Key result
High predicted adherence at OAC initiation is linked to ~33% lower 12-month ischaemic stroke risk.
Why the study?
Medication non-adherence is a major challenge in stroke prevention in AF, but no validated tool exists to identify patients at risk of non-adherence at OAC initiation.
Does high predicted medication adherence (MAS ≥80) reduce ischaemic stroke risk in adults with AF initiating OAC?
Cohort (n=11,233)
No
Does high predicted medication adherence (MAS ≥80) reduce ischaemic stroke risk in adults with AF initiating OAC?
In AF patients initiating OAC, low predicted medication adherence using the Medication Adherence Score is independently associated with increased ischaemic stroke risk, highlighting a potential tool for targeted adherence interventions.
May identify AF patients for adherence support at OAC initiation; hypothesis-generating, needs prospective trials before practice change.
BACKGROUND: Medication non-adherence is a major challenge in stroke prevention in atrial fibrillation (AF), yet no validated tool exists to identify patients at risk of non-adherence at the time of oral anticoagulation (OAC) initiation. METHODS: In this retrospective cohort study at a large tertiary centre in New York City (2015-2023), adults with AF and a CHA₂DS₂-VASc score ≥ 2 initiating OAC were included. Predicted medication adherence was quantified using the Medication Adherence Score (MAS), a validated algorithm incorporating demographic, socioeconomic, and geographic attributes, dichotomised as high (MAS ≥80) or low (MAS <80). The primary outcome was ischaemic stroke within 12 months, analysed using Fine-Gray competing-risk regression. RESULTS: Of 11,233 eligible patients, 4035 (35.9%) had high and 7198 (64.1%) had low predicted adherence. Most patients received a direct oral anticoagulant (DOAC, 70.3%), 10.7% received warfarin, and 19.0% switched agents. Ischaemic stroke occurred in 6.2% of patients. High predicted adherence was associated with significantly lower stroke risk (sHR 0.67; 95% CI 0.56-0.80), with 12-month cumulative incidences of 5.08% vs. 7.97%. Continuously modelled MAS confirmed a dose-response relationship (HR 0.98 per unit increase; 95% CI 0.97-0.99). Results were consistent after excluding patients with prior stroke (sHR 0.66; 95% CI 0.53-0.83). CONCLUSIONS: In AF patients initiating OAC, low predicted medication adherence is independently associated with increased ischaemic stroke risk. The MAS may support early identification of high-risk patients, enabling targeted adherence interventions at OAC initiation.
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Perdeck et al. (2026) conducted a cohort in Atrial fibrillation (n=11,233). High predicted medication adherence (MAS ≥80) vs. Low predicted medication adherence (MAS <80) was evaluated on Ischaemic stroke within 12 months (sHR 0.67, 95% CI 0.56-0.80). High predicted medication adherence at oral anticoagulation initiation was associated with a lower 12-month risk of ischaemic stroke compared to low predicted adherence (sHR 0.67; 95% CI 0.56-0.80).
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