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Review
. 1994 Dec:55 Suppl:3-15; discussion 16-7.

Evolutionary trends in the pharmacotherapeutic management of depression

Affiliations
  • PMID: 7814356
Review

Evolutionary trends in the pharmacotherapeutic management of depression

C B Nemeroff. J Clin Psychiatry. 1994 Dec.

Abstract

The past decade has brought an exponential increase in our knowledge of the pharmacotherapeutic management of depression. Much has been learned about the prevalence, risks, and course of depression in the general population, the elderly, and patients with comorbid medical illnesses and about the biological basis of depression. This article reviews evolving trends in the diagnosis and management of depression and evaluates the main classes of antidepressants. Although depression carries a high risk of morbidity and mortality, it is very treatable, and early diagnosis and early treatment are now emphasized. Antidepressant medication is continued after the patients' acute depressive symptoms resolve, sometimes for as long as 1 to 5 years to prevent relapse and recurrence of depression; in addition, full doses, rather than lower doses of antidepressant are prescribed for maintenance therapy. The armamentarium of antidepressants too has changed. In addition to monoamine oxidase inhibitors and tricyclic and tetracyclic antidepressants, the serotonin reuptake inhibitors fluoxetine, sertraline, and paroxetine are now available, as well as a group of antidepressants with atypical mechanisms of action that includes bupropion, trazodone, venlafaxin, and nefazodone. Although comparable in efficacy to the tricyclic antidepressants, these new drugs are safer and better tolerated because they are believed to act selectively on specific neurotransmitter systems.

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Comment in

  • Incentive bias?
    Gammon GD. Gammon GD. J Clin Psychiatry. 1996 Jun;57(6):265; author reply 267-9. J Clin Psychiatry. 1996. PMID: 8666565 No abstract available.
  • Incentive bias?
    Lane RM. Lane RM. J Clin Psychiatry. 1996 Jun;57(6):265-7; author reply 267-9. J Clin Psychiatry. 1996. PMID: 8666566 No abstract available.
  • SSRI optimal dose remains at issue.
    Rifkin A. Rifkin A. J Clin Psychiatry. 1997 Feb;58(2):87-8. doi: 10.4088/jcp.v58n0206d. J Clin Psychiatry. 1997. PMID: 9062381 No abstract available.
  • Continuing dialogue on incentive bias.
    Jefferson JW, Greist JH, Katielnick DJ. Jefferson JW, et al. J Clin Psychiatry. 1997 Oct;58(10):450-3. doi: 10.4088/jcp.v58n1008b. J Clin Psychiatry. 1997. PMID: 9375598 No abstract available.

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