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dc.contributor.authorHollander, E.
dc.contributor.authorStein, D.J.
dc.contributor.authorFineberg, Naomi
dc.contributor.authorMarteau, F.
dc.contributor.authorLegault, M.
dc.date.accessioned2010-07-07T10:11:29Z
dc.date.available2010-07-07T10:11:29Z
dc.date.issued2010
dc.identifier.citationHollander , E , Stein , D J , Fineberg , N , Marteau , F & Legault , M 2010 , ' Quality of Life Outcomes in Patients With Obsessive-Compulsive Disorder: Relationship to Treatment Response and Symptom Relapse ' , Journal of Clinical Psychiatry , vol. 71 , no. 6 , pp. 784-792 .
dc.identifier.issn0160-6689
dc.identifier.otherPURE: 193863
dc.identifier.otherPURE UUID: 46f71b75-0b75-479a-b59a-aa1530d78236
dc.identifier.otherdspace: 2299/4631
dc.identifier.otherScopus: 77953760019
dc.identifier.urihttp://hdl.handle.net/2299/4631
dc.descriptionOriginal article can be found at: http://www.psychiatrist.com/default2.asp Copyright Physicians Postgraduate Press, Inc. [Full text of this article is not available in the UHRA]
dc.description.abstractObjective: Data were analyzed from 2 prospective, double-blind, placebo-controlled trials of escitalopram in obsessive-compulsive disorder (OCD) to characterize the baseline levels of functional disability and impairment in health-related quality of life (HRQoL) and to assess the relationship between treatment outcomes (response or relapse) and disability or HRQoL. Method: Data from a 24-week, placebo-controlled, fixed-dose trial (N = 466) of escitalopram (10–20 mg/d) or paroxetine (40 mg/d) and from a 40-week, flexible-dose (escitalopram 10–20 mg/d), placebo-controlled relapse-prevention trial (N = 468) were analyzed. Obsessive-compulsive disorder symptoms (DSM-IV criteria) were assessed using the Yale-Brown Obsessive Compulsive Scale (YBOCS), functioning was assessed using the Sheehan Disability Scale (SDS), and HRQoL was assessed using the Medical Outcomes Study Short Form (SF-36). Baseline data were pooled for patients across both studies. For patients in the fixed-dose study, SDS and SF-36 scores were compared across treatment groups and for responders versus nonresponders. In the relapse-prevention trial, SDS and SF-36 scores were compared for relapsed versus nonrelapsed patients. Results: Patients with more severe baseline symptoms (YBOCS ≥ 27) reported significantly greater impairment on the SDS (P < .001) and SF-36 (except for bodily pain). Patients receiving escitalopram or paroxetine reported significant improvements on most SF-36 dimensions and on the SDS compared to placebo; however, improvements in work-related functioning were seen earlier for patients receiving escitalopram (20 mg/d). At the study endpoints, SDS and SF-36 scores were significantly better for patients who were responders (versus nonresponders) and for patients who did not relapse (versus relapsers). Conclusions: Obsessive-compulsive disorder is associated with significant impairment in functioning and HRQoL. Significant differences in disability and HRQoL between responders and nonresponders or relapsers and nonrelapsers suggest a relationship between symptomatic and functional outcomes.en
dc.language.isoeng
dc.relation.ispartofJournal of Clinical Psychiatry
dc.titleQuality of Life Outcomes in Patients With Obsessive-Compulsive Disorder: Relationship to Treatment Response and Symptom Relapseen
dc.contributor.institutionDepartment of Psychology
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.contributor.institutionDepartment of Psychology and Sports Sciences
dc.contributor.institutionSchool of Life and Medical Sciences
dc.description.statusPeer reviewed
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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