Kennedy Donna L, Kemp Harriet I, Ridout Deborah, Yarnitsky David, Rice Andrew S C
Pain Research, Department of Surgery and Cancer, Imperial College London, London, United Kingdom.
Population, Policy and Practice Programme, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
Pain. 2016 Nov;157(11):2410-2419. doi: 10.1097/j.pain.0000000000000689.
A systematic literature review was undertaken to determine if conditioned pain modulation (CPM) is reliable. Longitudinal, English language observational studies of the repeatability of a CPM test paradigm in adult humans were included. Two independent reviewers assessed the risk of bias in 6 domains; study participation; study attrition; prognostic factor measurement; outcome measurement; confounding and analysis using the Quality in Prognosis Studies (QUIPS) critical assessment tool. Intraclass correlation coefficients (ICCs) less than 0.4 were considered to be poor; 0.4 and 0.59 to be fair; 0.6 and 0.75 good and greater than 0.75 excellent. Ten studies were included in the final review. Meta-analysis was not appropriate because of differences between studies. The intersession reliability of the CPM effect was investigated in 8 studies and reported as good (ICC = 0.6-0.75) in 3 studies and excellent (ICC > 0.75) in subgroups in 2 of those 3. The assessment of risk of bias demonstrated that reporting is not comprehensive for the description of sample demographics, recruitment strategy, and study attrition. The absence of blinding, a lack of control for confounding factors, and lack of standardisation in statistical analysis are common. Conditioned pain modulation is a reliable measure; however, the degree of reliability is heavily dependent on stimulation parameters and study methodology and this warrants consideration for investigators. The validation of CPM as a robust prognostic factor in experimental and clinical pain studies may be facilitated by improvements in the reporting of CPM reliability studies.
进行了一项系统的文献综述,以确定条件性疼痛调制(CPM)是否可靠。纳入了关于成人CPM测试范式重复性的纵向英文观察性研究。两名独立评审员在六个领域评估了偏倚风险;研究参与;研究损耗;预后因素测量;结果测量;混杂因素以及使用预后研究质量(QUIPS)关键评估工具进行的分析。组内相关系数(ICC)小于0.4被认为较差;0.4至0.59为中等;0.6至0.75为良好;大于0.75为优秀。最终综述纳入了十项研究。由于研究之间存在差异,故不适合进行荟萃分析。在八项研究中调查了CPM效应的 session 间可靠性,其中三项研究报告为良好(ICC = 0.6 - 0.75),在这三项研究中的两项研究的亚组中报告为优秀(ICC > 0.75)。偏倚风险评估表明,在样本人口统计学、招募策略和研究损耗的描述方面,报告并不全面。缺乏盲法、对混杂因素缺乏控制以及统计分析缺乏标准化是常见问题。条件性疼痛调制是一种可靠的测量方法;然而,可靠性程度在很大程度上取决于刺激参数和研究方法,这值得研究人员考虑。CPM可靠性研究报告的改进可能有助于在实验性和临床疼痛研究中验证CPM作为一个强大的预后因素。