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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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10. S<strong>ed</strong>atives/Hypnotics and Benzodiazepines 231cat<strong>ed</strong>. A number <strong>of</strong> alternative treatments for anxiety are available, includingnonpharmacological treatments, antidepressants, and buspirone (Buspar), anons<strong>ed</strong>ating antianxiety m<strong>ed</strong>icine with no abuse potential. As a general principle,the use <strong>of</strong> psychotropic m<strong>ed</strong>icines, whether controll<strong>ed</strong> (e.g., benzodiazepines)or noncontroll<strong>ed</strong> substances (e.g., antidepressants or antipsychotics), isunlikely to produce a therapeutic benefit for the actively using addict<strong>ed</strong> patient.Stable abstinence is requir<strong>ed</strong> for these antianxiety m<strong>ed</strong>icines to produce therapeuticresults.For patients who have been stable in recovery (including recovering alcoholics)and ne<strong>ed</strong> treatment for anxiety, it is advisable not to use benzodiazepines,unless the physician can be sure that the patient uses the benzodiazepineonly as prescrib<strong>ed</strong> and in the absence <strong>of</strong> any nonm<strong>ed</strong>ical drug use,including alcohol use. For many recovering people, successful use <strong>of</strong> benzodiazepinesin the treatment <strong>of</strong> their anxiety disorders has not threaten<strong>ed</strong> theirsobriety. We have seen many more patients in recovery who do not want to useany controll<strong>ed</strong> substance and have done well with their anxiety problems, withoutusing a benzodiazepine (Ciraulo et al., 1996; Sattar & Bhatia, 2003).If a benzodiazepine is to be administer<strong>ed</strong> to a recovering person, it may beprudent to use one <strong>of</strong> the slow-onset m<strong>ed</strong>icines (e.g., oxazepam, clorazepate, orprazepam) and to include a family member, as well as the sponsor from a 12-step fellowship in the therapeutic alliance, to help ensure that there is no abuse<strong>of</strong> the benzodiazepine or any other drug, including alcohol.WithdrawalAll <strong>of</strong> the m<strong>ed</strong>icines that influence the GABA system show cross-tolerance andsimilar withdrawal patterns. Because <strong>of</strong> cross-tolerance within this class <strong>of</strong> s<strong>ed</strong>ativesand hypnotics, an alcoholic or barbiturate addict can be withdrawn underm<strong>ed</strong>ical supervision using a benzodiazepine. For the same reason, phenobarbitalcan be us<strong>ed</strong> to manage benzodiazepine withdrawal (Wesson, Smith, & Ling,2003). Compar<strong>ed</strong> to other benzodiazepines, however, alprazolam withdrawalmay be inadequately cover<strong>ed</strong> by substitution. Alprazolam detoxification shouldinclude an estimation <strong>of</strong> daily use and a slow withdrawal over a period <strong>of</strong> weeks.Clonazepam has been found to be helpful in this condition.The s<strong>ed</strong>atives/hypnotics withdrawal syndrome, including the potential forwithdrawal seizures on abrupt discontinuation, is also a phenomenon <strong>of</strong> thisclass <strong>of</strong> m<strong>ed</strong>icines, which argues against abrupt discontinuation <strong>of</strong> any <strong>of</strong> thesem<strong>ed</strong>icines after daily use for more than a few weeks. Cessation <strong>of</strong> use <strong>of</strong> thebenzodiazepines, along with the other s<strong>ed</strong>atives and hypnotics, can cause withdrawalseizures, because they are potent antiepilepsy drugs that raise the seizurethreshold. M<strong>ed</strong>icines that raise the seizure threshold, when abruptly discontinu<strong>ed</strong>,produce a rebound drop in the seizure threshold that may cause seizures,even in people who have not previously had an epileptic seizure.

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