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1B 期状态不足以优先考虑患有慢加急性肝衰竭的儿童进行肝移植。

Status 1B designation does not adequately prioritize children with acute-on-chronic liver failure for liver transplantation.

机构信息

Division of Critical Care MedicineChildren's Hospital of PhiladelphiaPhiladelphiaPennsylvaniaUSA.

Division of Gastroenterology and HepatologyPerelman School of MedicineUniversity of PennsylvaniaPhiladelphiaPennsylvaniaUSA.

出版信息

Liver Transpl. 2022 Aug;28(8):1288-1298. doi: 10.1002/lt.26436. Epub 2022 Apr 25.

Abstract

Acute-on-chronic liver failure (ACLF) is an acute decompensation of chronic liver disease leading to multiorgan failure and mortality. The objective of this study was to evaluate characteristics and outcomes of children with ACLF who are at the highest priority for liver transplantation (LT) on the United Network for Organ Sharing (UNOS) database-listed as status 1B. The characteristics and outcomes of 478 children with ACLF listed as status 1B on the UNOS LT waiting list from 2007-2019 were compared with children with similar or higher priority listing for transplant: 929 with acute liver failure (ALF) listed as status 1A and 808 with metabolic diseases and malignancies listed as status 1B (termed "non-ACLF"). Children with ACLF had comparable rates of cumulative organ failures compared with ALF (45% vs. 44%; p > 0.99) listings, but higher than non-ACLF (45% vs. 1%; p < 0.001). ACLF had the lowest LT rate (79%, 84%, 95%; p < 0.001), highest pre-LT mortality (20%, 11%, 1%; p < 0.001), and longest waitlist time (57, 3, 56 days; p < 0.001), and none recovered without LT (0%, 4%, 1%; p < 0.001). In survival analyses, ACLF was associated with an increased adjusted hazard ratio (HR) for post-LT mortality (HR, 1.50 vs. ALF [95% confidence interval, CI, 1.02-2.19; p = 0.04] and HR, 1.64 vs. non-ACLF [95% CI, 1.15-2.34; p = 0.01]). ACLF has the least favorable waitlist and post-LT outcomes of all patients who are status 1A/1B. Increased prioritization on the LT waiting list may offer children with ACLF an opportunity for enhanced outcomes.

摘要

急性慢性肝衰竭(ACLF)是慢性肝病的急性失代偿,导致多器官衰竭和死亡。本研究的目的是评估在器官共享联合网络(UNOS)数据库中列为 1B 级的最优先进行肝移植(LT)的 ACLF 患儿的特征和结局。比较了 2007 年至 2019 年在 UNOS LT 等待名单上列为 1B 级的 478 例 ACLF 患儿与具有类似或更高移植优先权的患儿的特征和结局:929 例急性肝衰竭(ALF)患儿列为 1A 级,808 例代谢疾病和恶性肿瘤患儿列为 1B 级(称为“非 ACLF”)。与 ALF 患儿(44%)相比,ACLF 患儿的累积器官衰竭发生率相当(45%,p>0.99),但高于非 ACLF 患儿(1%,p<0.001)。ACLF 的 LT 率最低(79%、84%、95%,p<0.001),LT 前死亡率最高(20%、11%、1%,p<0.001),等待名单时间最长(57、3、56 天,p<0.001),没有患儿在不进行 LT 的情况下恢复(0%、4%、1%,p<0.001)。在生存分析中,ACLF 与 LT 后死亡率的调整后危险比(HR)增加相关(HR,1.50 与 ALF [95%置信区间,CI,1.02-2.19;p=0.04],HR,1.64 与非 ACLF [95%CI,1.15-2.34;p=0.01])。在所有列为 1A/1B 的患者中,ACLF 的等待名单和 LT 后结局最不理想。在 LT 等待名单上给予更高的优先级可能为 ACLF 患儿提供改善结局的机会。

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