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优化未来 AKI 试验的设计和分析。

Optimizing the Design and Analysis of Future AKI Trials.

机构信息

Department of Anesthesia and Perioperative Care, Division of Critical Care Medicine, University of California San Francisco, San Francisco, California.

French Clinical Research Infrastructure Network, Investigation Network Initiative Cardiovascular and Renal Trialists, Nancy, France.

出版信息

J Am Soc Nephrol. 2022 Aug;33(8):1459-1470. doi: 10.1681/ASN.2021121605. Epub 2022 Jul 13.

Abstract

AKI is a complex clinical syndrome associated with an increased risk of morbidity and mortality, particularly in critically ill and perioperative patient populations. Most AKI clinical trials have been inconclusive, failing to detect clinically important treatment effects at predetermined statistical thresholds. Heterogeneity in the pathobiology, etiology, presentation, and clinical course of AKI remains a key challenge in successfully testing new approaches for AKI prevention and treatment. This article, derived from the "AKI" session of the "Kidney Disease Clinical Trialists" virtual workshop held in October 2021, reviews barriers to and strategies for improving the design and implementation of clinical trials in patients with, or at risk of, developing AKI. The novel approaches to trial design included in this review span adaptive trial designs that increase the knowledge gained from each trial participant; pragmatic trial designs that allow for the efficient enrollment of sufficiently large numbers of patients to detect small, but clinically significant, treatment effects; and platform trial designs that use one trial infrastructure to answer multiple clinical questions simultaneously. This review also covers novel approaches to clinical trial analysis, such as Bayesian analysis and assessing heterogeneity in the response to therapies among trial participants. We also propose a road map and actionable recommendations to facilitate the adoption of the reviewed approaches. We hope that the resulting road map will help guide future clinical trial planning, maximize learning from AKI trials, and reduce the risk of missing important signals of benefit (or harm) from trial interventions.

摘要

急性肾损伤(AKI)是一种复杂的临床综合征,与发病率和死亡率增加相关,尤其是在重症和围手术期患者人群中。大多数 AKI 临床试验的结果不确定,未能在预定的统计学阈值检测到具有临床意义的治疗效果。AKI 的病理生物学、病因、表现和临床病程存在异质性,这仍然是成功测试 AKI 预防和治疗新方法的一个关键挑战。本文源自 2021 年 10 月举行的“肾脏病临床试验人员”虚拟研讨会的“AKI”会议,讨论了在存在或有发展 AKI 风险的患者中改善临床试验设计和实施的障碍和策略。本综述中纳入的试验设计新方法涵盖了适应性试验设计,这些设计可以增加从每个试验参与者中获得的知识;实用试验设计,允许有效地招募足够数量的患者,以检测小但具有临床意义的治疗效果;以及平台试验设计,该设计使用一个试验基础设施同时回答多个临床问题。本综述还涵盖了临床试验分析的新方法,如贝叶斯分析和评估试验参与者对治疗的反应异质性。我们还提出了路线图和可操作的建议,以促进所审查方法的采用。我们希望由此产生的路线图将有助于指导未来的临床试验规划,最大限度地从 AKI 试验中学习,并降低错过试验干预重要获益(或危害)信号的风险。

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