Champagne S, Su J B, Unterseeh T, Elamine S, Elbaz N, Garot P, Dubois-Randé J L, Merlet P, Hittinger L, Teiger E
Fédération de cardiologie, hôpital Henri Mondor, Créteil.
Arch Mal Coeur Vaiss. 2003 Apr;96(4):332-8.
The NOGA-Biosense catheter-based mapping technique has been well studied experimentally in infarction model. However, chronic myocardial ischemia with this new device has not been well explored. Thus, the aim of our study was to assess electromechanical changes in a pig aneroid constricor model. To achieved this aim, ten pigs were studied 21 days after the implantation of an aneroid constrictor around the circumflex artery. Coronary reserve assess by intracoronary Doppler flow wire was reduced in the ischemic lateral area (ILA) compared with the nonischemic zone (NIZ) (1.3 +/- 0.1 in the ILA vs. 2.3 +/- 0.2 in the NSZ; p < 0.01). TM echocardiography was used to evaluate myocardial regional contractility under basal condition and after stress induced by rapid atrial pacing. In stress state, the ischemic zone showed an impaired contractility compared with basal state (wall thickening, 32.7 +/- 7.4% vs. 59.7 +/- 8.6%; p < 0.05) whereas the non ischemic zone did not (53.8 +/- 7.6% vs. 60.8 +/- 10.1%; p = ns). Constrast echography showed a decrease in contrast intensity in subendocardium of the ila compared with the niz (46.2 +/- 16.6 vs. 99.2 +/- 35.6; p = 0.03) in pacing. Ventricular mapping quantified unipolar (UV). bipolar (BV) voltage potentials and endocardial local shortening (LLS) in 9 left ventricular regions. In basal state, electrical potentials were preserved in both zones (UV: 9.1 +/- 1.8 mV in the ischemic vs 11.3 +/- 3.6 mV in the non ischemic zone; p = ns; BV: 4.2 +/- 1.1 mV in the ILA vs. 3.9 +/- 1.5 mV; p = ns). In contrast, LLS was significantly lower in the ischemic compared with non ischemic zone (6.4 +/- 5.4% vs. 17.9 +/- 3.0%, p < 0.001). In conclusion, ventricular mapping with the NOGA-Biosense system can identify the ischemic myocardium. In this pig model, the association of a preserved electrical activity and an impaired mechanical activity characterizes the ischemic myocardium. These findings could be interesting in this model in regard of the new developments of the system in particular in the field of angiogenesis.
基于NOGA - Biosense导管的标测技术已在梗死模型中进行了充分的实验研究。然而,使用这种新设备对慢性心肌缺血的研究尚未充分开展。因此,我们研究的目的是评估猪类无液限流器模型中的机电变化。为实现这一目标,在左旋支动脉周围植入类无液限流器21天后对10头猪进行了研究。与非缺血区(NIZ)相比,通过冠状动脉内多普勒血流导丝评估的缺血侧区(ILA)的冠状动脉储备降低(ILA为1.3±0.1,NSZ为2.3±0.2;p<0.01)。使用组织多普勒超声心动图评估基础状态下以及快速心房起搏诱导应激后的心肌区域收缩力。在应激状态下,与基础状态相比,缺血区的收缩力受损(室壁增厚,32.7±7.4%对59.7±8.6%;p<0.05),而非缺血区则没有(53.8±7.6%对60.8±10.1%;p=无显著性差异)。对比超声心动图显示,在起搏时,与NIZ相比,ILA的心内膜下对比剂强度降低(46.2±16.6对99.2±35.6;p=0.03)。心室标测量化了9个左心室区域的单极(UV)、双极(BV)电压电位和心内膜局部缩短(LLS)。在基础状态下,两个区域的电位均得以保留(UV:缺血区为9.1±1.8mV,非缺血区为11.3±3.6mV;p=无显著性差异;BV:ILA为4.2±1.1mV,NIZ为3.9±1.5mV;p=无显著性差异)。相比之下,与非缺血区相比,缺血区的LLS显著更低(6.4±5.4%对17.9±3.0%,p<0.001)。总之,使用NOGA - Biosense系统进行心室标测可以识别缺血心肌。在这个猪模型中,电活动保留与机械活动受损的关联是缺血心肌的特征。就该系统的新进展而言,尤其是在血管生成领域,这些发现可能具有重要意义。