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Published on: February 5, 2021
[Congenital anatomic gastrointestinal obstruction: prenatal diagnosis, morbidity and mortality]
G Bustos Lozano1, C Orbea Gallardo, O Domínguez García
1Servicios de Neonatología, Hospital Universitario 12 de Octubre, Madrid, España. gbustos.hdoc@salud.madrid.org
Insights
Congenital gastrointestinal obstruction morbidity and mortality are mainly linked to extraintestinal issues. Prenatal diagnosis for these obstructions is often late and has limited effectiveness, particularly for lower gastrointestinal sites.
Area of Science:
- Pediatric Surgery
- Neonatal Medicine
- Medical Genetics
Background:
- Congenital gastrointestinal obstruction presents significant challenges in neonates.
- Understanding associated morbidities and mortality is crucial for improving outcomes.
- The role of prenatal diagnosis in managing these conditions requires further evaluation.
Purpose of the Study:
- To detail the morbidity and mortality of congenital gastrointestinal obstruction.
- To evaluate the efficacy of prenatal diagnosis for these conditions.
- To analyze outcomes based on the obstruction's anatomical location.
Main Methods:
- A retrospective case series of 148 patients over 13 years (1990-2003).
- Obstruction sites categorized into three groups: gastric/duodenal/jejunal, ileal/colonic, and anorectal.
- Analysis of surgical interventions, associated syndromes, and diagnostic sensitivities.
Main Results:
- Overall mortality was 14.2%, significantly influenced by prematurity and extraintestinal malformations.
- Nosocomial sepsis (32%) and necrotizing enterocolitis (7%) were major morbidities.
- Prenatal diagnosis sensitivity varied by site (0.77 for upper GI, 0.04 for anorectal) and did not improve prognosis.
Conclusions:
- Extraintestinal problems are the primary drivers of morbidity and mortality in congenital gastrointestinal obstruction.
- Midgut volvulus and necrotizing enterocolitis represent severe intestinal complications.
- Prenatal diagnosis is often delayed and shows limited utility, especially for distal obstructions.
Objectives:
To describe the morbidity and mortality associated with congenital gastrointestinal obstruction, assess the usefulness of prenatal diagnosis, and analyze the results in relation to the site of obstruction.
Patients And Methods:
We performed a retrospective case series study of 148 patients in a 13-year period (1990-2003). Sites of obstruction was classified into three groups: I) gastric, duodenal or jejunal; II) ileal or colonic; III) anorectal.
Results:
There were 65 patients in group I, 38 in group II and 45 in group III. Surgery was performed in 137 patients. Trisomy was diagnosed in 15 patients, polymalformation syndrome in 16 patients, and cystic fibrosis in seven patients. More than one site of intestinal obstruction was found in 22 patients (15 %). Morbidity consisted of nosocomial sepsis in 32 %, necrotizing enterocolitis in 7 %, and short gut in 3.4 %. Prematurity (48 %) was associated with higher morbidity and mortality. Overall mortality was 14.2 %, mainly associated with other malformations and extraintestinal problems. When patients with other extraintestinal malformations were excluded, the highest mortality was found in group II (OR: 12.19; CI: 2.4-76.2). The overall sensitivity of prenatal diagnosis was 0.44 and the mean gestational age at diagnosis was 31.6 weeks (SD 5.2). According to the site of obstruction, sensitivity was 0.77 in group I, 0.39 in group II and 0.04 in group III. Prenatal diagnosis did not alter prognosis.
Conclusions:
Morbidity and mortality were strongly influenced by extraintestinal problems. The most severe intestinal complications were midgut volvulus and necrotizing enterocolitis. Prenatal diagnosis was late and showed good sensitivity only in group I.
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