Outcomes of Liver Transplantation in Infants: A Retrospective Cohort Study.

Transplantation proceedings Pub Date : 2024-12-01 Epub Date: 2024-11-30 DOI:10.1016/j.transproceed.2024.10.028
Halil Erbis, Eyyup Mehmet Kilinc, Aynur Camkiran Firat, Cigdem Aliosmanoglu, Mevlut Harun Agca, Ibrahim Aliosmanoglu
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Abstract

Background: Liver transplantation (LT) is a crucial treatment for infants with end-stage liver disease, yet specific data on LT outcomes in infants under 12 months old remain limited. This study aims to present the clinical course and outcomes of infants who underwent LT, assessing the impact of demographic and etiological differences on mortality and survival.

Methods: A retrospective analysis was conducted on 64 infants (< 12 months) who underwent LT between January 2019 and March 2024. Demographic, clinical, and laboratory data were collected from their medical records. LT-specific details, postoperative complications, and survival data were analyzed.

Results: The median age of the infants was 157 days, with 37 boys (57.8%) and 27 girls (42.2%). Biliary atresia was the most common diagnosis (85.9%), and seven infants had undergone a previous Kasai procedure. The median pediatric end-stage liver disease (PELD) score was 15.5. Left lateral segmentectomy was the predominant graft type (60.9%). The median pediatric intensive care unit (PICU) and hospital stays were 5 and 21 days, respectively. Complications occurred in 20 infants (31.3%), with vascular and biliary complication rates both at 12.5%. The overall mortality rate was 17.2%, with early (30-day) and late mortality rates of 6.3% and 10.9%, respectively. The median overall survival (OS) was 204.5 days, and the 1-year survival rate was 32.8%. Kaplan-Meier and log rank analyses showed no significant impact of sex, age, diagnostic groups, graft type, or surgical complications on OS (P > .05).

Conclusions: LT in infants can be performed with acceptable morbidity and mortality rates, particularly with increased experience and standardized protocols.

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婴儿肝移植的预后:一项回顾性队列研究。
背景:肝移植(LT)是终末期肝病婴儿的重要治疗方法,但关于12个月以下婴儿肝移植结局的具体数据仍然有限。本研究旨在介绍接受肝移植的婴儿的临床过程和结果,评估人口统计学和病因学差异对死亡率和生存率的影响。方法:回顾性分析2019年1月至2024年3月期间接受肝移植的64例< 12个月婴儿。从他们的医疗记录中收集人口统计、临床和实验室数据。分析lt特异性细节、术后并发症和生存数据。结果:患儿年龄中位数为157天,其中男孩37例(57.8%),女孩27例(42.2%)。胆道闭锁是最常见的诊断(85.9%),其中7名婴儿曾接受过Kasai手术。儿童终末期肝病(PELD)的中位评分为15.5分。左侧外侧节段切除术为主要移植类型(60.9%)。儿童重症监护病房(PICU)和住院时间的中位数分别为5天和21天。并发症20例(31.3%),其中血管和胆道并发症发生率均为12.5%。总死亡率为17.2%,早期(30天)和晚期死亡率分别为6.3%和10.9%。中位总生存期(OS)为204.5天,1年生存率为32.8%。Kaplan-Meier和log rank分析显示,性别、年龄、诊断组、移植物类型或手术并发症对OS无显著影响(P < 0.05)。结论:婴儿肝移植可以在可接受的发病率和死亡率下进行,特别是随着经验的增加和标准化的方案。
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