| Literature DB >> 35831022 |
Matthieu Legrand1,2, Sean M Bagshaw3, Jay L Koyner4, Ivonne H Schulman5, Michael R Mathis6, Juliane Bernholz7, Steven Coca8, Martin Gallagher9, Stéphane Gaudry2,10,11, Kathleen D Liu12, Ravindra L Mehta13, Romain Pirracchio14, Abigail Ryan15, Dominik Steubl16,17, Norman Stockbridge18, Fredrik Erlandsson19, Alparslan Turan20,21, F Perry Wilson22, Alexander Zarbock23, Michael P Bokoch24, Jonathan D Casey25, Patrick Rossignol2,26,27, Michael O Harhay28.
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.Entities:
Keywords: AKI; Bayesian; cluster; heterogeneity; pragmatic; randomized controlled trials
Mesh:
Year: 2022 PMID: 35831022 PMCID: PMC9342638 DOI: 10.1681/ASN.2021121605
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 14.978