Novartis Pharma AG, Basel, Switzerland.
Novartis Healthcare Pvt. Ltd., Hyderabad, India.
Eur J Health Econ. 2023 Apr;24(3):453-467. doi: 10.1007/s10198-022-01485-3. Epub 2022 Jul 5.
To summarize cost-effectiveness (CE) evidence of sacubitril/valsartan for the treatment of heart failure (HF) patients with reduced ejection fraction (HFrEF). The impact of different modeling approaches and parameters on the CE results is also described.
We conducted a systematic literature review using multiple databases: Embase; MEDLINE; MEDLINE-In Process; NIHR CRD database including DARE, NHS EED, and HTA databases; and the Cost Effectiveness Analysis registry. We also reviewed HTA countries' websites to identify CE reports of sacubitril/valsartan, published up to 25-July-2021. Articles published in English as full-texts, conference-abstracts, or HTA reports were included.
We included 44 CE models [39 from 37 publications (22 full-texts; 15 conference-abstracts) and 5 HTAs; Europe, n = 20; North and South Americas, n = 14; Asia and Australia, n = 10]. Most models adopted a Markov structure with constant transition probabilities of events (n = 27) or a mix of Markov and regression-based models (n = 16), with variations in structural assumptions and chosen parameters. Study authors concluded sacubitril/valsartan to be a cost-effective therapy in 37/41 models in chronic HFrEF patients and 2/3 models in hospitalized patients stabilized after an acute decompensation for HF. CE models showing sacubitril/valsartan not to be a cost-effective treatment generally modeled a shorter time horizon. Effect of sacubitril/valsartan on cardiovascular and all-cause mortality, cost, duration of effect and time horizon was the main model drivers.
Most evidence indicated sacubitril/valsartan is cost-effective in HFrEF. The use of a lifetime horizon is recommended in future models as HF is a chronic disease. Data on the CE of sacubitril/valsartan in the inpatient setting were limited and further research is warranted.
总结沙库巴曲缬沙坦治疗射血分数降低的心力衰竭(HFrEF)患者的成本效益(CE)证据。还描述了不同建模方法和参数对 CE 结果的影响。
我们使用多个数据库进行了系统的文献综述:Embase;MEDLINE;MEDLINE-In Process;NIHR CRD 数据库,包括 DARE、NHS EED 和 HTA 数据库;以及成本效益分析登记处。我们还审查了 HTA 国家的网站,以确定截至 2021 年 7 月 25 日发布的沙库巴曲缬沙坦的 CE 报告。纳入的文章为全文发表的文章、会议摘要或 HTA 报告,发表语言为英语。
我们纳入了 44 项 CE 模型[39 项来自 37 篇出版物(22 篇全文;15 篇会议摘要)和 5 项 HTA;欧洲,n=20;北美和南美,n=14;亚洲和澳大利亚,n=10]。大多数模型采用具有固定事件转移概率的 Markov 结构(n=27)或 Markov 和基于回归的模型的混合(n=16),结构假设和所选参数存在差异。研究作者得出结论,在慢性 HFrEF 患者中,沙库巴曲缬沙坦在 37/41 项模型中具有成本效益,在心力衰竭急性失代偿后稳定的住院患者中,2/3 项模型具有成本效益。表明沙库巴曲缬沙坦不是一种具有成本效益的治疗方法的 CE 模型通常设定了较短的时间范围。沙库巴曲缬沙坦对心血管和全因死亡率、成本、效果持续时间和时间范围的影响是模型的主要驱动因素。
大多数证据表明,沙库巴曲缬沙坦在 HFrEF 中具有成本效益。建议在未来的模型中使用终生时间范围,因为 HF 是一种慢性疾病。关于沙库巴曲缬沙坦在住院患者中的 CE 数据有限,需要进一步研究。