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A case study of the utilization of clozapine treatment for treatment‐resistant schizophrenia associated with 22q11.2 deletion syndrome

BACKGROUND: The optimal treatment strategy for patients with treatment‐resistant schizophrenia (TRS) associated with 22q11.2 deletion syndrome (DS) remains a subject of debate. CASE PRESENTATION: We present the case of a 40‐year‐old female patient diagnosed with TRS and 22q11.2DS who was effectively...

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Autores principales: Tsurue, Arisa, Funahashi, Hideki, Tsurue, Keiichi, Kawano, Masahiko, Ishida, Yasushi, Hirano, Yoji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275284/
https://www.ncbi.nlm.nih.gov/pubmed/36929244
http://dx.doi.org/10.1002/npr2.12333
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author Tsurue, Arisa
Funahashi, Hideki
Tsurue, Keiichi
Kawano, Masahiko
Ishida, Yasushi
Hirano, Yoji
author_facet Tsurue, Arisa
Funahashi, Hideki
Tsurue, Keiichi
Kawano, Masahiko
Ishida, Yasushi
Hirano, Yoji
author_sort Tsurue, Arisa
collection PubMed
description BACKGROUND: The optimal treatment strategy for patients with treatment‐resistant schizophrenia (TRS) associated with 22q11.2 deletion syndrome (DS) remains a subject of debate. CASE PRESENTATION: We present the case of a 40‐year‐old female patient diagnosed with TRS and 22q11.2DS who was effectively treated with clozapine. She was diagnosed with schizophrenia and mild intellectual disability during her adolescence; despite being hospitalized for a period of 10 years beginning in her 30s, she continued to exhibit symptoms of impulsivity, and explosive behavior, requiring periods of isolation. We ultimately decided to switch her medication to clozapine, which was administered with caution and gradually titrated upward, with no discernable adverse effects, resulting in a marked improvement in her symptoms and obviated the need for isolation. Subsequently, the patient's history of congenital heart disease and facial abnormalities prompted initial suspicions of a 22q11.2DS diagnosis, which was subsequently confirmed through genetic testing. CONCLUSION: Clozapine may serve as an efficacious pharmacological intervention for TRS patients with 22q11.2DS, including those of Asian descent.
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spelling pubmed-102752842023-06-17 A case study of the utilization of clozapine treatment for treatment‐resistant schizophrenia associated with 22q11.2 deletion syndrome Tsurue, Arisa Funahashi, Hideki Tsurue, Keiichi Kawano, Masahiko Ishida, Yasushi Hirano, Yoji Neuropsychopharmacol Rep Case Reports BACKGROUND: The optimal treatment strategy for patients with treatment‐resistant schizophrenia (TRS) associated with 22q11.2 deletion syndrome (DS) remains a subject of debate. CASE PRESENTATION: We present the case of a 40‐year‐old female patient diagnosed with TRS and 22q11.2DS who was effectively treated with clozapine. She was diagnosed with schizophrenia and mild intellectual disability during her adolescence; despite being hospitalized for a period of 10 years beginning in her 30s, she continued to exhibit symptoms of impulsivity, and explosive behavior, requiring periods of isolation. We ultimately decided to switch her medication to clozapine, which was administered with caution and gradually titrated upward, with no discernable adverse effects, resulting in a marked improvement in her symptoms and obviated the need for isolation. Subsequently, the patient's history of congenital heart disease and facial abnormalities prompted initial suspicions of a 22q11.2DS diagnosis, which was subsequently confirmed through genetic testing. CONCLUSION: Clozapine may serve as an efficacious pharmacological intervention for TRS patients with 22q11.2DS, including those of Asian descent. John Wiley and Sons Inc. 2023-03-16 /pmc/articles/PMC10275284/ /pubmed/36929244 http://dx.doi.org/10.1002/npr2.12333 Text en © 2023 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Tsurue, Arisa
Funahashi, Hideki
Tsurue, Keiichi
Kawano, Masahiko
Ishida, Yasushi
Hirano, Yoji
A case study of the utilization of clozapine treatment for treatment‐resistant schizophrenia associated with 22q11.2 deletion syndrome
title A case study of the utilization of clozapine treatment for treatment‐resistant schizophrenia associated with 22q11.2 deletion syndrome
title_full A case study of the utilization of clozapine treatment for treatment‐resistant schizophrenia associated with 22q11.2 deletion syndrome
title_fullStr A case study of the utilization of clozapine treatment for treatment‐resistant schizophrenia associated with 22q11.2 deletion syndrome
title_full_unstemmed A case study of the utilization of clozapine treatment for treatment‐resistant schizophrenia associated with 22q11.2 deletion syndrome
title_short A case study of the utilization of clozapine treatment for treatment‐resistant schizophrenia associated with 22q11.2 deletion syndrome
title_sort case study of the utilization of clozapine treatment for treatment‐resistant schizophrenia associated with 22q11.2 deletion syndrome
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275284/
https://www.ncbi.nlm.nih.gov/pubmed/36929244
http://dx.doi.org/10.1002/npr2.12333
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