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Umbilical hernia and clinical course of patients with bile duct atresia
Sofia Brenes-Guzmán1, Jean Pierre Aurelus1, Susana Aideé González-Chávez2
1Instituto Mexicano del Seguro Social, Centro Médico Nacional Siglo XXI, Hospital de Pediatría Dr. Silvestre Frenk Freund, Departamento de Cirugía Pediátrica. Ciudad de México, México.
Insights
Children with biliary atresia (BA) have a higher chance of developing umbilical hernias (UH). This co-occurrence is linked to more severe portal hypertension and related complications in BA patients.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Surgical Pediatrics
Background:
- Biliary atresia (BA) is the primary cause of pediatric cirrhosis, leading to significant morbidity and mortality.
- Complications such as gastrointestinal bleeding and portal hypertension are key concerns in BA.
- Umbilical hernia (UH) has known associations with portal hypertension and cirrhosis, but its specific role in BA progression is unclear.
Purpose of the Study:
- To determine the prevalence of coexisting biliary atresia and umbilical hernia (BA-UH).
- To describe the clinical evolution of patients with BA, comparing those with and without UH.
- To identify prognostic factors for morbidity and mortality in BA patients related to UH presence.
Main Methods:
- An observational, descriptive, retrospective, and longitudinal study.
- Inclusion of patients diagnosed with biliary atresia at a tertiary pediatric hospital.
- Analysis of BA-related variables and clinical outcomes stratified by the presence or absence of UH.
Main Results:
- The study included 56 patients with BA; 69.6% were female.
- Umbilical hernia coexisted with BA in 75% of cases.
- Patients with BA and UH showed significantly higher prevalence of portal hypertension (80.4%), collateral venous networks, gastrointestinal bleeding, ascites, and esophageal varices.
Conclusions:
- Biliary atresia patients have an increased likelihood of developing umbilical hernias.
- The presence of an umbilical hernia in BA patients correlates with advanced portal hypertension and its complications.
Background:
Bile atresia is children's leading cause of cirrhosis. Its high morbidity and mortality are explained by its complications, including gastrointestinal bleeding and portal hypertension. Umbilical hernia has been embryologically and clinically associated with portal hypertension and cirrhosis; however, the clinical evolution of patients with bile atresia and umbilical hernia is unknown, so the aim of the study is to describe this link.
Objective:
To determine the prevalence of the coexistence of AVB and HU in patients in a tertiary hospital, and describe the clinical evolution of these patients with respect to the presence/absence of HU as a strategy in the search for prognostic factors of morbidity and mortality.
Material And Methods:
This is an observational, descriptive, retrospective, and longitudinal study that included patients with bile atresia in a tertiary pediatric hospital. The variables related to bile atresia were analyzed, and the clinical evolution was described according to the presence or absence of UH.
Results:
56 patients with bile atresia were included, of which 69.6% were females. Portal hypertension occurred in 80.4%, with the presence of collateral venous network, gastrointestinal bleeding, ascites, and hepatomegaly being the indirect clinical data most often presented. The frequency of coexistence of umbilical hernia and bile atresia was 75%. Portal hypertension, collateral venous network, gastrointestinal bleeding, ascites, and small esophageal varices were the significantly more prevalent variables in patients with umbilical hernia.
Conclusions:
Patients with bile atresia have a greater possibility of developing umbilical hernia and that it is associated with a more advanced evolution of portal hypertension and its associated signs and complications.
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