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Second case report of successful electroconvulsive therapy for a patient with schizophrenia and severe hemophilia A
Electroconvulsive therapy (ECT) is used for medication-resistant and life-threatening mental disorders, and therefore it occupies an important position in psychiatric treatment. ECT reportedly increases intracranial pressure and is suspected of increasing the risk of intracranial hemorrhage, especia...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037299/ https://www.ncbi.nlm.nih.gov/pubmed/24876778 http://dx.doi.org/10.2147/NDT.S61816 |
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author | Saito, Nobuyoshi Shioda, Katsutoshi Nisijima, Koichi Kobayashi, Toshiyuki Kato, Satoshi |
author_facet | Saito, Nobuyoshi Shioda, Katsutoshi Nisijima, Koichi Kobayashi, Toshiyuki Kato, Satoshi |
author_sort | Saito, Nobuyoshi |
collection | PubMed |
description | Electroconvulsive therapy (ECT) is used for medication-resistant and life-threatening mental disorders, and therefore it occupies an important position in psychiatric treatment. ECT reportedly increases intracranial pressure and is suspected of increasing the risk of intracranial hemorrhage, especially in patients with hemorrhagic diseases such as hemophilia. A decrease in or loss of blood coagulation factors, including factor VIII and factor IX, are found in hemophilia A and B, respectively. Psychiatrists may hesitate to perform ECT on patients with bleeding tendencies, such as in hemophilia. Here, we report the successful use of ECT on a neuroleptic-resistant patient with schizophrenia and severe hemophilia A. We performed ECT 16 times supplemented with coagulation factor VIII to prevent intracranial and systematic hemorrhage. We administered factor VIII concentrates to the patient to keep factor VIII activity at 30%–40% during ECT. The patient did not show bleeding or other complications during the ECT sessions. We suggest that pretreatment with factor VIII can help manage the increased risks of intracranial and systematic bleeding during ECT that is present in patients with hemophilia A. The present report supports the idea of performing ECT safely on patients with hemophilia A by administering factor VIII. |
format | Online Article Text |
id | pubmed-4037299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40372992014-05-29 Second case report of successful electroconvulsive therapy for a patient with schizophrenia and severe hemophilia A Saito, Nobuyoshi Shioda, Katsutoshi Nisijima, Koichi Kobayashi, Toshiyuki Kato, Satoshi Neuropsychiatr Dis Treat Case Report Electroconvulsive therapy (ECT) is used for medication-resistant and life-threatening mental disorders, and therefore it occupies an important position in psychiatric treatment. ECT reportedly increases intracranial pressure and is suspected of increasing the risk of intracranial hemorrhage, especially in patients with hemorrhagic diseases such as hemophilia. A decrease in or loss of blood coagulation factors, including factor VIII and factor IX, are found in hemophilia A and B, respectively. Psychiatrists may hesitate to perform ECT on patients with bleeding tendencies, such as in hemophilia. Here, we report the successful use of ECT on a neuroleptic-resistant patient with schizophrenia and severe hemophilia A. We performed ECT 16 times supplemented with coagulation factor VIII to prevent intracranial and systematic hemorrhage. We administered factor VIII concentrates to the patient to keep factor VIII activity at 30%–40% during ECT. The patient did not show bleeding or other complications during the ECT sessions. We suggest that pretreatment with factor VIII can help manage the increased risks of intracranial and systematic bleeding during ECT that is present in patients with hemophilia A. The present report supports the idea of performing ECT safely on patients with hemophilia A by administering factor VIII. Dove Medical Press 2014-05-16 /pmc/articles/PMC4037299/ /pubmed/24876778 http://dx.doi.org/10.2147/NDT.S61816 Text en © 2014 Saito et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Case Report Saito, Nobuyoshi Shioda, Katsutoshi Nisijima, Koichi Kobayashi, Toshiyuki Kato, Satoshi Second case report of successful electroconvulsive therapy for a patient with schizophrenia and severe hemophilia A |
title | Second case report of successful electroconvulsive therapy for a patient with schizophrenia and severe hemophilia A |
title_full | Second case report of successful electroconvulsive therapy for a patient with schizophrenia and severe hemophilia A |
title_fullStr | Second case report of successful electroconvulsive therapy for a patient with schizophrenia and severe hemophilia A |
title_full_unstemmed | Second case report of successful electroconvulsive therapy for a patient with schizophrenia and severe hemophilia A |
title_short | Second case report of successful electroconvulsive therapy for a patient with schizophrenia and severe hemophilia A |
title_sort | second case report of successful electroconvulsive therapy for a patient with schizophrenia and severe hemophilia a |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4037299/ https://www.ncbi.nlm.nih.gov/pubmed/24876778 http://dx.doi.org/10.2147/NDT.S61816 |
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