Key result
Switching from well-controlled VKA to DOAC in atrial fibrillation improved average PACT-Q Convenience scores by 2.5 points (95% CI 0.3-4.7) at one year, but increased the risk of side-effects.
Why the study?
DOACs presumably affect quality of life less than VKAs due to fixed dosing without INR monitoring, but high TTR also reduces VKA impact on quality of life, leaving the effect of switching well-controlled patients uncertain.
Does switching from well-controlled VKA to DOAC improve quality of life in patients with atrial fibrillation?
RCT (n=241)
randomised
Does switching from well-controlled VKA to DOAC improve quality of life in patients with atrial fibrillation?
Switching from well-controlled VKA to DOAC in AF patients modestly improves anticoagulation-related convenience and satisfaction, but carries a risk of side-effects leading to VKA resumption.
Switching well-controlled VKA patients to DOAC yields modest convenience/satisfaction gains but side-effect risks; supports selective switching only for those dissatisfied with VKA.
BACKGROUND: Direct oral anticoagulants (DOAC) and vitamin K antagonists (VKA) prevent thromboembolism in atrial fibrillation (AF). DOAC have a fixed dosing regimen and obviate INR monitoring. Therefore, DOAC presumably affect quality of life (QoL) less than VKA. However, some VKA users appreciate the monitoring. A high time in the therapeutic range (TTR) leads to a lower impact on QoL. We assessed the influence of switching from well-controlled VKA to a DOAC on QoL. METHODS: In the GAInN study, 241 patients with AF, a TTR ≥ 70%, and neither bleeding nor thrombosis while on VKA were randomised to switching to DOAC (n = 121) or continuing VKA (n = 120). Health-related (SF-36) and anticoagulation-related QoL (PACT-Q) was assessed at baseline and after six and twelve months of follow-up. RESULTS AND CONCLUSION: SF-36 development did not differ between groups. After one year, average PACT-Q Convenience improvement was 2.5 (0.3-4.7) higher on DOAC. DOAC users were 6percentage points (95%CI -4-16) more likely to improve >5 points on Convenience; 22 pp. (95%CI 1-43) in patients who scored <95/100 at baseline. The probability to meaningfully improve on PACT-Q Satisfaction was 12 pp. (95%CI 0-25) higher on DOAC. However, 5 (4.1%) and 4 (3.3%) DOAC users resumed VKA because of side-effects and patient preference. Switching from well-controlled VKA to DOAC for AF leads to a higher probability of improved PACT-Q convenience and satisfaction, but also to a higher risk of side-effects. Arguably only patients who are not satisfied with VKA should switch, because they have more to gain by switching.
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Miert et al. (2020) conducted an RCT in Atrial fibrillation (n=241). Direct oral anticoagulants (DOAC) vs. Vitamin K antagonists (VKA) was evaluated on Health-related (SF-36) and anticoagulation-related QoL (PACT-Q) (MD 2.5, 95% CI 0.3-4.7). Switching from well-controlled VKA to DOAC in atrial fibrillation improved average PACT-Q Convenience scores by 2.5 points (95% CI 0.3-4.7) at one year, but increased the risk of side-effects.
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