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Factors Influencing the Route of
Administration for Epoetin Treatment Among Hemodialysis Patients in the United
States
June 6, 2006 - A forthcoming
article to be published in the July 2006 issue of the American Journal of Kidney
Diseases finds that physician decision-making for the delivery of epoetin
therapy is primarily influenced by the type of ownership and financial
incentives associated with dialysis centers. The study, Factors Influencing the
Route of Administration for Epoetin Treatment Among Hemodialysis Patients in the
United States, was conducted by authors from MTPPI and from the Boston VA.
Thamer et al. concluded that given the similar effectiveness but significantly
reduced dose associated with subcutaneous (SC) epoetin, this study suggests an
enormous opportunity for cost-savings for the Medicare program. All current
guidelines, including the U.S.-generated National Kidney Foundation Kidney
Disease Outcomes Quality Initiative (NKF-KDOQI) and the European and Canadian
national guidelines for anemia management, recommend SC administration for
hemodialysis patients based on best evidence. However, in the U.S. only 7% of
all hemodialysis patients receive epoetin via SC route with important
implications in terms of the dose, frequency of administration, costs, and,
potentially, outcomes. Despite this disparity between the recommended guidelines
and real world practice, few studies have examined the factors associated with
route of administration of epoetin therapy among hemodialysis patients.
Using data from a survey by the Centers of Medicaid&Medicare Services, Thamer et
al. identified 13,854 patients receiving hemodialysis in 3,069 dialysis
facilities from October-December 1999 and 2000. The authors found that in the
U.S., use of SC route of epoetin administration varied widely across the
country. After adjusting for patient sociodemographics and comorbidities, the
highest rates of SC therapy are found in the Midwest and West, among providers
not affiliated with chains, and in hospital-based and not-for-profit
freestanding units. Previous exposure to SC administration (as a predialysis or
peritoneal dialysis patient) predicted subsequent SC use; for-profit and large
chains were significantly less likely to use SC administration; and increased
use of injectable drugs overall (to maximize income) was associated with less SC
use.
Notably, Thamer et al. found that hemodialysis patients at freestanding
for-profit centers were significantly less likely to receive SC epoetin compared
to hemodialysis patients at not-for profit and hospital-based centers suggesting
that ownership of a health care facility influences clinical decision-making in
the treatment of anemia. Furthermore, the larger the chain, the smaller the
proportion of patients using SC route of epoetin administration. The authors
speculate that the volume discounts for supplies or drugs such as epoetin that
are typically provided to large chains may explain this finding. Given the
smaller profits associated with SC epoetin, treatment guidelines alone are not
likely to be effective in promoting SC route of administration. Since epoetin is
expensive, however, optimizing its therapeutic effect by using subcutaneous
administration could lead to substantial cost savings to the Medicare program;
one study found that SC use could result in annual per patient savings of
$1,761.
Research was supported in part by NIH grant R01-DK066011-01A2.
For more information on this article or other EPO-related research activities,
visit us at: www.mtppi.org
The Medical Technology and Practice Patterns Institute is an independent
non-profit institute whose mission is to provide research services related to
safety, clinical effectiveness, patient outcome, cost, and cost effectiveness of
new and emerging medical technologies. MTPPI has not received public or private
funding for work related to this analysis.
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