Why the study?
Real-world AF treatment often involves prescribing NOACs at lower or higher doses than recommended, but their efficacy and safety remained to be evaluated.
Does non-recommended dosage of NOACs reduce stroke or systemic thromboembolism in patients with atrial fibrillation compared to recommended doses?
Meta-Analysis (n=98,764)
Yes
Does non-recommended dosage of NOACs reduce stroke or systemic thromboembolism in patients with atrial fibrillation compared to recommended doses?
Relative Risk: 1.24 (95% CI 1.14–1.35)
p-value: p=<0.00001
Non-recommended dosing of NOACs in atrial fibrillation, whether low or high, is associated with worse efficacy (increased stroke/systemic embolism) without improving safety compared to guideline-recommended dosing.
Introduction: The real-world treatment of atrial fibrillation (AF) often involves the prescription of new oral anticoagulants (NOACs) using dosing both lower and higher than recommended guidelines. Our study aimed to evaluate the efficacy and safety of non-recommended dosage of NOACs in AF patients. Methods: A systematic search was performed for relevant studies across multiple electronic databases (PubMed, Embase, Cochrane Library, Clinical Trials Registry) from inception to May 1, 2021. Multicenter randomized trials and observational studies were selected with key reporting measures for inclusion involved efficacy outcomes including stroke or systemic thromboembolism along with safety endpoints assessing major or clinically relevant bleeding events. Results: A total of 11 eligible studies were included involving 48,648 patients receiving recommended dose of NOACs and 50,116 patients receiving non-recommended dosage. Compared to AF patients treated with recommended dose regimens, administration of low dose of NOACs was associated with higher risk of stroke/systemic embolism (RR = 1.24, 95% CI 1.14–1.35, P < 0.00001), but without reducing bleeding risk (RR = 1.18, 95% CI 0.91–1.53, P = 0.21) and a higher risk of all-cause mortality (RR = 1.58, 95% CI 1.25–1.99, P = 0.0001). Moreover, high dose of NOACs was associated with higher risk of stroke and systemic embolism efficacy (RR = 1.71, 95% CI 1.06–2.76, P = 0.03) and a non-significant trend to a greater risk of major or clinically relevant bleeding (RR = 1.57, 95% CI 0.96–2.58, P = 0.07). Conclusions: AF patients treated with low dose of NOACs showed equivalent safety but with worse efficacy compared with recommended dose. High dose of NOACs was not superior to recommended dose regimens in preventing stroke/systemic embolism outcomes in AF patients.
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Kong et al. (2021) conducted a meta-analysis in Atrial Fibrillation (n=98,764). Non-recommended dose of NOACs vs. Recommended dose of NOACs was evaluated on stroke or systemic thromboembolism (RR 1.24, 95% CI 1.14-1.35, p=<0.00001).
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