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Causes of Acidosis
List of causes of Acidosis
Following is a list of causes or underlying conditions (see also Misdiagnosis of underlying causes of Acidosis) that could possibly cause Acidosis includes:
- Diabetes
- Type 1 diabetes
- Diabetic Ketoacidosis
- Lactic Acidosis
- Renal Tubular Acidosis
- Lung disorders
- Kidney disorders
- Copperhead snake poisoning - lactic acidosis
- Renal rickets - acidosis
- Ondine's curse - acidosis
- Mitochondrial myopathy - lactic acidosis - lactic acidosis
- Intermediate cystinosis - acidic blood
- Hydroxyacyl-coa dehydrogenase, type 2, deficiency - lactic acidosis
- 3-alpha-hydroxyisobutyryl-CoA hydrolase deficiency - acidosis
- Starvitation
- Hypoxia
- Methanol toxicity
- Salicylate
- CNS depression
- Chronic obstructive lung disease
- Hepatic or renal failure
- Acidosis - see various types of acidosis
- Succinic acidemia - lactic acidosis, congenital - lactic acidosis
- Posthemorrhagic anemia - lactic acidosis
- Osteopetrosis - renal tubular acidosis - renal tubular acidosis
- Organic acidemia - acidosis
- Necrotizing enterocolitis - acidosis
- Myopathy with lactic acidosis and sideroblastic anemia - lactic acidosis
- Inborn urea cycle disorder - acidosis
- Hyperkalemic Renal Tubular Acidosis - acidosis
- Finnish lethal neonatal metabolic syndrome - lactic acidosis
- Fistula
- Alcohol
- Neuromuscular disorder
- Pyruvate dehydrogenase phosphatase deficiency - lactic acidosis
- Pyruvate carboxylase deficiency, Group B - acute metabolic acidosis
- MELAS - Lactic Acidosis
- Hereditary primary Fanconi disease - chronic acidosis
- Glycogen storage disease type 6 - ketosis
- Fanconi renotubular syndrome - acidosis
- Distal renal tubular acidosis
- Severe anaemia
- Medications
- Infection
- Classic Distal Renal Tubular Acidosis - acidosis
- Pyruvate carboxylase deficiency, Group C - ketosis
- Lipoamide dehydrogenase deficiency - ketoacidosis
- Carbon monoxide poisoning (type of Poisoning)
- Septicemic shock
- Hemorrhagic shock
- Toni-Fanconi syndrome type 1 - chronic acidosis
- Herbal Agent overdose - Germanium - lactic acidosis
- Complex 1 mitochondrial respiratory chain deficiency - acidosis
- Cardiomyopathy - hypotonia - lactic acidosis - lactic acidosis
- Apple seed poisoning - acidosis
- Osteopetrosis with renal tubular acidosis - renal tubular acidosis
- Mitochondrial neurogastrointestinal encephalopathy syndrome - lactic acidosis
- Metabolic disorders - lactic acidosis
- DEND syndrome - ketoacidosis
- Severe liver disease
- Hyperemesis Gravidarum - acidosis
- Chemical poisoning - Endothall - acidosis
- Biotinidase deficiency - ketoacidosis
- Proximal renal tubular acidosis - acidosis
- Intrinsic lung disease
- Sjogren's Syndrome - renal tubular acidosis
- Glycogen storage disease type 6A, due to phosphorylase kinase deficiency - ketosis
- Glomerulopathy with fibronectin deposits - renal tubular acidosis
- Acute tubulointerstitial nephritis and uveitis syndrome - renal tubular acidosis
- Ethanol ingestion
- Uremic
- Crotalidae snake poisoning - lactic acidosis
- Tiglic acidemia - acidosis
- Multiple carboxylase deficiency, propionic acidemia - acidosis
- Microvillus Inclusion Disease - acidosis
- Glycogen storage disease type 1C - lactic acidosis
- Fanconi-ichthyosis-dysmorphism - acidosis
- Cholera - acidosis
- Cataract and cardiomyopathy - lactic acidosis
- Acute glomerulonephritis
- Cardiogenic shock
- Shock
- Glycogen storage disease type 1D - lactic acidosis
- Fructose-1,6-bisphosphatase deficiency, hereditary - lactic acidosis
- Coenzyme Q cytochrome c reductase deficiency of - lactic acidosis
- 3-methylglutaconic aciduria, type 4 - lactic acidosis
- Severe diarrhoea
- Renal circulatory insufficiency
- Fanconi syndrome
- Renal failure
- Leukemia
- Tissue hypoxia
- Lowe oculocerebrorenal syndrome - renal tubular acidosis
- Wilson's Disease - renal tubular acidosis
- Von Gierke Disease - lactic acidosis
- Pyruvate decarboxylase deficiency - lactic acidosis
- Nephropathic cystinosis - acidic blood
- Mitochondrial encephalomyopathy - aminoacidopathy - lactic acidosis
- Colibacillosis - acidosis
- Hypotensive state
- Traumatic shock
- Severe exercise
- Starvation
More causes: see full list of causes for Acidosis
Acidosis as a complication of other conditions:
Other conditions that might have Acidosis as a complication may, potentially, be an underlying cause of Acidosis. Our database lists the following as having Acidosis as a complication of that condition:
- Cholera
- Classic Distal Renal Tubular Acidosis
- Cutler Syndrome
- Hyperemesis Gravidarum
- Hyperkalemic Renal Tubular Acidosis
- Proximal Renal Tubular Acidosis
- Renal Tubular Acidosis
Acidosis as a symptom:
Conditions listing Acidosis as a symptom may also be potential underlying causes of Acidosis. Our database lists the following as having Acidosis as a symptom of that condition:
- 3-alpha-hydroxyisobutyryl-CoA hydrolase deficiency
- Apple seed poisoning
- Chemical poisoning - Endothall
- Chemical poisoning - Strychnine
- Cholera
- Colibacillosis
- Complex 1 mitochondrial respiratory chain deficiency
- Fanconi renotubular syndrome
- Fanconi-ichthyosis-dysmorphism
- Fructose-1,6-bisphosphatase deficiency, hereditary
- Hyperemesis Gravidarum
- Hyperkalemic Renal Tubular Acidosis
- Inborn urea cycle disorder
- Lactic Acidosis
- Microvillus Inclusion Disease
- Multiple carboxylase deficiency, propionic acidemia
- NADH CoQ reductase, deficiency of
- Necrotizing enterocolitis
- Ondine syndrome
- Ondine's curse
- Organic acidemia
- Renal rickets
- Renal Tubular Acidosis
- Tiglic acidemia
Medications or substances causing Acidosis:
The following drugs, medications, substances or toxins are some of the possible
causes of Acidosis as a symptom.
This list is incomplete and various other drugs or substances
may cause your symptoms.
Always advise your doctor of any medications or treatments you are using,
including prescription, over-the-counter, supplements, herbal or alternative treatments.
- Bisac-Evac
- Bisacodyl Uniserts
- Bisco-Lax
- Carter’s Little Pills
- Clysodrast
- more drugs...»
See full list of 14 medications causing Acidosis
Drug interactions causing Acidosis:
When combined, certain drugs, medications, substances or toxins may react causing Acidosis as a symptom.
The list below is incomplete and various other drugs or substances may cause your symptoms. Always advise your doctor of any medications or treatments you are using, including prescription, over-the-counter, supplements, herbal or alternative treatments.
- Timolol, Ophthalmic and Acetazolamide interaction
- more interactions...»
Read more about medication causes of Acidosis
Related information on causes of Acidosis:
As with all medical conditions, there may be many causal factors. Further relevant information on causes of Acidosis may be found in:
Causes of Acidosis: Online Medical Books
16 MEDICAL BOOKS ONLINE! Review excerpts from medical books online, free, without registration, for more information about the causes of Acidosis.
Metabolic Acidosis:
Differential Diagnosis
(In A Page: Pediatric Signs and Symptoms)
- Increased anion gap (AG) metabolic acidosis, due to production of exogenous acid “MUDPILES”
- Methanol
- Uremia
- DKA
- Paraldehyde
- Ingestions/inborn errors of metabolism
- Lactic acidosis
- Ethylene glycol
- Salicylates
- Normal anion gap metabolic acidosis, due to bicarbonate loss in the GI tract or kidneys or impaired acid secretion by the kidney
–Diarrhea, other GI losses (very common)
–Type I (distal) renal tubular acidosis (RTA): Inability to excrete hydrogen ion, urine pH always high (>6.5), caused by a variety of medications, inherited forms, or renal insufficiency; often associated with low potassium and hypercalciuria
–Type II (proximal) RTA: Impaired reabsorption of bicarbonate from the proximal tubule, usually associated with other evidence of proximal tubule dysfunction (Fanconi syndrome), such as phosphaturia or glycosuria
–Type IV (hyperkalemic) RTA: Inadequate aldosterone production or inability to respond appropriately to aldosterone; commonly seen in patients with a history of obstructive uropathy or as a transient occurrence in patients with acute pyelonephritis
Source: In A Page: Pediatric Signs and Symptoms, 2007
Breath with fruity odor:
Medical causes
(Handbook of Signs & Symptoms (Third Edition))
❑ Anorexia nervosa. Severe weight loss associated with anorexia nervosa may produce fruity breath, usually with nausea, constipation, and cold intolerance as well as dental enamel erosion and scars or calluses in the dorsum of the hand, both related to induced vomiting.
❑ Ketoacidosis. Fruity breath odor accompanies alcoholic ketoacidosis, which is usually seen in poorly nourished alcoholics with vomiting, abdominal pain, and only minimal food intake over several days. Kussmaul's respirations begin abruptly and accompany dehydration, abdominal pain and distention, and absent bowel sounds. Blood glucose levels are normal or slightly decreased.
With diabetic ketoacidosis, fruity breath odor commonly occurs as ketoacidosis develops over 1 to 2 days. Other findings include polydipsia, polyuria, nocturia, a weak and rapid pulse, hunger, weight loss, weakness, fatigue, nausea, vomiting, and abdominal pain. Eventually, Kussmaul's respirations, orthostatic hypotension, dehydration, tachycardia, confusion, and stupor occur. Signs and symptoms may lead to coma.
Starvation ketoacidosis is a potentially life-threatening disorder that has a gradual onset. Besides fruity breath odor, typical findings include signs of cachexia and dehydration, a decreased LOC, bradycardia, and a history of severely limited food intake (anorexia nervosa).
Other causes
❑ Drugs. Any drug known to cause metabolic acidosis, such as nitroprusside and salicylates, can result in fruity breath odor.
❑ Low-carbohydrate diets. These diets, which encourage little or no carbohydrate intake, may cause ketoacidosis and the resulting fruity breath odor.
Source: Handbook of Signs & Symptoms (Third Edition), 2006
Metabolic acidosis:
Causes
(Professional Guide to Diseases (Eighth Edition))
Metabolic acidosis usually results from excessive fat burning in the absence of usable carbohydrates. This can be caused by diabetic ketoacidosis, chronic alcoholism, malnutrition, or a low-carbohydrate, high-fat diet — all of which produce more keto acids than the metabolic process can handle. Other causes include:
❑ anaerobic carbohydrate metabolism: a decrease in tissue oxygenation or perfusion (as occurs with pump failure after myocardial infarction, or with pulmonary or hepatic disease, shock, or anemia) forces a shift from aerobic to anaerobic metabolism, causing a corresponding rise in lactic acid level
❑ renal insufficiency and failure (renal acidosis): underexcretion of metabolized acids or inability to conserve base
❑ diarrhea and intestinal malabsorption: loss of sodium bicarbonate from the intestines, causing the bicarbonate buffer system to shift to the acidic side. For example, ureteroenterostomy and Crohn’s disease can also induce metabolic acidosis.
Less frequently, metabolic acidosis results from salicylate intoxication (overuse of aspirin), exogenous poisoning, or Addison’s disease with an increased excretion of sodium and chloride, and retention of potassium ions.
Source: Professional Guide to Diseases (Eighth Edition), 2005
Renal tubular acidosis:
Causes
(Professional Guide to Diseases (Eighth Edition))
Metabolic acidosis usually results from renal excretion of bicarbonate. However, metabolic acidosis associated with RTA results from a defect in the kidneys’normal tubular acidification of urine.
Distal RTA results from an inability of the distal tubule to secrete hydrogen ions against established gradients across the tubular membrane. This results in decreased excretion of titratable acids and ammonium, increased loss of potassium and bicarbonate in the urine, and systemic acidosis. Prolonged acidosis causes mobilization of calcium from bone and, eventually, hypercalciuria, predisposing the kidney to the formation of renal calculi. Distal RTA may be classified as primary or secondary.
❑ Primary distal RTA may occur sporadically or through a hereditary defect and is most prevalent in females, older children, adolescents, and young adults.
❑ Secondary distal RTA has been linked to many renal or systemic conditions, such as starvation, malnutrition, hepatic cirrhosis, and several genetically transmitted disorders.
Proximal RTA results from defective reabsorption of bicarbonate in the proximal tubule. This causes bicarbonate to flood the distal tubule, which normally secretes hydrogen ions, and leads to impaired formation of titratable acids and ammonium for excretion. Ultimately, metabolic acidosis results. Proximal RTA occurs in two forms:
❑ In primary proximal RTA, the reabsorptive defect is idiopathic and is the only disorder present.
❑ In secondary proximal RTA, the reabsorptive defect may be one of several defects and is due to proximal tubular cell damage from a disease such as Fanconi’s syndrome.
Source: Professional Guide to Diseases (Eighth Edition), 2005
Breath with fruity odor:
Medical causes
(Professional Guide to Signs & Symptoms (Fifth Edition))
Anorexia nervosa
Severe weight loss associated with anorexia nervosa may produce fruity breath odor, usually with nausea, constipation, and cold intolerance. Induced vomiting may cause dental enamel erosion and scars or calluses in the dorsum of the hand.
Ketoacidosis
Fruity breath odor accompanies alcoholic ketoacidosis, which is usually seen in poorly nourished alcoholics with a history of vomiting, abdominal pain, and only minimal food intake over several days. Kussmaul’s respirations begin abruptly and accompany dehydration, abdominal pain and distention, and absent bowel sounds. Blood glucose levels are normal or slightly decreased.
In diabetic ketoacidosis, fruity breath odor commonly acompanies the development of ketoacidosis over 1 to 2 days. Other findings include polydipsia, polyuria, nocturia, weak and rapid pulse, hunger, weight loss, weakness, fatigue, nausea, vomiting, and abdominal pain. Eventually, Kussmaul’s respirations, orthostatic hypotension, dehydration, tachycardia, confusion, and stupor occur. Signs and symptoms may lead to coma.
Starvation ketoacidosis is a potentially life-threatening disorder that has a gradual onset. Besides fruity breath odor, typical findings include signs of cachexia and dehydration, decreased LOC, bradycardia, and a history of anorexia nervosa.
Other causes
Drugs
Any drug known to cause metabolic acidosis, such as nitroprusside and salicylates, can result in fruity breath odor.
Low-carbohydrate diets
Diets that promote little or no carbohydrate intake may cause ketoacidosis and the resulting fruity breath odor.
Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006
Renal tubular acidosis:
Causes
(Handbook of Diseases)
Metabolic acidosis usually results from renal excretion of bicarbonate. However, metabolic acidosis associated with RTA results from a defect in the kidneys’normal tubular acidification of urine.
Distal RTA
Type I RTA results from an inability of the distal tubule to secrete hydrogen ions against established gradients across the tubular membrane. This results in decreased excretion of titratable acids and ammonium, increased loss of potassium and bicarbonate in the urine, and systemic acidosis.
Prolonged acidosis causes mobilization of calcium from bone and eventually hypercalciuria, predisposing the patient to the formation of renal calculi.
Distal RTA may be classified as primary or secondary:
❑ Primary distal RTA may occur sporadically or through a hereditary defect and is most prevalent in females, older children, adolescents, and young adults.
❑ Secondary distal RTA has been linked to many renal and systemic conditions, such as starvation, malnutrition, hepatic cirrhosis, and several genetically transmitted disorders.
Proximal RTA
Type II RTA results from defective reabsorption of bicarbonate in the proximal tubule. This causes bicarbonate to flood the distal tubule, which normally secretes hydrogen ions, and leads to impaired formation of titratable acids and ammonium for excretion. Ultimately, metabolic acidosis results.
Proximal RTA occurs in two forms:
❑ With primary proximal RTA, the reabsorptive defect is idiopathic and is the only disorder present.
❑ With secondary proximal RTA, the reabsorptive defect may be one of several defects and results from proximal tubular cell damage from a disease such as Fanconi’s syndrome.
Source: Handbook of Diseases, 2003
Respiratory acidosis:
Causes
(Handbook of Diseases)
Respiratory acidosis can result from airway obstruction or parenchymal lung disease, which interferes with alveolar ventilation, or from chronic obstructive pulmonary disease (COPD), asthma, severe adult respiratory distress syndrome, chronic bronchitis, large pneumothorax, extensive pneumonia, or pulmonary edema.
Hypoventilation compromises excretion of carbon dioxide produced through metabolism. The retained carbon dioxide then combines with water to form an excess of carbonic acid, decreasing the blood pH. As a result, the concentration of hydrogen ions in body fluids, which directly reflects acidity, increases.
In addition, several factors predispose the patient to respiratory acidosis:
❑ Drugs: Narcotics, anesthetics, hypnotics, and sedatives decrease the sensitivity of the respiratory center.
❑ Central nervous system (CNS) trauma: Medullary injury may impair ventilatory drive.
❑ Chronic metabolic alkalosis: Respiratory compensatory mechanisms attempt to normalize pH by decreasing alveolar ventilation.
❑ Neuromuscular disease (such as myasthenia gravis, Guillain-Barré syndrome, and poliomyelitis): Failure of respiratory muscles to respond properly to respiratory drive reduces alveolar ventilation.
Source: Handbook of Diseases, 2003
Breath odor, fruity:
Medical causes
(Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series)
Anorexia nervosa
. Severe weight loss associated with anorexia nervosa may produce fruity breath, usually with nausea, constipation, and cold intolerance as well as dental enamel erosion and scars or calluses in the dorsum of the hand, related to induced vomiting.Ketoacidosis
Fruity breath odor accompanies alcoholic ketoacidosis, which is usually seen in poorly nourished alcoholics with vomiting, abdominal pain, and only minimal food intake over several days. Kussmaul’s respirations begin abruptly and accompany dehydration, abdominal pain and distention, and absent bowel sounds. Blood glucose levels are normal or slightly decreased.With DKA, fruity breath odor commonly occurs as ketoacidosis develops over 1 to 2 days. Other findings include polydipsia, polyuria, nocturia, weak and rapid pulse, hunger, weight loss, weakness, fatigue, nausea, vomiting, and abdominal pain. Eventually, Kussmaul’s respirations, orthostatic hypotension, dehydration, tachycardia, confusion, and stupor occur. Signs and symptoms may lead to coma.
Starvation ketoacidosis is a potentially life-threatening disorder that has a gradual onset. Besides fruity breath odor, typical findings include signs of cachexia and dehydration, decreased LOC, bradycardia, and a history of severely limited food intake (anorexia nervosa).
Other causes
Drugs
Any drug known to cause metabolic acidosis, such as nitroprusside and salicylates, can result in fruity breath odor.Low-carbohydrate diets
Low-carbohydrate diets, which encourage little or no carbohydrate intake, may cause ketoacidosis and the resulting fruity breath odor.Source: Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series, 2007
Breath with fruity odor:
Medical causes
(Signs & Symptoms: A 2-in-1 Reference for Nurses)
Anorexia nervosa
Severe weight loss associated with anorexia nervosa may produce fruity breath, usually with nausea, constipation, and cold intolerance as well as dental enamel erosion and scars or calluses in the dorsum of the hand, both related to induced vomiting.
Ketoacidosis
Fruity breath odor accompanies alcoholic ketoacidosis, which is usually seen in poorly nourished alcoholics with vomiting, abdominal pain, and only minimal food intake over several days. Kussmaul’s respirations begin abruptly and accompany dehydration, abdominal pain and distention, and absent bowel sounds. Blood glucose levels are normal or slightly decreased.
With diabetic ketoacidosis, fruity breath odor commonly occurs as ketoacidosis develops over 1 to 2 days. Other findings include polydipsia, polyuria, nocturia, weak and rapid pulse, hunger, weight loss, weakness, fatigue, nausea, vomiting, and abdominal pain. Eventually, Kussmaul’s respirations, orthostatic hypotension, dehydration, tachycardia, confusion, stupor, and coma may occur.
Starvation ketoacidosis is a potentially life-threatening disorder that has a gradual onset. Besides fruity breath odor, typical findings include signs of cachexia and dehydration, decreased level of consciousness, bradycardia, and a history of severely limited food intake (anorexia nervosa).
Other causes
Drugs
Any drug known to cause metabolic acidosis, such as nitroprusside and salicylates, can result in fruity breath odor.
Low-carbohydrate diets
Low-carbohydrate diets, which encourage little or no carbohydrate intake, may cause ketoacidosis and a resulting fruity breath odor.
Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007
Breath with fruity odor:
Medical causes
(Nursing: Interpreting Signs and Symptoms)
Anorexia nervosa.Severe weight loss associated with anorexia nervosa may produce fruity breath, usually with nausea, constipation, and cold intolerance as well as dental enamel erosion and scars or calluses in the dorsum of the hand, both related to induced vomiting.
Ketoacidosis.Fruity breath odor accompanies alcoholic ketoacidosis, which is usually seen in poorly nourished alcoholics with vomiting, abdominal pain, and only minimal food intake over several days. Kussmaul's respirations begin abruptly and accompany dehydration, abdominal pain and distention, and absent bowel sounds. Blood glucose levels are normal or slightly decreased.
With diabetic ketoacidosis, fruity breath odor commonly occurs as ketoacidosis develops over 1 or 2 days. Other findings include polydipsia, polyuria, nocturia, a weak and rapid pulse, hunger, weight loss, weakness, fatigue, nausea, vomiting, and abdominal pain. Eventually, Kussmaul's respirations, orthostatic hypotension, dehydration, tachycardia, confusion, and stupor occur. Signs and symptoms may lead to coma.
Starvation ketoacidosis is a potentially life-threatening disorder that has a gradual onset. Besides fruity breath odor, typical findings include signs of cachexia and dehydration, a decreased LOC, bradycardia, and a history of severely limited food intake.
Other causes
Drugs.Any drug known to cause metabolic acidosis, such as nitroprusside and salicylates, can result in fruity breath odor.
Low-carbohydrate diets.These diets, which encourage little or no carbohydrate intake, may cause ketoacidosis and the resulting fruity breath odor.
Source: Nursing: Interpreting Signs and Symptoms, 2007
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