Nguyen Hiep, Dufour Robert, Caldwell-Tarr Amanda
Sunovion Pharmaceuticals, Marlborough, MA, USA.
Comprehensive Health Insights, Louisville, KY, USA.
Adv Ther. 2017 Mar;34(3):658-673. doi: 10.1007/s12325-016-0470-y. Epub 2017 Jan 11.
Anti-diabetes medication regimen adherence is a clinical challenge in elderly patients with type 2 diabetes (T2D) and other comorbidities associated with aging. Glucagon-like peptide-1 receptor agonists (GLP-1RA) therapies such as exenatide once weekly (QW), exenatide twice daily (BID), and liraglutide once daily (QD) are an increasingly used class of drugs with proven efficacy and tolerability. Real-world evidence on adherence to GLP-1RAs in elderly or disabled patients is limited. To further the understanding of this drug class, the current study examined medication adherence in Medicare patients aged ≥65 years with T2D initiating a GLP-1RA.
This retrospective cohort study used medical and pharmacy claims between 2010 and 2013 for Medicare members in a United States health plan diagnosed with T2D who were new initiators of either exenatide QW (n = 537), exenatide BID (n = 923), or liraglutide QD (n = 3,673). Included patients were between the ages of 65 and 89 and were continuously enrolled for 6 months pre- and post-index. Medication adherence was examined during the post-index period using proportion of days covered (PDC) ≥80% and ≥90%.
A significantly higher percentage of patients receiving exenatide QW had a PDC ≥80% (43.2%) versus exenatide BID (39.0%, P < 0.01) and liraglutide QD (35.0%, P < 0.001). The patients receiving exenatide QW were significantly more likely to reach a PDC of ≥90% (37.2%, P < 0.001) than those initiating exenatide BID (20.6%) or liraglutide QD (23.3%).
While results from this retrospective study suggest room for improvement in adherence to GLP-1RAs, medication adherence rates for patients initiating therapy with exenatide QW were higher than patients initiating therapy with exenatide BID or liraglutide QD. Further research is needed to validate these findings in other T2D patient populations.
AstraZeneca Pharmaceuticals.
对于患有2型糖尿病(T2D)以及其他与衰老相关合并症的老年患者而言,坚持抗糖尿病药物治疗方案是一项临床挑战。胰高血糖素样肽-1受体激动剂(GLP-1RA)疗法,如每周一次的艾塞那肽(QW)、每日两次的艾塞那肽(BID)以及每日一次的利拉鲁肽(QD),是一类使用日益广泛的药物,其疗效和耐受性已得到证实。关于老年或残疾患者坚持使用GLP-1RA的真实世界证据有限。为了进一步了解这类药物,本研究调查了年龄≥65岁、开始使用GLP-1RA的T2D医疗保险患者的药物依从性。
这项回顾性队列研究使用了2010年至2013年期间美国一家健康计划中被诊断为T2D且新开始使用艾塞那肽QW(n = 537)、艾塞那肽BID(n = 923)或利拉鲁肽QD(n = 3673)的医疗保险参保者的医疗和药房理赔数据。纳入的患者年龄在65岁至89岁之间,在索引前后连续参保6个月。在索引后期间,使用覆盖天数比例(PDC)≥80%和≥90%来检查药物依从性。
接受艾塞那肽QW治疗的患者中,PDC≥80%的比例(43.2%)显著高于接受艾塞那肽BID治疗的患者(39.0%,P < 0.01)和接受利拉鲁肽QD治疗的患者(35.0%,P < 0.001)。与开始使用艾塞那肽BID(20.6%)或利拉鲁肽QD(23.3%)的患者相比,接受艾塞那肽QW治疗的患者达到PDC≥90%的可能性显著更高(37.2%,P < 0.001)。
虽然这项回顾性研究的结果表明在坚持使用GLP-1RA方面仍有改进空间,但开始使用艾塞那肽QW治疗的患者的药物依从率高于开始使用艾塞那肽BID或利拉鲁肽QD治疗的患者。需要进一步研究以在其他T2D患者群体中验证这些发现。
阿斯利康制药公司。