A Smaller Sample Size Is Associated With Lower Rates of Reporting of Harms in Randomized Controlled Trials Cited in the AAOS Clinical Practice Guidelines for Anterior Cruciate Ligament Injuries

Ryan D. Stadler, Ryan Terrany, Suleiman Y. Sudah, Kathryn Whitelaw, Mariano E. Menendez, Charles J. Gatt, Ryan Plyler
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Abstract

Background: Randomized controlled trials (RCTs) significantly influence clinical decision-making, necessitating comprehensive reporting of trial outcomes. However, previous studies have demonstrated that reporting of harms among RCTs is often inadequate. Purpose/Hypothesis: The purpose of this study was to evaluate reporting of harms among RCTs cited within the American Academy of Orthopaedic Surgeons (AAOS) clinical practice guidelines (CPGs) for anterior cruciate ligament (ACL) injuries, with an emphasis on study characteristics associated with adherence. We hypothesized that >50% of these trials would have incomplete adherence to the checklist items outlined in the Consolidated Standards of Reporting Trials (CONSORT) extension for harms and that a larger sample size would be associated with greater compliance. Study Design: Cross-sectional study. Methods: We identified RCTs cited in the AAOS CPGs for the management of ACL injuries and assessed compliance with the 18-item CONSORT extension for harms checklist. Descriptive statistics were used to summarize overall adherence to the checklist items, and linear regression analysis evaluated adherence over time. Results: Our analysis included 116 RCTs, the majority of which were single-center studies (81.0%). Most trials had sample sizes of 50-100 patients (45.7%) or 101-500 patients (37.9%). On average, trials adhered to 9.25 of 18 CONSORT items (51.4%), with the most compliant study meeting 15 of 18 items (83.3%) and the least compliant meeting 3 of 18 items (16.7%). Overall, 18 RCTs (15.5%) reported ≤33% of items, and 22 RCTs (19.0%) reported ≥67% of items. Studies with >500 patients had significantly higher adherence compared with studies with <50 patients ( P = .046). There was no significant difference in adherence based on the disclosure of funding sources ( P = .85) or the implementation of blinding ( P = .37). Interrupted time series regression analysis demonstrated no significant change in reporting both before ( R 2 = 0.017; P = .62) and after ( R 2 = 0.21; P = .16) the release of the checklist in 2004. Conclusion: On average, RCTs cited within the AAOS CPGs for the management of ACL injuries adhered to 51.4% of CONSORT checklist requirements, with considerable variability across studies. Improvements in reporting practices are warranted to support evidence-based treatment decisions.
在AAOS前交叉韧带损伤临床实践指南中引用的随机对照试验中,较小的样本量与较低的危害报告率相关
背景:随机对照试验(RCTs)显著影响临床决策,需要对试验结果进行综合报告。然而,先前的研究表明,在随机对照试验中报告危害往往是不充分的。目的/假设:本研究的目的是评估美国骨科学会(AAOS)临床实践指南(CPGs)中引用的前交叉韧带(ACL)损伤的随机对照试验的危害报告,重点是与依从性相关的研究特征。我们假设这些试验中有50%不完全符合试验综合报告标准(CONSORT)扩展中列出的危害清单项目,并且样本量越大,依从性越高。研究设计:横断面研究。方法:我们检索了AAOS CPGs中引用的ACL损伤管理的随机对照试验,并评估了18项CONSORT扩展危害清单的依从性。描述性统计用于总结对检查表项目的总体依从性,线性回归分析评估随时间的依从性。结果:我们的分析包括116项随机对照试验,其中大多数为单中心研究(81.0%)。大多数试验的样本量为50-100例(45.7%)或101-500例(37.9%)。平均而言,18个CONSORT项目中有9.25个项目符合要求(51.4%),其中最符合的研究满足18个项目中的15个(83.3%),最不符合的研究满足18个项目中的3个(16.7%)。总体而言,18项rct(15.5%)报告了≤33%的项目,22项rct(19.0%)报告了≥67%的项目。500例患者的依从性明显高于50例患者(P = 0.046)。在资金来源披露(P = 0.85)或盲法实施(P = 0.37)的基础上,依从性无显著差异。中断时间序列回归分析显示,在此之前,两组报告均无显著变化(r2 = 0.017;P = 0.62)后(r2 = 0.21;P = .16) 2004年发布的检查表。结论:平均而言,在AAOS CPGs中引用的ACL损伤管理的随机对照试验遵守了51.4%的CONSORT清单要求,各研究之间存在相当大的差异。有必要改进报告做法,以支持循证治疗决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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