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ABSTRACTS - World Psychiatric Association

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the drug self-administration model the animal self administers the<br />

drug (intravenously or orally). Thus, these two animal models can be<br />

complementary and represent, so far, the most reliable tools to investigate<br />

neurobiology and possible therapies in drug addiction.<br />

RS33.2.<br />

NEW TARGETS FOR TREATING DRUG<br />

DEPENDENCE: THE ROLE OF THE AMYGDALA<br />

M. Cador<br />

Université Victor Segalen, Bordeaux, France<br />

Opiate withdrawal leads to the emergence of an aversive state that can<br />

be conditioned to a specific environment. Reactivation of these withdrawal<br />

memories has been suggested to be involved in relapse to drugseeking<br />

of abstinent opiate addicts. Among the limbic areas that are<br />

likely to mediate these features of opiate dependence, amygdala nuclei<br />

represent critical neural substrates. Using a conditioned place aversion<br />

paradigm (CPA), we have previously shown specific opposite patterns<br />

of reactivity in the basolateral (BLA) and the central (CeA) amygdala,<br />

when comparing the experience of acute opiate withdrawal with the<br />

re-exposure to a withdrawal-paired environment. These data gave<br />

clues about the potential mechanisms by which amygdala nuclei may<br />

be involved in withdrawal memories. To extend these results, the present<br />

study aimed to assess the cellular reactivity and plasticity of amygdala<br />

nuclei during the opiate withdrawal conditioning process. For<br />

this, we have quantified c-fos and arc expression using in situ<br />

hybridization in rats, following each of the three conditioning sessions<br />

during CPA, and after re-exposure to the withdrawal-paired environment.<br />

BLA output neurons showed an increase in the expression of the<br />

plasticity-related arc gene during conditioning that was also increased<br />

by re-exposure to the withdrawal-paired environment. Interestingly,<br />

the CeA showed an opposite pattern of responding, and the intercalated<br />

cell masses (ITC), a possible inhibitory interface between the BLA<br />

and CeA, showed a persistent activation of c-fos and arc mRNA. We<br />

report here specific c-fos and arc patterns of reactivity in amygdala<br />

nuclei during withdrawal conditioning. These findings improve our<br />

understanding of the involvement of the amygdala network in the formation<br />

and retrieval of withdrawal memories. Plasticity processes<br />

within BLA output neurons during conditioning may participate in<br />

increasing the BLA reactivity to conditioned stimuli, which could in<br />

turn (by the control of downstream nuclei) reinforce and drive the<br />

motivational properties of withdrawal over drug consumption.<br />

RS33.3.<br />

CLINICAL GOALS FOR DRUG ADDICTION THERAPY<br />

W. van den Brink<br />

University of Amsterdam, The Netherlands<br />

Both clinical experience and neurobiological evidence indicate that<br />

opioid dependence is a chronic relapsing disorder. Treatment objectives<br />

depend on the pursued goals: crisis intervention, abstinence-oriented<br />

treatment (detoxification and relapse prevention), or agonist<br />

maintenance treatment. The high quality of solid evidence in the literature<br />

demonstrates that there are numerous effective interventions<br />

available for the treatment of opioid dependence. Crisis intervention,<br />

frequently necessary owing to the high overdose rate, can be effectively<br />

handled with naloxone. Abstinence-oriented interventions are<br />

effective for only a few motivated patients with stable living conditions<br />

and adequate social support. Agonist maintenance treatment is<br />

considered the first line of treatment for opioid dependence. Numerous<br />

studies have shown efficacy for methadone and buprenorphine<br />

treatment, while maintenance with other agonists is also becoming<br />

available to a greater extent. Maintenance treatment with diamorphine<br />

should be made available for the small group of treatmentresistant,<br />

severely dependent addicts. Other harm-reduction measures<br />

can serve to engage individuals with opioid addiction who are<br />

not in treatment. In conclusion, opioid dependence is a chronic<br />

relapsing disease that is difficult to cure, but effective treatments are<br />

available to stabilize patients and reduce harm, thereby increasing life<br />

expectancy and quality of life.<br />

RS33.4.<br />

OPIOID DEPENDENCE AND PREGNANCY<br />

G. Fischer<br />

Department of Psychiatry and Psychotherapy, Medical University<br />

of Vienna, Austria<br />

The management of opioid dependence during pregnancy has<br />

received considerable attention over the past three decades. Recent<br />

peer-reviewed literature in the fields of pregnancy and opioid dependence<br />

and neonatal abstinence syndrome has been evaluated and discussed.<br />

Pregnant opioid-dependent women must be carefully managed<br />

to minimize harm to the fetus; therefore, standardized care for<br />

maternal health is required. In a multidisciplinary care system, opioid<br />

maintenance therapy is the recommended treatment approach during<br />

pregnancy. Equivalent attention must be given to the treatment of<br />

neonatal abstinence syndrome, which occurs in 55-94% of neonates<br />

after intrauterine opioid exposure with a 60% likelihood of requiring<br />

treatment. Heterogeneous rating scales as well as heterogeneous<br />

treatment approaches are often responsible for extended hospital<br />

stays. The interpretation of available literature is confounded by several<br />

methodological flaws. In general, there is still a lack of evidencebased<br />

study designs for pharmacological treatment of these patients<br />

as well as for the neonatal abstinence syndrome.<br />

RS33.5.<br />

PHARMACOLOGICAL VS. PSYCHOSOCIAL<br />

INTERVENTIONS IN THE THERAPY OF ADDICTION<br />

M. Davoli<br />

Department of Epidemiology, Local Health Unit E, Rome, Italy<br />

Several pharmacological approaches aimed at opioid detoxification<br />

are effective. Nevertheless, a majority of patients relapse to heroin use,<br />

and relapses are a substantial problem in the rehabilitation of heroin<br />

users. Some studies have suggested that the sorts of symptoms which<br />

are most distressing to addicts during detoxification are psychological<br />

rather than physiological. We explored the benefit from adding psychosocial<br />

interventions to detoxification treatments by searching the<br />

Cochrane Drugs and Alcohol Group trials register, the Cochrane Central<br />

Register of Controlled Trials (CENTRAL), PUBMED, EMBASE,<br />

CINAHL, PsycINFO and a reference list of articles. Nine studies<br />

involving people were included. These studies considered five different<br />

psychosocial interventions and two substitution detoxification<br />

treatments: methadone and buprenorphine. The results show promising<br />

benefit from adding any psychosocial treatment to any substitution<br />

detoxification treatment in terms of completion of treatment (RR<br />

1.68; 95% CI 1.11 to 2.55); use of opiate (RR 0.82; 95% CI 0.71 to<br />

0.93), results at follow-up (RR 2.43; 95% CI 1.61 to 3.66), and compliance<br />

(RR 0.48; 95% CI 0.38 to 0.59). Thus, psychosocial treatments<br />

offered in addition to pharmacological detoxification treatments are<br />

effective in terms of completion of treatment, use of opiate, results at<br />

follow-up and compliance. Limitations to this review are imposed by<br />

the heterogeneity of the assessment of outcomes. Because of lack of<br />

detailed information, no meta-analysis could be performed.<br />

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