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| Phân tích sống còn hiệu chỉnh rủi ro× | Ghép cặp điểm xu hướng× | |
|---|---|---|
| Lĩnh vực≠ | Dịch tễ học | Thống kê nghiên cứu |
| Họ | Process / pipeline | Process / pipeline |
| Năm ra đời≠ | 1972 (Cox regression); broader covariate-adjusted survival methods developed 1970s–1990s | 1983 |
| Người khởi xướng≠ | D. R. Cox (regression framework); extensions via Kaplan & Meier, Breslow, and others | Paul Rosenbaum and Donald Rubin |
| Loại≠ | Observational and experimental analytical method | Method |
| Công trình gốc≠ | Cox, D. R. (1972). Regression models and life-tables. Journal of the Royal Statistical Society, Series B, 34(2), 187–220. link ↗ | 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 ↗ |
| Tên gọi khác≠ | covariate-adjusted survival analysis, adjusted time-to-event analysis, risk-stratified survival analysis, adjusted Kaplan-Meier / Cox analysis | PSM, propensity score weighting, covariate balance |
| Liên quan≠ | 5 | 3 |
| Tóm tắt≠ | Risk-adjusted survival analysis estimates the time to an event of interest — such as death, relapse, or hospital readmission — while simultaneously accounting for baseline differences in patient characteristics (covariates). By incorporating confounders such as age, comorbidities, or disease severity, it produces hazard ratios, survival curves, and median survival estimates that are attributable to the factor of interest rather than to pre-existing risk differences between groups. | 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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