Bardy G H, Packer D L, German L D, Gallagher J J
Circulation. 1984 Sep;70(3):377-91. doi: 10.1161/01.cir.70.3.377.
During the electrophysiologic study of 435 patients referred for evaluation of Wolff-Parkinson-White syndrome, 42 (10%) had preexcited reciprocating tachycardia (defined as a macro-reentrant tachycardia that used an accessory atrioventricular [AV] pathway for antegrade conduction). The ages of the patients ranged from 9 to 67 years (27 +/- 14). Thirty-three were male patients, nine female, and eight had Ebstein's anomaly. Preexcited reciprocating tachycardia cycle length was 220 to 430 msec (294 +/- 42). Significant hemodynamic compromise in the laboratory directly related to preexcitated reciprocating tachycardia occurred in only one patient. However, in 10 patients a transformation to atrial fibrillation was seen after a spontaneously occurring premature atrial contraction. Only 17 of the 42 patients with preexcited reciprocating tachycardia during electrophysiologic study had the same tachycardia documented clinically. These 17 patients were more often younger with multiple accessory pathways and with no history of orthodromic reciprocating tachycardia when compared with 25 patients in whom preexcited reciprocating tachycardia could be induced only in the laboratory. Preexcited reciprocating tachycardia was induced in the laboratory in 22 of 374 (6%) patients with single accessory pathways and in 20 of 61 (33%) of those with multiple accessory pathways. In the 20 patients with multiple accessory pathways, the spectrum of reentrant circuits included fusion over two or more accessory pathways or fusion over both an accessory pathway and the AV node. In the 22 patients with a single accessory pathway and true antidromic reciprocating tachycardia, all but two episodes were at least 4 cm from the AV node. No patient with true antidromic reciprocating tachycardia had a posterior septal accessory AV pathway. Only in patients with multiple accessory pathways was the posterior septal accessory AV pathway used as the antegrade limb.
在对435例因预激综合征前来评估的患者进行电生理研究期间,42例(10%)发生了预激性折返性心动过速(定义为一种大折返性心动过速,其顺向传导使用一条房室旁道)。患者年龄9至67岁(27±14岁)。男性患者33例,女性9例,8例患有埃布斯坦畸形。预激性折返性心动过速的心动周期长度为220至430毫秒(294±42)。仅1例患者在实验室中出现了与预激性折返性心动过速直接相关的严重血流动力学损害。然而,10例患者在自发房性早搏后出现了房颤转变。在电生理研究期间,42例预激性折返性心动过速患者中只有17例临床上记录到了相同的心动过速。与25例仅在实验室中能诱发预激性折返性心动过速的患者相比,这17例患者更年轻,有多个旁道,且无顺向性折返性心动过速病史。在374例有单个旁道的患者中,22例(6%)在实验室中诱发了预激性折返性心动过速;在61例有多个旁道的患者中,20例(33%)诱发了该心动过速。在20例有多个旁道的患者中,折返环路的范围包括两条或更多条旁道之间的融合或一条旁道与房室结之间的融合。在22例有单个旁道且发生真正逆向性折返性心动过速的患者中,除2次发作外,所有发作距离房室结至少4厘米。没有真正逆向性折返性心动过速的患者有后间隔房室旁道。仅在有多个旁道的患者中,后间隔房室旁道被用作顺向支。