A cost-effectiveness analysis of peginterferon alfa-2b plus ribavirin for the treatment of naive patients with chronic hepatitis C

被引:55
作者
Buti, M
Medina, M
Casado, MA
Wong, JB
Fosbrook, L
Esteban, R
机构
[1] Hosp Valle De Hebron, Serv Hepatol, Dept Hepatol, Barcelona 08035, Spain
[2] Schering Plough Corp, Madrid, Spain
[3] Tufts Univ, Sch Med, Tufts New England Med Ctr, Tupper Res Inst,Dept Med,Div Clin Decis Making, Boston, MA 02111 USA
关键词
D O I
10.1046/j.1365-2036.2003.01453.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim: To estimate the cost-effectiveness of therapy and analyse the effect of therapy compliance in naive patients with chronic hepatitis C. Methods: A decision analysis using the Markov model was performed for four different therapeutic strategies using peginterferon alfa-2b plus ribavirin or interferon alfa-2b plus ribavirin. Clinical data were obtained from available published reports and from the Spanish health system perspective. Results: The incremental cost-effectiveness ratio of peginterferon alfa-2b plus ribavirin at a fixed dose, compared with interferon alfa-2b plus ribavirin, was 8478 euros per life year saved and 3737 euros per quality-adjusted life year gained. Good therapeutic compliance and weight-adjusted doses of ribavirin decreased the incremental cost-effectiveness ratio to 1636 euros per life year saved and 721 euros per quality-adjusted life year gained. In compliant genotype 1 patients, the incremental cost-effectiveness ratio decreased to 916 euros per life year saved and 404 euros per quality-adjusted life year gained, with an increase from 64 to 69 years in the threshold age at which therapy was cost-effective. The sensitivity analysis demonstrated that changes in the values of the most relevant parameters do not modify the study outcomes. Conclusion: From the clinical and pharmaco-economics perspective, the use of decision therapeutic analysis models suggests that the most effective therapy for chronic hepatitis C is peginterferon alfa-2b plus ribavirin adjusted to patient body weight and with good compliance, particularly in genotyped patients.
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页码:687 / 694
页数:8
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