So of course I had to ask him what was his goal hematocrit? The answer? 45-46% which would place him at higher risk for untoward events if he were in a similar demographic (notice the age differential). Still forewarned is forearmed so I emailed him the abstract to the study and asked him to review its applicability w/his hematologist.
In an analogous situation, testosterone is known to stimulate bone marrow production leading to secondary polycythemia. This is usually due to supraphysiologic levels so I always recommend smaller more frequent doses for those who take injectable testosterone. But if the hematocrit still runs high despite my best attempts to smooth out the peak & trough, I then recommend therapeutic phlebotomy to minimize this same risk of cardiovascular death & thrombotic events. Granted this study was performed on a population of patients w/PV, but it does make me wonder about its generalizability to secondary polycythemia.
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