Journal of Thrombosis and Thrombolysis

, Volume 44, Issue 4, pp 519–524 | Cite as

Oral factor Xa inhibitors for the treatment of left ventricular thrombus: a case series

  • Keaton S. Smetana
  • Jessie Dunne
  • Kevin Parrott
  • George A. Davis
  • Amy C. Schmelzer Collier
  • Mary Covell
  • Susan Smyth
Article

Abstract

Left ventricular thrombus (LVT) formation usually necessitates short term anticoagulation for thrombus resolution and to prevent embolic events. Historically, vitamin K antagonist therapy has been the treatment of choice. However, with the advent of direct acting anticoagulants, their role in the management of LVT is not clear. Patients were included if they had received rivaroxaban or apixaban for more than 1 day for LVT documented on imaging. The primary objective was resolution of LVT at 3 months based on assessment by an independent cardiologist review of initial and subsequent imaging results. The principle safety objective was to assess major or clinically relevant non-major bleeding using GUSTO, TIMI, and BARC bleeding criteria. During the 2-year study period seven patients were treated with rivaroxaban and three with apixaban. Two patients who had received apixaban and one on rivaroxaban were lost to follow up. In those with an initial and follow-up ECHO (n = 6) the median time to follow up imaging was 214 (IQR 33–414) days and complete LVT resolution was observed in 83% of patients. One patient on rivaroxaban had a bleeding events that was minimal (TIMI), Type 2 (BARC), or classified as mild (GUSTO) due to pulmonary hemorrhage. In those deemed not to be a candidate for vitamin K antagonist the use of rivaroxaban or apixaban may be a considered in the treatment of LVT. Further research in this area is needed to assess the efficacy and safety of using FXAI for treatment of LVT.

Keywords

Apixaban Factor Xa inhibitors Left ventricle Rivaroxaban Thrombosis 

Notes

Funding

No funding was obtained for the conduction of this study.

Compliance with ethical standards

Conflict of interest

All authors of this study have no direct or indirect conflicts of interest to disclose.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

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Copyright information

© Springer Science+Business Media, LLC 2017

Authors and Affiliations

  • Keaton S. Smetana
    • 1
  • Jessie Dunne
    • 2
  • Kevin Parrott
    • 3
  • George A. Davis
    • 2
  • Amy C. Schmelzer Collier
    • 4
  • Mary Covell
    • 2
  • Susan Smyth
    • 3
  1. 1.Department of Pharmaceutical ServicesThe Ohio State University Wexner Medical CenterColumbusUSA
  2. 2.Department of Pharmaceutical ServicesUniversity of Kentucky HealthCareLexingtonUSA
  3. 3.Division of Cardiovascular MedicineGill Heart and Vascular InstituteLexingtonUSA
  4. 4.Department of Internal MedicineUniversity of Kentucky HealthCareLexingtonUSA

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