带有结果过程的马尔可夫调制泊松过程的贝叶斯推理

Yu Luo, Chris Sherlock
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引用次数: 0

摘要

在医学研究中,了解结果测量的变化对于推断病人潜在健康状况的变化至关重要。虽然来自临床和行政系统的数据有望促进这一理解,但传统的疾病进展建模方法难以分析不定期收集的大量纵向数据,也无法解释个人健康状况越差,与医疗系统的互动就越频繁这一现象。此外,来自索赔和医疗系统的数据不提供死亡等终止事件的信息。为了应对这些挑战,我们从连续时间隐马尔可夫模型入手,将观察到的数据模拟为一种结果,其分布取决于代表潜在健康状况的潜在马尔可夫链的状态,从而理解疾病的进展。此外,我们还创建了一个额外的 "死亡 "状态,并通过一个额外的泊松过程(其速率取决于马尔可夫链的潜伏状态)来模拟未观测到的终止事件,即向该状态的转变。通过这种扩展,我们不仅可以根据所接受的护理类型,还可以根据不同观察事件的时间和频率对疾病严重程度和死亡进行建模。我们提出了一种精确的吉布斯取样器程序,该程序以完整路径为条件,交替对隐藏链的完整路径(整个观察窗口中的潜在健康状态)进行取样。当未观察到的终止事件在观察窗口早期发生时,就不会再有观察到的事件了,如果天真地使用只有 "活 "的健康状态的模型,就会导致参数估计的偏差;而我们加入了 "死 "的状态,则可以减轻这种偏差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bayesian inference for the Markov-modulated Poisson process with an outcome process
In medical research, understanding changes in outcome measurements is crucial for inferring shifts in a patient's underlying health condition. While data from clinical and administrative systems hold promise for advancing this understanding, traditional methods for modelling disease progression struggle with analyzing a large volume of longitudinal data collected irregularly and do not account for the phenomenon where the poorer an individual's health, the more frequently they interact with the healthcare system. In addition, data from the claim and health care system provide no information for terminating events, such as death. To address these challenges, we start from the continuous-time hidden Markov model to understand disease progression by modelling the observed data as an outcome whose distribution depends on the state of a latent Markov chain representing the underlying health state. However, we also allow the underlying health state to influence the timings of the observations via a point process. Furthermore, we create an addition "death" state and model the unobserved terminating event, a transition to this state, via an additional Poisson process whose rate depends on the latent state of the Markov chain. This extension allows us to model disease severity and death not only based on the types of care received but also on the temporal and frequency aspects of different observed events. We present an exact Gibbs sampler procedure that alternates sampling the complete path of the hidden chain (the latent health state throughout the observation window) conditional on the complete paths. When the unobserved, terminating event occurs early in the observation window, there are no more observed events, and naive use of a model with only "live" health states would lead to biases in parameter estimates; our inclusion of a "death" state mitigates against this.
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