Markov-modulated marked Poisson processes for modeling disease dynamics based on medical claims data

被引:1
|
作者
Mews, Sina [1 ,3 ]
Surmann, Bastian [2 ]
Hasemann, Lena [2 ]
Elkenkamp, Svenja [2 ]
机构
[1] Bielefeld Univ, Dept Business Adm & Econ, Bielefeld, Germany
[2] Bielefeld Univ, Dept Hlth Econ & Hlth Care Management, Bielefeld, Germany
[3] Bielefeld Univ, Dept Business Adm & Econ, Univ str 25, D-33615 Bielefeld, Germany
关键词
chronic obstructive pulmonary disease; continuous time; disease process; hidden Markov model; informative observation times; maximum likelihood; CHARLSON COMORBIDITY INDEX; PROGRESSION; TIMES;
D O I
10.1002/sim.9832
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We explore Markov-modulated marked Poisson processes (MMMPPs) as a natural framework for modeling patients' disease dynamics over time based on medical claims data. In claims data, observations do not only occur at random points in time but are also informative, that is, driven by unobserved disease levels, as poor health conditions usually lead to more frequent interactions with the health care system. Therefore, we model the observation process as a Markov-modulated Poisson process, where the rate of health care interactions is governed by a continuous-time Markov chain. Its states serve as proxies for the patients' latent disease levels and further determine the distribution of additional data collected at each observation time, the so-called marks. Overall, MMMPPs jointly model observations and their informative time points by comprising two state-dependent processes: the observation process (corresponding to the event times) and the mark process (corresponding to event-specific information), which both depend on the underlying states. The approach is illustrated using claims data from patients diagnosed with chronic obstructive pulmonary disease by modeling their drug use and the interval lengths between consecutive physician consultations. The results indicate that MMMPPs are able to detect distinct patterns of health care utilization related to disease processes and reveal interindividual differences in the state-switching dynamics.
引用
收藏
页码:3804 / 3815
页数:12
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