Estimating the Effects of Treatment Regimes over the Course of Chronic Disease: A Multi-state Causal Framework with Baseline Confounding
Ding, M.
Show abstract
The development of chronic disease is a long-term process that involves multiple endpoints, and few methods can assess the health benefits of a treatment regime over the disease course. Existing multi-state Cox models estimate survival risks by state over time, which are difficult to use when comparing the effectiveness of treatment regimes. A discrete-time split-state framework has been proposed, which divides disease states into substates by conditioning on past history. As this framework is both "memoryless" and "memorable", the time-specific transition parameters can be synthesized into summary measures, substate-specific life year (SSLY), multimorbidity-adjusted life year (MALY), and disease path. In this paper, based on this framework, we propose to investigate the causal effects of static and dynamic treatment regimes on health benefits over the entire disease course, under the assumptions of constant confounders from baseline and instantaneous effects of interventions on transition rates. Our method can identify the optimal treatment regime that generates the most benefits using MALY, and illustrate the mechanisms of treatment regimes affecting disease progression using SSLY and disease path. In the application, we evaluated the cardiovascular benefits of smoking cessation using data from the Atherosclerosis Risk in Communities (ARIC) study, where the course of heart disease was modeled in healthy (S0), at metabolic risk (S1), coronary heart disease (S2), heart failure (S3), and mortality states (S4). Compared to the regime "being a smoker in S0-S4", the MALY was 0.53 (95% CI: 0.21, 0.96), 6.10 (95% CI: 4.88, 7.19), and 4.34 (95% CI: 3.02, 5.47) years higher for the regimes "being a smoker in S0 and S1 and stop smoking if a person develops S2, S3, or S4", "no smoking in S0-S4", and "being a smoker at the start of intervention and stop smoking if age>65y", respectively. In summary, our method can evaluate the health benefits of treatment regimes over the disease course, and has the potential to improve the precision of chronic disease prevention.
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Analyses using multiple imputation need to consider missing data in auxiliary variables 92%
- Potential Biases in Test-Negative Design Studies of COVID-19 Vaccine Effectiveness Arising from the Inclusion of Asymptomatic Individuals 92%
- How Timing of Stay-at-home Orders and Mobility Reductions Impacted First-Wave COVID-19 Deaths in US Counties 91%
Similar papers in this journal
- Pathway-specific population attributable fractions 94%
- Causes of Outcome Learning: A causal inference-inspired machine learning approach to disentangling common combinations of potential causes of a health outcome 94%
- Estimation of time-varying causal effects with multivariable Mendelian randomization: some cautionary notes 93%
Similar papers in this journal
- Negative Control Exposures: Causal effect Identifiability and Use in Probabilistic-Bias and Bayesian Analyses with Unmeasured Confounders 94%
- Assessing Direct and Spillover Effects of Intervention Packages in Network-Randomized Studies 93%
- Causal Estimands for Infectious Disease Count Outcomes to Investigate the Public Health Impact of Interventions 92%
Similar papers in this journal
- A Double Machine Learning Approach for the Evaluation of COVID-19 Vaccine Effectiveness under the Test-Negative Design: Analysis of Québec Administrative Data 95%
- Efficient Estimation of Indirect Effects in Case-Control Studies Using a Unified Likelihood Framework 94%
- Multi-state network meta-analysis of cause-specific survival data 93%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.