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Reporting of key methodological and ethical aspects of cluster trials in hemodialysis require improvement: a systematic review

机译:报告血液透析中聚类试验的关键方法论和伦理方面需要改进:系统审查

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The hemodialysis setting is suitable for trials that use cluster randomization, where intact groups of individuals are randomized. However, cluster randomized trials (CRTs) are complicated in their design, analysis, and reporting and can pose ethical challenges. We reviewed CRTs in the hemodialysis setting with respect to reporting of key methodological and ethical issues. We conducted a systematic review of CRTs in the hemodialysis setting, published in English, between 2000 and 2019, and indexed in MEDLINE or Embase. Two reviewers extracted data, and study results were summarized using descriptive statistics. We identified 26 completed CRTs and five study protocols of CRTs. These studies randomized hemodialysis centers (n?=?17, 55%), hemodialysis shifts (n?=?12, 39%), healthcare providers (n?=?1, 3%), and nephrology units (n?=?1, 3%). Trials included a median of 28 clusters with a median cluster size of 20 patients. Justification for using a clustered design was provided by 15 trials (48%). Methods that accounted for clustering were used during sample size calculation in 14 (45%), during analyses in 22 (71%), and during both sample size calculation and analyses in 13 trials (42%). Among all CRTs, 26 (84%) reported receiving research ethics committee approval; patient consent was reported in 22 trials: 10 (32%) reported the method of consent for trial participation and 12 (39%) reported no details about how consent was obtained or its purpose. Four trials (13%) reported receiving waivers of consent, and the remaining 5 (16%) provided no or unclear information about the consent process. There is an opportunity to improve the conduct and reporting of essential methodological and ethical issues in future CRTs in hemodialysis. We conducted this systematic review using a pre-specified protocol that was not registered.
机译:血液透析设置适用于使用群集随机化的试验,其中完整的个体组随机化。然而,集群随机试验(CRT)在其设计,分析和报告方面复杂,并且可以构成道德挑战。我们在报告关键方法论和道德问题时审查了血液透析环境中的CRT。我们对血液透析环境中的CRT进行了系统审查,2000年至2019年间,在英语之间发表,并在Medline或Embase中索引。两个审阅者提取数据,并使用描述性统计来概述研究结果。我们确定了26个已完成的CRT和五项学习协议的CRT。这些研究随机化血液透析中心(n?= 17,55%),血液透析移位(n?= 12,39%),医疗保健提供者(n?=?1,3%)和肾病单位(n?=? 1,3%)。试验包括28个簇的中位数,中位数为20名患者。使用聚集设计的理由由15项试验提供(48%)。在22(71%)的分析期间,在14(45%)的样品尺寸计算期间使用算用于聚类的方法,并且在样本量计算和13项试验中分析(42%)。在所有CRT中,26名(84%)报告接受研究伦理委员会批准;患者同意于22项试验中报告:10(32%)报告了试验参与的同意的方法,12名(39%)报告了有关如何获得同意的细节或其目的。四项试验(13%)报告收到同意的豁免,其余5(16%)提供了有关同意进程的无关信息尚未清楚或不清楚。有机会改善血液透析中未来CRT的基本方法论和道德问题的行为和报告。我们使用未注册的预先指定的协议进行了此系统审查。

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