Selecting an antiarrhythmic agent for atrial fibrillation should be a patient-specific, data-driven decision

被引:15
作者
Reiffel, JA
机构
[1] Columbia Univ, Dept Med, Div Cardiol, Clin Electrophysiol Serv, New York, NY USA
[2] New York & Presbyterian Hosp, New York, NY USA
关键词
D O I
10.1016/S0002-9149(98)00588-8
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Selecting an antiarrhythmic agent for atrial fibrillation (AF) should be a patient-specific decision. When possible, it should be based on sound rationale and available clinical data. This article details many of the thought processes that must go into this decision process and offers some suggested algorithmic starting points based on these considerations. With a patient's first episode of AF, termination is appropriate, bur antiarrhythmic therapy should usually be withheld in order to assess the recurrence pattern. However, if severe hemodynamic or ischemic intolerance would make recurrence a serious risk, or if an early symptomatic recurrence is highly likely, antiarrhythmic therapy would be appropriate. Acute AF may terminate spontaneously or may be terminated iatrogenically. The latter may be achieved by direct current or pharmacologic approaches. The risks, benefits, and optimum utility of these approaches are addressed in the article. Infrequent recurrences may be created with cardioversion; frequent or severely symptomatic episodes are best created with attempts at suppression with chronic antiarrhythmic drug administration. Since the therapeutic efficacy of maintaining sinus rhythm is similar for the currently available agents, the drug selection process should be based in large part on safety and convenience considerations. The factors underlying this selection process and one suggested algorithm for drug choice are provided in this article. (C)1998 by Excerpta Medica, Inc.
引用
收藏
页码:72N / 80N
页数:9
相关论文
共 65 条
[1]
Aliot E, 1996, AM J CARDIOL, V77, pA66
[3]
PREVENTION OF SYMPTOMATIC RECURRENCES OF PAROXYSMAL ATRIAL-FIBRILLATION IN PATIENTS INITIALLY TOLERATING ANTIARRHYTHMIC THERAPY - A MULTICENTER, DOUBLE-BLIND, CROSSOVER STUDY OF FLECAINIDE AND PLACEBO WITH TRANSTELEPHONIC MONITORING [J].
ANDERSON, JL ;
GILBERT, EM ;
ALPERT, BL ;
HENTHORN, RW ;
WALDO, AL ;
BHANDARI, AK ;
HAWKINSON, RW ;
PRITCHETT, ELC .
CIRCULATION, 1989, 80 (06) :1557-1570
[4]
FLECAINIDE ACETATE FAR PAROXYSMAL SUPRAVENTRICULAR TACHYARRHYTHMIAS [J].
ANDERSON, JL ;
PLATT, ML ;
GUARNIERI, T ;
FOX, TL ;
MASER, MJ ;
PRITCHETT, ELC ;
KAY, GN ;
PLUMB, VJ ;
EPSTEIN, AE ;
BUBIEN, RS ;
BHANDARI, AK ;
LEON, C ;
BRINKLEY, AM ;
ROSIN, BL ;
MCCABE, E ;
DATORRE, S ;
DEBORDE, R ;
HAFFAJEE, C ;
RUFINO, K ;
DEGON, C ;
WEBB, CR ;
BIELINSKI, KA ;
DUNBAR, D ;
HEDGES, M ;
FJELDOOSPERBECK, K ;
GOMES, JA ;
WINTERS, S ;
PE, E ;
FOSTER, JR ;
WOELFEL, A ;
CULLINANE, L ;
MCCARTHY, EA ;
CHRISTIE, LG ;
CARLSON, KL ;
ALPERT, BL ;
FECIK, CM ;
MORENO, F ;
JOHNSON, L ;
SUMMERS, K ;
ELLENBOGEN, KA ;
MARTIN, ML ;
HART, WL ;
FRIEDMAN, NJ ;
NEUMANN, S ;
LAIDLAW, JC ;
STOLLINGS, L ;
CULLEN, MT ;
DONAHUE, PA ;
HAHN, MA ;
HAWKINSON, RW .
AMERICAN JOURNAL OF CARDIOLOGY, 1994, 74 (06) :578-584
[5]
[Anonymous], 1989, NEW ENGL J MED, V321, P406
[6]
LONG-TERM ORAL PROPAFENONE THERAPY FOR SUPPRESSION OF REFRACTORY SYMPTOMATIC ATRIAL-FIBRILLATION AND ATRIAL-FLUTTER [J].
ANTMAN, EM ;
BEAMER, AD ;
CANTILLON, C ;
MCGOWAN, N ;
GOLDMAN, L ;
FRIEDMAN, PL .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1988, 12 (04) :1005-1011
[7]
Bellandi F, 1996, G Ital Cardiol, V26, P379
[8]
Rhythm management in atrial fibrillation - With a primary emphasis on pharmacological therapy: Part 1 [J].
Blitzer, M ;
Costeas, C ;
Kassotis, J ;
Reiffel, JA .
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, 1998, 21 (03) :590-602
[9]
Boissel J P, 1981, Eur Heart J, V2, P49
[10]
PROPAFENONE FOR CONVERSION OF RECENT-ONSET ATRIAL-FIBRILLATION - A CONTROLLED COMPARISON BETWEEN ORAL LOADING DOSE AND INTRAVENOUS ADMINISTRATION [J].
BORIANI, G ;
CAPUCCI, A ;
LENZI, T ;
SANGUINETTI, M ;
MAGNANI, B .
CHEST, 1995, 108 (02) :355-358