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Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

Clinical Textbook of Addictive Disorders 3rd ed - R. Frances, S. Miller, A. Mack (Guilford, 2005) WW

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606 V. TREATMENTS FOR ADDICTIONScal trials for efficacy in humans have shown excellent safety, adequate antibodydevelopment, and r<strong>ed</strong>uctions in cocaine abuse (Kosten et al., 2002; Kosten &O’Connor, 2003).INTERFACE OF PSYCHIATRIC COMORBIDITYAND SUBSTANCE USE DISORDERSPsychotropic m<strong>ed</strong>ication treatment <strong>of</strong> dually diagnos<strong>ed</strong> patients is similar tothat <strong>of</strong> psychiatric patients without SUDs, with several caveats. Patients withpsychotic disorders treat<strong>ed</strong> with m<strong>ed</strong>ications that block dopamine receptorsmay develop postsynaptic dopaminergic supersensitivity, which has been demonstrat<strong>ed</strong>in animal studies (Kosten, 1997). This supersensitivity may enhanceeuphoria from a wide range <strong>of</strong> abus<strong>ed</strong> drugs. Furthermore, patients withchronic psychotic disorders <strong>of</strong>ten experience negative symptoms <strong>of</strong> schizophreniaand dysphoria that may be exacerbat<strong>ed</strong> by conventional neuroleptics. Thesepatients will benefit from selection <strong>of</strong> an atypical neuroleptic that lacks strongdopaminergic antagonism (Kosten & Zi<strong>ed</strong>onis, 1997). Patients with psychoticdisorders who are also alcoholic should be carefully evaluat<strong>ed</strong> before beingtreat<strong>ed</strong> with disulfiram, a dopamine beta-hydroxylase inhibitor that could exacerbatepsychosis in such patients.Attention-deficit/hyperactivity disorder (ADHD) can occur as a comorbidcondition in cocaine abusers who may self-m<strong>ed</strong>icate with this stimulant.Cocaine use in this population is <strong>of</strong>ten describ<strong>ed</strong> as ingestion <strong>of</strong> small amounts<strong>of</strong> cocaine taken intermittently throughout the day rather than the classicbinge pattern characteriz<strong>ed</strong> by use <strong>of</strong> multiple doses <strong>of</strong> cocaine in rapid successiondescrib<strong>ed</strong> by those with primary cocaine dependence. Treatment withstandard agents us<strong>ed</strong> for ADHD, including stimulant m<strong>ed</strong>ications, may result incessation <strong>of</strong> cocaine use.Depressive disorders are common in those with cocaine and alcohol us<strong>ed</strong>isorders. SRIs may be a good choice for these patients because they are lesslikely to have significant cardiovascular interactions with cocaine and to belethal in overdose. Monoamine oxidase inhibitors (MAOIs) should never beus<strong>ed</strong> in cocaine abusers, because <strong>of</strong> the risk <strong>of</strong> hypertensive crisis. Benzodiazepinesshould be us<strong>ed</strong> with caution in those with cormorbid psychiatric andSUDs, and particularly in alcoholic patients, because <strong>of</strong> cross-tolerance withalcohol and additive effects if combin<strong>ed</strong> with alcohol. Benzodiazepines may berequir<strong>ed</strong> initially to stabilize patients with exacerbation <strong>of</strong> psychosis or severeagitation but should be taper<strong>ed</strong> as antipsychotics and/or mood stabilizersbecome therapeutic. Alcoholic patients with anxiety disorders can usually beeffectively treat<strong>ed</strong> with serotonergic agents (SRIs or partial agonists) or, insome cases, tricyclic antidepressants.

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