Sydney Musculoskeletal Health, The Kolling Institute, School of Medicine, Faculty of Medicine and Health, University of Sydney, Sydney, and Royal North Shore Hospital, St. Leonards, New South Wales, Australia.
Erasmus MC, University Medical Centre Rotterdam, Rotterdam, The Netherlands.
Arthritis Care Res (Hoboken). 2024 Feb;76(2):208-224. doi: 10.1002/acr.25212. Epub 2023 Oct 25.
We undertook this study to evaluate potential predictors of placebo response with intra-articular (IA) injections for knee/hip osteoarthritis (OA) using individual participant data (IPD) from existing trials.
Randomized placebo-controlled trials evaluating IA glucocorticoid or hyaluronic acid published to September 2018 were selected. IPD for disease characteristics and outcome measures were acquired. Potential predictors of placebo response included participant characteristics, pain severity, intervention, and trial design. Placebo response was defined as at least a 20% reduction in baseline pain. Logistic regression models and odds ratios were computed as effect measures to evaluate patient and pain mechanisms and then pooled using a random effects model. Generalized mixed-effect models were applied to intervention and trial characteristics.
Of 56 eligible trials, 6 shared data, and these were combined with the existing 4 OA Trial Bank studies, yielding 10 studies with IPD of 621 placebo participants for analysis. In the total placebo population, at short-term follow-up, the use of local anesthetic and ultrasound guidance were associated with reduced odds of placebo response. At midterm follow-up, mid- to long-term trial duration was associated with increased odds of placebo response, and worse baseline function scores were associated with reduced odds of a placebo response.
The administration of local anesthetics or ultrasound guidance may reduce IA placebo response at short-term follow-up. At midterm follow-up, participants with worse baseline function scores may be less likely to respond to IA placebo, and mid- to long-term trial duration may enhance the placebo response. Further studies are required to corroborate these potential predictors of IA placebo response.
我们开展了这项研究,旨在使用现有的临床试验个体参与者数据(IPD)评估膝关节/髋关节骨关节炎(OA)关节内(IA)注射的安慰剂反应的潜在预测因子。
选择了截止到 2018 年 9 月评估 IA 糖皮质激素或透明质酸的随机安慰剂对照试验。获取了疾病特征和结局测量的 IPD。安慰剂反应的潜在预测因子包括参与者特征、疼痛严重程度、干预措施和试验设计。安慰剂反应定义为基线疼痛至少降低 20%。计算了逻辑回归模型和优势比作为效应测量值,以评估患者和疼痛机制,然后使用随机效应模型进行汇总。应用广义混合效应模型来评估干预措施和试验特征。
在 56 项合格的试验中,有 6 项共享数据,并与现有的 4 项 OA 试验银行研究合并,得出 10 项研究,共 621 名安慰剂参与者的 IPD 进行分析。在总安慰剂人群中,短期随访时,使用局部麻醉剂和超声引导与降低安慰剂反应的几率相关。中期随访时,试验持续时间较长与安慰剂反应几率增加相关,基线功能评分较差与降低安慰剂反应几率相关。
在短期随访时,给予局部麻醉剂或超声引导可能会降低 IA 安慰剂反应。在中期随访时,基线功能评分较差的参与者可能不太可能对 IA 安慰剂产生反应,并且中至长期的试验持续时间可能会增强安慰剂反应。需要进一步的研究来证实这些 IA 安慰剂反应的潜在预测因子。