Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Feb 28;39(1):142.
doi: 10.1007/s00383-023-05424-y.

Prognostic factors and outcomes of Kasai portoenterostomy (KPE): nine-year experience from a lower-middle income country

Affiliations
Review

Prognostic factors and outcomes of Kasai portoenterostomy (KPE): nine-year experience from a lower-middle income country

Nipun Wickramasekara et al. Pediatr Surg Int. .

Abstract

Purpose: Outcome data after Kasai portoenterostomy (KPE) reported worldwide show considerable regional and institutional variation. It is not known whether the same standards of outcomes reported in western world can be replicated in resource-poor countries.

Methods: We reviewed 79 patients of which 43 had completed a 2-year minimum follow-up. Two cohorts were based on age at KPE. The median age at surgery was 60 days.

Results: Clearance of jaundice (COJ) at 3 months was 20.93% and was not affected by age at surgery (p = 0.295). Four patients (9.3%) received liver transplant and 16 patients (37.21%) were recorded dead at a median age of 7 months. Native liver survival (NLS) was 53.49% and overall survival (OS) was 62.79%. Kaplan-Meier estimated 4- and 6-year NLS were 55.8% and 49.6%, respectively. There was a significant difference in the NLS between early and late surgery groups.

Conclusion: While causes for low COJ need to be explored, these data reaffirm that early surgery has a significant favorable effect on survival. NLS was comparable with data from the developed world, whereas low OS is explained by limited access to transplant. Thus, where the survival depends on native liver longevity, emphasis should be on as early KPE as possible.

Keywords: Biliary atresia; Jaundice; Kasai portoenterostomy; Native liver survival.

PubMed Disclaimer

References

    1. Sasaki H, Nio M, Okubo R, Murai Y (2021) Japanese biliary atresia registry. Springer, Singapore, pp 19–26
    1. Nio M, Ohi R, Miyano T, Saeki M, Shiraki K, Tanaka K (2003) Five- and 10-year survival rates after surgery for biliary atresia: a report from the Japanese biliary atresia registry. J Pediatr Surg 38:997–1000. https://doi.org/10.1016/S0022-3468(03)00178-7 - DOI - PubMed
    1. Petersen C, Harder D, Abola Z, Becker T, Chardot C, Davenport M, Deutschmann A, Khelif K, Kobayashi H, Kvist N, Leonhardt J, Melter M, Pakarinen M, Pawlowska J, Petersons A, Pfister ED, Rygl M, Schreiber R, Kelly D (2008) European biliary atresia registries: Summary of a symposium. Eur J Ped Surg 18:111–116. https://doi.org/10.1055/s-2008-1038479 - DOI
    1. Luthufdeen I, Waidyanatha S (2016) A study on cholestasis in infants less than six months of age presenting to lady ridgeway hospital for children, Colombo. Sri Lanka J Child Health 45:34. https://doi.org/10.4038/sljch.v45i1.8083 - DOI
    1. Hartley J, Davenport M, Kelly D (2009) Biliary atresia. Lancet 374:1704–1713. https://doi.org/10.1016/S0140-6736(09)60946-6 - DOI - PubMed

LinkOut - more resources