Antipsychotic Agents for the Treatment of Substance Use Disorders in Patients With and Without Comorbid Psychosis

被引:35
作者
Zhornitsky, Simon [1 ]
Rizkallah, Elie [1 ,2 ]
Pampoulova, Tania [1 ,2 ]
Chiasson, Jean-Pierre [2 ]
Stip, Emmanuel [1 ]
Rompre, Pierre-Paul [1 ]
Potvin, Stephane [1 ]
机构
[1] Univ Montreal, Fernand Seguin Res Ctr, Dept Psychiat, Fac Med, Montreal, PQ H1N 3V2, Canada
[2] Clin Nouveau Depart, Montreal, PQ, Canada
关键词
dual diagnosis; substance dependence; antipsychotic agent; schizophrenia; alcohol; stimulants; cannabis; PLACEBO-CONTROLLED TRIAL; BRAIN-STIMULATION REWARD; DOUBLE-BLIND TRIAL; COCAINE DEPENDENCE; ALCOHOL-DEPENDENCE; ATYPICAL ANTIPSYCHOTICS; BIPOLAR DISORDER; WITHDRAWAL SYNDROME; SMOKING-CESSATION; PILOT TRIAL;
D O I
10.1097/JCP.0b013e3181e7810a
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Substance dependence has serious negative consequences upon society such as increased health care costs, loss of productivity, and rising crime rates. Although there is some preliminary evidence that atypical antipsychotic agents may be effective in treating substance dependence, results have been mixed, with some studies demonstrating positive and others negative or no effect. The present study was aimed at determining whether this disparity originates from that reviewers separately discussed trials in patients with (DD) and without (SD) comorbid psychosis. Using electronic databases, we screened the relevant literature, leaving only studies that used a randomized, double-blind, placebo-controlled or case-control design that had a duration of 4 weeks or longer. A total of 43 studies were identified; of these, 23 fell into the category of DD and 20 into the category of SD. Studies in the DD category suggest that atypical antipsychotic agents, especially clozapine, may decrease substance use in individuals with alcohol and drug (mostly cannabis) use disorders. Studies in the SD category suggest that atypical antipsychotic agents may be beneficial for the treatment of alcohol dependence, at least in some subpopulations of alcoholics. They also suggest that these agents are not effective at treating stimulant dependence and may aggravate the condition in some cases.
引用
收藏
页码:417 / 424
页数:8
相关论文
共 104 条
[1]   Comparison of olanzapine to risperidone in substance-abusing individuals with schizophrenia [J].
Akerele, Evaristo ;
Levin, Frances R. .
AMERICAN JOURNAL ON ADDICTIONS, 2007, 16 (04) :260-268
[2]  
[Anonymous], ADICCIONES
[3]  
[Anonymous], 2014, COCHRANE DB SYST REV, DOI DOI 10.1002/14651858.CD000031.PUB3
[4]  
[Anonymous], COCHRANE DATABASE SY
[5]   A randomized, multicenter, double-blind, placebo-controlled study of the efficacy and safety of aripiprazole for the treatment of alcohol dependence [J].
Anton, Raymond F. ;
Kranzler, Henry ;
Breder, Christopher ;
Marcus, Ronald N. ;
Carson, William H. ;
Han, Jian .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2008, 28 (01) :5-12
[6]   Tiospirone and the reinforcing effects of cocaine in the conditioned place preference paradigm in rats [J].
Arolfo, MP ;
McMillen, BA .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2000, 52 (08) :977-981
[7]   Reactivity to laboratory stress provocation predicts relapse to cocaine [J].
Back, Sudie E. ;
Hartwell, Karen ;
DeSantis, Stacia M. ;
Saladin, Michael ;
McRae-Clark, Aimee L. ;
Price, Kimber L. ;
Maria, Megan M. Moran-Santa ;
Baker, Nathaniel L. ;
Spratt, Eve ;
Kreek, Mary Jeanne ;
Braly, Kathleen T. .
DRUG AND ALCOHOL DEPENDENCE, 2010, 106 (01) :21-27
[8]  
Bailey Katharine P, 2004, J Psychosoc Nurs Ment Health Serv, V42, P14
[9]   REWARD SYSTEM DEPRESSION FOLLOWING CHRONIC AMPHETAMINE - ANTAGONISM BY HALOPERIDOL [J].
BARRETT, RJ ;
WHITE, DK .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1980, 13 (04) :555-559
[10]   The efficacy of the dopamine D2/D3 antagonist tiapride in maintaining abstinence:: a randomized, double-blind, placebo-controlled trial in 299 alcohol-dependent patients [J].
Bender, Stefan ;
Scherbaum, Norbert ;
Soyka, Michael ;
Ruether, Eckart ;
Mann, Karl ;
Gastpar, Markus .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2007, 10 (05) :653-660