Department of Health Research Methods, Evidence, and Impact (HEI), Faculty of Health Sciences, McMaster University, Hamilton, Canada.
Ted Rogers Centre for Heart Research, Toronto General Hospital Research Institute, Toronto, Canada.
J Med Econ. 2021 Jan-Dec;24(1):1318-1326. doi: 10.1080/13696998.2021.2003804.
The present cost-consequence analysis compared estimated hospitalization costs in a Canadian setting with insulin degludec (degludec) versus insulin glargine 100 units/mL (glargine U100) in patients with type 2 diabetes (T2D) at high cardiovascular (CV) risk.
Medical terms were mapped across the different vocabularies, in order to assign unit costs from eligible hospital abstracts in Canadian Institute for Health Information data (International Statistical Classification of Diseases and Related Health Problems, 10 Revision, Canada) to serious adverse events (SAEs; Medical Dictionary for Regulatory Activities) from the randomized DEVOTE trial comparing the two insulins degludec and glargine. Mean annual costs of SAE-related hospitalizations were estimated by treatment, the cost difference (degludec - glargine U100) was bootstrapped to compute confidence intervals (CIs) and -values, and the cost ratio (degludec/glargine U100) was estimated using a Tweedie distribution.
The mean annual cost per patient for SAE-related hospitalizations was 4,074 CAD with degludec and 4,569 CAD with glargine U100 (cost difference: -495, 95% confidence interval [CI]: -966; -24, = .039), for a cost ratio of 0.89 (95% CI: 0.81; 0.98, = .016). Overall, cost ratios from sensitivity analyses varying individual methodological assumptions were consistent with the main analysis. Of the system organ classes from DEVOTE SAEs, were the largest contributor to the costs savings with degludec versus glargine U100.
In patients with T2D at high CV risk, our findings suggest that there are likely to be lower hospitalization costs with degludec versus glargine U100 based on the SAEs observed in DEVOTE and in a Canadian setting.
本成本-后果分析比较了加拿大环境中 2 型糖尿病(T2D)高心血管(CV)风险患者使用胰岛素德谷胰岛素(degludec)与胰岛素甘精 100 单位/毫升(glargine U100)的估计住院费用。
通过映射不同词汇表中的医学术语,将加拿大健康信息研究所数据(国际疾病分类和相关健康问题第十版,加拿大)中合格住院摘要的单位成本分配给比较两种胰岛素德谷胰岛素和甘精的随机 DEVOTE 试验中的严重不良事件(SAE;监管活动医学词典)。通过治疗估计与 SAE 相关的住院费用,通过 bootstrap 计算成本差异(degludec-glargine U100)的置信区间(CI)和 - 值,并使用 Tweedie 分布估计成本比(degludec/glargine U100)。
与 SAE 相关的住院费用,德谷胰岛素患者的年平均费用为 4074 加元,甘精 U100 患者为 4569 加元(成本差异:-495,95%CI:-966;-24, = .039),成本比为 0.89(95%CI:0.81;0.98, = .016)。总的来说,从不同方法假设变化的敏感性分析的成本比与主要分析一致。在 DEVOTE SAE 的系统器官分类中,与 SAE 相关的住院费用节省的最大贡献者是德谷胰岛素与甘精 U100 相比。
在高 CV 风险的 T2D 患者中,我们的研究结果表明,基于 DEVOTE 和加拿大环境中观察到的 SAE,与甘精 U100 相比,德谷胰岛素的住院费用可能更低。