Landstedt-Hallin Lena, Gundgaard Jens, Ericsson Åsa, Ellfors-Zetterlund Susanne
a Karolinska Institutet, Department of Clinical Sciences, Division of Medicine , Danderyd Hospital , Stockholm , Sweden.
b Novo Nordisk A/S , Søborg, Denmark.
Curr Med Res Opin. 2017 Apr;33(4):647-655. doi: 10.1080/03007995.2016.1277194. Epub 2017 Jan 20.
Health economic analysis from a healthcare and societal point of view was conducted to assess the cost-effectiveness of insulin degludec (IDeg) after switching from other basal insulins in people with type 1 diabetes.
This was a prospective, open-label, single arm, observational follow-up from August 2013 to October 2015 of 476 consecutive patients at Danderyd Hospital (Stockholm, Sweden) who switched to IDeg from other basal insulins (99% basal insulin analogs). The IMS CORE Diabetes Model (CDM) was used to predict the cost-effectiveness of life-long treatment with IDeg vs. other basal insulins, based on a Swedish setting.
Mean (SD) duration of follow-up was 21.7 (6.0) weeks. Mean HbA decreased by 2.7 mmol/mol, mean basal insulin dose decreased by 13.1% (p < .0001), and mean bolus insulin dose decreased by 7.5% (p < .0001) after switching. Frequencies of non-severe daytime hypoglycemia and non-severe nocturnal hypoglycemia decreased by 12% (p = .0127) and 53% (p < .0001) respectively and severe hypoglycemia was reduced by 62% (p = .0225). The CDM predicted a gain in life expectancy of 0.33 years, a discounted gain in quality-adjusted life-years (QALYs) of 0.54, and lower estimated direct lifetime healthcare costs of SEK 22,757 for patients switching to IDeg. The incremental cost-effectiveness ratio (ICER) showed IDeg as dominant (i.e. higher effectiveness with a lower cost). Sensitivity analyses confirmed the results.
Based on this prospective, real-world, follow-up and using the CDM, it was estimated that switching to IDeg from other basal insulins translated into QALY gains including improved life expectancy and health-related quality of life, as well as dominant ICER, meaning cost-savings for the healthcare system. However, the study is limited by its observational design. Extrapolation into the future is only estimated since the actual treatment effect cannot be projected with certainty.
从医疗保健和社会角度进行健康经济分析,以评估1型糖尿病患者从其他基础胰岛素转换为德谷胰岛素(IDeg)后的成本效益。
这是一项前瞻性、开放标签、单臂观察性随访研究,于2013年8月至2015年10月对瑞典斯德哥尔摩丹德吕德医院连续476例从其他基础胰岛素(99%为基础胰岛素类似物)转换为IDeg的患者进行。基于瑞典的情况,使用IMS核心糖尿病模型(CDM)预测IDeg与其他基础胰岛素终身治疗的成本效益。
平均(标准差)随访时间为21.7(6.0)周。转换后,平均糖化血红蛋白(HbA)下降2.7 mmol/mol,平均基础胰岛素剂量下降13.1%(p <.0001),平均餐时胰岛素剂量下降7.5%(p <.0001)。非严重日间低血糖和非严重夜间低血糖的发生率分别下降了12%(p = 0.0127)和53%(p <.0001),严重低血糖减少了62%(p = 0.0225)。CDM预测,转换为IDeg的患者预期寿命增加0.33年,质量调整生命年(QALY)的贴现增益为0.54,估计直接终身医疗保健成本降低22,757瑞典克朗。增量成本效益比(ICER)显示IDeg具有优势(即效果更好且成本更低)。敏感性分析证实了结果。
基于这项前瞻性、真实世界的随访研究并使用CDM,估计从其他基础胰岛素转换为IDeg可带来QALY增益,包括预期寿命和健康相关生活质量的改善,以及具有优势的ICER,这意味着医疗保健系统可节省成本。然而,该研究受其观察性设计的限制。由于无法确定预测实际治疗效果,对未来的推断仅为估计值。