Comparar métodos
Examine os métodos selecionados lado a lado; as linhas que diferem ficam destacadas.
| Estimador de Pareamento Dinâmico× | Propensity Score Matching× | |
|---|---|---|
| Área≠ | Inferência causal | Estatística para pesquisa |
| Família≠ | Regression model | Process / pipeline |
| Ano de origem≠ | 2010 | 1983 |
| Autor original≠ | Lechner & Miquel (2010); building on Heckman, Ichimura & Todd (1998) | Paul Rosenbaum and Donald Rubin |
| Tipo≠ | Nonparametric causal inference / matching | Method |
| Fonte seminal≠ | 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 ↗ |
| Outros nomes≠ | dynamic treatment matching, sequential matching estimator, dynamic selection-on-observables, DME | PSM, propensity score weighting, covariate balance |
| Relacionados≠ | 6 | 3 |
| Resumo≠ | The Dynamic Matching Estimator extends standard matching methods to settings where treatment is assigned sequentially over multiple periods. Instead of a single treatment decision, units receive or forgo treatment at each time point, and the estimator identifies causal effects of entire treatment histories by matching on time-varying covariates and past treatment paths, under sequential conditional independence assumptions. | 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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