An overview of psychotropic drug-drug interactions

被引:96
|
作者
Sandson, NB
Armstrong, SC
Cozza, KL
机构
[1] Tual Forest Grove Hosp, Ctr Geriatr Psychiat, Forest Grove, OR 97116 USA
[2] Sheppard Pratt Hlth Syst, Div Educ & Residency Training, Towson, MD USA
[3] Univ Maryland, Sheppard Pratt Psychiat Residency Program, Baltimore, MD 21201 USA
[4] Univ Maryland, Dept Psychiat, Med Syst, Baltimore, MD 21201 USA
[5] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[6] Walter Reed Army Med Ctr, Dept Med, Infect Dis Serv, Washington, DC 20307 USA
[7] Uniformed Serv Univ Hlth Sci, Bethesda, MD 20814 USA
关键词
D O I
10.1176/appi.psy.46.5.464
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The psychotropic drug-drug interactions most likely to be relevant to psychiatrists' practices are examined. The metabolism and the enzymatic and P-glycoprotein inhibition/induction profiles of all antidepressants, antipsychotics, and mood stabilizers are described; all clinically meaningful drug-drug interactions between agents in these psychotropic classes, as well as with frequently encountered nonpsychotropic agents, are detailed; and information on the pharmacokinetic/pharmacodynamic results, mechanisms, and clinical consequences of these interactions is presented. Although the range of drug-drug interactions involving psychotropic agents is large, it is a finite and manageable subset of the much larger domain of all possible drug-drug interactions. Sophisticated computer programs will ultimately provide the best means of avoiding drug-drug interactions. Until these programs are developed, the best defense against drug-drug interactions is awareness and focused attention to this issue.
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收藏
页码:464 / 494
页数:31
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