Chinushi M, Tagawa M, Kasai H, Abe A, Taneda K, Washizuka T, Aizawa Y
First Department of Internal Medicine, Niigata University School of Medicine, Japan.
Jpn Heart J. 2000 May;41(3):313-24. doi: 10.1536/jhj.41.313.
To study the role of antitachycardia burst pacing in patients with reentrant pleomorphic ventricular tachycardia (VT) associated with non-coronary artery diseases, the efficacy of antitachycardia pacing and appropriate antitachycardia pacing cycle length were evaluated in each pleomorphic VT morphology of seven patients. Seven patients were included in this study. Clinically documented pleomorphic VTs were reproduced in an electrophysiologic study. For each VT, rapid ventricular pacing was attempted from the apex of the right ventricle at a cycle length which was 20 ms shorter than that of VT and repeated after a decrement of the cycle length in steps of 10 ms until the VT was terminated or accelerated. All 16 VTs could be entrained by the rapid pacing, and 13 of the 16 VTs (81%) were terminated, whereas pacing-induced acceleration was observed in the other 3 VTs of the 3 patients. VT cycle length (VTCL), block cycle length (BCL) which was defined as the longest VT interrupting paced cycle length, %BCL/VTCL and entrainment zone which was defined as VTCL minus BCL, varied in each VT morphology of each patient. In two patients, antitachycardia pacing was effective in all VT morphologies and the maximum difference of the %BCL/VTCL among the pleomorphic VTs was less than 10%. Thus, antitachycardia pacing seemed to be beneficial for these patients. In the other 5 patients, a difference of more than 10% in %BCL/VTCL was observed among the pleomorphic VT morphologies and/or at least one VT morphology showed pacing-induced acceleration. Compared to the 13 terminated VTs, three accelerated VTs had a wide entrainment zone [160 +/- 44 vs 90 +/- 48 ms, p < 0.04] and small %BCL/VTCL [61 +/- 6 vs 77 +/- 11%,p<0.03]. In pleomorphic VTs associated with non-coronary artery diseases, responses to rapid pacing was not uniform; VT might be terminable or accelerated even in the same patient. We need to pay close attention when programming antitachycardia pacing in patients with pleomorphic VT.
为研究抗心动过速猝发起搏在非冠状动脉疾病相关的折返性多形性室性心动过速(VT)患者中的作用,对7例患者每种多形性VT形态的抗心动过速起搏疗效及合适的抗心动过速起搏周期长度进行了评估。本研究纳入了7例患者。在电生理研究中重现了临床记录的多形性VT。对于每种VT,尝试从右心室心尖以比VT周期长度短20 ms的周期长度进行快速心室起搏,并在周期长度每次递减10 ms后重复,直至VT终止或加速。所有16次VT均能被快速起搏拖带,16次VT中的13次(81%)被终止,而在3例患者的另外3次VT中观察到起搏诱发的加速。VT周期长度(VTCL)、定义为最长的VT中断起搏周期长度而得的阻滞周期长度(BCL)、%BCL/VTCL以及定义为VTCL减去BCL的拖带区,在每位患者的每种VT形态中各不相同。在2例患者中,抗心动过速起搏对所有VT形态均有效,多形性VT之间%BCL/VTCL的最大差异小于10%。因此,抗心动过速起搏似乎对这些患者有益。在另外5例患者中,多形性VT形态之间观察到%BCL/VTCL的差异超过10%,和/或至少一种VT形态显示起搏诱发的加速。与13次终止的VT相比,3次加速的VT有较宽的拖带区[(l60±44)对(90±48)ms,p<〇.〇4]和较小的%BCL/VTCL[(61±6)对(77±11)%,p<〇.〇3]。在非冠状动脉疾病相关的多形性VT中,对快速起搏的反应并不一致;即使在同一患者中,VT也可能被终止或加速。在为多形性VT患者设置抗心动过速起搏时,我们需要密切关注。