The impact of blinding on trial results: A systematic review and meta-analysis

Tyler Pitre, Sarah Kirsh, Tanvir Jassal, Mason Anderson, Adelia Padoan, Alexander Xiang, Jasmine Mah, Dena Zeraatkar
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Abstract

Background

Blinding—the concealment of the arm to which participants have been randomized—is an important consideration for assessing the risk of bias of randomized trials. A growing body of evidence has, however, yielded inconsistent results on whether trials without blinding produce biased findings.

Objective

To conduct a systematic review and meta-analysis of the evidence addressing whether trials with and without blinding produce different results.

Methods

We searched MEDLINE, EMBASE, Cochrane Reviews, JBI EBP, and Web of Science, from inception to May 2022, for studies comparing the results of trials with and without blinding. Pairs of reviewers, working independently and in duplicate, reviewed search results for eligible studies and extracted data. We pooled the results of studies comparing trials with and without blinding of patients, healthcare providers/investigators, and outcome assessors/adjudicators using frequentist random-effects meta-analyses. We coded study results such that a ratio of odds ratio < 1 and difference in standardized mean difference < 0 indicate that trials without blinding overestimate the beneficial effects of treatments.

Results

We identified 47 eligible studies. For dichotomous outcomes, we found low certainty evidence that trials without blinding of patients and healthcare providers and trials without blinding of patients may slightly overestimate the beneficial effects of treatments. We found moderate certainty evidence that trials without blinding of outcome assessors overestimate the beneficial effects of treatments. For continuous outcomes, we found low certainty evidence that trials without blinding of patients and healthcare providers may overestimate the beneficial effects of treatments. We found moderate certainty evidence that trials without blinding of outcome assessors/adjudicators probably overestimate the beneficial effects of treatments.

Conclusion

Our systematic review and meta-analysis suggest that blinding may influence trial results in select situations—although the findings are of low certainty and the magnitude of effect is modest. In the absence of high-certainty evidence suggesting that trials with and without blinding produce similar results, investigators should be cautious about interpreting the results of trials without blinding.

Abstract Image

盲法对试验结果的影响:系统综述和荟萃分析
背景盲法是评估随机试验偏倚风险的一个重要考虑因素。然而,越来越多的证据表明,在没有盲法的试验是否会产生有偏见的结果方面,结果并不一致。目的对有盲法和无盲法试验是否产生不同结果的证据进行系统回顾和荟萃分析。方法从开始到2022年5月,我们在MEDLINE、EMBASE、Cochrane Reviews、JBI EBP和Web of Science上搜索了比较有盲法和无盲法试验结果的研究。成对的评审员,独立和重复工作,评审合格研究的搜索结果和提取的数据。我们使用频率随机效应荟萃分析汇总了对患者、医疗保健提供者/研究人员和结果评估者/裁决者进行盲法和非盲法试验比较的研究结果。我们对研究结果进行了编码,使得比值比 <; 1和标准化平均差的差异 <; 0表明没有盲法的试验高估了治疗的有益效果。结果我们确定了47项符合条件的研究。对于二分法的结果,我们发现了低确定性的证据,即没有对患者和医疗保健提供者进行盲法试验和没有对患者进行盲法的试验可能会略微高估治疗的有益效果。我们发现了适度的确定性证据,即没有对结果评估者进行盲法的试验高估了治疗的有益效果。对于持续的结果,我们发现了低确定性的证据,即没有对患者和医疗保健提供者进行盲法的试验可能高估了治疗的有益效果。我们发现了适度的确定性证据,即没有对结果评估者/裁决者进行盲法的试验可能高估了治疗的有益效果。结论我们的系统综述和荟萃分析表明,在某些情况下,盲法可能会影响试验结果——尽管研究结果的确定性很低,影响程度也不大。在缺乏高确定性证据表明有盲法和无盲法的试验产生相似结果的情况下,研究人员应谨慎解释无盲法试验的结果。
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