StATS: Stratified Cox regression models (March 22, 2005)
Someone sent me an email asking about a Cox regression model that included a strata for clinics. What's the best way to handle strata? That's a tricky question to answer. The first question you might want to ask is whether it makes sense to include the clinic factor as a strata at all. When you include strata, you allow the Cox model to estimate an entirely separate hazard function for each clinic. That's quite different from including clinic as a fixed effect in the Cox regression model, where you would be assuming that the clinics differ only in that the hazard function for one clinic is a multiple of the hazard function for the other clinic.
Thernau and Grambsch describe it well in their book on survival analysis.
Analysis of multicenter clinical trials frequently uses stratification. Because of varying patient populations and referral patterns, the different clinical centers in the trial are likely to have difference baseline survival curves, ones that do not have simple parallel relationships. Strata play a role similar to blocks in randomized block designs analyzed by two-factor analysis of variance. (page 44).
Using a stratified Cox model could lead to a loss of power or precision, because you are using more of the data to estimate separate hazard functions and that leaves less of the data for your other research hypotheses. But perhaps assuming that the clinics only differ by a multiplicative constant is an oversimplification. A third approach is to treat clinics as a random effect. This leads to a frailty model, which you cannot run in SPSS, but which is available with other software programs.
The rule is to choose a model that is as simple as possible, but not too simple. Perhaps your sample size might also help you decide about the complexity of the model. Do you have lots of data to spare so that estimating separate hazard functions is a luxury you can easily afford? Also, take a look at the Kaplan-Meier curves for each clinic. Do they show unusual patterns, such as one clinic having very high early mortality, but the second clinic eventually catching up?
There's no easy answer to this question, but remember that just because you used a stratified sample, that does not mean that your strata have to be accounted for in a particular way. Think hard about including clinics as a fixed effect or as a random effect as an alternative.
The other thing to keep in mind is that there are probably several approaches to your data set that would be easy to defend in a peer-reviewed publication. Choose a reasonable approach, and don't worry so much about the choices you didn't make. If a peer-reviewer tells you to use a different model, that's actually good news. When the reviewers start nitpicking your model and don't mention bigger issues, you are probably only one step away from publishing.
This page was written by Steve Simon while working at Children's Mercy Hospital. Although I do not hold the copyright for this material, I am reproducing it here as a service, as it is no longer available on the Children's Mercy Hospital website. Need more information? I have a page with general help resources. You can also browse for pages similar to this one at Category: Survival analysis.