Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/15304
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dc.contributor.authorChanpattana W.
dc.contributor.authorChakrabhand M.L.S.
dc.contributor.authorSackeim H.A.
dc.contributor.authorKitaroonchai W.
dc.contributor.authorKongsakon R.
dc.contributor.authorTechakasem P.
dc.contributor.authorBuppanharun W.
dc.contributor.authorTuntirungsee Y.
dc.contributor.authorKirdcharoen N.
dc.date.accessioned2021-04-05T04:33:28Z-
dc.date.available2021-04-05T04:33:28Z-
dc.date.issued1999
dc.identifier.issn10950680
dc.identifier.other2-s2.0-0042203177
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/15304-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0042203177&partnerID=40&md5=f93704b31edb63012ba41372ce6fac6b
dc.description.abstractIn patients with treatment-resistant schizophrenia (TRS), this study compared the efficacy of continuation treatment with flupenthixol alone, continuation electroconvulsive therapy (ECT) alone, and combined continuation ECT and flupenthixol. One hundred fourteen TRS patients received acute treatment (Phase I) with bilateral ECT and flupenthixol (12-24 mg/day). Fifty-eight patients met remitter criteria, including clinical stability during a 3-week stabilization period, and were eligible for the continuation treatment study (Phase II). Fifty-one patients enrolled in the single-blind Phase II continuation trial, and were randomized to the three treatment groups. The duration of the Phase II study was 6 months. Assessments of outcome included the Brief Psychiatric Rating Scale, Global Assessment of Functioning, and the Mini-Mental State Examination. Forty-five patients either relapsed or completed the Phase II study, and six patients dropped out. Among completers, 6 of 15 (40%) patients relapsed in the combined continuation ECT and flupenthixol group. In both the group treated with continuation ECT alone and that with flupenthixol alone, 14 of 15 (93%) patients relapsed. Analyses of intent-to-treat and completer samples demonstrated a marked advantage for the combination treatment condition in relapse prevention. Furthermore, all eight patients who received maintenance ECT combined with neuroleptic medication (Phase III study) maintained therapeutic benefits during the follow-up period of 3-17 months after the continuation treatment study. Among TRS patients who respond to acute combination treatment with ECT and neuroleptic therapy, continuation of this combination treatment is more effective in relapse prevention than use of ECT or neuroleptic therapy alone.
dc.subjectflupentixol
dc.subjectneuroleptic agent
dc.subjectadult
dc.subjectarticle
dc.subjectclinical trial
dc.subjectcontrolled clinical trial
dc.subjectcontrolled study
dc.subjectelectroconvulsive therapy
dc.subjectfemale
dc.subjecthuman
dc.subjectmale
dc.subjectmethodology
dc.subjectmiddle aged
dc.subjectmultimodality cancer therapy
dc.subjectprospective study
dc.subjectrandomized controlled trial
dc.subjectrecurrent disease
dc.subjectschizophrenia
dc.subjectsingle blind procedure
dc.subjectAdult
dc.subjectAntipsychotic Agents
dc.subjectCombined Modality Therapy
dc.subjectElectroconvulsive Therapy
dc.subjectFemale
dc.subjectFlupenthixol
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectProspective Studies
dc.subjectRecurrence
dc.subjectSchizophrenia
dc.subjectSingle-Blind Method
dc.titleContinuation ECT in treatment-resistant schizophrenia: A controlled study
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of ECT. Vol 15, No.3 (1999), p.178-192
Appears in Collections:Scopus 1983-2021

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