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应激(心碎)心肌病的自然病史和广泛的临床表现。

Natural history and expansive clinical profile of stress (tako-tsubo) cardiomyopathy.

机构信息

Hypertrophic Cardiomyopathy Center and Cardiovascular Research Division, Minneapolis Heart Institute Foundation, Minneapolis, Minnesota 55407, USA.

出版信息

J Am Coll Cardiol. 2010 Jan 26;55(4):333-41. doi: 10.1016/j.jacc.2009.08.057.

Abstract

OBJECTIVES

This study was designed to define more completely the clinical spectrum and consequences of stress cardiomyopathy (SC) beyond the acute event.

BACKGROUND

Stress cardiomyopathy is a recently recognized condition characterized by transient cardiac dysfunction with ventricular ballooning.

METHODS

Clinical profile and outcome were prospectively assessed in 136 consecutive SC patients.

RESULTS

Patients were predominantly women (n = 130; 96%), but 6 were men (4%). Ages were 32 to 94 years (mean age 68 +/- 13 years); 13 (10%) were <or=50 years of age. In 121 patients (89%), SC was precipitated by intensely stressful emotional (n = 64) or physical (n = 57) events, including 22 associated with sympathomimetic drugs or medical/surgical procedures; 15 other patients (11%) had no evident stress trigger. Twenty-five patients (18%) were taking beta-blockers at the time of SC events. Three diverse ventricular contraction patterns were defined by cardiovascular magnetic resonance (CMR) imaging, usually with rapid return to normal systolic function, although delayed >2 months in 5%. Right and/or left ventricular thrombi were identified in 5 patients (predominantly by CMR imaging), including 2 with embolic events. Three patients (2%) died in-hospital and 116 (85%) have survived, including 5% with nonfatal recurrent SC events. All-cause mortality during follow-up exceeded a matched general population (p = 0.016) with most deaths occurring in the first year.

CONCLUSIONS

In this large SC cohort, the clinical spectrum was heterogeneous with about one-third either male, <or=50 years of age, without a stress trigger, or with in-hospital death, nonfatal recurrence, embolic stroke, or delayed normalization of ejection fraction. Beta-blocking drugs were not absolutely protective and SC was a marker for increased noncardiac mortality. These data support expanded management and surveillance strategies including CMR imaging and consideration for anticoagulation.

摘要

目的

本研究旨在更全面地定义应激性心肌病(SC)在急性事件之外的临床谱和后果。

背景

应激性心肌病是一种新近被认识的疾病,其特征为短暂性心室功能障碍伴心室球囊样变。

方法

前瞻性评估了 136 例连续 SC 患者的临床特征和结局。

结果

患者主要为女性(n=130;96%),但有 6 例为男性(4%)。年龄为 32 至 94 岁(平均年龄 68±13 岁);13 例(10%)年龄≤50 岁。在 121 例(89%)患者中,SC 由强烈的精神(n=64)或躯体应激(n=57)事件诱发,包括 22 例与拟交感神经药物或医疗/手术有关;15 例其他患者(11%)无明显应激触发因素。25 例(18%)在发生 SC 时正在服用β受体阻滞剂。心血管磁共振(CMR)成像定义了 3 种不同的心室收缩模式,通常迅速恢复正常的收缩功能,尽管有 5%的患者延迟超过 2 个月。5 例患者(主要通过 CMR 成像)发现右心室和/或左心室血栓,包括 2 例有栓塞事件。3 例(2%)患者住院期间死亡,116 例(85%)存活,其中 5%发生非致命性复发性 SC 事件。随访期间全因死亡率超过匹配的一般人群(p=0.016),大多数死亡发生在第一年。

结论

在本大规模 SC 队列中,临床谱呈异质性,约三分之一为男性、≤50 岁、无应激触发因素、或住院期间死亡、非致命性复发、栓塞性脑卒中或射血分数延迟正常。β受体阻滞剂并非绝对保护因素,SC 是心脏外死亡率增加的标志物。这些数据支持扩大管理和监测策略,包括 CMR 成像和考虑抗凝治疗。

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