Manolis A S, Katsaros C, Cokkinos D V
Department of Cardiology, Tzaneio State Hospital, Athens, Greece.
Eur Heart J. 1992 Nov;13(11):1489-95. doi: 10.1093/oxfordjournals.eurheartj.a060091.
To study the electrophysiological effects of oral propafenone on accessory pathways and determine the potential for catecholamine-mediated reversal of these effects, comprehensive electrophysiology studies (EPS) were conducted in 11 patients with manifest (n = 9) or concealed (n = 2) pre-excitation syndrome. EPS were performed at baseline (in the drug-free state), after oral propafenone loading, and with isoproterenol infusion during propafenone therapy. The study group included 10 men and 1 woman with a mean age of 39 +/- 13 years, who presented with symptoms of palpitations (n = 6), presyncope (n = 3) and syncope (n = 2). The clinical arrhythmia was atrioventricular reciprocating tachycardia (n = 6), atrial flutter/fibrillation (n = 3), or both (n = 2). During the baseline EPS the accessory pathway location was identified as left (n = 6) or septal (n = 5). The mean anterograde effective refractory period was 265 +/- 42 ms, the shortest pre-excited RR interval 259 +/- 20 ms and the retrograde refractory period 258 +/- 39 ms. Orthodromic atrioventricular reciprocating tachycardia was induced in 10 patients (mean cycle length = 324 +/- 31 ms). Antidromic reciprocating tachycardia was induced in one patient (cycle length = 340 ms). In all the 11 patients EPS were repeated after 4 days of oral propafenone loading (668 +/- 226 mg daily) when drug steady state was expected to have been achieved. One additional patient had baseline EPS but developed clinical arrhythmia recurrences after propafenone loading and thus he was excluded from the study; follow-up EPS were conducted on procainamide.(ABSTRACT TRUNCATED AT 250 WORDS)
为研究口服普罗帕酮对旁路的电生理效应,并确定儿茶酚胺介导逆转这些效应的可能性,对11例显性(n = 9)或隐匿性(n = 2)预激综合征患者进行了全面的电生理研究(EPS)。EPS在基线(无药状态)、口服普罗帕酮负荷后以及普罗帕酮治疗期间静脉输注异丙肾上腺素时进行。研究组包括10名男性和1名女性,平均年龄39±13岁,表现为心悸症状(n = 6)、先兆晕厥(n = 3)和晕厥(n = 2)。临床心律失常为房室折返性心动过速(n = 6)、心房扑动/颤动(n = 3)或两者皆有(n = 2)。在基线EPS期间,旁路位置确定为左侧(n = 6)或间隔(n = 5)。平均前传有效不应期为265±42毫秒,最短预激RR间期为259±20毫秒,逆传不应期为258±39毫秒。10例患者诱发了顺向房室折返性心动过速(平均周期长度 = 324±31毫秒)。1例患者诱发了逆向折返性心动过速(周期长度 = 340毫秒)。在11例患者中,口服普罗帕酮负荷4天(每日668±226毫克)后,预计达到药物稳态时重复进行EPS。另外1例患者进行了基线EPS,但在普罗帕酮负荷后出现临床心律失常复发,因此被排除在研究之外;对普鲁卡因胺进行了随访EPS。(摘要截断于250字)