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Метааналитическое рандомизированное клиническое исследование×Мета-анализ индивидуальных данных пациентов×
ОбластьЭпидемиологияСинтез доказательств
СемействоProcess / pipelineProcess / pipeline
Год появления1976 (Glass coinage of meta-analysis); 1993 (Cochrane Collaboration formalization)1990s
Автор методаGene V. Glass (meta-analysis method); Cochrane Collaboration (systematic RCT pooling standards)Cochrane Collaboration, Pioneered by Stewart & Clarke
ТипQuantitative evidence-synthesis designMethod
Основополагающий источникHiggins, J. P. T., Thomas, J., Chandler, J., Cumpston, M., Li, T., Page, M. J., & Welch, V. A. (Eds.). (2019). Cochrane Handbook for Systematic Reviews of Interventions (2nd ed.). Wiley-Blackwell. ISBN: 978-1119536628Stewart, L. A., Clarke, M. J., & Cochrane IPD Meta-analysis Methods Group. (2015). Practical methodology of meta-analyses (including IPD) of randomised trials reporting time to event data. Cochrane Database of Systematic Reviews, 2015(10), MR000027. link ↗
Другие названияmeta-analytic RCT, MA-RCT, meta-analysis of RCTs, pooled randomized trial analysisIPD Meta-Analysis, Participant-Level Data Synthesis, One-Stage Meta-Analysis
Связанные31
СводкаA meta-analytic randomized clinical trial is a formal evidence-synthesis method that identifies, appraises, and statistically combines the results of multiple randomized clinical trials addressing the same clinical question. By pooling trial-level data, it produces a single, more precise estimate of treatment effect and quantifies between-trial heterogeneity, sitting at the apex of the evidence hierarchy for evaluating healthcare interventions.Individual patient data meta-analysis (IPD-MA) is a systematic synthesis method where researchers obtain and analyze raw data at the patient level from multiple randomized controlled trials, rather than relying on published summary statistics (aggregate data). Pioneered by the Cochrane Collaboration and formalized by Stewart, Clarke, and Riley, IPD-MA is considered the gold standard for evidence synthesis because it enables consistent outcome definition across trials, robust subgroup analysis, and detection of treatment-covariate interactions. Though time-intensive and resource-demanding, IPD-MA provides the most reliable estimates of intervention effects and is preferred for critical clinical decisions, particularly for identifying which patients benefit most from treatment.
ScholarGateНабор данных
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ScholarGateСравнение методов: Meta-analytic Randomized Clinical Trial · Individual Patient Data Meta-Analysis. Получено 2026-06-19 из https://scholargate.app/ru/compare