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恩格列净与利拉鲁肽治疗2型糖尿病合并已确诊心血管疾病患者的成本效益

The Cost-Effectiveness of Empagliflozin Versus Liraglutide Treatment in People with Type 2 Diabetes and Established Cardiovascular Disease.

作者信息

Ehlers Lars Holger, Lamotte Mark, Monteiro Sofia, Sandgaard Susanne, Holmgaard Pia, Frary Evan C, Ejskjaer Niels

机构信息

Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

IQVIA Real World Solutions, Zaventem, Belgium.

出版信息

Diabetes Ther. 2021 May;12(5):1523-1534. doi: 10.1007/s13300-021-01040-y. Epub 2021 Apr 15.

Abstract

INTRODUCTION

The increasing financial burden associated with diabetes treatment presents a challenge to healthcare systems worldwide. Recently, clinical guidelines have focussed on patients with type 2 diabetes (T2D) and established cardiovascular disease (CVD) and recommend a sodium-glucose co-transporter 2 (SGLT2) inhibitor or a glucagon-like peptide 1 (GLP-1) receptor agonist as second-line treatment after metformin or independently of baseline glycated haemogloblin A1c (HbA1c). In Danish clinical guidelines, empagliflozin and liraglutide are highlighted owing to their positive impact on mortality. Thus, this study aimed to assess the cost-effectiveness of empagliflozin plus standard of care (SoC) versus liraglutide plus SoC in Danish patients with T2D and established CVD using a lifetime and 5-year horizon.

METHODS

The IQVIA Core Diabetes Model (CDM) was calibrated to reproduce the clinical event rates observed in the cardiovascular outcome trial EMPA-REG OUTCOME. Network meta-analysis provided the relative risks for cardiovascular outcomes with empagliflozin versus liraglutide. Microvascular outcomes were predicted by standard CDM risk equations. The relative treatment effect was assumed for 9 years after which treatment was switched to basal-bolus therapy. The CDM was populated with Danish costs of events and drug costs at price-level 2019. Discounting of 4% was applied.

RESULTS

Over a lifetime horizon, CDM projected 9.858 and 9.667 life years, 6.162 and 5.976 quality-adjusted life years (QALY) and DKK 478,026 (€64,079) and DKK 500,025 (€67,027) in total costs for empagliflozin plus SoC and liraglutide plus SoC, respectively. For a 5-year horizon, the results were 4.189 and 4.140 life years, 2.746 and 2.655 QALY, as well as DKK 123,413 (€16,543) and DKK 161,783 (€21,687), respectively. Empagliflozin was the dominant treatment alternative. Sensitivity analyses showed the robustness of these results.

CONCLUSION

The cost-effectiveness analysis suggests that empagliflozin plus SoC is dominant compared to liraglutide plus SoC in Denmark over both lifetime and 5-year horizons.

摘要

引言

糖尿病治疗相关的经济负担日益加重,给全球医疗系统带来了挑战。最近,临床指南聚焦于2型糖尿病(T2D)合并已确诊心血管疾病(CVD)的患者,并推荐钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂或胰高血糖素样肽1(GLP-1)受体激动剂作为二甲双胍之后的二线治疗药物,或独立于基线糖化血红蛋白A1c(HbA1c)使用。在丹麦临床指南中,恩格列净和利拉鲁肽因其对死亡率的积极影响而受到关注。因此,本研究旨在评估恩格列净加标准治疗(SoC)与利拉鲁肽加SoC相比,在丹麦T2D合并已确诊CVD患者中的成本效益,评估期限为终身和5年。

方法

对艾昆纬核心糖尿病模型(CDM)进行校准,以重现心血管结局试验EMPA-REG OUTCOME中观察到的临床事件发生率。网络荟萃分析提供了恩格列净与利拉鲁肽相比的心血管结局相对风险。微血管结局通过标准CDM风险方程进行预测。假设相对治疗效果持续9年,之后治疗转换为基础-餐时胰岛素治疗方案。CDM纳入了2019年价格水平的丹麦事件成本和药物成本。采用4%的贴现率。

结果

在终身评估期限内,CDM预测恩格列净加SoC和利拉鲁肽加SoC的总生命年数分别为9.858年和9.667年,质量调整生命年(QALY)分别为6.162年和5.976年,总成本分别为478,026丹麦克朗(64,079欧元)和500,025丹麦克朗(67,027欧元)。在5年评估期限内,结果分别为4.189年和4.140年生命年,2.746年和2.655年QALY,以及123,413丹麦克朗(16,543欧元)和161,783丹麦克朗(21,68)欧元。恩格列净是主要的治疗选择。敏感性分析表明这些结果具有稳健性。

结论

成本效益分析表明,在丹麦,无论是终身还是5年评估期限内,恩格列净加SoC相比于利拉鲁肽加SoC都具有优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6904/8099952/f2ef0e6ec280/13300_2021_1040_Fig1_HTML.jpg

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