

    a. “Burning” pain—ulcer

    b. “Agony”—pancreatitis

    c. “Shearing” or “tearing”—abdominal aortic aneurysm

    d. “Colicky” or “cramping”—cholecystitis, bowel obstruction, urolithiasis, irritable bowel syndrome

    e. “Constant ache”—appendicitis, peritonitis, herpes zoster

    4. R: Radiation or Referred—pain from appendicitis, simple colic, and bowel obstruction from strangulation or volvulus is often first felt in the epigastrium. Abdominal causes may result in referred or radiating pain to extraabdominal sites:

    a. Abdominal aortic aneurysm—to the midback

    b. Biliary colic—to the right scapula

    c. Renal colic—to the costovertebral angles, testicle, or thigh

    d. Hernias—to the genitalia

    5. Extraabdominal pathology can cause referred pain to the abdomen.

    a. Cardiac ischemia—to the epigastrium

    b. Scrotal pathology—to the abdomen

    6. S: Severity—level of intensity (some use a 1–10 scale)

     7. T: Time or Temporal relationships—with meals, after bowel movement, menses, and so on

     B. Past medical history. Is there a history of previous abdominal or pelvic surgery? Prior abdominal surgery increases the risk for bowel incarceration, obstruction, and strangulation. Fallopian tube surgery and prior pelvic inflammatory disease (PID) increase a woman’s risk for ectopic pregnancy (Chapter 11.3).

    C. Review of systems. Are there associated symptoms that point to a specific etiology? Chills and fever suggest infectious causes (UTI, PID, prostatitis, and pneumonia). Emesis occurring before the onset of pain is associated with appendicitis; with the onset of pain, cholecystitis or urolithiasis; after onset of pain, gastroenteritis. Late onset or feculent emesis suggests bowel obstruction; bilious emesis occurs in cholecystitis. Postprandial right upper quadrant pain is common in cholecystitis. Diarrhea with a recent travel history suggests dysentery or parasitic infections. Genitourinary complaints (dysuria, frequency, hematuria, vaginal discharge, and dypareunia) should prompt evaluation for UTI, sexually transmitted disease, and PID.

    Physical examination

    A thorough, targeted physical examination, directed by a complete history, leads to a correct diagnosis in most cases (2).

    Complete vital signs are essential. Tachycardia or hypotension can indicate hypovolemia and the need for urgent intervention (Chapter 7.12). Rapid, shallow breaths occur with peritoneal irritation. Inspect the abdomen for distention (obstruction), pulsations (AAA), or scars from past surgery. High-pitched hyperactive bowel sounds occur with bowel obstruction. Palpation and percussion help localize tenderness, organomegaly, and masses. Pain with movement, rebound tenderness, or rigidity are indicative of peritonitis and should prompt surgical consultation.

    Cardiovascular, pulmonary, and digital rectal and genitourinary examinations should be included in all evaluations of significant abdominal pain. The pelvic examination must be done to exclude ectopic pregnancy and PID. Among patients in whom pregnancy is a possibility, the presence of peritoneal signs, cervical motion tenderness, or lateral (or bilateral) abdominal or pelvic tenderness should raise concern about possible ectopic pregnancy (3).

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Calf Pain: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

    A. Pain characteristics. What is the pattern of onset, quality, location, duration, and intensity of the pain? What, if anything, helps relieve the pain? A report of a sensation of being “clubbed in the back of the leg” or “shot in the calf,” along with an audible pop or snap sound, suggests an acute Achilles tendon rupture (ATR) (1). Cramping calf pain may indicate a metabolic disturbance or a denervating disease. Numbness and burning pain or an electric-shock sensation, may indicate a neurological process. A “creeping and crawling” sensation deep within the muscles of the legs and thighs that is somewhat relieved with movement of the extremity is suggestive of restless leg syndrome (RLS).

     B. Preceding events. Was the pain preceded by any specific activity or trauma? Any recent prolonged inactivity? Unilateral calf pain after a period of immobility, especially in the presence of risk factors (e.g., lower extremity venous disease, oral contraceptive use), is DVT until proved otherwise. If the patient presents with a history of direct trauma to the calf, a compartment syndrome or intramuscular hematoma should be suspected. Pain occurring at night and disrupting sleep is suggestive of RLS or arterial disease.

     C. Associated symptoms. Coexisting symptoms can help to differentiate the cause of the pain. Any fever or back or knee pain should be noted. Ask about leg swelling, bruising, weakness, tingling, or other changes in sensation.

    D. Pertinent medical history. Does the patient smoke? Is there a history of any form of arthritis, or a Baker’s cyst? Any recent hip, knee, gynecologic, or lower abdominal surgery? Is the patient pregnant or postpartum? Pertinent medical illnesses include peripheral vascular disease, varicosities, malignancy, hematologic disorders, and diabetes. Acquired immune deficiency syndrome has been associated with a syndrome of calf pain, swelling, and tenderness along with cutaneous hyperesthesia to light touch. The syndrome is believed to be caused by hyperalgesic thrombophlebitis (2).

    E. Family history. A family history of DVT or inherited causes of hypercoagulability increase the risk for DVT (3).

    Physical examination (PE)

     A. Initial PE. Is the patient febrile? Inspect the patient’s back and check the curvature of the spine. Examine both legs from the groin and buttocks down for size, symmetry, skin color, pigmentation, hair distribution, and venous pattern. Note any skin lesions. Palpate lower extremity pulses and check for edema. Assess capillary refill. Note the temperature of the leg, especially over the area of pain. Palpate the calf for localized tenderness or a cord, which can indicate a superficial or deep thrombophlebitis. Feel for any increased firmness of the calf muscles. Palpate for masses, swelling, or tenderness in the lower back and entire leg. Check the mobility and flexibility of the spine and note if movement provokes any distal pain or weakness. Examine the knee and ankle joints on the affected side. Assess joint range of motion (ROM) and muscle strength. Check lower extremity reflexes and perform a good peripheral sensory examination.

     B. Additional PE. If evaluation suggests arterial insufficiency, assess for postural color changes by elevating the patient’s leg 60°. If ATR is suspected, perform a Thompson test. With the patient prone, squeeze the calf muscle just distal to its maximal girth. Plantar flexion of the foot is the normal result, indicating an intact Achilles tendon. A positive Homan or Lowenberg sign is suggestive of DVT. However, these signs are neither sensitive or specific for the diagnosis (4,5).

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Chronic Pelvic Pain: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

     As with any pain, the onset, duration, and pattern of the pain must be assessed. The location, intensity, character, and radiation are important historical elements. Aggravating or relieving factors are important, especially as they relate to the urinary, musculoskeletal, or gastrointestinal systems as well as the relationship of pain to sexual activity or menstruation. Systemic symptoms such as fatigue and anorexia are often present. A medication history (e.g., use of birth control pills or over-the-counter medications) should be obtained. The past obstetric, gynecologic, and general surgical histories are extremely important.

    It should be noted that women with a history of pelvic inflammatory disease are four times more likely to develop chronic pelvic pain. The list of possibilities for the condition is substantial. A person with intestinal, sexual, urinary, musculoskeletal, and systemic symptoms may be suffering from a psychiatric disorder (e.g., depression) and an acknowledged or remote history of sexual abuse. Often this information is possible to obtain only when the provider creates an atmosphere of mutual respect and trust.

    Dyspareunia is often present. Cyclic pain that is related to menstruation usually points to a gynecologic problem. Pain referred to the anterior thigh, pain associated with irregular uterine bleeding, or new onset dysmenorrhea may have a uterine or ovarian cause. Urethral tenderness, dysuria, or bladder pain suggests interstial cystitis or a urethral problem (Chapter 10.1). Pain on defecation, melana, bloody stools, or abdominal pain with alternating diarrhea and constipation can point toward pelvic floor problems, irritable bowel syndrome, or inflammatory bowel diseases.

    Physical examination

     A. The general condition of the patient should be noted. Does the patient look chronically ill, which may suggest a pelvic lesion or an inflammatory bowel disorder? Does the patient appear anxious, stressed, or inappropriate?

     1. Can the patient point to the pain with one finger? If so, this can indicate that the pain may have a discrete source.

    2. An examination of the lower back, sacral area, and coccyx, including a neuologic examination of the lower extremities, is necessary. Herniated disc, exaggerated lumbar lordosis, and spondylolisthesis can all cause pelvic pain.

     3. Examine the abdomen, looking for surgical scars, distension, and palpable tenderness, particularly in the epigastrium, flank, back, or bladder.

     B. A thorough pelvic examination is the most important part of the evaluation.

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Hip Pain: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

    A. Pain characteristics. What is the exact location of the pain? Pain arising from the lumbar spine is perceived in the buttock and, less commonly, in the groin and anterior thigh. This must be differentiated from radicular pain arising from the spine. True hip pain more often localizes to the anterior midgroin or midthigh area. Lateral hip or thigh pain most likely represents trochanteric bursitis (1). How is the pain described? A “snapping” type discomfort is most commonly caused by iliotibial band syndrome. Constant pain can indicate infection or cancer.

    B. Involved joints. Hip osteoarthritis (OA) can have a monarticular onset, or other joints may be involved. Of hip OA patients, 20% will develop bilateral involvement.

    C. Precipitating factors. Has there been a recent fall or other trauma? In an elderly or an osteoporotic patient, hip fracture can occur after a very minor incident. A contusion over the greater trochanter can lead to persistent bursitis; a contusion over the iliac crest, to a tear of the muscle aponeurosis. Has there been any preceding athletic or overuse activity that could cause muscle strain? Ischial bursitis usually develops after prolonged sitting.

    D. Other symptoms. Bacterial involvement of the hip joint can be accompanied by fever and shaking chills (2). Other symptoms may be present in cancer, pelvic, intraabdominal, or retroperitoneal pathology. Sciatica commonly accompanies trochanteric bursitis.

     E. Past medical history. Any prior hip problems or hip surgery? A patient with a hip replacement may develop loosening of prosthetic components, which can be a source of pain, or can seed the joint during a recent infection or invasive procedure. Aseptic necrosis of the femoral head is more likely in patients with sickle cell disease. Previous occult hip fracture or delayed treatment, can also lead to aseptic necrosis. Patients receiving long-term steroids may manifest constant hip pain. Congenital or developmental defects are found in 80% of patients with hip OA.

    Physical examination

     A. General. If referred pain is suspected, evaluate the appropriate organ system. Palpate the groin and thigh for hernias, lymph nodes, and vascular cords. Assess gait. An unwillingness to bear weight suggests fracture, even with a negative preliminary x-ray finding. Check the neurovascular status of the distal extremity after any traumatic episode.

     B. Musculoskeletal. Observe the involved extremity. In femoral neck fractures, the involved leg may appear slightly shortened and externally rotated. Intertrochanteric fractures can cause the involved leg to be internally rotated and shortened. Evaluate the spine, including the straight leg raise test, if spinal pathology is being considered. Compression of the patient’s pelvis with the patient side lying may localize pain to the sacroiliac joint. Check for leg length discrepancy by measuring each extremity from the anterior superior iliac spine (ASIS) to the medial malleolus; for hip joint shortening, measure from the ASIS to the greater trochanter.

    Palpate the greater trochanter, ischial tuberosity, and surrounding muscle groups for tenderness. The hip joint is not easily palpated; palpable warmth is produced only when intensely inflamed. Document joint range of motion. Nondisplaced or impacted fractures may not be painful, except at extremes of motion. Pain in all directions suggests intraarticular disease. Pain arising from the hip is typically elicited at the extreme ranges of motion, as well as with motion against resistance. With the patient supine, bend the uninvolved leg at the knee and hip and bring it toward the chest. Watch the opposite hip for flexion (Thomas test), indicating a flexion contracture of that hip. Loss of internal rotation occurs early in OA, followed by the loss of extension, adduction, and flexion. Pain and an inability to fully abduct or extend the hip can also be seen in rheumatoid arthritis (RA). Trochanteric bursitis may present with pain on external rotation only. Muscle strain (e.g., a “groin pull”) will produce pain on passive stretch or resisted contraction of the involved muscles only. In iliotibial band syndrome, the “snapping” of the band may be audible and palpable as the hip is flexed and extended. Document any muscle weakness or muscle atrophy.

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Knee Pain: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

    A. Age and etiology. The patient’s age is an important factor in determining the likelihood of certain knee problems. Because of stronger ligaments, avulsion fracture (anterior intercondylar eminence of the tibia, tibia tubercle) is more common in younger age groups, whereas ligamentous rupture occurs in older persons. Patellar dislocations and apophysitis are more likely in growing adolescents.

     B. Trauma. Understanding the mechanism of injury and estimating the acceleration or deceleration and torsional forces across the knee joint, predict the likelihood of occult fractures and internal derangement. Patients describing a popping sensation during a rotational or twisting injury, followed by an immediate swelling, usually have internal derangement of either meniscal or ligamentous components, or both. Locking of the knee suggests a “bucklehandle” meniscal tear obstructing normal hingejoint activity of the femoraltibial joint.

     C. Alleviating or exacerbating factors. Patellofemoral syndrome (PFS) or chrondromalacia patella is associated with anterior knee pain that worsens going up or down stairs or with prolonged sitting. Morning stiffness that improves with mild activity, but worsens as the day progresses, is typical of degenerative arthritis (osteoarthritis). The stiffness of rheumatoid arthritis (RA) generally does not improve with activity. Patients with multiple joint pains should be questioned about fever or skin rash to rule out infectious or inflammatory joint disease.

    Physical examination

    Both knees, as well as the hip, ankle, and foot on the affected side, should be examined. The knees are inspected for symmetry, signs of quadriceps or calf wasting, and any obvious swellings, discoloration, or pallor. Thigh, knee, calf circumference, and leg length are measured to document any asymmetry. Measurement of the quadriceps or Q angle (normal <15°) is important to evaluate anterior knee pain. Inability to perform full knee flexion and extension will highlight any effusion. Neurovascular supply should also be evaluated.

    In nonacute circumstances, the suprapatellar bursa is milked to determine if effusion is present. The patellar apprehension test may detect patellar dislocation; the patellar grind test is used to detect PFS. Evaluation of patellofemoral tracking within the femoral groove also helps make the latter diagnosis as the patella will track laterally in PFS, leading to the characteristic “jockey cap” patella. The knee should be carefully palpated for tenderness of the patellotibial insertion (Osgood-Schlatter’s disease), the body of the infrapatellar tendon (tendinitis), the insertion of the tendon on the patella (Sinding-Larsen-Johannson disease), medial and lateral joint line (potential meniscal pathology), pes anserine bursa (bursitis), or iliotibial band insertion. Plica, a painful, thickened band of exuberant synovium, can also be diagnosed by palpitation of the medial and lateral joint lines.

    Ligamentous testing is done next. Test the posterior cruciate ligament through the posterior drawer sign. Use the Lachman test for the anterior cruciate ligament, or, in obese patients, the anterior drawer sign. The medial collateral ligament is tested in zero and 15° of flexion by applying a valgus stress to the knee. The lateral collateral ligament is tested similarly using a varus stress. McMurray’s test may detect a meniscal tear. A duck walk test can also be used to look for a posterior meniscal tear. The patient’s gait is observed, specifically looking for forefoot varus and heel valgus, Morton’s foot deformity, and femoral anteversion, all of which can accentuate valgus stress on the knee and lead to a painful overuse syndrome. >

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Neck Pain: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

    A. General. Patient age and occupation are important. An individual’s job can involve awkward or prolonged body positioning (1). Some of the conditions listed in Table 12.8 can present with fever or with constitutional or other musculoskeletal symptoms. More diagnosis-specific symptoms may be present (e.g., chest pain with a myocardial infarction).

    B. Pain characteristics. What is the character, location, frequency, and duration of pain? Tumors of the cervical spine can present with unremitting neck pain that is worse at night. Referred neck pain from intrathoracic pathology is more often located anteriorly.

    C. Precipitating factors. Any prior history of neck problems? Has there been any preceding neck trauma or change in work or avocational activities? A history of collision trauma may warrant consideration of concurrent head injury. Is there any relationship of the pain to a particular neck position or movement? Careful questioning may be needed to uncover this latter information, but it is crucial to determining the mechanism of pain production. Have there been any emotional stressors?

    D. Associated symptoms. Is headache present? Any paresthesia, dyskinesia, or weakness of the trunk or upper or lower extremities? Bladder dysfunction can occur with a central spinal cord injury. What is the distribution of any radicular pain? An increase in radicular symptoms with coughing or sneezing suggests nerve root impingement (2).

    Physical examination

     A. General. After any cervical spine injury, order an x-ray study first to rule out an unstable injury. Assess gait, which can be impaired with a cervical myelopathy. Notice neck posture (3). Torticollis can occur secondary to trauma, muscle strain, vertebral subluxation, viral infection or from a psychogenic cause. Examine other head and neck structures (e.g., lymph nodes) and the temporomandibular joints (1). Look for meningeal signs, if appropriate.

     B. Musculoskeletal examination. Palpate for muscle tenderness or spasm in the neck and head. Tender trigger points may be found in fibromyalgia. Assess active and passive range of motion (ROM) of the neck and shoulders. ROM is not affected with referred sources of pain. Decreased passive ROM may be seen in rheumatoid arthritis (RA), ankylosing spondylitis (AS), disseminated idiopathic skeletal hyperostosis (DISH), compression fractures, and cervical spondylosis. Active contraction or stretching of strained muscles or ligaments will precipitate pain.

     C. Neurologic examination. Include the examination of cranial nerves, motor function, tone, and reflexes of the upper and lower extremities. Look for muscle atrophy. Check pinprick and light touch sensation in the upper extremities, looking for a dermatomal pattern of loss. Evaluate cerebellar, vibration, and position sense in the legs. The exact level of nerve root involvement cannot be precisely known from the physical examination because of overlapping innervation (2) (Table 12.9). A Spurling’s test (extension and rotation of the head and neck while applying downward pressure to the top of the head) that precipitates radicular symptoms is very suggestive of nerve root pathology (1).

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Pleuritic Pain: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

    A. Characteristics of the pleuritic pain. What is the acuity of the pain, its location, and exacerbating features?

     1. Acute onset suggests sudden development as viral or idiopathic pleurisy, PE, pneumonia, or pneumothorax.

    Insidious onset suggests a slower inflammatory or irritative process usually resulting in a pleural effusion with the pain generally diminishing as fluid accumulates (Chapter 8.4).

    2. Pleuritic chest pain localizes above the underlying pleural pathology through intercostal innervation.

     3. Through phrenic innervation, shoulder pain can indicate ipsilateral diaphragmatic involvement, usually by abdominal pathology (Table 8.1).

     4. Substernal pain improved by leaning forward suggests pericarditis (Chapter 7.1).

    5. Provocation of pain by shoulder movement indicates a musculoskeletal cause.

    B. Focused review of systems. What symptoms or history accompany the pain that might suggest a respiratory infection, PE, or malignancy? A nonproductive cough is nonspecific, and a productive cough suggests infection. Hemoptysis suggests malignancy, tuberculosis, or pulmonary embolism. A fever suggests infection but can occur with PE. Recent surgery or lower extremity trauma or swelling increase the risk for PE. Unexplained weight loss suggests malignancy or tuberculosis (TB).

    C. Past medical history. Past history can provide clues to the cause including malignancy, recent myocardial infarction, uremia, lupus, and rheumatoid arthritis.

    D. Other history. Inquire about oral contraceptives (PE risk), TB, or asbestos exposure.

    Physical examination

     A. Focused physical examination. This should include vital signs with attention to temperature and respiratory rate and examination of the chest. Tenderness to palpation indicates a musculoskeletal cause. Dullness to percussion suggests pleural effusion or parenchymal pathology and hyperresonant percussion indicates pneumothorax. On auscultation, a pleural friction rub is the only sign of pleurisy; crackles suggest pneumonia; and decreased breath sounds indicate pneumothorax or effusion. The examination result is frequently normal.

     B. Additional physical examination. Abdominal tenderness can suggest a subdiaphragmatic process (Table 8.2, Abdominal). Lower extremity edema, tenderness, or Homans’ sign can imply deep vein thrombosis (DVT) and PE. Lymphadenopathy can represent lymphoma or metastatic disease.

    » READ BOOK EXCERPT ONLINE »

    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Shoulder Pain: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

    A. Characteristics of the pain. What is the onset, location, radiation, severity, and duration of the pain? Is there any instability, weakness, stiffness, or locking? Are there exacerbating or alleviating maneuvers? Has there been any associated trauma? What was the mechanism of injury? Any associated neurologic or systemic symptoms? Is there a history of prior shoulder problems? Are other joints involved?

    Physical examination

    Observe the shoulder for symmetry, motion, and signs of injury. Palpate all bony structures [including the acromioclavicular (AC) joint and bicipital groove]; check cervical spine range of motion (ROM) and the neurovascular status of the affected arm. If fracture is suspected, obtain an x-ray study. If finding on the x-ray is negative, proceed with passive and active ROM testing of the shoulder. Assess muscle strength and perform provocative tests for specific suspected pathology (Table 12.12) (1).

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Scrotal Pain: History
    (The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter)

     A. Trauma rarely causes significant damage to the testicle. Traumatic damage is extremely rare in prepubertal patients (4). Unless the testicle is ruptured or a secondary torsion occurs, pain from trauma usually resolves in less than 1 hour (4). Severe pain or evidence of testicular rupture associated with minor trauma is suggestive of occult tumor (1,4).

     B. Symptoms and disease course

    1. Testicular torsion is the most common cause of scrotal pain in first year of life (3). It is frequently misdiagnosed as colic, or an intraabdominal disorder. The highest incidence occurs between the ages of 12 to 18 years (5). Testicular torsion causes acute pain with testicular swelling and scrotal erythema, and nausea and vomiting are common.

    2. Torsion of testicular appendage. Torsion is common between the ages of 10 to 15 years; however, it is rare in neonates and adults (5). Pain can last several days with malaise and may not localize to the scrotum initially, but presents as lower abdominal pain.

     3. Epididymitis is the most common cause of acute scrotal pain in adults (1). It is rare in prepubertal children (5). In infants or young children, suspect urogenital anomaly or dysfunction (3). The onset can be abrupt or insidious. Fever, voiding symptoms, or both are common (4). Scrotal edema and erythema can occur, but less commonly than that seen with torsion (5).

     4. Orchitis is usually caused by extension of epididymitis inflammation to the testis (4). Mumps orchitis, which is seen only after puberty in 20% of mumps cases, is usually unilateral (70%). It is declining in the United States because of immunization (5).

     C. Sexual activity is an important factor in all age groups. In prepubertal children, rule out abuse or self-experimentation. In adolescents and adults, infection and trauma can occur from sexual practices. A good history is especially important.

    D. Recurrent pain. A history of previous ipsilateral pain is associated with a 44% incidence of testicular torsion (1). Consider multiple causes. Is previous pain similar or different from the current episode?

     E. Infection. Look for a history of urinary tract infection (UTI), dribbling, urgency, dysuria, and incomplete emptying (Chapter 10.1). Consider reflux, obstruction, chronic prostatitis, and unusual sexual practices.

     F. Concurrent illness. Possibilities include Henoch–Schönlein purpura, mononucleosis, Buerger’s disease, coxsackie B virus, and polyarteritis nodosa (1,4). Also consider incarcerated hernia or thrombosed varicocele (1).

    Physical examination

     A. Observation. Especially in the very young, it is important to quietly observe the patient before initiating an examination (4). Is he quiet or active? Playing or fussing? Is there guarding?

     B. Referred pain. The neonate or young child with abdominal pain always deserves an examination of the scrotum (2,4).

    C. Scrotum. Edema and redness are found in torsion and epididymitis. They occur early in testicular torsion. If pain is present longer than 24 hours and no scrotal changes are noted, torsion is unlikely (4). Discoloration suggests trauma but it can also be seen with delayed diagnosis of torsion and epididymitis. Check for the cremasteric reflex, which rules out testicular torsion if present on the painful side (2,4). Its presence must be demonstrated on the nonpainful side to be reliable indicator. Unilateral swelling without skin changes suggests hernia or hydrocele (4). In torsion, pain increases when the scrotum is elevated; it decreases with epididymitis (Prehn’s sign) (5) (Chapter 10.7).

    D. Penis. Look for discharge, redness, and trauma. Partial hypospadius suggests possible other genitourinary anomalies. A higher incidence of UTI is seen in the uncircumcised neonate.

     E. Testes. Are they present or absent? Examine the inguinal canal. Evaluate for high versus low, transverse versus vertical lie. High, transverse testicle suggests torsion (4). Evaluate size, shape, and tenderness. The testicle with torsion will become swollen early in the process, however, the appendage with torsion does not cause a difference is testicular size (2). Feel and look for a palpable mass on the margin of the testis. Transilluminate for the “blue dot sign” to diagnosis torsion in the appendage (4,5). Does tenderness involve the entire testicle or is it asymmetric (4)?

     F. Other. Rule out other causes, examine skin for petechiae, and look for adenopathy. Examine the abdomen and flank for a source of referred pain or signs of trauma. Fever is not usually present with a testicular torsion (unless delayed), but can be found in epididymitis (4).

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    Source: The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter, 2000

    Seizures: Differential Overview

    (Field Guide to Bedside Diagnosis)

    ❑ Generalized (grand mal)

    ❑ Partial (focal)

    ❑ Complex partial (temporal lobe)

    ❑ Absence (petit mal)

    ❑ Vasovagal syncope

    ❑ Myoclonic

    ❑ Akinetic (drop attacks)

    ❑ Psychomotor

    ❑ Pseudoseizures

    Diagnostic Approach

    When the patient is found unresponsive, the differential is seizure versus syncope. Interviewing witnesses is crucial to ascertain the diagnosis. Seizures can be distinguished by color (cyanosis in seizure, pallor in syncope), aura, injury from falling, protracted tonic-clonic activity, tongue biting, urinary incontinence, and slow recovery of consciousness (seizure). Confusion, headache, and drowsiness are sequelae of seizure, whereas physical weakness and a clear sensorium occur with syncope. Seizures often have a promontory aura, such as an odor, and syncope has a prodrome of tunnel vision. Seizures are followed by eye closure, rotation of the head side-to-side, and prolonged, motionless unresponsiveness.

    General precipitating factors include sleep deprivation, systemic disease such as renal failure, metabolic/electrolyte disorder such as hypoglycemia or hyponatremia, alcohol use, or drug use. Elicit a history of febrile seizures or prior head trauma. Common causes of recurrent seizures in previously controlled patients include alcohol use, intercurrent infection, and missed medication doses.

    A neurological examination will indicate whether there is an underlying structural problem as evidenced by mild hemiparesis, reflex asymmetry, or extensor plantar response. Seizures are more common in slowly growing cerebral lesions, such as low-grade glioma or meningioma.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Chronic/Recurrent Abdominal Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    ❑ Irritable bowel syndrome

    ❑ Peptic ulcer disease

    ❑ Cholecystitis

    ❑ Chronic pancreatitis

    ❑ Inflammatory bowel disease

    ❑ Intermittent mesenteric ischemia

    ❑ Pancreatic cancer

    ❑ Gastric cancer

    ❑ Endometriosis

    ❑ Recurrent intestinal obstruction

    ❑ Sickle cell anemia

    ❑ Radiculopathy

    ❑ Adrenal insufficiency

    ❑ Lead poisoning

    ❑ Porphyria

    Diagnostic Approach

    Examining a patient during an episode of pain is important for diagnosis. A significant proportion of patients with chronic abdominal pain will remain undiagnosed despite extensive testing. For these patients, repeated history and examination, during which one looks for new symptoms or any change in the pattern of symptoms, may eventually yield a formulation.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Pleuritic Chest Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    ❑ Costochondritis

    ❑ Pneumonia

    ❑ Rib fracture

    ❑ Pulmonary embolism

    ❑ Pleurisy

    ❑ Pneumothorax

    ❑ Pericarditis

    ❑ Lung cancer

    ❑ Pneumomediastinum

    ❑ Splenic infarction

    Diagnostic Approach

    Pleuritic chest pain, intensified by a deep breath, usually has a pulmonary or chest wall origin. Cardiac pain is almost never pleuritic (LR 0.2), sharp or stabbing (LR 0.3), positional (LR 0.3) or reproduced by palpation (LR 0.3).

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Scrotal Pain/Swelling: Differential Overview
    (Field Guide to Bedside Diagnosis)

    Pain Predominant

    ❑ Epididymitis

    ❑ Testicular torsion

    ❑ Prostatitis

    ❑ Referred pain

    ❑ Trauma

    ❑ Orchitis

    ❑ Torsion of the appendix testis

    ❑ Inguinal hernia/incarcerated

    Swelling Predominant

    ❑ Varicocele

    ❑ Inguinal hernia

    ❑ Hydrocele

    ❑ Spermatocele

    ❑ Sebaceous cyst

    ❑ Testicular cancer

    Diagnostic Approach

    Testicular torsion, a medical emergency, should be the primary consideration in a patient with an acutely painful scrotum; however, epididymitis is a more common cause than torsion by 10:1. Reduction in pain by manual elevation of the testicle (Phren sign) helps to distinguish epididymitis from testicular torsion. A cremasteric reflex is absent in testicular torsion but present in torsion of the appendix testis.

    Testicular cancer must be definitively ruled out whenever a firm induration or mass is found to be contiguous with the testicle.

    Referred pain can be differentiated from scrotal pathology by a normal testicular examination.

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    Source: Field Guide to Bedside Diagnosis, 2007

    Acute Nonpleuritic Chest Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    ❑ Chest wall pain

    ❑ Angina

    ❑ Unstable angina

    ❑ Myocardial infarction

    ❑ Gastroesophageal reflux

    ❑ Herpes zoster

    ❑ Thoracic root compression

    ❑ Panic disorder

    ❑ Aortic stenosis

    ❑ Aortic dissection

    ❑ Mediastinal mass

    ❑ Biliary disease

    Diagnostic Approach

    It is essential to maintain a high index of suspicion (low threshold for investigation) for critical problems; however, most chest pain has a benign cause. The patient with myocardial ischemia often is reluctant to label the symptom as “pain.” Instead descriptors are used such as squeezing, pressure, tightness, fullness, a heavy weight on the chest, burning (attributed to indigestion),
    or a toothache (when jaw radiation is present). A closed fist held to the sternum is commonly employed to explain the symptoms. Pleuritic chest pain, intensified by a deep breath, usually has a pulmonary or chest wall origin. Recurrent episodic pain or persistent pain lasting days is unlikely to represent a critical problem. Pain lasting a few seconds or pain that is sharp or stabbing in quality is almost never ischemic, especially if reproducible by palpation
    or movement.

    Syncope with chest pain should raise suspicion of aortic dissection,
    ruptured aortic aneurysm, pulmonary embolism, or critical aortic stenosis. “Angor anomie,” a sense of impending doom, is found in serious conditions such as myocardial infarction, pulmonary embolism, aortic dissection, and to a lesser extent, panic disorder. Sternal pain may be caused by xiphoidalgia, myelomatosis, ankylosing spondylitis, osteomyelitis, or traumatic fracture.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Ear Pain/Discharge: Differential Overview
    (Field Guide to Bedside Diagnosis)

    Ear Pain

    ❑ Acute otitis media

    ❑ Acute otitis externa

    ❑ Eustachian dysfunction

    ❑ Temporomandibular joint arthritis

    ❑ Traumatic tympanic membrane rupture

    ❑ Foreign body, external auditory canal

    ❑ Erysipelas

    ❑ Herpes zoster oticus

    ❑ Dental abscess

    ❑ Frostbite

    ❑ Relapsing polychondritis

    ❑ Malignant otitis externa

    ❑ Acute mastoiditis

    ❑ Nasopharyngeal cancer

    Ear Discharge

    ❑ Otitis externa

    ❑ Eczematoid dermatitis

    ❑ Low-viscosity cerumen

    ❑ Otitis media with perforation

    ❑ Foreign body

    ❑ Psoriasis

    ❑ Herpes zoster oticus

    Diagnostic Approach

    If ear pain is present without ear findings, consider referred pain from the tonsils, teeth, trachea, or temporomandibular joint. Ear pain may be an early sign of nasopharyngeal carcinoma. Lesions of the anterior portion of the tongue refer pain in front of the ear whereas the posterior one-third of the tongue refers pain to within the ear.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Facial / Dental / Temporomandibular Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    ❑ Maxillary sinusitis

    ❑ Dental infection

    ❑ Temporomandibular joint dysfunction

    ❑ Myofascial masseter pain

    ❑ Migraine

    ❑ Trigeminal neuralgia

    ❑ Frontal sinusitis

    ❑ Ethmoid sinusitis

    ❑ Sphenoid sinusitis

    ❑ Parotitis

    ❑ Parotid calculus

    ❑ Orbital fracture

    ❑ Mandibular fracture

    ❑ Maxillary fracture

    ❑ Myocardial infarction

    ❑ Connective tissue disease

    ❑ Temporal arteritis

    ❑ Cavernous sinus thrombosis

    ❑ Glossopharyngeal neuralgia

    Diagnostic Approach

    The V1 ophthalmic branch of the trigeminal innervates the forehead, cornea (corneal reflex), dorsum of the nose, and anterior cranial dura. The V2 maxillary branch innervates the upper lip, lateral nose, upper cheek, anterior temple, upper jaw and teeth, roof of the mouth, and middle cranial dura. The V3 mandibular branch innervates the lower lip, chin, posterior cheek, external ear, mucosa of the lower mouth, anterior two-thirds of the tongue, and parts of the anterior and middle cranial dura.

    Pain provoked by hot, cold, or sweet foods is usually dental in origin. Neuralgia may produce a similar pain, but the pain will have a refractory period after an initial response. Pain increased by chewing suggests trigeminal neuralgia, temporomandibular joint pain, or jaw claudication. Pain increased by swallowing and taste is consistent with glossopharyngeal neuralgia. Objective sensory loss persisting after the pain is an important clue to organic disease.

    Epidemiologic studies reveal that temporomandibular joint tenderness is common, occurring in 35% of asymptomatic people, clicking in 25%, crepitus in 8%, and jaw deviation in 15%.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Low Back Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    ❑ Musculoligamentous strain

    ❑ Lumbar disc herniation

    ❑ Osteoarthritis

    ❑ Compression fracture

    ❑ Pyelonephritis

    ❑ Secondary gain

    ❑ Scoliosis

    ❑ Spondylolisthesis

    ❑ Metastatic cancer

    ❑ Spinal stenosis

    ❑ Transverse process fracture

    ❑ Pancreatic cancer

    ❑ Ankylosing spondylitis

    ❑ Sacroiliitis

    ❑ Aortic dissection

    ❑ Cauda equina syndrome

    ❑ Vertebral osteomyelitis

    ❑ Epidural abscess

    Diagnostic Approach

    Radicular pain has such a high sensitivity for nerve root compression that its absence makes important disc herniation unlikely. Not all radicular pain is due to a herniated disc however. Other causes include spinal stenosis, ligamentous hypertrophy, deep lumbar muscle spasm, and deep trochanteric bursitis.

    Back pain at rest or unassociated with posture/movement should increase the suspicion of tumor, fracture, infection, or referred visceral pain. Spinal tenderness is a sensitive but not specific indicator. Clues to metastatic cancer include a history of cancer, unexplained weight loss, and signs of cord compression, such as motor weakness of the legs, urinary or fecal incontinence, and absent anal reflex. Recent bacterial infection, injection drug use, or immune suppression (from steroids, chemotherapy, or HIV) should raise suspicion for infection. Fever occurs in osteomyelitis (50%), epidural abscess (83%), and tuberculosis (27%).

    A red flag for fracture in a young adult is major trauma, such as a fall from a height or a motor vehicle accident. In older adults, minor trauma or strenuous lifting can cause a compression fracture.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Acute Abdominal Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    Generalized/Periumbilical

    ❑ Gastroenteritis

    ❑ Obstipation

    ❑ Small bowel obstruction

    ❑ Large bowel obstruction

    ❑ Mesenteric ischemia

    ❑ Peritonitis

    ❑ Abdominal aortic dissection

    ❑ Sickle cell crisis

    Right Upper Quadrant/Epigastrium

    ❑ Hepatitis

    ❑ Biliary colic

    ❑ Peptic ulcer disease

    ❑ Pyelonephritis

    ❑ Acute cholecystitis

    Right Lower Quadrant

    ❑ Appendicitis

    ❑ Inflammatory bowel disease

    ❑ Salpingitis

    ❑ Rectus abdominus muscle strain

    ❑ Ureteral calculus

    ❑ Ruptured corpus luteum cyst

    ❑ Ruptured ectopic pregnancy

    ❑ Ovarian torsion

    Left Upper Quadrant

    ❑ Pancreatitis

    ❑ Splenic infarction

    ❑ Pyelonephritis

    ❑ Myocardial infarction

    Left Lower Quadrant

    ❑ Inflammatory bowel disease

    ❑ Diverticulitis

    ❑ Salpingitis

    ❑ Rectus abdominus muscle strain

    ❑ Ureteral calculus

    ❑ Ovarian torsion

    ❑ Ruptured corpus luteum cyst

    ❑ Ruptured ectopic pregnancy

    ❑ Sigmoid volvulus

    Diagnostic Approach

    Acute abdominal pain is a classic symptom that can herald conditions ranging from the trivial to the life-threatening. The accurate diagnosis and timely management of abdominal pain requires an understanding of the mechanisms of pain, recognition of typical patterns of clinical presentation, a broad differential of common causes, and an index of suspicion for variant presentations and unusual causes. The ultimate disposition decision may require a repeated history and physical examination over several hours. Narcotic analgesics should be withheld until a diagnosis is established because they can mask the expression of diagnostic characteristics of the disease. History indicates the diagnosis in 85% to 90% of cases. Consider organs located in the region of maximal pain and the time-course of onset. An intrathoracic source must always be considered with upper abdominal pain. Physical examination can demonstrate peritoneal inflammation and rebound tenderness by eliciting pain with gentle percussion of the abdomen as opposed to sharp release of the depressed hand. Muscular rigidity or “guarding” is an early sign of peritoneal inflammation. Auscultation may reveal silence, consistent with ileus or advanced peritonitis, hyperactive high-pitched sounds with early bowel obstruction, or a friction rub with splenic infarct or hepatic metastases. Pelvic and rectal examinations are mandatory in every patient who has abdominal pain.

    Parietal pain, caused by inflammation of the parietal peritoneum, is
    a sharp, steady, aching pain, well-localized over the inflamed area, and
    accentuated by pressure. Tonic reflex spasm of the abdominal musculature is present. Visceral pain, caused by obstruction of a hollow viscera, is classically intermittent and cramping, but distension may produce dull, steady pain. The patient with visceral pain will writhe incessantly, while the patient with parietal pain lies still in bed. Referred pain is aching and perceived to be near the surface, accompanied by skin hyperalgesia and increased tone of the abdominal wall. Vascular occlusion can be recognized by severe pain out of proportion to physical findings in a patient with vascular disease or atrial fibrillation. Visceral pain is perceived at the level the nerves enter the spinal cord. An example is gallbladder pain which may be first perceived at the scapula, then later in the right upper quadrant when the somatically innervated overlying parietal peritoneum is inflamed.

    If the patient is well one moment, then has excruciating pain, which is maximal at onset, consider a ruptured hollow viscera or a vascular event, such as myocardial infarction or ruptured aortic aneurysm.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Acute Knee Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    ❑ Osteoarthritis

    ❑ Patellofemoral pain

    ❑ Collateral ligament sprain

    ❑ Meniscal tear

    ❑ Anterior cruciate tear

    ❑ Infrapatellar quadriceps tendinitis

    ❑ Acute monoarticular arthritis

    ❑ Prepatellar bursitis

    ❑ Anserine bursitis

    ❑ Hamstring injury

    ❑ Baker cyst

    ❑ Septic joint

    ❑ Iliotibial band syndrome

    ❑ Hemarthrosis

    ❑ Patellar fracture

    ❑ Patellar dislocation

    ❑ Osteochondritis desiccans

    ❑ Osteonecrosis

    Diagnostic Approach

    Careful questioning about the mechanism of injury is most important. Overuse injury or undue stress caused by unbalanced walking is a common source. A sensation of “giving away” on stepping down is a symptom of posterior horn meniscus or anterior cruciate tear. Joint line pain is seen in osteoarthritis, high-grade collateral ligament injury, meniscal tear, and tibial plateau fracture. Pain located medially several centimeters below this is due to anserine bursitis or low-grade medial collateral ligament injury. Anterior knee pain is found in injury to the quadriceps mechanism or large joint effusions. Popliteal pain is usually due to a large knee effusion.

    Systematically stress the knee in each direction, looking for pain and/or laxity, comparing with the contralateral side. The range of motion may be limited by effusion, by a meniscal tear, or by a loose body. True locking, with ability to flex but not extend fully, occurs 10 degrees short of full extension. A McMurray maneuver is performed by rotating the tibia on the femur medially with the knee flexed at 90 degrees and then extending the knee, then repeating the process with lateral rotation. A painful “clunk” with medial rotation indicates a lateral meniscus tear, and the same finding with lateral rotation suggests a medial meniscus tear. An anterior drawer sign is elicited as pain and a laxity when the tibia is pulled forward with the knee at 90 degrees, indicating anterior cruciate injury. A Lachman manuver, performed at 15 degrees flexion, is more sensitive. With effusion the hollows of the knee are filled, and a transmitted fluid wave can be elicited.

    In acute knee injury, the Ottawa Knee Rule minimizes the number of x-rays without missing a significant fracture. Obtain an x-ray if: (a) age is >54, (b) there is tenderness at the head of the fibula, (c) there is isolated patellar tenderness, (d) there is an inability to flex the knee to 90 degrees, or (e) there is an inability to bear weight immediately and take four steps in the E.R.

    Palpable clicks are not necessarily pathologic; they may be caused by the semitendinosus tendon slipping over the medial condyle or the iliotibial band slipping over the lateral condyle.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Ankle/Foot Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    Ankle Pain

    ❑ Ankle sprain

    ❑ Fibular fracture

    ❑ Achilles tendinitis

    ❑ Acute gout

    Foot Pain

    ❑ Plantar fasciitis

    ❑ Acute gout

    ❑ Hallux valgus (bunion)

    ❑ Sciatica

    ❑ Metatarsalgia

    ❑ Metatarsal stress fracture

    ❑ Tibialis anterior tendinitis

    ❑ Pes planus

    ❑ Calcaneal fracture

    ❑ Interdigital neuroma

    ❑ Posterior tibial nerve entrapment

    ❑ Compartment syndrome

    Diagnostic Approach

    In acute ankle injury, ability to bear weight for four steps and absence of bone tenderness at the posterior edge or the tip of either malleolus rule out a significant fracture (Ottawa ankle rule).

    In acute foot injury, ability to bear weight for four steps and absence of bone tenderness at the navicular or the base of the fifth metatarsal rule out a significant midfoot fracture (Ottawa foot rule).

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Elbow Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    ❑Lateral epicondylitis

    ❑Olecranon bursitis

    ❑Medial epicondylitis

    ❑Bicipitoradialis tendinitis

    ❑Cubital tunnel syndrome

    ❑Radial head fracture

    ❑Septic arthritis

    ❑Gout

    ❑Osteoarthritis

    ❑Elbow dislocation

    ❑Ruptured distal biceps tendon

    ❑Epitrochlear lymphadenitis

    ❑Cervical radiculopathy

    Diagnostic Approach

    Pain arising from within the elbow joint is poorly localized between the lateral epicondyle and the olecranon, and there is inability to straighten the elbow. Referred pain to the elbow is vague, not affected by elbow movement, but increased by movement of the neck or shoulder.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Eye Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    ❑ Conjunctivitis

    ❑ Corneal abrasion

    ❑ Foreign body

    ❑ Sinusitis

    ❑ Migraine

    ❑ Acute glaucoma

    ❑ Orbital cellulitis

    ❑ Zoster prodrome

    ❑ Orbital fracture

    ❑ Keratitis

    ❑ Scleritis

    ❑ Iritis

    ❑ Optic neuritis

    ❑ Temporal arteritis

    Diagnostic Approach

    A foreign body sensation occurs with a foreign body, corneal abrasion, or keratoconjunctivitis sicca. Itching is associated with allergic and vernal conjunctivitis. Photophobia occurs with iritis and herpes simplex keratitis. Deep pain suggests acute glaucoma or posterior scleritis. Pain on eye movement is found with optic neuritis, sinusitis, and influenza.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Flank Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    ❑ Ureteral calculus

    ❑ Acute pyelonephritis

    ❑ Latissimus strain

    ❑ Perinephric abscess

    ❑ Renal infarction

    ❑ Renal trauma

    ❑ Renal cancer

    ❑ Mononeuritis

    ❑ Papillary necrosis

    Diagnostic Approach

    Renal pain occurs with stretching of the capsule and distension of the collecting system. The pain is usually severe and aching, with nausea, vomiting, and ileus. There may be hyperesthesia in the T 9 to 10 dermatome.

    Ureteral pain begins in the costovertebral angle and radiates to the lower abdomen, upper thigh, testis, or labia. The pain is excruciating, with crescendo waves of colic. The patient writhes but is unable to obtain relief. Hyperesthesia over the T 12 dermatome often occurs along with tenderness over the kidney or ureter.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Hip Pain: Differential Overview
    (Field Guide to Bedside Diagnosis)

    ❑Hip osteoarthritis

    ❑Trochanteric bursitis

    ❑Ischial bursitis

    ❑Iliopectineal bursitis

    ❑Iliopsoas bursitis

    ❑Nerve root compression

    ❑Meralgia paresthetica

    ❑Obturator inflammation

    ❑Iliac apophysitis

    ❑Hip fracture

    ❑Aortoiliac insufficiency

    ❑Polymyalgia rheumatica

    ❑Ankylosing spondylitis

    ❑Septic arthritis

    ❑Osteonecrosis

    ❑Sacroiliitis

    Diagnostic Approach

    Pain arising from the hip joint is aggrevated with or after use, particularly weight-bearing, and improved with rest. In contrast, constant pain, particularly pain at night, should suggest an infectious, inflammatory, or neoplastic process.

    In disease of the hip joint, the earliest limitation is internal rotation with the hip hyperextended. The hip joint is palpated just below the inguinal ligament lateral to the femoral artery. Tenderness and/or crepitance are usually felt there with movement. Manual internal and external rotation of the hip with the knee and hip in flexion usually reproduces pain as does concussion of the heel with the examiner’s palm.

    » READ BOOK EXCERPT ONLINE »

    Source: Field Guide to Bedside Diagnosis, 2007

    Complex regional pain syndrome: Diagnostic tests
    (Handbook of Diseases)

    There is no laboratory test for CRPS, so the diagnosis is based on the patient’s history and clinical findings. A history of injury to an extremity may point to CRPS. Bone X-rays may aid in ruling out other conditions, such as osteomyelitis and stress fractures, which cause similar signs and symptoms. With early diagnosis, prognosis improves.

    » READ BOOK EXCERPT ONLINE »

    Source: Handbook of Diseases, 2003

    Myoclonus: History
    (Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series)

    If the patient is stable, evaluate his level of consciousness and mental status. Ask about the frequency, severity, location, and circumstances of the myoclonus. Has he ever had a seizure? If so, did myoclonus precede it? Is the myoclonus ever precipitated by a sensory stimulus? 

    Physical examination

    During the physical examination, check for muscle rigidity and wasting, and test deep tendon reflexes. Evaluate level of consciousness and mental condition. Perform a complete neurologic and musculoskeletal assessment.

    » READ BOOK EXCERPT ONLINE »

    Source: Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series, 2007

    Seizures, generalized tonic-clonic: History
    (Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series)

    Obtain the patient’s medical history. Has he had generalized or focal seizures before? If so, how frequently? Do other family members have seizures? Is the patient receiving drug therapy? Is he compliant? Ask about sleep deprivation and emotional or physical stress at the time the seizure occurred. Ask about the use of alcohol or illicit drugs.

    If you didn’t witness the seizure, obtain a description from the patient’s family. Ask when it started and how long it lasted. Did the patient report unusual sensations before the seizure began? Did the seizure start in one area of the body and spread, or did it affect the entire body immediately? Did the patient fall on a hard surface? Did his eyes or head turn? Did he turn blue? Did he lose bladder control? Did he have other seizures before recovering? Does he complain of headache and muscle soreness?

    Physical examination

    If the patient may have sustained a head injury, perform a complete neurologic examination, observing closely for loss of consciousness, unequal or nonreactive pupils, and focal neurologic signs. Assess his vital signs. Is he increasingly difficult to arouse when you check on him at 20-minute intervals? Examine his arms, legs, and face (including tongue) for injury, residual paralysis, or limb weakness.

    » READ BOOK EXCERPT ONLINE »

    Source: Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series, 2007

    Abdominal pain: History
    (Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series)

    If the patient’s condition permits, obtain his history. Ask whether he has had this type of pain before. Because some patients report abdominal pain as indigestion or gas pain, it’s important to ask the patient to describe his pain in detail. For example, is it dull, sharp, stabbing, or burning? Ask him where the pain is located and whether it radiates to other areas. If a language barrier exists between you and the patient, use a pain rating scale with visual cues such as faces.

    Ask the patient about factors that relieve the pain or make it worse. For example, do movement, coughing, exertion, vomiting, eating, elimination, or walking relieve the pain or worsen it? Ask him when the pain began and whether it’s intermittent or constant. If pain is intermittent, ask about the duration of a typical episode.

    Intermittent, cramping abdominal pain suggests obstruction of a hollow organ. Constant, steady abdominal pain suggests organ perforation, ischemia, or inflammation or blood in the peritoneal cavity.

    Ask the patient about substance abuse and a history of vascular, GI, GU, or reproductive disorders. Ask the female patient about the date of her last menses, changes in her menstrual pattern, or dyspareunia.

    Ask the patient about appetite changes. Ask about the onset and frequency of nausea or vomiting. Has he experienced increased flatulence, constipation, diarrhea, or changes in stool consistency? When was the patient’s last bowel movement? Ask about urinary frequency, urgency, or pain. Is the urine cloudy or pink?

    Physical examination

    Obtain the patient’s vital signs, and assess skin turgor and mucous membranes. Inspect his abdomen for distention or visible peristaltic waves and, if indicated, measure his abdominal girth.

    Auscultate for bowel sounds in all four quadrants for at least 10 to 15 seconds and characterize their motility. Listen for systolic bruits in such locations as the abdominal aorta, renal artery, or iliac artery. (See Auscultating for vascular sounds.)

    Percuss all quadrants, noting the percussion sounds.

    ALERT: Abdominal percussion or palpation is contraindicated in patients with suspected abdominal aortic aneurysm, those who have received abdominal organ transplants, and children with suspected Wilms’tumor. If performing abdominal percussion or palpation in patients with suspected appendicitis, use extreme caution to avoid precipitating a rupture.

    Palpate the entire abdomen for masses, rigidity, and tenderness. Involuntary rigidity is generally asymmetrical, evident on inspiration and expiration, unaffected by relaxation techniques, and painful when the patient sits up using his abdominal muscles alone. Check for costovertebral angle (CVA) tenderness, abdominal tenderness with guarding, and rebound tenderness. Peritonitis and appendicitis can cause rebound tenderness. Because appendicitis may be accompanied by increased abdominal wall resistance and guarding, perform the maneuver for rebound tenderness only once — repeating the maneuver can rupture an inflamed appendix. (See Eliciting rebound tenderness, page 4.)

    » READ BOOK EXCERPT ONLINE »

    Source: Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series, 2007

    Back pain: History
    (Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series)

    Ask the patient where the pain is located; back pain in some areas can signal the presence of a life-threatening condition.

    Act Now: If the patient reports acute, severe back pain, quickly obtain his vital signs and perform a rapid evaluation to rule out life-threatening causes. If he describes deep lumbar pain unaffected by activity, observe for a pulsating epigastric mass. Presence of this sign may indicate a dissecting abdominal aortic aneurysm. Withhold food and fluids because the patient may require emergency surgery. Prepare for I.V. fluid replacement and oxygen administration.

    If he reports severe epigastric pain that radiates through the abdomen to the back, assess for absent bowel sounds and abdominal rigidity and tenderness. These symptoms may indicate a perforated ulcer or acute pancreatitis. Start an I.V. line for fluids and medications, administer oxygen, insert a nasogastric tube, and withhold food.

    If the patient complains of scapular area back pain, especially if accompanied by shortness of breath or diaphoresis, give oxygen via a nasal cannula or mask and obtain a 12-lead electrocardiogram to rule out myocardial infarction.

    After you have ruled out potential life-threatening causes of back pain, continue to obtain the patient’s history. Observe him for expressions of pain while gathering information. Ask about previous injuries and illnesses, dietary habits, alcohol intake, and cigarette smoking. Inquire about medications, including past and present prescriptions, use of over-the-counter drugs, and disease processes or pain control regimens.

    Ask the patient about the onset of his back pain. Were there precipitating factors? Ask the patient to rate the pain on a standardized pain scale. Ask him for details about the pain — is it burning, stabbing, throbbing, or aching? Constant or intermittent? If it’s intermittent, does it occur at a specific time of day? Does the pain radiate? Is there associated weakness? Does he experience repetitive pain or different types of pain? What, if anything, lessens the pain? What aggravates it? The patient’s answers will help identify the cause of his back pain. For example, visceral referred back pain is indicated if the patient states that the pain isn’t affected by activity and rest. In contrast, spondylogenic-referred back pain is likely if the pain increases with activity and decreases with rest. Pain of neoplastic origin is indicated if the patient reports that he can obtain relief by walking and that the pain increases at night.

    Physical examination

    Perform a thorough physical examination. Observe skin color, especially in the patient’s legs, and palpate skin temperature. Palpate femoral, popliteal, posterior tibial, and pedal pulses. Ask the patient about unusual sensations in the legs, such as numbness and tingling. If pain doesn’t prevent standing, observe the patient’s posture — does he stand erect or lean toward one side? Observe the level of the shoulders and pelvis and the curvature of the back. Ask the patient to bend forward, backward, and from side to side while you palpate for paravertebral muscle spasms. Note rotation of the spine on the trunk. Palpate the dorsolumbar spine for point tenderness. Then ask the patient to walk — first on his heels, then on his toes (stand close by during these tests so that you can assist the patient if he falls). Weakness may reflect a muscular disorder or spinal nerve root irritation.

    Place the patient in a sitting position to evaluate and compare patellar tendon (knee), Achilles tendon, and Babinski’s reflexes. (See How to elicit Babinski’s reflex.) Evaluate the strength of the extensor hallucis longus by asking the patient to keep his great toe firmly in place against resistance. Measure leg length and hamstring and quadriceps muscles bilaterally. Note a difference of more than ⅜"(1 cm) in muscle size, especially in the calf.

    To reproduce leg and back pain, assist the patient into a supine position on the examining table. Grasp his heel and slowly lift his leg. If he feels pain, note its exact location and the angle between the table and his leg when it occurs. Repeat this maneuver with the opposite leg. Pain along the sciatic nerve may indicate disk herniation or sciatica.

    Note the range of motion of the hip and knee. Palpate the flanks and percuss with your fingertips or fist to reveal the presence of costovertebral angle (CVA) tenderness.

    » READ BOOK EXCERPT ONLINE »

    Source: Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series, 2007

    Chest pain: History
    (Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series)

    Ask the patient to rate the pain using a standardized pain rating scale. Is the pain a dull, aching, pressurelike sensation, or sharp, stabbing, and knifelike? Is it constant or intermittent? If it’s intermittent, ask how long an episode lasts. Ask him about precipitating, aggravating, or alleviating factors. Review the patient’s history for cardiac or pulmonary disease, chest trauma, intestinal disease, or sickle cell anemia. Ask about medications he’s taking, if any, including recent dosage or schedule changes.

    ALERT: Chest pain in perimenopausal women may be difficult to diagnose because it may present atypically. Fatigue, nausea, dyspnea, and shoulder or neck pain are symptoms more likely to signal an MI in women than in men.

    Physical examination

    Take the patient’s vital signs, noting tachypnea, fever, tachycardia, oxygen saturation, paradoxical pulse, and hypertension or hypotension. Check for jugular vein distention and peripheral edema. Observe the patient’s breathing pattern, and inspect his chest for asymmetrical expansion. Auscultate his lungs for pleural friction rub, crackles, rhonchi, wheezing, or diminished or absent breath sounds. Next, auscultate for murmurs, clicks, gallops, or pericardial friction rub. Palpate for lifts, heaves, thrills, gallops, tactile fremitus, and abdominal masses or tenderness.

    » READ BOOK EXCERPT ONLINE »

    Source: Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series, 2007

    Eye pain: History
    (Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series)

    If the patient’s eye pain doesn’t result from a chemical burn, take a complete history. Have the patient describe the pain fully. Is it an ache or a sharp pain? How long does it last? Is it accompanied by burning, itching, or discharge? Find out when it began. Is it worse in the morning or late in the evening? Ask about recent trauma or surgery, especially if the patient complains of sudden, severe pain. Does he have headaches? If so, find out how often and at what time of day they occur.

    Physical examination

    During the physical examination, don’t manipulate the eye if you suspect trauma. Carefully assess the lids and conjunctiva for redness, inflammation, and swelling. Then examine the eyes for ptosis or exophthalmos. Finally, test visual acuity with and without correction, and assess extraocular movements. Characterize any discharge. (See Examining the external eye.)

    » READ BOOK EXCERPT ONLINE »

    Source: Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series, 2007

    Flank pain: History
    (Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series)

    If the patient’s condition isn’t critical, take a thorough history. Ask about the pain’s onset and apparent precipitating events. Have him describe the pain’s location, intensity, pattern, and duration. Find out if anything aggravates or alleviates it.

    Ask the patient about any changes in his normal pattern of fluid intake and urine output. Explore his history for urinary tract infection (UTI) or obstruction, renal disease, or recent streptococcal infection.

    Physical examination

    During the physical examination, palpate the patient’s flank area and percuss the CVA to determine the extent of pain.

    » READ BOOK EXCERPT ONLINE »

    Source: Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series, 2007

    Jaw pain: History
    (Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series)

    Begin the patient history by asking the patient to describe the pain’s character, intensity, and frequency. When did he first notice the jaw pain? Where on the jaw does he feel pain? Does the pain radiate to other areas? Sharp or burning pain arises from the skin or subcutaneous tissues. Causalgia, an intense burning sensation, usually results from damage to the fifth cranial, or trigeminal, nerve. This type of superficial pain is easily localized, unlike dull, aching, boring, or throbbing pain, which originates in muscle, bone, or joints. Also ask about aggravating or alleviating factors.

    Ask about recent trauma, surgery, or procedures, especially dental work. Ask about associated signs and symptoms, such as joint or chest pain, dyspnea, palpitations, fatigue, headache, malaise, anorexia, weight loss, intermittent claudication, diplopia, and hearing loss. (Keep in mind that jaw pain may accompany more characteristic signs and symptoms of life-threatening disorders, such as chest pain in a patient with an MI.)

    Physical examination

    Focus your physical examination on the jaw. Inspect the painful area for redness, and palpate for edema or warmth. Facing the patient directly, look for facial asymmetry indicating swelling. Check the TMJs by placing your fingertips just anterior to the external auditory meatus and asking the patient to open and close, and to thrust out and retract his jaw. Note the presence of crepitus, an abnormal scraping or grinding sensation in the joint. (Clicks heard when the jaw is widely spread apart are normal.) How wide can the patient open his mouth ? Less than 1⅛" (3 cm) or more than 2⅜" (6 cm) between upper and lower teeth is abnormal. Next, palpate the parotid area for pain and swelling, and inspect and palpate the oral cavity for lesions, elevation of the tongue, or masses.

    » READ BOOK EXCERPT ONLINE »

    Source: Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series, 2007

    Neck pain: History
    (Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series)

    If the patient hasn’t sustained trauma, inquire about the severity and onset of his neck pain. Where specifically in the neck does he feel pain? Does anything relieve or worsen the pain? Is there a particular event that precipitates the pain? Also, ask about the development of other symptoms such as headaches. Next, focus on the patient’s current and past illnesses and injuries, diet, drug history, and family health history.

    Physical examination

    Thoroughly inspect the patient’s neck, shoulders, and cervical spine for swelling, masses, erythema, and ecchymoses. Assess active range of motion (ROM) in his neck by having him perform flexion, extension, rotation, and lateral side bending. Note the degree of pain produced by these movements. Examine his posture, and test and compare bilateral muscle strength. Check the sensation in his arms, and assess his hand grasp and arm reflexes. Attempt to elicit Brudzinski’s and Kernig’s signs if there isn’t a history of neck trauma, and palpate the cervical lymph nodes for enlargement. (See Neck pain: Causes and associated findings.)

    » READ BOOK EXCERPT ONLINE »

    Source: Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series, 2007

    Myoclonus: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    If the patient is stable, evaluate level of consciousness (LOC) and mental status. Ask about the frequency, severity, location, and circumstances of myoclonus. Has he ever had a seizure? If so, did myoclonus precede it? Is the myoclonus ever precipitated by a sensory stimulus?

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Seizures, complex partial: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    If you witness a complex partial seizure, never attempt to restrain the patient. Instead, lead him gently to a safe area. (Exception: Don’t approach him if he’s angry or violent.) Calmly encourage him to sit down, and remain with him until he’s fully alert. After the seizure, ask him if he experienced an aura. Record all observations and findings.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Seizures, generalized tonic-clonic: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    If you didn’t witness the seizure, obtain a description from the patient’s companion. Ask when the seizure started and how long it lasted. Did the patient report any unusual sensations before the seizure began? Did the seizure start in one area of the body and spread, or did it affect the entire body right away? Did the patient fall on a hard surface? Did his eyes or head turn? Did he turn blue? Did he lose bladder control? Did he have any other seizures before recovering? Does he complain of headache and muscle soreness? Is he increasingly difficult to arouse when you check on him at 20-minute intervals?

    Next, obtain a history. Has the patient ever had generalized or focal seizures before? If so, do they occur frequently? Do other family members also have them? Is the patient receiving drug therapy? Is he compliant? Also, ask about sleep deprivation and emotional or physical stress at the time the seizure occurred.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Seizures, simple partial: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    Record the patient’s seizure activity in detail; your data may be critical in locating the lesion in the brain. Does the patient turn his head and eyes? If so, to what side? Where does movement first start? Does it spread? Because a partial seizure may become generalized, you’ll need to watch closely for loss of consciousness, bilateral tonicity and clonicity, cyanosis, tongue biting, and urinary incontinence. (See “Seizures, generalized tonic-clonic,” page 598.)

    After the seizure, ask the patient to describe exactly what he remembers, if anything, about the seizure. Then obtain a history. Ask the patient what happened before the seizure. Can he describe an aura or did he recognize its onset? If so, how — by a smell, a visual disturbance, or a sound or visceral phenomenon, such as an unusual sensation in his stomach? How does this seizure compare with others he has had?

    Also, explore fully any history, recent or remote, of head trauma. Check for a history of stroke or recent infection, especially with fever, headache, or a stiff neck.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Abdominal pain: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    If the patient has no life-threatening signs or symptoms, take his history. Ask him if he has had this type of pain before. Have him describe the pain — for example dull, sharp, stabbing, or burning. Ask if anything relieves the pain or makes it worse. Ask the patient if the pain is constant or intermittent and when the pain began. Constant, steady abdominal pain suggests organ perforation, ischemia, or inflammation or blood in the peritoneal cavity. Intermittent, cramping abdominal pain suggests the patient may have obstruction of a hollow organ.

    If the pain is intermittent, find out the duration of a typical episode. In addition, ask the patient where the pain is located and if it radiates to other areas.

    Find out if movement, coughing, exertion, vomiting, eating, elimination, or walking worsens or relieves the pain. The patient may report abdominal pain as indigestion or gas pain, so have him describe it in detail.

    Ask the patient about substance abuse and any history of vascular, GI, GU, or reproductive disorders. Ask the female patient about the date of her last menses, changes in her menstrual pattern, or dyspareunia.

    Ask the patient about appetite changes. Ask about the onset and frequency of nausea or vomiting. Find out about increased flatulence, constipation, diarrhea, and changes in stool consistency. When was his last bowel movement? Ask about urinary frequency, urgency, or pain. Is his urine cloudy or pink?

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Arm pain: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    If the patient reports arm pain after an injury, take a brief history of the injury from the patient. Then quickly assess him for severe injuries requiring immediate treatment. If you’ve ruled out severe injuries, check pulses, capillary refill time, sensation, and movement distal to the affected area because circulatory impairment or nerve injury may require immediate surgery. Inspect the arm for deformities, assess the level of pain, and immobilize the arm to prevent further injury.

    If the patient reports continuous or intermittent arm pain, ask him to describe it and to relate when it began. Is the pain associated with repetitive or specific movements or positions? Ask him to point out other painful areas because arm pain may be referred. For example, arm pain commonly accompanies the characteristic chest pain of myocardial infarction, and right shoulder pain may be referred from the right-upper-quadrant abdominal pain of cholecystitis. Ask the patient if the pain worsens in the morning or in the evening, if it prevents him from performing his job, and if it restricts any movements. Also ask if heat, rest, or drugs relieve it. Finally, ask about any preexisting illnesses, a family history of gout or arthritis, and current drug therapy.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Back pain: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    If life-threatening causes of back pain are ruled out, continue with a complete history. Be aware of the patient’s expressions of pain as you do so.

    CULTURAL CUE:A patient’s cultural background may impact his response to pain. For example, a patient of Irish descent may have a stoic response. A Jewish patient or one of Italian descent may be more vocal. The Navajo patient may view pain as a way of life. A patient of Filipino descent may regard pain as a chance to atone for past transgressions.

    Obtain a medical history, including past injuries and illnesses, and a family history. Ask about diet and alcohol intake. Also, take a drug history, including past and present prescriptions and over-the-counter drugs as well as herbal remedies.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Breast pain: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    Begin by asking the patient if breast pain is constant or intermittent. For either type, ask about onset and character. If it’s intermittent, determine the relationship of pain to the phase of the menstrual cycle. Is the patient a nursing mother? If not, ask about any nipple discharge and have her describe it. Is she pregnant? Has she reached menopause? Has she recently experienced any flulike symptoms or sustained any injury to the breast? Has she noticed any change in breast shape or contour?

    Ask your patient to describe the pain. She may describe it as sticking, stinging, shooting, stabbing, throbbing, or burning. Determine if the pain affects one breast or both, and ask the patient to point to the painful area.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Chest pain: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    If the chest pain isn’t severe, proceed with the history. Ask if the patient feels diffuse pain or can point to the painful area. Sometimes a patient won’t perceive the sensation he’s feeling as pain, so ask whether he has any discomfort radiating to his neck, jaw, arms, or back. If he does, ask him to describe it. Is it a dull, aching, pressurelike sensation? A sharp, stabbing, knifelike pain? Does he feel it on the surface or deep inside? Find out whether it’s constant or intermittent. If it’s intermittent, how long does it last? Ask if movement, exertion, breathing, position changes, or eating certain foods worsens or helps relieve the pain. Does anything in particular seem to bring it on?

    Review the patient’s history for cardiac or pulmonary disease, chest trauma, intestinal disease, or sickle cell anemia. Find out which medications he’s taking, if any, and ask about recent dosage or schedule changes.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Eye pain: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    If the patient’s eye pain doesn’t result from a chemical burn, take a complete history. Have the patient describe the pain fully. Is it an ache or a sharp pain? How long does it last? Is it accompanied by burning, itching, or discharge? Find out when it began. Is it worse in the morning or late in the evening? Ask about recent trauma or surgery, especially if the patient complains of sudden, severe pain. Does he have headaches? If so, find out how often and at what time of day they occur.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Facial pain: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    Begin by characterizing the patient’s facial pain. Is it stabbing, throbbing, or dull? When did it begin? How long has it lasted? What relieves or worsens it? Ask the patient to point to the painful area. If facial pain is recurrent, have the patient describe a typical episode. Review the patient’s medical and dental history, noting especially previous head trauma, dental disease, and infection.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Flank pain: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    If the patient’s condition isn’t critical, take a thorough history. Ask about the pain’s onset and apparent precipitating events. Have him describe the pain’s location, intensity, pattern, and duration. Find out if anything aggravates or alleviates it.

    Ask the patient about any changes in his normal pattern of fluid intake and urine output. Explore his history for urinary tract infection (UTI) or obstruction, renal disease, or recent streptococcal infection.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Jaw pain: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    Begin the patient history by asking the patient to describe the pain’s character, intensity, and frequency. When did he first notice the jaw pain? Did it arise suddenly or gradually? Where on the jaw does he feel pain? Does the pain radiate to other areas?

    Sharp or burning pain arises from the skin or subcutaneous tissues. Causalgia, an intense burning sensation, usually results from damage to the fifth cranial, or trigeminal, nerve. This type of superficial pain is easily localized, unlike dull, aching, boring, or throbbing pain, which originates in muscle, bone, or joints.

    Ask about recent trauma, surgery, or procedures, especially dental work. Ask about associated signs and symptoms, such as joint or chest pain, dyspnea, palpitations, fatigue, headache, malaise, anorexia, weight loss, intermittent claudication, diplopia, and hearing loss. Also ask about aggravating or alleviating factors.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Neck pain: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    If the patient hasn’t sustained trauma, find out the severity and onset of his neck pain. Where specifically in the neck does he feel pain? Does anything relieve or worsen the pain? Is there any particular event that precipitates the pain? Also ask about the development of other symptoms such as headaches. Next, focus on the patient’s current and past illnesses and injuries, diet, drug history, and family health history.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Rectal pain: History
    (Signs & Symptoms: A 2-in-1 Reference for Nurses)

    Ask the patient to describe the pain. Is it sharp or dull, burning or knifelike? How often does it occur? Ask if the pain is worse during or immediately after defecation. Does the patient avoid having bowel movements because of anticipated pain? Find out what alleviates the pain.

    Be sure to ask appropriate questions about the development of any associated signs and symptoms. For example, does the patient experience bleeding along with rectal pain? If so, find out how frequently this occurs and whether the blood appears on the toilet tissue, on the surface of the stool, or in the toilet bowl. Is the blood bright or dark red? Also, ask whether the patient has noticed other drainage, such as mucus or pus, and whether he’s experiencing constipation or diarrhea. Ask when he last had a bowel movement. Obtain a dietary history.

    » READ BOOK EXCERPT ONLINE »

    Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

    Seizures: Clinical Features and Diagnosis
    (The Diagnostic Approach to Symptoms and Signs in Pediatrics)

    Febrile Seizures

  • Can be definedas a seizure occurring in child <6 yrs of age associatedwith a temperature >38°C without evidence of intracranialinfection or acute systemic metabolic disorder. These seizures areuncommon before 6 mos of age.
  • Can be categorized as simple or complex.Most febrile seizures are simple and consist of single, brief, generalizedseizures with tonic-clonic or clonic movements lasting several minutes,although they can last as long as 15 mins. If they occur in a series,duration is <30 mins. Complex febrile seizures last >15mins, can occur in a prolonged series for several hours, and maybe focal.
  • Common clinical dilemma, especiallyin infants, is whether febrile seizure could indicate presence ofmeningitis or encephalitis. Lumbar puncture should be performedif these infections are suspected. This is especially importantin infants <18 mos of age, when physical exam is not asreliable as in older children.
  • Hypoxic-Ischemic Encephalopathy

  • Most commoncause of neonatal seizures is hypoxic-ischemic encephalopathy.
  • In most cases asphyxia occurs beforeor during delivery. History of toxemia, abruptio placenta, cordprolapse, fetal bradycardia, meconium staining, or prolonged failureto establish spontaneous respiration can be presumptive evidenceof intrauterine hypoxia.
  • In infants and children, hypoxic-ischemicencephalopathy may occur from suffocation, near drowning, shock,and cardiorespiratory arrest from any cause.
  • Brain Disorders

    Cerebral Malformations

    Seizures may arise from malformations ofthe brain. Some examples are polymicrogyria, holoprosencephaly,and cortical heterotopias. MRI is diagnostic.

    Intracranial Infection

    Infections (e.g., bacterial meningitis, encephalitis,and brain abscess) may be associated with seizures. See Chap. 3, Alteration in Consciousness.

    Intracranial Hemorrhage

  • Hypoxiais major factor in development of intraventricular hemorrhage inpreterm infants, whereas subarachnoid hemorrhage usually occursas result of difficult labor or delivery in near-term infants.
  • In infants and children, head traumais most common cause of intracranial hemorrhage.
  • Head U/S, CT, and MRI areuseful in localizing and defining extent of hemorrhage. Study performeddepends on age of child and clinical circumstances. ≥1 modalitymay be necessary.
  • Other

    Brain tumors, cerebrovascular disorders,neurocutaneous disorders, and neurodegenerative diseases also maycause seizures. See Chap. 3,Alteration in Consciousness; Chap. 13, Developmental Delay;and Chap. 25, Headache.

    Hypertensive Encephalopathy

  • Severe generalizedheadache and visual disturbances (e.g., blurring of vision) maybe symptoms of severe hypertension.
  • Seizures also may occur; however, itis impossible to predict at what BP level seizures will occur.
  • BP should be measured in every individualwho has a seizure (see Chap.32, Hypertension).
  • Drugs and Toxins

  • Ingestionof the following substances may produce seizures: theophylline,phenothiazines, tricyclic antidepressants, camphor, glutethimide,benzene, acetylsalicylic acid, morphine, codeine, cocaine, heroin,amphetamines, and lead.
  • History and physical exam may be diagnostic.
  • Urine or serum level of implicateddrug, chemical, or heavy metal confirms diagnosis.
  • Metabolic Disorders

    Hypoglycemia

  • Can be definedas blood glucose concentration of <40 mg/dL afterinitial 2–3 hrs of life.
  • Clinical manifestations of hypoglycemiain the neonate include jitteriness, tremors, lethargy, poor feeding,apnea, seizures, and alteration of consciousness. In infancy andchildhood, clinical findings include anxiety, hunger, headache,vomiting, sweating, fatigue, lassitude, seizures, and alterationof consciousness.
  • Principal Causes of Hypoglycemia

    1. Transientneonatal hypoglycemia
      1. Associated with decreased substrate or enzymefunction
      2. Associated with hyperinsulinemia
    2. Persistent hypoglycemia in infants,children, or adolescents
      1. Hyperinsulinemia
      2. Hormone deficiency
      3. Ketotic hypoglycemia
      4. Drugs or toxins
        1. Insulin
        2. Salicylates
        3. Propranolol
        4. Alcohol
        5. Oral hypoglycemic agents
      5. Hepatic disease
        1. Hepatitis
        2. Cirrhosis
        3. Reye syndrome
    3. Metabolic disorders
      1. Glycogenstorage diseases (types O, I, III,VI)
      2. Disorders of gluconeogenesis
      3. Galactosemia
      4. Hereditary fructose intolerance
      5. Maple syrup urine disease
      6. Tyrosinemia
      7. Propionic acidemia
      8. Methylmalonic acidemia
      9. Medium-chain acyl-CoA dehydrogenasedeficiency
    4. Systemic disorders
      1. Septicemia
      2. Malnutrition
      3. Malabsorption
      4. Burns
      5. Shock

    Transient Neonatal Hypoglycemia

  • Transienthypoglycemia may occur in neonates because of inadequate substrate(liver glycogen, muscle protein, body fat) or lack of fully developedenzyme systems to sustain glucose production.
  • Most common in infants who are premature,small for gestational age, or the smaller of twins, but it alsocan occur in infants born to toxemic mothers and infants who experiencesevere respiratory distress.
  • Maternal diabetes mellitus and perinatalasphyxia are most common causes of transient neonatal hyperinsulinemia.
  • Resolution of hypoglycemia usuallyoccurs in 2–3 days with milk feedings or infusion of intravenousglucose.
  • Persistent Hypoglycemia in Infants, Children, or Adolescents

    Hyperinsulinemia

  • Most commoncause of persistent hypoglycemia in infancy is hyperinsulinism,which can occur from birth to 18 mos of age.
  • It should be suspected in a macrosomicinfant with severe nonketotic hypoglycemia who requires glucoseinfusion of >10–15 mg/kg/minto maintain normal serum glucose concentration. When blood glucoseconcentration is <40 mg/dL, inappropriate increasein serum insulin (>10 μU/mL) is considereddiagnostic.
  • Once presence of hyperinsulinemia hasbeen established through spontaneous or fasting-induced hypoglycemia,specific cause should be investigated by clinical, biochemical,and molecular genetic means.
  • Causes include genetic defects of beta-cellregulation and focal lesions (islet cell adenoma, focal islet cellhyperplasia).
  • Hormonal Deficiency

  • Causes ofhypoglycemia associated with endocrine deficiency include adrenalinsufficiency with or without growth hormone deficiency.
  • When hypoglycemia is discovered, bloodsample should be drawn for possible cortisol, growth hormone, thyroidhormone (thyroxine), thyroid-stimulating hormone, insulin, and adrenocorticotropichormone measurements. These tests should be performed if other clinicalsigns suggest hormonal deficiency or if no other cause can be foundfor hypoglycemia.
  • Ketotic Hypoglycemia

  • Hypoglycemiaassociated with ketonuria may occur in children 18 mos–5yrs of age as response to prolonged fast.
  • At time of hypoglycemia, serum insulinconcentration is appropriately low (≥5–10 μU/mL),which excludes hyperinsulinism.
  • Prolonged fast of 12–18 hrsusually reproduces hypoglycemia in susceptible individuals.
  • Drugs or Toxins

  • Insulinin excessive dosage may cause severe hypoglycemia. So may salicylateintoxication, which increases insulin secretion and may possiblyinterfere with gluconeogenesis.
  • Propranolol, a beta-adrenergic blockingagent, may cause hypoglycemia in children who have decreased oralintake from prolonged fasting or illness.
  • Because ethyl alcohol impairs gluconeogenesis,hypoglycemia may occur 6–8 hrs after acute alcohol ingestionor as early as 1 hr after ingestion in a young child, especiallyif the child has not been fed for several hours. In this circumstance,a blood alcohol level confirms diagnosis.
  • Hepatic Disease

    Hepatitis, cirrhosis, and Reye syndrome alsomay be associated with hypoglycemia. See Chap. 3, Alteration in Consciousness; Chap. 30, Hepatomegaly;and Chap. 36, Jaundice.

    Metabolic Disorders

    Glycogen Storage Diseases (Types O, I, III, VI)

  • Glycogenstorage disease type 0 is autosomal-recessive disorder caused bydeficiency in enzyme activity of hepatic glycogen synthetase.
  • Gene locus has been mapped to chromosome12p12.2.
  • Hypoglycemia and seizures occur withfasting. Serum insulin concentration is appropriately low.
  • Liver biopsy with enzyme assay confirmsdiagnosis.
  • Hypoglycemia and hepatomegaly may occurwith glycogen storage diseases types I, III, and VI (see Chap. 30, Hepatomegaly).
  • Disorders of Gluconeogenesis

    Fructose 1,6-Diphosphatase Deficiency

  • Resultsin hypoglycemia only during caloric restriction (e.g., with intercurrentillness or in fasting state).
  • Gene locus of this autosomal-recessivedisorder has been mapped to chromosome 9q22.2-q22.3.
  • Characteristic features include hepatomegaly,failure to thrive, ketonuria, and lactic acidosis.
  • Liver biopsy with enzyme assay is diagnostic.
  • Phosphoenolpyruvate Carboxykinase Deficiency

  • Severe fastinghypoglycemia, which may occur during first day of life, can occurwith this enzyme deficiency.
  • Diagnosis is made by enzyme assay fromliver biopsy.
  • Other

    Galactosemia, hereditary fructose intolerance,maple syrup urine disease, tyrosinemia, propionic acidemia, methylmalonicacidemia, and fatty acid oxidation disorders (especially medium-chainacyl-CoA dehydrogenase deficiency) are discussed in Chap. 3, Alteration in Consciousness,and Chap. 36, Jaundice.

    Systemic Disorders

    Septicemia, malnutrition, malabsorption,burns, and shock also may be associated with hypoglycemia.

    Hypocalcemia

  • May be definedas total serum calcium concentration of <7 mg/dLin preterm infants and <8 mg/dL in infants andchildren. Ionized calcium concentration of <3 mg/dLis also abnormal.
  • Clinical features include poor feeding,tremulousness, lethargy, vomiting, cramps, abdominal distension,seizures, apnea, and tetany (in non-neonates).
  • Suspicion of hypocalcemia should beconfirmed with measurement of total and ionized serum calcium. Agentsthat complex calcium in blood (e.g., citrate and long-chain freefatty acids) can reduce serum ionized calcium without a decreasein serum calcium.
  • In neonatal period, hypocalcemia mayoccur during first 1–2 days of life (early) or toward endof first week of life (late). Early form can occur in very-low-birth-weightinfants, infants with perinatal asphyxia, and infants of diabeticmothers. Hypoparathyroidism and maternal hyperparathyroidism areother causes of early hypocalcemia.
  • Late occurrence of hypocalcemia maybe due to intake of high-phosphate milk, decreased calcium intestinalabsorption, hypoparathyroidism, and hypomagnesemia. Failure of hypocalcemiato respond to intravenous calcium should suggest coexisting hypomagnesemia.
  • Principal causes of hypocalcemia ininfants and children include decreased intake (nutritional), diminishedintestinal absorption of calcium, excessive calcium excretion (hypercalciuria),chronic renal failure, drugs (furosemide), excessive use of sodiumphosphate enemas, hypoparathyroidism, and vitamin D deficiency.The latter 2 disorders are discussed in the next section.
  • Hypoparathyroidism

  • Causes includefamilial hypoparathyroidism, DiGeorge syndrome, postsurgical hypoparathyroidism,autoimmune disease, resistance to parathyroid hormone, and idiopathic.
  • Diagnosis is confirmed by low serumcalcium, high serum phosphorous, and low serum parathyroid hormoneconcentrations. Specific cause needs to be investigated.
  • Vitamin D Deficiency

  • Deficiencyof vitamin D intake or defect in its metabolism may lead to hypocalcemia. Resultof these disturbances is rickets, which involves failure of bonemineralization. Most infantile rickets occurs in exclusively breast-fedterm babies who are not exposed to the sun.
  • Other causes of rickets include

  • Vitamin Dmalabsorption
  • Defective vitamin D synthesis (acquired25-hydroxylase deficiency from liver disease)
  • Congenital l-alpha-hydroxylase deficiency(also called vitamin D–dependent rickets)
  • Acquired l-alpha-hydroxylase deficiency(chronic renal failure)
  • Altered vitamin D metabolism from anticonvulsanttherapy (phenobarbital, phenytoin)
  • Hypophosphatemia (familial vitaminD–resistant rickets)
  • Dietary phosphate deficiency
  • Multiple renal tubular defects (Fanconisyndrome)
  • Clinical manifestations of ricketsdepend on age of child and degree of mineral depletion. Mild involvementmay only cause biochemical changes, whereas more severe involvementusually produces some of the following physical findings: frontalbossing, craniotabes, delayed closure of the fontanelles and sutures,enlarged costochondral junctions, enlarged wrists and ankles, bilateralbowing of the legs, lumbar lordosis, and diminished growth.
  • Radiographic changes include cuppingand fraying of metaphyses of rapidly growing bone, decreased densityof shafts of long bones, and pathologic fractures.
  • Lab findings in rickets include normalor low serum calcium, low serum phosphorus (except with renal osteodystrophy),and high serum alkaline phosphatase.
  • Specific cause must be investigated.
  • Hypomagnesemia

  • Occurs whenserum magnesium concentration is <1.5 mg/dL.
  • Clinical signs include tremors, nystagmus,seizures, and muscle weakness (chronic).
  • Causes of neonatal magnesium deficiencyinclude

  • Decreasedmagnesium intake (maternal magnesium deficiency, small-for-gestational ageinfants)
  • Diminished intestinal absorption (extensivesmall intestine resection)
  • Increased magnesium losses (chronicdiarrhea, extrahepatic biliary atresia, neonatal hepatitis, decreasedrenal tubular reabsorption)
  • Drugs (aminoglycosides, diuretics)
  • Maternal hyperparathyroidism
  • Increased phosphate intake
  • In infants and children, causes include

  • Chronic diarrhea
  • Intestinal malabsorption
  • Chronic renal disease, drugs (aminoglycosides,diuretics, cisplatin, cyclosporine)
  • Diabetes mellitus
  • Hyponatremia

  • Definedas serum sodium concentration of <130 mEq/L.
  • In low-birth-weight infants, diureticsgiven for chronic lung disease is common cause.
  • Other causes in neonates include excessivehypotonic replacement of fluid losses, hypovolemia with loss ofsodium in excess of water, and inappropriate secretion of antidiuretichormone. The latter may occur with hypoxic-ischemic encephalopathy,intracranial hemorrhage, and bacterial meningitis.
  • Frequent cause in young infants isfeeding of large amounts of water without any electrolyte. Anothercause is persistent diarrhea with loss of sodium in excess of water.
  • Hypernatremia

  • Definedas serum sodium >150 mEq/L.
  • In low-birth-weight infants, hypernatremiais usually due to severe insensible water loss or treatment of metabolicacidosis with large amounts of sodium bicarbonate.
  • Main causes in infancy and childhoodinclude diarrhea with water losses out of proportion to sodium losses,extensive burns, diabetes insipidus, and chronic renal disease.
  • Uremia

    Various factors may cause seizures in childrenwith uremia, including uremia itself, hypocalcemia, hyponatremia,and hypertension.

    Bilirubin Encephalopathy (Kernicterus)

    Infants with kernicterus often have high-pitchedcry, poor feeding, decreased movements, opisthotonus, and seizures.Survivors usually have deafness, choreoathetosis, spasticity, andpsychomotor retardation (see Chap.3, Alteration in Consciousness).

    Pyridoxine Dependency

  • Pyridoxine(vitamin B6) dependency, a rare cause ofintractable neonatal seizures, usually presents in neonatal period,often during first day of life. Biochemical defect is unknown.
  • Seizures can be of any type. If noimmediate cause of neonatal seizures can be found and if they failto respond to usual therapy, trial of intravenous pyridoxine maybe given.
  • Cessation of seizures under EEG monitoringis best way to confirm diagnosis.
  • Inborn Errors of Metabolism

    These disorders include galactosemia, hereditaryfructose intolerance, glycogen storage diseases, disorders of gluconeogenesis,and organic acidemias (maple syrup urine disease, disorders of fattyacid oxidation). They are mentioned in the section Hypoglycemia and discussedin Chap. 3, Alteration in Consciousness,and Chap. 13, Developmental Delay.

    Selected Epileptic Syndromes

    In addition to conditions discussed below,childhood absence epilepsy causes seizures. There are also unknowncauses.

    Neonatal Seizures

  • Manifestationsof seizures in neonates may be different from those in infants andchildren. Neonatal seizures are often subtle and change from momentto moment. They rarely occur as isolated events but usually occurrepeatedly over a few hours or days. Generalized tonic-clonic seizuresrarely if ever occur in neonates. Main seizure types in neonatesare subtle (associated motor automatisms), clonic (focal or multifocal),tonic (focal or generalized), and myoclonic (focal, multifocal,generalized).

  • Mostcommon type of neonatal seizure is subtle, which may involve eyechanges (conjugate eye deviation, eye fluttering, blinking), mouthmovements (chewing, sucking, drooling, tongue thrusting), autonomicchanges (tachycardia, BP changes, pupillary dilatation), or apnea.Usually unassociated with ictal EEG changes, except when tonic eyedeviation occurs.
  • Clonic seizures involve rhythmic jerkingof 1 part of body that may be focal or multifocal. Focal seizurein neonates does not necessarily signify focal brain pathology.Can occur with generalized metabolic disturbance (e.g., hypoglycemia).Ictal EEG usually shows rhythmic discharges.
  • Tonic seizures involve extension oflimbs and are usually generalized. Seen most commonly with severebrain injury (hypoxic-ischemic encephalopathy, intracranial hemorrhage)and is usually not accompanied by ictal EEG changes.
  • Myoclonic seizures are characterizedby rapid isolated jerks of entire body or body parts. Usually signifiessevere brain injury (e.g., hypoxic-ischemic encephalopathy). Mayevolve into infantile spasms. Generalized myoclonic seizures areusually associated with abnormal ictal EEG, whereas it is unusualto see ictal changes with focal or multifocal myoclonic seizures.
  • Benign Neonatal Epilepsy

  • Benign formof neonatal seizures has been described in some families. Genetictransmission is autosomal-dominant and 2 genetic loci have beenmapped.
  • Seizures are often mixed, with tonicand clonic movements and motor automatisms.
  • Neurologic exam is normal.
  • Spontaneous remission usually occursafter several months.
  • Infantile Spasms (West Syndrome)

  • Infantilespasms, a form of generalized epilepsy, usually begin at 4–8mos of age.
  • The flexor spasm (salaam or jackknifeattacks) with sudden flexion of head, neck, and trunk, lasts a fewseconds and tends to occur in repetitive series of attacks, whichmay number up to several hundred episodes in 1 day.
  • Usual EEG finding is hypsarrhythmiapattern, which consists of high-voltage, irregular slow waves withspike-and-wave complexes.
  • Hypoxic-ischemic encephalopathy, perinatalinfections, cerebral dysgenesis, and various genetic (tuberous sclerosis)and metabolic disorders (phenylketonuria) are common causes of thistype of epilepsy.
  • Lennox-Gastaut Syndrome

  • Characterizedby seizures, developmental delay, and characteristic EEG pattern.It is not a pathologic entity, but rather diffuse encephalopathywith many causes (e.g., perinatal asphyxia, cerebral malformation,head trauma, CNS infection, metabolic disorders, and neurodegenerativediseases).
  • Seizures usually begin in children <3yrs of age and are difficult to control.
  • More than 1 seizure type may occur,and most common types are tonic-clonic, tonic, and myoclonic.
  • EEG usually shows bilateral, generalized,synchronous sharp and slow-wave discharges.
  • Benign Focal Epilepsy with Centrotemporal Spikes

  • Most commonsyndrome of simple partial epilepsy in childhood. Onset is usually2–14 yrs of age, with peak at 9–10 yrs.
  • Seizures are primarily motor and predominantlyaffect face and oropharyngeal musculature, often lasting 30–60secs and occurring usually while asleep or upon awakening.
  • Neurologic exam is normal. TypicalEEG shows repetitive spike focus in centrotemporal area.
  • Recurrences after 16 yrs of age areunusual.
  • Temporal Lobe Epilepsy

  • Temporallobe seizures are most common cause of partial complex seizuresin adolescents.
  • Usually preceded by aura, which mayconsist of head deviation and posturing in children <2 yrsof age, epigastric sensation associated with fear in young children,and hallucinations in older children.
  • Onset is often noted by staring episodes,lip smacking, or chewing movements.
  • Duration is usually 1–2 mins,which is longer than with absence seizures. Period of confusionor tiredness usually follows.
  • MRI may reveal anatomic abnormality(e.g., hamartoma, slow-growing glioma, cyst, arteriovenous malformation,or mesial temporal sclerosis).
  • Juvenile Myoclonic Epilepsy

  • Usual onsetis 12–18 yrs of age.
  • Myoclonic jerks affect mainly shouldersand arms and rarely lower extremities.
  • Consciousness is usually preserved.
  • Tonic-clonic or absence seizures alsomay occur.
  • Sleep deprivation and photic stimulationcan trigger this type of seizure.
  • Characteristic EEG shows generalizedspike/polyspike-and-wake discharges.
  • Posttraumatic Epilepsy

  • Head traumacan cause seizures at any age.
  • Risk of seizures is related to severityof trauma. Children with cerebral contusion, intracerebral hematoma,or loss of consciousness for >24 hrs are at risk for developingseizures.
  • Generalized or focal seizures can occuras acute reaction of the brain to trauma, in 1–2 wks followingtrauma, or months later.
  • Diagnostic Approach

    Neonatal Seizures

    Phenomena That May Be Confused with Seizures

    Determining whether a seizure has occurredmay be difficult in some neonates. Seizures may consist of clonicmovements, tonic posturing of extremity, repetitive random or suckingmovements, or eye deviation. Recurrent apnea also may occur as amanifestation of a seizure disorder, but it is rarely the only manifestation.Jitteriness and benign myoclonic phenomena must be distinguishedfrom seizures.

    Jitteriness

    Jitteriness is stimulus sensitive and hasa tremulous quality. It ceases when extremity is held.

    Benign Neonatal Sleep Myoclonus

  • Occurs duringdrowsiness and sleep but not during wakefulness.
  • Consists of isolated jerking movementsof arm or leg.
  • Pathologic myoclonic jerks in newbornsare not related to sleep; face and trunk may be involved, and EEGis abnormal.
  • Evaluation

  • Historyand physical exam suggest most likely causes of neonatal seizures.
  • Certain tests should be performed initially:CBC with differential; blood glucose and urea nitrogen; and serumelectrolytes, creatinine, calcium, phosphorus, and magnesium.
  • If meningitis or septicemia is suspected,spinal fluid analysis with appropriate cultures, blood culture,UA, and urine culture should be performed.
  • Imaging of brain with head U/Splus CT or MRI is useful for suspected brain malformations and intracranialhemorrhage.
  • The following tests should be consideredfor suspected metabolic disorders: serum ammonia, lactate, pyruvate,carnitine, liver function tests, amino acids, blood pH, and PCO2;urine for reducing sugars, ketones, and organic acid analysis; andcerebrospinal fluid glycine. Simultaneous video-EEG recording mayclarify whether seizures are occurring and if so, what type theyare.
  • Blood glucose determination confirmspresence of hypoglycemia.

  • With symptomatic hypoglycemia, intravenousglucose should be given, but before glucose is given, blood sampleshould be drawn and held for subsequent tests.
  • Serum insulin level of >10μU/mL in presence of hypoglycemia is evidence forhyperinsulinemia.
  • Serum cortisol level of <10μg/dL suggests adrenal insufficiency. Low serum cortisoland growth hormone levels suggest pituitary disease.
  • Presence of hepatomegaly suggests galactosemia,hereditary fructose intolerance, or glycogen storage disease (typesI, III, VI). Urine positive for reducing sugars occurs with galactosemiaand hereditary fructose intolerance.
  • If diagnosis is uncertain and seizuresdo not respond to therapy, 100–200 mg of intravenous pyridoxinemay be given, while monitoring clinical and EEG responses.
  • Postneonatal Seizures

    Phenomena That May Be Confused with Seizures

    Clinical phenomena that may be confused withseizures are syncope, breath-holding spells, tics, benign paroxysmalvertigo, pseudoseizures, night terrors, migraine, and spasmus nutans.Manifestations of each are briefly described and contrasted withthose of seizures.

    Syncope

  • May be precededby dizziness or nausea. There is loss of postural tone, and individual collapses.Bradycardia and lowered BP occur in neurocardiogenic syncope (commonfaint).
  • History may include evidence of anxiety,hyperventilation, systemic illness, fasting, or prolonged standing,especially in warm weather or in closed quarters.
  • Tonic-clonic movements are uncommon,and urine incontinence is rare.
  • After episode, confusion is uncommonand amnesia does not occur.
  • Breath-Holding Spells

  • Unusualbefore 6 mos of age and usually cease by 6 yrs of age.
  • Pallid breath holding, which is consideredvariant of neurocardiogenic syncope, usually follows acute painor an injury. Infant or child becomes pale and loses consciousness;however, complete recovery occurs in 1–2 mins.
  • More common is cyanotic breath-holdingspell, where infant or child cries, holds breath during expiration,and turns dusky until breathing occurs again. Prolonged episodemay result in tonic-clonic movements and loss of consciousness.
  • Tics

    Recurrent involuntary movements that maymimic seizures. No loss or change in consciousness or postictalphenomena occur. Verbal tics also occur, especially in Tourettesyndrome.

    Benign Paroxysmal Vertigo

  • Usuallydevelops in children 2–6 yrs of age.
  • Sudden episodes are associated withfalling, refusing to walk, nausea, vomiting, and nystagmus. Duringthe episode, ability to communicate and talk is retained.
  • Episodes may last seconds to minutesand can occur daily or every few months.
  • Pseudoseizures (Nonepileptic Events)

  • Typicallyoccur at 10–18 yrs of age and are more common in girls.They may be seen, however, in children as young as 4–6yrs of age.
  • These events represent a form of conversionreaction, sometimes as a result of physical or sexual abuse.
  • Episodes can mimic generalized tonic-clonic,tonic, and complex partial seizures, but they differ from true seizuresin several ways. Onset of movements gradually builds up to paroxysmcompared with sudden onset of epileptic attack. Motor movementsare not true clonic movements but range from quivering to flailingof extremities. Postures and verbalizations are unusual.
  • Afterward, most individuals becomeimmediately responsive and do not experience postictal state.
  • Urination and tongue biting are infrequentbut may occur. Episodes never occur during sleep and only infrequentlywhen child is alone.
  • Ictal EEG shows no paroxysmal discharges.
  • Pseudoseizures also can occur in individualswho have true seizures.
  • Night Terrors

    Common in children 5–7 yrs of age,particularly in boys, and occur during slow-wave sleep. Childrenscream, thrash around, and appear frightened. Seem unaware of theirparents and surroundings. Difficult to console and do not rememberepisode. In contrast, nightmares occur during rapid eye movement sleep,and children can often recall episode.

    Migraine

  • Transientconfusional states and focal neurologic signs may occur during migraine episode.
  • Family history of migraine usuallyexists.
  • Migraine and seizures may occur insame individual, so careful evaluation is important.
  • Spasmus Nutans

    Characterized by triad of head nodding, nystagmus,and torticollis.

    Evaluation

  • Once ithas been established that a seizure has occurred, seizure type andcause must be determined if possible. Direct observation or carefulhistory may permit physician to determine seizure type, but thisis not always possible, and EEG is often helpful.
  • Age of onset, type of seizure, medicalhistory, circumstances in which seizure occurs, and physical examhelp determine whether patient has epileptic syndrome. Importantto recognize particular epileptic syndrome to determine appropriatetherapy and prognosis as well as to assess genetic risk.
  • Child who presents with fever and seizureusually has either febrile seizure or intracranial infection (meningitisor encephalitis).
  • Lumbar puncture should be performedin any child with suspected meningitis or encephalitis.
  • Because clinical exam is more reliablein child >18 mos of age than in younger infant, lumbarpuncture may not be necessary in older child with simple febrileseizure who appears otherwise well and has normal physical exam.
  • With occurrence of nonfebrile seizure,serum sodium, glucose, calcium, magnesium, creatinine, and bloodurea nitrogen should be measured. Approach to hypoglycemia has alreadybeen discussed. EEG should be performed except for child with typicalfebrile seizure.
  • History of head trauma suggests presenceof contusion, skull fracture, or intracranial hemorrhage. Childabuse is frequent cause of head trauma, and other clues (e.g., obviousbruising) may be seen. Shaking injury may produce extensive traumawith no visible evidence of injury.
  • With history of head trauma and seizure,CT should be performed.
  • With evidence of increased intracranialpressure or focal findings including focal seizures, intracranialmass lesion should be suspected and CT or MRI should be performed.MRI is preferred over CT for diagnosis of small hamartomas or othermalformations, neuronal migrational disorders, and mesial temporalsclerosis.
  • Drug or poison ingestion is anotherpossible cause of acute seizure, and history may be diagnostic.Otherwise, urine toxicology screen may confirm diagnosis.
  • Cerebral angiography is useful in thediagnosis of a vascular lesion (e.g., cerebral aneurysm or arteriovenousmalformation).
  • Other tests should be ordered, dependingon presence of other findings (e.g., progressive neurologic syndrome).
  • If uncertain whether seizures are occurring,simultaneous video-EEG recording can be performed. Although EEGis useful to help confirm diagnosis of epilepsy and classify typeof seizures, normal interictal EEG may occur with epilepsy and abnormalEEG does not confirm diagnosis unless seizure has been clinicallyrecognized. EEG should be recorded during wakefulness and sleep,and maneuvers that may activate seizure activity (e.g., hyperventilation,photic stimulation, and sleep deprivation) should be performed.
  • >>>>>>>>>>>>>

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    Source: The Diagnostic Approach to Symptoms and Signs in Pediatrics, 2006

    Abdominal Pain: Clinical Features and Diagnosis: Acute Abdominal Pain
    (The Diagnostic Approach to Symptoms and Signs in Pediatrics)

    Neonates

    Colic

    Historically thought of as cause of abdominalpain but now conceptualized more broadly. See Chap. 11, Crying and Irritability.

    Necrotizing Enterocolitis

  • Infantsappear ill and usually have abdominal distension and often evidenceof GI bleeding.
  • Progression of illness commonly resultsin bowel infarction and often perforation.
  • See Chap.22, Gastrointestinal Bleeding).
  • Gastrointestinal Obstruction or Perforation of Any Viscus

  • Reasonableassumption is that neonates with GI tract obstruction or perforationof viscus have abdominal pain, which may be expressed by persistentcrying and irritability.
  • Vomiting and abdominal distension areprominent findings.
  • Common causes of obstruction in neonatesare pyloric stenosis, intestinal atresia, volvulus with malrotation,meconium ileus, and congenital aganglionic megacolon.
  • See Chap.55, Regurgitation and Vomiting.
  • Infants

    Gastroenteritis

  • Usual presentingfeatures are vomiting, diarrhea, abdominal pain, and fever.
  • Rotavirus is most common pathogen.Frequent bacterial pathogens include Salmonella, Shigella, and Campylobacterspecies.
  • Detection of rotavirus antigen in stoolby enzyme immunoassay is diagnostic. Positive stool culture is diagnosticof bacterial infection.
  • See Chap.14, Diarrhea.
  • Viral Illness

  • Many virusescan produce illnesses that may be accompanied by mild nonspecificabdominal pain. Some viruses produce disease in respiratory tractand include rhinoviruses, respiratory syncytial virus, parainfluenzaviruses, influenza viruses, and adenoviruses.
  • Illness is usually mild and self-limitedand resolves in 3–7 days.
  • Clinical findings include fever, rhinorrhea,cough, headache, anorexia, vomiting, mild sore throat, and myalgia.
  • Diagnosis is usually clinical; however,viral culture or polymerase chain reaction of nasal secretions canoften identify specific virus.
  • Incarcerated Inguinal Hernia

  • Common causeof intestinal obstruction.
  • Painful, tender mass is palpable ininguinal area with extension at times into scrotum.
  • Persistent vomiting, abdominal distension,and inability to reduce hernia suggest intestinal obstruction.
  • Surgery should be performed immediatelyif hernia cannot be reduced and bowel obstruction is suspected.If hernia can be reduced, surgery is usually planned in severaldays, after edema has diminished.
  • Intussusception

  • Clinicalfindings are intermittent abdominal pain, vomiting, abdominal mass,and currant jelly stools.
  • Not only is air-contrast enema diagnostic,but in many cases it also may be therapeutic.
  • Trauma, Including Child Abuse

  • Many abdominalinjuries are mild and cause only abdominal wall musculoskeletal pain.
  • More serious abdominal injuries includecontusion, laceration, or rupture of spleen, liver, kidney, or intestine.Pancreatic and major vessel injuries are less common.
  • Splenic injury causes tenderness andoccasionally splenic enlargement secondary to hematoma formation.CT is best method for diagnosing contusion, laceration, or ruptureof spleen.
  • With significant liver injury, serumaminotransferase levels are usually >3–5 timesnormal level. CT is the best method to determine type and degreeof liver injury.
  • Hematuria and flank pain may occurwith kidney injury. With history of mild trauma and possibilityof isolated renal injury, excretory urography may be performed.
  • If more serious injury has occurredwith possible involvement of other abdominal organs, CT is radiologicprocedure of choice. Elevated serum amylase level suggests pancreaticinjury, which can be delineated by CT.
  • Pelvic trauma may injure pelvis, bladder,urethra, or rectum.

  • Rectal exam should be performed to determinewhether rectal laceration has occurred.
  • Pelvic tenderness or pain may indicatepelvic fracture, which can be confirmed by plain radiography.
  • Bladder and urethral injuries may causesuprapubic pain and hematuria.
  • If blood is seen at meatus, prostateis higher than normal position, or there is evidence of scrotaltrauma, urethrography should be performed.
  • Child abuse should be suspected wheneverany unexplained injuries, burns, or fractures occur. Typical skinlesions include bruises in varying stages of healing, especiallyon face, back, chest and abdomen, and different types of scars indicativeof burns or trauma with various implements.
  • Stabilization of patient with significantabdominal trauma is first priority.
  • After history and physical exam, thefollowing tests should be performed:

  • CBC with differential
  • Analysis of serum electrolytes, glucose,creatinine, amylase, aspartate and alanine aminotransferases, andblood urea nitrogen
  • Radiography of chest and abdomen
  • Cervical spine and pelvic radiographyshould be performed if indicated. In serious cases, abdominal CTshould be considered because it is most efficient and effectivemethod to investigate significant abdominal trauma.
  • Other

    Less common causes of abdominal pain in infantsinclude appendicitis, cow milk protein sensitivity, lactose intolerance,GI obstruction, sickle cell pain episodes, lead poisoning, and neoplasms.

    Preschool Children

    Constipation

  • Definedas difficult and painful passage of hard stools.
  • Abdominal pain is usually intermittent,crampy, and generalized.
  • Stool may be palpable on abdominalor rectal exam.
  • After bowel movement, pain and palpablestool masses disappear.
  • See Chap.9, Constipation.
  • Urinary Tract Infection

  • Lower abdominal,suprapubic, or flank pain associated with dysuria suggests presenceof urinary tract infection.
  • Fever and vomiting are common findings.
  • Pyuria suggests diagnosis, which isconfirmed by positive urine culture.
  • See Chap.15, Dysuria.
  • Pneumonia

  • May producereferred epigastric or periumbilical abdominal pain, especiallyif inflammation occurs in lower lobes of lung.
  • Fever, cough, tachypnea, and pleuriticpain suggest its presence.
  • Chest radiography is usually confirmatory.
  • See Chap.10, Cough.
  • Lactose Intolerance

  • Common inpreschool and school-aged children, especially African-Americanand Hispanic children.
  • Clinical manifestations include diarrheaand recurrent abdominal pain in those individuals who have low lactaseactivity and who ingest large amounts of lactose-containing products.
  • See Chap.14, Diarrhea.
  • Sickle Cell Pain Episodes

  • Vasoocclusiveepisode may cause mild-to-severe abdominal pain. Chest, back, and extremitypain also may occur.
  • Diagnosis can be confirmed by Hgb electrophoresis.
  • Food Poisoning

  • Resultsfrom ingestion of food contaminated with bacteria.
  • Crampy abdominal pain, diarrhea, andvomiting are typical features.
  • Recovery usually occurs in 1–2days.
  • History and physical exam suggest diagnosis.Positive stool culture or culture of suspected contaminated foodconfirms diagnosis.
  • See Chap.14, Diarrhea.
  • Diabetic Ketoacidosis

  • Can be initialpresentation of insulin-dependent diabetes mellitus.
  • Omission of insulin, acute illness,and emotional stress can be predisposing factors to diabetic ketoacidosis.
  • History of polyphagia, polydipsia,and polyuria of <1 mo's duration is usually found.Mild nonspecific abdominal pain and vomiting also may occur.
  • Kussmaul respirations are compensatoryphenomena of severe metabolic acidosis.
  • Severe illness may produce alterationin mental status that ranges from drowsiness to coma.
  • Presence of glucosuria, ketonuria,hyperglycemia, and metabolic acidosis confirm diagnosis.
  • Gastrointestinal Obstruction

  • Should besuspected with presence of persistent bilious vomiting and abdominal pain.
  • In this age group, common causes includeincarcerated inguinal hernia and surgical adhesions.
  • Henoch-Schönlein Purpura

  • Common causeof vasculitis in childhood.
  • Characterized by purpuric rash on buttocksand lower legs, abdominal pain, GI bleeding, transient migratoryarthritis of large joints, and hematuria.
  • Diagnosis is usually clinical.
  • See Chap.28, Hematuria.
  • Neoplasm

  • Wilms tumor,neuroblastoma, and lymphoma usually present with abdominal masses, butabdominal pain also may occur, especially with Wilms tumor.
  • See Chap.1, Abdominal Masses.
  • Drugs and Toxins

  • Acute ingestionof significant amounts of alcohol, iron, lead, or aspirin may produce abdominalpain.
  • History and measurement of toxic agentin blood are diagnostic.
  • School-Aged Children and Adolescents

  • Common causesof abdominal pain in this age group are gastroenteritis, viral illness, constipation,urinary tract infection, pneumonia, trauma, and sickle cell disease,as discussed previously.
  • Functional abdominal pain, which isusually chronic, is discussed below.
  • Acute Appendicitis

  • Occurs mostcommonly between 5 and 15 yrs of age but can occur in children <2 yrs.
  • First clinical manifestation is usuallycrampy periumbilical pain with shift in pain to right lower quadrantduring next few hours and is due to irritation of parietal peritoneumby small amount of fluid from inflamed appendix.
  • Location of appendix determines locationof pain.
  • Retrocecal appendix may irritate psoasmuscle; retrocolic appendix may cause pain in right flank.
  • Pelvic appendix may produce mild abdominalpain yet distinct tenderness on rectal exam.
  • Irritation of rectosigmoid colon byinflammatory fluid may cause mild diarrhea; irritation of uretermay cause dysuria.
  • Low-grade fever usually occurs withnonperforated appendix, whereas perforation usually produces sickerchild with higher fever, more vomiting, and more severe abdominalpain because of peritonitis or a localized abscess. Abdomen is distendedand tender, and signs of septic shock may be present. Children <2yrs are more likely to present with peritonitis and septic shock.
  • Abdominal findings depend on when childis seen during course of illness. Early in illness, right lowerquadrant tenderness may be found. With progression of illness, involuntaryspasm and rebound tenderness occur.
  • Child favors right side of abdomenand walks bent over. Climbing up on exam table, coughing, or jumpingup and down aggravate pain and indicate peritoneal inflammation.
  • Leukocytosis is common.
  • Results of UA either are normal orshow pyuria because of inflammation of ureter.
  • Abdominal radiography may occasionallyshow fecalith, edema of lateral abdominal wall, concave lumbar scoliosis,dilated cecum with air-fluid level, or localized ileus in rightlower quadrant.
  • Diagnosis is usually clinical. Otherstudies are unnecessary if findings are characteristic
  • In equivocal cases, abdominal U/Sor CT may be helpful.
  • With suspected appendicitis, surgeryshould be performed, as it is only definitive way to confirm diagnosis.
  • Appendiceal colic can cause recurrentepisodes of acute right lower quadrant pain. Drinking fluids oreating usually exacerbate the pain within 5–15 mins. Findingof maximum tenderness at McBurney point is evidence for this disorder.No lab tests are diagnostic.
  • Resolution of pain after removal ofappendix is confirmatory.
  • Peptic Ulcer Disease

  • May occurin stomach or duodenum.
  • Ulcer development is related to gastritiscaused by Helicobacter pylori.
  • Secondary ulcers usually occur in stomachand may be due to septicemia, burns, head injury, or NSAIDs.
  • Abdominal pain typically occurs inepigastric area and can awaken individual from sleep.
  • In many cases, food or antacids relievepain.
  • Vomiting and GI bleeding (heme-positivestools, hematemesis, melena) also may occur.
  • Physical exam can be normal or revealepigastric tenderness.
  • Method of choice to identify ulceris endoscopy.
  • Biliary Tract Disease

    Acute Cholecystitis

  • Usuallyrelated to presence of gallstones.
  • Clinical findings include right upperquadrant pain, vomiting, and low-grade fever. Enlarged gallbladdermay be palpable in right upper quadrant.
  • Abdominal U/S usually showsgallstones and thickened gallbladder wall.
  • Cholescintigraphy may be performedif individual is obese or has gas-filled loops of bowel.
  • Biliary Colic

  • Resultsfrom acute obstruction of cystic or common bile duct, usually by stone.
  • Pain is in right upper quadrant orepigastric region.
  • Associated symptoms often include nausea,vomiting, and jaundice.
  • Plain abdominal radiograph may showstones in some cases; otherwise, abdominal U/S is usuallydiagnostic.
  • Pancreatitis

  • Common causesinclude viral infection, blunt trauma, cystic fibrosis, and idiopathic etiologies.
  • Abdominal pain is usually epigastricand can range from mild to severe. Eating usually aggravates thepain.
  • Other clinical findings include fever,anorexia, nausea, and vomiting. Epigastric tenderness may be foundon exam. Serum amylase and lipase concentrations are usually increased.
  • Abdominal U/S and CT are usefulin demonstrating any abnormalities of pancreas.
  • Obstructive Uropathy

  • Any typeof obstructive uropathy may produce abdominal pain.
  • Most common type is ureteropelvic junctionobstruction, which may present with abdominal pain or recurringattacks of flank pain along with nausea and vomiting.
  • Various tests may be used to evaluateurinary tract obstruction including renal U/S, voiding cystourethrography,intravenous urography, and diuretic renography.
  • Urolithiasis

  • Characterizedby acute flank pain and hematuria.
  • At time of presentation, excretoryurography is useful for diagnosis of radiolucent stones and demonstrationof level of obstruction.
  • See Chap.28, Hematuria.
  • Intraabdominal Abscess

  • May occurwith localization of inflammatory process within abdominal cavity.
  • Common causes in pediatric populationare appendiceal abscesses.
  • Tender mass may be palpable on rectalexam with pelvic abscess. Leakage of abscess usually produces seriousillness with associated gram-negative septicemia.
  • Abdominal U/S or CT is usuallydiagnostic.
  • Primary Bacterial Peritonitis

  • May be associatedwith infection of preexisting ascites, which may be associated with nephroticsyndrome or chronic liver disease.
  • May occur spontaneously without anyprior underlying disease process.
  • S. pneumoniae, S. pyogenes, and gram-negativeenteric bacteria (e.g., E. coli) are common pathogens.
  • Usual clinical findings are fever,abdominal pain, and tenderness, especially with movement (coughing,jumping up and down). Vomiting and abdominal distension also mayoccur.
  • Paracentesis with Gram stain and cultureof fluid may reveal pathogen.
  • Other

  • For inflammatorybowel disease, see Chap. 14,Diarrhea.
  • For hepatitis, see Chap. 36, Jaundice.
  • Adolescent Girls

    Primary Dysmenorrhea

  • Common problemin adolescence.
  • Crampy lower abdominal pain usuallybegins 1–3 yrs after onset of menarche.
  • Occurs with menses or 1–2days before menses and may last a few hours or several days. Nausea,vomiting, headache, lower backache, thigh pain, nervousness, anddizziness also may occur.
  • Usually diagnosis of exclusion.
  • Mittelschmerz

  • Definedas lower abdominal pain that occurs at menstrual mid-cycle and lastsminutes, several hours, or (rarely) 2–3 days.
  • Pain may be due to spillage of fluidfrom follicular cyst during ovulation, which irritates peritoneum.
  • Timing of pain provides most importantdiagnostic clue.
  • Pelvic Inflammatory Disease

  • N. gonorrhoeaeand C. trachomatis are most common pathogens.
  • Clinical manifestations include vaginaldischarge, lower abdominal pain, cervical motion tenderness, adnexaltenderness, and fever. Occasionally, mass (abscess) may be palpablein adnexa or cul-de-sac.
  • Positive cervical culture is diagnostic.Laparoscopy may be necessary to confirm chronic disease.
  • Ovarian Disorders

  • Bleedinginto ovarian cyst or rupture of cyst may cause acute lower quadrantpain and tenderness.
  • Pain usually disappears within a dayafter rupture of physiologic cyst, whereas pain, nausea, vomiting,and fever may persist with other cysts.
  • Abdominal U/S may be diagnostic;otherwise, diagnosis may be confirmed by laparoscopy or at timeof surgery.
  • Torsion of ovarian cyst or fallopiantube (less common) may produce unilateral lower abdominal pain andpalpable mass.
  • In older children and adolescents,torsion is more likely with ovarian tumor. Other findings includenausea, vomiting, and fever.
  • Abdominal U/S usually demonstratescyst or tumor.
  • Endometriosis

  • Definedas presence of endometrial glands and stroma outside normal locationof uterine lining.
  • Usual presenting feature is pelvicpain, which may be cyclic or acyclic.
  • Pelvic exam in adolescents usuallyreveals mild-to-moderate tenderness rather than nodules or massesoften found in adult women.
  • If trial of NSAIDs followed by cyclicoral contraceptives fails to relieve pain, laparoscopy with biopsyshould be performed to confirm diagnosis.
  • Genital Malformations with Obstruction

  • Uterineand vaginal malformations that cause obstruction of genital tractmay produce pelvic pain, which is often chronic.
  • Lesions include imperforate hymen,transverse vaginal septum, vaginal or cervical atresia, and noncommunicatinguterine horn.
  • Pelvic U/S and MRI are usefulin defining anatomy of these lesions.
  • Complications of Pregnancy

  • Crampy abdominalpain and mild uterine bleeding are common findings with threatenedabortion. History usually includes ≥1 missed menstrual cycles.Internal os is closed, and no tissue has been expelled.
  • With incomplete abortion, uterine bleeding,painful uterine contractions, and passage of tissue fragments areusual findings. Presence of fever and pelvic pain during any stageof spontaneous or induced abortion suggests a septic abortion.
  • Any female with delayed menstrual period,lower abdominal pain, and abnormal vaginal bleeding should be suspectedof having ectopic pregnancy. There may be no history of missed menstrual periodor abnormal bleeding. Results of hCG urine pregnancy test are usuallypositive.
  • Pelvic U/S may be helpfulin demonstrating presence of ectopic pregnancy.
  • Positive culdocentesis with nonclottingblood also suggests ectopic pregnancy.
  • Laparoscopy or laparotomy confirmsdiagnosis.
  • Diagnostic Approach: Acute Abdominal Pain

  • Completehistory and reliable physical exam are far more valuable than anylab test or radiograph in diagnosis.
  • Ability of physician to make diagnosislargely depends on consideration of all possibilities, knowledgeof how they present, and planned orderly approach.
  • Age, type of onset, character and locationof pain, and associated findings are useful in diagnosis.
  • Abdominal pain of sudden onset is mostlikely to occur with intussusception, perforation of viscus, ortorsion of fallopian tube or ovary. Pain of gradual onset usuallyoccurs with appendicitis, pancreatitis, and cholecystitis. Severeintermittent pain may occur with gastrointestinal, genitourinary,or biliary tract obstruction.
  • Pain of peritonitis is diffuse, constant,and exacerbated by movement.
  • More recurrent or chronic pain usuallyoccurs with constipation, sickle cell pain episodes, and inflammatorybowel disease.
  • Lesions of stomach, duodenum, pancreas,and biliary tract commonly cause epigastric pain. Small bowel andproximal colon lesions usually produce umbilical pain. Distal colonlesions may cause hypogastric pain, whereas rectal lesions may producesacral pain.
  • Irritation of diaphragm may cause shoulderpain, and gallbladder disease may produce pain at right scapula.
  • Lesions involving ureter or femalegenital tract may produce lower abdominal and pelvic pain.
  • Most important diagnostic goal is todistinguish abdominal pain that may be life threatening.

  • 2 clinicalcircumstances represent potentially serious disease and requireimmediate investigation: (a) abdominal pain associated with biliousvomiting, persistent vomiting, or abdominal distension, and (b)abdominal pain associated with either localized or diffuse reboundtenderness. Very few clinical problems require such urgent operativeintervention that orderly approach needs to be abandoned. Only exceptionis massive exsanguinating hemorrhage.
  • Children in whom the diagnosis is uncertainshould be admitted to hospital and observed.

  • Period of active observation is extremeimportance and is safe.
  • Most causes can be diagnosed at thebedside by careful and often repeated clinical observations.
  • Initial lab tests are CBC with differential,UA, urine culture, analysis of stool for blood, ESR, chest and abdominalradiography, and abdominal U/S.
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    Source: The Diagnostic Approach to Symptoms and Signs in Pediatrics, 2006

    Back Pain: Clinical Features and Diagnosis
    (The Diagnostic Approach to Symptoms and Signs in Pediatrics)

    Congenital

  • Congenitalspine anomalies, including absence of lumbar pedicle, spinal fusion,or spinal stenosis, are unusual causes of back pain.
  • Plain radiographs are useful for diagnosis.In some cases, MRI is necessary for diagnosis.
  • Developmental

    Scoliosis

    Idiopathic scoliosis may be associated withmild back pain, particularly after long activity. When scoliosisis associated with more severe back pain, other underlying disordersshould be considered (e.g., infection, herniated disc, spondylolysis,spondylolisthesis, and tumor).

    Scheuermann Disease

  • Disorderof unknown cause that usually occurs in older children and adolescentsinvolved in athletics.
  • Most common site is thoracolumbar area,although thoracic or lumbar spine may be affected alone. Pain isusually worse with forward flexion and relieved by rest.
  • Spine radiographs show increased kyphosiswith anterior wedging of ≥1 vertebrae, irregular vertebral endplates, and disc herniation upward or downward into adjacent vertebra(Schmorl node).
  • Trauma

    Musculoskeletal

  • Muscle strainis common cause of back pain and is usually result of improper conditioning,heavy lifting, overuse in sport-related activity, or contusion.
  • History of trauma followed by spasmof paraspinous muscles and limited range of motion of spine suggestdiagnosis. Tenderness over vertebrae may indicate fracture.
  • Although spine radiographs are usuallydiagnostic, some fractures may not be visible, and technetium bonescan can be useful in localization of occult fracture.
  • Herniated Disc

  • Most commonin individuals who participate in vigorous athletic activities.
  • Trauma is often predisposing factor.
  • Most commonly involved discs are thosebetween L4 and L5 and L5 and S1.
  • Intermittent or constant lower backor buttock pain with radiation down the leg is most common presentation.Limp and disturbed gait are frequent findings.
  • Sneezing, coughing, or laughing mayaggravate pain.
  • There is limitation of movement oflumbosacral spine and often spasm of paraspinous muscles.
  • Straight leg raising test is usuallyabnormal.
  • Decreased sensation in L4–S1dermatome and motor weakness are variable findings.
  • MRI confirms diagnosis.
  • Spondylolysis

  • Definedas fracture of pars interarticularis of vertebral arch, which occursprimarily in older children and adolescents, especially in thoseparticipating in gymnastics, dance, or weight lifting.
  • Usual location is lumbar spine, andless commonly thoracic spine.
  • Pain is especially aggravated by extensionmovements of leg. There is localized tenderness and limited rangeof motion of spine.
  • Plain radiographs usually demonstratedefect.
  • Spondylolisthesis

  • Involvessame defect as spondylolysis, but there is also forward slippageof 1 vertebra on the other, usually L5 on S1.
  • Plain radiographs are usually diagnostic.
  • Slipped Vertebral Epiphysis

  • Posteriorrim of inferior epiphysis, usually L4, and adjacent disc are displacedinto spinal canal.
  • Pain usually occurs after heavy lifting.
  • Diagnosis may be confirmed by plainradiographs or CT.
  • Spinal Epidural Hematoma

  • May occurafter a fall, another injury, or spontaneously in children withbleeding disorders.
  • Pain is usually followed by signs ofspinal cord compression.
  • CT or MRI is diagnostic.
  • Infection/Inflammation

    Discitis

  • Thoughtto result from bacterial or low-grade viral infection and usuallyoccurs in preschool or school-age children.
  • Most common sites of infection aredisc spaces in lumbar region.
  • Affected children may have low back,hip, or lower abdominal pain; limp or reluctance to walk; and sometimesfever. Localized tenderness over involved disc space, spasm of adjacentmuscles, and pain with straight leg raising are usually found.
  • Early in course of illness, plain radiographsare normal; later, they show narrowing of disc space with irregularerosions and sclerosis of vertebral end plates. Nuclear scintigraphyshows increased uptake in vertebral bodies on each side of involveddisc space. CT or MRI may be useful in atypical or questionablecases by confirming presence of disc space narrowing and vertebralend-plate destruction.
  • Although controversy exists about whetherdisc space aspirate should be performed, in some cases S. aureuscan be cultured from disc space aspirate or blood.
  • Disc Space Calcification

  • Rare lesionin pediatric population. Although pathogenesis is uncertain, itmay follow nonspecific inflammatory reaction of disc space. Mostcommonly involved area is cervical spine.
  • There is cervical or thoracic pain,localized tenderness over disc space, muscle spasm, and occasionalfever.
  • Plain radiographs show calcification.
  • Osteomyelitis

  • Most commonpathogen causing osteomyelitis of spine is S. aureus. Other pathogens includeS. pneumoniae, group A Streptococcus, E. coli, P. aeruginosa, andSalmonella species.
  • Localized back pain, tenderness overinvolved vertebrae, restriction of spine motion, and fever are commonfindings. There is usually leukocytosis and increased sedimentationrate.
  • Plain radiographs may be normal earlyin course of illness, but after about 10 days, radiologic findingsinclude disc space narrowing, decreased height of vertebra, andsclerotic/lytic lesions of vertebral body, pedicles, orneural arches. Extension into soft tissues can produce paravertebralmass. Nuclear scintigraphy usually shows increased uptake earlyin illness.
  • Bone aspirate or biopsy may revealpathogen, and blood cultures also may be positive.
  • Tuberculosis of Spine

  • Much lesscommon than pyogenic infection.
  • Thoracic spine is most common siteof involvement, with pain radiating to intercostal areas. Involvementof cervical spine may produce neck pain and torticollis, whereaslumbar spine involvement may produce lower back pain and limp. Feveralso may occur.
  • Plain radiographs show destructionand collapse of vertebrae with narrowing of disc spaces.
  • Involvement of spinal cord at any levelmay produce extremity weakness.
  • Diagnosis should be considered in childrenwho have history of exposure or who live in endemic area and whohave persistent back or neck pain.
  • CBC, sedimentation rate, chest radiograph,Mantoux test, early morning gastric aspirates, and bone biopsy foracid-fast bacilli and culture should be performed.
  • Iliac Osteomyelitis

  • Uncommoninfection.
  • Clinical manifestations include lowback pain, fever, and tenderness over ilium.
  • Nuclear scintigraphy shows increaseduptake. Bone aspirate or biopsy is diagnostic.
  • Sacroiliac Joint Infection

  • Most commonpathogen is S. aureus. Prior pelvic fracture is risk factor.
  • Usually presents with pain in lowerback, hip, or buttock; limp; and fever. Flexion, abduction, andexternal rotation of leg cause sacroiliac pain if joint is involved.
  • Plain radiographs may be normal earlyin illness, but within 10 days, lytic and sclerotic changes of bonemargins and widening of joint space are usually seen. Nuclear scintigraphyshows increased uptake in affected bone.
  • Aspiration or open biopsy is usuallyrequired to establish specific diagnosis. Blood culture also mayreveal pathogen.
  • Juvenile Rheumatoid Arthritis

  • Can affectthe spine at any level and cause persistent back pain and decreasedrange of motion. Most commonly involved area is cervical spine.
  • Plain radiographs of cervical spinemay show atlantoaxial displacement, ankylosis of apophyseal joints,and narrowing of disc spaces.
  • See Chap.37, Limp
  • Ankylosing Spondylitis

  • Disorderof unknown cause that primarily affects boys >8 yrs.
  • Most common feature is arthritis oflower extremity joints, which may include hips, knees, ankles, andfeet. Back pain and limitation of motion of lumbosacral spine orsacroiliac joints also can occur.
  • Diagnostic clue is presence of enthesitis,especially involving heel.
  • Plain radiographs of lumbosacral spineand sacroiliac joints may show changes consistent with sacroiliitis.
  • Slit-lamp exam should be performedbecause uveitis can occur.
  • HLA-B27 antigen is positive in about90% of cases. Antinuclear antibody and rheumatoid factorare usually negative.
  • Spinal Epidural Abscess

  • Rare infectionin childhood that can be acute or chronic.
  • Most common pathogen is S. aureus.Predisposing factors include local wound infection, decubitus ulcer,or spine surgery.
  • Back pain, localized spine tenderness,tender spinal mass, and fever are common findings. Lumbosacral involvementmay produce buttock and leg pain with leg weakness, impaired sensation,decreased deep tendon reflexes, and impaired bowel and bladder function.
  • Radiographs of spine are usually normalbut sometimes show evidence of osteomyelitis. CT or MRI may be diagnostic.
  • Diagnosis is confirmed at surgery.
  • Sickle Cell Disease

  • Back painmay occur in sickle cell vasoocclusive episode and is usually musculoskeletalin origin. Infarction of posterior ribs or vertebrae may cause backpain and bone tenderness.
  • Can usually be demonstrated by bonescintigraphy.
  • Neoplasm

  • Tumors ofthe spine or spinal cord are uncommon in pediatric population.
  • Clinical features include persistentpain sometimes waking child during night, sciatic pain, painfulscoliosis, localized tenderness, palpable mass, lower extremityweakness, sensory changes, and bowel or bladder disturbances.
  • Histologic diagnosis is necessary exceptfor perhaps osteoid osteoma.
  • Vertebral Tumors

  • Most commonbenign tumor of spine is osteoid osteoma.

  • Pain often awakens child from sleep.
  • Localized tenderness and scoliosisalso may occur.
  • Spine radiograph shows small radiolucentarea surrounded by sclerosis.
  • Osteoblastoma has same histology asosteoid osteoma but is larger.
  • Aneurysmal bone cyst may affect posteriorelements of spine, vertebral bodies, or ribs, causing pain and sometimespalpable mass.

  • Commonlyoccurs in adolescence.
  • Spine radiograph shows cyst with finetrabeculae and thin cortex.
  • MRI shows extent of tumor and any neuralcompression.
  • Eosinophilic granuloma commonly presentswith persistent thoracic back pain in adolescence. Radiographs showcircumscribed area of osteolysis and any vertebral collapse.
  • Most common primary malignant bonetumors affecting spine are osteogenic sarcoma and Ewing sarcoma.Common metastatic lesions include neuroblastoma, Wilms tumor, leukemia,and lymphoma. Usual findings are persistent pain, bone tenderness,fever, and weight loss. Spine radiographs, nuclear scintigraphy,CT, and MRI are useful in locating and defining the extent of thetumor.
  • Intraspinal Tumors

  • May arisewithin spinal cord (astrocytoma, ependymoma), within dura but outside spinalcord (neurofibroma, lipoma, dermoid), and outside dura (commonly,extension of paravertebral neuroblastoma).
  • May present with spinal pain with radiationto specific dermatome, leg or arm weakness, limp or difficulty walking,and bowel or bladder disturbance. Clinical findings include weaknessor spasticity of extremities, decreased sensation, pathologic reflexes,relaxation of anal sphincter, and scoliosis.
  • Spine radiographs are useful, but CTand MRI help locate and define extent of lesion.
  • Referred Pain

  • Infection/inflammationor mass in abdominal, thoracic, retroperitoneal, or pelvic regionscan cause referred back pain. Examples are pneumonia, pyelonephritis,pancreatitis, appendicitis, cholecystitis, and hydronephrosis.
  • History and physical exam suggest thesediagnoses, which are discussed in other chapters.
  • Psychogenic

  • Back paincan be due to anxiety, depression, hypochondriasis, or conversionreaction.
  • Pain is nonspecific and nonlocalizing.
  • Physical and neurologic exams, CBC,sedimentation rate, and spine radiographs are normal.
  • Psychosocial history provides cluesto diagnosis.
  • Diagnostic Approach

  • History,physical exam, and spine radiographs are usually diagnostic of congenital spineanomalies, fractures, Scheuermann disease, spondylolysis, and spondylolisthesis.
  • MRI is procedure of choice to confirmdiagnosis of herniated disc.
  • Fever usually occurs with inflammatorydisorder or infection affecting spine. When fever accompanies backpain, CBC and erythrocyte sedimentation rate should be performed.
  • Nuclear scintigraphy is useful, especiallywith suspected osteomyelitis, discitis, or sacroiliac joint infection.
  • Aspirate or biopsy of lesion shouldbe strongly considered with suspected osteomyelitis. Blood culturemay reveal organism, but yield is often low.
  • Spine radiographs are useful in diagnosisof vertebral spine and intraspinal masses.
  • CT and MRI are valuable in diagnosingtumors as well as spinal epidural abscess.
  • For all tumors except possibly osteoidosteoma, histologic exam is necessary for diagnosis.
  • » READ BOOK EXCERPT ONLINE »

    Source: The Diagnostic Approach to Symptoms and Signs in Pediatrics, 2006

    Chest Pain: Clinical Features and Diagnosis
    (The Diagnostic Approach to Symptoms and Signs in Pediatrics)

    Musculoskeletal Disorders

    Muscle

    Trauma

  • Normal activitycan strain chest wall musculature.
  • Participation in athletics or overexertionalso may injure specific muscle groups of chest wall.
  • Blunt trauma from accidents, athleticinjuries, or physical abuse can cause chest wall contusions.
  • Stitch

  • Definedas sharp pain occurring in upper quadrants of abdomen under costalmargin during strenuous activity.
  • Resolves when exercise is over.
  • Stress on peritoneal ligaments is thoughtto be the cause.
  • Precordial Catch

  • Also calledTexidor twinge and defined as benign self-limited disorder of unknown cause.
  • Characterized by acute onset of sharppain, usually localized over cardiac apex and occurring at restor with mild activity.
  • Usually lasts up to 1 min but may befollowed by dull ache.
  • Deep inspiration may aggravate pain.
  • Sickle Cell Pain Episodes

    Chest pain can occur during vasoocclusiveepisode and usually involves muscle ache.

    Bone/Cartilage

    Trauma

  • Accidentalor nonaccidental trauma may produce rib fractures.
  • Localized bone tenderness suggestsrib contusion or fracture.
  • Chest radiography should be performed.
  • Costochondritis

  • Common causeof chest pain in adolescence.
  • Localized pain and tenderness occurover the affected costochondral junction. Left fourth and fifthjunctions are most commonly involved.
  • Sickle Cell Disease (Thoracic Bone Infarction)

  • Chest painmay occur as result of thoracic bone infarction that may affectribs, sternum, or vertebrae.
  • Nuclear scintigraphy can demonstrateinfarction.
  • Slipping-Rib Syndrome

  • Pain isthought to arise from eighth, ninth, or tenth ribs overriding theone above.
  • Diagnosis may be confirmed by graspingcostal margin and pulling anteriorly to reproduce pain (hookingmaneuver). Same maneuver may produce palpable click as cartilagesslip over one another.
  • Tietze Syndrome

  • Syndromeof unknown cause characterized by swelling at right sternoclavicularor second sternochondral junction.
  • Pain may last for weeks with frequentremissions and exacerbations.
  • Osteomyelitis

  • Localizedpain and tenderness along with fever characterize osteomyelitisof sternum or rib.
  • S. aureus is most common pathogen.
  • Nonspecific lab findings are leukocytosisand increased erythrocyte sedimentation rate.
  • Although chest radiograph may be normalearly in illness, nuclear scintigraphy reveals localized uptakeof radionuclide.
  • In 10–14 days, chest radiographyshows periosteal bone formation and destructive lesions.
  • Bone aspiration or biopsy is usuallydiagnostic.
  • Neoplasm

  • Bone tumorsof chest wall are rare; however, neoplastic disease may cause localized ribor sternal pain.
  • Acute lymphoblastic leukemia may involvesternum or ribs. Chest pain is not infrequent during course of thisillness but is rarely presenting symptom. Metastatic neuroblastomaalso may cause bone pain.
  • See Chap.1, Abdominal Masses and Chap. 38, Lymphadenopathy.
  • Trachea and Proximal Bronchi Disorders

  • Tracheobronchialpain usually occurs in neck or chest where inflammation is.
  • See Chap.10, Cough.
  • Parietal Pleura Disorders

    Intercostal nerves conduct pain impulsesfrom parietal pleura to spinal cord.

    Pneumonia

  • Most commoncause of pleuritic chest pain is pneumonia.
  • Pain is localized, sharp, stabbing,and knifelike and usually occurs with inspiration. Shallow breathsminimize pain, whereas laughing and coughing aggravate it. Pleuralfriction rub indicates pleural involvement.
  • Chest radiograph shows infiltrate andsometimes pleural effusion.
  • See Chap.10, Cough).
  • Pleurodynia

  • Self-limitedillness usually caused by enteroviral infection.
  • Fever and paroxysms of sharp chestpain without evidence of pneumonia are usual presenting clinicalfeatures. Pain usually subsides within 1 wk.
  • Positive pharyngeal viral culture or4-fold increase in antibody titer is diagnostic.
  • Empyema

  • Definedas presence of pus in pleural space and usually occurs from extensionof bacterial pneumonia.
  • Most common pathogen in pediatric populationis S. pneumoniae.
  • High spiking fever, respiratory distress,and occasional chest pain characterize empyema. Usually no breathsounds are heard over affected area.
  • Chest radiograph shows effusion, butthoracentesis must be performed for specific diagnosis. Analysisof fluid should include white cell and differential counts; Gramand acid-fast stains; protein; glucose; and aerobic, anaerobic,fungal, and acid-fast cultures.
  • Pneumothorax

  • Definedas accumulation of air in pleural space.
  • Common causes include penetrating woundsof chest, rib fracture, positive pressure ventilation, pneumonia,cystic fibrosis, and idiopathic.
  • Although chest pain is acute, unilateral,and severe, degree of respiratory distress depends on how largepneumothorax is. Large pneumothorax results in hyperresonance topercussion on involved side.
  • Chest radiography is diagnostic.
  • Hemothorax

  • Definedas collection of blood in pleural space.
  • Most common cause is trauma, surgicalor nonsurgical.
  • Degree of respiratory distress dependson size of hemothorax. Decreased breath sounds and dullness to percussionover affected side of chest usually occur.
  • Chest radiograph that shows collapseof lung surrounded by opacification suggests presence of hemothorax.
  • Diagnosis is confirmed by thoracentesis.
  • Pneumomediastinum

  • Definedas presence of air or gas in mediastinum that can cause acute, severechest pain that may be referred to back, shoulders, and neck.
  • Palpation of subcutaneous air in softtissues of chest wall or neck signifies presence of mediastinalemphysema.
  • Common causes include pneumothoraxwith dissection of air into mediastinum, asthma, cystic fibrosis,and chest trauma with disruption of tracheobronchial tree.
  • Chest radiography is diagnostic.
  • Postpericardiotomy Syndrome

  • Thoughtto be immunologic reaction associated with introduction or reactivationof virus at time of intrapericardial surgery.
  • Usually occurs 1–3 wks aftersurgery in children >2 yrs.
  • Clinical manifestations include fever,chest pain, pericardial and pleural effusions, and sometimes pulmonaryparenchymal disease. Sharp or dull pain is precordial in locationand worsens with inspiration and lying down. Pleural and pericardialfriction rubs may be heard, unless there are significant effusions.
  • Pericardial effusions can be life threateningif they are large.
  • Serum may be positive for antiheartantibody.
  • Average duration of illness is 2–3wks, but recurrences sometimes occur months or years later.
  • Pulmonary Embolism

  • Definedas thrombus or any foreign material (e.g., air or fat) in pulmonaryarteries that causes obstruction of pulmonary blood flow.
  • Risk factors in pediatric populationinclude deep venous thrombosis, central venous catheter, prolongedimmobilization, ventriculoatrial shunt, right-sided endocarditis,intravenous drug use, septicemia, and severe dehydration.
  • Chest pain associated with pulmonaryembolism is acute and can be pleuritic or nonpleuritic. Usuallyassociated with dyspnea. Other findings include sweating, nausea,vomiting, palpitations, syncope, and anxiety.
  • Physical exam commonly reveals tachycardia,dyspnea or tachypnea, and fever. Other findings include crackles,wheezes, pleural friction rub, prominent RV impulse, accentuatedpulmonary closure sound, S4 gallop, systolic ejection murmur alongsternal border, hepatomegaly, and edema.
  • Chest radiograph is normal or showsconsolidation, atelectasis, or pleural effusion.
  • ECG findings include ST-segment orT-wave changes in right precordial leads and RV hypertrophy.
  • Pulmonary isotope lung perfusion scanthat shows bilateral segmental defects strongly suggests presenceof pulmonary emboli, whereas normal scan effectively excludes pulmonaryemboli. If scan is abnormal, ventilation (xenon) scan should beperformed. With pulmonary emboli, perfusion scan should be abnormaland ventilation scan normal.
  • MRI also may be useful in diagnosisof pulmonary embolism. If diagnosis is still uncertain, pulmonaryangiogram is best way to establish presence of pulmonary embolism.
  • Neoplasm

  • Primarychest neoplasms are rare in children.
  • Chest pain is usually secondary topleural metastases, which can occur with Wilms tumor, osteogenicsarcoma, neuroblastoma, or rhabdomyosarcoma.
  • Chest radiography may show mass ormetastases.
  • Chest CT locates and defines extentof mass or metastases.
  • Histologic diagnosis is definitive.
  • Cardiac Disorders

  • Cardiacdisorders that cause chest pain usually produce myocardial ischemiaor inflammation of parietal pericardium.
  • Middle and inferior cardiac nervesconduct myocardial pain impulses to upper thoracic rami, sympatheticchain, and spinal cord. Pain impulses from upper parietal pericardiumtravel along intercostal nerves, and those from lower pericardiumtravel along phrenic nerves and then to spinal cord.
  • Myocardial Ischemia Including Infarction

  • Myocardialischemia causes angina, which has been described as gripping, crushing, sharp,knifelike pain in retrosternal or left chest areas that usuallyfollows exercise or exertion and is relieved by rest. Pain may betransmitted to neck, shoulder, arm, or back. In some cases, myocardialinfarction may occur. Tachypnea, tachycardia, gallop rhythm, sweating,nausea, and vomiting are common findings.
  • Causes of myocardial ischemia includesevere aortic stenosis, coronary artery anomalies (including anomalouscoronary artery from pulmonary artery), myocarditis, cardiomyopathy,Kawasaki disease, familial dysproteinemias, and cocaine use.
  • ECG changes may indicate myocardialischemia or injury. ECG leads overlying subepicardial or transmuralischemic area show inverted T waves. Symmetric tall peaked T wavesare seen in leads overlying subendocardial ischemic area. Leadsoverlying subendocardial injury show ST depression with concaveor flat contour, whereas those overlying subepicardial injury showST elevation with upwardly convex or concave contour. Within hoursto days of myocardial infarction, Q waves and inverted T waves appearin leads overlying infarction.
  • 2-D echocardiogram may show local orgeneralized myocardial dysfunction.
  • Elevation of creatine kinase MB fractionor troponin T is usually found with destruction of myocardial tissue.
  • Nuclear scintigraphy of myocardiummay show decreased local uptake.
  • Cardiac catheterization and angiographyare necessary in some cases for definitive diagnosis.
  • Pericarditis

  • Most commoncauses in children are viral infection, acute rheumatic fever, andpostpericardiotomy syndrome. Less common are purulent pericarditis,uremia, systemic lupus erythematosus, juvenile rheumatoid arthritis,and radiation therapy.
  • Triad of fever, chest pain, and pericardialfriction rub signify pericarditis.
  • Chest pain is usually acute and substernalwith radiation to neck, shoulders, and arms. Sitting up and leaningforward eases pain, whereas deep breathing, coughing, and lyingdown aggravate it.
  • ECG shows elevated ST segments in nearlyall leads that progress to T-wave flattening and inversion in someof the leads, which may persist for months after acute lesion hasresolved.
  • 2-D echocardiography commonly revealspericardial effusion.
  • Mitral Valve Prolapse

  • Associationof chest pain and mitral valve prolapse has been seriously questioned, bothin adults and children. Mechanism of pain, which is ill definedand usually nonexertional, is uncertain. Other causes of chest painshould be considered in children with chest pain and mitral valveprolapse.
  • Midsystolic click or late systolicmurmur (mitral incompetence) or both are heard at apex.
  • M-mode or 2-D echocardiography confirmsdiagnosis of mitral valve prolapse.
  • Arrhythmias

  • Supraventriculartachycardia may cause some chest discomfort as well as cardiac failure.
  • Sinus tachycardia or premature ventricularcontractions have been associated with palpitations.
  • Important to differentiate by historywhether child is having chest pain or different sensation causedby palpitations.
  • ECG rhythm strip confirms diagnosisof arrhythmia. If cardiac rhythm is normal, Holter monitoring maybe useful.
  • With intermittent chest pain and suspectedarrhythmia, event recorder is another useful diagnostic technique.
  • Diaphragm Disorders

  • Intercostalnerves conduct impulses from peripheral diaphragm to spinal cord. Phrenicnerves (C3–C5) conduct pain impulses from central diaphragmto spinal cord.
  • With diaphragmatic irritation, painmay radiate to lower chest or shoulder, depending on extent of involvement.
  • Possible causes include subphrenicor hepatic abscess and perihepatitis (Fitz-Hugh-Curtis syndrome).
  • Gastrointestinal Disorders

    Esophagus

    Gastroesophageal Reflux

  • Common causeof transient chest pain is reflux of gastric contents from stomachinto esophagus. Severe reflux may lead to esophagitis with persistentchest pain.
  • Monitoring for 24 hrs with esophagealpH probe can determine presence and severity of reflux. Endoscopywith biopsy can diagnose esophagitis.
  • See Chap.55, Regurgitation and Vomiting).
  • Caustic Ingestion

  • Ingestionof caustic substances may cause sharp or burning pain in midsternaland lower chest.
  • Esophagoscopy is diagnostic.
  • Foreign Body

  • Foreignbody lodged in esophagus commonly causes choking, drooling, anddifficulty swallowing. Associated dull ache also may occur.
  • Chronically impacted foreign body maycause esophagitis.
  • If foreign body is radiopaque, maybe seen on chest radiograph. Otherwise, filling defect may be seenon esophagram.
  • Esophagoscopy is diagnostic for chronicallyimpacted foreign body.
  • Hiatal Hernia

  • Definedas sliding hernia with gastroesophageal junction lying above diaphragm.
  • Symptoms of hiatal hernia are thoseof gastroesophageal reflux with epigastric and lower chest paincommonly occurring after meals.
  • Sometimes large hiatal hernia may beseen on plain radiograph with retrocardiac mass extending to rightlateral chest wall.
  • Upper GI series is diagnostic.
  • Spasm

  • May causechoking episodes during feeding, difficulty in swallowing, and substernal chestache.
  • May be related to stress, rapid eating,and drinking cold liquids.
  • Upper GI series with video playbackcapability is diagnostic.
  • Tear

  • Persistentsevere vomiting may produce acute esophageal tear, which causeschest pain along with hematemesis.
  • Esophagoscopy is diagnostic.
  • Referred Pain

  • Gastritis,peptic ulcer disease, cholecystitis, and pancreatitis may causereferred chest pain.
  • See Chap.2, Abdominal Pain.
  • Neurologic Disorders

    Intercostal Nerve

    Trauma

    Injury to intercostal nerve may produce painin dermatome supplied by nerve.

    Herpes Zoster Neuritis

  • Herpes zostercan cause painful, vesicular lesions along ≥1 dermatomes correspondingto intercostal nerves.
  • Positive viral culture of lesion isconfirmatory.
  • Dorsal Root

  • Trauma (fractures)or spinal disease (tumor, osteomyelitis, epidural abscess) can involvecervical or upper thoracic dorsal roots and cause chest pain.
  • Pain often occurs with body motionor after coughing, sneezing, or laughing. Hypesthesia to pin prickor light touch may be found in affected dermatomes.
  • Useful diagnostic tests include cervicaland thoracic spine radiographs, nuclear scintigraphy, CT, and MRI.
  • Psychologic Disorders

  • Anxietywith or without hyperventilation, depression, school phobia, hypochondriasis,and conversion reactions are common causes of chest pain, especiallyin adolescence.
  • Pain has no particular characteristicsand usually diminishes once patients can talk about problem andreceive reassurance that they are not seriously ill.
  • Hyperventilation attacks are most commonin girls and may produce air hunger, dizziness, syncope, palpitations,and paresthesias.
  • Generally, specific stressful situationthat is related to onset of chest pain can be identified.
  • Family history of chest pain and occurrenceof recurrent somatic complaints (e.g., headache and abdominal pain)are also common.
  • To make diagnosis of psychogenic chestpain, positive clinical psychologic evidence must exist.
  • Onset of pain in association with stressfulemotional situation suggests that pain is manifestation of psychologicproblem.
  • In general, psychologic symptoms donot occur in isolation but are accompanied by other signs of unhappinessand anxiety.
  • Psychosocial history is most usefulclinical tool in making diagnosis of psychogenic chest pain.
  • Idiopathic Chest Pain

  • Most commoncause of chest pain in childhood and adolescence is idiopathic.Such pain is nonspecific but may be recurrent or chronic.
  • This is diagnosis of exclusion.
  • Diagnostic Approach

  • Most commoncauses of chest pain in pediatric population are idiopathic, musculoskeletal,and psychologic.
  • If complaint has been present for >6mos, organic cause is less likely.
  • History and physical exam are diagnosticin many cases.
  • Chest radiography should be performedwith localized rib or bone pain, any respiratory distress, or suspectedpulmonary disorder.
  • With suspected heart disease, ECG shouldbe performed.
  • 2-D echocardiography may be necessary,depending on suspected diagnosis.
  • Psychologic causes must be substantiatedby clinical psychologic evidence.
  • Children in whom no definite causecan be found are more likely to complain recurrently, presumablyfor secondary gain.
  • In adolescence, chest pain is frequentcomplaint, but it is usually benign. Knowledge about recent lifeevents and individual's beliefs about the symptom are importantin managing this problem.
  • » READ BOOK EXCERPT ONLINE »

    Source: The Diagnostic Approach to Symptoms and Signs in Pediatrics, 2006

    Myoclonus: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    If the patient is stable, evaluate his level of consciousness (LOC) and mental status. Ask about the frequency, severity, location, and circumstances of myoclonus. Has he ever had a seizure? If so, did myoclonus precede it? Is myoclonus ever precipitated by a sensory stimulus? During the physical examination, check for muscle rigidity and wasting, and test deep tendon reflexes. Then perform a neurologic examination.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Breast pain [Mastalgia]: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    Begin by asking the patient if breast pain is constant or intermittent. For either type, ask about onset and character. If it's intermittent, determine the relationship of pain to the phase of the menstrual cycle. Is the patient breast-feeding? If not, ask about any nipple discharge and have her describe it. Is she pregnant? Has she reached menopause? Has she recently experienced flulike symptoms or sustained injury to the breast? Has she noticed a change in breast shape or contour?

    Ask the patient to describe the pain. She may describe it as sticking, stinging, shooting, stabbing, throbbing, or burning. Determine if the pain affects one breast or both, and ask the patient to point to the painful area.

    Instruct the patient to place her arms at her sides, and inspect the breasts. Note their size, symmetry, and contour and the appearance of the skin. Remember that breast shape and size vary and that breasts normally change during menses, pregnancy, and lactation and with aging. Are the breasts red or edematous? Are the veins prominent?

    Note the size, shape, and symmetry of the nipples and areolae. Do you detect ecchymosis, a rash, ulceration, or a discharge? Do the nipples point in the same direction? Do you see signs of retraction, such as skin dimpling or nipple inversion or flattening? Repeat your inspection, first with the patient's arms raised above her head and then with her hands pressed against her hips.

    Palpate the breasts, first with the patient seated and then with her lying down and a pillow placed under her shoulder on the side being examined. Use the pads of your fingers to compress breast tissue against the chest wall. Proceed systematically from the sternum to the midline and from the axilla to the midline, noting any warmth, tenderness, nodules, masses, or irregularities. Palpate the nipple, noting tenderness and nodules, and check for discharge. Palpate axillary lymph nodes, noting any enlargement.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Eye pain [Ophthalmalgia]: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    If the patient's eye pain doesn't result from a chemical burn, take a complete history. Have the patient describe the pain fully. Is it an ache or a sharp pain? How long does it last? Is it accompanied by burning, itching, or discharge? Find out when it began. Is it worse in the morning or late in the evening? Ask about recent trauma or surgery, especially if the patient complains of sudden, severe pain. Does the patient wear contact lenses? How often are they removed or replaced if they're disposable? Does he have headaches? If so, find out how often and at what time of day they occur.

    During the physical examination, don'tmanipulate the eye if you suspect trauma. Carefully assess the lids and conjunctiva for redness, inflammation, and swelling. Then examine the eyes for ptosis or exophthalmos. Finally, test visual acuity with and without correction, and assess extraocular movements. Characterize any discharge. (See Examining the external eye.)

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Seizures, absence: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    If you suspect a patient is having an absence seizure, evaluate its occurrence and duration by reciting a series of numbers and then asking him to repeat them after the attack ends. If the patient has had an absence seizure, he can't do this. Alternatively, if the seizures are occurring within minutes of each other, ask the patient to count for about 5 minutes. He'll stop counting during a seizure and resume when it's over. Look for accompanying automatisms. Find out if the family has noticed a change in behavior or deteriorating schoolwork.

    Next, perform a complete neurologic examination.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Seizures, complex partial: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    If you witness a complex partial seizure, never attempt to restrain the patient. Instead, lead him gently to a safe area. (Exception: Don't approach him if he's angry or violent.) Calmly encourage him to sit down, and remain with him until he's fully alert. After the seizure, ask him if he experienced an aura. Record all observations and findings. Obtain a history. Has the patient experienced a seizure in the past? Has he had a recent head injury? Has he experienced any fever, headaches, or periods of confusion? Obtain a complete drug history. Take his vital signs and perform a complete neurologic examination.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Seizures, generalized tonic-clonic: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    If you didn't witness the patient's seizure, obtain a description from his companion. Ask when the seizure started and how long it lasted. Did the patient report unusual sensations before the seizure began? Did the seizure start in one area of the body and spread, or did it affect the entire body right away? Did the patient fall on a hard surface? Did his eyes or head turn? Did he turn blue? Did he lose bladder control? Did he have other seizures before recovering?

    If the patient may have sustained a head injury, observe him closely for loss of consciousness, unequal or nonreactive pupils, and focal neurologic signs. Does he complain of headache and muscle soreness? Is he increasingly difficult to arouse when you check on him at 20-minute intervals? Examine his arms, legs, and face (including tongue) for injury, residual paralysis, or limb weakness.

    Next, obtain a history. Has the patient ever had generalized or focal seizures before? If so, do they occur frequently? Do other family members also have them? Is the patient receiving drug therapy? Is he compliant? Also, ask about sleep deprivation and emotional or physical stress at the time the seizure occurred.

    Next, assess the patient's level of consciousness (LOC) and proceed with a complete neurologic examination.

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    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Seizures, simple partial: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    Be sure to record the patient's seizure activity in detail; your data may be critical in locating the lesion in the brain. Does the patient turn his head and eyes? If so, to what side? Where does movement first start? Does it spread? Because a partial seizure may become generalized, you'll need to watch closely for loss of consciousness, bilateral tonicity and clonicity, cyanosis, tongue biting, and urinary incontinence. (See “Seizures, generalized tonic-clonic,” page 552.)

    After the seizure, ask the patient to describe exactly what he remembers, if anything, about the seizure. Check the patient's LOC, and test for residual deficits (such as weakness in the involved extremity) and sensory disturbances.

    Then obtain a history. Ask the patient what happened before the seizure. Can he describe an aura or did he recognize its onset? If so, how—by a smell, a vision disturbance, or a sound or visceral phenomenon such as an unusual sensation in his stomach? How does this seizure compare with others he has had?

    Also, explore fully any history—recent or remote—of head trauma. Check for a history of stroke or recent infection, especially with fever, headache, or stiff neck.

    Perform a complete neurologic examination.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Abdominal pain: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    If the patient has no life-threatening signs or symptoms, take his history. Ask him if he has had this type of pain before. Have him describe the pain in his own words. Ask him if the pain is dull, sharp, stabbing, or burning and to rate his pain on a scale, such as the visual analog scale, FACES pain scale, or verbal numeric scale for intensity of pain. Ask if anything relieves the pain or makes it worse. Ask the patient if the pain is constant or intermittent and when the pain began. Constant, steady abdominal pain suggests organ perforation, ischemia, or inflammation or blood in the peritoneal cavity. Intermittent, cramping abdominal pain suggests that the patient may have obstruction of a hollow organ.

    If pain is intermittent, find out the duration of a typical episode. In addition, ask the patient to point where the pain is located and if it radiates to other areas.

    Find out if movement, coughing, exertion, vomiting, eating, elimination, or walking worsens or relieves the pain. The patient may report abdominal pain as indigestion or gas pain, so have him describe it in detail.

    Ask the patient about substance abuse and any history of vascular, GI, GU, or reproductive disorders. Ask the female patient about the date of her last menstrual cycle, changes in her menstrual pattern, or dyspareunia.

    Ask the patient about appetite changes. Ask about the onset and frequency of nausea or vomiting. Find out about increased flatulence, constipation, diarrhea, and changes in stool consistency. When was the last bowel movement? Ask about urinary frequency, urgency, or pain. Is the urine cloudy or pink?

    Perform a physical examination. Take the patient's vital signs, and assess skin turgor and mucous membranes. Inspect his abdomen for distention or visible peristaltic waves and, if indicated, measure his abdominal girth.

    Auscultate for bowel sounds and characterize their motility. Percuss all quadrants, noting the percussion sounds. Palpate the entire abdomen for masses, rigidity, and tenderness. Check for costovertebral angle (CVA) tenderness, abdominal tenderness with guarding, and rebound tenderness.

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    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Arm pain: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    If the patient reports arm pain after an injury, take a brief history of the injury from the patient. Quickly assess him for severe injuries requiring immediate treatment. If you've ruled out severe injuries, check pulses, capillary refill time, sensation, and movement distal to the affected area because circulatory impairment or nerve injury may require immediate surgery. Inspect the arm for deformities, assess the level of pain, and immobilize the arm to prevent further injury.

    If the patient reports continuous or intermittent arm pain, ask him to describe it and to relate when it began. Is the pain associated with repetitive or specific movements or positions? Ask him to point out other painful areas because arm pain may be referred. For example, arm pain commonly accompanies the characteristic chest pain of myocardial infarction, and right shoulder pain may be referred from the right upper quadrant abdominal pain of cholecystitis. Ask the patient if the pain worsens in the morning or in the evening, if it prevents him from performing his job, and if it restricts movement. Ask if heat, rest, or drugs relieve it. Finally, ask about preexisting illnesses, a family history of gout or arthritis, and current drug therapy.

    Next, perform a focused examination. Observe the way the patient walks, sits, and holds his arm. Inspect the entire arm, comparing it with the opposite arm for symmetry, movement, and muscle atrophy. (It's important to know if the patient is right- or left-handed.) Palpate the entire arm for swelling, nodules, and tender areas. In both arms, compare active range of motion, muscle strength, and reflexes.

    If the patient reports numbness or tingling, check his sensation to vibration, temperature, and pinprick. Compare bilateral hand grasps and shoulder strength to detect weakness.

    If a patient has a cast, splint, or restrictive dressing, check for circulation, sensation, and mobility distal to the dressing. Ask the patient about edema and if the pain has worsened within the last 24 hours.

    Examine the neck for pain on motion, point tenderness, muscle spasms, or arm pain when the neck is extended with the head toward the involved side.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Back pain: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    If life-threatening causes of back pain are ruled out, continue with a complete history and physical examination. Be aware of the patient's expressions of pain as you do so. Obtain a medical history, including past injuries, surgeries, and illnesses, and a family history. Ask about diet and alcohol intake. Take a drug history, including past and present prescriptions, over-the-counter drugs, and herbal medicines. Ask the patient to rate the pain according to a pain scale and describe the type and location of his pain.

    Next, perform a thorough physical examination. Observe skin color, especially in the patient's legs, and palpate skin temperature. Palpate femoral, popliteal, posterior tibial, and pedal pulses. Ask about unusual sensations in the legs, such as numbness and tingling. Observe the patient's posture if pain doesn't prohibit standing. Does he stand erect or tend to lean toward one side? Observe the level of the shoulders and pelvis and the curvature of the back. Ask the patient to bend forward, backward, and from side to side while you palpate for paravertebral muscle spasms. Note rotation of the spine on the trunk. Palpate the dorsolumbar spine for point tenderness. Then ask the patient to walk—first on his heels, then on his toes; protect him from falling as he does so. Weakness may reflect a muscular disorder or spinal nerve root irritation. Place the patient in a sitting position to evaluate and compare patellar tendon (knee), Achilles tendon, and Babinski's reflexes. Evaluate the strength of the extensor hallucis longus by asking the patient to hold up his big toe against resistance. Measure leg length and hamstring and quadriceps muscles bilaterally. Note a difference of more than 3⁄89 (1 cm) in muscle size, especially in the calf.

    To reproduce leg and back pain, position the patient in a supine position on the examining table. Grasp his heel and slowly lift his leg. If he feels pain, note its exact location and the angle between the table and his leg when it occurs. Repeat this maneuver with the opposite leg. Pain along the sciatic nerve may indicate disk herniation or sciatica. Note the range of motion of the hip and knee.

    Palpate the flanks and percuss with the fingertips or perform fist percussion to elicit costovertebral angle tenderness.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Chest pain: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    If the chest pain isn't severe, proceed with the history. Ask if the patient feels diffuse pain or can point to the painful area. Ask when the pain began and if the patient ever experienced this type of pain in the past. Sometimes a patient won't perceive the sensation he's feeling as pain, so ask whether he has any discomfort radiating to his neck, jaw, arms, or back. If he does, ask him to describe it. Is it a dull, aching, pressurelike sensation? A sharp, stabbing, knifelike pain? Does he feel it on the surface or deep inside? Ask him to rate the pain on a pain scale. Find out whether it's constant or intermittent. If it's intermittent, how long does it last? Ask if movement, exertion, breathing, position changes, or eating certain foods worsens or helps relieve the pain. Does anything in particular seem to bring it on?

    Review the patient's history for cardiac or pulmonary disease, chest trauma, intestinal disease, or sickle cell anemia. Find out which medications he's taking, if any, and ask about recent dosage or schedule changes.

    Take the patient's vital signs, noting tachypnea, fever, tachycardia, oxygen saturation, paradoxical pulse, and hypertension or hypotension. Place the patient on a cardiac monitor and evaluate his heart rhythm. Also, look for jugular vein distention and peripheral edema. Note the feel of his skin. Is it cool and clammy or warm and diaphoretic? Auscultate his chest for extra heart sounds. Observe the patient's breathing pattern, and inspect his chest for asymmetrical expansion. Auscultate his lungs for pleural friction rub, crackles, rhonchi, wheezing, or diminished or absent breath sounds. Next, auscultate for murmurs, clicks, gallops, or pericardial friction rub. Palpate for lifts, heaves, thrills, gallops, tactile fremitus, and abdominal masses or tenderness.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Flank pain: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    If the patient's condition isn't critical, take a thorough history. Ask about the onset of his pain and apparent precipitating events. Have him describe the pain's location, intensity, pattern, and duration. Find out if anything aggravates or alleviates it.

    Ask the patient about changes in his normal pattern of fluid intake and urine output. Explore his history for a urinary tract infection (UTI) or obstruction, renal disease, or recent streptococcal infection.

    During the physical examination, palpate the patient's flank area and percuss the CVA to determine the extent of pain.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Jaw pain: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    Begin the patient history by asking him to describe the pain's character, intensity, and frequency. When did he first notice the jaw pain? Where on the jaw does he feel pain? Does the pain radiate to other areas? Sharp or burning pain arises from the skin or subcutaneous tissues. Causalgia, an intense burning sensation, usually results from damage to the fifth cranial, or trigeminal, nerve. This type of superficial pain is easily localized, unlike dull, aching, boring, or throbbing pain, which originates in muscle, bone, or joints. Also ask about aggravating or alleviating factors.

    Ask about recent trauma, surgery, or procedures, especially dental work. Ask about associated signs and symptoms, such as joint or chest pain, dyspnea, palpitations, fatigue, a headache, malaise, anorexia, weight loss, intermittent claudication, diplopia, and hearing loss. (Keep in mind that jaw pain may accompany more characteristic signs and symptoms of life-threatening disorders such as chest pain in a patient with an MI.)

    Focus your physical examination on the jaw. Inspect the painful area for redness, and palpate for edema or warmth. Facing the patient directly, look for facial asymmetry indicating swelling. Check the TMJs by placing your fingertips just anterior to the external auditory meatus and asking the patient to open and close, and to thrust out and retract his jaw. Note the presence of crepitus, an abnormal scraping or grinding sensation in the joint. (Clicks heard when the jaw is widely spread apart are normal.) How wide can the patient open his mouth? Less than 1 1⁄89 (3 cm) or more than 23⁄89 (6 cm) between the upper and lower teeth is abnormal. Next, palpate the parotid area for pain and swelling, and inspect and palpate the oral cavity for lesions, elevation of the tongue, or masses.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Neck pain: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    If the patient hasn't sustained trauma, find out the severity and onset of his neck pain. Where specifically in the neck does he feel pain? Does anything relieve or worsen the pain? Does any particular event precipitate the pain? Also, ask about other symptoms, such as headaches or back pain. Next, focus on the patient's current and past illnesses and injuries, diet, drug history, and family health history.

    Thoroughly inspect the patient's neck, shoulders, and cervical spine for swelling, masses, erythema, and ecchymoses. Assess active range of motion (ROM) in his neck by having him perform flexion, extension, rotation, and lateral side bending. Note the degree of pain produced by these movements. Examine his posture, and test and compare bilateral muscle strength. Check the sensation in his arms, and assess his hand grasp and arm reflexes. Attempt to elicit Brudzinski's and Kernig's signs if there isn't a history of neck trauma, and palpate the cervical lymph nodes for enlargement.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Rectal pain: History and physical examination
    (Nursing: Interpreting Signs and Symptoms)

    Begin by taking the patient's history. Ask him to describe the pain. Is it sharp or dull, burning or knifelike? How often does it occur? Ask if the pain is worse during or immediately after defecation. Does the patient avoid having bowel movements because of anticipated pain? Find out what alleviates the pain.

    Be sure to ask appropriate questions about the development of associated signs and symptoms. For example, does the patient experience bleeding along with rectal pain? If so, find out how frequently this occurs and whether the blood appears on the toilet tissue, on the surface of the stools, or in the toilet bowl. Is the blood bright or dark red? Also, ask whether the patient has noticed other drainage, such as mucus or pus, and whether he's experiencing constipation or diarrhea. Ask when he last had a bowel movement. Obtain a dietary and drug history.

    Then inspect the rectal area for bleeding; abnormal drainage, such as pus; or protrusions, such as skin tags or thrombosed hemorrhoids. Also, check for inflammation and other lesions. A rectal examination may be necessary.

    » READ BOOK EXCERPT ONLINE »

    Source: Nursing: Interpreting Signs and Symptoms, 2007

    Abdominal Pain, Generalized: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    If the onset is acute, a general surgeon should be consulted at the outset. Ominous signs include boardlike rigidity, rebound tenderness, and shock with nausea and vomiting. Hyperactive bowel sounds of a high-pitched tinkling character with distention and obstipation suggest intestinal obstruction. In contrast, normal bowel sounds, little distention, good vital signs, and minimal tenderness suggest gastroenteritis or other diffuse irritation of the bowel. It is wise to pass a nasogastric tube and attach to suction and proceed with a CBC, urinalysis, an immediate flat plate and upright of the abdomen, chest x-ray, serum amylase and lipase levels, and chemistry panel. Sometimes, lateral decubitus films are necessary to reveal the stepladder pattern of intestinal obstruction. A pregnancy test should be ordered if age and gender dictates it. If these tests fail to confirm the clinical diagnosis and the patient’s condition is deteriorating, it is probably wise to proceed immediately with an exploratory laparotomy. If the patient’s condition is stable, one may order more diagnostic tests depending on the location of the pain and other symptoms and signs. For example, if the pain seems more localized to the RUQ, a gallbladder ultrasound or nuclear scan may be ordered. If it is still considered generalized, perhaps a CT scan of the abdomen and pelvis is indicated. Monitoring vital signs and doing repeated CBCs, serum amylase levels, and flat plates of the abdomen are useful in borderline cases.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    LOW BACK PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    Our first priority in a patient who presents with low back pain is to rule out anything serious such as a herniated disc or cauda equina tumor. A pelvic and rectal examination must be performed to exclude a pelvic tumor or prostate carcinoma. A careful neurologic examination must be done. If one is too busy to do that, referral to an orthopedic surgeon or neurologist is indicated. The neurologic examination should include an SLR test, femoral stretch test, careful sensory examination, and an assessment for asymmetric reflexes. It is wise to carefully measure the thighs and calves to reveal muscular atrophy. Any findings to support a diagnosis of radiculopathy are a reasonable indication for a CT scan or MRI of the lumbar spine. However, it may be wise to have a neurologist or neurosurgeon examine the patient first because these tests are expensive. If the patient has normal neurologic, pelvic, and rectal examinations, it is perfectly legitimate to manage the patient conservatively for a while without any testing other than clinical. Close follow-up is important in these cases, however. Should the pain persist despite rest and conservative treatment, a more thorough diagnostic workup is indicated regardless of the lack of objective findings. This will include plain films or CT scan and an arthritis panel.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    ARM PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The association of other symptoms and signs found on a good history and physical examination is most important in pinpointing the diagnosis. Thus, arm pain with tenderness and limitation of motion at the elbow suggests tennis elbow, gout, or rheumatoid arthritis. Arm pain with loss of sensation in the distribution of the median nerve suggests carpal tunnel syndrome. Injection of lidocaine into bursa or trigger points may be diagnostic. The laboratory workup should include x-rays of the involved area and of the cervical spine, especially if there is a radicular distribution of the pain. If there are focal neurologic signs, a neurologist should be consulted before ordering an MRI: A cervical rib will not be missed in this way. An ECG and myocardial enzymes may be necessary to exclude a myocardial infarct, and an exercise tolerance test will help to exclude coronary insufficiency. Arteriogram, phlebogram, lymphangiogram, electromyogram with nerve conduction studies, myelogram, and nerve blocks will be necessary in specific cases.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    Breast Pain: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The diagnosis of a painful breast is usually made by taking a careful history. What drugs is the patient taking? Associated symptoms and signs (see sections on bloody discharge, page 306 and swelling, page 74) are also important. A culture of the discharge, mammography, and determination of serum, estrogen, and prolactin levels may be important, but referral to an endocrinologist is wise when the history does not provide a simple solution, especially when the pain is bilateral. Biopsy (frozen section) is necessary when tumor is suspected and mammography is equivocal, because faith in mammography has declined somewhat in recent years.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    CHEST PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    A possible myocardial infarction must be the first consideration in all adults with acute chest pain, especially if there are significant alterations of the vital signs. Consequently, serial ECGs, serial cardiac enzymes, and hospitalization will often be necessary. After this condition has been excluded, we can turn our attention to the other possibilities. Arterial blood gases, chest x-ray, and a lung scan may be ordered to exclude a pulmonary embolism. Pulmonary angiography may be necessary in some cases. A chest x-ray may be ordered to rule out pneumonia. Acute chest pain related to esophagitis is often relieved by swallowing lidocaine viscus, an extremely useful tool in the differential diagnosis. Relief of the pain with nitroglycerin under the tongue or by spray will support the diagnosis of coronary insufficiency. Tenderness of the costochondral junctions with relief on lidocaine injection into the point of maximum tenderness suggests Tietze syndrome (costochondritis). In cases of chronic chest pain, an exercise tolerance test with thallium scan should be done to rule out coronary insufficiency or myocardial infarction. It may be wise to do immediate coronary angiography if the condition deteriorates so that balloon angiography, bypass surgery, or reperfusion therapy may be initiated. Dissecting aneurysm is revealed by CT scan or MRI of the chest.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    ELBOW PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    In the approach to the diagnosis, the traumatic conditions and arthritic disorders will probably stand out. A diagnostic dilemma occurs when the elbow looks normal and has good movement. Nevertheless, most of these cases are caused by tennis elbow, myositis, and fasciitis. Thus, a simple injection at the trigger point will assist the diagnosis and give the patient immediate and sometimes lasting relief. If this is unsuccessful, referral to an orthopedic surgeon is wise.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    Epigastric Pain: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The approach to the diagnosis of midepigastric pain is identical to that for generalized abdominal pain .

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    EYE PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The approach to the diagnosis of eye pain involves a careful search for inflammation of the various anatomic structures; then a drop or two of fluorescent dye is inserted and the cornea inspected for lacerations, herpes ulcers, and foreign bodies. Finally, tonometry may be done. Referral to an ophthalmologist is often necessary, but the astute clinician will want to x-ray the sinuses, ask about a history of migraine, do a visual field, and rule out systemic diseases beforehand.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    FACIAL PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The approach to the diagnosis of face pain includes a careful history and physical with a good neurologic examination. The sinuses are transilluminated, and x-rays may be performed. The teeth and occlusion are examined carefully and possibly x-rayed. A histamine test may be indicated. The busy physician may want to refer the patient to a neurologist immediately, but this will obviously take away the challenge.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    FLANK PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The diagnosis of flank pain usually involves careful examination of the urine and a urine culture, an IVP, and plain films of the abdomen and spine. If these are negative, bone scans, arteriogram, and other tests listed below may be required. CT has eliminated the need for exploratory laparotomy in many cases.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    GROIN PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    In the approach to the diagnosis of groin pain, a mass or tender structure is usually present in the groin. If the mass is a lymph node, careful examination of the genitalia and lower extremities will often show the cause, but a urethral or vaginal smear and culture may be necessary to show gonorrhea. Investigation of the genitourinary (GU) tract and the GI tract for causes of referred pain is then undertaken. If the mass is reducible, a hernia is likely and referral to a surgeon is in order. Incarcerated hernias, of course, demand immediate referral.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    HAND AND FINGER PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    In diagnosis, most of these conditions will be obvious on inspection. The difficulty arises when the hand looks normal. Then one must check for the following:

    1. Carpal tunnel syndrome by tapping the volar aspect of the wrist (Tinel sign)
    2. Brachial plexus neuralgia and scalenus anticus syndrome by Adson tests
    3. Causalgia by stellate ganglion block to see if pain is relieved
    4. Cervical spine disease by a roentgenogram, possibly a myelogram or magnetic resonance imaging (MRI), and nerve blocks of the various roots. Referral to a neurologist is often necessary. In early RA, the joints may be normal on inspection, but pain and stiffness of the hands and fingers in the morning is an excellent clue.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    HIP PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The history and physical examination will allow differentiation of many of the conditions listed above. For example, the history of trauma suggests sprain, fracture, or contusion. Remember that fractures of the hip can occur in elderly persons without a history of trauma. A positive straight-leg-raise (SLR) test suggests a herniated disc or other cauda equina pathology. X-ray of hip and lumbosacral spine will help rule out fracture or osteoarthritis, but CT scan, bone scan, or MRI may be necessary. If x-rays and laboratory examinations are negative, a trial of lidocaine injections into the greater trochanter bursa or other trigger points may be diagnostic.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    JOINT PAIN: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    The approach to the diagnosis of joint pain includes a careful history and examination for other signs such as swelling, redness, and hyperthermia of the joints. If the joint pain is worse in the morning, consider RA. If multiple joints are involved, look for RA, lupus, and osteoarthritis. Single joint involvement suggests gonorrhea, septic arthritis, tuberculosis, or gout, among other things. Small joints are involved more frequently in RA, Reiter syndrome, and lupus, although the large joints are more frequently involved in osteoarthritis, gonorrhea, tuberculosis, and other infections. Remember, however, that both osteoarthritis and gonorrhea may involve the small joints of the hands and feet. Rheumatic fever presents a migratory arthritis; this is a helpful differential point. When the knee joint is involved, the astute clinician will always examine for a torn or subluxated meniscus and loose cruciate or collateral ligaments. MRI or arthroscopy will pin down this diagnosis. Listed below are the most valuable diagnostic tests. Synovial fluid analysis for uric acid and calcium pyrophosphate, the character of the mucin clot, a white cell count, and culture can be done in the office and may make the diagnosis almost immediately. This may eliminate the need for hospitalization. A therapeutic trial of aspirin or colchicine is useful in diagnosing rheumatic fever and gout, respectively. If the joint fluid examination is nonspecific and no systemic signs of infection are evident, the injection of steroids into the joint is reasonable while the physician waits for the results of more sophisticated diagnostic tests.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007

    Left Lower Quadrant Pain: Approach to the Diagnosis
    (Differential Diagnosis in Primary Care)

    There is no doubt about the value of a good history and physical examination, including both the rectal and pelvic areas. After this, the signs and symptoms should be summarized and grouped together; in many cases, this technique will pinpoint the diagnosis. The laboratory workup can now proceed. In acute cases, the physician should order a flat plate of the abdomen, CBC, urinalysis (and examine it him or herself), and serum amylase level before exploratory surgery. A pregnancy test is ordered in women of childbearing age. In chronic cases, sigmoidoscopy, barium enema, upper GI series, small-bowel follow-through, and stool examination for blood, ova, and parasites should be done before culdoscopy, peritoneoscopy, or colonoscopy is contemplated. An exploratory laparotomy remains a useful diagnostic tool even in chronic cases of LLQ pain.

    » READ BOOK EXCERPT ONLINE »

    Source: Differential Diagnosis in Primary Care, 2007


     » Next page: Signs of Restless Legs Syndrome

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