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Venous Thromboembolism as an Adverse Effect During Treatment With Olanzapine: A Case Series
Objective: Venous thromboembolism (VTE) is a serious multifactorial disorder. Patients with severe mental illness have a higher risk of developing the condition compared to the general population. Methods: We observed 10 cases of VTE in patients with mental illness who were treated with the antipsyc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529840/ https://www.ncbi.nlm.nih.gov/pubmed/31156478 http://dx.doi.org/10.3389/fpsyt.2019.00330 |
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author | Masopust, Jiri Bazantova, Vera Kuca, Kamil Klimova, Blanka Valis, Martin |
author_facet | Masopust, Jiri Bazantova, Vera Kuca, Kamil Klimova, Blanka Valis, Martin |
author_sort | Masopust, Jiri |
collection | PubMed |
description | Objective: Venous thromboembolism (VTE) is a serious multifactorial disorder. Patients with severe mental illness have a higher risk of developing the condition compared to the general population. Methods: We observed 10 cases of VTE in patients with mental illness who were treated with the antipsychotic drug olanzapine. The diagnosis of VTE was made at the University Hospital Hradec Kralove (UH HK) from 2004 to 2013. VTE was objectively determined by imaging techniques (duplex ultrasonography, CT angiography) and laboratory tests (D-dimer). The average age was 46 years. The clinical manifestation of VTE was deep vein thrombosis in nine cases, including one case of simultaneous pulmonary embolism and one case of a concurrent ischemic cerebrovascular accident (iCVA). None of our patients had a history of malignant disease, trauma, or surgery. Results: Apart from antipsychotic medication, all the patients had clinical or laboratory risk factors for VTE. The most frequent clinical risk factors were obesity (n = 7) and smoking (n = 6). The most frequent laboratory risk factors were increased levels of FVIII (n = 4), mild hyperhomocysteinemia (n = 3), and factor V Leiden mutation (n = 2). VTE developed within 3 months after antipsychotic drug initiation in three patients and within 6 months in three patients. Conclusion: Olanzapine can be considered a precipitating factor for VTE formation. When olanzapine is administered, we need to monitor for clinical signs and symptoms of VTE, especially when other risk factors are present. |
format | Online Article Text |
id | pubmed-6529840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65298402019-05-31 Venous Thromboembolism as an Adverse Effect During Treatment With Olanzapine: A Case Series Masopust, Jiri Bazantova, Vera Kuca, Kamil Klimova, Blanka Valis, Martin Front Psychiatry Psychiatry Objective: Venous thromboembolism (VTE) is a serious multifactorial disorder. Patients with severe mental illness have a higher risk of developing the condition compared to the general population. Methods: We observed 10 cases of VTE in patients with mental illness who were treated with the antipsychotic drug olanzapine. The diagnosis of VTE was made at the University Hospital Hradec Kralove (UH HK) from 2004 to 2013. VTE was objectively determined by imaging techniques (duplex ultrasonography, CT angiography) and laboratory tests (D-dimer). The average age was 46 years. The clinical manifestation of VTE was deep vein thrombosis in nine cases, including one case of simultaneous pulmonary embolism and one case of a concurrent ischemic cerebrovascular accident (iCVA). None of our patients had a history of malignant disease, trauma, or surgery. Results: Apart from antipsychotic medication, all the patients had clinical or laboratory risk factors for VTE. The most frequent clinical risk factors were obesity (n = 7) and smoking (n = 6). The most frequent laboratory risk factors were increased levels of FVIII (n = 4), mild hyperhomocysteinemia (n = 3), and factor V Leiden mutation (n = 2). VTE developed within 3 months after antipsychotic drug initiation in three patients and within 6 months in three patients. Conclusion: Olanzapine can be considered a precipitating factor for VTE formation. When olanzapine is administered, we need to monitor for clinical signs and symptoms of VTE, especially when other risk factors are present. Frontiers Media S.A. 2019-05-15 /pmc/articles/PMC6529840/ /pubmed/31156478 http://dx.doi.org/10.3389/fpsyt.2019.00330 Text en Copyright © 2019 Masopust, Bazantova, Kuca, Klimova and Valis http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Psychiatry Masopust, Jiri Bazantova, Vera Kuca, Kamil Klimova, Blanka Valis, Martin Venous Thromboembolism as an Adverse Effect During Treatment With Olanzapine: A Case Series |
title | Venous Thromboembolism as an Adverse Effect During Treatment With Olanzapine: A Case Series |
title_full | Venous Thromboembolism as an Adverse Effect During Treatment With Olanzapine: A Case Series |
title_fullStr | Venous Thromboembolism as an Adverse Effect During Treatment With Olanzapine: A Case Series |
title_full_unstemmed | Venous Thromboembolism as an Adverse Effect During Treatment With Olanzapine: A Case Series |
title_short | Venous Thromboembolism as an Adverse Effect During Treatment With Olanzapine: A Case Series |
title_sort | venous thromboembolism as an adverse effect during treatment with olanzapine: a case series |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529840/ https://www.ncbi.nlm.nih.gov/pubmed/31156478 http://dx.doi.org/10.3389/fpsyt.2019.00330 |
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