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Outcomes of Kidney Transplant Patients with Atypical Hemolytic Uremic Syndrome Treated with Eculizumab: A Systematic Review and Meta-Analysis

机译:依库丽单抗治疗非典型溶血性尿毒症综合征肾移植患者的疗效:系统评价和荟萃分析

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摘要

Background: Kidney transplantation in patients with atypical hemolytic uremic syndrome (aHUS) is frequently complicated by recurrence, resulting in thrombotic microangiopathy in the renal allograft and graft loss. We aimed to assess the use of eculizumab in the prevention and treatment of aHUS recurrence after kidney transplantation. Methods: Databases (MEDLINE, EMBASE and Cochrane Database) were searched through February 2019. Studies that reported outcomes of adult kidney transplant recipients with aHUS treated with eculizumab were included. Estimated incidence rates from the individual studies were extracted and combined using random-effects, generic inverse variance method of DerSimonian and Laird. Protocol for this systematic review has been registered with PROSPERO (International Prospective Register of Systematic Reviews; no. CRD42018089438). Results: Eighteen studies (13 cohort studies and five case series) consisting of 380 adult kidney transplant patients with aHUS who received eculizumab for prevention and treatment of post-transplant aHUS recurrence were included in the analysis. Among patients who received prophylactic eculizumab, the pooled estimated incidence rates of recurrent thrombotic microangiopathy (TMA) after transplantation and allograft loss due to TMA were 6.3% (95%CI: 2.8–13.4%, I2 = 0%) and 5.5% (95%CI: 2.9–10.0%, I2 = 0%), respectively. Among those who received eculizumab for treatment of post-transplant aHUS recurrence, the pooled estimated rates of allograft loss due to TMA was 22.5% (95%CI: 13.6–34.8%, I2 = 6%). When the meta-analysis was restricted to only cohort studies with data on genetic mutations associated with aHUS, the pooled estimated incidence of allograft loss due to TMA was 22.6% (95%CI: 13.2–36.0%, I2 = 10%). We found no significant publication bias assessed by the funnel plots and Egger’s regression asymmetry test (p > 0.05 for all analyses). Conclusions: This study summarizes the outcomes observed with use of eculizumab for prevention and treatment of aHUS recurrence in kidney transplantation. Our results suggest a possible role for anti-C5 antibody therapy in the prevention and management of recurrent aHUS.
机译:背景:非典型溶血性尿毒症综合征(aHUS)患者的肾脏移植经常因复发而复杂化,导致同种异体肾血栓形成性微血管病和移植物丢失。我们旨在评估依库丽单抗在预防和治疗肾移植术后aHUS复发中的用途。方法:搜索数据库(MEDLINE,EMBASE和Cochrane数据库)至2019年2月。研究报告了接受依库丽单抗治疗的aHUS成人肾移植受者的结局。提取各个研究的估计发病率,并使用随机效应,DerSimonian和Laird的通用逆方差方法进行组合。该系统评价的规程已在PROSPERO(国际系统评价预期登记册; CRD42018089438)中注册。结果:分析包括18项研究(13项队列研究和5个病例系列),其中包括380例接受eculizumab预防和治疗移植后aHUS复发的成年肾移植aHUS患者。在接受预防性依库丽单抗治疗的患者中,移植后复发血栓性微血管病(TMA)和因TMA引起的同种异体移植损失的合并估计发生率为6.3%(95%CI:2.8–13.4%,I 2 = 0%)和5.5%(95%CI:2.9–10.0%,I 2 = 0%)。在接受依库丽单抗治疗的移植后aHUS复发患者中,因TMA引起的同种异体移植总损失率为22.5%(95%CI:13.6–34.8%,I 2 = 6%) 。当荟萃分析仅限于具有与aHUS相关的基因突变数据的队列研究时,由TMA引起的同种异体移植损失的合并估计发生率为22.6%(95%CI:13.2–36.0%,I 2 = 10%)。通过漏斗图和Egger回归不对称检验,我们发现没有明显的出版偏倚(所有分析的p> 0.05)。结论:本研究总结了使用依库丽单抗预防和治疗肾移植术后aHUS复发所观察到的结果。我们的结果表明抗C5抗体疗法在预防和管理复发性aHUS中可能发挥作用。

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