Literature DB >> 8318682

Cost implications to Medicare of recombinant erythropoietin therapy for the anemia of end-stage renal disease.

N R Powe1, R I Griffiths, E B Bass.   

Abstract

The purpose of this study was to estimate the net cost effect to Medicare of the increasing use of recombinant human erythropoietin (EPO) instead of red blood cell transfusions or androgens in the management of anemia for the approximately 100,000 hemodialysis patients in the U.S. End-Stage Renal Disease (ESRD) program. A computerized decision model that takes into account the effectiveness and possible side effects of transfusions, androgens, and EPO and predicts 1- and 5-yr direct medical costs to Medicare associated with each therapy was constructed. Probability estimates for clinical events were derived from the literature. Costs were assigned by use of the amounts Medicare pays providers of ESRD care for: (1) use of EPO, transfusions, and androgens; and (2) health care services related to the treatment of anemia (including complications of treatment and possible reductions in morbidity). For every 10,000 hemodialysis patients treated with EPO, net Medicare expenditures will be much greater than if only transfusions are used by $42,530,000 at 1 yr (6% of ESRD program costs) and by $118,050,000 at 5 yr and also much greater than if androgens are used (by $42,700,000 at 1 yr and $118,370,000 at 5 yr). The increase in cost was highly sensitive to the dose of EPO; moderately sensitive to changes in estimated anemia response rates for EPO, frequency of EPO-induced vascular access clotting, and reduction in cardiovascular or overall morbidity; and slightly sensitive to transfusion rates, estimated anemia response rates for androgens, frequency of EPO-induced seizure or hypertensive complications (stroke, myocardial infarction), frequency of transfusion-related viral infection, and frequency of androgen-induced virilization. Considering both effectiveness and side effects of alternative treatments for the anemia of ESRD, it was projected that the increasing use of EPO will markedly increase the cost to Medicare of ESRD medical care.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8318682     DOI: 10.1681/ASN.V3101660

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  6 in total

Review 1.  Low-dosage epoetin in maintenance haemodialysis: costs and quality-of-life improvement.

Authors:  D C Harris
Journal:  Pharmacoeconomics       Date:  1994-01       Impact factor: 4.981

2.  Patients, populations and policy: patient outcomes in chronic kidney disease.

Authors:  N R Powe
Journal:  Trans Am Clin Climatol Assoc       Date:  2001

3.  Reconciling decision models with the real world. An application to anaemia of renal failure.

Authors:  Y C Shih; T L Kauf
Journal:  Pharmacoeconomics       Date:  1999-05       Impact factor: 4.981

Review 4.  Androgen therapy for anemia in elderly uremic patients.

Authors:  J F Navarro; C Mora
Journal:  Int Urol Nephrol       Date:  2001       Impact factor: 2.370

5.  Gene therapy for long-term expression of erythropoietin in rats.

Authors:  W R Osborne; N Ramesh; S Lau; M M Clowes; D C Dale; A W Clowes
Journal:  Proc Natl Acad Sci U S A       Date:  1995-08-15       Impact factor: 11.205

6.  A review of the first year of Medicare coverage of erythropoietin.

Authors:  R I Griffiths; N R Powe; J Greer; G de Lissovoy; G F Anderson; P K Whelton; A J Watson; P W Eggers
Journal:  Health Care Financ Rev       Date:  1994
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.