Preventing Stroke, Premature Death and Cognitive Decline in a Broader Community of Patients With Atrial Fibrillation

Designed with a Patient and Public Involvement Team, DaRe2THINK is an individual-patient, open-label, event-driven randomised trial with 1:1 allocation to DOAC or no additional therapy (usual care). Automated screening will occur of over 12 million patients in England, with targeted recruitment to practices with eligible patients, regular updates to General Practitioners, simple processes for centre inclusion and patient randomisation, remote e-consent and no additional visits for any patient. The primary outcome is a comprehensive composite of any thromboembolic event, ascertained entirely using electronic healthcare records within both primary and secondary NHS care across the nation. All endpoint data will follow a pre-published coding manual for extracted electronic healthcare data. The key secondary outcome is the change in patient-reported cognitive function, using remote technology solutions to save time for clinical staff and patients. DaRe2THINK will carefully assess and validate safety outcomes relating to major and minor bleeding. A systematic health economic analysis will determine NHS and societal cost-effectiveness of DOAC therapy in this younger population of patients with AF. DaRe2THINK will initially run over a 5-year period (outcomes as listed below), with longer-term outcomes (in particular cardiovascular death, cognitive function and vascular dementia) reassessed at 10 years.

Inclusion criteria

• Diagnosis of AF (previous, current or chronic)
• Age at enrolment ≥55 years to ≤73 years

Exclusion criteria

based on coding in Primary Care:

• Prior documented stroke, transient ischaemic attack or systemic thromboembolism.
• Combination of multiple known risk factors for stroke where oral anticoagulation would ordinarily be started, including: Heart failure; Hypertension; Age 65 years or older; Diabetes mellitus; Previous myocardial infarction, peripheral artery disease or aortic plaque; and/or Female gender.
• Any prior history of intracranial bleeding.
• Prior major bleeding requiring hospitalisation in the last 3 years.
• Condition that poses a significant risk for bleeding (within 12 months) including gastrointestinal ulceration, brain/spinal/ophthalmic injury or surgery, arteriovenous malformations or vascular aneurysms, major intraspinal or intracerebral vascular abnormalities, hepatic disease associated with coagulopathy, known or suspected oesophageal varices, and cancers with high bleeding risk.
• Estimated glomerular filtration rate <30 mL/min/1.73m2 measured within the last 12 months.
• Patients receiving systemic treatment with azole-antimycotics within the last 3 months (ketoconazole, itraconazole, voriconazole and posaconazole).
• Documented diagnosis of dementia.
• Hypersensitivity or known intolerance to direct oral anticoagulants.

Exclusion criteria

based on review by Primary Care staff:

• Currently receiving an anticoagulant.
• Any clinical indication for anticoagulation.
• Active clinically-significant bleeding.
• Life expectancy estimated <2 years.
• Participant unable or unwilling to provide informed consent for access and linkage of past and future electronic healthcare records.
• Currently participating in another clinical trial.
• Women of childbearing potential.