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基因工程药物的药物经济学

Pharmacoeconomics of genetically engineered drugs.

作者信息

Jones-Grizzle A J, Bootman J L

机构信息

College of Pharmacy, Center for Pharmaceutical Economics, University of Arizona, Tucson.

出版信息

Pharmacoeconomics. 1992 Jan;1(1):45-53. doi: 10.2165/00019053-199201010-00009.

Abstract

Biotechnology is a rapidly developing area of drug development which has great growth potential. Development of genetically engineered drugs is very expensive and as these products become available the impact on healthcare costs could be vast. The cost-benefit ratio of biotechnology products needs to be established, but few relevant pharmacoeconomic studies are available. Issues in pharmacoeconomic analysis of genetically engineered drugs can be exemplified by the data available for alteplase, epoetin and interferon alpha-2b. One study concluded that thrombolysis with streptokinase rather than alteplase would substantially reduce the percentage of total hospital costs that were not reimbursed. However, differences in efficacy were not accounted for. Based on the superior efficacy of alteplase, a more extensive pharmacoeconomic analysis found that alteplase was more cost-effective than streptokinase when the agents were combined with aggressive reocclusion management. However, this conclusion may be altered by the finding of a more recent study that streptokinase may be at least as effective as alteplase. Economic factors involved in epoetin treatment of anaemia associated with chronic renal disease have been studied thoroughly. However, cost-effectiveness or cost-benefit analysis was not attempted, and improvement in quality of life with epoetin therapy also needs to be considered, to facilitate cost-utility analysis. Compared with chlorambucil, the use of interferon alpha-2b for hairy cell leukaemia resulted in significant direct and indirect cost savings, in a retrospective cost-benefit analysis.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

生物技术是药物研发中一个快速发展的领域,具有巨大的增长潜力。基因工程药物的研发成本非常高昂,随着这些产品的问世,对医疗成本的影响可能巨大。需要确定生物技术产品的成本效益比,但相关的药物经济学研究却很少。基因工程药物的药物经济学分析问题可以通过阿替普酶、促红细胞生成素和干扰素α-2b的现有数据来说明。一项研究得出结论,用链激酶而非阿替普酶进行溶栓可大幅降低未报销的总住院费用百分比。然而,未考虑疗效差异。基于阿替普酶的卓越疗效,一项更广泛的药物经济学分析发现,当这些药物与积极的再闭塞管理相结合时,阿替普酶比链激酶更具成本效益。然而,最近一项研究发现链激酶可能至少与阿替普酶一样有效,这一结论可能会改变。促红细胞生成素治疗慢性肾病相关性贫血所涉及的经济因素已得到充分研究。然而,未尝试进行成本效益或成本效益分析,并且还需要考虑促红细胞生成素治疗对生活质量的改善,以促进成本效用分析。在一项回顾性成本效益分析中,与苯丁酸氮芥相比,使用干扰素α-2b治疗毛细胞白血病可显著节省直接和间接成本。(摘要截选于250字)

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