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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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230 III. SUBSTANCES OF ABUSEAlthough a long half-life may be beneficial in r<strong>ed</strong>ucing the spe<strong>ed</strong> <strong>of</strong> onsetand severity <strong>of</strong> benzodiazepine withdrawal on abrupt discontinuation, it can bemore problematic in other situations. An increase in motor vehicle crashinvolvement was found in elderly persons using long half-life benzodiazepines,whereas use <strong>of</strong> shorter half-life benzodiazepines show<strong>ed</strong> no increase in the probability<strong>of</strong> crashes in elderly persons compar<strong>ed</strong> to same-age persons who did notuse a benzodiazepine (Hemmelgarn, Suissa, Huang, Boivin, & Pinard, 1997;Wang, Bohn, Glynn, Mogun, & Avom, 2001).ReinforcementThree additional aspects <strong>of</strong> benzodiazepine pharmacology are relevant to thetreatment <strong>of</strong> addict<strong>ed</strong> patients: reinforcement, withdrawal, and tolerance.Reinforcement is the potential for these m<strong>ed</strong>icines to be abus<strong>ed</strong> or “lik<strong>ed</strong>” byalcoholics and drug addicts. In controll<strong>ed</strong> studies, benzodiazepines are not reinforcingor “lik<strong>ed</strong>” by either normal or anxious subjects. For example, normaland anxious subjects, given a choice between placebos and benzodiazepines,more <strong>of</strong>ten choose the placebo in double-blind acute dose experiments, regardless<strong>of</strong> the specific benzodiazepine given. In contrast, subjects with a history <strong>of</strong>addiction in double-blind studies prefer benzodiazepines—especially at highdoses—to placebos. Studies have demonstrat<strong>ed</strong> that people with a history <strong>of</strong>addiction show a greater preference for interm<strong>ed</strong>iate-acting barbiturates andstimulants, as well as narcotics, than for benzodiazepines. Thus, the benzodiazepinesare reinforcing for alcoholics and drug addicts (though not for anxiouspeople or for people who do not have a history <strong>of</strong> addiction). The benzodiazepinesare relatively weak reinforcers compar<strong>ed</strong> to opiates, stimulants, andbarbiturates among alcoholics and drug addicts.This research confirms the common clinical observation that benzodiazepinesare rarely drugs <strong>of</strong> choice among addict<strong>ed</strong> people for their euphoriceffects (DuPont, 1984, 1988). Although it remains unclear why alcoholics anddrug addicts react differently to the benzodiazepines than do normal or anxioussubjects, this phenomenon exists with all abus<strong>ed</strong> drugs. It is not limit<strong>ed</strong> to thebenzodiazepines. Normal subjects in double-blind studies do not generally“like” abus<strong>ed</strong> drugs, including stimulants, narcotics, and even alcohol. Peoplewho are not addict<strong>ed</strong> to alcohol and other drugs do not like the feeling <strong>of</strong> beingintoxicat<strong>ed</strong>. Whether addict<strong>ed</strong> people learn to like the intoxicat<strong>ed</strong> feeling orwhether they have some innate (perhaps genetically determin<strong>ed</strong>) differencethat explains this characteristic response to alcohol and controll<strong>ed</strong> substancesremains an unanswer<strong>ed</strong> question <strong>of</strong> great importance to the prevention <strong>of</strong>addiction.When it comes to the outpatient treatment <strong>of</strong> anxiety in patients withactive addiction (e.g., current or recent abuse <strong>of</strong> alcohol or other drugs), the use<strong>of</strong> a controll<strong>ed</strong> substance, including benzodiazepines, is generally contraindi-

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