摘要
目的:评价与普通干扰素相比,聚乙二醇干扰素α-2a对于不同基因型的中国慢性丙型肝炎患者的经济性。方法:将慢性丙型肝炎患者分为基因1型和非基因1型,分别构建疾病进展Markov模型,比较聚乙二醇干扰素α-2a和普通干扰素的长期成本-效用,并对结果进行敏感性分析。结果:与普通干扰素相比,聚乙二醇干扰素α-2a对于基因1型患者成本更低(183 631.14元vs 212 703.42元)、效用更高(14.06QALY vs 12.32 QALY),聚乙二醇干扰素α-2a更具有经济性;对于非基因1型患者,聚乙二醇干扰素α-2a成本更高(112 770.18元vs 111 025.80元)、效用更高(15.01 QALY vs 14.51 QALY),增量成本-效用比3 488.76元/QALY(低于中国阈值),聚乙二醇干扰素α-2a更具有经济性。敏感性分析与基础分析一致。结论:对于不同基因型中国慢性丙型肝炎患者,聚乙二醇干扰素α-2a均为更经济的治疗方案。
Objective: To evaluate the pharmacoeconomics of pegylated interferon α-2a and interferon based on Chinese patients with different genotypes of chronic hepatitis C. Methods: The chronic hepatitis C patients were divided into genotype 1 and non-genotype 1. Markov models were built,respectively,to simulate developmental process of chronic hepatitis C in Chinese patients. We evaluated the cost and utility of pegylated interferon α-2a and interferon by running 50 cycles of the models,and carried out sensitivity analysis. Results:Cost-utility analysis results showed that for patients with genotype 1 chronic hepatitis C,pegylated interferon α-2a had lower cost( 183 631. 14 RMB vs 212 703. 42 RMB) and higher utility( 14. 06 QALY vs 12. 32 QALY),which proved that pegylated interferon α-2a was cost-effective. With regard to non-genotype 1 patients,pegylated interferonα-2a had higher cost( 112 770. 18 RMB vs 111 025. 80 RMB) and higher utility( 15. 01 QALY vs 14. 51 QALY),and the incremental cost-utility ratio was 3 488. 76 RMB/QALY( lower than Chinese threshold),so pegylated interferon α-2a was cost-effective. In the sensitivity analysis,the results were similar with base case analysis.Conclusion: Pegylated interferon α-2a is more cost-effctive than interferon for patients with both genotype 1 and non-genotype 1 chronic hepatitis C in China.
作者
陈平钰
刘国恩
徐菲
马爱霞
CHEN Ping-yu LIU Guo-en XU Fei MA Ai-xia(School of International Pharmaceutical Business, China Pharmaceutical University, Nanjing 211198, China China Center for Health Economic Research, Peking University, Beijing 100871, China School of Public Health, Fadan University, Shanghai 200433, China)
出处
《中国新药杂志》
CAS
CSCD
北大核心
2017年第15期1736-1743,共8页
Chinese Journal of New Drugs