Psychotropic drugs, cardiac arrhythmia, and sudden death

被引:145
作者
Witchel, HJ
Hancox, JC
Nutt, DJ
机构
[1] Univ Bristol, Sch Med Sci, Dept Physiol, Bristol BS8 1TD, Avon, England
[2] Univ Bristol, Sch Med Sci, Cardiovasc Res Labs, Bristol BS8 1TD, Avon, England
[3] Univ Bristol, Sch Med Sci, Psychopharmacol Unit, Bristol BS8 1TD, Avon, England
关键词
D O I
10.1097/00004714-200302000-00010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A variety of drugs targeted towards the central nervous system are associated with cardiac side effects, some of which are linked with reports of arrhythmia and sudden death. Some psychotropic drugs, particularly tricyclic antidepressants (TCAs) and antipsychotic agents, are correlated with iatrogenic prolongation of the QT interval of the electrocardiogram (ECG). In turn, this is associated with the arrhythmia torsades de pointes (UP). This review discusses the association between psychotropic agents, arrhythmia and sudden death and, focusing on TCAs and antipsychotics, considers their range of cellular actions on the heart; potentially pro-arrhythmic interactions between psychotropic and other medications are also considered. At the cellular level TCAs, such as imipramine and amitriptyline, and antipsychotics, such as thioridazine, are associated with inhibition of potassium channels encoded by HERG. In many cases this cellular action correlates with ECG changes and a risk of TdP. However, not all psychotropic agents that inhibit HERG at the cellular level are associated equally with QT prolongation in patients, and the potential for QT prolongation is not always equally correlated with UP. Differences in risk between classes of psychotropic drugs, and between individual drugs within a class, may result from additional cellular effects of particular agents, which may influence the consequent effects of inhibition of repolarizing potassium current.
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页码:58 / 77
页数:20
相关论文
共 238 条
[1]   MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia [J].
Abbott, GW ;
Sesti, F ;
Splawski, I ;
Buck, ME ;
Lehmann, WH ;
Timothy, KW ;
Keating, MT ;
Goldstein, SAN .
CELL, 1999, 97 (02) :175-187
[2]   Effects of newer atypical antipsychotics on autonomic neurocardiac function: A comparison between amisulpride, olanzapine, sertindole, and clozapine [J].
Agelink, MW ;
Majewski, T ;
Wurthmann, C ;
Lukas, K ;
Ullrich, H ;
Linka, T ;
Klieser, E .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2001, 21 (01) :8-13
[3]   PHENOTHIAZINE-INDUCED T-WAVE ABNORMALITIES - EFFECTS OF OVERNIGHT FASTING [J].
ALVAREZM.SC ;
FRANK, MJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1973, 224 (13) :1730-1733
[4]   HETEROGENEITY WITHIN THE VENTRICULAR WALL - ELECTROPHYSIOLOGY AND PHARMACOLOGY OF EPICARDIAL, ENDOCARDIAL, AND M-CELLS [J].
ANTZELEVITCH, C ;
SICOURI, S ;
LITOVSKY, SH ;
LUKAS, A ;
KRISHNAN, SC ;
DIDIEGO, JM ;
GINTANT, GA ;
LIU, DW .
CIRCULATION RESEARCH, 1991, 69 (06) :1427-1449
[5]   Effect of sertraline on protein binding of warfarin [J].
Apseloff, G ;
Wilner, KD ;
Gerber, N ;
Tremaine, LM .
CLINICAL PHARMACOKINETICS, 1997, 32 (Suppl 1) :37-42
[6]   MAGNESIUM AND CARDIOVASCULAR-DISEASE [J].
ARSENIAN, MA .
PROGRESS IN CARDIOVASCULAR DISEASES, 1993, 35 (04) :271-310
[7]  
AVERY D, 1976, ARCH GEN PSYCHIAT, V33, P1029
[8]   Electrocardiographic effects of fluoxetine and doxepin in patients with major depressive disorder [J].
Baker, B ;
Dorian, P ;
Sandor, P ;
Shapiro, C ;
Schell, C ;
Mitchell, J ;
Irvine, MJ .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1997, 17 (01) :15-21
[9]   ELECTROCARDIOGRAPHIC CHANGES INDUCED BY PHENOTHIAZINE DRUGS [J].
BAN, TA ;
STJEAN, A .
AMERICAN HEART JOURNAL, 1965, 70 (04) :575-&
[10]   EVALUATION OF THE POTENTIAL FOR INTERACTIONS OF PAROXETINE WITH DIAZEPAM, CIMETIDINE, WARFARIN, AND DIGOXIN [J].
BANNISTER, SJ ;
HOUSER, VP ;
HULSE, JD ;
KISICKI, JC ;
RASMUSSEN, JGC .
ACTA PSYCHIATRICA SCANDINAVICA, 1989, 80 :102-106