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The Comparison of Aripiprazole and Risperidone Augmentation in Selective Serotonin Reuptake Inhibitor-Refractory Obsessive-Compulsive Disorder: a Single-Blind, Randomised Study

dc.authorid Selvi, Yavuz/0000-0003-0218-6796
dc.authorscopusid 6603309359
dc.authorscopusid 36630069500
dc.authorscopusid 15829049500
dc.authorscopusid 6506893612
dc.authorscopusid 36718861100
dc.authorscopusid 57196709155
dc.authorwosid Selvi, Yavuz/Glt-0029-2022
dc.authorwosid Aydin, Adem/Khy-0854-2024
dc.authorwosid Özdemir, Osman/Abi-1650-2020
dc.contributor.author Selvi, Yavuz
dc.contributor.author Atli, Abdullah
dc.contributor.author Aydin, Adem
dc.contributor.author Besiroglu, Lutfullah
dc.contributor.author Ozdemir, Pinar
dc.contributor.author Ozdemir, Osman
dc.date.accessioned 2025-05-10T16:49:06Z
dc.date.available 2025-05-10T16:49:06Z
dc.date.issued 2011
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Selvi, Yavuz] Yuzuncu Yil Univ, Sch Med, Dept Psychiat, Fac Med, TR-65300 Van, Turkey; [Aydin, Adem] Educ & Res Hosp, Dept Psychiat, Van, Turkey en_US
dc.description Selvi, Yavuz/0000-0003-0218-6796 en_US
dc.description.abstract Objective To investigate the comparative efficacy of aripiprazole and risperidone as augmenting agents in the treatment of obsessive-compulsive disorder (OCD) patients who did not show a >= 35% decrease in the Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) after 12-week monotherapy with selective serotonin reuptake inhibitors (SSRIs). Methods The study consists of two different periods of treatment: a 12-week prospective period to determine resistance to SSRI treatment and an 8-week single-blind addition period for refractory patients only. Ninety patients were randomly assigned to receive one of the SSRI treatments. Sixty-nine patients (76.6%) completed the 12-week SSRI monotherapy period. Forty-one patients (59.4%) were considered refractory and were randomised to receive either risperidone (20 patients, 3 mgr daily) or aripiprazole (21 patients, 15 mgr daily) as augmentation to SSRI treatment. Sixteen patients (76.2%) in the aripiprazole group and 18 patients (84%) in the risperidone group completed the 8-week treatment period. Results Eight patients (50%) in aripiprazole and 13 patients (72.2%) in risperidone group met response criteria of Y-BOCS decrease >= 35% at the end of the study. The risperidone group showed a significant improvement in Y-BOCS obsession scores compared with aripiprazole. Conclusions The present findings suggest that risperidone may be more effective than aripiprazole. Copyright (C) 2011 John Wiley & Sons, Ltd. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1002/hup.1169
dc.identifier.endpage 57 en_US
dc.identifier.issn 0885-6222
dc.identifier.issn 1099-1077
dc.identifier.issue 1 en_US
dc.identifier.pmid 21308781
dc.identifier.scopus 2-s2.0-79953245254
dc.identifier.scopusquality Q3
dc.identifier.startpage 51 en_US
dc.identifier.uri https://doi.org/10.1002/hup.1169
dc.identifier.uri https://hdl.handle.net/20.500.14720/1723
dc.identifier.volume 26 en_US
dc.identifier.wos WOS:000288947300008
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Obsessive-Compulsive Disorder en_US
dc.subject Antipsychotic en_US
dc.subject Treatment-Refractory en_US
dc.title The Comparison of Aripiprazole and Risperidone Augmentation in Selective Serotonin Reuptake Inhibitor-Refractory Obsessive-Compulsive Disorder: a Single-Blind, Randomised Study en_US
dc.type Article en_US

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