In general the approach proposed is reasonably sensible. However, there is panel data available for the time dependent covariates. It therefore seems possible to fit a time continuous Markov model to the data using methods appropriate for panel data (e.g. Kalbfleisch and Lawless, 1985). This approach has the advantage that the exact time of the death events can still be used.
The authors rely on categorization throughout. While this seems necessary for the time dependent covariates, there seems scope for using multinomial logit models for other covariates. Similarly, by allowing a different mortality probability for each combination of covariates they are effectively fitting covariate models with interactions (i.e. the effect of being in covariate level 2 compared to 1, is different depending on which level(s) of the other time dependent covariate(s) a subject is in). While such interactions may be necessary, it might be better to allow simpler models where only the evolution of the time dependent covariates is kept general. This is another advantage of a continuous time model since covariate effects could remain on the hazard (transition intensity) scale as in the Cox PH model.
Finally, the authors give a partial justification of the use of a time homogeneous Markov model through the Cox PH model having an approximately constant baseline hazard. It should be noted that a time homogeneous Markov model does not imply a constant absorption hazard (unless the model begins in the quasi-stationary distribution). Conversely, while a constant hazard might suggest homogeneity more than non-homogeneity, it is nevertheless possible to construct non-homogeneous processes with constant (or near constant) marginal absorption hazards. The authors do however report a
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