“…As a result of fixed dosing, no need for routine laboratory monitoring, few drug interactions, at least equal efficacy to vitamin K antagonists and lower risks of bleeding, DOACs (dabigatran, apixaban, rivaroxaban and edoxaban) have become the oral anticoagulants of choice in several conditions, including AF, in the general population and patients with mild to moderate CME: Renal medicine CKD. 3,4,7,21 However, all DOACs have an element of renal excretion. Although patients with advanced CKD/ESKD have been generally excluded from the large DOAC clinical trials, 3 on the basis of pharmacological modelling, rivaroxaban, apixaban and edoxaban have been approved for use in Europe for patients with severe CKD ( Table 2 ).…”