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Fast apixaban-related resolution of left ventricular thrombi in a patient with dilated cardiomyopathy
Waldemar Elikowski1, Magorzata Małek-Elikowska2, Natalia Fertała1
1Department of Internal Medicine, Józef Struś Hospital, Poznań, Poland.
Insights
Direct-acting oral anticoagulants like apixaban show rapid resolution of left ventricular thrombi (LVTs) in patients with dilated cardiomyopathy. This case highlights apixaban
Area of Science:
- Cardiology
- Pharmacology
Background:
- Left ventricular thrombi (LVTs) are a significant risk in patients with left ventricular dysfunction and cardiomyopathies, particularly dilated cardiomyopathy (DCM).
- Systemic embolization is a major complication associated with LVTs.
- Direct-acting oral anticoagulants (DOACs) have not been extensively studied for LVT treatment, with limited case reports available.
Observation:
- A 53-year-old male with DCM presented with heart failure exacerbation and multiple apical LVTs.
- Treatment with apixaban was initiated, with dosage adjusted based on creatinine levels.
- Echocardiography revealed gradual resolution of LVTs starting from day 3.
Findings:
- Complete resolution of LVTs was observed within one week of apixaban therapy.
- No instances of systemic embolization occurred during the treatment period.
- This represents the fastest reported resolution of LVTs with apixaban and the first description of DOAC use for multiple LVTs.
Implications:
- Apixaban demonstrates potential efficacy in rapidly resolving LVTs in patients with DCM.
- This case suggests DOACs, specifically apixaban, may be a viable treatment option for multiple LVTs.
- Further systematic investigation is warranted to confirm the safety and efficacy of DOACs in managing LVTs.
Abstract:
Left ventricular thrombi (LVTs) develop most often in patients with post-myocardial left ventricular dysfunction and in cardiomyopathies, particularly in dilated cardiomyopathy (DCM). They constitute a danger of systemic embolization. So far, direct-acting oral anticoagulants (DOACs), including apixaban - a selective inhibitor of active Factor X, have not been systematically investigated in patients with LVTs; study comparing the efficacy of apixaban and warfarin has been undertaken only recently. A few case reports or case series presenting patients with LVTs treated with DOACs are available in the literature. The authors described a case of a 53-year-old male with DCM, hospitalized due to heart failure exacerbation. In echocardiography, apart from typical features of DCM, three apical LVTs connected with false tendons were revealed. Treatment with apixaban was introduced, initially in a dose of 2.5 mg twice daily, as creatinine concentration was 2.0 mg/dl, and after 2 days - when creatinine concentration dropped, the dose was augmented to 5 mg twice a day. Gradual resolution of LVTs was observed from day 3; they disappeared completely after one week. There were no symptoms of systemic embolization. The patient was discharged with advice to take apixaban permanently. To the best of the authors knowledge, the case presented is the fastest resolution of LVTs during therapy with apixaban reported in the literature and the first description of DOAC use for multiple LVTs.
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