Please use this identifier to cite or link to this item: https://doi.org/10.4088/JCR.12m08093
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dc.titleA randomized, double-blind, placebo-controlled trial of pramipexole augmentation in treatment-resistant major depressive disorder
dc.contributor.authorCusin, C.
dc.contributor.authorIovieno, N.
dc.contributor.authorIosifescu, D.V.
dc.contributor.authorNierenberg, A.A.
dc.contributor.authorFava, M.
dc.contributor.authorRush, A.J.
dc.contributor.authorPerlis, R.H.
dc.date.accessioned2014-11-26T09:03:30Z
dc.date.available2014-11-26T09:03:30Z
dc.date.issued2013-07
dc.identifier.citationCusin, C.,Iovieno, N.,Iosifescu, D.V.,Nierenberg, A.A.,Fava, M.,Rush, A.J.,Perlis, R.H. (2013-07). A randomized, double-blind, placebo-controlled trial of pramipexole augmentation in treatment-resistant major depressive disorder. Journal of Clinical Psychiatry 74 (7) : e636-e641. ScholarBank@NUS Repository. <a href="https://doi.org/10.4088/JCR.12m08093" target="_blank">https://doi.org/10.4088/JCR.12m08093</a>
dc.identifier.issn01606689
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/110478
dc.description.abstractBackground: Multiple treatments for patients with major depressive disorder (MDD) have demonstrated efficacy, but up to one-third of individuals with MDD do not achieve symptomatic remission despite various interventions. Existing augmentation or combination strategies can have substantial safety concerns that may limit their application. Method: This study investigated the antidepressant efficacy ofa flexible dose of the dopamine agonist pramipexole as an adjunct to standard antidepressant treatment in an 8-week, randomized, double-blind, placebo-controlled trial conducted in a tertiary-level depression center. We randomized 60 outpatients (aged 18 to 75 years) with treatment-resistant nonpsychotic MDD (diagnosed according to OSM-IY) to either pramipexole (n 30) or placebo (n 30).Treatment resistance was defined as continued depression (Montgomery-Asberg Depression Rating Scale [MADRS] score > 18) despite treatment with at least 1 prior antidepressant in the current depressive episode. Patients were recruited between September 2005 and April 2008. The primary outcome measure was the MADRS score. Results:The analyses that used a mixed-effects linear regression model indicated a modest but statistically significant benefit for pramipexole (P=.038). The last- observation-carried- forward analyses indicated that 40% and 33% of patients randomized to augmentation with pramipexole achieved response (x2=1.2, P=.27) and remission (x2=0.74, P=.61), respectively, compared to 27% and 23% with placebo; however, those differences were not statistically significant. Augmentation with pramipexole was well-tolerated, with no serious adverse effects identified. Conclusion: For patients who have failed to respond to standard antidepressant therapies, pramipexole is a safe and potentially efficacious augmentation strategy. © Copyright 2013 Physicians Postgraduate Press, Inc.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.4088/JCR.12m08093
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentDUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE
dc.description.doi10.4088/JCR.12m08093
dc.description.sourcetitleJournal of Clinical Psychiatry
dc.description.volume74
dc.description.issue7
dc.description.pagee636-e641
dc.description.codenJCLPD
dc.identifier.isiutNOT_IN_WOS
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