Maccabelli Giuseppe, Tsiachris Dimitris, Silberbauer John, Esposito Antonio, Bisceglia Caterina, Baratto Francesca, Colantoni Caterina, Trevisi Nicola, Palmisano Anna, Vergara Pasquale, De Cobelli Francesco, Del Maschio Alessandro, Della Bella Paolo
Arrhythmia Unit and Electrophysiology Laboratories, San Raffaele University Hospital, Milan, Italy
Arrhythmia Unit and Electrophysiology Laboratories, San Raffaele University Hospital, Milan, Italy.
Europace. 2014 Sep;16(9):1363-72. doi: 10.1093/europace/euu017. Epub 2014 Feb 20.
We present clinical, electroanatomical mapping (EAM), imaging, and catheter ablation (CA) strategies in patients with myocarditis-related ventricular tachycardia (VT).
Between January 2010 and July 2012, 26 consecutive patients underwent imaging-guided CA of myocarditis-related ventricular arrhythmias, 23 of 26 using a combined endo-epicardial approach. Segment per segment correspondence of late enhanced (LE) scar localization with EAM scar was assessed in all patients with available uni/bipolar maps (n = 19). Induced VTs were targeted prior to substrate modification. Late potentials (LPs) abolition constituted a procedural endpoint independently from VT inducibility. Clinical monomorphic VT was induced in 15 of 26 patients (57.7%) and was associated with epicardial LPs in 10 of 15, completely abolished in 7 of 10 patients. Of the 10 patients rendered non-inducible VTs were ablated epicardially in 7. Late potentials were also detected in 7 of 11 initially non-inducible patients and completely abolished in 4. After a median follow-up of 23 (15-31) months, 20 of 26 patients (76.9%) remained free from VT recurrence. Bipolar mapping revealed low-voltage scar (<1.5 mV) in 1 patient endocardially and in 14 of 19 epicardially. Unipolar mapping revealed low-voltage scar (<8 mV) in 12 of 19 patients endocardially and in 18 of 19 epicardially. Correspondence of LE scar localization with endocardial bipolar scar was 1%, with endocardial unipolar scar 23.7%, with epicardial bipolar scar 39.8%, and with epicardial unipolar scar 66.2%.
Pre-procedural scar imaging and EAM findings support the necessity of an epicardial approach in patients with prior myocarditis. Epicardial unipolar mapping (<8 mV) is superior in scar identification and CA based on substrate modification is safe and effective in this setting.
我们介绍了心肌炎相关室性心动过速(VT)患者的临床、电解剖标测(EAM)、影像学及导管消融(CA)策略。
2010年1月至2012年7月期间,26例连续患者接受了影像学引导下的心肌炎相关室性心律失常的CA治疗,26例中的23例采用了心内膜-心外膜联合方法。在所有有单极/双极标测图的患者(n = 19)中评估延迟强化(LE)瘢痕定位与EAM瘢痕的逐段对应关系。在进行基质改良之前对诱发的VT进行靶向治疗。消除晚期电位(LP)构成了独立于VT诱发性的手术终点。26例患者中有15例(57.7%)诱发了临床单形性VT,其中15例中的10例与心外膜LP相关,10例患者中的7例完全消除。在10例不能诱发VT的患者中,7例在心外膜进行了消融。在最初11例不能诱发VT的患者中,7例也检测到了晚期电位,4例完全消除。中位随访23(15 - 31)个月后,26例患者中有20例(76.9%)未出现VT复发。双极标测显示1例患者心内膜有低电压瘢痕(<1.5 mV),19例中的14例心外膜有低电压瘢痕。单极标测显示19例患者中有12例心内膜有低电压瘢痕(<8 mV),19例中的18例心外膜有低电压瘢痕。LE瘢痕定位与心内膜双极瘢痕的对应率为1%,与心内膜单极瘢痕的对应率为23.7%,与心外膜双极瘢痕的对应率为39.8%,与心外膜单极瘢痕的对应率为66.2%。
术前瘢痕成像和EAM结果支持既往有心肌炎的患者采用心外膜途径的必要性。心外膜单极标测(<8 mV)在瘢痕识别方面更具优势,基于基质改良的CA在这种情况下是安全有效的。