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dc.contributor.author Bitter, István
dc.contributor.author Dossenbach MR
dc.contributor.author Brook S
dc.contributor.author Feldman PD
dc.contributor.author Metcalfe S
dc.contributor.author Gagiano CA
dc.contributor.author Füredi, János
dc.contributor.author Bartko G
dc.contributor.author Janka, Zoltán
dc.contributor.author Banki CM
dc.contributor.author Kovacs G
dc.contributor.author Breier A
dc.contributor.author for the Olanzapine HGCK Study Group
dc.date.accessioned 2018-01-03T08:24:10Z
dc.date.available 2018-01-03T08:24:10Z
dc.date.issued 2004
dc.identifier 10744231049
dc.identifier.citation pagination=173-180; journalVolume=28; journalIssueNumber=1; journalTitle=PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/4515
dc.description.abstract Clozapine has been the gold standard for treatment of patients with refractory schizophrenia but is associated with serious safety liabilities. This has prompted the search for therapeutic alternatives for treatment-resistant schizophrenia. The objective of this study was to compare the efficacy and safety of olanzapine versus clozapine in schizophrenic patients who failed to respond adequately to antipsychotic medication or who experienced intolerable adverse effects associated with the medication. This 18-week, randomized, double-blind, parallel study compared treatment with either olanzapine (5-25 mg/day, n=75) or clozapine (100-500 mg/day, n=72) in patients with schizophrenia who were nonresponsive to, or intolerant of, standard acceptable antipsychotic therapy. At the 18-week endpoint, no statistically significant differences were found between olanzapine and clozapine in any efficacy measure used: Positive and Negative Syndrome Scale (PANSS) total, positive, negative, or general psychopathology or Clinical Global Impression severity (CGI-S). Response rates based on the criteria of Kane et al. [Arch. Gen. Psychiatry 45 (1988) 789] were also not significantly different between olanzapine-treated (57.9%) and clozapine-treated patients (60.8%). There were no significant differences in measurements of extrapyramidal symptoms or electrocardiography, and no clinically and statistically significant changes were seen in vital signs or laboratory measures in either group. Both treatments were well tolerated. Olanzapine demonstrated similar efficacy to clozapine in patients who had failed previous treatment because of lack of efficacy (treatment resistance) or intolerable side effects (treatment intolerance). Olanzapine therefore presents a safe alternative in the treatment of refractory schizophrenia.
dc.relation.ispartof urn:issn:0278-5846
dc.title Olanzapine versus clozapine in treatment-resistant or treatment-intolerant schizophrenia
dc.type Journal Article
dc.date.updated 2017-10-03T12:53:59Z
dc.language.rfc3066 en
dc.identifier.mtmt 1280699
dc.identifier.wos 000187938800021
dc.identifier.pubmed 14687871
dc.contributor.department SZTE/ÁOK/Pszichiátriai Klinika
dc.contributor.department SE/AOK/K/Pszichiátriai és Pszichoterápiás Klinika [2015.12.31]
dc.contributor.institution Szegedi Tudományegyetem
dc.contributor.institution Semmelweis Egyetem
dc.mtmt.swordnote Olanzapine HGCK Study Group


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