FIECON Ltd, 3 College Yard, Lower Dagnall Street, Hertfordshire, St Albans, AL3 4PA, UK.
Portola Pharmaceuticals, Inc, South San Francisco, CA, USA.
Pharmacoeconomics. 2019 May;37(5):701-714. doi: 10.1007/s40273-018-0757-8.
Studies show that the risk of venous thromboembolism (VTE) continues post-discharge in nonsurgical patients with acute medical illness. Betrixaban is the first anticoagulant approved in the United States (US) for VTE prophylaxis extending beyond hospitalization.
The aim was to establish whether betrixaban for VTE prophylaxis in nonsurgical patients with acute medical illness at risk of VTE in the US is cost-effective compared with enoxaparin.
A cost-effectiveness analysis was conducted, estimating the cost per quality-adjusted life-year (QALY) gained with betrixaban (35-42 days) compared with enoxaparin (6-14 days) from a US payer perspective over a lifetime horizon. A decision tree (DT) estimated primary VTE events, thrombotic events, and treatment complications in the first 3 months based on data from the phase III Acute Medically Ill VTE Prevention with Extended Duration Betrixaban study. A Markov model estimated recurrent events and long-term complication risks from published literature. EuroQoL-5 Dimensions utility data and costs inflated to 2017 US dollars (US$) were from published literature. Results were discounted at 3.0% per annum. Deterministic and probabilistic sensitivity analyses explored uncertainty.
Betrixaban dominated enoxaparin, with savings of US$784 and increased QALYs of 0.017 per patient. In addition, betrixaban dominated enoxaparin across all sensitivity analyses, but was most sensitive to utilities and DT probabilities. Furthermore, probabilistic sensitivity analysis found that betrixaban was more cost-effective than enoxaparin at all willingness-to-pay thresholds.
Betrixaban can be considered cost-effective for nonsurgical patients with acute medical illness at risk of VTE, requiring longer VTE prophylaxis from hospitalization through post-discharge.
研究表明,非外科急性内科疾病患者出院后静脉血栓栓塞(VTE)风险仍持续存在。贝曲西班是首个获美国批准用于延长住院后 VTE 预防的抗凝药物。
旨在评估贝曲西班用于有 VTE 风险的非外科急性内科疾病患者 VTE 预防是否优于依诺肝素,是否具成本效益。
从美国支付者角度,采用终生时间范围,对贝曲西班(35-42 天)和依诺肝素(6-14 天)进行成本效果分析,评估贝曲西班的成本效果,即每获得一个质量调整生命年(QALY)的成本,与依诺肝素比较。采用决策树(DT),根据 III 期急性内科疾病患者 VTE 预防延长疗程贝曲西班研究的数据,在 3 个月内估计主要 VTE 事件、血栓事件和治疗并发症。采用马尔可夫模型,根据已发表文献,估计复发事件和长期并发症风险。采用已发表文献的 EuroQoL-5 维度效用数据和成本,换算成 2017 年的美元(US$)。结果按每年 3.0%贴现。确定性和概率敏感性分析探索了不确定性。
贝曲西班优于依诺肝素,节省了 784 美元,每位患者的 QALY 增加了 0.017。此外,贝曲西班在所有敏感性分析中均优于依诺肝素,但对效用和 DT 概率最敏感。此外,概率敏感性分析发现,贝曲西班在所有支付意愿阈值上都比依诺肝素更具成本效益。
贝曲西班可用于需要延长住院至出院后 VTE 预防的有 VTE 风险的非外科急性内科疾病患者,具有成本效益。