糖尿病和动脉粥样硬化性心血管疾病患者钠-葡萄糖共转运蛋白2抑制剂的处方模式和相关因素

CMAJ open Pub Date : 2023-05-01 DOI:10.9778/cmajo.20220039
Aya F Ozaki, Dennis T Ko, Alice Chong, Jiming Fang, Clare L Atzema, Peter C Austin, Therese A Stukel, Karen Tu, Jacob A Udell, David Naimark, Gillian L Booth, Cynthia A Jackevicius
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引用次数: 2

摘要

背景:钠-葡萄糖共转运蛋白-2 (SGLT2)抑制剂是2型糖尿病和动脉粥样硬化性心血管疾病(CVD)患者的心脏保护剂。由于人们对SGLT2抑制剂在动脉粥样硬化性心血管疾病中的应用知之甚少,我们研究了SGLT2抑制剂的处方趋势,并确定了处方模式中的潜在差异。方法:2016年4月至2020年3月,我们在加拿大安大略省开展了一项观察性研究,使用相关的基于人群的健康数据,研究对象是65岁及以上伴有2型糖尿病和动脉粥样硬化性心血管疾病的患者。为了检查SGLT2抑制剂(canagliflozin, dapagliflozin和empagliflozin)的流行处方,我们从4月1日至3月31日(2016/17,2017/18,2018/19和2019/20)构建了4个横断面年度队列。我们按年度和亚组估计了SGLT2抑制剂处方的流行情况,并使用多变量logistic回归确定了与SGTL2抑制剂处方相关的因素。结果:我们的整个队列中有208 303例患者(中位年龄74.0岁[四分位数间距68.0-80.0岁],其中132 196例(63.5%)为男性)。尽管SGLT2抑制剂的处方随着时间的推移而增加,从7.0%增加到20.1%,他汀类药物的处方最初是SGLT2抑制剂处方的10倍,后来是SGLT2抑制剂处方的3倍。在2019/20年度,75岁及以上人群的SGLT2抑制剂处方比75岁以下人群低约50% (12.9% vs . 28.3%, p < 0.001),女性比男性低约50% (15.3% vs . 22.9%, p < 0.001)。年龄75岁及以上、女性、心力衰竭和肾脏疾病史以及低收入是SGLT2抑制剂处方减少的独立因素。在内科专家中,看内分泌科医生和家庭医生比看心脏病科医生更能影响SGLT2抑制剂的处方。我们发现在2019/20年度,每5名糖尿病和动脉粥样硬化性心血管疾病患者中就有1名使用SGLT2抑制剂,而每5名患者中有4名使用他汀类药物。尽管SGLT2抑制剂的处方在研究期间有所增加,但在年龄、性别、社会经济地位、合并症和医生专业方面的差异仍然存在。
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Prescribing patterns and factors associated with sodium-glucose cotransporter-2 inhibitor prescribing in patients with diabetes mellitus and atherosclerotic cardiovascular disease.

Background: Sodium-glucose cotransporter-2 (SGLT2) inhibitors are cardioprotective agents in patients with type 2 diabetes mellitus and atherosclerotic cardiovascular disease (CVD). Since little is known about their uptake in atherosclerotic CVD, we examined SGLT2 inhibitor prescribing trends and identified potential disparities in prescribing patterns.

Methods: We conducted an observational study using linked population-based health data in Ontario, Canada, from April 2016 to March 2020 of patients aged 65 years or older with concomitant type 2 diabetes and atherosclerotic CVD. To examine prevalent prescribing of SGLT2 inhibitors (canagliflozin, dapagliflozin and empagliflozin), we constructed 4 cross-sectional yearly cohorts from Apr. 1 to Mar. 31 (2016/17, 2017/18, 2018/19 and 2019/20). We estimated prevalent SGLT2 inhibitor prescribing by year and by subgroups, and identified factors associated with SGTL2 inhibitor prescribing using multivariable logistic regression.

Results: There were 208 303 patients in our overall cohort (median age 74.0 yr [interquartile range 68.0-80.0 yr], 132 196 [63.5%] male). Although SGLT2 inhibitor prescribing increased over time, from 7.0% to 20.1%, statin prescribing was initially 10-fold higher and later threefold higher than SGLT2 inhibitor prescribing. In 2019/20, SGLT2 inhibitor prescribing was roughly 50% lower among those aged 75 years or older than among those younger than 75 years (12.9% v. 28.3%, p < 0.001) and in women than in men (15.3% v. 22.9%, p < 0.001). Age 75 years or older, female sex, history of heart failure and kidney disease, and low income were independent factors of lower SGLT2 inhibitor prescribing. Among physician specialists, visits to endocrinologists and family physicians were stronger factors of SGLT2 inhibitor prescribing than cardiologist visits.

Interpretation: We found that 1 in 5 patients with diabetes and atherosclerotic CVD were prescribed SGLT2 inhibitors in 2019/20, whereas statins were prescribed for 4 of every 5 patients. Although SGLT2 inhibitor prescribing increased over the study period, disparities in adoption by age, sex, socioeconomic status, comorbidities and physician specialty remained.

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