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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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13. Pathological Gambling and Other “Behavioral” Addictions 309between gambling and alcohol use disorders (Cunningham-Williams, Cottler,Compton, & Spitznagel, 1998; Welte, Barnes, Wieczorek, Tidwell, & Parker,2001). A Canadian epidemiological survey estimat<strong>ed</strong> that the relative risk foran alcohol use disorder is increas<strong>ed</strong> 3.8-fold when disorder<strong>ed</strong> gambling is present(Grant, Kushner, & Kim, 2002), and odds ratios ranging from 3.3 to23.1 have been report<strong>ed</strong> between PG and alcohol abuse/dependence in U.S.population-bas<strong>ed</strong> studies (Cunningham-Williams et al., 1998; Welte et al.,2001).TreatmentGiven the high rates <strong>of</strong> placebo response <strong>of</strong>ten observ<strong>ed</strong> in treatment trials <strong>of</strong>PG, the treatment section focuses on findings from double-blind, placebocontroll<strong>ed</strong>trials (see Table 13.2).AntidepressantsSRIs are the most well-studi<strong>ed</strong> pharmacotherapy for PG. In a double-blindstudy with one subject, 125 mg/day <strong>of</strong> clomipramine result<strong>ed</strong> in significantimprovement. The patient sustain<strong>ed</strong> improvement for 28 weeks on a dose <strong>of</strong>175 mg/day (Grant, Kim, & Potenza, 2003). Fluvoxamine has demonstrat<strong>ed</strong>mix<strong>ed</strong> results in two placebo-controll<strong>ed</strong>, double-blind studies, with one 16-week crossover study supporting its efficacy at an average dose <strong>of</strong> 207 mg/day(Hollander et al., 2000), and a second 6-month parallel-arm study with highrates <strong>of</strong> dropout finding no significant difference in response to active or placebodrug (Blanco, Petkova, Ibanez, & Saiz-Ruiz, 2002).Paroxetine at doses between 20 and 60 mg/day (average end-<strong>of</strong>-study dose= 52 mg/day) has been shown in a short-term, parallel-arm, placebo-controll<strong>ed</strong>,double-blind study to be well-tolerat<strong>ed</strong> and efficacious in the treatment <strong>of</strong> PG(Kim, Grant, Adson, Shin, & Zaninelli, 2002). However, a 16-week multicenterstudy <strong>of</strong> paroxetine did not find a statistically significant differencebetween active drug and placebo, perhaps in part due to the high placeboresponse rate (48% to placebo, 59% to active drug) (Grant, Kim, Potenza, etal., 2003). A similarly high placebo response rate was seen in a recent studyusing sertraline (Saiz-Ruiz et al., <strong>2005</strong>).Opioid AntagonistsGiven their ability to modulate dopaminergic transmission in the mesolimbicpathway, mu opioid receptor antagonists have been investigat<strong>ed</strong> in the treatment<strong>of</strong> PG. Initially, open-label treatment suggest<strong>ed</strong> the efficacy <strong>of</strong> naltrexone,an FDA-approv<strong>ed</strong> treatment for alcohol dependence, in r<strong>ed</strong>ucing theintensity <strong>of</strong> urges to gamble, gambling thoughts, and gambling behavior when

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