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Clozapine-Related Thromboembolic Events
Elisa Pallares Vela1, Prashil Dave2, Ivan Cancarevic3
1General Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Clozapine use, an antipsychotic for schizophrenia, is linked to rare but fatal venous thromboembolism (VTE). Most VTE events occurred within six months, especially in patients with comorbidities and risk factors.
Area of Science:
- Pharmacology
- Clinical Medicine
- Psychiatry
Background:
- Clozapine is a critical atypical antipsychotic for treatment-resistant schizophrenia.
- Venous thromboembolism (VTE) is a rare, potentially fatal side effect associated with clozapine use.
- Understanding the VTE risk in clozapine users is crucial for patient safety.
Purpose of the Study:
- To summarize current evidence on the risk of VTE in patients using clozapine.
- To analyze case reports of VTE onset in clozapine users over the last two decades.
- To identify patient characteristics, risk factors, and outcomes associated with clozapine-induced VTE.
Main Methods:
- Conducted a literature search of PubMed (MeSH) and Google Scholar for the past 20 years.
- Included human studies and case reports focusing on clozapine use at the time of VTE onset.
- Analyzed 42 case reports for demographic data, clozapine dosage, VTE onset timing, comorbidities, concomitant medications, and outcomes.
Main Results:
- The average age of affected patients was 42.9 years, with a male predominance (71.43%).
- VTE onset typically occurred within the first six months of clozapine use (71.8%), with an average dose of 285.62 mg/day.
- A high percentage of patients had comorbidities (70.37%) and VTE risk factors (87.5%); mortality was 32.5%, with clozapine discontinuation in 60% of cases.
Conclusions:
- VTE associated with clozapine can occur across a wide dose range, with a notable incidence within the first six months of treatment.
- Patients prescribed clozapine often have pre-existing risk factors for VTE, necessitating careful consideration of this risk.
- Further research is needed to clarify the precise risk of VTE in clozapine users and evaluate the efficacy of thromboprophylaxis.
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