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dc.contributor.authorTrivedi, Madhukar H.
dc.contributor.authorDunner, David L.
dc.contributor.authorKornstein, Susan G.
dc.contributor.authorThase, Michael E.
dc.contributor.authorZajecka, John M.
dc.contributor.authorRothschild, Anthony J.
dc.contributor.authorFriedman, Edward S.
dc.contributor.authorShelton, Richard C.
dc.contributor.authorKeller, Martin B.
dc.contributor.authorKocsis, James H.
dc.contributor.authorGelenberg, Alan J.
dc.date2022-08-11T08:10:27.000
dc.date.accessioned2022-08-23T17:09:52Z
dc.date.available2022-08-23T17:09:52Z
dc.date.issued2010-11-01
dc.date.submitted2011-03-08
dc.identifier.citationJ Affect Disord. 2010 Nov;126(3):420-9. Epub 2010 May 26. <a href="http://dx.doi.org/10.1016/j.jad.2010.04.011">Link to article on publisher's site</a>
dc.identifier.issn0165-0327 (Linking)
dc.identifier.doi10.1016/j.jad.2010.04.011
dc.identifier.pmid20510459
dc.identifier.urihttp://hdl.handle.net/20.500.14038/45918
dc.description.abstractBACKGROUND: Psychosocial outcomes from the Prevention of Recurrent Episodes of Depression with Venlafaxine ER for Two Years (PREVENT) study were evaluated. METHODS: Adult outpatients with recurrent major depressive disorder (MDD) and response or remission following 6-month continuation treatment with venlafaxine extended release (ER) were randomized to receive venlafaxine ER or placebo for 1 year. Patients without recurrence on venlafaxine ER during year 1 were randomized to venlafaxine ER or placebo for year 2. Psychosocial functioning was assessed using the Quality of Life Enjoyment and Satisfaction Questionnaire-Short Form (Q-LES-Q), Life Enjoyment Scale-Short Version (LES-S), Social Adjustment Scale-Self-Report (SAS-SR) total and individual factors, Short Form Health Survey (SF-36) (vitality, social functioning, and role function-emotional items), and Longitudinal Interval Follow-up Evaluation (LIFE). RESULTS: At year 1 end, better overall psychosocial functioning was seen among patients randomly assigned to venlafaxine ER (n=129) vs placebo (n=129), with significant differences at end point on SF-36 role function-emotional, Q-LES-Q, and SAS-SR total, and work, house work, social/leisure, and extended-family factor scores (p LIMITATIONS: Patients with chronic MDD or treatment resistance were excluded and long-term specialist care was a financial incentive for treatment compliance. Discontinuation-related adverse events may have compromised the integrity of the treatment blind. CONCLUSIONS: For patients with recurrent MDD, 2 years' maintenance therapy with venlafaxine ER may improve psychosocial functioning vs placebo.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=20510459&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.jad.2010.04.011
dc.subjectAdult
dc.subjectAntidepressive Agents, Second-Generation
dc.subjecteffects
dc.subjectCyclohexanols
dc.subjectDelayed-Action Preparations
dc.subjectDepressive Disorder, Major
dc.subjectFemale
dc.subjectHumans
dc.subjectLong-Term Care
dc.subjectLongitudinal Studies
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectQuality of Life
dc.subjectQuestionnaires
dc.subjectRecurrence
dc.subject*Social Adjustment
dc.subjectPsychiatry
dc.titlePsychosocial outcomes in patients with recurrent major depressive disorder during 2 years of maintenance treatment with venlafaxine extended release
dc.typeJournal Article
dc.source.journaltitleJournal of affective disorders
dc.source.volume126
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/psych_pp/445
dc.identifier.contextkey1858216
html.description.abstract<p>BACKGROUND: Psychosocial outcomes from the Prevention of Recurrent Episodes of Depression with Venlafaxine ER for Two Years (PREVENT) study were evaluated.</p> <p>METHODS: Adult outpatients with recurrent major depressive disorder (MDD) and response or remission following 6-month continuation treatment with venlafaxine extended release (ER) were randomized to receive venlafaxine ER or placebo for 1 year. Patients without recurrence on venlafaxine ER during year 1 were randomized to venlafaxine ER or placebo for year 2. Psychosocial functioning was assessed using the Quality of Life Enjoyment and Satisfaction Questionnaire-Short Form (Q-LES-Q), Life Enjoyment Scale-Short Version (LES-S), Social Adjustment Scale-Self-Report (SAS-SR) total and individual factors, Short Form Health Survey (SF-36) (vitality, social functioning, and role function-emotional items), and Longitudinal Interval Follow-up Evaluation (LIFE).</p> <p>RESULTS: At year 1 end, better overall psychosocial functioning was seen among patients randomly assigned to venlafaxine ER (n=129) vs placebo (n=129), with significant differences at end point on SF-36 role function-emotional, Q-LES-Q, and SAS-SR total, and work, house work, social/leisure, and extended-family factor scores (p</p> <p>LIMITATIONS: Patients with chronic MDD or treatment resistance were excluded and long-term specialist care was a financial incentive for treatment compliance. Discontinuation-related adverse events may have compromised the integrity of the treatment blind.</p> <p>CONCLUSIONS: For patients with recurrent MDD, 2 years' maintenance therapy with venlafaxine ER may improve psychosocial functioning vs placebo.</p>
dc.identifier.submissionpathpsych_pp/445
dc.contributor.departmentDepartment of Psychiatry
dc.source.pages420-9


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