Abnormal Liver Biopsies of Donor Grafts in Pediatric Liver Transplantation: How Do They Fare?

IF 1.1 4区 医学 Q3 SURGERY
Jason Guo, Jorge A Sanchez-Vivaldi, Madhukar S Patel, Benjamin K Wang, Andrew D Shubin, Yash Kadakia, Jigesh A Shah, Malcolm MacConmara, Steven Hanish, Parsia A Vagefi, Christine S Hwang
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Abstract

BACKGROUND Little is known about outcomes of pediatric patients transplanted using donor liver grafts with abnormal biopsy results. We assessed donor liver biopsy data to report characteristics and outcomes of abnormal livers transplanted in pediatric patients. MATERIAL AND METHODS We identified pediatric patients who received a liver transplant from a biopsied deceased donor between 2015 and 2022 using the national database UNOS Standard Transplant Analysis and Research files. Recipients were excluded if they received multi-organ transplants or were lost to follow-up. Livers with ≤5% macrosteatosis, no fibrosis, and no inflammation were classified as normal livers (NL). Allografts with >5% macrosteatosis, any fibrosis, or any inflammation were considered abnormal livers (AL). Donor and recipient demographic data and outcomes were examined. RESULTS Of the 3808 total pediatric liver transplants in the study period, there were 213 biopsied donor liver allografts transplanted into pediatric recipients. Of those, 114 were NL and 99 were AL. 35.4% (35/99) of the AL had >5% macrosteatosis with a mean of 7.6±11.4%, 64.6% (64/99) had any inflammation, and 18.2% (18/99) had any fibrosis. AL donors were significantly older than NL donors. AL recipients had higher PELD scores. There were no significant differences in length of stay, rejection rates and causes, or allograft survival between AL and NL. Multivariable analysis revealed that inflammation was independently associated with a significantly greater risk for graft failure. CONCLUSIONS Outcomes of abnormal livers are excellent. Inflammation was an independent risk factor for poor graft prognosis. Donor biopsies in pediatric liver transplantation can be a useful adjunct to assess outcomes.

小儿肝移植中供体移植物的异常肝活检:他们的表现如何?
背景 对使用活检结果异常的供体肝脏移植物进行移植的儿科患者的治疗效果知之甚少。我们评估了供体肝脏活检数据,以报告儿科患者移植的异常肝脏的特征和结果。材料和方法 我们利用国家数据库 UNOS 标准移植分析和研究档案,确定了 2015 年至 2022 年间接受过已故供体活检肝移植的儿科患者。如果受者接受了多器官移植或失去随访,则排除在外。大骨节病≤5%、无纤维化、无炎症的肝脏被归类为正常肝脏(NL)。大骨质增生>5%、有纤维化或炎症的同种异体肝被视为异常肝(AL)。对供体和受体的人口统计学数据及结果进行了研究。结果 在研究期间进行的3808例小儿肝移植中,有213例经活检的供体肝脏同种异体移植物移植给了小儿受体。其中,114 例为 NL 型,99 例为 AL 型。35.4%(35/99)的AL有>5%的大骨节病,平均为7.6±11.4%,64.6%(64/99)有任何炎症,18.2%(18/99)有任何纤维化。AL供体的年龄明显高于NL供体。AL受者的PELD评分较高。AL和NL在住院时间、排斥反应发生率和原因以及异体移植物存活率方面没有明显差异。多变量分析表明,炎症与移植物失败的风险显著增加密切相关。结论 异常肝脏的治疗效果非常好。炎症是导致移植物预后不良的独立风险因素。小儿肝移植中的供体活检可作为评估预后的有用辅助手段。
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来源期刊
CiteScore
2.50
自引率
0.00%
发文量
79
审稿时长
>12 weeks
期刊介绍: Annals of Transplantation is one of the fast-developing journals open to all scientists and fields of transplant medicine and related research. The journal is published quarterly and provides extensive coverage of the most important advances in transplantation. Using an electronic on-line submission and peer review tracking system, Annals of Transplantation is committed to rapid review and publication. The average time to first decision is around 3-4 weeks. Time to publication of accepted manuscripts continues to be shortened, with the Editorial team committed to a goal of 3 months from acceptance to publication. Expert reseachers and clinicians from around the world contribute original Articles, Review Papers, Case Reports and Special Reports in every pertinent specialty, providing a lot of arguments for discussion of exciting developments and controversies in the field.
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