Сравнение методов
Просматривайте выбранные методы рядом; строки с различиями подсвечены.
| Мета-регрессионный быстрый обзор× | Мета-регрессионный мета-анализ× | |
|---|---|---|
| Область | Наукометрия | Наукометрия |
| Семейство | Process / pipeline | Process / pipeline |
| Год появления≠ | 2000s–2010s (convergence of rapid review and meta-regression) | 1993–1999 |
| Автор метода≠ | Meta-regression: Simon Thompson & Stephen Sharp (1999); Rapid review methodology: Cochrane, WHO, and health technology assessment bodies (2000s onward) | Stephen G. Thompson & Simon J. Sharp (systematic framework); earlier work by Berlin, Longnecker & Greenland (1993) |
| Тип≠ | Quantitative evidence synthesis variant | Quantitative evidence synthesis with covariate modeling |
| Основополагающий источник | Thompson, S. G., & Sharp, S. J. (1999). Explaining heterogeneity in meta-analysis: A comparison of methods. Statistics in Medicine, 18(20), 2693–2708. DOI ↗ | Thompson, S. G., & Sharp, S. J. (1999). Explaining heterogeneity in meta-analysis: a comparison of methods. Statistics in Medicine, 18(20), 2693–2708. DOI ↗ |
| Другие названия | rapid review with meta-regression, accelerated meta-regression review, rapid synthesis with meta-regression, RRMR | meta-regression, meta-analytic regression, weighted regression meta-analysis, MR-MA |
| Связанные≠ | 5 | 4 |
| Сводка≠ | A meta-regression-based rapid review is an accelerated evidence synthesis that combines the time-efficient protocols of a rapid review with meta-regression analysis to identify which study-level or population-level characteristics explain variability in effect sizes across included studies. By streamlining search and screening steps without sacrificing the explanatory power of regression modeling, this approach delivers actionable heterogeneity insights under decision-making time constraints. | Meta-regression-based meta-analysis extends standard meta-analysis by fitting a weighted regression model in which study-level characteristics (moderators) predict observed effect sizes. Rather than simply pooling effects, this approach asks why effects vary across studies — linking heterogeneity in outcomes to differences in population, intervention, design, or measurement features. It is the primary tool for explaining between-study variance in quantitative evidence synthesis. |
| ScholarGateНабор данных ↗ |
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