Real-world causal evidence for planned predictive enrichment in critical care trials: A scoping review.

IF 1.9 4区 医学 Q2 ANESTHESIOLOGY Acta Anaesthesiologica Scandinavica Pub Date : 2024-01-01 Epub Date: 2023-08-30 DOI:10.1111/aas.14321
Benjamin Skov Kaas-Hansen, Anders Granholm, Praleene Sivapalan, Carl Thomas Anthon, Olav Lilleholt Schjørring, Mathias Maagaard, Maj-Brit Nørregaard Kjaer, Jesper Mølgaard, Karen Louise Ellekjaer, Steen Kåre Fagerberg, Theis Lange, Morten Hylander Møller, Anders Perner
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Abstract

Background: Randomised clinical trials in critical care are prone to inconclusiveness due, in part, to undue optimism about effect sizes and suboptimal accounting for heterogeneous treatment effects. Although causal evidence from rich real-world critical care can help overcome these challenges by informing predictive enrichment, no overview exists.

Methods: We conducted a scoping review, systematically searching 10 general and speciality journals for reports published on or after 1 January 2018, of randomised clinical trials enrolling adult critically ill patients. We collected trial metadata on 22 variables including recruitment period, intervention type and early stopping (including reasons) as well as data on the use of causal evidence from secondary data for planned predictive enrichment.

Results: We screened 9020 records and included 316 unique RCTs with a total of 268,563 randomised participants. One hundred seventy-three (55%) trials tested drug interventions, 101 (32%) management strategies and 42 (13%) devices. The median duration of enrolment was 2.2 (IQR: 1.3-3.4) years, and 83% of trials randomised less than 1000 participants. Thirty-six trials (11%) were restricted to COVID-19 patients. Of the 55 (17%) trials that stopped early, 23 (42%) used predefined rules; futility, slow enrolment and safety concerns were the commonest stopping reasons. None of the included RCTs had used causal evidence from secondary data for planned predictive enrichment.

Conclusion: Work is needed to harness the rich multiverse of critical care data and establish its utility in critical care RCTs. Such work will likely need to leverage methodology from interventional and analytical epidemiology as well as data science.

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重症监护试验中计划的预测性浓缩的真实因果证据:范围综述。
背景:重症监护领域的随机临床试验容易产生不确定性,部分原因是对效应大小过于乐观,以及对异质性治疗效果的考虑不够理想。尽管来自丰富真实世界重症监护的因果证据可以为丰富预测提供信息,从而帮助克服这些挑战,但目前还没有这方面的综述:我们进行了一次范围界定综述,系统检索了 10 种普通期刊和专业期刊,以获取 2018 年 1 月 1 日或之后发表的、纳入成年重症患者的随机临床试验报告。我们收集了 22 个变量的试验元数据,包括招募期、干预类型和早期停止(包括原因),以及使用二手数据中的因果证据进行计划性预测富集的数据:我们筛选了 9020 条记录,纳入了 316 项独特的 RCT,共有 268563 名随机参与者。173项(55%)试验测试了药物干预,101项(32%)测试了管理策略,42项(13%)测试了设备。入组时间的中位数为 2.2 年(IQR:1.3-3.4 年),83% 的试验的随机参与者少于 1000 人。36项试验(11%)仅限于COVID-19患者。在55项(17%)提前终止的试验中,有23项(42%)采用了预先确定的规则;无效、入组缓慢和安全问题是最常见的终止原因。所纳入的研究性试验中,没有一项试验使用了二级数据中的因果证据来进行有计划的预测性充实:需要努力利用丰富的重症监护数据,并确定其在重症监护 RCT 中的用途。这项工作可能需要利用介入和分析流行病学以及数据科学的方法。
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来源期刊
CiteScore
4.30
自引率
9.50%
发文量
157
审稿时长
3-8 weeks
期刊介绍: Acta Anaesthesiologica Scandinavica publishes papers on original work in the fields of anaesthesiology, intensive care, pain, emergency medicine, and subjects related to their basic sciences, on condition that they are contributed exclusively to this Journal. Case reports and short communications may be considered for publication if of particular interest; also letters to the Editor, especially if related to already published material. The editorial board is free to discuss the publication of reviews on current topics, the choice of which, however, is the prerogative of the board. Every effort will be made by the Editors and selected experts to expedite a critical review of manuscripts in order to ensure rapid publication of papers of a high scientific standard.
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