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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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650 V. TREATMENTS FOR ADDICTIONSfor drug dependence (Rounsaville & Kosten, 2000). Barriers to access to methadonemaintenance include both limit<strong>ed</strong> patient and community acceptance <strong>of</strong>methadone, and regulatory restrictions and the lack <strong>of</strong> availability in manyareas <strong>of</strong> the country. Development <strong>of</strong> alternative maintenance agents, andespecially agents that can be more readily administer<strong>ed</strong> with r<strong>ed</strong>uc<strong>ed</strong> clinicattendance and outside <strong>of</strong> traditional methadone maintenance settings, mayaddress some <strong>of</strong> the problems associat<strong>ed</strong> with limit<strong>ed</strong> access to treatment.Buprenorphine, a partial mu agonist and kappa antagonist, represents apromising alternative to methadone and was recently approv<strong>ed</strong> by the FDA.Because <strong>of</strong> its unique pharmacological properties, there may be a number <strong>of</strong>advantages to its use, compar<strong>ed</strong> to either methadone or levo-alpha-acetylmethadol (LAAM), as a maintenance agent for the treatment <strong>of</strong> opioiddependence settings. Ceiling effects at higher buprenorphine doses result in alower risk <strong>of</strong> overdose compar<strong>ed</strong> with methadone, and buprenorphine may alsohave a r<strong>ed</strong>uc<strong>ed</strong> abuse liability in opiate-dependent individuals (thus, less likelihoodfor diversion), because its use may precipitate withdrawal symptoms(Strain, Preston, Liebson, & Bigelow, 1995; Walsh, Preston, Bigelow, & Stitzer,1995). Withdrawal symptoms following abrupt discontinuation <strong>of</strong> buprenorphineare also usually relatively mild (Cowan & Lewis, 1995; Fudala, Jaffe, Dax,& Johnson, 1990). Results <strong>of</strong> random assignment, double-blind clinical trialsgenerally support the safety and dose-dependent efficacy <strong>of</strong> buprenorphinemaintenance (Fudala et al., 2003; Ling, Wesson, Charavastra, & Klett, 1996;Schottenfeld, Pakes, Oliveto, Zi<strong>ed</strong>onis, & Kosten, 1997).Because buprenorphine have been made available only recently, very fewstudies have been done to identify pr<strong>ed</strong>ictors <strong>of</strong> patient response to methadoneversus buprenorphine, or the minimal and optimal intensity <strong>of</strong> behavioral treatmentto be administer<strong>ed</strong> in conjunction with these maintenance agents. However,it is likely that the same principles as those found in the methadone literatureregarding use <strong>of</strong> behavioral therapies to enhance outcome with theseagents as will emerge over time.Naltrexone–Agonist TreatmentOpioid antagonist treatment (naltrexone) <strong>of</strong>fers many potential advantagesover methadone maintenance: It is nonaddicting and can be prescrib<strong>ed</strong> withoutconcerns about diversion, it has a benign side-effect pr<strong>of</strong>ile, and it may be lesscostly, in terms <strong>of</strong> demands on pr<strong>of</strong>essionals and patients’ time, than the dailyor near-daily clinic visits requir<strong>ed</strong> for methadone maintenance (Rounsaville,1995). Most important are behavioral aspects <strong>of</strong> the treatment, because unreinforc<strong>ed</strong>opiate use allows extinction <strong>of</strong> relationships between cues and druguse. While naltrexone treatment is likely to be attractive only to a minority <strong>of</strong>opioid addicts (Cornish et al., 1997), naltrexone’s unique properties make it animportant alternative to methadone maintenance.

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