Bell Kelly F, Cappell Katherine, Liang Michael, Kong Amanda M
The time of study, a Director, Health Economics and Outcomes Research, AstraZeneca, Wilmington, DE.
Director, Custom Data Analytics, Truven Health Analytics, an IBM Company, Ann Arbor, MI.
Am Health Drug Benefits. 2017 Jun;10(4):165-174.
Patients with type 2 diabetes treated with pharmacotherapy should be adherent to and persistent with their medications to experience glycemic control and prevent associated complications.
To compare medication adherence and persistence among patients with type 2 diabetes who are newly initiating a sodium-glucose cotransporter 2 (SGLT-2) inhibitor or a sulfonylurea.
This was a retrospective, observational cohort study using the MarketScan claims databases. The patients who were selected for the study had newly initiated treatment with an SGLT-2 inhibitor or a sulfonylurea between January 1, 2015, and December 31, 2015 (index date; class of earliest medication is defined as the index class); were aged ≥18 years on the index date; were continuously enrolled with health insurance for 12 months before and 6 months after (ie, follow-up) the index date; and had ≥1 baseline diagnoses of type 2 diabetes. Study exclusions were type 1 diabetes, pregnancy, and gestational diabetes. Medication adherence was measured by the proportion of days covered (PDC) with the index class during the follow-up period and dichotomized as adherent (PDC ≥80%) or nonadherent. Persistence was defined as the number of days from the index date until a >60-day continuous gap in days without the index drug class (ie, discontinuation) or the end of follow-up. A propensity score model was used to match patients receiving an SGLT-2 inhibitor to patients receiving a sulfonylurea in a 1:1 ratio based on patient characteristics. Logistic (ie, adherence) and Cox (ie, persistence) regression models were fit to the matched samples.
Initially, the study included 17,724 patients who received an SGLT-2 inhibitor and 25,490 patients who received a sulfonylurea. After propensity score matching, 13,657 patients remained in each cohort. Compared with patients receiving a sulfonylurea, a statistically significantly greater percentage of patients receiving an SGLT-2 inhibitor were adherent to therapy (61.4% vs 53.9%, respectively; odds ratio of adherence, 1.364; 95% confidence interval [CI], 1.30-1.43; <.001) and persistent (76.1% vs 68.9%, respectively; hazard ratio of discontinuation, 0.746; 95% CI, 0.71-0.78; <.001).
Maintaining adherence to and persistence with antidiabetes medication is vital to glycemic control among patients with type 2 diabetes. In this real-world study, patients who newly initiated treatment with SGLT-2 inhibitors were more likely to adhere to treatment and persist with the initiated therapy than similar patients who newly initiated treatment with sulfonylureas.
接受药物治疗的2型糖尿病患者应坚持并持续用药,以实现血糖控制并预防相关并发症。
比较新开始使用钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂或磺脲类药物的2型糖尿病患者的用药依从性和持续性。
这是一项使用MarketScan理赔数据库的回顾性观察性队列研究。入选本研究的患者在2015年1月1日至2015年12月31日期间新开始使用SGLT-2抑制剂或磺脲类药物(索引日期;最早用药类别定义为索引类别);在索引日期时年龄≥18岁;在索引日期前12个月和索引日期后6个月(即随访期)连续参加医疗保险;并且有≥1次2型糖尿病的基线诊断。研究排除标准为1型糖尿病、妊娠和妊娠期糖尿病。用药依从性通过随访期内索引类别药物的覆盖天数比例(PDC)来衡量,并分为依从(PDC≥80%)或不依从。持续性定义为从索引日期到无索引药物类别连续间隔>60天(即停药)或随访结束的天数。使用倾向评分模型根据患者特征将接受SGLT-2抑制剂的患者与接受磺脲类药物的患者按1:1比例进行匹配。将逻辑回归(即依从性)和Cox回归(即持续性)模型应用于匹配后的样本。
最初,该研究纳入了17724例接受SGLT-2抑制剂的患者和25490例接受磺脲类药物的患者。倾向评分匹配后,每个队列中仍有13657例患者。与接受磺脲类药物的患者相比接受SGLT-2抑制剂的患者中,在治疗依从性方面,统计学上显著更高比例的患者为依从(分别为61.4%和53.9%;依从性比值比,1.364;95%置信区间[CI],1.30 - 1.43;P<.001),在持续性方面(分别为76.1%和68.9%;停药风险比,0.746;95% CI,0.71 - 0.78;P<.001)。
维持抗糖尿病药物的依从性和持续性对于2型糖尿病患者的血糖控制至关重要。在这项真实世界研究中,新开始使用SGLT-2抑制剂治疗的患者比新开始使用磺脲类药物治疗的类似患者更有可能坚持治疗并持续接受起始治疗。