Neumann P J, Hermann R C, Kuntz K M, Araki S S, Duff S B, Leon J, Berenbaum P A, Goldman P A, Williams L W, Weinstein M C
Program on the Economic Evaluation of Medical Technology, Center for Risk Analysis, Harvard School of Public Health, Boston, MA 02115, USA.
Neurology. 1999 Apr 12;52(6):1138-45. doi: 10.1212/wnl.52.6.1138.
To demonstrate the use of cost-effectiveness analysis to assess the economic impact of donepezil in the treatment of mild or moderate AD.
Cost-effectiveness analyses show the relationship between resources used (costs) and health benefits achieved (effects) for an intervention compared with an alternative strategy.
We developed a model to estimate the incremental cost-effectiveness of donepezil compared with no treatment. We determined costs per quality-adjusted life-years gained, a measurement that enhances the comparability of diverse studies. The model projects the progression of AD patients into more severe disease stages and into nursing homes. Data from a randomized clinical trial of donepezil were used to assess the drug's impact on the 6-week probabilities of progression. Data on the costs and health-related quality of life associated with different disease stages and settings were taken from published estimates and our companion cross-sectional study, respectively.
Donepezil costs are partially offset by a reduction in the costs of care due to enhancement in cognitive functioning and the delay to more costly disease stages and settings. The magnitude of this cost offset and of the effect of donepezil on health-related quality of life depends on the model's assumptions about the duration of the drug effect, where controlled data are lacking. If the drug effect exceeds 2 years, the model predicts that for mild AD the drug would pay for itself in terms of cost offsets.
The results of the cost-effectiveness model presented here suggest that donepezil may be cost-effective but additional controlled data on long-term drug efficacy are needed.
证明使用成本效益分析来评估多奈哌齐治疗轻度或中度阿尔茨海默病(AD)的经济影响。
成本效益分析显示了与替代策略相比,一种干预措施所使用的资源(成本)与所实现的健康效益(效果)之间的关系。
我们建立了一个模型来估计多奈哌齐与未治疗相比的增量成本效益。我们确定了每获得一个质量调整生命年的成本,这一衡量标准提高了不同研究之间的可比性。该模型预测了AD患者进展到更严重疾病阶段并进入疗养院的情况。多奈哌齐随机临床试验的数据用于评估该药物对6周进展概率的影响。与不同疾病阶段和环境相关的成本及健康相关生活质量的数据分别取自已发表的估计值和我们的配套横断面研究。
由于认知功能的改善以及延迟到成本更高的疾病阶段和环境,护理成本的降低部分抵消了多奈哌齐的成本。这种成本抵消的幅度以及多奈哌齐对健康相关生活质量的影响取决于模型对药物效果持续时间的假设,而这方面缺乏对照数据。如果药物效果超过2年,模型预测对于轻度AD,该药物在成本抵消方面将实现自给自足。
此处提出的成本效益模型结果表明,多奈哌齐可能具有成本效益,但需要更多关于长期药物疗效的对照数据。