Badianyama Marheb, Mutyaba Arthur, Tsabedze Nqoba
Division of Cardiology, Department of Internal Medicine, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2193, South Africa.
J Cardiovasc Dev Dis. 2025 Jul 24;12(8):282. doi: 10.3390/jcdd12080282.
Despite the increased mortality due to ST-segment elevation myocardial infarction (STEMI) in South Africa (SA), SA lacks comprehensive data on STEMI clinical outcomes. This study aimed to determine the 30-day and one-year all-cause mortality rates of STEMI patients presenting to our hospital. This was a one-year prospective single-centre study of STEMI patients presenting to the Charlotte Maxeke Johannesburg Hospital in SA between December 2021 and August 2023. We compared the baseline clinical characteristics, reperfusion strategies, and in-hospital, 30-day, and one-year clinical outcomes of survivors and non-survivors. This cohort included 378 STEMI participants. The in-hospital, 30-day, and one-year all-cause mortality rates were 6.6% (n = 25), 10.1% (n = 38), and 17.2% (n = 65), respectively. The pharmacoinvasive strategy was the most used reperfusion therapy (n = 150, 39.7%). On adjusted multivariate Cox regression analysis, a Killip class >2 was the strongest independent predictor of 30-day [HR 5.61, 95% CI 2.83-11.12; < 0.001] and one-year all-cause mortality [HR 1.72, 95% CI 1.26-2.34; = 0.001]. Although mortality has increased, our mortality rates were comparable to outcomes from high-income countries but significantly lower than reports from other low- or middle-income countries. Importantly, there were no significant differences in 30-day and one-year survival outcomes between the different reperfusion strategies.
尽管南非因ST段抬高型心肌梗死(STEMI)导致的死亡率有所上升,但南非缺乏关于STEMI临床结局的全面数据。本研究旨在确定我院STEMI患者的30天和1年全因死亡率。这是一项为期一年的前瞻性单中心研究,研究对象为2021年12月至2023年8月期间在南非约翰内斯堡夏洛特·马克塞克医院就诊的STEMI患者。我们比较了幸存者和非幸存者的基线临床特征、再灌注策略以及住院期间、30天和1年的临床结局。该队列包括378名STEMI参与者。住院期间、30天和1年的全因死亡率分别为6.6%(n = 25)、10.1%(n = 38)和17.2%(n = 65)。药物侵入性策略是最常用的再灌注治疗方法(n = 150,39.7%)。在调整后的多变量Cox回归分析中,Killip分级>2是30天[HR 5.61,95%CI 2.83 - 11.12;<0.001]和1年全因死亡率[HR 1.72,95%CI 1.26 - 2.34;= 0.001]的最强独立预测因素。尽管死亡率有所上升,但我们的死亡率与高收入国家的结果相当,但显著低于其他低收入或中等收入国家的报告。重要的是,不同再灌注策略之间的30天和1年生存结局没有显著差异。