Venous Thromboembolism as an Adverse Effect During Treatment With Olanzapine: A Case Series
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
31156478
PubMed Central
PMC6529840
DOI
10.3389/fpsyt.2019.00330
Knihovny.cz E-zdroje
- Klíčová slova
- antipsychotics, olanzapine, risk factors, side effects, venous thromboembolism,
- Publikační typ
- časopisecké články MeSH
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.
Biomedical Research Center University Hospital Hradec Kralove Hradec Kralove Czechia
Department of Chemistry Faculty of Science University of Hradec Kralove Hradec Kralove Czechia
Zobrazit více v PubMed
Di Nisio M, van Es N, Buller HR. Deep vein thrombosis and pulmonary embolism. Lancet (2016) 388:3060–73. 10.1016/S0140-6736(16)30514-1 PubMed DOI
Heit JA, Spencer FA, White RH. The epidemiology of venous thromboembolism. J Thromb Thrombolysis (2016) 41:3–14. 10.1007/s11239-015-1311-6 PubMed DOI PMC
Cohen AT, Agnelli G, Anderson FA, Arcelus JI, Berqvist D, Brecht JG, et al. Venous thromboembolism (VTE) in Europe. Thromb Haemost (2007) 98:756–64. 10.1160/TH07-03-0212 PubMed DOI
Lijfering WM, Rosendaal FR, Cannegieter SC. Risk factors for venous thrombosis—current understanding from an epidemiological point of view. Br J Haematol (2010) 149:824–33. 10.1111/j.1365-2141.2010.08206.x PubMed DOI
Masopust J, Maly R, Andrys C, Valis M, Bazant J, Hosak L. Markers of thrombogenesis are activated in unmedicated patients with acute psychosis: a matched case control study. BMC Psychiatry (2011) 11:2. 10.1186/1471-244X-11-2 PubMed DOI PMC
Masopust J, Maly R, Andrys C, Valis M, Bazant J, Hosak L. The dynamics of haemostatic parameters in acute psychotic patients: a one-year prospective study. Psychiatr Danub (2013) 25:142–8. PubMed
Khandaker GM, Cousins L, Deakin J, Lennox BR, Yolken R, Jones PB. Inflammation and immunity in schizophrenia: implications for pathophysiology and treatment. Lancet Psychiatry (2015) 2:258–70. 10.1016/S2215-0366(14)00122-9 PubMed DOI PMC
Hagg S, Bate A, Stahl M, Spigset O. Associations between venous thromboembolism and antipsychotics. Drug Saf (2008) 31:685–94. 10.2165/00002018-200831080-00005 PubMed DOI
Jonsson AK, Schill J, Olsson H, Spigset O, Hagg S. Venous thromboembolism during treatment with antipsychotics: a review of current evidence. CNS Drugs (2018) 32:47–64. 10.1007/s40263-018-0495-7 PubMed DOI PMC
Barbui C, Conti V, Cipriani A. Antipsychotic drug exposure and risk of venous thromboembolism: a systematic review and meta-analysis of observational studies. Drug Saf (2014) 37:79–90. 10.1007/s40264-013-0127-6 PubMed DOI
Zhang R, Dong L, Shao F, Tan X, Ying K. Antipsychotics and venous thromboembolism risk: a meta-analysis. Pharmacopsychiatry (2011) 44:183–8. 10.1055/s-0031-1280814 PubMed DOI
Masopust J, Maly R, Valis M. Risk of venous thromboembolism during treatment with antipsychotic agents. Psychiatry Clin Neurosci (2012) 66:541–52. 10.1111/pcn.12001 PubMed DOI
Wu CS, Lin CC, Chang CM, Wu KY, Liang HY, Huang YW, et al. Antipsychotic treatment and the occurrence of venous thromboembolism: a 10-year nationwide registry study. J Clin Psychiatry (2013) 74:918–24. 10.4088/JCP.12m08117 PubMed DOI
Ishiguro C, Wang X, Li L, Jick S. Antipsychotic drugs and risk of idiopathic venous thromboembolism: a nested case–control study using the CPRD. Pharmacoepidemiol Drug Saf (2014) 23:1168–75. 10.1002/pds.3699 PubMed DOI
Shulman M, Njoku IJ, Manu P. Thrombotic complications of treatment with antipsychotic drugs. Minerva Med (2013) 104:175–84 PubMed
Kamijo Y, Soma K, Nagai T, Kurihara K, Ohwada T. Acute massive pulmonary thromboembolism associated with risperidone and conventional phenothiazines. Circ J (2003) 67:46–8. 10.1253/circj.67.46 PubMed DOI
Rosendaal FR. Venous thrombosis: the role of genes, environment, and behavior. Hematol Am Soc Hematol Educ Program (2005) 2005:1–12. 10.1182/asheducation-2005.1.1 PubMed DOI
Bhanji NH, Chouinard G, Hoffman L, Margolese HC. Seizures, coma, and coagulopathy following olanzapine overdose. Can J Psychiatry (2005) 50:126–7. 10.1177/070674370505000214 PubMed DOI
Wallaschofski H, Eigenthaler M, Kiefer M, Donne M, Hentschel B, Gertz HJ, et al. Hyperprolactinemia in patients on antipsychotic drugs causes ADP-stimulated platelet activation that might explain the increased risk for venous thromboembolism: pilot study. J Clin Psychopharmacol (2003) 23:479–83. 10.1097/01.jcp.0000088914.24613.51 PubMed DOI
Borch KH, Braekkan SK, Mathiesen EB, Njolstad I, Wilsgaard T, Stormer J, et al. Abdominal obesity is essential for the risk of venous thromboembolism in the metabolic syndrome: the Tromso study. J Thromb Haemost (2009) 7:739–45. 10.1111/j.1538-7836.2008.03234.x PubMed DOI
Christiansen SC, Lijfering WM, Naess IA, Hammerstrom J, van Hylckama Vlieg A, Rosendaal FR, et al. The relationship between body mass index, activated protein C resistance and risk of venous thrombosis. J Thromb Haemost (2012) 10:1761–7. 10.1111/j.1538-7836.2012.04828.x PubMed DOI
Morange PE, Alessi MC. Thrombosis in central obesity and metabolic syndrome: mechanisms and epidemiology. Thromb Haemost (2013) 110:669–80. 10.1160/TH13-01-0075 PubMed DOI
Hem E, Steen O, Opjordsmoen S. Thrombosis associated with physical restraints. Acta Psychiatr Scand (2001) 103:73–5. 10.1034/j.1600-0447.2001.00082.x PubMed DOI
Parker C, Coupland C, Hippisley-Cox J. Antipsychotic drugs and risk of venous thromboembolism: nested case–control study. BMJ (2010) 341:c4245. 10.1136/bmj.c4245 PubMed DOI
De Hert M, Correll CU, Bobes J, Cetkovich-Bakmas M, Cohen D, Asai I, et al. Physical illness in patients with severe mental disorders. World Psychiatry (2011) 10:52–77. 10.1002/j.2051-5545.2011.tb00014.x PubMed DOI PMC
Maly R, Masopust J, Hosak L, Konupcikova K. Assessment of risk of venous thromboembolism and its possible prevention in psychiatric patients. Psychiatry Clin Neurosci (2008) 62:3–8. 10.1111/j.1440-1819.2007.01773.x PubMed DOI