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. 2022 Nov 7;11(21):6601.
doi: 10.3390/jcm11216601.

Surgical and Medical Aspects of the Initial Treatment of Biliary Atresia: Position Paper

Affiliations

Surgical and Medical Aspects of the Initial Treatment of Biliary Atresia: Position Paper

Mark Davenport et al. J Clin Med. .

Abstract

Biliary atresia, a fibro-obliterative disease of the newborn, is usually initially treated by Kasai portoenterostomy, although there are many variations in technique and different options for post-operative adjuvant medical therapy. A questionnaire on such topics (e.g., open vs. laparoscopic; the need for liver mobilisation; use of post-operative steroids; use of post-operative anti-viral therapy, etc.) was circulated to delegates (n = 43) of an international webinar (Biliary Atresia and Related Diseases-BARD) held in June 2021. Respondents were mostly European, but included some from North America, and represented 18 different countries overall. The results of this survey are presented here, together with a commentary and review from an expert panel convened for the meeting on current trends in practice.

Keywords: Kasai operation; adjuvant therapy; biliary atresia; corticosteroids; cytomegalovirus; ursodeoxycholic acid.

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Conflict of interest statement

The authors declare no conflict of interest.

References

    1. Nizery L., Chardot C., Sissaoui S., Capito C., Henrion-Caude A., Debray D., Girard M. Biliary atresia: Clinical advances and perspectives. Clin. Res. Hepatol. Gastroenterol. 2016;40:281–287. doi: 10.1016/j.clinre.2015.11.010. - DOI - PubMed
    1. Scottoni F., Davenport M. Biliary atresia: Potential for a new decade. Semin. Pediatr. Surg. 2020;29:150940. doi: 10.1016/j.sempedsurg.2020.150940. - DOI - PubMed
    1. Harpavat S., Finegold M.J., Karpen S.J. Patients with biliary atresia have elevated direct/conjugated bilirubin levels shortly after birth. Pediatrics. 2011;128:e1428–e1433. doi: 10.1542/peds.2011-1869. - DOI - PMC - PubMed
    1. Jiang J., Wang J., Shen Z., Lu X., Chen G., Huang Y., Dong R., Zheng S. Serum MMP-7 in the diagnosis of biliary atresia. Pediatrics. 2019;144:e20190902. doi: 10.1542/peds.2019-0902. - DOI - PubMed
    1. Wu J.F., Jeng Y.M., Chen H.L., Ni Y.-H., Hsu H.-Y., Chang M.-H. Quantification of serum matrix metallopeptide 7 levels may assist in the diagnosis and predict the outcome for patients with biliary atresia. J. Pediatr. 2019;208:30–37.e1. doi: 10.1016/j.jpeds.2018.12.006. - DOI - PubMed

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