Identifying Preoperative Clinical Characteristics of Unexpected Gastrointestinal Perforation in Infants-A

Adinda G H Pijpers1,2,3, Ramon R Gorter1, Laurens D Eeftinck Schattenkerk1

  • 1Department of Pediatric Surgery, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.

PubMed

Insights

Infants with unexpected gastrointestinal perforation (GIP) are at higher risk for small bowel perforation if they are premature or have low birth weight. Colon perforations warrant screening for Hirschsprung disease and cystic fibrosis.

Area of Science:

  • Pediatric Surgery
  • Neonatal Care
  • Gastroenterology

Background:

  • Unexpected pneumoperitoneum in infants signifies gastrointestinal perforation (GIP), a critical surgical emergency.
  • Preoperative localization of GIP is challenging, impacting surgical strategy due to differences between small bowel and colon perforations.

Purpose of the Study:

  • To characterize preoperative patient factors in infants with unexpected GIP.
  • To differentiate between small bowel and colon perforations.
  • To identify underlying causes of GIP in this cohort.

Main Methods:

  • Retrospective analysis of infants (≤ 6 months) with unexpected pneumoperitoneum undergoing surgery (1996-2024).
  • Statistical analysis (chi-squared, t-tests, Bonferroni correction) to compare perforation locations.
  • Review of preoperative characteristics and final diagnoses.

Main Results:

  • 51 infants presented with unexpected GIP; 26 small bowel, 22 colon, 3 stomach perforations.
  • Small bowel perforations were associated with prematurity, low birth weight (<1000g), respiratory support, and lower arterial pH.
  • Colon perforations showed higher incidence of pneumatosis intestinalis and were linked to Hirschsprung disease and cystic fibrosis.

Conclusions:

  • Prematurity and low birth weight (<1000g) increase the risk of small bowel perforation in infants with GIP.
  • Colon perforations necessitate further investigation for Hirschsprung disease and cystic fibrosis.
Abstract

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