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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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8. Marijuana, Hallucinogens, and Club Drugs 169KETAMINESpecial K, Super K, Vitamin K, or just plain K, are all names for the nonanalgesicanesthetic ketamine. Ketamine was first manufactur<strong>ed</strong> in 1965. Veterinariansand p<strong>ed</strong>iatric surgeons still legally manufacture it, primarily for therapeutic use;recent crackdowns on the illegal distribution <strong>of</strong> ketamine from these sourceshave l<strong>ed</strong> to the increas<strong>ed</strong> smuggling <strong>of</strong> it from foreign sources. The recreationaluse <strong>of</strong> ketamine probably began in the 1960s and was first describ<strong>ed</strong> in detail byLilly (1978). Since that time, its popularity has continu<strong>ed</strong> to rise (Cooper,1996; Dotson, Ackerman, & West, 1995; Graeme, 2000).Ketamine is classifi<strong>ed</strong> as a dissociative anesthetic. As this classificationimplies, the drug causes a dose-dependent dissociative episode, with feelings <strong>of</strong>fragmentation, detachment, and what one user has describ<strong>ed</strong> as “psychic/physical/spiritualscatter.” Use <strong>of</strong> ketamine imparts a disconnection from awareness<strong>of</strong> stimuli from the general environment. This includes but is not limit<strong>ed</strong> topain.HistoryKetamine was first manufactur<strong>ed</strong> in 1965 at the University <strong>of</strong> Michigan andmarket<strong>ed</strong> under the name <strong>of</strong> Ketalar. It is most commonly available in 10-ml(100 mg/ml) liquid-containing vials (Fort Dodge Laboratories, 1997). It is aclose chemical cousin <strong>of</strong> phencyclidine, also known as PCP or angel dust. PCPhas physiological properties that made it advantageous as an anesthetic. PCPdoes not cause the kind <strong>of</strong> cardiac arrhythmias and respiratory depression inherentin classical anesthetics. PCP also had a number <strong>of</strong> severe limitations as ananesthetic, most significantly, that it causes a high degree <strong>of</strong> psychotic and violentreactions (National Institute on Drug Abuse, 1979). These effects occur atan alarmingly high rate (50%) and may persist for as long as 10 days (Crider,1986; Meyer, Greifenstein, & DeVault, 1959). Ketamine produces minimal cardiacand respiratory effects, and its anesthetic and behavioral effects remit soonafter administration (Moretti, Hassan, Goodman, & Meltzer, 1984; Pandit,Kothary, & Kumar, 1980). The m<strong>ed</strong>ication continues to have therapeutic usefulness,principally with children and animals.Since the 1970s, ketamine has been a drug us<strong>ed</strong> for “recreational” purposes.Although the distinction is by no means complete, ketamine users clusterinto two distinct subtypes. The first type uses ketamine in a solitary fashion;the second type uses the drug in a social setting, although the effects <strong>of</strong> the drugdo not promote sociability. These are the young clubgoers and “ravers” (Weir,2000). Ketamine is especially popular at circuit parties and thus a favorite <strong>of</strong> gayurbanites (Lee & McDowell, 2003).Ketamine is commercially available as a liquid. About 90% <strong>of</strong> ketaminecomes from divert<strong>ed</strong> veterinary sources (National Institute on Drug Abuse,

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