Favale S, Minafra F, Massari V, Tritto M, Rizzon P
Division of Cardiology, University of Bari, Italy.
Int J Cardiol. 1991 Feb;30(2):209-14. doi: 10.1016/0167-5273(91)90097-9.
Electrophysiologic intracardiac and noninvasive transesophageal testing, used to evaluate parameters of anterograde conduction across the accessory pathway, the refractory period and shortest atrial cycle length with 1:1 conduction over the pathway, were compared to assess the reliability of the noninvasive technique in identifying patients with Wolff-Parkinson-White syndrome, at risk of rapid ventricular response during atrial fibrillation when this arrhythmia is not inducible. Sixteen patients with Wolff-Parkinson-White syndrome were submitted both to invasive and transesophageal atrial stimulation. We evaluated both the functional and effective refractory periods of the accessory pathway, using the same drive cycle length, and the shortest cycle length with 1:1 atrioventricular conduction over the accessory pathway. There were no differences between the parameters obtained by intracardiac atrial stimulation and by transesophageal atrial stimulation. The two approaches correlated well: mean functional refractory periods of the accessory pathway were 285 +/- 42 msec and 289 +/- 32 msec, respectively (NS, r = 0.88); mean effective refractory periods of the accessory pathway were 267 +/- 41 msec and 271 +/- 32 msec, respectively (NS, r = 0.89); mean shortest cycle lengths with 1:1 conduction over the accessory pathway were 255 +/- 48 msec and 255 +/- 44 msec, respectively (NS, r = 0.94). These data demonstrate the reliability of transesophageal atrial stimulation in estimating the parameters for anterograde conduction across an accessory pathway. These results, and the already documented ability of transesophageal atrial stimulation to induce atrial fibrillation, suggest this noninvasive technique should be taken as a first approach in screening patients with Wolff-Parkinson-White syndrome.(ABSTRACT TRUNCATED AT 250 WORDS)
采用心内电生理和无创经食管检测来评估经旁路前向传导参数、不应期以及 1:1 经旁路传导时的最短心房周期长度,比较这两种检测方法以评估无创技术在识别预激综合征患者中的可靠性,这些患者在房颤不可诱发时存在快速心室反应风险。16 例预激综合征患者接受了有创和经食管心房刺激。我们使用相同的驱动周期长度评估旁路的功能和有效不应期,以及经旁路 1:1 房室传导时的最短周期长度。心内心房刺激和经食管心房刺激所获得的参数之间没有差异。两种方法相关性良好:旁路的平均功能不应期分别为 285±42 毫秒和 289±32 毫秒(无显著性差异,r = 0.88);旁路的平均有效不应期分别为 267±41 毫秒和 271±32 毫秒(无显著性差异,r = 0.89);经旁路 1:1 传导时的平均最短周期长度分别为 255±48 毫秒和 255±44 毫秒(无显著性差异,r = 0.94)。这些数据证明了经食管心房刺激在估计经旁路前向传导参数方面的可靠性。这些结果,以及已记录的经食管心房刺激诱发房颤的能力,表明这种无创技术应作为筛查预激综合征患者的首选方法。(摘要截短为 250 字)