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S194. CLOZAPINE AND ELECTROCONVULSIVE THERAPY AUGMENTATION IN ADOLESCENTS WITH TREATMENT-RESISTANT SCHIZOPHRENIA
BACKGROUND: Early onset schizophrenia is associated unfavorable treatment response and psychosocial outcome. Clozapine or Electroconvulsive Therapy (ECT) have suggested that these therapies may have an important role in treatment in treatment resistant schizophrenia in adolescents. The aim of this s...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234453/ http://dx.doi.org/10.1093/schbul/sbaa031.260 |
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author | Jeong Park, Kee Kim, Hyo-Won |
author_facet | Jeong Park, Kee Kim, Hyo-Won |
author_sort | Jeong Park, Kee |
collection | PubMed |
description | BACKGROUND: Early onset schizophrenia is associated unfavorable treatment response and psychosocial outcome. Clozapine or Electroconvulsive Therapy (ECT) have suggested that these therapies may have an important role in treatment in treatment resistant schizophrenia in adolescents. The aim of this study was to compare effectiveness between clozapine and ECT augmentation in adolescents with treatment-resistant schizophrenia. METHODS: We retrospectively reviewed the electronic medical records of 27 adolescents with treatment-resistant schizophrenia (age 15.6±1.4 years; 16 boys, 59.3%) who were treated with clozapine or clozapine plus ECT. Effectiveness was measured with the Clinical Global Impressions–Severity (CGI-S) and/or Clinical Global Impressions–Improvement (CGI-I) scales at baseline, and after 2, 4 and 8 weeks. Treatment response was defined as a CGI-S < 3 or CGI-I < 3. RESULTS: The 21 adolescents treated with clozapine alone (age 15.5±1.2 years; 14 boys, 66.7%), and six adolescents treated with clozapine plus ECT (age 16.0±2.1 years; 2 boys, 33.3%) were compared their treatment effectiveness. The 13 adolescents (61.0%) in clozapine alone group and four adolescents (66.7%) in clozapine plus ECT group met the treatment response criterion. Three (50.0%) of adolescents with clozapine plus ECT group experienced mild post ictal confusion and two (9.5%) of adolescents with clozapine alone group experienced mild reduction of WBC and ANC. DISCUSSION: Our results suggest that clozapine and ECT augmentation could be one of safe and effective treatment in adolescents with treatment-resistant schizophrenia. |
format | Online Article Text |
id | pubmed-7234453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72344532020-05-23 S194. CLOZAPINE AND ELECTROCONVULSIVE THERAPY AUGMENTATION IN ADOLESCENTS WITH TREATMENT-RESISTANT SCHIZOPHRENIA Jeong Park, Kee Kim, Hyo-Won Schizophr Bull Poster Session I BACKGROUND: Early onset schizophrenia is associated unfavorable treatment response and psychosocial outcome. Clozapine or Electroconvulsive Therapy (ECT) have suggested that these therapies may have an important role in treatment in treatment resistant schizophrenia in adolescents. The aim of this study was to compare effectiveness between clozapine and ECT augmentation in adolescents with treatment-resistant schizophrenia. METHODS: We retrospectively reviewed the electronic medical records of 27 adolescents with treatment-resistant schizophrenia (age 15.6±1.4 years; 16 boys, 59.3%) who were treated with clozapine or clozapine plus ECT. Effectiveness was measured with the Clinical Global Impressions–Severity (CGI-S) and/or Clinical Global Impressions–Improvement (CGI-I) scales at baseline, and after 2, 4 and 8 weeks. Treatment response was defined as a CGI-S < 3 or CGI-I < 3. RESULTS: The 21 adolescents treated with clozapine alone (age 15.5±1.2 years; 14 boys, 66.7%), and six adolescents treated with clozapine plus ECT (age 16.0±2.1 years; 2 boys, 33.3%) were compared their treatment effectiveness. The 13 adolescents (61.0%) in clozapine alone group and four adolescents (66.7%) in clozapine plus ECT group met the treatment response criterion. Three (50.0%) of adolescents with clozapine plus ECT group experienced mild post ictal confusion and two (9.5%) of adolescents with clozapine alone group experienced mild reduction of WBC and ANC. DISCUSSION: Our results suggest that clozapine and ECT augmentation could be one of safe and effective treatment in adolescents with treatment-resistant schizophrenia. Oxford University Press 2020-05 2020-05-18 /pmc/articles/PMC7234453/ http://dx.doi.org/10.1093/schbul/sbaa031.260 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Poster Session I Jeong Park, Kee Kim, Hyo-Won S194. CLOZAPINE AND ELECTROCONVULSIVE THERAPY AUGMENTATION IN ADOLESCENTS WITH TREATMENT-RESISTANT SCHIZOPHRENIA |
title | S194. CLOZAPINE AND ELECTROCONVULSIVE THERAPY AUGMENTATION IN ADOLESCENTS WITH TREATMENT-RESISTANT SCHIZOPHRENIA |
title_full | S194. CLOZAPINE AND ELECTROCONVULSIVE THERAPY AUGMENTATION IN ADOLESCENTS WITH TREATMENT-RESISTANT SCHIZOPHRENIA |
title_fullStr | S194. CLOZAPINE AND ELECTROCONVULSIVE THERAPY AUGMENTATION IN ADOLESCENTS WITH TREATMENT-RESISTANT SCHIZOPHRENIA |
title_full_unstemmed | S194. CLOZAPINE AND ELECTROCONVULSIVE THERAPY AUGMENTATION IN ADOLESCENTS WITH TREATMENT-RESISTANT SCHIZOPHRENIA |
title_short | S194. CLOZAPINE AND ELECTROCONVULSIVE THERAPY AUGMENTATION IN ADOLESCENTS WITH TREATMENT-RESISTANT SCHIZOPHRENIA |
title_sort | s194. clozapine and electroconvulsive therapy augmentation in adolescents with treatment-resistant schizophrenia |
topic | Poster Session I |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234453/ http://dx.doi.org/10.1093/schbul/sbaa031.260 |
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