British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, Scotland.
St James Hospital, Dublin, Ireland.
JAMA Cardiol. 2024 Oct 1;9(10):928-933. doi: 10.1001/jamacardio.2024.2356.
Sudden death is a leading cause of death after acute myocardial infarction (AMI). The Prospective ARNi vs ACE Inhibitor Trial to Determine Superiority in Reducing Heart Failure Events After MI (PARADISE-MI) and Valsartan in Acute Myocardial Infarction (VALIANT) trials enrolled patients with pulmonary congestion and/or left ventricular dysfunction after AMI. Whether the prognosis in such patients has changed over time has not been examined.
To compare the rate of sudden death/resuscitated cardiac arrest (RCA) after AMI in the PARADISE-MI and VALIANT trials.
DESIGN, SETTING, AND PARTICIPANTS: This was a secondary analysis of multicenter randomized clinical trials enrolling patients after AMI. In the primary analysis, the VALIANT cohort was restricted to patients with "PARADISE-MI-like" characteristics (eg, at least 1 augmenting risk factor and no history of heart failure). The baseline characteristics of people in both trials were compared. The VALIANT trial enrolled from December 1998 to June 2001, and the PARADISE-MI trial enrolled between December 2016, and March 2020. The median follow-up in the VALIANT and PARADISE-MI trials was 24.7 and 22 months, respectively. People with AMI, complicated by pulmonary congestion and/or left ventricular dysfunction, were included in the analysis.
Sudden death after AMI.
A total of 5661 patients were included in the PARADISE-MI cohort (mean [SD] age, 63.7 [11.5] years; 4298 male [75.9%]), 9617 were included in the VALIANT (PARADISE-MI-like) cohort (mean [SD] age, 66.1 [11.5] years; 6504 male [67.6%]), and 14 703 patients were included in the VALIANT (total) cohort (mean [SD] age, 64.8 [11.8] years; 10 133 male [68.9%]). In the PARADISE-MI-like cohort of the VALIANT trial, 707 of 9617 participants (7.4%) experienced sudden death/RCA. A total of 148 of 5661 people (2.6%) in the PARADISE-MI trial experienced sudden death/RCA. Sudden death rates were highest in the first month after infarction in both trials: 19.3 (95% CI, 16.4-22.6) per 100 person-years in the VALIANT trial and 9.5 (95% CI, 7.0-12.7) per 100 person-years in the PARADISE-MI trial, and these rates declined steadily thereafter. Compared with the VALIANT cohort, people in the PARADISE-MI trial were more often treated with percutaneous coronary intervention for their qualifying AMI and received a β-blocker, statin, and mineralocorticoid receptor antagonist more frequently.
After AMI, the risk of sudden death/RCA was highest in the first month, declining rapidly thereafter. Results revealed that compared with counterparts from 20 years ago, the rate of sudden death/RCA in patients with a reduced left ventricular ejection fraction and/or pulmonary congestion was 2- to 3-fold lower in people receiving contemporary management. Interventions to further protect people in the highest risk first month after infarction are needed.
ClinicalTrials.gov Identifier: NCT02924727.
急性心肌梗死(AMI)后,猝死是导致死亡的主要原因之一。前瞻性 ARNi 与 ACE 抑制剂试验以确定在 MI 后降低心力衰竭事件的优势(PARADISE-MI)和缬沙坦在急性心肌梗死(VALIANT)试验中招募了 AMI 后出现肺充血和/或左心室功能障碍的患者。尚未研究此类患者的预后是否随时间而改变。
比较 PARADISE-MI 和 VALIANT 试验中 AMI 后猝死/复苏性心脏骤停(RCA)的发生率。
设计、地点和参与者:这是对多中心随机临床试验的二次分析,招募 AMI 后患者。在主要分析中,VALIANT 队列仅限于具有“PARADISE-MI 样”特征的患者(例如,至少有 1 个增强风险因素且无心力衰竭病史)。比较了两项试验中人群的基线特征。VALIANT 试验于 1998 年 12 月至 2001 年 6 月招募,PARADISE-MI 试验于 2016 年 12 月至 2020 年 3 月招募。VALIANT 和 PARADISE-MI 试验的中位随访时间分别为 24.7 个月和 22 个月。包括 AMI 合并肺充血和/或左心室功能障碍的患者。
AMI 后猝死。
共纳入 5661 名 PARADISE-MI 队列患者(平均[SD]年龄,63.7[11.5]岁;4298 名男性[75.9%]),9617 名患者纳入 VALIANT(PARADISE-MI 样)队列(平均[SD]年龄,66.1[11.5]岁;6504 名男性[67.6%]),14703 名患者纳入 VALIANT(总)队列(平均[SD]年龄,64.8[11.8]岁;10133 名男性[68.9%])。在 VALIANT 试验的 PARADISE-MI 样队列中,9617 名参与者中有 707 名(7.4%)经历了猝死/RCA。PARADISE-MI 试验中 5661 人中共有 148 人(2.6%)经历了猝死/RCA。两项试验中,梗死后第一个月的猝死率最高:VALIANT 试验中为每 100 人年 19.3(95%CI,16.4-22.6),PARADISE-MI 试验中为每 100 人年 9.5(95%CI,7.0-12.7),此后稳步下降。与 VALIANT 队列相比,PARADISE-MI 试验中的患者更常接受经皮冠状动脉介入治疗其合格的 AMI,并更频繁地接受β受体阻滞剂、他汀类药物和盐皮质激素受体拮抗剂治疗。
AMI 后,RCA 的猝死风险在第一个月最高,此后迅速下降。结果表明,与 20 年前的患者相比,在接受当代治疗的射血分数降低和/或肺充血患者中,猝死/RCA 的发生率降低了 2 至 3 倍。需要进一步采取干预措施,以保护在梗死后最高风险的第一个月的人群。
ClinicalTrials.gov 标识符:NCT02924727。