Delwel G O, Sprenger M J W
College voor zorgverzekeringen, Prof. J. H. Bavincklaan 2, 1183 AT Amstelveen.
Ned Tijdschr Geneeskd. 2002 Jun 8;146(23):1068-71.
In the light of rising expenditure on drugs and health care, a transparent, rational and careful decision-making process is required for the reimbursement of drugs. In the Netherlands, the Ministry of Health intends using pharmaco-economics in this process, i.e., new drugs will not only be judged on their clinical efficacy but also on their cost-effectiveness. Guidelines for pharmaco-economic research in the Netherlands have been published. According to these guidelines, a pharmaco-economic study must contain a cost-effectiveness analysis and/or a cost-utility analysis. In addition, a budgetary impact analysis is required. By 2005, all new drugs with therapeutic added value must supply a pharmaco-economic evaluation in order to apply for reimbursement. It will be the Minister of Health who decides whether a new drug will be reimbursed.
鉴于药品和医疗保健支出不断增加,药品报销需要一个透明、合理且谨慎的决策过程。在荷兰,卫生部打算在此过程中运用药物经济学,也就是说,新药不仅要根据其临床疗效进行评判,还要考量其成本效益。荷兰已发布了药物经济学研究指南。根据这些指南,一项药物经济学研究必须包含成本效益分析和/或成本效用分析。此外,还需要进行预算影响分析。到2005年,所有具有治疗附加值的新药必须提供药物经济学评估,以便申请报销。决定一种新药是否能获得报销的将是卫生部长。