ELECTROPHYSIOLOGIC EFFECTS AND EFFICACY OF CIBENZOLINE IN PATIENTS WITH SUPRAVENTRICULAR TACHYCARDIA

被引:3
作者
FUJIKI, A
MIZUMAKI, K
TANI, M
YOSHIDA, S
SASAYAMA, S
机构
[1] The Second Department of Internal Medicine, Toyama Medical and Pharmaceutical University, Toyama
关键词
ACCESSORY PATHWAY; ATRIOVENTRICULAR REENTRANT TACHYCARDIA; ATRIOVENTRICULAR NODAL REENTRANT TACHYCARDIA; CIBENZOLINE;
D O I
10.1097/00005344-199209000-00006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Electrophysiologic effects of intravenous (i.v.) cibenzoline were evaluated in 18 patients with accessory pathways or dual atrioventricular (AV) nodal pathways (12 men and 6 women with a mean age of 44 +/- 18 years). Twelve patients had accessory AV pathways, including 6 patients with a manifest accessory pathway. Six patients had AV nodal reentrant tachycardia (AVNRT). Electrophysiologic studies were performed before and after cibenzoline (1.4 mg/kg i.v.) infusion for 5 min. Sinus cycle length did not change significantly after cibenzoline administration. Cibenzoline increased both the AH (85 +/- 20 vs. 91 +/- 21 ms, p < 0.05) and HV intervals (41 +/- 10 ms vs. 53 +/- 11 ms, p < 0.001). Neither the atrial nor ventricular effective refractory period (ERP) was altered by cibenzoline. Complete block in the accessory pathway occurred antegradely in 4 patients and retrogradely in 1 patient. Cibenzoline prevented induction of AV reentrant tachycardia (AVRT) in 3 of 8 patients with sustained orthodromic AVRT by abolishing retrograde accessory pathway conduction or prolonging the retrograde accessory pathway ERP. Of 5 patients who continued to have inducible AVRT before and after cibenzoline administration, the tachycardia cycle length was increased in 3, mainly due to the increase in retrograde accessory pathway conduction time. Cibenzoline prevented induction of sustained AVNRT in 4 of 5 patients by prolonging the minimum pacing cycle length, maintaining 1:1 ventriculoatrial (VA) conduction through the retrograde fast AVN pathway or shortening the antegrade fast AVN pathway ERP equal to the slow AVN pathway. In one patient who had an uncommon type of AVNRT, sustained tachycardia was induced by cibenzoline. We conclude that the effects of i.v. cibenzoline at a dose of 1.4 mg/kg on suppression of initiation of paroxysmal supraventricular tachycardia are due mainly to the effects of class I antiarrhythmic agents and not class IV agents according to the Vaughan Williams classification. Cibenzoline may prevent both AVRT and AVNRT by suppressing retrograde VA conduction in selected patients.
引用
收藏
页码:375 / 379
页数:5
相关论文
共 15 条
[1]  
ARENA JP, 1987, J PHARMACOL EXP THER, V240, P441
[2]   SERIAL ELECTROPHYSIOLOGIC TESTING OF MULTIPLE-DRUGS IN PATIENTS WITH ATRIOVENTRICULAR NODAL REENTRANT PAROXYSMAL TACHYCARDIA [J].
BAUERNFEIND, RA ;
WYNDHAM, CR ;
DHINGRA, RC ;
SWIRYN, SP ;
PALILEO, E ;
STRASBERG, B ;
ROSEN, KM .
CIRCULATION, 1980, 62 (06) :1341-1349
[3]   PHARMACOKINETICS AND PHARMACODYNAMICS OF INTRAVENOUS CIBENZOLINE IN NORMAL VOLUNTEERS [J].
BRAZZELL, RK ;
KHOO, KC ;
SZUNA, AJ ;
SANDOR, D ;
AOGAICHI, K ;
WILLS, RJ .
JOURNAL OF CLINICAL PHARMACOLOGY, 1985, 25 (06) :418-423
[4]   CLINICAL EFFICACY AND ELECTROPHYSIOLOGIC EFFECTS OF CIBENZOLINE THERAPY IN PATIENTS WITH VENTRICULAR ARRHYTHMIAS [J].
BROWNE, KF ;
PRYSTOWSKY, EN ;
ZIPES, DP ;
CHILSON, DA ;
HEGER, JJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1984, 3 (03) :857-864
[5]  
FUJIKI A, 1989, AM HEART J, V118, P1057
[6]   DETERMINATION OF CIBENZOLINE IN PLASMA AND URINE BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
HACKMAN, MR ;
LEE, TL ;
BROOKS, MA .
JOURNAL OF CHROMATOGRAPHY, 1983, 273 (02) :347-356
[7]  
Josephson ME, 1979, CLIN CARDIAC ELECTRO
[8]  
KUHLKAMP V, 1990, AM J CARDIOL, V5, P628
[9]  
MASSE C, 1984, ARCH INT PHARMACOD T, V269, P219