Clinical studies and the National Kidney Foundation-Dialysis Outcomes Quali
ty Initiative guidelines suggest that a target hematocrit of 33% to less th
an 36% is appropriate for patient benefit. Previous studies have shown an a
ssociation of lower risks for death and hospitalization when hematocrits we
re 33% to less than 36%, In this study, we assessed the relationship betwee
n hematocrit value and associated Medicare expenditures, analyzing incident
Medicare hemodialysis patients from January 1, 1991, through June 30, 1995
. All patients survived at least 90 days to normalize eligibility and an ad
ditional B-month entry period to assess comorbidity and hematocrit values,
All patients were followed up from July 1, 1991, through December 31, 1996,
We assessed the association between hematocrit values in the 6-month entry
period and the Medicare-allowable Part A and Part B per-member-per-month (
PMPM) expenditures in the follow-up period, controlling for other variables
, including patient demographic characteristics, comorbid conditions, and s
everity of disease. We found that hematocrits of 33% to less than 36% and 3
6% and higher were associated with lower Medicare-allowable payments in the
follow-up period. Compared with reference patients with hematocrits of 30%
to less than 33%, the Medicare-allowable PMPM expenditures were significan
tly greater for patients with hematocrits less than 27% and 27% to less tha
n 30% (12.7% and 5.3%, respectively), and the Medicare-allowable PMPMs were
significantly less for patients with hematocrits of 33% to less than 36% a
nd 36% and higher (6.0% and 8.2%, respectively). Although these findings su
ggest that the treatment of anemia may be associated with significant savin
gs in total patient Medicare expenditures, caution should be considered bec
ause these findings are associations and should not be deemed as showing ca
usality. (C) 2000 by the National Kidney Foundation, Inc.