Predictors of relapse in a study of duloxetine treatment for patients with generalized anxiety disorder
Objective Data from a relapse prevention study of duloxetine treatment for adults with generalized anxiety disorder (GAD) were examined to identify predictors of relapse. Methods Patients responding to 6 months of open‐label duloxetine treatment were randomized to continuation with duloxetine or wit...
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Veröffentlicht in: | Human psychopharmacology 2011-04, Vol.26 (3), p.258-266 |
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description | Objective
Data from a relapse prevention study of duloxetine treatment for adults with generalized anxiety disorder (GAD) were examined to identify predictors of relapse.
Methods
Patients responding to 6 months of open‐label duloxetine treatment were randomized to continuation with duloxetine or withdrawal to placebo for a 6‐month double‐blind continuation phase (duloxetine, N = 216; placebo, N = 213). Post hoc analyses compared time to GAD relapse during continuation phase by using predictor variables that included patient demographics, symptom severity measures (Hamilton Anxiety Scale Scores [HAMA], Hospital Anxiety and Depression Scale), functional outcomes, and visual analogue scale (VAS) pain measures. Univariate and multivariate analyses were performed using predictor variables from time of randomization into the continuation, withdrawal phase.
Results
Severity of anxiety symptoms, degree of functional impairment, and severity of pain at time of randomization were significantly predictive of likelihood of relapse during the continuation phase. Multivariate backwards elimination analysis of significant univariate predictors identified HAMA item one (anxious mood) ≥1 and severity of pain while awake (≥30 on VAS) as the strongest predictors of GAD relapse.
Conclusions
For patients with GAD responding to open‐label treatment with duloxetine, residual symptoms related to anxious mood, pain severity, and psychosocial function were associated with increased relapse risk, although the greatest risk was associated with anxious mood and increased severity of pain while awake. Copyright © 2011 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/hup.1211 |
format | Article |
fullrecord | <record><control><sourceid>proquest_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_swepub_ki_se_543634</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1017968584</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4301-47cbd0b0a2f379877c2e529954d7e3ddba60c552180d742c5ed94da631aba8e3</originalsourceid><addsrcrecordid>eNqNkU9v1DAQxS0EoktB4hMgH7mk-G9sH1EFXUQFlSjlaDnxpDXNxsF2tLt8erJq2J6QOM3Tm5-eZvQQek3JGSWEvbubxjPKKH2CVpQYU1Gi1FO0IlrLqmaMnaAXOf8kZN4R8xydMForLYxYodurBD60JaaMY4cT9G7MgMOAHc5l8vuD66c-7qCEAXBJ4MoGhoK7mPDoSph1xttQ7vAtDJBcH36Dx27YBSh77EOOyUN6iZ51rs_wapmn6Prjh-vzdXX59eLT-fvLqhWc0EqotvGkIY51XBmtVMtAMmOk8Aq4942rSSslo5p4JVgrwRvhXc2pa5wGfoqqh9i8hXFq7JjCxqW9jS7YxbqfFVgpeM3FzL994McUf02Qi92E3ELfuwHilC0lVJlaS_1fKKWaaWMe0TbFnBN0xzsosYfC7FyYPRQ2o2-W1KnZgD-Cfxt6_Ggbetj_M8iuv18tgQsfcoHdkXfp3taKK2l_fLmwQvCbG_p5bb_xP7sBr9k</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1011182899</pqid></control><display><type>article</type><title>Predictors of relapse in a study of duloxetine treatment for patients with generalized anxiety disorder</title><source>MEDLINE</source><source>Wiley Online Library All Journals</source><creator>Bodkin, J. Alexander ; Allgulander, Christer ; Llorca, Pierre M. ; Spann, Melissa E. ; Walker, Daniel J. ; Russell, James M. ; Ball, Susan G.</creator><creatorcontrib>Bodkin, J. Alexander ; Allgulander, Christer ; Llorca, Pierre M. ; Spann, Melissa E. ; Walker, Daniel J. ; Russell, James M. ; Ball, Susan G.</creatorcontrib><description>Objective
Data from a relapse prevention study of duloxetine treatment for adults with generalized anxiety disorder (GAD) were examined to identify predictors of relapse.
Methods
Patients responding to 6 months of open‐label duloxetine treatment were randomized to continuation with duloxetine or withdrawal to placebo for a 6‐month double‐blind continuation phase (duloxetine, N = 216; placebo, N = 213). Post hoc analyses compared time to GAD relapse during continuation phase by using predictor variables that included patient demographics, symptom severity measures (Hamilton Anxiety Scale Scores [HAMA], Hospital Anxiety and Depression Scale), functional outcomes, and visual analogue scale (VAS) pain measures. Univariate and multivariate analyses were performed using predictor variables from time of randomization into the continuation, withdrawal phase.
Results
Severity of anxiety symptoms, degree of functional impairment, and severity of pain at time of randomization were significantly predictive of likelihood of relapse during the continuation phase. Multivariate backwards elimination analysis of significant univariate predictors identified HAMA item one (anxious mood) ≥1 and severity of pain while awake (≥30 on VAS) as the strongest predictors of GAD relapse.
Conclusions
For patients with GAD responding to open‐label treatment with duloxetine, residual symptoms related to anxious mood, pain severity, and psychosocial function were associated with increased relapse risk, although the greatest risk was associated with anxious mood and increased severity of pain while awake. Copyright © 2011 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0885-6222</identifier><identifier>ISSN: 1099-1077</identifier><identifier>EISSN: 1099-1077</identifier><identifier>DOI: 10.1002/hup.1211</identifier><identifier>PMID: 21678494</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Adult ; Anxiety ; Anxiety Disorders - diagnosis ; Anxiety Disorders - drug therapy ; Anxiety Disorders - psychology ; Clinical trials ; Data processing ; Demography ; Depression ; Double-Blind Method ; Duloxetine ; Duloxetine Hydrochloride ; Female ; generalized anxiety disorder ; Glutamate decarboxylase ; Hospitals ; Humans ; Male ; Middle Aged ; Mood ; Multivariate analysis ; Pain ; placebo ; Predictive Value of Tests ; predictors of relapse ; Secondary Prevention ; Thiophenes - therapeutic use ; Treatment Outcome ; Withdrawal</subject><ispartof>Human psychopharmacology, 2011-04, Vol.26 (3), p.258-266</ispartof><rights>Copyright © 2011 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4301-47cbd0b0a2f379877c2e529954d7e3ddba60c552180d742c5ed94da631aba8e3</citedby><cites>FETCH-LOGICAL-c4301-47cbd0b0a2f379877c2e529954d7e3ddba60c552180d742c5ed94da631aba8e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhup.1211$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhup.1211$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21678494$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:122921100$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Bodkin, J. Alexander</creatorcontrib><creatorcontrib>Allgulander, Christer</creatorcontrib><creatorcontrib>Llorca, Pierre M.</creatorcontrib><creatorcontrib>Spann, Melissa E.</creatorcontrib><creatorcontrib>Walker, Daniel J.</creatorcontrib><creatorcontrib>Russell, James M.</creatorcontrib><creatorcontrib>Ball, Susan G.</creatorcontrib><title>Predictors of relapse in a study of duloxetine treatment for patients with generalized anxiety disorder</title><title>Human psychopharmacology</title><addtitle>Hum. Psychopharmacol Clin Exp</addtitle><description>Objective
Data from a relapse prevention study of duloxetine treatment for adults with generalized anxiety disorder (GAD) were examined to identify predictors of relapse.
Methods
Patients responding to 6 months of open‐label duloxetine treatment were randomized to continuation with duloxetine or withdrawal to placebo for a 6‐month double‐blind continuation phase (duloxetine, N = 216; placebo, N = 213). Post hoc analyses compared time to GAD relapse during continuation phase by using predictor variables that included patient demographics, symptom severity measures (Hamilton Anxiety Scale Scores [HAMA], Hospital Anxiety and Depression Scale), functional outcomes, and visual analogue scale (VAS) pain measures. Univariate and multivariate analyses were performed using predictor variables from time of randomization into the continuation, withdrawal phase.
Results
Severity of anxiety symptoms, degree of functional impairment, and severity of pain at time of randomization were significantly predictive of likelihood of relapse during the continuation phase. Multivariate backwards elimination analysis of significant univariate predictors identified HAMA item one (anxious mood) ≥1 and severity of pain while awake (≥30 on VAS) as the strongest predictors of GAD relapse.
Conclusions
For patients with GAD responding to open‐label treatment with duloxetine, residual symptoms related to anxious mood, pain severity, and psychosocial function were associated with increased relapse risk, although the greatest risk was associated with anxious mood and increased severity of pain while awake. Copyright © 2011 John Wiley & Sons, Ltd.</description><subject>Adult</subject><subject>Anxiety</subject><subject>Anxiety Disorders - diagnosis</subject><subject>Anxiety Disorders - drug therapy</subject><subject>Anxiety Disorders - psychology</subject><subject>Clinical trials</subject><subject>Data processing</subject><subject>Demography</subject><subject>Depression</subject><subject>Double-Blind Method</subject><subject>Duloxetine</subject><subject>Duloxetine Hydrochloride</subject><subject>Female</subject><subject>generalized anxiety disorder</subject><subject>Glutamate decarboxylase</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mood</subject><subject>Multivariate analysis</subject><subject>Pain</subject><subject>placebo</subject><subject>Predictive Value of Tests</subject><subject>predictors of relapse</subject><subject>Secondary Prevention</subject><subject>Thiophenes - therapeutic use</subject><subject>Treatment Outcome</subject><subject>Withdrawal</subject><issn>0885-6222</issn><issn>1099-1077</issn><issn>1099-1077</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9v1DAQxS0EoktB4hMgH7mk-G9sH1EFXUQFlSjlaDnxpDXNxsF2tLt8erJq2J6QOM3Tm5-eZvQQek3JGSWEvbubxjPKKH2CVpQYU1Gi1FO0IlrLqmaMnaAXOf8kZN4R8xydMForLYxYodurBD60JaaMY4cT9G7MgMOAHc5l8vuD66c-7qCEAXBJ4MoGhoK7mPDoSph1xttQ7vAtDJBcH36Dx27YBSh77EOOyUN6iZ51rs_wapmn6Prjh-vzdXX59eLT-fvLqhWc0EqotvGkIY51XBmtVMtAMmOk8Aq4942rSSslo5p4JVgrwRvhXc2pa5wGfoqqh9i8hXFq7JjCxqW9jS7YxbqfFVgpeM3FzL994McUf02Qi92E3ELfuwHilC0lVJlaS_1fKKWaaWMe0TbFnBN0xzsosYfC7FyYPRQ2o2-W1KnZgD-Cfxt6_Ggbetj_M8iuv18tgQsfcoHdkXfp3taKK2l_fLmwQvCbG_p5bb_xP7sBr9k</recordid><startdate>201104</startdate><enddate>201104</enddate><creator>Bodkin, J. Alexander</creator><creator>Allgulander, Christer</creator><creator>Llorca, Pierre M.</creator><creator>Spann, Melissa E.</creator><creator>Walker, Daniel J.</creator><creator>Russell, James M.</creator><creator>Ball, Susan G.</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TK</scope><scope>ADTPV</scope><scope>AOWAS</scope></search><sort><creationdate>201104</creationdate><title>Predictors of relapse in a study of duloxetine treatment for patients with generalized anxiety disorder</title><author>Bodkin, J. Alexander ; Allgulander, Christer ; Llorca, Pierre M. ; Spann, Melissa E. ; Walker, Daniel J. ; Russell, James M. ; Ball, Susan G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4301-47cbd0b0a2f379877c2e529954d7e3ddba60c552180d742c5ed94da631aba8e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Anxiety</topic><topic>Anxiety Disorders - diagnosis</topic><topic>Anxiety Disorders - drug therapy</topic><topic>Anxiety Disorders - psychology</topic><topic>Clinical trials</topic><topic>Data processing</topic><topic>Demography</topic><topic>Depression</topic><topic>Double-Blind Method</topic><topic>Duloxetine</topic><topic>Duloxetine Hydrochloride</topic><topic>Female</topic><topic>generalized anxiety disorder</topic><topic>Glutamate decarboxylase</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mood</topic><topic>Multivariate analysis</topic><topic>Pain</topic><topic>placebo</topic><topic>Predictive Value of Tests</topic><topic>predictors of relapse</topic><topic>Secondary Prevention</topic><topic>Thiophenes - therapeutic use</topic><topic>Treatment Outcome</topic><topic>Withdrawal</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bodkin, J. Alexander</creatorcontrib><creatorcontrib>Allgulander, Christer</creatorcontrib><creatorcontrib>Llorca, Pierre M.</creatorcontrib><creatorcontrib>Spann, Melissa E.</creatorcontrib><creatorcontrib>Walker, Daniel J.</creatorcontrib><creatorcontrib>Russell, James M.</creatorcontrib><creatorcontrib>Ball, Susan G.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><collection>SwePub</collection><collection>SwePub Articles</collection><jtitle>Human psychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bodkin, J. Alexander</au><au>Allgulander, Christer</au><au>Llorca, Pierre M.</au><au>Spann, Melissa E.</au><au>Walker, Daniel J.</au><au>Russell, James M.</au><au>Ball, Susan G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predictors of relapse in a study of duloxetine treatment for patients with generalized anxiety disorder</atitle><jtitle>Human psychopharmacology</jtitle><addtitle>Hum. Psychopharmacol Clin Exp</addtitle><date>2011-04</date><risdate>2011</risdate><volume>26</volume><issue>3</issue><spage>258</spage><epage>266</epage><pages>258-266</pages><issn>0885-6222</issn><issn>1099-1077</issn><eissn>1099-1077</eissn><abstract>Objective
Data from a relapse prevention study of duloxetine treatment for adults with generalized anxiety disorder (GAD) were examined to identify predictors of relapse.
Methods
Patients responding to 6 months of open‐label duloxetine treatment were randomized to continuation with duloxetine or withdrawal to placebo for a 6‐month double‐blind continuation phase (duloxetine, N = 216; placebo, N = 213). Post hoc analyses compared time to GAD relapse during continuation phase by using predictor variables that included patient demographics, symptom severity measures (Hamilton Anxiety Scale Scores [HAMA], Hospital Anxiety and Depression Scale), functional outcomes, and visual analogue scale (VAS) pain measures. Univariate and multivariate analyses were performed using predictor variables from time of randomization into the continuation, withdrawal phase.
Results
Severity of anxiety symptoms, degree of functional impairment, and severity of pain at time of randomization were significantly predictive of likelihood of relapse during the continuation phase. Multivariate backwards elimination analysis of significant univariate predictors identified HAMA item one (anxious mood) ≥1 and severity of pain while awake (≥30 on VAS) as the strongest predictors of GAD relapse.
Conclusions
For patients with GAD responding to open‐label treatment with duloxetine, residual symptoms related to anxious mood, pain severity, and psychosocial function were associated with increased relapse risk, although the greatest risk was associated with anxious mood and increased severity of pain while awake. Copyright © 2011 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>21678494</pmid><doi>10.1002/hup.1211</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Anxiety Anxiety Disorders - diagnosis Anxiety Disorders - drug therapy Anxiety Disorders - psychology Clinical trials Data processing Demography Depression Double-Blind Method Duloxetine Duloxetine Hydrochloride Female generalized anxiety disorder Glutamate decarboxylase Hospitals Humans Male Middle Aged Mood Multivariate analysis Pain placebo Predictive Value of Tests predictors of relapse Secondary Prevention Thiophenes - therapeutic use Treatment Outcome Withdrawal |
title | Predictors of relapse in a study of duloxetine treatment for patients with generalized anxiety disorder |
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