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Date:   Tue, 20 Sep 2011 07:02:16 -0400
Reply-To:   William Shakespeare <shakespeare_1040@HOTMAIL.COM>
Sender:   "SAS(r) Discussion" <SAS-L@LISTSERV.UGA.EDU>
From:   William Shakespeare <shakespeare_1040@HOTMAIL.COM>
Subject:   Study design
Content-Type:   text/plain; charset=ISO-8859-1

Suppose there’s a situation where Treatment A and never Treatment B is always administered to a cohort, there then occurs a change in practice, and Treatment B and never Treatment A is administered to a different cohort. An investigator wishes to compare the incidence of a disease across these cohorts. What does this prove other than the incidences are similar/different? There are so many threats to internal validity there’s no way anyone can make any causal attribution for the differences. This is certainly the unspoken goal of such a study. Do any of you face this situation? What do you say? What is the standard design for such a situation? There is not really the possibility of a case-control study after the change of practice since there really is not a relevant control group because everyone gets the same treatment. Even if you could find appropriate controls a case-control study would be a poor choice because those designs are geared more toward elucidating the factors associated with disease rather than the effectiveness of treatment. Has anyone ever seen case-control studies used to evaluate treatments in a retrospective sense?


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