Publication:
Acute phase results from storm, a multicountry observational study of bipolar disorder treatment and outcomes

dc.contributor.authorTreuer, Tamás
dc.contributor.authorOrûc, Lilijana
dc.contributor.authorLoza, Nasser
dc.contributor.authorEl Saidi, Mohammed A.
dc.contributor.authorKovacs, Zoltán
dc.contributor.authorGülseren, Şeref Abdurrahman
dc.contributor.authorSaylan, Mete I.
dc.contributor.authorColman, Samuel A.
dc.contributor.authorHarrison, Gavan A.
dc.contributor.buuauthorAkkaya, Cengiz
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentPsikiyatri Ana Bilim Dalı
dc.contributor.scopusid14061855100
dc.date.accessioned2024-04-03T05:46:48Z
dc.date.available2024-04-03T05:46:48Z
dc.date.issued2007-12
dc.descriptionBu çalışma, 09-13 Temmuz 2006 tarihlerinde Chicago[ABD] düzenlenen 25. Congress of the Collegium-Internationale-Neuro-Psychopharmacologicum (CINP)/29th Annual Meeting of the Canadian-College-of-Neuropsychopharmacology Kongresi‘nde bildiri olarak sunulmuştur.
dc.description.abstractObjectives: This prospective observational study examined the outcomes associated with the treatment of bipolar mania in clinical practice settings in a diverse range of countries: Bosnia, Slovenia, Slovakia, Egypt, Saudi Arabia and Turkey. Particular emphasis was placed on investigating outcomes associated with treatment regimens including and excluding the atypical antipsychotic olanzapine. Subjects and Methods: In- and outpatients initiating or changing oral medication for the treatment of bipolar mania were grouped into two treatment cohorts: (1) olanzapine (N=569), and (2) non-olanzapine (N=325). Clinical outcome measures included change in Clinical Global Impressions-Bipolar Version Severity of Illness scale (CGI-BP), Young Mania Rating Scale (YAMS) and Hamilton Depression Rating scale-5 item (HAMD-5) scores, and response and remission rates. Outcomes were analysed by conventional linear or logistic regression, adjusted for potential confounders, using last observation carried forward (LOCF) at endpoint, and a marginal structural model (MSAI) approach to account for treatment switching. Results from the 12-week acute phase are presented. Results: Clinical improvements were observed in both cohorts. While no marked differences were apparent between the groups in adjusted mean baseline to LOCF endpoint change, longitudinal analysis of these variables using MSM averaged over all visits indicated greater improvements in the olanzapine versus non-olanzapine cohort in CGI-BP Overall (-0.26, p<.001), CGI-BP Mania (-0.19, p<.001), CGI-BP Depression (-0.10, p=.003), CGI Psychosis (-0.14, p=.001), YAMS (-1.70, p<.001), and HAMD-5 (-0.40, p<.001) scores. Conclusions: Inclusion of olanzapine after initiating or switching treatment for bipolar mania appeared to be beneficial during treatment in terms of symptom improvement.
dc.description.sponsorshipCollegium Int Neuro Psychopharmacol; Canadian Coll Neuro Psychopharmacol
dc.identifier.citationAkkaya, C. vd. (2007). "Acute phase results from storm, a multicountry observational study of bipolar disorder treatment and outcomes". Psychiatria Danubina, 25. Congress of the Collegium-Internationale-Neuro-Psychopharmacologicum (CINP)/29th Annual Meeting of the Canadian-College-of-Neuropsychopharmacology, 19(4), 282-295.
dc.identifier.endpage295
dc.identifier.issn0353-5053
dc.identifier.issue4
dc.identifier.pubmed18000479
dc.identifier.scopus2-s2.0-36448974917
dc.identifier.startpage282
dc.identifier.urihttps://hdl.handle.net/11452/40921
dc.identifier.volume19
dc.identifier.wos000253849300003
dc.indexed.wosSCIE
dc.indexed.wosSSCI
dc.indexed.wosCPCISSH
dc.indexed.wosCPCIS
dc.language.isoen
dc.publisherMedicinska Naklada
dc.relation.journalPsychiatria Danubina
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAntipsychotic
dc.subjectSTORM
dc.subjectBipolar disorder
dc.subjectObservational study
dc.subjectMania
dc.subjectOlanzapine
dc.subjectOlanzapine
dc.subjectAntipsychotics
dc.subjectMania
dc.subjectSchizophrenia
dc.subjectScale
dc.subjectPsychiatry
dc.subject.emtreeAnticonvulsive agent
dc.subject.emtreeAntidepressant agent
dc.subject.emtreeAtypical antipsychotic agent
dc.subject.emtreeCarbamazepine
dc.subject.emtreeChlorpromazine
dc.subject.emtreeCholinergic receptor blocking agent
dc.subject.emtreeClozapine
dc.subject.emtreeHaloperidol
dc.subject.emtreeLithium salt
dc.subject.emtreeNeuroleptic agent
dc.subject.emtreeOlanzapine
dc.subject.emtreeQuetiapine
dc.subject.emtreeRisperidone
dc.subject.emtreeTranquilizer
dc.subject.emtreeValproic acid
dc.subject.emtreeAdult
dc.subject.emtreeAkathisia
dc.subject.emtreeAmnesia
dc.subject.emtreeArticle
dc.subject.emtreeBipolar disorder
dc.subject.emtreeBipolar mania
dc.subject.emtreeBosnia and herzegovina
dc.subject.emtreeClinical global impression scale
dc.subject.emtreeClinical practice
dc.subject.emtreeClinical trial
dc.subject.emtreeCombination chemotherapy
dc.subject.emtreeConcentration loss
dc.subject.emtreeControlled clinical trial
dc.subject.emtreeControlled study
dc.subject.emtreeDisease severity
dc.subject.emtreeDizziness
dc.subject.emtreeDrug withdrawal
dc.subject.emtreeDystonia
dc.subject.emtreeEgypt
dc.subject.emtreeFemale
dc.subject.emtreeGastrointestinal symptom
dc.subject.emtreeHamilton scale
dc.subject.emtreeHospital patient
dc.subject.emtreeHuman
dc.subject.emtreeInsomnia
dc.subject.emtreeLinear regression analysis
dc.subject.emtreeLogistic regression analysis
dc.subject.emtreeLongitudinal study
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMale
dc.subject.emtreeMenstruation disorder
dc.subject.emtreeMonotherapy
dc.subject.emtreeMulticenter study
dc.subject.emtreeNocturia
dc.subject.emtreeObservational study
dc.subject.emtreeOutpatient
dc.subject.emtreeParkinsonism
dc.subject.emtreePolyuria
dc.subject.emtreePrognosis
dc.subject.emtreePsychosis
dc.subject.emtreeRemission
dc.subject.emtreeSaudi arabia
dc.subject.emtreeSedation
dc.subject.emtreeSexual dysfunction
dc.subject.emtreeSide effect
dc.subject.emtreeSlovakia
dc.subject.emtreeSlovenia
dc.subject.emtreeSymptom
dc.subject.emtreeTardive dyskinesia
dc.subject.emtreeTreatment duration
dc.subject.emtreeTreatment outcome
dc.subject.emtreeTreatment response
dc.subject.emtreeTremor
dc.subject.emtreeTurkey (republic)
dc.subject.emtreeWeight gain
dc.subject.meshAcute disease
dc.subject.meshAdministration, oral
dc.subject.meshAdult
dc.subject.meshAnticonvulsants
dc.subject.meshAntimanic agents
dc.subject.meshAntipsychotic agents
dc.subject.meshBenzodiazepines
dc.subject.meshBipolar disorder
dc.subject.meshCohort studies
dc.subject.meshCross-cultural comparison
dc.subject.meshDrug therapy, combination
dc.subject.meshDrug utilization
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshLong-term care
dc.subject.meshMale
dc.subject.meshMiddle aged
dc.subject.meshPersonality inventory
dc.subject.meshProspective studies
dc.subject.meshPsychiatric status rating scales
dc.subject.meshTreatment outcome
dc.subject.scopusBipolar Disorder; Mania; Mixed State
dc.subject.wosPsychiatry
dc.titleAcute phase results from storm, a multicountry observational study of bipolar disorder treatment and outcomes
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Psikiyatri Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atScopus

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