Abushanab Dina, Al-Badriyeh Daoud, Liew Danny, Ademi Zanfina
School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia; Drug Information Department, Hamad Medical Corporation, Doha, Qatar.
College of Pharmacy, QU Health, Qatar University, Doha, Qatar.
Curr Probl Cardiol. 2022 Jun;47(6):100852. doi: 10.1016/j.cpcardiol.2021.100852. Epub 2021 Apr 6.
Sodium-glucose cotransporter 2 (SGLT2) inhibitors have shown to reduce cardiovascular events and mortality in patients with type 2 diabetes mellitus (T2DM), but they are currently not used as first-line therapy in clinical practice. This study sought to evaluate the cost-effectiveness of first-line empagliflozin plus standard care for patients with newly diagnosed T2DM and existing cardiovascular disease (CVD). A decision-analytic Markov model with one-year cycles and a lifetime time horizon was developed from the perspective of the Qatari healthcare system to compare first-line empagliflozin combined with metformin versus metformin monotherapy for patients aged 50 to 79 years with T2DM and existing CVD. Two health states were considered: 'Alive with CVD and T2DM' and 'Dead'. Patients could experience non-fatal myocardial infarction, non-fatal stroke, hospitalization for heart failure, hospitalization for unstable angina, and cardiovascular or non-cardiovascular death. Model inputs were ascertained from published and publicly available sources in Qatar. Costs and outcomes were discounted at 3% per annum. Sensitivity analyses were conducted to evaluate parameter uncertainty. The model predicted that adding empagliflozin to current standard care led to additional 1.9 years of life saved (YoLS) and 1.5 quality-adjusted life year (QALYs) per person, and an incremental cost of QAR 56,869 (USD 15,619), which equated to an incremental cost-effectiveness ratio of QAR 30,675 (USD 8,425) per YoLS and QAR 39,245 (USD 10,779) per QALY. Sensitivity analyses showed the findings to be robust. First-line empagliflozin combined with metformin appears to be a cost-effective therapeutic option for patients with T2DM and CVD.
钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂已被证明可降低2型糖尿病(T2DM)患者的心血管事件和死亡率,但目前在临床实践中未被用作一线治疗。本研究旨在评估一线恩格列净加标准治疗方案对新诊断的T2DM合并现有心血管疾病(CVD)患者的成本效益。从卡塔尔医疗保健系统的角度开发了一个为期一年周期、具有终身时间跨度的决策分析马尔可夫模型,以比较一线恩格列净联合二甲双胍与二甲双胍单药治疗对年龄在50至79岁的T2DM合并现有CVD患者的效果。考虑了两种健康状态:“患有CVD和T2DM存活”和“死亡”。患者可能经历非致命性心肌梗死、非致命性中风、因心力衰竭住院、因不稳定型心绞痛住院以及心血管或非心血管死亡。模型输入数据来自卡塔尔已发表和公开可用的资料。成本和结果按每年3%进行贴现。进行敏感性分析以评估参数不确定性。该模型预测,在当前标准治疗中添加恩格列净可使每人额外节省1.9年的生命(YoLS)和1.5个质量调整生命年(QALY),增量成本为56,869卡塔尔里亚尔(15,619美元),这相当于每YoLS的增量成本效益比为30,675卡塔尔里亚尔(8,425美元),每QALY为39,245卡塔尔里亚尔(10,779美元)。敏感性分析表明研究结果具有稳健性。一线恩格列净联合二甲双胍似乎是T2DM合并CVD患者具有成本效益的治疗选择。