Yu Xiangyou, Hao Yan, Zhu Zhanfang, Zhang Wei, Liu Bo, Ma Meijuan, Zhang Xuejun, Wei Na, Wang Junkui, Liu Fuqiang
Department of Cardiology, Shaanxi Provincial People's Hospital, Youyi West Road, Xi'an, 710068, Shaanxi Province, People's Republic of China.
Department of Endocrinology, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi Province, People's Republic of China.
Clin Drug Investig. 2023 Apr;43(4):241-250. doi: 10.1007/s40261-023-01253-y. Epub 2023 Mar 16.
Approximately 38 million people worldwide experience heart failure (HF), with more than 10 million in China. Heart failure exacerbations are the main cause of HF hospitalization, and hospitalizations are the main driver of HF-associated costs. Vericiguat is recommended to treat patients who have had worsening HF despite guideline-directed medical therapy. However, the cost effectiveness of adding vericiguat to the standard treatment of this population in China remains unclear. The objective of this study was to investigate the cost effectiveness of adding vericiguat to standard treatment in patients with HF in the Chinese population METHODS: A lifetime Markov model with a 1-month cycle length was developed to compare the cost effectiveness of vericiguat plus standard treatment versus standard treatment alone in Chinese patients with HF with reduced ejection fraction following an HF exacerbation, from the perspective of Chinese healthcare providers. The clinical data were obtained from the VICTORIA study. The cost was accessed from our institution or studies conducted in China. The primary outcome was the incremental cost-effectiveness ratio, representing incremental cost per incremental quality-adjusted life-year (QALY). Vericiguat was considered highly cost effective if the incremental cost-effectiveness ratio obtained was lower than 12,551 USD/QALY, cost effective if the incremental cost-effectiveness ratio was between 12,551 and 37,654.5 USD/QALY, and not cost effective if the incremental cost-effectiveness ratio was higher than 37,654.5 USD/QALY. A scenario analysis, one-way sensitivity analysis, and probabilistic sensitivity analysis were performed to test the robustness of the results.
For a 67-year-old patient with HF following an HF exacerbation, the lifetime cost was 17,721 USD if vericiguat plus standard treatment was given, compared to 7907 USD if standard treatment alone was prescribed. The corresponding effectiveness was 2.20 QALY and 2.10 QALY, respectively. The incremental cost-effectiveness ratio of vericiguat plus standard treatment versus standard treatment alone in Chinese patients with HF was 89,429 USD/QALY, higher than the willingness-to-pay threshold of 37654.5 USD/QALY. The scenario analysis and sensitivity analysis showed the robustness of our results.
The addition of vericiguat to the treatment regimen of Chinese patients with HF with reduced ejection fraction following an HF exacerbation resulted in an incremental cost-effectiveness ratio of $89,429 USD/QALY compared to standard treatment. This incremental cost-effectiveness ratio exceeds the willingness-to-pay threshold and thus, vericiguat was deemed not cost effective in the Chinese population.
全球约有3800万人患有心力衰竭(HF),中国有超过1000万人患病。心力衰竭恶化是HF住院的主要原因,而住院是HF相关费用的主要驱动因素。对于尽管接受了指南指导的药物治疗但心力衰竭仍恶化的患者,推荐使用维立西呱进行治疗。然而,在中国,将维立西呱添加到该人群的标准治疗中的成本效益仍不明确。本研究的目的是调查在中国人群中,将维立西呱添加到HF患者标准治疗中的成本效益。方法:建立了一个周期长度为1个月的终身马尔可夫模型,从中国医疗服务提供者的角度,比较维立西呱加标准治疗与单纯标准治疗在中国射血分数降低的HF加重患者中的成本效益。临床数据来自VICTORIA研究。成本数据来自我们机构或在中国进行的研究。主要结局是增量成本效益比,即每增加一个质量调整生命年(QALY)的增量成本。如果获得的增量成本效益比低于12,551美元/QALY,则认为维立西呱具有高成本效益;如果增量成本效益比在12,551至37,654.5美元/QALY之间,则具有成本效益;如果增量成本效益比高于37,654.5美元/QALY,则不具有成本效益。进行了情景分析、单因素敏感性分析和概率敏感性分析,以检验结果的稳健性。
对于一名HF加重后患有HF的67岁患者,如果给予维立西呱加标准治疗,终身成本为17,721美元,而仅开标准治疗时为7907美元。相应的效果分别为2.20 QALY和2.10 QALY。在中国HF患者中,维立西呱加标准治疗与单纯标准治疗相比的增量成本效益比为89,429美元/QALY,高于支付意愿阈值37,654.5美元/QALY。情景分析和敏感性分析表明了我们结果的稳健性。
在HF加重后射血分数降低的中国HF患者的治疗方案中添加维立西呱,与标准治疗相比,增量成本效益比为89,429美元/QALY。该增量成本效益比超过了支付意愿阈值,因此,维立西呱在中国人群中被认为不具有成本效益。