Gautam Vipul, Kumar Vikram, Agarwal Shaleen, Gupta Subhash
Department of Pediatric Hepatology, Centre for Liver and Biliary Sciences, Max Super Speciality Hospital, Saket, New Delhi, India.
Department of Liver Transplant Surgery, Centre for Liver and Biliary Sciences, Max Super Speciality Hospital, Saket, New Delhi, India.
J Clin Exp Hepatol. 2024 May-Jun;14(3):101340. doi: 10.1016/j.jceh.2023.101340. Epub 2023 Dec 22.
In recent years, paediatric ABO incompatible (ABOi) living donor liver transplant (LT) has shown promising outcomes and can potentially eliminate organ shortage. This study aims to report paediatric ABOi LT experience, including short- and long-term outcomes.
It is a single-centre retrospective study. Out of 108 LTs, 20 were done in children. We compared the outcomes between ABOi (n = 20) and non-ABOi (n = 220) paediatric living donor liver transplantation (LDLT) performed during the study period. All the children received pre-LT desensitization therapy comprising rituximab and plasmapheresis targeting pre-LT isohemagglutinin (IHA) titres of ≤1:16.
Out of 239 paediatric LDLTs from 2017 to 2022, 19 children (11 females) underwent 20 ABOi LTs (including one retransplant with an ABOi domino allograft) at a median age of 12 (12, 51) months, with the majority being biliary atresia (60%). The median change in CD19 cell%, CD20 cell%, and IHA titres after rituximab from day -14 to day -1 (before LT) was satisfactory. In the first 3 months following LT, acute cellular rejection, culture-proven sepsis, and biliary and vascular complications were seen in 10%, 20%, 20%, and 15%, respectively. None of the ABOi LT recipients developed antibody-mediated rejection. ABOi LT recipients, as compared to non-ABOi LT recipients, had a higher incidence of bile leaks and prolonged hospital stay, with the rest of the complications, including biliary strictures and long-term outcomes, being comparable. At a median follow-up of 21 (14, 33) months, 4 children expired (21%).
ABOi LT in children shows excellent outcomes and can be performed safely with prior desensitization when a compatible liver is unavailable.
近年来,儿科ABO血型不相容(ABOi)活体肝移植(LT)已显示出良好的效果,并有可能缓解器官短缺问题。本研究旨在报告儿科ABOi肝移植的经验,包括短期和长期结果。
这是一项单中心回顾性研究。在108例肝移植中,有20例是儿童肝移植。我们比较了研究期间进行的ABOi(n = 20)和非ABOi(n = 220)儿科活体肝移植(LDLT)的结果。所有儿童在肝移植前均接受了脱敏治疗,包括利妥昔单抗和血浆置换,目标是使肝移植前同种血凝素(IHA)滴度≤1:16。
在2017年至2022年的239例儿科LDLT中,19名儿童(11名女性)接受了20例ABOi肝移植(包括1例ABOi多米诺同种异体肝再次移植),中位年龄为12(12, 51)个月,大多数为胆道闭锁(60%)。利妥昔单抗治疗后第-14天至第-1天(肝移植前)CD19细胞%、CD20细胞%和IHA滴度的中位变化令人满意。肝移植后的前3个月,急性细胞排斥反应、培养证实的败血症、胆道和血管并发症的发生率分别为10%、20%、20%和15%。没有ABOi肝移植受者发生抗体介导的排斥反应。与非ABOi肝移植受者相比,ABOi肝移植受者胆汁漏的发生率更高,住院时间更长,其余并发症,包括胆道狭窄和长期结果,具有可比性。中位随访21(14, 33)个月时,4名儿童死亡(21%)。
儿童ABOi肝移植显示出良好的效果,在没有合适肝脏的情况下,预先进行脱敏治疗可以安全地进行。