Variceal Bleeds in Patients with Biliary Atresia

Daan B van Wessel*, Mauri Witt, Niels Bax, Henkjan J Verkade, René Scheenstra, Ruben H de Kleine, Jan B Hulscher

*Corresponding author voor dit werk

    OnderzoeksoutputAcademicpeer review

    12 Citaten (Scopus)
    60 Downloads (Pure)

    Samenvatting

    Introduction Portal hypertension often occurs in biliary atresia (BA). The subsequent development of esophageal varices and bleeding from these varices are a well-known complication. We aim to describe the incidence and severity of variceal bleeding in patients with BA. In addition, we describe the characteristics of patients who experienced variceal bleeds.

    Materials and Methods We included all infants treated for BA at our center between March 1987 and August 2015. Variceal bleeding was defined as hematemesis and/or melena with presence of varices at endoscopy. Findings at endoscopy and ultrasound, laboratory tests, clearance of jaundice, fibrosis-grade at Kasai portoenterostomy, and several varices prediction scores were documented. Routine endoscopies were not performed.

    Results In this study, 74 patients were included. During follow-up, 18 out of 74 patients (24%) developed variceal bleeding at an age of 9 months (range, 4-111). Twelve patients were listed for liver transplantation at the time of bleeding. Patients who did not clear their jaundice developed variceal bleeds more often and earlier in life. Bleeds were treated with sclerotherapy, banding, or octreotide. Four patients did not receive treatment. No bleeding-related mortality occurred.

    Conclusion One-fourth of the children diagnosed with BA experience variceal bleeds during follow-up. Most of these children are younger than 1 year and often already listed for transplantation. Major complications did not occur after variceal bleeding.

    Originele taal-2English
    Pagina's (van-tot)439-444
    Aantal pagina's6
    TijdschriftEuropean Journal of Pediatric Surgery
    Volume28
    Nummer van het tijdschrift5
    Vroegere onlinedatum28-jun.-2017
    DOI's
    StatusPublished - okt.-2018

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