Comparer des méthodes
Examinez les méthodes sélectionnées côte à côte ; les lignes qui diffèrent sont mises en évidence.
| Appariement dynamique par score de propension× | Appariement par score de propension× | |
|---|---|---|
| Domaine≠ | Inférence causale | Statistiques de recherche |
| Famille≠ | Regression model | Process / pipeline |
| Année d'origine≠ | 1986-2010 | 1983 |
| Auteur d'origine≠ | Robins (1986) on sequential treatments; Lechner & Miquel (2010) on dynamic matching | Paul Rosenbaum and Donald Rubin |
| Type≠ | Sequential causal matching | Method |
| Source fondatrice≠ | Lechner, M., & Miquel, R. (2010). Identification of the effects of dynamic treatments by sequential conditional independence assumptions. Empirical Economics, 39(1), 111-137. DOI ↗ | Rosenbaum, P. R., & Rubin, D. B. (1983). The central role of the propensity score in observational studies for causal effects. Biometrika, 70(1), 41–55. DOI ↗ |
| Alias≠ | dynamic PSM, sequential propensity score matching, longitudinal propensity matching, DPSM | PSM, propensity score weighting, covariate balance |
| Apparentées≠ | 6 | 3 |
| Résumé≠ | Dynamic Propensity Score Matching (DPSM) extends classic propensity score matching to settings where treatment is assigned repeatedly over time and earlier treatment choices influence later ones. It estimates the causal effect of entire treatment sequences or regime changes by constructing matched comparisons at each decision point using the full history of covariates and prior treatments. | Propensity score matching (PSM) is a method for reducing confounding bias in observational studies by balancing baseline characteristics between treatment groups, simulating randomization. Developed by Rosenbaum and Rubin (1983), it estimates the probability of receiving treatment given observed covariates, then matches or weights treated and control individuals with similar treatment probabilities. Widely used in medicine, epidemiology, and policy evaluation when randomized trials are infeasible or unethical, enabling estimation of treatment effects while controlling for selection bias. |
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