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反向性应激性心肌病:全面综述

Reverse Takotsubo cardiomyopathy: a comprehensive review.

作者信息

Awad Hamza H, McNeal Ashley R, Goyal Hemant

机构信息

Department of Community Medicine/Internal Medicine, Mercer University School of Medicine, Macon, GA, USA.

Medical Student, Mercer University School of Medicine, Macon, GA, USA.

出版信息

Ann Transl Med. 2018 Dec;6(23):460. doi: 10.21037/atm.2018.11.08.

Abstract

Takotsubo cardiomyopathy (TTC) was first described in Japan in the 1980s. It is described as an acute but often reversible left ventricular (LV) dysfunction mainly triggered by emotional or physical stress. Multiple variants of TTC have been reported including reverse Takotsubo cardiomyopathy (rTTC) which is a variant characterized by the basal akinesis/hypokinesis associated with apical hyperkinesis that resolves spontaneously. The hallmark of rTTC is a clinical presentation similar to an acute coronary syndrome (ACS), with no evident obstructive coronary artery disease. The incidence of TTC is estimated to be 2% of all troponin-positive patients presenting with suspected ACS. The proportion of patients presenting with the rTTC variant out of all TTC patients in published literature has been variable, ranging from 1-23%. Reverse Takotsubo has been associated with younger age, less decrease in left ventricular ejection fraction (LVEF), and more neurological disease compared to the TTC. While the exact mechanism of rTTC is unknown, hypothesized mechanisms include catecholamine cardiotoxicity, coronary artery spasm, coronary microvasculature impairment, and estrogen deficiency. Patients with rTTC typically present with chest pain and/or dyspnea after an emotional or physically stressful event. rTTC can also be triggered by intracranial hemorrhage, general anesthesia, or neurological conditions. Diagnosis of rTTC requires the presence of LV basal hypokinesis/akinesis, new electrocardiogram (EKG) abnormalities or elevated cardiac troponin, and absence of obstructive coronary disease, pheochromocytoma, or myocarditis. Management of rTTC is similar to that of TTC, which is predominantly supportive with the treatment of complications. The recurrence rate of rTTC is around 10%. The most common complications of rTTC include myocarditis, pleural and pericardial effusions, and development of LV thrombi. The best predictors of mortality include decreased LVEF, development of atrial fibrillation, and neurologic disease.

摘要

应激性心肌病(TTC)于20世纪80年代在日本首次被描述。它被描述为一种主要由情绪或身体应激引发的急性但通常可逆的左心室(LV)功能障碍。已报道了多种TTC变体,包括反转型应激性心肌病(rTTC),这是一种以基底运动减弱/运动减退伴心尖运动增强为特征且可自发缓解的变体。rTTC的标志是临床表现类似于急性冠状动脉综合征(ACS),且无明显的阻塞性冠状动脉疾病。据估计,TTC在所有疑似ACS的肌钙蛋白阳性患者中占2%。在已发表文献中,rTTC变体患者在所有TTC患者中所占比例各不相同,范围为1%至23%。与TTC相比,反转型应激性心肌病与更年轻的年龄、左心室射血分数(LVEF)下降较少以及更多的神经系统疾病相关。虽然rTTC的确切机制尚不清楚,但推测的机制包括儿茶酚胺心脏毒性、冠状动脉痉挛、冠状动脉微血管损伤和雌激素缺乏。rTTC患者通常在情绪或身体应激事件后出现胸痛和/或呼吸困难。rTTC也可由颅内出血、全身麻醉或神经系统疾病引发。rTTC的诊断需要存在左心室基底运动减退/运动不能、新的心电图(EKG)异常或心肌肌钙蛋白升高,且无阻塞性冠状动脉疾病、嗜铬细胞瘤或心肌炎。rTTC的管理与TTC相似,主要是支持性治疗并处理并发症。rTTC的复发率约为10%。rTTC最常见的并发症包括心肌炎、胸腔和心包积液以及左心室血栓形成。死亡率的最佳预测因素包括LVEF降低、房颤的发生和神经系统疾病。

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