Why the study?
DOAC prescriptions in clinical practice frequently deviate from trial-established indications, notably through inappropriate underdosing that increases thromboembolic risk and hospitalization.
This position paper emphasizes the importance of prescribing appropriate doses of DOACs in patients with non-valvular atrial fibrillation to avoid increased risks of stroke and systemic thromboembolism.
Answers are grounded in this paper and cite their sources.
Ensure approved DOAC doses in non-valvular AF unless criteria met; reinforces guideline-directed prescribing to minimize thromboembolic risk.
The appropriateness of prescribing direct oral anticoagulants [dabigatran, rivaroxaban, apixaban, and edoxaban (DOACs)] is regulated on the criteria established in Phase III trials. These criteria are reported in the summary of the product characteristics of the four DOACs. In clinical practice, prescriptions are not always in compliance with established indications. In particular, the use of lower doses than those recommended in drug data sheets is not uncommon. Literature data show that the inappropriate prescription of reduced doses causes drug underexposure and up to a three-fold increase in the risk of stroke/ischaemic transient attack, systemic thromboembolism, and hospitalization. Possible causes of the deviation between the dose that should be prescribed and that prescribed in the real world include erroneous prescription, an overstated haemorrhagic risk perception, and the presence of frail and complex patients in clinical practice who were not included in pivotal trials, which makes it difficult to apply study results to the real world. For these reasons, we summarize DOAC indications and contraindications. We also suggest the appropriate use of DOACs in common clinical scenarios, in accordance with what international guidelines and national and international health regulatory bodies recommend.
No takes yet. Share an insight, caveat, or question.
Mocini et al. (2022) conducted a review in Non-valvular atrial fibrillation. Direct oral anticoagulants (DOACs) was evaluated. Inappropriate prescription of reduced DOAC doses causes drug underexposure and up to a three-fold increase in the risk of stroke, systemic thromboembolism, and hospitalization.
Synapse has enriched 10 related papers. Consider them for comparative context: