Antidepressant: Difference between revisions
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===Recurrence of illness after discontinuation=== | |||
The recurrence risk for depression or panic was shorter if antidepressants were discontinued over 7 days or less.<ref name="pmid20478876">{{cite journal| author=Baldessarini RJ, Tondo L, Ghiani C, Lepri B| title=Illness risk following rapid versus gradual discontinuation of antidepressants. | journal=Am J Psychiatry | year= 2010 | volume= 167 | issue= 8 | pages= 934-41 | pmid=20478876 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20478876 | doi=10.1176/appi.ajp.2010.09060880 }} </ref> | |||
==References== | ==References== | ||
<references/> | <references/> | ||
Revision as of 22:59, 8 September 2010
Antidepressant medications are "mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions. Several monoamine oxidase inhibitors are useful as antidepressants apparently as a long-term consequence of their modulation of catecholamine levels. The tricyclic compounds useful as antidepressive agents (tricyclic antidepressant) also appear to act through brain catecholamine systems. A third group (second-generation antidepressant agents) is a diverse group of drugs including some that act specifically on serotonergic systems."[1]
Mechanism of action
Depression may be due to the monoamine-deficiency hypothesis, which is a "deficiency in serotonin or norepinephrine neurotransmission in the brain."[2]
Classification
Tricyclic antidepressants
Tricyclic antidepressants are "substances that contain a fused three-ring moiety and are used in the treatment of depression. These drugs block the uptake of norepinephrine and serotonin into axon terminals and may block some subtypes of serotonin, adrenergic, and histamine receptors. However the mechanism of their antidepressant effects is not clear because the therapeutic effects usually take weeks to develop and may reflect compensatory changes in the central nervous system."[3]
Heterocyclic antidepressants
Heterocyclic antidepressants include trazadone and bupropion, and more recently, mirtazapine and nefazadone which are based on trazadone[4]
Second-generation antidepressants
Second-generation antidepressants are a "structurally and mechanistically diverse group of drugs that are not tricyclics or monoamine oxidase inhibitors. The most clinically important appear to act selectively on serotonergic systems, especially by inhibiting serotonin reuptake."[5]
Monoamine oxidase inhibitors
Monoamine oxidase inhibitors are a "chemically heterogeneous group of drugs that have in common the ability to block oxidative deamination of naturally occurring monoamines".[6]
Effectiveness
The effectiveness is antidepressants depends on the severity of a patient's depression. This relationship may be due to thedeclining effect of placebo among more severely depressed patients.[7]
| American Psychiatric Association classification of severity[8] | Hamilton Depression Rating Scale (HDRS) | Number needed to treat | Clinical significance (NICE)[9] |
|---|---|---|---|
| Mild to moderate | < 19 | 16 | No |
| Severe | 19 - 22 | 11 | No |
| Very severe | > 22 | 4 | Yes |
Adverse effects
Neuroleptic malignant syndrome
Serotonin syndrome
Recurrence of illness after discontinuation
The recurrence risk for depression or panic was shorter if antidepressants were discontinued over 7 days or less.[10]
References
- ↑ Anonymous (2024), Antidepressant (English). Medical Subject Headings. U.S. National Library of Medicine.
- ↑ Belmaker RH, Agam G (2008). "Major depressive disorder". N. Engl. J. Med. 358 (1): 55–68. DOI:10.1056/NEJMra073096. PMID 18172175. Research Blogging.
- ↑ Anonymous (2024), Tricyclic Antidepressive Agents (English). Medical Subject Headings. U.S. National Library of Medicine.
- ↑ Katzung, Bertram G. (2006). “Antidepressant Agents”, Basic and Clinical Pharmacology, 10th. New York: McGraw-Hill Medical Publishing Division. ISBN 0-07-145153-6.
- ↑ Anonymous (2024), Second-generation antidepressants (English). Medical Subject Headings. U.S. National Library of Medicine.
- ↑ Anonymous (2024), Monoamine Oxidase Inhibitors (English). Medical Subject Headings. U.S. National Library of Medicine.
- ↑ 7.0 7.1 Lo B (2010). "Commentary: Conflict of interest policies: an opportunity for the medical profession to take the lead.". Acad Med 85 (1): 9-11. DOI:10.1097/ACM.0b013e3181c46e96. PMID 20042812. Research Blogging.
- ↑ First, Michael B. (2007). Handbook of Psychiatric Measures, Second Edition. American Psychiatric Publishing, Inc. ISBN 1-58562-218-4.
- ↑ National Institute for Clinical Excellence. Depression: Management of Depression in Primary and Secondary Care. London, England: National Institute for Clinical Excellence; 2004.
- ↑ Baldessarini RJ, Tondo L, Ghiani C, Lepri B (2010). "Illness risk following rapid versus gradual discontinuation of antidepressants.". Am J Psychiatry 167 (8): 934-41. DOI:10.1176/appi.ajp.2010.09060880. PMID 20478876. Research Blogging.