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基于高斯个体患者数据的荟萃分析:两阶段还是非两阶段?

Meta-analysis of Gaussian individual patient data: Two-stage or not two-stage?

机构信息

London Hub for Trials Methodology Research, MRC Clinical Trials Unit at UCL, London, UK.

Ashkirk, UK.

出版信息

Stat Med. 2018 Apr 30;37(9):1419-1438. doi: 10.1002/sim.7589. Epub 2018 Jan 18.

Abstract

Quantitative evidence synthesis through meta-analysis is central to evidence-based medicine. For well-documented reasons, the meta-analysis of individual patient data is held in higher regard than aggregate data. With access to individual patient data, the analysis is not restricted to a "two-stage" approach (combining estimates and standard errors) but can estimate parameters of interest by fitting a single model to all of the data, a so-called "one-stage" analysis. There has been debate about the merits of one- and two-stage analysis. Arguments for one-stage analysis have typically noted that a wider range of models can be fitted and overall estimates may be more precise. The two-stage side has emphasised that the models that can be fitted in two stages are sufficient to answer the relevant questions, with less scope for mistakes because there are fewer modelling choices to be made in the two-stage approach. For Gaussian data, we consider the statistical arguments for flexibility and precision in small-sample settings. Regarding flexibility, several of the models that can be fitted only in one stage may not be of serious interest to most meta-analysis practitioners. Regarding precision, we consider fixed- and random-effects meta-analysis and see that, for a model making certain assumptions, the number of stages used to fit this model is irrelevant; the precision will be approximately equal. Meta-analysts should choose modelling assumptions carefully. Sometimes relevant models can only be fitted in one stage. Otherwise, meta-analysts are free to use whichever procedure is most convenient to fit the identified model.

摘要

通过荟萃分析进行定量证据综合是循证医学的核心。由于有充分的记录,个体患者数据的荟萃分析比汇总数据更受重视。通过访问个体患者数据,分析不受“两阶段”方法(合并估计值和标准误差)的限制,而是可以通过将单个模型拟合到所有数据上来估计感兴趣的参数,即所谓的“一阶段”分析。关于一阶段和两阶段分析的优缺点存在争议。一阶段分析的论点通常指出,可以拟合更广泛的模型,并且整体估计可能更精确。两阶段分析的一方强调,可以在两阶段中拟合的模型足以回答相关问题,因为在两阶段方法中,建模选择较少,因此犯错的机会较少。对于正态数据,我们考虑了在小样本环境下灵活性和精度的统计论点。关于灵活性,仅能在一阶段拟合的几种模型可能对大多数荟萃分析从业者没有太大兴趣。关于精度,我们考虑固定效应和随机效应荟萃分析,并且发现,对于做出某些假设的模型,拟合该模型使用的阶段数无关紧要;精度将大致相等。荟萃分析人员应谨慎选择建模假设。有时相关模型只能在一阶段拟合。否则,荟萃分析人员可以自由使用最方便拟合已识别模型的程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef1e/5901423/7d019127898e/SIM-37-1419-g001.jpg

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