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Prevalence and Incidence of Cyclic vomiting syndrome

Prevalance of Cyclic vomiting syndrome:

1 in 50 children (perhaps) ... see also overview of Cyclic vomiting syndrome.

Prevalance Rate:

approx 1 in 50 or 2.00% or 5.4 million people in USA [Source statistic for calcuation: "1 in 50 children (perhaps)" -- see also general information about data sources]

Cyclic vomiting syndrome: Rare Disease

Cyclic vomiting syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Cyclic vomiting syndrome, or a subtype of Cyclic vomiting syndrome, affects less than 200,000 people in the US population.

Cyclic vomiting syndrome Prevalence: Book Excerpts

Prevalance of Cyclic vomiting syndrome:

No one knows for sure how many people have CVS, but medical researchers believe that more people may have the disorder than is commonly thought (as many as 1 in 50 children in one study). (Source: excerpt from Cyclic Vomiting Syndrome: NIDDK)

Prevalence/Incidence of Cyclic vomiting syndrome: Online Medical Books

16 MEDICAL BOOKS ONLINE! Review excerpts from medical books online, free, without registration, for more information about the prevalence and/or incidence of Cyclic vomiting syndrome.

Vomiting - Case 3-1: 7-Week-Old Boy: III. Incidence and Epidemiology of Methemoglobinemia
(Pediatric Complaints and Diagnostic Dilemmas)

Although methemoglobinemia is a rare condition in pediatrics, it can cause significant cyanosis and even death. Methemoglobin is a derivative of normal hemoglobin in which the iron component has been oxidized from the ferrous (Fe 2+) to the ferric (Fe3+) state. The oxidized iron (Fe3+) is unable to reversibly bind oxygen. Therefore, the oxidation of hemoglobin to methemoglobin produces a functional anemia by impairing the ability of the blood to transport oxygen. Methemoglobin occurs regularly in the body but rarely exceeds levels of 2% of the total hemoglobin because of antioxidant reactions in the body that reduce methemoglobin back to hemoglobin. The most important of these antioxidant reactions uses either reduced nicotinamide adenine dinucleotide (NADH) –cytochrome b5 reductase or NADH phosphate (NADPH)–methemoglobin reductase. NADPH-methemoglobin reductase also reduces methylene blue, an action that has important therapeutic implications, as described in the treatment section below.
Methemoglobin levels increase when there is a disturbance in the balance between the oxidation and reduction of heme iron. Infants are at an increased risk for methemoglobinemia for two main reasons: (a) young infants have a lower level of the reductase enzymes, and (b) fetal hemoglobin is more easily oxidized than adult hemoglobin. Methemoglobinemia can be caused by exposure to oxidant drugs, development of acidosis, or inherited conditions. The most common oxidizing agents in acquired methemoglobinemia are sulfonamides, aniline dyes, chlorates, quinones, benzocaine, lidocaine, metoclopramide, and phenytoin. Ingestion of well water nitrates can also cause methemoglobinemia. Gastroenteritis with acidosis can cause methemoglobinemia in infants, especially when nitrite-forming bacteria such as Escherichia coli and Campylobacter jejuni are present. Less common causes are inherited deficiencies of erythrocyte methemoglobin reductase or the presence of M hemoglobin.

» READ BOOK EXCERPT ONLINE »

Source: Pediatric Complaints and Diagnostic Dilemmas, 2003

Vomiting - Case 3-2: 9-Month-Old Girl: III. Incidence and Epidemiology of Supraventricular Tachycardia
(Pediatric Complaints and Diagnostic Dilemmas)

SVT is a generic term encompassing a group of cardiac arrhythmias that originate above the atrioventricular (AV) node. It is the most common sustained accelerated nonsinus tachyarrhythmia, with an incidence of 1 per 250 to 1,000 children. SVT can be diagnosed by EKG during an episode. Episodes can be captured by means of a diagnostic EKG, a 24-hour Holter monitor, or transtelephonic monitoring. Two mechanisms account for virtually all cases of SVT: (a) an abnormal or enhanced normal automatic rhythm and (b) a reentrant rhythm. Approximately 75% of patients with a reentrant rhythm exhibit findings of preexcitation, with a shortened PR interval and initial slurred upstroke of the QRS (delta wave). Children younger than 12 years of age are more likely to have an accessory AV connection in adolescence, nodal reentry tachycardia increases in frequency.
Reentrant rhythms account for 90% of all cases of SVT. Two separate conducting pathways must be present, either AV or within the atrium, that lead to a cyclic pattern of excitation resulting in SVT. Atrial reentry rhythms may lead to either atrial fibrillation or atrial flutter. AV reentrant rhythms may be either through the AV node (nodal) or associated with an accessory AV pathway termed the bundle of Kent. Tachycardia may result from transmission of the impulse antegrade through the AV node-His-Purkinje system, through the myocardium retrograde, and through the accessory pathway completing the circuit. This orthodromic reciprocating tachycardia (ORT) is the most common pattern seen in Wolf-Parkinson-White syndrome and results in the typical narrow-complex QRS tachycardia. Rarely, the antegrade impulse travels via the accessory pathway and retrograde through the AV node-His-Purkinje system, resulting in antidromic reciprocating tachycardia (ART).
Preexcitation occurs in 75% of individuals with accessory pathways. This implies that the accessory pathway can conduct the impulse in antegrade fashion, from the atria to the ventricle. Bypassing the intrinsic delay of the AV node results in a shortened PR interval and a slurred upstroke of the QRS, the so-called delta wave. Twenty-five percent of accessory pathways transmit impulses only in retrograde fashion, from the ventricle to the atrium, resulting in a normal resting EKG (i.e., with no evidence of preexcitation).
SVT secondary to increased automaticity or atrial and junctional ectopic tachycardias occurs more commonly in children with postoperative congenital heart disease or cardiomyopathies.

» READ BOOK EXCERPT ONLINE »

Source: Pediatric Complaints and Diagnostic Dilemmas, 2003

Vomiting - Case 3-6: 10-Month-Old Girl: III. Incidence and Epidemiology of Hirschsprung's Disease
(Pediatric Complaints and Diagnostic Dilemmas)

Hirschsprung initially reported this condition in 1888, but it was not until the 1920s that the absence of ganglion cells in the distal gastrointestinal tract was discovered. Hirschsprung 's disease has an incidence of 1 in 5,000 live births, with a male predominance of almost 4:1. Ninety percent of cases occur in full-term infants, and it is the most common cause of lower intestinal obstruction in neonates. A family history is noted in 7%, and if the cecum is involved the proportion rises to 21%. Hirschsprung 's disease occurs in up to 10% of patients with Down syndrome and is associated with other conditions such as Smith-Lemli-Opitz syndrome, Waardenburg syndrome, congenital deafness, Laurence-Moon-Biedl-Bardet syndrome, and Ondine 's curse.
Hirschsprung's disease is caused by the failed cephalocaudal migration of neural crest cells during the 5th through 12th week of gestation. The absence of neurons begins at the anus and extends proximally. This defect is limited to the rectal and sigmoid area in 75% of patients and includes the total colon in only 8%. Absence of these neural crest cells interrupts the inhibitory parasympathetic nerves in the myenteric plexus, thereby inhibiting relaxation and causing unopposed contraction.

» READ BOOK EXCERPT ONLINE »

Source: Pediatric Complaints and Diagnostic Dilemmas, 2003

About prevalence and incidence statistics:

The term 'prevalence' of Cyclic vomiting syndrome usually refers to the estimated population of people who are managing Cyclic vomiting syndrome at any given time. The term 'incidence' of Cyclic vomiting syndrome refers to the annual diagnosis rate, or the number of new cases of Cyclic vomiting syndrome diagnosed each year. Hence, these two statistics types can differ: a short-lived disease like flu can have high annual incidence but low prevalence, but a life-long disease like diabetes has a low annual incidence but high prevalence. For more information see about prevalence and incidence statistics.


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