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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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Effects on Reproductive Functioning20. <strong>Addictive</strong> <strong>Disorders</strong> in Women 441Whereas single doses <strong>of</strong> alcohol have little effect on sex hormone levels inwomen, chronic heavy drinking leads to inhibition <strong>of</strong> ovulation, infertility, anda variety <strong>of</strong> reproductive and sexual dysfunctions (Blume & Zilberman, 2004).Consumption <strong>of</strong> alcohol by women suppresses both sexual arousal andorgasmic function in a dose–response fashion. The physiological reality is contraryto the widely held cultural belief that alcohol is an aphrodisiac for women(Blume, 1991). This belief <strong>of</strong>ten leads alcoholic women to expect that theyne<strong>ed</strong> alcohol to perform and enjoy the sexual act, in spite <strong>of</strong> their alcoholrelat<strong>ed</strong>sexual problems. The clinician can help such women by explaining thattheir drinking has depress<strong>ed</strong> rather than enhanc<strong>ed</strong> their sexual responsiveness,and that in the presence <strong>of</strong> a loving relationship, they will find sex more enjoyablein recovery than they did while drinking (Gavaler, Rizzo, & Rossaro,1993).Cocaine and amphetamines are widely believ<strong>ed</strong> by their users to be sexualstimulants, whereas chronic use is <strong>of</strong>ten associat<strong>ed</strong> with loss <strong>of</strong> sexual desire andinhibit<strong>ed</strong> orgasm. In addition, cocaine use has been associat<strong>ed</strong> with menstrualalterations, galactorrhea, infertility, hyperprolactinemia, and increas<strong>ed</strong> levels <strong>of</strong>luteinizing hormones in women (Mendelson, Sholar, Siegel, & Mello, 2001).Heroin use has been report<strong>ed</strong> to suppress both ovulation and sexual desire, ashas abuse <strong>of</strong> s<strong>ed</strong>ative drugs (Zilberman & Blume, 2004).Fetal Alcohol and Drug EffectsFetal alcohol syndrome (FAS), a combination <strong>of</strong> birth defects producing lifelongdisability, is currently estimat<strong>ed</strong> to affect about 1–3 infants for every 1,000live births in the Unit<strong>ed</strong> States. FAS is thus among the three most frequentbirth defects resulting in mental retardation, with a prevalence similar to Downsyndrome and spina bifida. A diagnosis <strong>of</strong> FAS is bas<strong>ed</strong> on the co-occurrence <strong>of</strong>pre- and postnatal growth deficiency, structural facial abnormalities, and centralnervous system dysfunctions, including poor coordination, mental retardation,and/or behavioral dyscontrol. In addition, a wide variety <strong>of</strong> other birthdefects affecting vision, hearing, and other body systems are <strong>of</strong>ten seen in thesechildren. Although the full FAS syndrome is seen almost exclusively in the <strong>of</strong>fspring<strong>of</strong> alcoholic women who drink heavily (an average <strong>of</strong> six or more drinksper day) during pregnancy, women who drink at lower levels are at risk for fetalalcohol effects such as miscarriage, low birthweight, birth defects, and behavioralabnormalities (Warren et al., 2001). The prevalence <strong>of</strong> fetal alcoholeffects is thought to be many times greater than that <strong>of</strong> FAS.Fetal damage is also associat<strong>ed</strong> with other drug use and abuse (Singer et al.,2002). Cigarette smoking during pregnancy is implicat<strong>ed</strong> as an important factor

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