Heart Center and Center for Population Health Research, Turku University Hospital and University of Turku, Turku, Finland.
Turku Clinical Research Center, Turku University Hospital, Turku, Finland.
Eur Heart J Cardiovasc Pharmacother. 2023 Feb 2;9(2):156-164. doi: 10.1093/ehjcvp/pvac064.
Effective statin therapy is a cornerstone of secondary prevention after myocardial infarction (MI). Real-life statin dosing is nevertheless suboptimal and largely determined early after MI. We studied long-term outcome impact of initial statin dose after MI.
Consecutive MI patients treated in Finland who used statins early after index event were retrospectively studied (N = 72 401; 67% men; mean age 68 years) using national registries. High-dose statin therapy was used by 26.3%, moderate dose by 69.2%, and low dose by 4.5%. Differences in baseline features, comorbidities, revascularisation, and usage of other evidence-based medications were adjusted for with multivariable regression. The primary outcome was major adverse cardiovascular or cerebrovascular event (MACCE) within 10 years. Median follow-up was 4.9 years. MACCE was less frequent in high-dose group compared with moderate dose [adjusted hazard ratio (HR) 0.92; P < 0.0001; number needed to treat (NNT) 34.1] and to low dose [adj.HR 0.81; P < 0.001; NNT 13.4] as well as in moderate-dose group compared with low dose (adj.HR 0.88; P < 0.0001; NNT 23.4). Death (adj.HR 0.87; P < 0.0001; NNT 23.6), recurrent MI (adj.sHR 0.91; P = 0.0001), and stroke (adj.sHR 0.86; P < 0.0001) were less frequent with a high- vs. moderate-dose statin. Higher initial statin dose after MI was associated with better long-term outcomes in subgroups by age, sex, atrial fibrillation, dementia, diabetes, heart failure, revascularisation, prior statin usage, or usage of other evidence-based medications.
Higher initial statin dose after MI is dose-dependently associated with better long-term cardiovascular outcomes. These results underline the importance of using a high statin dose early after MI.
有效的他汀类药物治疗是心肌梗死后二级预防的基石。然而,实际生活中的他汀类药物剂量并不理想,并且在很大程度上是在心肌梗死后早期确定的。我们研究了心肌梗死后初始他汀类药物剂量对长期预后的影响。
我们使用国家登记处对芬兰接受他汀类药物治疗的连续心肌梗死患者进行了回顾性研究(N=72401;67%为男性;平均年龄 68 岁),这些患者在指数事件后早期使用了他汀类药物。高剂量他汀类药物治疗的使用率为 26.3%,中剂量为 69.2%,低剂量为 4.5%。使用多变量回归调整了基线特征、合并症、血运重建以及其他循证药物的使用差异。主要结局是 10 年内主要不良心血管或脑血管事件(MACCE)。中位随访时间为 4.9 年。与中剂量组相比,高剂量组的 MACCE 发生率较低[调整后的危险比(HR)0.92;P<0.0001;需要治疗的人数(NNT)34.1],与低剂量组相比,MACCE 发生率也较低[调整后的 HR 0.81;P<0.001;NNT 13.4],与中剂量组相比,低剂量组的 MACCE 发生率也较低[调整后的 HR 0.88;P<0.0001;NNT 23.4]。死亡(调整后的 HR 0.87;P<0.0001;NNT 23.6)、复发性心肌梗死(调整后的 sHR 0.91;P=0.0001)和中风(调整后的 sHR 0.86;P<0.0001)的发生率较低与高剂量他汀类药物相关。在年龄、性别、心房颤动、痴呆、糖尿病、心力衰竭、血运重建、既往他汀类药物使用或其他循证药物使用的亚组中,较高的初始他汀类药物剂量与更好的长期预后相关。
心肌梗死后较高的初始他汀类药物剂量与更好的长期心血管结局呈剂量依赖性相关。这些结果强调了在心肌梗死后早期使用高剂量他汀类药物的重要性。