Agbla Schadrac C, DiazOrdaz Karla
Department of Medical Statistics, London School of Hygiene and Tropical Medicine (LSHTM), London, UK.
Clin Trials. 2018 Jun;15(3):294-304. doi: 10.1177/1740774518761666. Epub 2018 Apr 2.
Treatment non-adherence in randomised trials refers to situations where some participants do not receive their allocated treatment as intended. For cluster randomised trials, where the unit of randomisation is a group of participants, non-adherence may occur at the cluster or individual level. When non-adherence occurs, randomisation no longer guarantees that the relationship between treatment receipt and outcome is unconfounded, and the power to detect the treatment effects in intention-to-treat analysis may be reduced. Thus, recording adherence and estimating the causal treatment effect adequately are of interest for clinical trials.
To assess the extent of reporting of non-adherence issues in published cluster trials and to establish which methods are currently being used for addressing non-adherence, if any, and whether clustering is accounted for in these.
We systematically reviewed 132 cluster trials published in English in 2011 previously identified through a search in PubMed.
One-hundred and twenty three cluster trials were included in this systematic review. Non-adherence was reported in 56 cluster trials. Among these, 19 reported a treatment efficacy estimate: per protocol in 15 and as treated in 4. No study discussed the assumptions made by these methods, their plausibility or the sensitivity of the results to deviations from these assumptions.
The year of publication of the cluster trials included in this review (2011) could be considered a limitation of this study; however, no new guidelines regarding the reporting and the handling of non-adherence for cluster trials have been published since. In addition, a single reviewer undertook the data extraction. To mitigate this, a second reviewer conducted a validation of the extraction process on 15 randomly selected reports. Agreement was satisfactory (93%).
Despite the recommendations of the Consolidated Standards of Reporting Trials statement extension to cluster randomised trials, treatment adherence is under-reported. Among the trials providing adherence information, there was substantial variation in how adherence was defined, handled and reported. Researchers should discuss the assumptions required for the results to be interpreted causally and whether these are scientifically plausible in their studies. Sensitivity analyses to study the robustness of the results to departures from these assumptions should be performed.
随机试验中的治疗不依从是指一些参与者未按预期接受分配的治疗。对于整群随机试验,随机化单位是一组参与者,不依从可能发生在整群或个体层面。当出现不依从时,随机化不再保证治疗接受与结局之间的关系是无混杂的,并且在意向性分析中检测治疗效果的效能可能会降低。因此,记录依从性并充分估计因果治疗效果对临床试验具有重要意义。
评估已发表的整群试验中不依从问题的报告程度,确定目前正在使用哪些方法(如果有的话)来解决不依从问题,以及在这些方法中是否考虑了整群因素。
我们系统回顾了2011年以英文发表的132项整群试验,这些试验先前通过在PubMed中检索确定。
本系统评价纳入了123项整群试验。56项整群试验报告了不依从情况。其中,19项报告了治疗效果估计值:15项采用符合方案分析,4项采用实际治疗分析。没有研究讨论这些方法所做的假设、其合理性或结果对偏离这些假设的敏感性。
本评价纳入的整群试验的发表年份(2011年)可被视为本研究的一个局限性;然而,自那时以来,尚未发布关于整群试验中不依从报告和处理的新指南。此外,由一名审阅者进行数据提取。为了减轻这一影响,另一名审阅者对15份随机选择的报告进行了提取过程验证。一致性令人满意(93%)。
尽管《报告试验的统一标准》声明扩展到了整群随机试验,但治疗依从性的报告不足。在提供依从性信息的试验中,依从性的定义、处理和报告方式存在很大差异。研究人员应讨论为使结果能够进行因果解释所需的假设,以及这些假设在其研究中是否具有科学合理性。应进行敏感性分析,以研究结果对偏离这些假设的稳健性。