Morady F, DiCarlo L A, Baerman J M, de Buitleir M
Am J Cardiol. 1986 Jun 1;57(15):1269-73. doi: 10.1016/0002-9149(86)90203-1.
Coupling intervals of extrastimuli that induced 57 previously documented unimorphic ventricular tachycardias (VTs) were compared with coupling intervals that induced 57 episodes of polymorphic VT or ventricular fibrillation (VF) in patients without a documented or suspected history of polymorphic VT or VF. Programmed stimulation was performed with the patient in the drug-free state, with 1 to 3 extrastimuli and 2 basic drive cycle lengths (600 or 500 ms, and 400 ms) at 2 right ventricular sites; stimuli were twice diastolic threshold. The mean coupling intervals of the first, second and third extrastimuli that induced nonclinical VT/VF (241 +/- 19, 185 +/- 19 and 173 +/- 24 ms, respectively, mean +/- standard deviation) were significantly shorter than the corresponding coupling intervals that induced the clinical VTs (266 +/- 25, 228 +/- 32 and 214 +/- 27 ms, respectively, p less than 0.001 for each). Regardless of the basic drive cycle length, the shortest coupling interval required to induce a clinical VT was 180 ms. Depending on the drive cycle length, 29 to 70% of nonclinical VT/VF induced by 3 extrastimuli required a coupling interval of less than 180 ms to induce. Therefore, a lower limit of coupling intervals may be identified below which only nonclinical VT/VF is induced by programmed stimulation. Restriction of coupling intervals to this lower limit may allow for significant improvement in specificity without compromise in the sensitivity of programmed ventricular stimulation protocols.
将诱发57例先前记录的单形性室性心动过速(VT)的期外刺激的耦合间期,与诱发57例多形性VT或室颤(VF)发作的耦合间期进行比较,这些患者无多形性VT或VF的记录或疑似病史。在患者处于无药状态下进行程序刺激,在右心室两个部位施加1至3个期外刺激和2个基础驱动周期长度(600或500毫秒以及400毫秒);刺激强度为舒张期阈值的两倍。诱发非临床VT/VF的第一、第二和第三期外刺激的平均耦合间期(分别为241±19、185±19和173±24毫秒,均值±标准差)显著短于诱发临床VT的相应耦合间期(分别为266±25、228±32和214±27毫秒,每组p均小于0.001)。无论基础驱动周期长度如何,诱发临床VT所需的最短耦合间期为180毫秒。根据驱动周期长度,由3个期外刺激诱发的非临床VT/VF中有29%至70%需要小于180毫秒的耦合间期来诱发。因此,可以确定一个耦合间期下限,低于该下限,程序刺激仅诱发非临床VT/VF。将耦合间期限制在该下限可能会在不损害程序心室刺激方案敏感性的情况下显著提高特异性。