Department of Cardiology, Angiology and Pneumology, Heidelberg University Hospital, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.
DZHK (German Centre for Cardiovascular Research), Partner Site Heidelberg/Mannheim, Heidelberg, Germany.
Clin Res Cardiol. 2024 Mar;113(3):446-455. doi: 10.1007/s00392-023-02317-x. Epub 2023 Oct 16.
Left ventricular (LV) thrombus formation is a common but potentially serious complication, typically occurring after myocardial infarction. Due to perceived high thromboembolic risk and lack of safety data, stress cardiac magnetic resonance (CMR) imaging especially with dobutamine is usually avoided despite its high diagnostic yield. This study aimed to investigate the characteristics, safety and outcome of patients with LV thrombus undergoing dobutamine or vasodilator stress CMR.
Patients undergoing stress CMR with concomitant LV thrombus were retrospectively included. Risk factors, comorbidities, and previous embolic events were recorded. Periprocedural safety was assessed for up to 48 h following the examination. Major adverse cardiac events (MACE) 12 months before the diagnosis were compared to 12 months after the exam and between patients and a matched control group. Additionally, patients were followed up for all-cause mortality.
95 patients (78 male, 65 ± 10.7 years) were included. Among them, 43 patients underwent dobutamine (36 high-dose, 7 low-dose) and 52 vasodilator stress CMR. Periprocedural safety was excellent with no adverse events. During a period of 24 months, 27 MACE (14.7%) occurred in patients and controls with no statistical difference between groups. During a median follow-up of 33.7 months (IQR 37.6 months), 6 deaths (6.3%) occurred. Type of stress agent, thrombus mobility, or protrusion were not correlated to embolic events or death.
The addition of a stress test to a CMR exam is safe and does increase the generally high cardioembolic event rate in LV thrombus patients. Therefore, it is useful to support reperfusion decision-making.
左心室(LV)血栓形成是一种常见但潜在严重的并发症,通常发生在心肌梗死后。由于认为血栓栓塞风险高且缺乏安全性数据,尽管诊断效果高,但通常避免使用多巴酚丁胺或血管扩张剂负荷心脏磁共振(CMR)成像。本研究旨在调查接受多巴酚丁胺或血管扩张剂负荷 CMR 的 LV 血栓形成患者的特征、安全性和结局。
回顾性纳入接受负荷 CMR 检查并伴有 LV 血栓形成的患者。记录风险因素、合并症和以前的栓塞事件。检查后 48 小时内评估围手术期安全性。比较诊断前 12 个月和诊断后 12 个月的主要不良心脏事件(MACE),并比较患者与匹配对照组之间的 MACE。此外,对所有患者进行全因死亡率随访。
共纳入 95 例患者(78 例男性,65±10.7 岁)。其中,43 例接受多巴酚丁胺(36 例高剂量,7 例低剂量),52 例接受血管扩张剂负荷 CMR。围手术期安全性极佳,无不良事件发生。在 24 个月的时间内,27 例患者(14.7%)和对照组发生 MACE,但组间无统计学差异。在 33.7 个月(IQR 37.6 个月)的中位随访期间,6 例患者(6.3%)死亡。负荷试验类型、血栓活动度或突出度与栓塞事件或死亡无相关性。
在 CMR 检查中增加负荷试验是安全的,确实会增加 LV 血栓形成患者通常较高的心源性栓塞事件发生率。因此,有助于支持再灌注决策。