Population-based studies of maintenance hemodialysis patients have demonstr
ated a reproducible relationship between the dose of hemodialysis and morta
lity and morbidity outcomes. In these analyses, which have aggregated hemod
ialysis patient subgroups, improved outcomes are associated with greater do
ses of hemodialysis. However, remarkable counterintuitive findings are obse
rved if patients are analyzed by subgroups based on their race, gender, and
anthropometric and blood-based biomarkers of nutritional state. For exampl
e, blacks generally receive lower doses of hemodialysis than whites, but en
joy relatively improved survival; patients who receive the highest doses of
hemodialysis have an increased death risk; and the dose response curve bet
ween hemodialysis and survival is altered based on the patients' body mass
index. These seemingly paradoxical relationships between hemodialysis dose
and patient survival can be explained because of the use of mathematical ur
ea kinetic constructs as clinical outcome predictors; they integrate a meas
ure of solute removal (K x t) with an anthropometric surrogate of nutrition
, the urea distribution volume (V). Both these measures have an independent
influence on patient survival and in some clinical circumstances are of un
equal power as clinical outcome predictors. These complex interactions must
be kept in perspective as clinical care is delivered in the context of hem
odialysis dose.