قارن الطرق
راجع الطرق التي اخترتها جنبًا إلى جنب؛ الصفوف المختلفة مميَّزة.
| تحليل المخاطر المتنافسة البايزي× | نموذج البقاء متعدد الحالات× | |
|---|---|---|
| المجال≠ | علم الأوبئة | تحليل البقاء |
| العائلة≠ | Process / pipeline | Survival analysis |
| سنة النشأة≠ | 1980s–2000s (classical CR: 1970s; Bayesian extension: 1990s–2000s) | 1978 |
| صاحب الطريقة≠ | Various; Bayesian formulation advanced by Gelfand, Dey, Larson, and Dinse among others | Andersen, P.K. & Keiding, N. (foundational framework); popularised by Putter, Fiocco & Geskus (2007) |
| النوع≠ | Bayesian survival/time-to-event model | Semi-parametric hazard model |
| المصدر التأسيسي≠ | Larson, M. G., & Dinse, G. E. (1985). A mixture model for the regression analysis of competing risks data. Applied Statistics, 34(3), 201–211. DOI ↗ | Putter, H., Fiocco, M. & Geskus, R.B. (2007). Tutorial in Biostatistics: Competing Risks and Multi-State Models. Statistics in Medicine, 26(11), 2389–2430. DOI ↗ |
| الأسماء البديلة≠ | Bayesian cause-specific hazard model, Bayesian subdistribution hazard model, BCRA, Bayesian cumulative incidence analysis | illness-death model, multi-state transition model, Çok Durumlu Model (Multi-State / Illness-Death) |
| ذات صلة≠ | 3 | 4 |
| الملخص≠ | Bayesian competing risks analysis is a time-to-event method for settings where subjects can fail from more than one mutually exclusive cause — such as death from cancer versus death from cardiovascular disease — and prior knowledge or small-sample uncertainty makes a Bayesian framework advantageous. It extends classical competing risks models (cause-specific hazards and cumulative incidence functions) by placing probability distributions over unknown parameters and updating those distributions with observed data, yielding full posterior inference for each failure type. | The multi-state model is a generalised survival framework, formalised in the work of Andersen and Keiding and brought to wide biostatistical practice by Putter, Fiocco and Geskus (2007), that models individuals moving through multiple distinct health states — for example, healthy, ill and dead — over time. A separate hazard function is estimated for each possible transition, and transition probabilities are recovered via the product-integral of the cumulative transition intensities. |
| ScholarGateمجموعة البيانات ↗ |
|
|