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法国扩大标准器官捐献者肾脏移植中的低温治疗(HYPOREME):一项多中心、随机对照试验。

Hypothermia for expanded criteria organ donors in kidney transplantation in France (HYPOREME): a multicentre, randomised controlled trial.

出版信息

Lancet Respir Med. 2024 Sep;12(9):693-702. doi: 10.1016/S2213-2600(24)00117-6. Epub 2024 Jun 11.

Abstract

BACKGROUND

Expanded criteria donors help to increase graft availability, but provide organs with an increased risk of delayed graft function. We aimed to investigate whether donor hypothermia decreases the risk of delayed graft function compared with normothermia.

METHODS

We did this multicentre, randomised, controlled, parallel-arm trial at 53 intensive care units and transplant centres in France. We included expanded criteria donors in whom death was diagnosed based on neurological criteria, in compliance with French law, and the recipients of their kidney grafts. Eligible expanded criteria donors were older than 60 years or were aged 50-59 years and had at least two other risk factors (history of hypertension, creatinine >132 μmol/L, or cerebrovascular cause of death). Donors were randomly assigned to hypothermia (34-35°C) or normothermia (36·5-37·5°C). Machine perfusion was used routinely. Randomisation was done using a computer-generated, interactive, web-response system, in permuted blocks (block size six), stratified by centre. Outcome assessors were masked; investigator masking was not feasible. The primary outcome was the proportion of kidney recipients with delayed graft function, defined as renal replacement therapy within 7 days after transplantation, assessed in the modified intention-to-treat (mITT) population, which included all recipients who received at least one kidney from an expanded criteria donor, with the exception of those under guardianship. Secondary outcomes in expanded criteria donors were the number of organs recovered and transplanted, kidney function, body temperature, total volume of fluids administered, blood pressure and need for vasopressors and inotropes, and adverse events (cardiovascular events, metabolic disturbances, and coagulation disorders). Secondary outcomes in kidney recipients were duration of hospital stay, kidney graft function and vital status at day 7, day 28, 3 months, and 1 year after transplantation, and adverse events (infections, cardiovascular events, and surgical complications). Secondary outcomes were assessed in the mITT population. The trial was registered at ClinicalTrials.gov, NCT03098706.

FINDINGS

Between Nov 9, 2017, and March 3, 2021, 365 donors were randomly assigned, of whom 298 (151 [51%] male, 147 [49%] female) provided kidneys to 526 recipients (323 [61%] male, 203 [39%] female). 251 recipients in the hypothermia group and 275 recipients in the normothermia group were included in the analysis. Graft function was delayed in 40 (16%) of 251 recipients in the hypothermia group and 58 (21%) of 275 recipients in the normothermia group (odds ratio 0·71 [95% CI 0·44-1·13]; p=0·14; absolute difference -5·2% [95% CI 11·8-1·5]). Compared with donors in the normothermia group, donors in the hypothermia group had higher highest mean arterial pressure (115 mm Hg [SD 22] vs 108 mm Hg [20]; p=0·001). 1 year after transplantation, recipients in the hypothermia group had a lower mean creatinine concentration (152·4 μmol/L [SD 59·1] vs 169·7 μmol/L [51·4]; p=0·0351) and a higher mean creatinine clearance (42·3 mL/min/1·73 m [15·8] vs 40·5 mL/min/1·73 m [17·9]; p=0·0414) than those in the normothermia group. No significant differences between groups were identified for any other secondary outcomes.

INTERPRETATION

Hypothermia in expanded criteria donors whose organs were routinely stored using machine perfusion did not decrease the frequency of delayed kidney graft function. However, hypothermia was associated with a lower serum creatinine concentration and a higher creatinine clearance 1 year after transplantation.

FUNDING

French Ministry of Health and French Intensive Care Society.

摘要

背景

扩大标准供者有助于增加移植物的可获得性,但也会增加移植物延迟功能恢复的风险。我们旨在研究与常温相比,供者低温是否会降低延迟移植物功能恢复的风险。

方法

我们在法国的 53 个重症监护病房和移植中心进行了这项多中心、随机、对照、平行臂试验。我们纳入了根据法国法律,基于神经学标准诊断死亡的扩大标准供者,以及他们的肾移植物的受者。符合条件的扩大标准供者年龄大于 60 岁或年龄为 50-59 岁,且至少有其他两个危险因素(高血压病史、肌酐>132 μmol/L 或脑血管死亡原因)。供者被随机分配到低温(34-35°C)或常温(36.5-37.5°C)组。常规使用机器灌注。使用计算机生成的、交互式的、网络响应系统进行随机分组,采用区组随机化(区组大小为 6),按中心分层。结局评估者设盲;研究者设盲不可行。主要结局是接受扩大标准供者肾移植的受者中延迟移植物功能的比例,定义为移植后 7 天内需要肾脏替代治疗,在改良意向治疗(mITT)人群中评估,该人群包括所有接受至少一个扩大标准供者供肾的受者,不包括受监护的受者。扩大标准供者的次要结局包括器官采集和移植的数量、肾功能、体温、总输液量、血压以及对血管加压药和正性肌力药的需求,以及不良事件(心血管事件、代谢紊乱和凝血障碍)。肾移植受者的次要结局包括移植后 7 天、28 天、3 个月和 1 年的住院时间、肾移植物功能和生存状态,以及不良事件(感染、心血管事件和手术并发症)。次要结局在 mITT 人群中进行评估。该试验在 ClinicalTrials.gov 注册,NCT03098706。

结果

在 2017 年 11 月 9 日至 2021 年 3 月 3 日期间,365 名供者随机分配,其中 298 名(151 名[51%]男性,147 名[49%]女性)为 526 名受者(323 名[61%]男性,203 名[39%]女性)提供了肾脏。低温组 251 名受者和常温组 275 名受者纳入分析。低温组 251 名受者中 40 名(16%)和常温组 275 名受者中 58 名(21%)发生移植物功能延迟(比值比 0.71[95%CI 0.44-1.13];p=0.14;绝对差异-5.2%[95%CI 11.8-1.5])。与常温组供者相比,低温组供者的平均动脉压最高(115mmHg[22] vs 108mmHg[20];p=0.001)。移植后 1 年,低温组受者的平均肌酐浓度(152.4μmol/L[59.1] vs 169.7μmol/L[51.4];p=0.0351)和肌酐清除率(42.3mL/min/1.73m[15.8] vs 40.5mL/min/1.73m[17.9];p=0.0414)均高于常温组。两组在其他次要结局方面无显著差异。

解释

在常规使用机器灌注储存器官的扩大标准供者中,低温并没有降低延迟肾移植功能的发生率。然而,低温与移植后 1 年时血清肌酐浓度降低和肌酐清除率升高有关。

资助

法国卫生部和法国重症监护学会。

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