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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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172 III. SUBSTANCES OF ABUSEIn the 1970s, GHB was available commercially as a sleep aid. It has som<strong>ed</strong>emonstrat<strong>ed</strong> therapeutic efficacy, particularly in the treatment <strong>of</strong> narcolepsy(Lammers et al., 1993; Mamelak, Scharf, & Woods, 1986; Scrima, Hartman,Johnson, Thomas, & Hiller, 1990). In 1990, after reports indicat<strong>ed</strong> that GHBmight have contribut<strong>ed</strong> to the hospitalization <strong>of</strong> several California youth, theFDA bann<strong>ed</strong> it. GHB has an extremely small therapeutic index, and as little asdouble the euphorigenic dose may cause serious central nervous system (CNS)depression. In recent years, it has been associat<strong>ed</strong> with numerous incidents <strong>of</strong>respiratory depression and coma. Increasing numbers <strong>of</strong> deaths have beenlink<strong>ed</strong> to GHB (Li, Stokes, & Woeckner, 1998).The legal status <strong>of</strong> GHB is complicat<strong>ed</strong>. Recently, GHB, under the brandname Xyrem, was classifi<strong>ed</strong> as a Sch<strong>ed</strong>ule III controll<strong>ed</strong> substance, but with specialregulations. The company that makes and markets the m<strong>ed</strong>ication hasdevelop<strong>ed</strong> a rigorous system that makes Xyrem available to patients from a singlespecialty pharmacy. Both physicians and patients must receive an <strong>ed</strong>ucationprogram from the manufacturer, Orphan M<strong>ed</strong>ical, before obtaining Xyrem.Orphan M<strong>ed</strong>ical has work<strong>ed</strong> closely with the FDA, the Drug EnforcementAdministration (DEA), and law enforcement agencies to develop strict distributionand risk-management controls design<strong>ed</strong> to restrict access to Xyrem tothe intend<strong>ed</strong> patient population (Tunnicliff & Raess, 2002). Illicit use <strong>of</strong>Xyrem is subject to penalties reserv<strong>ed</strong> for Sch<strong>ed</strong>ule I drugs.Most <strong>of</strong> the GHB sold in the Unit<strong>ed</strong> States is <strong>of</strong> the bootleg variety, manufactur<strong>ed</strong>by nonpr<strong>of</strong>essionals. In fact, it is relatively easy to manufacture, andInternet sites devot<strong>ed</strong> to explaining the process can be found readily, althoughthey are sometimes cleverly conceal<strong>ed</strong>.Physiological EffectsGHB is ingest<strong>ed</strong> orally, absorb<strong>ed</strong> rapidly, and reaches peak plasma concentrationsin 20–60 minutes (Vickers, 1969). The typical recreational dosage is0.75–1.5 g; higher dosages result in increas<strong>ed</strong> effects. The high lasts for no morethan 3 hours and report<strong>ed</strong>ly has few lasting effects. Repeat<strong>ed</strong> use <strong>of</strong> the drug canprolong its effects.Users <strong>of</strong> the drug report that GHB induces a pleasant state <strong>of</strong> relaxation andtranquility. Frequently report<strong>ed</strong> effects are placidity, mild euphoria, and anenhanc<strong>ed</strong> tendency to verbalize. GHB, like MDMA, has also been describ<strong>ed</strong> as asensual drug. Its effects have been liken<strong>ed</strong> to alcohol, another GABA-like drug(McCabe, Layne, Sayler, Slusher, & Bessman, 1971). Users report a feeling <strong>of</strong>mild numbing and pleasant disinhibition. This effect may account for the reportsthat GHB enhances the experience <strong>of</strong> sex. The dose–response curve for GHB isexce<strong>ed</strong>ingly steep. The LD 50is estimat<strong>ed</strong> at perhaps only five times the intoxicatingdosage (Vickers, 1969). Furthermore, the drug has synergistic effects withalcohol and probably other drugs as well. Therefore, small increases in the

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