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| Αντιστοίχιση Βαθμολογίας Προδιάθεσης Ενισχυμένη με Μηχανική Μάθηση× | Αντιστοίχιση Βαθμολογίας Προδιάθεσης× | |
|---|---|---|
| Πεδίο≠ | Αιτιακή Συμπερασματολογία | Ερευνητική Στατιστική |
| Οικογένεια≠ | Regression model | Process / pipeline |
| Έτος προέλευσης≠ | 2004 | 1983 |
| Δημιουργός≠ | McCaffrey, Ridgeway & Morral (2004); Westreich, Lessler & Funk (2010) | Paul Rosenbaum and Donald Rubin |
| Τύπος≠ | Causal inference / matching | Method |
| Θεμελιώδης πηγή≠ | McCaffrey, D. F., Ridgeway, G., & Morral, A. R. (2004). Propensity score estimation with boosted regression for evaluating causal effects in observational studies. Psychological Methods, 9(4), 403-425. 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 ↗ |
| Εναλλακτικές ονομασίες≠ | ML-PSM, boosted propensity score matching, ML-augmented PSM, nonparametric propensity score matching | PSM, propensity score weighting, covariate balance |
| Συναφείς≠ | 6 | 3 |
| Σύνοψη≠ | Machine learning-augmented propensity score matching (ML-PSM) replaces the traditional logistic regression used to estimate propensity scores with flexible machine learning algorithms — such as gradient boosted trees, random forests, or LASSO — to better capture complex, nonlinear relationships among covariates. The resulting richer propensity scores improve covariate balance and reduce bias in the estimated average treatment effect on the treated (ATT). | 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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