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奥地利应激性心肌病(心尖球形综合征)。

Stress-induced cardiomyopathy (Tako-Tsubo syndrome) in Austria.

机构信息

Wilhelminenhospital, Vienna, Austria.

出版信息

Eur Heart J Acute Cardiovasc Care. 2013 Jun;2(2):137-46. doi: 10.1177/2048872613483592.

Abstract

BACKGROUND

Tako-Tsubo syndrome (TS) is a still rarely diagnosed clinical syndrome, which is characterized by acute onset of chest pain, transient cardiac dysfunction with (frequently) reversible wall motion abnormalities (WMAs), but with no relevant obstructive coronary artery disease.

METHODS AND RESULTS

Among 179 consecutive patients with proven diagnosis of TS that were retrospectively analysed in this multicentre registry, women represented the majority of patients (94%) while only 11 men (6%) developed TS. Mean age was 69.1±11.5 years (range 35-88 years). Cardinal symptoms of TS, which led to admission, were acute chest pain (82%) and dyspnoea (32%), respectively. All patients demonstrated typical WMAs, whereby four different types of WMAs could be defined: (1) a more common apical type of TS (n=89; 50%); (2) a combined apical and midventricular form of TS (n=23; 13%); (3) the midventricular TS (n=6; 3%); and (4) an unusual type of basal WMAs of the left ventricle (n=3). Only in 101 patients (57%), a clear causative trigger for onset of symptoms could be identified. In-hospital cardiovascular complications occurred in 25 patients (14%) and consisted of cardiac arrhythmias in 10 patients (40%), cardiogenic shock in six patients (24%), cardiac decompensation in eight patients (32%) and cardiovascular death in one patient, respectively. Echocardiographic control of left ventricular function after the initial measurement was available in almost 70% of the patients: complete recovery of WMAs was found in 73 patients (58.87%); 49 patients (39.52%) showed persistent WMAs. Recurrences of TS were only seen in four patients. During the follow-up period, 13 patients died: three of cardiovascular causes and 10 of non-cardiac causes. In-hospital mortality was 0.6%, 30-day mortality was 1.3% and 2-year mortality was 6.7%.

CONCLUSIONS

This study represents to date the largest series of patients suffering from TS in Austria and worldwide. Similar to others, in our series the prevalence of TS was significantly higher in women than in men, while in contrast to other studies, the apical type of TS was detected most frequently. The similar clinical presentation of TS patients to the clinical picture of acute myocardial infarction demonstrates the importance of immediate coronary angiography for adequate differential diagnosis of TS. TS is not necessarily a benign disease due to cardiovascular complications as well as persistent WMAs with delayed recovery.

摘要

背景

心肌应变综合征(Takotsubo 综合征,TS)是一种临床诊断仍较为罕见的综合征,其特征为胸痛急性发作、短暂性心功能障碍伴(常为)可逆性壁运动异常(WMA),但不存在相关的阻塞性冠状动脉疾病。

方法和结果

在这项多中心回顾性研究中,对 179 例确诊为 TS 的连续患者进行了分析,女性占多数(94%),仅有 11 名男性(6%)患有 TS。平均年龄为 69.1±11.5 岁(范围 35-88 岁)。导致住院的 TS 的主要症状分别为急性胸痛(82%)和呼吸困难(32%)。所有患者均表现出典型的 WMA,可定义为 4 种不同类型的 WMA:(1)更常见的 TS 心尖型(n=89;50%);(2)TS 心尖和中段联合型(n=23;13%);(3)中段 TS(n=6;3%);(4)左心室不常见的基底段 WMA 型(n=3)。仅在 101 例患者(57%)中,能够明确识别出症状发作的明确诱因。25 例患者(14%)发生院内心血管并发症,包括 10 例患者(40%)的心律失常、6 例患者(24%)的心源性休克、8 例患者(32%)的心功能不全和 1 例患者的心血管死亡。几乎 70%的患者可获得初始测量后的左心室功能超声心动图检查结果:73 例患者(58.87%)的 WMA 完全恢复;49 例患者(39.52%)存在持续性 WMA。仅在 4 例患者中观察到 TS 复发。在随访期间,13 例患者死亡:3 例心血管原因,10 例非心血管原因。院内死亡率为 0.6%,30 天死亡率为 1.3%,2 年死亡率为 6.7%。

结论

这项研究是迄今为止在奥地利和全球范围内 TS 患者最大系列的研究。与其他研究相似,我们的研究中 TS 在女性中的发病率明显高于男性,而与其他研究不同的是,心尖型 TS 最为常见。TS 患者的临床表现与急性心肌梗死的临床表现相似,这表明立即进行冠状动脉造影对于正确的 TS 鉴别诊断至关重要。由于心血管并发症以及延迟恢复的持续性 WMA,TS 不一定是良性疾病。

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