Long-term outcome for children undergoing open hepatico-jejunostomy for choledochal malformations: a 43-year

M V Stern1, G Boroni2,3, F Parolini2,3

  • 1Department of Pediatric Surgery, "Spedali Civili" Children's Hospital, Brescia, Italy. mariavittoria.stern@gmail.com.

PubMed

Insights

Surgical excision of choledochal malformations (CMs) in children yields excellent long-term outcomes and quality of life (QoL). However, late complications necessitate careful, long-term follow-up protocols for pediatric surgery patients.

Area of Science:

  • Pediatric Surgery
  • Hepatobiliary Surgery
  • Congenital Malformations

Background:

  • Choledochal malformations (CMs) are rare congenital anomalies of the biliary tract.
  • Long-term outcomes and quality of life (QoL) after surgical correction in pediatric patients require further investigation.

Purpose of the Study:

  • To evaluate the long-term results and QoL in pediatric patients who underwent surgery for CMs.
  • To analyze the incidence and timing of long-term postoperative complications (POCs) after CMs surgery.

Main Methods:

  • Retrospective analysis of 113 pediatric patients with CMs treated between 1980 and 2022.
  • Focus on long-term POCs (occurring ≥5 years post-surgery) and adult QoL assessment.
  • Comparison of QoL with a matched control group.

Main Results:

  • Open excision with Roux-en-Y hepaticojejunostomy (HJ) was performed in all patients.
  • Median follow-up was 8.95 years; 8.9% experienced major long-term POCs, presenting a median of 11 years post-surgery.
  • Adult QoL was comparable to controls; no biliary malignancies were observed.

Conclusions:

  • Open complete excision of CMs with HJ provides excellent long-term results.
  • Severe complications can manifest many years after surgery, highlighting the need for precise transitional care follow-up.
  • International collaboration is recommended to establish standardized follow-up protocols for CMs patients.
Abstract

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