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房间传导阻滞患者的心房兴奋性与传导

Atrial excitability and conduction in patients with interatrial conduction defects.

作者信息

Simpson R J, Foster J R, Gettes L S

出版信息

Am J Cardiol. 1982 Dec;50(6):1331-7. doi: 10.1016/0002-9149(82)90471-4.

Abstract

Prolongation of P-wave duration is an accepted indicator of an interatrial conduction disturbance and may predispose patients to atrial arrhythmias. This study was performed to monitor electrophysiologic characteristics of the atria in patients with a prolonged P-wave duration. Atrial excitability and conduction times were compared in 7 patients with a P-wave duration of less than 115 ms (Group I), and 13 patients with a duration of greater than of equal to 115 ms (Group II). In contrast of the Group I patients, most of the 13 patients in Group II had atrial arrhythmias, including sinus nodal dysfunction (3 patients) and a history of atrial fibrillation or ectopic atrial tachycardia (6 patients). Electrophysiologic differences between the 2 groups included a higher late diastolic threshold in Group II (0.8 +/- 0.2 mA versus 1.3 +/- 0.2 mA; p less than 0.005), and a greater increase in intraatrial conduction time (5 +/- 10 ms versus 30 +/- 20 ms; p less than 0.005) and interatrial conduction time (5 +/- 15 ms versus 30 +/- 15 ms; p less than 0.05) of early premature responses. There were no differences between the 2 groups in refractory periods, shape of the strength interval curve, or conduction times of premature responses occurring late in diastole. These abnormalities in conduction time and excitability found in patients with a prolonged P-wave duration may predispose to the initiation of certain atrial tachyarrhythmias.

摘要

P波时限延长是公认的房内传导障碍指标,可能使患者易患房性心律失常。本研究旨在监测P波时限延长患者心房的电生理特征。比较了7例P波时限小于115毫秒的患者(第一组)和13例P波时限大于或等于115毫秒的患者(第二组)的心房兴奋性和传导时间。与第一组患者不同,第二组的13例患者中大多数患有房性心律失常,包括窦房结功能障碍(3例)以及有房颤或异位房性心动过速病史(6例)。两组之间的电生理差异包括:第二组舒张晚期阈值较高(0.8±0.2毫安对1.3±0.2毫安;p<0.005),房内传导时间(5±10毫秒对30±20毫秒;p<0.005)和房内传导时间(5±15毫秒对30±15毫秒;p<0.05)的早期早搏反应增加幅度更大。两组在不应期、强度-间期曲线形状或舒张晚期出现的早搏反应传导时间方面无差异。P波时限延长患者中发现的这些传导时间和兴奋性异常可能易引发某些房性快速心律失常。

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