首页> 外文期刊>PACE: Pacing and clinical electrophysiology >Characterization of the electroanatomic substrate for monomorphic ventricular tachycardia in patients with nonischemic cardiomyopathy.
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Characterization of the electroanatomic substrate for monomorphic ventricular tachycardia in patients with nonischemic cardiomyopathy.

机译:非缺血性心肌病患者单形性室性心动过速的电解剖基底特征。

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摘要

Ventricular arrhythmias are common in the setting of nonischemic cardiomyopathy. The etiology for the cardiomyopathy is frequently not identified and the label of "idiopathic" is applied. Interstitial fibrosis with conduction system involvement and associated left bundle branch block characterizes the disease process in some patients and the mechanism for monomorphic ventricular tachycardia is commonly bundle branch reentry. However, most patients with nonischemic cardiomyopathy have VT due to myocardial reentry and demonstrate marked myocardial fibrosis and electrogram abnormalities. Although patient specific, the overall distribution of electroanatomic abnormalities appears to be equal on the endocardium and epicardium. The extent of electrogram abnormalities appears to parallel arrhythmia presentation and/or inducibility. Patients with sustained uniform morphology VT have the most extensive endocardial and epicardial electrogram abnormalities. Magnetic electroanatomic voltage mapping provides a powerful tool to characterize the location and extent of the arrhythmia substrate. Basal left ventricular myocardial involvement, as indexed by the location of contiguous electrogram abnormalities, is common in patients with sustained VT and left ventricular cardiomyopathy. The relatively equal distribution of electrogram abnormalities on the endocardium and epicardium, and the results of mapping and ablation attempts, suggest that critical parts of the reentrant circuit may be epicardial. Unique features of the electroanatomic substrate associated with cardiomyopathy due to Chagas' disease, sarcoidosis, and arrhythmogenic right ventricular dysplasia are also discussed.
机译:室性心律失常在非缺血性心肌病中很常见。心肌病的病因常常无法确定,并贴上“特发性”标签。伴有传导系统参与的间质纤维化和相关的左束支传导阻滞是某些患者疾病进程的特征,单形性室性心动过速的机制通常是束支折返。然而,大多数非缺血性心肌病患者由于心肌再入而发生室速,并表现出明显的心肌纤维化和心电图异常。尽管是患者特定的,但在心内膜和心外膜上,电解剖异常的总体分布似乎是相等的。电描记图异常的程度似乎与并行的心律不齐表现和/或可诱导性有关。持续性统一形态室速的患者具有最广泛的心内膜和心外膜电图异常。电磁解剖电压映射提供了一个强大的工具来表征心律不齐基质的位置和范围。持续性VT和左心室心肌病的患者常见于基础左心室心肌受累,以连续的电描记图异常的位置为指标。心电图异常在心内膜和心外膜上的相对均等分布以及映射和消融尝试的结果表明,折返回路的关键部位可能是心外膜。还讨论了由于恰加斯氏病,结节病和致心律失常的右心室发育不良所致的心肌病相关的电解剖基底的独特特征。

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