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Inguinal hernias associated with biliary atresia
1Department of Paediatric Surgery, King's College Hospital, London, United Kingdom. a.zani@ich.ucl.ac.uk
Insights
Infants with biliary atresia (BA) have a higher incidence of inguinal hernias, likely due to liver fibrosis and increased abdominal pressure. This finding suggests a link between liver disease severity and hernia development in BA patients.
Area of Science:
- Pediatric Surgery
- Hepatology
- Gastroenterology
Background:
- Biliary atresia (BA) in infants can lead to hepatic fibrosis and ascites.
- Ascites in BA patients may increase the risk of developing inguinal hernias.
Purpose of the Study:
- To investigate the incidence of inguinal hernias in infants diagnosed with biliary atresia.
- To explore potential correlations between inguinal hernias and clinical factors in BA infants.
Main Methods:
- Retrospective review of biliary atresia (BA) infants diagnosed between 2006 and 2010 at a single center.
- Comparison of BA infants with inguinal hernias versus those without, analyzing clinical data and outcomes.
- Statistical analysis using nonparametric tests with significance set at p ≤ 0.05.
Main Results:
- 10 out of 123 (8.1%) infants with BA developed inguinal hernias.
- No significant differences were found in age at Kasai portoenterostomy, cytomegalovirus status, corticosteroid use, or need for liver transplant.
- Infants with inguinal hernias showed a higher aspartate aminotransferase-to-platelet ratio, indicating more severe liver fibrosis (p = 0.02).
Conclusions:
- Biliary atresia infants exhibit a high incidence of inguinal hernias.
- The occurrence of inguinal hernias appears associated with the degree of liver fibrosis and likely ascites and intra-abdominal pressure in BA infants.
- This study is the first to report this association, highlighting a potential complication of BA related to liver disease severity.
Introduction:
Infants with biliary atresia (BA) develop a degree of hepatic fibrosis as a consequence of their cholangiopathy. Some of them present clinically evident ascites that might predispose to inguinal hernias. We aimed to investigate whether infants with BA have a higher incidence of inguinal hernias.
Methods:
Single-center retrospective review of all BA infants diagnosed between January 2006 and December 2010. Infants with a clinical diagnosis of inguinal hernia were identified and compared with those without. Data were expressed as median (range) and compared with nonparametric statistical tests. p ≤ 0.05 was regarded as significant.
Results:
A total of 123 infants underwent Kasai portoenterostomy (KP) during the period. Of these, 10 (8.1%) infants (7 boys) developed inguinal hernias (bilateral n = 4, right n = 5, left n = 1); 9 were repaired (at KP [n = 3] and post-KP [n = 6] at 15 [7 to 30] days) using nonabsorbable sutures, and 1 died before repair. There was no difference in median age at KP (66 vs. 58 days, p = 0.31); cytomegalovirus (IgM positive) status (p = 1.0); use of postoperative corticosteroids (p = 0.49); or ultimate need for liver transplant (p = 1.0). However, aspartate aminotransferase-to-platelet ratio (surrogate marker of liver fibrosis) was higher in hernia infants (2.0 vs. 1.0; p = 0.02). Recurrence has not been identified at a follow-up of 27 months (4 to 55).
Conclusions:
This is the first report to suggest that BA infants have a high incidence of inguinal hernias, which seems related to degree of liver fibrosis at presentation and presumably degree of ascites and increased intra-abdominal pressure.
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