Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1997-10-21
pubmed:abstractText
In depression that is resistant to tricyclic antidepressant (TCA) therapy, the substitution of a selective serotonin re-uptake inhibitor (SSRI), clomipramine, or a monoamine oxidase (MAO) inhibitor has been recommended. However, adding an additional antidepressant medication from a different drug class may produce even more rapid efficacy. In this regard, the combination of a MAO inhibitor or a SSRI plus a TCA has been shown to be of value in treatment-resistant depression (TRD). In this report, we examined the efficacy of clomipramine augmentation in 20 patients who failed to respond to either a MAO inhibitor or fluoxetine therapy for at least a 6-week period, and compared this to a third group given MAO inhibitor plus a conventional TCA. Two out of 9 (22%) MAO inhibitor/clomipramine patients and 4 out of 11 (36%) fluoxetine/clomipramine patients improved (Fisher's Exact test, P = ns), compared to 3 out of 7 (43%) patients taking MAO inhibitor/TCA (P = ns). However, the MAO inhibitor/clomipramine group experienced significantly more adverse events which necessitated stopping treatment (56%) when compared to the fluoxetine/clomipramine (9%) and compared to the MAO inhibitor/TCA group (0%) (chi 2 = 8.9, df = 2, P < 0.05). These adverse events included several cases of serotonin syndrome of mild to moderate severity. These observations indicate that clomipramine augmentation of a failed MAO inhibitor trial is of marginal efficacy (compared to augmentation with a conventional TCA) and should be employed with extreme caution.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1091-4269
pubmed:author
pubmed:issnType
Print
pubmed:volume
5
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
84-90
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:9262938-Adult, pubmed-meshheading:9262938-Aged, pubmed-meshheading:9262938-Akathisia, Drug-Induced, pubmed-meshheading:9262938-Analysis of Variance, pubmed-meshheading:9262938-Antidepressive Agents, Tricyclic, pubmed-meshheading:9262938-Chi-Square Distribution, pubmed-meshheading:9262938-Clomipramine, pubmed-meshheading:9262938-Cross-Sectional Studies, pubmed-meshheading:9262938-Depressive Disorder, pubmed-meshheading:9262938-Drug Interactions, pubmed-meshheading:9262938-Drug Resistance, pubmed-meshheading:9262938-Drug Therapy, Combination, pubmed-meshheading:9262938-Female, pubmed-meshheading:9262938-Humans, pubmed-meshheading:9262938-Male, pubmed-meshheading:9262938-Mental Disorders, pubmed-meshheading:9262938-Middle Aged, pubmed-meshheading:9262938-Monoamine Oxidase Inhibitors, pubmed-meshheading:9262938-Prospective Studies, pubmed-meshheading:9262938-Retrospective Studies, pubmed-meshheading:9262938-Serotonin, pubmed-meshheading:9262938-Serotonin Uptake Inhibitors, pubmed-meshheading:9262938-Syndrome, pubmed-meshheading:9262938-Treatment Outcome
pubmed:year
1997
pubmed:articleTitle
Clomipramine augmentation in treatment-resistant depression.
pubmed:affiliation
Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, USA.
pubmed:publicationType
Journal Article, Clinical Trial, Research Support, Non-U.S. Gov't