Department of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota.
Heart Rhythm. 2013 Oct;10(10):1509-15. doi: 10.1016/j.hrthm.2013.06.010. Epub 2013 Jun 14.
Imaging myocardial activation from noninvasive body surface potentials promises to aid in both cardiovascular research and clinical medicine.
To investigate the ability of a noninvasive 3-dimensional cardiac electrical imaging technique for characterizing the activation patterns of dynamically changing ventricular arrhythmias during drug-induced QT prolongation in rabbits.
Simultaneous body surface potential mapping and 3-dimensional intracardiac mapping were performed in a closed-chest condition in 8 rabbits. Data analysis was performed on premature ventricular complexes, couplets, and torsades de pointes (TdP) induced during intravenous administration of clofilium and phenylephrine with combinations of various infusion rates.
The drug infusion led to a significant increase in the QT interval (from 175 ± 7 to 274 ± 31 ms) and rate-corrected QT interval (from 183 ± 5 to 262 ± 21 ms) during the first dose cycle. All the ectopic beats initiated by a focal activation pattern. The initial beat of TdPs arose at the focal site, whereas the subsequent beats were due to focal activity from different sites or 2 competing focal sites. The imaged results captured the dynamic shift of activation patterns and were in good correlation with the simultaneous measurements, with a correlation coefficient of 0.65 ± 0.02 averaged over 111 ectopic beats. Sites of initial activation were localized to be ~5 mm from the directly measured initiation sites.
The 3-dimensional cardiac electrical imaging technique could localize the origin of activation and image activation sequence of TdP during QT prolongation induced by clofilium and phenylephrine in rabbits. It offers the potential to noninvasively investigate the proarrhythmic effects of drug infusion and assess the mechanisms of arrhythmias on a beat-to-beat basis.
从无创体表面电位成像心肌激活有望在心血管研究和临床医学中都有所帮助。
研究一种无创的 3 维心脏电成像技术,以在兔体内氯菲安明和苯肾上腺素诱导的 QT 间期延长期间,对动态变化的室性心律失常的激活模式进行特征描述。
在 8 只闭胸兔中进行同步体表电位图和 3 维心内图描记。在静脉注射氯菲安明和苯肾上腺素时,通过各种输注率的组合,对室性早搏、成对搏动和尖端扭转型室性心动过速(TdP)进行数据分析。
药物输注导致 QT 间期(从 175±7 增加至 274±31 ms)和校正 QT 间期(从 183±5 增加至 262±21 ms)在第一剂量循环中显著增加。所有异位搏动均由局灶性激活模式引发。TdP 的初始搏动起源于局灶部位,而随后的搏动则是由于来自不同部位或 2 个竞争局灶部位的局灶性活动所致。成像结果捕捉到激活模式的动态变化,并与同步测量结果有很好的相关性,111 个异位搏动的平均相关系数为 0.65±0.02。初始激活部位定位于距直接测量起始部位约 5mm 处。
3 维心脏电成像技术可定位氯菲安明和苯肾上腺素诱导兔 QT 间期延长时 TdP 的激活起源和激活顺序。它提供了一种无创性研究药物输注致心律失常作用和逐搏评估心律失常机制的潜力。