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比较两种延迟策略对严重急性肾损伤(AKIKI 2)患者开始肾脏替代治疗的效果:一项多中心、开放标签、随机、对照试验。

Comparison of two delayed strategies for renal replacement therapy initiation for severe acute kidney injury (AKIKI 2): a multicentre, open-label, randomised, controlled trial.

机构信息

Département de réanimation médico-chirurgicale, APHP Hôpital Avicenne, Bobigny, France; Health Care Simulation Center, UFR SMBH, Université Sorbonne Paris Nord, Bobigny, France; Common and Rare Kidney Diseases, Sorbonne Université, INSERM, UMR-S 1155, Paris, France; Investigation Network Initiative-Cardiovascular and Renal Clinical Trialists, Bobigny, France.

INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Département de Santé Publique, Centre de Pharmacoépidémiologie (Cephepi), Sorbonne Université, Hôpital Pitié Salpêtrière, Paris, France.

出版信息

Lancet. 2021 Apr 3;397(10281):1293-1300. doi: 10.1016/S0140-6736(21)00350-0.

Abstract

BACKGROUND

Delaying renal replacement therapy (RRT) for some time in critically ill patients with severe acute kidney injury and no severe complication is safe and allows optimisation of the use of medical devices. Major uncertainty remains concerning the duration for which RRT can be postponed without risk. Our aim was to test the hypothesis that a more-delayed initiation strategy would result in more RRT-free days, compared with a delayed strategy.

METHODS

This was an unmasked, multicentre, prospective, open-label, randomised, controlled trial done in 39 intensive care units in France. We monitored critically ill patients with severe acute kidney injury (defined as Kidney Disease: Improving Global Outcomes stage 3) until they had oliguria for more than 72 h or a blood urea nitrogen concentration higher than 112 mg/dL. Patients were then randomly assigned (1:1) to either a strategy (delayed strategy) in which RRT was started just after randomisation or to a more-delayed strategy. With the more-delayed strategy, RRT initiation was postponed until mandatory indication (noticeable hyperkalaemia or metabolic acidosis or pulmonary oedema) or until blood urea nitrogen concentration reached 140 mg/dL. The primary outcome was the number of days alive and free of RRT between randomisation and day 28 and was done in the intention-to-treat population. The study is registered with ClinicalTrial.gov, NCT03396757 and is completed.

FINDINGS

Between May 7, 2018, and Oct 11, 2019, of 5336 patients assessed, 278 patients underwent randomisation; 137 were assigned to the delayed strategy and 141 to the more-delayed strategy. The number of complications potentially related to acute kidney injury or to RRT were similar between groups. The median number of RRT-free days was 12 days (IQR 0-25) in the delayed strategy and 10 days (IQR 0-24) in the more-delayed strategy (p=0·93). In a multivariable analysis, the hazard ratio for death at 60 days was 1·65 (95% CI 1·09-2·50, p=0·018) with the more-delayed versus the delayed strategy. The number of complications potentially related to acute kidney injury or renal replacement therapy did not differ between groups.

INTERPRETATION

In severe acute kidney injury patients with oliguria for more than 72 h or blood urea nitrogen concentration higher than 112 mg/dL and no severe complication that would mandate immediate RRT, longer postponing of RRT initiation did not confer additional benefit and was associated with potential harm.

FUNDING

Programme Hospitalier de Recherche Clinique.

摘要

背景

对于患有严重急性肾损伤且没有严重并发症的危重患者,延迟一段时间开始肾脏替代治疗(RRT)是安全的,并且可以优化医疗设备的使用。主要的不确定性仍然在于可以安全推迟多长时间开始 RRT。我们的目的是检验以下假设,即更延迟的开始策略会导致更多的无 RRT 天数,而不是延迟策略。

方法

这是一项在法国 39 个重症监护病房进行的非盲、多中心、前瞻性、开放标签、随机对照试验。我们监测患有严重急性肾损伤(定义为肾脏疾病:改善全球结果 3 期)的危重患者,直到他们出现少尿超过 72 小时或血尿素氮浓度高于 112mg/dL。然后,患者被随机分配(1:1)到延迟策略组或更延迟策略组。在更延迟的策略中,RRT 开始的时间推迟到强制性指征(明显高钾血症或代谢性酸中毒或肺水肿)或血尿素氮浓度达到 140mg/dL。主要结局是随机化至第 28 天之间存活且无 RRT 的天数,这是在意向治疗人群中进行的。该研究在 ClinicalTrials.gov 上注册,NCT03396757,现已完成。

结果

在 2018 年 5 月 7 日至 2019 年 10 月 11 日期间,对 5336 名评估患者中,有 278 名患者接受了随机分组;137 名患者被分配到延迟策略组,141 名患者被分配到更延迟策略组。两组之间与急性肾损伤或 RRT 相关的并发症的数量相似。在延迟策略组中,无 RRT 天数的中位数为 12 天(IQR 0-25),在更延迟策略组中为 10 天(IQR 0-24)(p=0·93)。多变量分析显示,与延迟策略相比,更延迟策略的 60 天死亡风险比为 1.65(95%CI 1.09-2.50,p=0·018)。与急性肾损伤或肾替代治疗相关的并发症数量在两组之间没有差异。

解释

对于少尿持续超过 72 小时或血尿素氮浓度高于 112mg/dL 且没有严重并发症需要立即开始 RRT 的严重急性肾损伤患者,进一步延迟 RRT 开始时间并没有带来额外的益处,反而可能造成伤害。

资助

医院临床研究计划。

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