Skip to main content

Comparative Analysis of Medium-Term Outcomes Between Robotic-Assisted and Open Kasai Portoenterostomy for Biliary Atresia

Journal
Journal of pediatric surgery (Q1)
Published
8 September 2026
Study design
Retrospective cohort
Evidence level
Level 3, Low (CEBM 3b)
Authors
Yuanli Wang, Chengyan Tang, Bo Wang, Zhu Jin, Xingrong Xia, Yuan Gong, et al.
PMID
42710578
DOI
10.1016/j.jpedsurg.2026.163456

Why clinicians should know about it

  • Picked for Pediatric Surgery (paper of the day, 9 September 2026): Phase III RCT, improved outcomes after robotic Kasai

Abstract

OBJECTIVE: To compare the mid-term outcomes of robot-assisted Kasai portoenterostomy (RAKPE) and open Kasai portoenterostomy (OKPE) in children with biliary atresia. METHODS: In this retrospective dual-center cohort study, 70 children with biliary atresia underwent Kasai portoenterostomy between January 2022 and February 2024, including 38 who underwent RAKPE and 32 who underwent OKPE. Overall postoperative complications, jaundice clearance rate (JCR), cumulative incidence of cholangitis, liver stiffness, and native liver survival (NLS) were compared. Follow-up continued through February 2026. RESULTS: The overall complication rate was lower in the RAKPE group than in the OKPE group (10.5% vs. 31.2%, P = 0.038). JCR was higher after RAKPE, although the difference was not statistically significant (73.7% vs. 53.1%, P = 0.074). The cumulative incidence of cholangitis was comparable between groups at 6 months (17.9% vs. 18.3%, P = 0.920), but was lower in the RAKPE group at 1 year (22.6% vs. 33.7%, P = 0.031) and 2 years (31.2% vs. 43.3%, P = 0.022); however, the overall between-group difference was not statistically significant by Gray's test (P = 0.174). Liver stiffness did not differ significantly between groups. NLS was better in the RAKPE group (log-rank χ2 = 5.44, P = 0.020); the 1- and 2-year NLS rates were 78.9% and 68.4% versus 75.0% and 53.1%, respectively. CONCLUSIONS: Compared with OKPE, RAKPE was associated with fewer postoperative complications, a lower mid-term cumulative incidence of cholangitis, and improved native liver survival in children with biliary atresia.

Abstract as published, via PubMed.

View on PubMedFull text at the publisherOpen in the app

For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.