dc.contributor.author | Hollander, E. | |
dc.contributor.author | Stein, D.J. | |
dc.contributor.author | Fineberg, Naomi | |
dc.contributor.author | Marteau, F. | |
dc.contributor.author | Legault, M. | |
dc.date.accessioned | 2010-07-07T10:11:29Z | |
dc.date.available | 2010-07-07T10:11:29Z | |
dc.date.issued | 2010 | |
dc.identifier.citation | Hollander , 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.issn | 0160-6689 | |
dc.identifier.other | dspace: 2299/4631 | |
dc.identifier.uri | http://hdl.handle.net/2299/4631 | |
dc.description | Original 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.abstract | Objective: 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.iso | eng | |
dc.relation.ispartof | Journal of Clinical Psychiatry | |
dc.title | Quality of Life Outcomes in Patients With Obsessive-Compulsive Disorder: Relationship to Treatment Response and Symptom Relapse | en |
dc.contributor.institution | Department of Psychology | |
dc.contributor.institution | Centre for Health Services and Clinical Research | |
dc.contributor.institution | School of Life and Medical Sciences | |
dc.contributor.institution | Cognitive Neuropsychology | |
dc.contributor.institution | Department of Clinical, Pharmaceutical and Biological Science | |
dc.description.status | Peer reviewed | |
rioxxterms.type | Journal Article/Review | |
herts.preservation.rarelyaccessed | true | |