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Venous Thromboembolism as an Adverse Effect During Treatment With Olanzapine: A Case Series

dc.contributor.authorMasopust, Jiri
dc.contributor.authorBazantova, Vera
dc.contributor.authorKuča, Kamil
dc.contributor.authorKlimova, Blanka
dc.contributor.authorValis, Martin
dc.date.accessioned2026-08-18T12:31:36Z
dc.date.issued2019
dc.description.abstractObjective: 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.eng
dc.description.abstract-translatedObjective: 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.cze
dc.formatp. 1-6
dc.identifier.doi10.3389/fpsyt.2019.00330
dc.identifier.issn1664-0640
dc.identifier.obd43875205
dc.identifier.scopus2-s2.0-85068220655
dc.identifier.urihttps://hdl.handle.net/20.500.12603/3145
dc.identifier.wos000468147700001
dc.language.isoeng
dc.peerreviewedyes
dc.publicationstatuspostprint
dc.publisherFRONTIERS MEDIA SA
dc.relation.ispartofFRONTIERS IN PSYCHIATRY, volume 10, issue: MAYeng
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fpsyt.2019.00330/full
dc.rights.accessOpen Access
dc.rights.licenseCC BY
dc.source.urlhttps://www.frontiersin.org/articles/10.3389/fpsyt.2019.00330/full
dc.subjectantipsychoticseng
dc.subjectolanzapineeng
dc.subjectvenous thromboembolismeng
dc.subjectside effectseng
dc.subjectrisk factorseng
dc.subjectantipsychotikacze
dc.subjectolanzapincze
dc.subjectvenózní tromboembolismuscze
dc.subjectvedlejší efektycze
dc.subjectrizikové faktorycze
dc.titleVenous Thromboembolism as an Adverse Effect During Treatment With Olanzapine: A Case Serieseng
dc.title.alternativeVenózní tromboembolie jako nežádoucí účinek během léčby přípravkem Olanzapin: Série případůcze
dc.typearticle

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