Human Performance Laboratory, KNB 222, Faculty of Kinesiology, University of Calgary, Calgary, Alberta, T2N 1N4, Canada.
Department of Chiropractic, Macquarie University, Building C5C West, Sydney, 2109, Australia.
Musculoskelet Sci Pract. 2017 Aug;30:34-41. doi: 10.1016/j.msksp.2017.05.002. Epub 2017 May 11.
While spinal manipulative therapy (SMT) is recommended for the treatment of spinal disorders, concerns exist about adverse events associated with the intervention. Adequate reporting of adverse events in clinical trials would allow for more accurate estimations of incidence statistics through meta-analysis. However, it is not currently known if there are factors influencing adverse events reporting following SMT in randomized clinical trials (RCTs). Thus our objective was to investigate predictive factors for the reporting of adverse events in published RCTs involving SMT. The Physiotherapy Evidence Database (PEDro) and Cochrane Central Register of Controlled Trials (CENTRAL) were searched for RCTs involving SMT. Domains of interest included: sample size; publication date relative to the 2010 CONSORT statement; risk of bias; the region treated; and number of intervention sessions. 7398 records were identified, of which 368 articles were eligible for inclusion. A total of 140 (38.0%) articles reported on adverse events. Articles were more likely to report on adverse events if they possessed larger sample sizes, were published after the 2010 CONSORT statement, had a low risk of bias and involved multiple intervention sessions. The region treated was not a significant predictor for reporting on adverse events. Predictors for reporting on adverse events included larger sample size, publication after the 2010 CONSORT statement, low risk of bias and trials involving multiple intervention sessions. We recommend that researchers focus on developing robust methodologies and participant follow-up regimens for RCTs involving SMT.
虽然脊柱手法治疗(SMT)被推荐用于治疗脊柱疾病,但人们对该干预措施相关的不良事件仍存在担忧。临床试验中充分报告不良事件将允许通过荟萃分析更准确地估计发病率统计数据。然而,目前尚不清楚是否存在影响 SMT 后随机临床试验(RCT)中不良事件报告的因素。因此,我们的目的是研究发表的涉及 SMT 的 RCT 中报告不良事件的预测因素。检索了 Physiotherapy Evidence Database(PEDro)和 Cochrane Central Register of Controlled Trials(CENTRAL)中的 RCT。感兴趣的领域包括:样本量;与 2010 年 CONSORT 声明相关的出版日期;偏倚风险;治疗区域;以及干预次数。共确定了 7398 条记录,其中 368 篇文章符合纳入标准。共有 140(38.0%)篇文章报告了不良事件。如果文章具有较大的样本量、在 2010 年 CONSORT 声明之后发表、偏倚风险较低且涉及多次干预,则更有可能报告不良事件。治疗区域并不是报告不良事件的显著预测因素。报告不良事件的预测因素包括较大的样本量、在 2010 年 CONSORT 声明之后发表、低偏倚风险和涉及多次干预的试验。我们建议研究人员专注于为涉及 SMT 的 RCT 开发稳健的方法和参与者随访方案。