Wood Stephen, Magliano Dianna J, Bell J Simon, Shaw Jonathan E, Ilomäki Jenni
Centre for Medicine Use and Safety, Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, Melbourne, VIC, Australia.
Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
Front Pharmacol. 2021 Dec 14;12:794273. doi: 10.3389/fphar.2021.794273. eCollection 2021.
To investigate the incidence of, and factors associated with addition and switching of glucose-lowering medications within 12-months of initiating metformin or a sulfonylurea for type 2 diabetes (T2D). We identified 109,573 individuals aged 18-99 years who initiated metformin or a sulfonylurea between July 2013 and April 2015 using Australian National Diabetes Service Scheme (NDSS) data linked with national dispensing data. Cox proportional hazards regression was used to estimate adjusted hazard ratios (HRs) with 95% confidence intervals (CI) for factors associated with time to addition to or switch from metformin or sulfonylurea over a 12-months follow-up. Treatment addition or switching occurred in 18% and 4% of individuals who initiated metformin and in 28% and 13% of individuals who initiated sulfonylureas. Median time to addition was 104 days for metformin and 82 days for sulfonylureas. Median time to switching was 63 days for metformin and 52 days for sulfonylureas. Congestive heart failure, nicotine dependence, end stage renal disease and dispensing of systemic corticosteroids were associated with higher likelihood of treatment additions and switching in individuals initiating metformin. Antipsychotic dispensing was associated with a higher likelihood of treatment addition in individuals initiating sulfonylureas. Women initiating metformin were less likely to receive treatment additions but more likely to switch treatment than men. Nearly one quarter of Australians who initiate treatment for T2D with metformin or sulfonylureas switch or receive additional treatment within 12-months, with those who initiate sulfonylureas more likely to switch or receive additional treatment than those who initiate metformin.
为调查在开始使用二甲双胍或磺脲类药物治疗2型糖尿病(T2D)的12个月内,降糖药物加用及换药的发生率和相关因素。我们利用与国家配药数据相关联的澳大利亚国家糖尿病服务计划(NDSS)数据,识别出109,573名年龄在18 - 99岁之间、于2013年7月至2015年4月开始使用二甲双胍或磺脲类药物的个体。采用Cox比例风险回归分析,估计在12个月随访期内与二甲双胍或磺脲类药物加用或换药时间相关因素的调整风险比(HR)及95%置信区间(CI)。开始使用二甲双胍的个体中,18%加用了药物,4%换用了药物;开始使用磺脲类药物的个体中,28%加用了药物,13%换用了药物。二甲双胍加用药物的中位时间为104天,磺脲类药物为82天。二甲双胍换药的中位时间为63天,磺脲类药物为52天。充血性心力衰竭、尼古丁依赖、终末期肾病和全身性糖皮质激素的配药与开始使用二甲双胍的个体加用药物及换药的可能性较高相关。抗精神病药物配药与开始使用磺脲类药物的个体加用药物的可能性较高相关。开始使用二甲双胍的女性加用药物的可能性较小,但换药的可能性比男性大。近四分之一开始使用二甲双胍或磺脲类药物治疗T2D的澳大利亚人在12个月内换药或接受额外治疗,开始使用磺脲类药物的人比开始使用二甲双胍的人更有可能换药或接受额外治疗。