Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, VIC, Australia.
Centre for Medicine Use and Safety, Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, Melbourne, VIC, Australia.
Adv Ther. 2019 Nov;36(11):3265-3278. doi: 10.1007/s12325-019-01077-3. Epub 2019 Sep 3.
Non-adherence and non-persistence to diabetes medications are associated with worse clinical outcomes. In this study, we aimed to characterise the 1-year switching, adherence, and persistence patterns among people with diabetes aged 18 years and older prescribed sodium-glucose co-transporter 2 inhibitors (SGLT2is) in Australia.
Using data from Australia's national Pharmaceutical Benefits Scheme (PBS), we identified 11,981 adults (mean age 60.9 years; 40.5% female) newly initiated on SGLT2is (5993 dapagliflozin; 5988 empagliflozin) from September 2015 to August 2017. Adherence was assessed via the proportion of days covered (PDC), persistence was defined as the continuous use of SGLT2i without a gap of ≥ 90 days, and switching was defined as the first change from dapagliflozin to empagliflozin or vice versa. Generalised linear models (GLMs) were used to compare the adherence (PDC = continuous), logistic regression models were used to compare the likelihoods of being adherent (PDC ≥ 0.80), and Cox proportional hazard models were used to compare the likelihoods of persistence and switching between people prescribed empagliflozin and dapagliflozin.
Overall, 65.8% (7879/11,981) of people dispensed SGLT2is were adherent (PDC ≥ 0.80) and 72.1% (8644/11,981) were persistent at 12 months. The mean PDC was 0.79 ± 0.27. The use of empagliflozin was associated with higher adherence (PDC = continuous) [odds ratio (OR) 1.04, 95% confidence interval (CI) 1.03-1.05], being adherent (OR 1.39, 95% CI 1.29-1.51), and persisting for 12 months [hazard ratio (HR) 1.14, 95% CI 1.06-1.22] compared with dapagliflozin. Only 4.3% (509/11,981) of people switched between the SGLT2i. Compared with dapagliflozin, people initiated on empagliflozin were less likely to switch [HR 0.46, 95% CI 0.38-0.55].
A considerable proportion of Australians prescribed SGLT2is were non-adherent or non-persistent. However, empagliflozin was associated with better adherence and persistence rates and a lower likelihood of switching compared with dapagliflozin.
糖尿病药物的不依从和不持续使用与更差的临床结局相关。在这项研究中,我们旨在描述 2015 年 9 月至 2017 年 8 月期间澳大利亚新开始使用钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)的 18 岁及以上糖尿病患者的 1 年转换、依从性和持续使用模式。
我们使用澳大利亚国家药品福利计划(PBS)的数据,确定了 11981 名新开始使用 SGLT2i(达格列净 5993 名;恩格列净 5988 名)的成年人(平均年龄 60.9 岁;40.5%为女性)。通过比例天数覆盖(PDC)来评估依从性,将连续使用 SGLT2i 而没有≥90 天的间隔定义为持续使用,将从达格列净转换为恩格列净或反之的第一次转换定义为转换。使用广义线性模型(GLMs)比较依从性(PDC=连续),使用逻辑回归模型比较依从性(PDC≥0.80)的可能性,使用 Cox 比例风险模型比较恩格列净和达格列净处方患者的持续使用和转换的可能性。
总体而言,7879/11981(65.8%)名使用 SGLT2i 的患者依从性(PDC≥0.80),72.1%(8644/11981)名患者在 12 个月时持续使用。平均 PDC 为 0.79±0.27。与达格列净相比,使用恩格列净与更高的依从性(PDC=连续)[比值比(OR)1.04,95%置信区间(CI)1.03-1.05]、更高的依从性(OR 1.39,95%CI 1.29-1.51)和 12 个月的持续使用[风险比(HR)1.14,95%CI 1.06-1.22]相关。只有 509/11981(4.3%)名患者在 SGLT2i 之间转换。与达格列净相比,起始使用恩格列净的患者转换的可能性更低[HR 0.46,95%CI 0.38-0.55]。
相当比例的澳大利亚 SGLT2i 处方患者不依从或不持续使用。然而,与达格列净相比,恩格列净与更高的依从性和持续率以及更低的转换可能性相关。