...
首页> 外文期刊>BMC Medical Research Methodology >Simulation-based power calculations for planning a two-stage individual participant data meta-analysis
【24h】

Simulation-based power calculations for planning a two-stage individual participant data meta-analysis

机译:基于仿真的功率计算,用于计划两阶段个体参与者数据的荟萃分析

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Researchers and funders should consider the statistical power of planned Individual Participant Data (IPD) meta-analysis projects, as they are often time-consuming and costly. We propose simulation-based power calculations utilising a two-stage framework, and illustrate the approach for a planned IPD meta-analysis of randomised trials with continuous outcomes where the aim is to identify treatment-covariate interactions. The simulation approach has four steps: (i) specify an underlying (data generating) statistical model for trials in the IPD meta-analysis; (ii) use readily available information (e.g. from publications) and prior knowledge (e.g. number of studies promising IPD) to specify model parameter values (e.g. control group mean, intervention effect, treatment-covariate interaction); (iii) simulate an IPD meta-analysis dataset of a particular size from the model, and apply a two-stage IPD meta-analysis to obtain the summary estimate of interest (e.g. interaction effect) and its associated p-value; (iv) repeat the previous step (e.g. thousands of times), then estimate the power to detect a genuine effect by the proportion of summary estimates with a significant p-value. In a planned IPD meta-analysis of lifestyle interventions to reduce weight gain in pregnancy, 14 trials (1183 patients) promised their IPD to examine a treatment-BMI interaction (i.e. whether baseline BMI modifies intervention effect on weight gain). Using our simulation-based approach, a two-stage IPD meta-analysis has
机译:研究人员和资助者应考虑计划中的个人参与者数据(IPD)元分析项目的统计能力,因为它们通常既费时又费钱。我们提出了利用两阶段框架的基于仿真的功率计算,并说明了以连续结果为目标的随机试验的计划IPD元分析方法,其目的是确定治疗之间的相互作用。模拟方法包括四个步骤:(i)为IPD荟萃分析中的试验指定基础(数据生成)统计模型; (ii)使用容易获得的信息(例如来自出版物)和先验知识(例如有希望获得IPD的研究数量)来指定模型参数值(例如对照组平均值,干预效果,治疗协变量相互作用); (iii)从模型中模拟一个特定大小的IPD元分析数据集,并进行两阶段IPD元分析,以获得感兴趣的汇总估算值(例如,交互作用)及其相关的p值; (iv)重复前一步骤(例如数千次),然后通过具有明显p值的摘要估算值的比例来估算检测出真实效果的能力。在一项计划进行的生活方式干预措施以减少孕妇体重增加的IPD荟萃分析中,有14个试验(1183例患者)承诺其IPD检查治疗与BMI的相互作用(即基线BMI是否改变了对体重增加的干预作用)。使用我们基于仿真的方法,两阶段IPD荟萃分析具有<?60%的功效,可检测出体重增加10单位时体重增加1公斤的减少。其他十项已发表的试验(包含1761名患者)的其他IPD可以将功效提高到80%以上,但前提是必须进行固定效果的荟萃分析。对预后因素进行预先指定的调整将进一步提高功能。 BMI不正确的二分法将使功耗降低20%以上,类似于立即将IPD从十项试验中丢弃。基于仿真的功率计算可以为IPD项目的计划和资金提供依据,应常规使用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号