Summary
The prevention and treatment of venous thromboembolism (VTE) remains a clinical challenge,
primarily owing to drawbacks associated with the use of heparins and vitamin K antagonists
(VKAs). These and other factors, including a growing elderly population, mean that
VTE presents a continuing burden to patients and physicians. Anticoagulant therapy
is a fundamental approach for VTE management. Non- VKA oral anticoagulants, including
the factor Xa inhibitors apixaban, edoxaban and rivaroxaban, and the thrombin inhibitor
dabigatran, have been studied in phase III trials across a spectrum of thromboembolic
disorders. These agents offer simplified care, with similar or improved efficacy and
safety outcomes compared with heparins and vitamin K antagonists. There are several
factors a physician must consider when prescribing an anticoagulant. An important
consideration with all anticoagulant use is bleeding risk, especially in high-risk
groups such as the elderly or those with renal impairment or cancer. In orthopaedic
patients, other risks include a need for surgical revision or blood transfusion, or
wound complications. Therefore, the clinical benefits of an anticoagulant should ideally
be balanced with any risks associated with the therapy. Quantitative benefit–risk
assessments are lacking, and owing to differences in trial design the non-VKA oral
anticoagulants cannot be compared directly. Based on trial and “reallife” data, this
review will summarise the clinical data for the non-VKA oral anticoagulants in the
prevention and treatment of VTE, focusing on the balance between the benefits and
risks of anticoagulation with these drugs, and their potential impact on VTE management.
Keywords
Benefit–risk assessment - non-VKA oral anticoagulants - real-life - thromboprophylaxis
- venous thromboembolism