Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA.
Cardiovasc Drugs Ther. 2018 Oct;32(5):453-461. doi: 10.1007/s10557-018-6816-8.
Patients with diabetes mellitus (DM) have a high risk for cardiovascular disease (CVD) events after an acute myocardial infarction (AMI). High-intensity statins reduce CVD risk following AMI among patients with and without DM.
We determined the proportion of Medicare beneficiaries 66 to 75 years of age taking a low/moderate-intensity statin with (n = 6718) and without (n = 6414) DM who titrated to a high-intensity statin dosage (i.e., atorvastatin 40 or 80 mg, or rosuvastatin 20 or 40 mg) following an AMI hospitalization in 2014-2015. All patients had a pharmacy claim for a statin fill within 365 days prior to, and within 30 days after their AMI hospitalization. We excluded beneficiaries without Medicare fee-for-service coverage including pharmacy benefits during the study period and those with a pharmacy claim for a high-intensity statin prior to their AMI.
The first statin fill following hospital discharge was for a high-intensity dosage among 37.7% and 44.4% of patients with and without DM, respectively. After multivariable adjustment, the risk ratio (RR) for titrating to a high-intensity statin comparing patients with versus without DM was 1.01 (95% CI 0.96, 1.06). Among patients whose first statin fill post-AMI was for a low/moderate-intensity dosage, 7.5% of those with DM titrated to a high-intensity statin within 182 days, compared with 9.2% of those without DM (multivariable-adjusted RR 0.90 [95% CI 0.75, 1.08]).
Most patients taking a low/moderate-intensity statin were not titrated to a high-intensity dosage following AMI irrespective of their diabetes status, potentially leaving substantial residual risk for recurrent CVD events.
糖尿病(DM)患者在急性心肌梗死(AMI)后发生心血管疾病(CVD)事件的风险较高。高强度他汀类药物可降低合并或不合并 DM 的 AMI 患者的 CVD 风险。
我们确定了在 2014-2015 年 AMI 住院期间,66 至 75 岁的 Medicare 受益人中服用低/中强度他汀类药物(n=6718)和未服用(n=6414)DM 的患者中,有多少患者将剂量调整为高强度他汀类药物(即阿托伐他汀 40 或 80mg,或瑞舒伐他汀 20 或 40mg)。所有患者在 AMI 住院前 365 天内和住院后 30 天内均有他汀类药物的配药记录。我们排除了在研究期间没有 Medicare 按服务收费(包括药房福利)覆盖的受益人和在 AMI 之前有高强度他汀类药物配药记录的受益人的患者。
出院后首次开具的他汀类药物中有 37.7%和 44.4%的 DM 患者和非 DM 患者分别为高强度剂量。经多变量调整后,DM 患者与非 DM 患者相比,调整为高强度他汀类药物的风险比(RR)为 1.01(95%置信区间 0.96,1.06)。在首次 AMI 后开具的他汀类药物为低/中强度剂量的患者中,7.5%的 DM 患者在 182 天内调整为高强度他汀类药物,而无 DM 的患者为 9.2%(多变量调整 RR 0.90 [95%置信区间 0.75,1.08])。
大多数服用低/中强度他汀类药物的患者在 AMI 后未调整为高强度剂量,无论其糖尿病状况如何,这可能会使 CVD 事件的复发风险大大增加。