mhollanders wrote:Okay, I was under the impression that you could actually make the state transitions interpretable by implementing something like the loglink function on it.
You can use the log-link as a 'way around' the hard-coded restrictions in MARK on specifying the interval lengths explicitly (which is the normal way forward for unequal intervals), but, just because you
can do something mechanically doesn't mean you necessarily will come up with an estimate that you can make sense of.
Yes, I've read and re-read those sections, and I do understand the principle, and I was wondering if there's a way around it.
In my opinion, a qualified 'no'. If you knew a priori something about transition probabilities (which might be possible for disease models) there are some technical things you can do that would allow you to do some of what you're after, but again, only given said informatioon, and perhaps some strong assumptions. If the variation in intervals among primary samples is relatively small, perhaps you might feel comfortable holding your nose. But if the difference(s) are large, relative to the process you're trying to model, you might be setting yourself up.
Not everyone is so pessimistic (Jim Nichols, for example, has worked on a problem of this sort, and for the system in question, he felt the assumptions were reasonable), but I tend to err on the side of caution.
Does this imply that one should really steer clear of multistate models that have unequal time intervals? Or is there still a way to analyse the data to get some meaningful results about the state transitions?
In my opinion, a qualified 'yes' to steering clear, and a qualified 'maybe' to the 'is there anything I can do?' query. To the former, if its me, I either 'get the design right in the first place', or I deecide how long I can go holding my nose (if I absolutely have to proceed). Knowing the challenges of meaningfully applying MS models (and permutations thereto), you should strive to conduct a sampling protocol where the intervals between primary samples is the same over the course of the study (or, at least nearly so). Unfortunately, as might be the situation you're faced with, the data weren't collected this way, and you're left wondering what to do. Low hanging fruit is to model unequal intervals, present estimates, and then do a *lot* of arm-waving about uncertianty in what comes out the other end. Not particularly satisfying, but might be what you have.
The other brick you can pile on (piling up bricks not being the best way to 'build a scientific house') is to try simulating under various plausibility scenarios, and see how much trouble you might get into by trying to explicitly model unequal intervals. Again, in the disease context, where transitions might be modelled as a function of various things, this might be possible (although, in my personal experience with this sort of stuff -- in an earlier incarantion I did some work with disease models -- the transition structure for most disease systems is semi-Markov, making most of the standard MS approaches pretty bogus -- including my own early attempts -- since they typically assume simple first-order Markov. For alternate and arguably better approaches, see work by Langrock and King).
Quoting Darryl MacKenzie: '
these methods are statistical, not magical'. Meaning, in context, that 'statistical cleverness' can't always 'magically' pull good stuff from data collected under a less-than-optimal design.