急性冠状动脉综合征后的残余风险和复发事件趋势分析:队列研究

Timothy C Shuey, Stephen Voyce, Laney K. Jones, Alicia Johns, Caroline F. deRichemond, Scott A. LeMaire, Braxton Lagerman, Shikhar Agarwal
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引用次数: 0

摘要

背景:目前尚缺乏对急性冠状动脉综合征(ACS)入院后复发主要不良心血管事件(MACE)的残余风险因素进行全面的真实世界分析。本研究的目标是1)描述急性冠状动脉综合征(ACS)后的结果、风险因素和药物处方模式的人群趋势;2)确定与复发性 MACE 相关的因素:对一家大型综合医疗系统在 2015-2021 年间收治的 4884 名 ACS 后患者进行了一项回顾性队列研究,以探讨复发性 MACE(ACS、脑血管事件、全因死亡率和非计划性血管重建)、可改变的风险因素趋势和药物治疗处方模式之间的关系。根据患者在首次住院后是否再次发生 MACE,将其分为两个队列。数据通过程序从电子病历中提取获得。进行了描述性统计。使用广义线性模型评估风险因素趋势,并在时间点之间进行配对比较。结果:ACS 后的中位随访时间为 31.2 个月。28%的患者再次发生MACE。尽管95.9%的患者接受了高强度他汀类药物处方,但仍有40%的患者未达到低密度脂蛋白胆固醇70毫克/分升的目标,仅有11.6%和2.6%的患者分别接受了依折麦布或9型抑制性单克隆抗体。虽然30.0%的患者在所有时间点的甘油三酯均≥150 mg/dL,但≤6%的患者接受了任何非他汀类甘油三酯降低疗法,0.6%的患者接受了伊可新戊酯疗法。持续高甘油三酯血症(≥150 mg/dL)与 ACS 后 6 个月、12 个月和 24 个月的复发性 MACE 相关(p<0.05),这些时间点的相对风险介于 1.20-1.35 之间。结论:这项研究表明,ACS 后需要更全面的护理,以解决残留的心脏代谢风险因素和指定疗法的次优处方模式。需要采取有针对性的策略来解决高甘油三酯血症问题,以降低心血管风险。
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Analysis of Residual Risk and Recurrent Event Trends Following Acute Coronary Syndrome: A Cohort Study
Background: A comprehensive real-world analysis of residual risk factors for recurrent major adverse cardiovascular events (MACE) following hospital admission for acute coronary syndrome (ACS) is lacking. The objectives of this study were: 1) to describe population trends for outcomes, risk factors, and medication prescribing patterns post-ACS and 2) to identify factors associated with recurrent MACE. Methods: A retrospective cohort study of 4,884 post-ACS patients admitted at a large integrated healthcare system between 2015-2021 was performed to investigate the relationship between recurrent MACE (ACS, cerebrovascular events, all-cause mortality, and unplanned revascularization), modifiable risk factor trends, and medical therapy prescribing patterns. Patients were separated into 2 cohorts based upon whether they experienced recurrent MACE following the initial hospitalization. Data were obtained via programmatic extraction from the electronic health record. Descriptive statistics were performed. Generalized linear models were used to assess risk factor trends and pairwise comparisons were performed between time points. Results: Median length of follow-up after ACS was 31.2 months. Recurrent MACE occurred in 28% of patients. Despite 95.9% of all patients receiving prescriptions for high-intensity statins, >40% did not achieve LDL-C goal of <70 mg/dL, and only 11.6% and 2.6% of all patients were prescribed ezetimibe or proprotein convertase subtilisin kexin type 9 inhibiting monoclonal antibodies, respectively. Although >30.0% of patients had triglycerides ≥150 mg/dL at all time points, ≤6% were prescribed any non-statin triglyceride lowering therapy and 0.6% were prescribed icosapent ethyl. Persistent hypertriglyceridemia (≥150 mg/dL) was associated with recurrent MACE at 6-, 12-, and 24-months post-ACS (p<0.05), and the relative risk ranged between 1.20-1.35 at those timepoints. Conclusions: This study demonstrates the need for more comprehensive post-ACS care to address residual cardiometabolic risk factors and suboptimal prescribing patterns for indicated therapies. Targeted strategies are needed to address hypertriglyceridemia for cardiovascular risk reduction.
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