Association of Hemometabolic Trajectory and Mortality: Insights From the Cardiogenic Shock Working Group Registry

IF 6.7 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Cardiac Failure Pub Date : 2024-10-01 DOI:10.1016/j.cardfail.2024.06.019
WISSAM KHALIFE MD , MANREET K. KANWAR MD , JACOB ABRAHAM MD , SONG LI MD , KEVIN JOHN MD , SHASHANK S. SINHA MD, MSC , ELRIC ZWECK MD , BORUI LI MA , ARTHUR R. GARAN MD , JAIME HERNANDEZ-MONTFORT MD , YIJING ZHANG MA , VAN-KHUE TON MD, PhD , MAYA GUGLIN MD, PhD , RACHNA KATARIA MD , GAVIN W. HICKEY MD , SARASCHANDRA VALLABHAJOSYULA MD , CHLOE KONG MA , MARYJANE FARR MD , JUSTIN FRIED MD , SHELLEY HALL MD , NAVIN K. KAPUR MD
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Abstract

Cardiogenic shock (CS) is a hemodynamic syndrome that can progress to systemic metabolic derangements and end-organ dysfunction. Prior studies have reported hemodynamic parameters at the time of admission to be associated with mortality but hemodynamic trajectories in CS have not been well described. We studied the association between hemodynamic profiles and their trajectories and in-hospital mortality in patients with CS due to heart failure (HF-CS) and acute myocardial infarction (MI-CS). Using data from the large multicenter Cardiogenic Shock Working Group (CSWG) registry, we analyzed hemodynamic data obtained at the time of pulmonary artery catheter (PAC) insertion (dataset at baseline) and at PAC removal or death (dataset at final time point). Univariable regression analyses for prediction of in-hospital mortality were conducted for baseline and final hemodynamic values, as well as the interval change (delta-P). Data was further analyzed based on CS etiology and survival status. A total of 2260 patients with PAC data were included (70% male, age 61 ± 14 years, 61% HF-CS, 27% MI-CS). In-hospital mortality was higher in the MI-CS group (40.1%) compared with HF-CS (22.4%, P < .01). In the HF-CS cohort, survivors exhibited lower right atrial pressure (RAP), pulmonary artery pressure (PAP), cardiac output/index (CO/CI), lactate, and higher blood pressure (BP) than nonsurvivors at baseline. In this cohort, during hospitalization, improvement in metabolic (aspartate transaminase, lactate), BP, hemodynamic (RAP, pulmonary artery pulsatility index [PAPi], pulmonary artery compliance for right-sided profile and CO/CI for left-sided profile), had association with survival. In the MI-CS cohort, a lower systolic BP and higher PAP at baseline were associated with odds of death. Improvement in metabolic (lactate), BP, hemodynamic (RAP, PAPi for right-sided profile and CO/CI for left-sided profile) were associated with survival. In a large contemporary CS registry, hemodynamic trajectories had a strong association with short-term outcomes in both cohorts. These findings suggest the clinical importance of timing and monitoring hemodynamic trajectories to tailor management in patients with CS.
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血液代谢轨迹与死亡率的关系:心源性休克工作组登记册的启示。
心源性休克(CS)是一种血流动力学综合征,可发展为全身代谢紊乱和终末器官功能障碍。先前的研究报告显示,入院时的血流动力学参数与死亡率有关,但对 CS 的血流动力学轨迹还没有很好的描述。我们研究了心力衰竭(HF-CS)和急性心肌梗死(MI-CS)导致的 CS 患者的血液动力学特征及其轨迹与院内死亡率之间的关系。我们利用大型多中心心源性休克工作组(CSWG)登记处的数据,分析了插入肺动脉导管(PAC)时(基线数据集)和拔除 PAC 或死亡时(最终时间点数据集)获得的血液动力学数据。针对基线和最终血流动力学值以及间隔变化(delta-P)进行了预测院内死亡率的单变量回归分析。根据 CS 病因和存活状况对数据进行了进一步分析。共纳入了 2260 名有 PAC 数据的患者(70% 为男性,年龄为 61 ± 14 岁,61% 为高频 CS,27% 为心肌梗死 CS)。MI-CS组的院内死亡率(40.1%)高于HF-CS组(22.4%,P < .01)。在 HF-CS 组群中,与基线时的非幸存者相比,幸存者的右心房压 (RAP)、肺动脉压 (PAP)、心输出量/指数 (CO/CI)、乳酸较低,血压 (BP) 较高。在该队列中,住院期间代谢(天冬氨酸转氨酶、乳酸盐)、血压、血液动力学(RAP、肺动脉搏动指数[PAPi]、右侧肺动脉顺应性和左侧肺动脉顺应性)的改善与存活率有关。在 MI-CS 队列中,基线收缩压较低和肺动脉搏动指数较高与死亡几率有关。代谢(乳酸)、血压、血液动力学(RAP、右侧血压曲线的 PAPi 和左侧血压曲线的 CO/CI)的改善与存活率相关。在一项大型当代 CS 登记中,两个队列的血液动力学轨迹都与短期预后密切相关。这些研究结果表明,对血流动力学轨迹进行计时和监测以调整 CS 患者的治疗方案具有重要的临床意义。
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来源期刊
Journal of Cardiac Failure
Journal of Cardiac Failure 医学-心血管系统
CiteScore
7.80
自引率
8.30%
发文量
653
审稿时长
21 days
期刊介绍: Journal of Cardiac Failure publishes original, peer-reviewed communications of scientific excellence and review articles on clinical research, basic human studies, animal studies, and bench research with potential clinical applications to heart failure - pathogenesis, etiology, epidemiology, pathophysiological mechanisms, assessment, prevention, and treatment.
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