Descriptive epidemiology of alimentary tract atresia

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J Harris1, B Källén, E Robert

  • 1California Birth Defects Monitoring Program, Emeryville 94608, USA.

Teratology
|July 1, 1995
PubMed

Insights

Infants with alimentary tract atresia, including esophageal, gut, and anal atresia, show varied epidemiological traits. Early disturbances in intestinal development likely cause a significant portion of these congenital malformations.

Area of Science:

  • Pediatric Surgery
  • Medical Genetics
  • Epidemiology

Background:

  • Alimentary tract atresia encompasses esophageal, small and large gut, and anal atresia, representing significant congenital malformations in infants.
  • Epidemiological data on these conditions are crucial for understanding their occurrence and potential causes.

Purpose of the Study:

  • To investigate the epidemiological characteristics of infants diagnosed with alimentary tract atresia.
  • To analyze racial differences, co-occurrence of atresia types, and associations with other factors like maternal age and chromosomal anomalies.

Main Methods:

  • Utilized data from three malformation registries, covering over 4.5 million births.
  • Identified 3,550 infants with alimentary atresia and analyzed epidemiological variables including sex ratio, twinning, maternal factors, and associated malformations.

Main Results:

  • The overall rate of alimentary atresia was approximately 8 per 10,000 births, with 4.7% of infants having multiple atresia types.
  • Observed racial disparities: higher rates of esophageal atresia in whites and gastrointestinal atresia in Black infants.
  • Found variations in registered rates between programs, partly due to ascertainment differences.

Conclusions:

  • A significant proportion of alimentary atresia cases are attributed to early disturbances in intestinal morphogenesis.
  • While shared mechanisms exist, distinct etiologies likely contribute to the observed epidemiological differences within atresia subgroups.

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