Skip to content
cardio.webdr
ToolsSpecialtiesEchoHeart sounds
ToolsSpecialtiesEchoHeart soundsFavoritesPrivate notes
cardio.webdr

Clinical clarity, in seconds. Built for focused decisions—not data collection.

Patient inputs stay on this device.
ExploreAll toolsSpecialtiesEchocardiographyHeart sounds
Your workspaceFavoritesPrivate notesCalculation historyOffline access
PlatformAboutFAQDevelopersFeedbackContact
© 2026 CardioWebdr Clinical support, not a substitute for judgment.PrivacyTermsStorageSupportReport an issue
All tools/Atrial Fibrillation & Stroke Prevention Scores
Interactive worksheet5 clinical inputsPatient data not stored

ARISTOTLE-based Stroke Risk (Appraisal of Risk in AF) Calculator

Appraisal of Risk in AF (ARISTOTLE-based) Score: Explanation and Clinical Context The ARISTOTLE-based risk score for atrial fibrillation was developed from the ARISTOTLE trial population to predict 1-year risk of stroke or systemic embolism in patients with AF. The model is based on easily obtainable clinical variables including age, prior stroke or transient ischemic attack (TIA), hypertension, diabetes mellitus, an

Interactive worksheet

Clinical inputs

0/5 filled
Inputs stay on this device
Active structured worksheetActive local worksheet: mapped inputs can be completed, validated, copied, saved, and exported on this device. No numerical score is asserted unless its formula is independently reproducible.
Clinical contextWhy this tool matters and how to interpret it

Understand the result,
not just the number.

Appraisal of Risk in AF (ARISTOTLE-based) Score: Explanation and Clinical Context The ARISTOTLE-based risk score for atrial fibrillation was developed from the ARISTOTLE trial population to predict 1-year risk of stroke or systemic embolism in patients with AF. The model is based on easily obtainable clinical variables including age, prior stroke or transient ischemic attack (TIA), hypertension, diabetes mellitus, and heart failure or reduced left ventricular ejection fraction. The score uses a weighted linear model derived from Cox proportional hazards regression in the ARISTOTLE trial, allowing estimation of individualized 1-year stroke risk.

Predicted risk is categorized as low (<1.5%), intermediate (1.5–3.0%), and high (>3.0%), supporting decision-making for anticoagulation therapy. This tool provides a more precise alternative to traditional risk scores such as CHA₂DS₂-VASc, by reflecting empirically derived hazard ratios in a contemporary trial population treated with anticoagulants.

Evidence & references1 primary source mapped
  1. Source 1

    Patel MR, et al. Apixaban versus warfarin in patients with atrial fibrillation. N Engl J Med. 2011;365:981–992. Hijazi Z, et al. Biomarker-based risk scores for predicting stroke and bleeding in patients with atrial fibrillation: insights from the ARISTOTLE trial. Eur Heart J. 2016;37:1230–1237. Wallentin L, et al. Application of ABC-AF stroke and bleeding risk scores in contemporary clinical practice. Thromb Haemost. 2020;120:748–756.

Clinical discussionModerated, tool-specific conversation

Loading discussion…

Moderated before publishingNever include patient identifiers.

Workspace mode

Structured worksheet

Active local worksheet: mapped inputs can be completed, validated, copied, saved, and exported on this device. No numerical score is asserted unless its formula is independently reproducible.

On this pageWorksheet Clinical context References Discussion

Privacy by default

Inputs, results, favorites, and notes remain in your browser unless you explicitly export them.

Privacy details
Report formula or content issue
Continue exploring

Related clinical tools

More in this specialty
Score mapped

ORBIT Bleeding Score Calculator

Atrial Fibrillation & Stroke Prevention Scores
Score mapped

C2HEST Score Calculator

Atrial Fibrillation & Stroke Prevention Scores
Interactive worksheet

ABC Stroke Risk Score Calculator

Atrial Fibrillation & Stroke Prevention Scores
Score mapped

HATCH Score (AF Progression) Calculator

Atrial Fibrillation & Stroke Prevention Scores
Clinical structure and calculation context point directly to Source 1; additional primary references remain listed for auditability.