Simpson K, Hatziandreu E J, Andersson F, Shakespeare A, Oleksy I, Tosteson A N
University of North Carolina at Chapel Hill, USA.
Pharmacoeconomics. 1994 Dec;6(6):553-62. doi: 10.2165/00019053-199406060-00008.
A cost-effectiveness model was developed on the basis of early clinical trial results from the US reporting sustained CD4+ cell response in patients receiving zalcitabine in addition to zidovudine. This model was then adapted and applied to 5 European countries to assess the comparative cost effectiveness of adding zalcitabine to antiviral treatment for AIDS patients. The countries included in the modelling effort were Switzerland, France, Italy, Germany and the UK. The model used a Markov state-transition process to estimate the rate of acute opportunistic disease episodes, lifetime medical treatment costs, and survival for populations of AIDS patients with baseline CD4+ counts of less than 300/microliters. Physician panels in each country developed standard treatment algorithms and adjusted the epidemiological data to reflect the AIDS profile of each country. Economic consultants provided cost data. Results from this exploratory data analysis show that if CD4+ counts correlate with the incidence of opportunistic disease episodes as expected, the combined use of zalcitabine and zidovudine for a 1-year period should be cost effective.
根据美国早期临床试验结果开发了一个成本效益模型,该结果报告了接受扎西他滨联合齐多夫定治疗的患者中CD4+细胞持续反应情况。然后,该模型被调整并应用于5个欧洲国家,以评估在艾滋病患者抗病毒治疗中添加扎西他滨的相对成本效益。建模工作所涵盖的国家包括瑞士、法国、意大利、德国和英国。该模型采用马尔可夫状态转换过程来估计基线CD4+计数低于300/微升的艾滋病患者群体的急性机会性疾病发作率、终身医疗费用和生存率。每个国家的医师小组制定了标准治疗算法,并调整了流行病学数据以反映每个国家的艾滋病概况。经济顾问提供了成本数据。这项探索性数据分析的结果表明,如果CD4+计数与机会性疾病发作率如预期那样相关,那么扎西他滨和齐多夫定联合使用1年应该具有成本效益。