Arai Riku, Murata Nobuhiro, Saito Yuki, Kojima Keisuke, Fukamachi Daisuke, Okumura Yasuo
Division of Cardiology, Department of Medicine, Nihon University School of Medicine.
Circ J. 2024 Oct 2. doi: 10.1253/circj.CJ-24-0522.
The short-term mortality associated with veno-arterial extracorporeal membrane oxygenation combined with the Impella device (termed ECPELLA) for acute myocardial infarction complicated by cardiogenic shock (AMI-CS) remains unclear.
The Japanese Registry for Percutaneous Ventricular Assist Devices (J-PVAD) includes data on all patients treated with an Impella in Japan. We extracted data for 922 AMI-CS patients who underwent ECPELLA support and conducted an exploratory analysis focusing on 30-day mortality. The median age of patients was 69 years, and 83.8% were male. The overall 30-day mortality was 46.1%. Factors associated with mortality included age >80 years, in-hospital cardiac arrest, systolic blood pressure <90 mmHg, serum creatinine >1.5 mg/dL, and serum lactate >4.0 mmol/L. In patients aged >80 years with any of these factors, mortality was significantly higher than in those without, ranging from 57.5% to 64.9%. The J-PVAD score assigns 1 point per predictor, with a C-statistic of 0.620 (95% confidence interval 0.586-0.654). The 30-day mortality was 20.0% for a J-PVAD score of 0, increasing to 70.0% for a score of 5.
The J-PVAD data indicate high short-term mortality in AMI-CS patients treated with ECPELLA, particularly among older patients. Further studies are needed to validate this risk stratification in this patient subset.
静脉-动脉体外膜肺氧合联合Impella装置(称为ECPELLA)用于治疗急性心肌梗死合并心源性休克(AMI-CS)的短期死亡率仍不明确。
日本经皮心室辅助装置注册研究(J-PVAD)纳入了日本所有接受Impella治疗患者的数据。我们提取了922例接受ECPELLA支持的AMI-CS患者的数据,并针对30天死亡率进行了探索性分析。患者的中位年龄为69岁,男性占83.8%。30天总体死亡率为46.1%。与死亡率相关的因素包括年龄>80岁、院内心脏骤停、收缩压<90 mmHg、血清肌酐>1.5 mg/dL以及血清乳酸>4.0 mmol/L。在年龄>80岁且存在上述任何因素的患者中,死亡率显著高于无这些因素的患者,范围为57.5%至64.9%。J-PVAD评分每个预测因素计1分,C统计量为0.620(95%置信区间0.586 - 0.654)。J-PVAD评分为0时,30天死亡率为20.0%,评分为5时则增至70.0%。
J-PVAD数据表明,接受ECPELLA治疗的AMI-CS患者短期死亡率较高,尤其是老年患者。需要进一步研究以验证该患者亚组中的这种风险分层。