Quetiapine treatment in early psychosis: 1 year outcomes
Identifieur interne : 000262 ( Istex/Corpus ); précédent : 000261; suivant : 000263Quetiapine treatment in early psychosis: 1 year outcomes
Auteurs : L. Kopala ; H. Woodley ; L. A. Campbell ; J. Gallant ; Q. Rui ; H. Milliken ; D. WhitehornSource :
- Acta Psychiatrica Scandinavica [ 0001-690X ] ; 2002-09.
Abstract
Objective To determine clinical response, dosing and adverse events associated with quetiapine treatment in early psychosis.
Url:
DOI: 10.1034/j.1600-0447.106.s413.1_12.x
Links to Exploration step
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<abstract><p>Method 40 Patients (33 men; 7 women; mean age 23.75) with schizophrenia spectrum disorders and less than 6 months previous exposure to antipsychotic treatment, entered an open label, 2 years, flexible dose trial and were assessed with PANSS, CGI, GAF, SOFAS, ESRS, BMI and ocular exams at baseline and 6 month intervals thereafter.</p>
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<abstract><p>Results Among 30 patients who enrolled >1 years ago, 19 (63%) completed 1‐year assessment. Dropouts were due to insufficient clinical response (13%), nonadherence (13%) and personal choice (10%). At 1 year, significant improvement was observed on the PANSS, CGI, GAF and SOFAS. Mean dose was 559 (±207) mg/day. No drug induced EPS was noted and EPS present at baseline was reduced. Mean change in BMI was 17% (±22). No ocular changes were observed.</p>
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<abstract><p>Conclusions Quetiapine was well tolerated. Clinical response was similar to that achieved with other second generation antipsychotic agents in the same early psychosis programme.</p>
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<abstractGroup><abstract type="main" xml:lang="en"><p><b>Objective </b>
To determine clinical response, dosing and adverse events associated with quetiapine treatment in early psychosis.</p>
<p><b>Method </b>
40 Patients (33 men; 7 women; mean age 23.75) with schizophrenia spectrum disorders and less than 6 months previous exposure to antipsychotic treatment, entered an open label, 2 years, flexible dose trial and were assessed with PANSS, CGI, GAF, SOFAS, ESRS, BMI and ocular exams at baseline and 6 month intervals thereafter.</p>
<p><b>Results </b>
Among 30 patients who enrolled >1 years ago, 19 (63%) completed 1‐year assessment. Dropouts were due to insufficient clinical response (13%), nonadherence (13%) and personal choice (10%). At 1 year, significant improvement was observed on the PANSS, CGI, GAF and SOFAS. Mean dose was 559 (±207) mg/day. No drug induced EPS was noted and EPS present at baseline was reduced. Mean change in BMI was 17% (±22). No ocular changes were observed.</p>
<p><b>Conclusions </b>
Quetiapine was well tolerated. Clinical response was similar to that achieved with other second generation antipsychotic agents in the same early psychosis programme.</p>
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<abstract>Objective To determine clinical response, dosing and adverse events associated with quetiapine treatment in early psychosis.</abstract>
<abstract>Method 40 Patients (33 men; 7 women; mean age 23.75) with schizophrenia spectrum disorders and less than 6 months previous exposure to antipsychotic treatment, entered an open label, 2 years, flexible dose trial and were assessed with PANSS, CGI, GAF, SOFAS, ESRS, BMI and ocular exams at baseline and 6 month intervals thereafter.</abstract>
<abstract>Results Among 30 patients who enrolled >1 years ago, 19 (63%) completed 1‐year assessment. Dropouts were due to insufficient clinical response (13%), nonadherence (13%) and personal choice (10%). At 1 year, significant improvement was observed on the PANSS, CGI, GAF and SOFAS. Mean dose was 559 (±207) mg/day. No drug induced EPS was noted and EPS present at baseline was reduced. Mean change in BMI was 17% (±22). No ocular changes were observed.</abstract>
<abstract>Conclusions Quetiapine was well tolerated. Clinical response was similar to that achieved with other second generation antipsychotic agents in the same early psychosis programme.</abstract>
<relatedItem type="host"><titleInfo><title>Acta Psychiatrica Scandinavica</title>
</titleInfo>
<genre type="journal">journal</genre>
<identifier type="ISSN">0001-690X</identifier>
<identifier type="eISSN">1600-0447</identifier>
<identifier type="DOI">10.1111/(ISSN)1600-0447</identifier>
<identifier type="PublisherID">ACPS</identifier>
<part><date>2002</date>
<detail type="volume"><caption>vol.</caption>
<number>106</number>
</detail>
<detail type="supplement"><caption>Suppl. no.</caption>
<number>s413</number>
</detail>
<extent unit="pages"><start>69</start>
<end>106</end>
</extent>
</part>
</relatedItem>
<identifier type="istex">0FF823DD25A3ADED2D36B9D5592A032B04E0425C</identifier>
<identifier type="DOI">10.1034/j.1600-0447.106.s413.1_12.x</identifier>
<identifier type="ArticleID">ACPSPO119_12</identifier>
<recordInfo><recordContentSource>WILEY</recordContentSource>
<recordOrigin>Blackwell publishers</recordOrigin>
</recordInfo>
</mods>
</metadata>
<serie></serie>
</istex>
</record>
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