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首页> 外文期刊>Circulation. Arrhythmia and electrophysiology >Lack of uniform progression of endocardial scar in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy and ventricular tachycardia.
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Lack of uniform progression of endocardial scar in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy and ventricular tachycardia.

机译:心律失常性右室发育异常/心肌病和室性心动过速患者心内膜瘢痕缺乏统一进展。

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BACKGROUND: The endocardial substrate for ventricular arrhythmias in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is thought to be caused by a progressive degenerative process. Many clinical decisions and treatment plans are guided by this pathophysiologic assumption, but the extent of progression of macroscopic endocardial scar and right ventricular (RV) dilatation have not been assessed. METHODS AND RESULTS: Eleven patients with ARVD/C and ventricular tachycardia had 2 detailed sinus rhythm electroanatomic endocardial voltage maps (average, 291+/-122 points per map; range, 114 to 558 points) performed a mean of 57 months apart (minimum, 9 months) as part of ventricular tachycardia ablation procedures. Voltage-defined scar (<1.5 mV) and RV volume were measured by area and volume measurement software and compared. Two of the 11 patients had a clear increase in scar area (47 cm(2); 32 cm(2)) confirmed by visual inspection. The remaining 9 (81%; 95% CI, 48% to 98%) patients had no increase (<10-cm(2) difference) in scar area between studies. In contrast, 10 of the 11 patients had a significant increase in RV volume, with an average increase of 24% (212+/-67 mL to 263+/-52 mL; P< or =0.01). CONCLUSIONS: In patients with ARVD/C and ventricular tachycardia, progressive RV dilatation is the rule, and rapid progression of significant macroscopic endocardial scar occurs in only a subset of patients. These results have important management implications, suggesting that efforts to prevent RV dilatation in this population are needed and that an aggressive substrate-based ablation strategy offers the potential to provide long-term ventricular tachycardia control.
机译:背景:心律失常性右室发育不良/心肌病(ARVD / C)患者的心律失常的心内膜基质被认为是由进行性退行性过程引起的。许多临床决策和治疗计划均以这种病理生理学假设为指导,但是尚未评估宏观心内膜瘢痕和右心室(RV)扩张的程度。方法和结果:11例ARVD / C和室性心动过速患者均制作了2份详细的窦性心律电解剖心内膜电压图(平均每幅图291 +/- 122点;范围114至558点),平均相隔57个月(最低) ,9个月)作为室速消融程序的一部分。通过面积和体积测量软件测量电压定义的疤痕(<1.5 mV)和RV体积并进行比较。通过视觉检查确认,11例患者中有2例疤痕面积明显增加(47 cm(2); 32 cm(2))。其余9例(81%; 95%CI,48%至98%)患者之间的疤痕面积没有增加(差异小于10-cm(2))。相比之下,这11例患者中有10例的RV体积显着增加,平均增加24%(212 +/- 67 mL至263 +/- 52 mL; P <或= 0.01)。结论:在患有ARVD / C和室性心动过速的患者中,进行性RV扩张是规则,并且仅一部分患者会发生明显的宏观心内膜瘢痕。这些结果具有重要的管理意义,表明需要努力预防该人群的RV扩张,并且基于基质的积极消融策略提供了长期控制心室心动过速的潜力。

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