Bardy G H, Poole J E, Kudenchuk P J, Dolack G L, Kelso D, Mitchell R
Department of Medicine, University of Washington, Seattle.
Circulation. 1993 Jun;87(6):1889-96. doi: 10.1161/01.cir.87.6.1889.
Multiprogrammable antiarrhythmia devices can treat monomorphic ventricular tachycardia (VT) with autodecremental overdrive pacing and/or with low-energy cardioversion. These two methods provide the opportunity to decrease patient discomfort typically experienced with high-energy pulses. Although both therapies are known to be effective, controversy persists over their relative safety and efficacy.
The purpose of this study was to examine the safety and efficacy of autodecremental overdrive pacing and low-energy cardioversion in reproducibly terminating monomorphic VT in 24 patients with multiprogrammable antiarrhythmia devices. The protocol required that identical ECG morphology VT be reproducibly induced four times to assess the outcome of antitachycardia pacing and cardioversion twice for each patient in a randomized fashion. Each episode of VT was induced via the implanted device. Autodecremental overdrive pacing initially began with seven stimuli at 97% of the VT cycle length, decrementing by 10 msec per stimulus to a minimum coupling interval of 200 msec. If ineffective, autodecremental overdrive pacing was allowed to iterate three more times for a total of four pacing interventions. With each iteration, one stimulus was added to the pacing train. Similarly, with low-energy cardioversion, up to four therapeutic attempts were made, beginning with a 0.2-J pulse. If ineffective, pulse energy was increased to 0.4, 1.0, and finally 2.0 J. All interventions were automatic without human interference. VT (cycle length, 306 +/- 42 msec) was repeatedly terminated in 15 of 24 patients (63%) by autodecremental overdrive pacing and in 18 of 24 patients (75%) by low-energy cardioversion (p = 0.53). Eight of the 24 patients (33%) had their VT terminated repeatedly by both therapies. VT accelerated to faster VT or ventricular fibrillation by autodecremental overdrive pacing in four of 24 patients (17%) and by low-energy cardioversion in five of 24 (21%) (p = 0.88). Only one of the 24 patients (4%) accelerated with both therapies. No patient was unaffected by either therapy.
In the manner programmed, autodecremental overdrive pacing and low-energy cardioversion have similar efficacy and acceleration rates. Response to one therapy does not predict response to the other.
多程控抗心律失常装置可通过自动递减超速起搏和/或低能量心脏复律来治疗单形性室性心动过速(VT)。这两种方法为减轻患者通常因高能量脉冲而产生的不适提供了机会。尽管已知这两种治疗方法均有效,但关于它们的相对安全性和疗效仍存在争议。
本研究的目的是检验自动递减超速起搏和低能量心脏复律在24例使用多程控抗心律失常装置的患者中可重复性终止单形性VT的安全性和疗效。该方案要求以可重复性方式诱发相同心电图形态的VT 4次,以便对每位患者的抗心动过速起搏和心脏复律结果进行随机评估,各进行2次。每次VT发作均通过植入装置诱发。自动递减超速起搏最初从以VT周期长度的97%发放7次刺激开始,每次刺激递减10毫秒,直至最小耦合间期为200毫秒。如果无效,允许自动递减超速起搏再重复3次,总共进行4次起搏干预。每次重复时,在起搏序列中增加1次刺激。同样,对于低能量心脏复律,从0.2焦耳的脉冲开始,最多进行4次治疗尝试。如果无效,将脉冲能量增加到0.4、1.0,最后增加到2.0焦耳。所有干预均为自动进行,无需人工干预。24例患者中有15例(63%)通过自动递减超速起搏反复终止VT,18例(75%)通过低能量心脏复律反复终止VT(p = 0.53)。24例患者中有8例(33%)的VT通过两种治疗方法均反复终止。24例患者中有4例(17%)的VT通过自动递减超速起搏加速为更快的VT或心室颤动,24例中有5例(21%)通过低能量心脏复律加速(p = 0.88)。24例患者中只有1例(4%)在两种治疗方法下均加速。没有患者对两种治疗方法均无反应。
按照设定的方式,自动递减超速起搏和低能量心脏复律具有相似的疗效和加速率。对一种治疗方法的反应不能预测对另一种治疗方法的反应。