Psychopharmacology of smoking cessation in patients with mental illness
Notice bibliographique
Résumé
A 48-year-old male smoker (35 cigarettes a day for 30 years) with major depressive disorder stabilized on citalopram, 40 mg once daily, wished to quit smoking. Whenever he quit “cold turkey,” he relapsed owing to intolerable anxiety and depression that twice met criteria for an acute depressive episode. His psychiatrist added bupropion SR, 150 mg twice daily. He was advised to quit within 2 weeks. His anxiety increased within a few days of quitting but resolved with a reduction in caffeine consumption. He discontinued bupropion after 12 months. He gained 1 kg, remained euthymic and had occasional mild cravings with minimal anxiety. Tobacco causes almost 48 000 premature deaths in Canada annually (Makomaski and Kaiserman, Can J Public Health 2004;95:38-44). Those with past-month psychiatric diagnoses consume 44% of all cigarettes (Lasser et al, JAMA 2000;284:2606-10). This significant association is due to a combination of genetic (e.g., P50 deficits in schizophrenia corrected by nicotine), environmental (e.g., pro-smoking policies in patient group homes) and other factors (e.g., “self-medicating behaviours” to reduce anxiety and depression; the use of cigarettes as rewards to shape behaviour). The adverse effects are amplified by obesity and metabolic changes owing to psychotropic drugs and poverty. Fortunately, there is a 50% risk reduction in coronary events within 1 year of quitting and a significant reduction in the risk of developing lung disease and cancer in the long-term. Bupropion has a large effect size in permanent smoking cessation (19 trials, odds ratio 2.06, 95% confidence interval 1.77–2.40) independent of its antidepressant effects (Hughes et al, Cochrane Database Syst Rev 2004;[4]:{type:entrez-nucleotide,attrs:{text:C31,term_id:30294550,term_text:C31}}C31), with 15% quitting permanently with minimal weight gain. It is also effective in smokers with depression and schizophrenia (Dudas and George, Essent Psychopharmacol 2005;6:158-72). Bupropion may stabilize the dopaminergic reward system and competitively antagonize nicotine at central α4β2 nicotinic receptors (Warner and Shoaib, Addict Biol 2005;10:219-31). Clinically, subjects report decreased cravings and cigarette taste aversion. Responders tend to be moderately dependent male smokers who have tried to quit previously (Hurt et al, Addict Behav 2002;27:493-507). Smokers with the low activity variant (CT/TT group) of CYP2B6 are less likely to be abstinent than are smokers with normal activity variants (CC group) (χ2 = 5.0, p < 0.02) (Munafo et al, Pharmacogenomics 2005; 6:211-23). Bupropion is safe in combination with most neurotropic drugs because it is primarily metabolized by CYP 2B6. However, dose reduction in concomitant caffeine, benzodiazepines and neuroleptic drugs (especially clozapine) may be warranted, because polyaromatic hydrocarbons present in smoke induce CYP 1A2. The induction reverses within days to weeks after smoking cessation. Doses of 150 mg or 300 mg are effective within 3 weeks, but there are no studies with higher doses. Motivated smokers may also respond after 4 weeks of therapy. Thereafter, nicotine replacement therapy may be added. Relapse is common on stopping the medication, even after a year, necessitating longer-term use in some smokers (Hays et al, Ann Intern Med 2001;135:423-33). Insomnia can be minimized by timing the second dose to be no later than 6 hours before bed. Seizures (1/2000) can be prevented by not exceeding the recommended dose and by observing contraindications. In conclusion, psychiatrists have the ability to treat smokers in their practice with a common psychiatric medication with good efficacy. Peter Selby, MBBS, CCFP, FASAM Addictions Program Centre for Addiction and Mental Health Departments of Family and Community Medicine, Psychiatry and Public Health Sciences University of Toronto Toronto, Ont.
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Comment cette classification a été obtenuedéplier
Prédiction machine sur la base complète
Imitation des enseignantsNi prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.
Scores du classifieur distillé par catégorie (deux têtes)
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,000 | 0,001 |
| Méta-épidémiologie (sens strict) | 0,000 | 0,000 |
| Méta-épidémiologie (sens large) | 0,000 | 0,000 |
| Bibliométrie | 0,000 | 0,000 |
| Études des sciences et des technologies | 0,000 | 0,000 |
| Communication savante | 0,000 | 0,000 |
| Science ouverte | 0,000 | 0,000 |
| Intégrité de la recherche | 0,000 | 0,001 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,002 | 0,000 |
Scores machine (provisoires)
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
score_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».