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应激性心肌病:一种酷似急性心肌梗死的急性可逆性心肌病。

Takotsubo cardiomyopathy: an acute and reversible cardiomyopathy mimicking acute myocardial infarction.

作者信息

Middlemost Shirley, Mabin Thomas

机构信息

Vergelegen Medi-Clinic, Somerset West, Western Cape.

出版信息

Cardiovasc J Afr. 2008 Jan-Feb;19(1):33-8.

PMID:18320087
Abstract

Takotsubo cardiomyopathy is an acute, reversible form of left ventricular dysfunction precipitated by emotional or physical stress. The condition is important to recognise as it mimics acute myocardial infarction and acute coronary syndrome. Most patients are female and postmenopausal. Presenting symptoms include severe chest pain, acute dyspnoea, hypotension or even cardiogenic shock. The ECG changes are suggestive of an acute coronary syndrome with T-wave inversion with/without ST elevation, most often in the precordial leads. The syndrome is characterised by a sudden onset of transient extensive akinesia of the left ventricle, often involving all three major coronary artery territories, in the absence of significant coronary artery stenosis. The wall motion typically involves the apex of the left ventricle with hyperkinesis of the base of the heart. Variant forms have recently been described where the wall motion abnormality involves the mid-ventricular wall with hyperkinesis of the base and apex, or the base of the heart with hyperkinesis of the apex. Characteristically, there is only a limited release of cardiac enzymes disproportionate to the extent of regional wall motion abnormality. Transient right ventricular dysfunction may occur and is associated with more complications, longer hospitalisation and worse left ventricular systolic dysfunction. Serial echocardiography is useful to document improvement in cardiac function. The pathogenesis is unclear. Transient mid-cavity obstruction has been invoked with subsequent myocardial stunning in the akinetic segments. Treatment is supportive. The most effective long-term management remains to be defined. Although the prognosis is good with recovery of ventricular function at about three weeks, some patients have died. The syndrome may recur.

摘要

应激性心肌病是一种由情绪或身体应激诱发的急性、可逆性左心室功能障碍形式。认识到这种疾病很重要,因为它可模仿急性心肌梗死和急性冠状动脉综合征。大多数患者为绝经后女性。临床表现包括严重胸痛、急性呼吸困难、低血压甚至心源性休克。心电图改变提示急性冠状动脉综合征,表现为T波倒置伴/不伴ST段抬高,最常见于胸前导联。该综合征的特征是左心室突然出现短暂的广泛运动减弱,常累及所有三个主要冠状动脉供血区域,而无明显冠状动脉狭窄。室壁运动通常累及左心室心尖,同时心底运动增强。最近描述了一些变异形式,其中室壁运动异常累及心室中层,心底和心尖运动增强,或者心底运动增强而心尖运动增强。其特点是心肌酶释放有限,与局部室壁运动异常程度不成比例。可能会出现短暂性右心室功能障碍,且与更多并发症、更长住院时间和更严重的左心室收缩功能障碍相关。系列超声心动图有助于记录心脏功能的改善情况。其发病机制尚不清楚。有人提出短暂性心腔中部梗阻,随后在运动减弱节段出现心肌顿抑。治疗以支持治疗为主。最有效的长期管理方法仍有待确定。虽然约三周时心室功能恢复,预后良好,但仍有一些患者死亡。该综合征可能复发。

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