School of Social and Community Medicine, University of Bristol, Bristol, UK (SD, NJW, AEA)
Department of Health Sciences, University of Leicester, Leicester, UK (AJS)
Med Decis Making. 2013 Jul;33(5):618-40. doi: 10.1177/0272989X13485157.
In meta-analysis, between-study heterogeneity indicates the presence of effect-modifiers and has implications for the interpretation of results in cost-effectiveness analysis and decision making. A distinction is usually made between true variability in treatment effects due to variation in patient populations or settings and biases related to the way in which trials were conducted. Variability in relative treatment effects threatens the external validity of trial evidence and limits the ability to generalize from the results; imperfections in trial conduct represent threats to internal validity. We provide guidance on methods for meta-regression and bias-adjustment, in pairwise and network meta-analysis (including indirect comparisons), using illustrative examples. We argue that the predictive distribution of a treatment effect in a "new" trial may, in many cases, be more relevant to decision making than the distribution of the mean effect. Investigators should consider the relative contribution of true variability and random variation due to biases when considering their response to heterogeneity. In network meta-analyses, various types of meta-regression models are possible when trial-level effect-modifying covariates are present or suspected. We argue that a model with a single interaction term is the one most likely to be useful in a decision-making context. Illustrative examples of Bayesian meta-regression against a continuous covariate and meta-regression against "baseline" risk are provided. Annotated WinBUGS code is set out in an appendix.
在荟萃分析中,研究间异质性表明存在效应修饰因子,并且对成本效益分析和决策中结果的解释具有重要意义。通常会区分由于患者人群或环境的变化而导致的治疗效果的真正变异性,以及与试验进行方式有关的偏倚。相对治疗效果的变异性会威胁到试验证据的外部有效性,并限制从结果中进行推广的能力;试验实施中的不完美之处代表着内部有效性的威胁。我们提供了有关成对和网络荟萃分析(包括间接比较)中荟萃回归和偏差调整方法的指导,使用了说明性示例。我们认为,在许多情况下,“新”试验中治疗效果的预测分布可能比平均效果的分布更能为决策提供依据。研究人员在考虑对异质性的反应时,应考虑真实变异性和由于偏倚导致的随机变异的相对贡献。在网络荟萃分析中,当存在或怀疑试验水平的效应修饰协变量时,可能会有多种类型的荟萃回归模型。我们认为,具有单个交互项的模型最有可能在决策背景下有用。提供了针对连续协变量和针对“基线”风险的贝叶斯荟萃回归的说明性示例。在附录中列出了带注释的 WinBUGS 代码。