THE COST-EFFECTIVENESS OF TREATMENT WITH LAMIVUDINE AND ZIDOVUDINE COMPARED WITH ZIDOVUDINE ALONE - A COMPARISON OF MARKOV MODEL AND TRIAL DATA ESTIMATES

Citation
J. Mauskopf et al., THE COST-EFFECTIVENESS OF TREATMENT WITH LAMIVUDINE AND ZIDOVUDINE COMPARED WITH ZIDOVUDINE ALONE - A COMPARISON OF MARKOV MODEL AND TRIAL DATA ESTIMATES, American journal of managed care, 4(7), 1998, pp. 1004-1012
Citations number
34
Categorie Soggetti
Heath Policy & Services","Medicine, General & Internal
Journal title
American journal of managed care
ISSN journal
10880224 → ACNP
Volume
4
Issue
7
Year of publication
1998
Pages
1004 - 1012
Database
ISI
SICI code
1096-1860(1998)4:7<1004:TCOTWL>2.0.ZU;2-E
Abstract
In this paper, we present a Markov model for estimating the cost-effec tiveness of combination therapy with lamivudine (LMV) and zidovudine ( ZDV) compared with ZDV alone. We also compare the predictions of the M arkov model for the impact of combination therapy on trial period cost s with the actual impact of combination therapy on selected trial peri od costs estimated from data collected during the clinical trials. In the Markov model, disease stages were defined by CD4 cell count, Based on clinical trial data for patients with CD4 counts higher than 100 c ells/mm(3), the model assumed that the CD4 cell count level could be m aintained above the level at the initiation of therapy for 6.5 months with monotherapy and for 18 months with combination therapy. After thi s period, transition rates for natural disease progression were used. Incremental lifetime costs and quality-adjusted rife years gained with LMV/ZDV compared with ZDV alone were estimated for cohorts of patient s initiating antiretroviral therapy at four different CD4 cell count s tages. Cost per life year gained varied from $10,000 to $18,000, and c ost per quality-adjusted life year gained varied from $14,000 to $27,0 00, In both cases, the combination therapy was more cost-effective whe n started earlier in disease progression. These estimates were not sen sitive to changes in key parameter values. In addition, the model was used to estimate the impact of combination therapy on healthcare costs during the trial period; these estimated costs were compared with dat a on the cost of resource use collected during the clinical trial for hospital stays, unscheduled visits, medications, and outpatient proced ures, Both the Markov model estimates and the trial data estimates for the trial period showed cost savings in other medical costs, though t hese were not large enough to completely offset the increased cost for antiretroviral therapy. The model estimates were more conservative th an the estimates based on the trial data.