Studies on the mechanism of a fatal clarithromycin-pimozide interaction in a patient with Tourette syndrome

被引:59
作者
Flockhart, DA
Drici, MD
Kerbusch, T
Soukhova, N
Richard, E
Pearle, PL
Mahal, SK
Babb, VJ
机构
[1] Georgetown Univ, Med Ctr, Div Clin Pharmacol, Dept Med, Washington, DC 20007 USA
[2] Georgetown Univ, Med Ctr, Dept Pharmacol, Washington, DC 20007 USA
[3] Washington Hosp Ctr, Dept Neurol, Washington, DC 20010 USA
[4] US FDA, Off Epidemiol & Biostat, Div Pharmacovigilance & Epidemiol, Rockville, MD 20857 USA
关键词
D O I
10.1097/00004714-200006000-00005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The authors report in detail the case of a 27-year-old man who experienced sudden cardiac death 2 days after coprescription of the neuroleptic pimozide and the macrolide antibiotic clarithromycin after the documentation of a prolonged QT interval. To determine the prevalence of this interaction, the authors referred to the Spontaneous Reporting System of the Food and Drug Administration and identified one similar case in which clarithromycin was coprescribed with pimozide and sudden cardiac death occurred shortly thereafter. In addition, the search identified 39 cases of cardiac arrhythmia associated with pimozide, 11 with pimozide alone, and 6 with clarithromycin alone, 1 of which had a positive rechallenge. The mechanism of the interaction between clarithromycin and pimozide seems to involve the inhibition of the hepatic metabolism of pimozide by the macrolide. The authors demonstrated that clarithromycin is able to inhibit the metabolism of pimozide in human liver microsomal preparations (K-i = 7.65 +/- 1.18 mu M) and that pimozide, but not clarithromycin or its primary metabolite, is able to prolong the electrocardiac QT interval in a dose-dependent manner in the isolated perfused rabbit heart. The increase was 9.6 +/- 1.1% in male hearts (N = 5) and 13.4 +/- 1.2% in female hearts (N = 4) (p < 0.05).
引用
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页码:317 / 324
页数:8
相关论文
共 49 条
[1]   KETOCONAZOLE AND SULFAPHENAZOLE AS THE RESPECTIVE SELECTIVE INHIBITORS OF P4503A AND 2C9 [J].
BALDWIN, SJ ;
BLOOMER, JC ;
SMITH, GJ ;
AYRTON, AD ;
CLARKE, SE ;
CHENERY, RJ .
XENOBIOTICA, 1995, 25 (03) :261-270
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   DEBRISOQUINE SPARTEINE HYDROXYLATION GENOTYPE AND PHENOTYPE - ANALYSIS OF COMMON MUTATIONS AND ALLELES OF CYP2D6 IN A EUROPEAN POPULATION [J].
BROLY, F ;
GAEDIGK, A ;
HEIM, M ;
EICHELBAUM, M ;
MORIKE, K ;
MEYER, UA .
DNA AND CELL BIOLOGY, 1991, 10 (08) :545-558
[4]  
CHEN Y, 1995, CLIN PHARMACOL THER, V57, P194
[5]   SELECTIVE INACTIVATION OF CYTOCHROME-P-450 ISOZYMES BY SUICIDE SUBSTRATES [J].
DEMONTELLANO, PRO ;
MICO, BA ;
MATHEWS, JM ;
KUNZE, KL ;
MIWA, GT ;
LU, AYH .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1981, 210 (02) :717-728
[6]  
DEMORAIS SMF, 1994, J BIOL CHEM, V269, P15419
[7]   GENETIC-ANALYSIS OF THE S-MEPHENYTOIN POLYMORPHISM IN A CHINESE POPULATION [J].
DEMORAIS, SMF ;
GOLDSTEIN, JA ;
XIE, HG ;
HUANG, SL ;
LU, YQ ;
XIA, H ;
XIAO, ZS ;
ILE, N ;
ZHOU, HH .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1995, 58 (04) :404-411
[8]   Effect of clarithromycin on the pharmacokinetics and pharmacodynamics of pimozide in healthy poor and extensive metabolizers of cytochrome P450 2D6 (CYP2D6) [J].
Desta, Z ;
Kerbusch, T ;
Flockhart, DA .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1999, 65 (01) :10-20
[9]  
Desta Z, 1999, J FORENSIC SCI, V44, P231
[10]  
Desta Z, 1998, J PHARMACOL EXP THER, V285, P428