Houston Methodist Orthopedic and Sports Medicine, Houston, Texas, U.S.A.
Department of Orthopaedic Surgery, Duke University School of Medicine, Durham, North Carolina, U.S.A.
Arthroscopy. 2020 Oct;36(10):2750-2762.e2. doi: 10.1016/j.arthro.2020.05.001. Epub 2020 May 14.
To determine the limitations of randomized sham surgery-controlled trials in orthopaedic sports medicine and fidelity of the trials' conclusions.
Randomized placebo surgery-controlled trials in orthopaedic sports medicine were included in this Preferred Reporting Items for Systematic Reviews and Meta-Analyses-guided systematic review. Several aspects of investigation design and conduct were analyzed: genetic analysis for propensity to placebo response, equipoise of informed consent process, geography of trial subjects, percentage of eligible subjects willing to be randomized, changes from protocol publication to results publication, and perioperative complications.
Seven sham surgery-controlled trials (845 subjects [370 knees, 449 shoulders, 26 elbows]; 5 from Europe, 1 from North America, and 1 from Australia; all superiority model, efficacy design) were analyzed. There were consistent methodologic deficiencies across studies. No studies reported genetic analysis of susceptibility to placebo response. Three studies (43%) were underpowered. Crossover rates ranged from 8% to 36%, which led to un-blinding in up to 100% of subjects. There were low enrollment rates of eligible subjects (up to 57% refused randomization). Follow-up was short term (2 years or less in all but one study). Complication rates ranged from 0% to 12.5%, with complications occurring in both groups (no significant difference between groups in any study).
Randomized sham-controlled studies in orthopaedic sports medicine have significant methodologic deficiencies that may invalidate their conclusions. Randomized trial design (with or without placebo control) may be optimized through the inclusion of per-protocol analysis, blinding index, equivalence or noninferiority trial design, and a nontreatment group.
Level II Systematic Review of Level II studies.
确定骨科运动医学中随机假手术对照试验的局限性和试验结论的真实性。
本研究为系统综述,纳入骨科运动医学中随机安慰剂手术对照试验。分析了调查设计和实施的几个方面:对安慰剂反应倾向的遗传分析、知情同意过程的均衡性、试验对象的地理位置、愿意随机分组的合格受试者的百分比、从方案发表到结果发表的变化以及围手术期并发症。
分析了 7 项假手术对照试验(845 例患者[370 膝,449 肩,26 肘];5 项来自欧洲,1 项来自北美,1 项来自澳大利亚;均为优效性模型,疗效设计)。研究之间存在一致的方法学缺陷。没有研究报告对安慰剂反应易感性的遗传分析。3 项研究(43%)的效力不足。交叉率为 8%至 36%,这导致多达 100%的受试者失去了盲法。合格受试者的入组率较低(最多有 57%的人拒绝随机分组)。随访时间较短(所有研究均为 2 年或更短,除 1 项研究外)。并发症发生率为 0%至 12.5%,两组均有并发症发生(任何研究中两组之间均无显著差异)。
骨科运动医学中的随机假手术对照研究存在明显的方法学缺陷,可能使结论无效。随机试验设计(有无安慰剂对照)可以通过包含方案分析、盲法指数、等效性或非劣效性试验设计以及非治疗组来优化。
二级系统综述,包含二级研究。