Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore.
Singapore Institute for Clinical Sciences, Agency for Science, Technology and Research , Singapore 117609, Singapore.
Biometrics. 2024 Jul 1;80(3). doi: 10.1093/biomtc/ujae075.
Time-to-event data are often recorded on a discrete scale with multiple, competing risks as potential causes for the event. In this context, application of continuous survival analysis methods with a single risk suffers from biased estimation. Therefore, we propose the multivariate Bernoulli detector for competing risks with discrete times involving a multivariate change point model on the cause-specific baseline hazards. Through the prior on the number of change points and their location, we impose dependence between change points across risks, as well as allowing for data-driven learning of their number. Then, conditionally on these change points, a multivariate Bernoulli prior is used to infer which risks are involved. Focus of posterior inference is cause-specific hazard rates and dependence across risks. Such dependence is often present due to subject-specific changes across time that affect all risks. Full posterior inference is performed through a tailored local-global Markov chain Monte Carlo (MCMC) algorithm, which exploits a data augmentation trick and MCMC updates from nonconjugate Bayesian nonparametric methods. We illustrate our model in simulations and on ICU data, comparing its performance with existing approaches.
时间事件数据通常以离散的尺度记录,其中多个竞争风险是事件的潜在原因。在这种情况下,应用具有单一风险的连续生存分析方法会导致有偏估计。因此,我们提出了一种用于具有离散时间的竞争风险的多元 Bernoulli 探测器,涉及多元变化点模型在特定原因的基线风险上。通过对变化点数量和位置的先验,我们在风险之间施加了变化点之间的依赖性,同时允许对其数量进行数据驱动的学习。然后,在这些变化点的条件下,使用多元 Bernoulli 先验来推断涉及哪些风险。后验推断的重点是特定原因的风险率和风险之间的依赖性。这种依赖性通常是由于随时间变化的特定于主体的变化而导致的,这些变化会影响所有风险。通过定制的局部-全局马尔可夫链蒙特卡罗(MCMC)算法进行完整的后验推断,该算法利用数据增强技巧和非共轭贝叶斯非参数方法的 MCMC 更新。我们在模拟和 ICU 数据中说明了我们的模型,并与现有方法进行了比较。