This review summarizes clinical trial data and guideline recommendations for the management of venous thromboembolism and atrial fibrillation in patients with active cancer.
Patients with active cancer at risk of or experiencing venous thromboembolism (VTE) or atrial fibrillation (AF)
Anticoagulation strategies including direct oral anticoagulants (DOACs), low molecular weight heparins (LMWH), and warfarin
This review summarizes current evidence and provides a practical approach to the use of DOACs, LMWH, and warfarin for managing VTE and AF in patients with active cancer.
Patients with active cancer are at an increased risk of arterial and venous thromboembolism (VTE) and bleeding events. Historically, in patients with cancer, low molecular weight heparins have been preferred for treatment of VTE, whereas warfarin has been the standard anticoagulant for stroke prevention in patients with atrial fibrillation (AF). More recently, direct oral anticoagulants (DOACs) have been demonstrated to reduce the risk of venous and arterial thromboembolism in large randomized clinical trials of patients with VTE and AF, respectively, thus providing an attractive oral dosing option that does not require routine laboratory monitoring. In this review, we summarize available clinical trial data and guideline recommendations, and outline a practical approach to anticoagulation management of VTE and AF in cancer.
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Ramya Mosarla
NYU Langone Health
Muthiah Vaduganathan
Brigham and Women's Hospital
Arman Qamar
NorthShore University HealthSystem
Journal of the American College of Cardiology
Harvard University
Brigham and Women's Hospital
Massachusetts General Hospital
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Mosarla et al. (Fri,) conducted a review in Cancer with venous thromboembolism and atrial fibrillation. Anticoagulation strategies (DOACs, LMWH, warfarin) was evaluated. This review summarizes clinical trial data and guideline recommendations for the management of venous thromboembolism and atrial fibrillation in patients with active cancer.
synapsesocial.com/papers/6a2391a96a2ea72b41a620c9 — DOI: https://doi.org/10.1016/j.jacc.2019.01.017
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