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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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9. Cocaine and Stimulants 209ence now appears to be differentially affecting poor, minority individuals wholive in the inner city. This same population is overrepresent<strong>ed</strong> in the AIDSpopulation. This confluence is not surprising, because both sex risk (includingsex workers) and ne<strong>ed</strong>le risk are associat<strong>ed</strong> with chronic use <strong>of</strong> cocaine. Ittherefore appears that these two epidemics are interconnect<strong>ed</strong> in a way thatdeserves close attention.At the same time, there may be reason for cautious optimism with regardto the long-term effects <strong>of</strong> prenatal exposure to cocaine. Some <strong>of</strong> the earlyclaims <strong>of</strong> devastating physical consequences to “crack babies” have proven tobe exaggerat<strong>ed</strong>; experts in the perinatal addiction field now consider that manyfactors (e.g., poverty, poor maternal nutrition/health, smoking, and exposure toviolence) combine to influence development. Molecular mechanisms <strong>of</strong> developmentalneuroadaptation are at the same time beginning to be studi<strong>ed</strong>. In thefuture, we hope to understand better the physiological basis for the observ<strong>ed</strong>clinical events.In the basic sciences area, we have come to understand more about theinteractions <strong>of</strong> various neurotransmitters, drug reinforcement, and the rewardpathway. Receptors are being subtyp<strong>ed</strong> and clon<strong>ed</strong>. Signal transduction pathways,with their longer range on protein synthesis and genetic regulation, arebeing explor<strong>ed</strong>. We are beginning to make inroads in our understanding <strong>of</strong> sensitizationand tolerance. Although pharmacological treatments for cocaineaddiction have not yet proven successful in clinical trials, there are many excitingnew avenues <strong>of</strong> pursuit. These prospects for pharmacological interventionare bas<strong>ed</strong> on the remarkable advances in neuroscience being made in thisdecade.Researchers also have been hard at work testing psychotherapeutic solutionsto this complex problem. Cocaine dependence should not be view<strong>ed</strong> inisolation from other psychiatric conditions and life problems. Rather, we mustconsider how best to address the problem in the presence <strong>of</strong> other psychoactivesubstance use and non-substance-use Axis I and Axis II disorders. Dependingon the larger clinical picture, successful treatment may require multiple orhighly select therapies that are match<strong>ed</strong> to the patient’s pathology and adaptivestrengths and resources. It is clear that a “one size fits all” approach to treatment<strong>of</strong> cocaine dependence is inappropriate; instead, an array <strong>of</strong> assessment tools isnecessary to determine patient ne<strong>ed</strong>s, along with a menu <strong>of</strong> cost-effective andreadily available therapeutic strategies. Although American Society <strong>of</strong> AddictionM<strong>ed</strong>icine (H<strong>of</strong>fman, Halikas, Mee-Lee, & We<strong>ed</strong>man, 1991) criteria facilitatepatient placement in an appropriate treatment setting bas<strong>ed</strong> on addictionseverity, they provide little guidance in terms <strong>of</strong> specific interventions to b<strong>ed</strong>eliver<strong>ed</strong> within those settings. <strong>Clinical</strong> research aim<strong>ed</strong> at developing therapiesfor specific subtypes <strong>of</strong> cocaine addicts in a variety <strong>of</strong> settings is the most promisingapproach we now have.

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