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🫀 STROKE RISK CALCULATOR

CHA₂DS₂-VA Score Calculator

Stroke risk in non-valvular Atrial Fibrillation · ESC 2024 updated score (female sex removed) · Anticoagulation guidance · Annual stroke risk % · DOAC recommendations

⚡ Updated for ESC 2024 — CHA₂DS₂-VA replaces CHA₂DS₂-VASc
Patient Risk Factors
Tick all that apply. Score calculates automatically.
For non-valvular AF only. Patients with valvular AF (mechanical heart valve or moderate-severe mitral stenosis) require anticoagulation regardless of score.
CHA₂DS₂-VA Score
0
Max score: 9
⚠️ Clinical scores aid — not replace — clinical judgement. Always assess individual bleeding risk and patient preferences before initiating anticoagulation.
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Tick risk factors to see score
Then click Get Full Risk Assessment for detailed guidance

CHA₂DS₂-VA Score: Complete Clinical Guide

What changed in ESC 2024, how to calculate the score, annual stroke risk percentages, anticoagulation thresholds and DOAC selection — with ESC 2024, Lancet, PMC and Eur Heart J references

What Is the CHA₂DS₂-VA Score?

The CHA₂DS₂-VA score is a clinical prediction rule used to estimate the annual risk of thromboembolic stroke in patients with non-valvular atrial fibrillation (AF). It is used to guide the decision of whether to initiate oral anticoagulation therapy — the most important intervention available to prevent AF-related stroke, which accounts for approximately 20–30% of all ischaemic strokes globally.

The score was formally adopted in the 2024 ESC Guidelines for the Management of Atrial Fibrillation (Van Gelder et al., Eur Heart J 2024) as an updated, simplified version of the widely-used CHA₂DS₂-VASc score — with one critical change: female sex has been removed as a risk variable.

⚡ What Changed in ESC 2024 — CHA₂DS₂-VA vs CHA₂DS₂-VASc

Key change: Female sex (the "Sc" component) has been REMOVED from the score.
The ESC 2024 guidelines state: "The inclusion of gender complicates clinical practice both for healthcare professionals and patients. It also omits individuals who identify as non-binary, transgender, or are undergoing sex hormone therapy."

The evidence behind this change comes from multiple large studies. A landmark nationwide UK study of over 1 million primary care patients (Yoshimura et al., Europace 2024) demonstrated that removing female sex from the score did not compromise its ability to discriminate thromboembolic events. A Finnish national registry study of AF patients confirmed that the CHA₂DS₂-VA score showed comparable predictive accuracy to CHA₂DS₂-VASc across different ethnicities and socioeconomic groups (Teppo et al., Lancet Reg Health Eur 2024).

ComponentCHA₂DS₂-VASc (old)CHA₂DS₂-VA (ESC 2024)
C — Congestive Heart Failure+1+1
H — Hypertension+1+1
A₂ — Age ≥75+2+2
D — Diabetes Mellitus+1+1
S₂ — Prior Stroke / TIA / TE+2+2
V — Vascular Disease+1+1
A — Age 65–74+1+1
Sc — Female Sex+1REMOVED ✓
Maximum Score99

Annual Stroke Risk by Score

ScoreAnnual Stroke RiskRisk LevelESC 2024 Recommendation
0~0%Very LowNo anticoagulation recommended
1~1.3%Low–ModerateConsider OAC (Class IIa) — individualised decision
2~2.2%Moderate–HighOAC recommended (Class I)
3~3.2%HighOAC strongly recommended
4~4.0%HighOAC strongly recommended
5~6.7%HighOAC strongly recommended
6~9.8%Very HighOAC strongly recommended
≥7>10%Very HighOAC essential; consider referral
Stroke rates from Lip GYH et al. Chest 2010; ESC 2024 Guidelines. OAC = oral anticoagulant. Rates in non-anticoagulated patients.

Preferred DOACs in Non-Valvular AF (ESC 2024 — Class I)

When anticoagulation is indicated, ESC 2024 strongly recommends Direct Oral Anticoagulants (DOACs) over Vitamin K Antagonists (warfarin) for non-valvular AF, unless contraindicated. DOACs offer comparable or superior efficacy with a significantly lower risk of intracranial haemorrhage.

DOACStandard DoseReduced DoseRenal Monitoring
Apixaban5mg BD2.5mg BD if ≥2: age ≥80, weight ≤60kg, Cr ≥133Annually
Rivaroxaban20mg OD with evening meal15mg OD if CrCl 15–49Annually
Dabigatran150mg BD110mg BD if age ≥80 or high bleeding riskEvery 6–12 months
Edoxaban60mg OD30mg OD if CrCl 15–50, wt ≤60kg, or P-gp inhibitorAnnually
Always verify with current BNF / drug SPC. DOACs are contraindicated in mechanical heart valves and moderate-severe mitral stenosis — use warfarin in these cases.
🚫 Anticoagulation Contraindications
  • Active major bleeding
  • Recent haemorrhagic stroke (<1–3 months)
  • Severe thrombocytopaenia (<50 × 10⁹/L)
  • Severe liver disease / coagulopathy
  • Pregnancy (use LMWH instead)
💊 Use Warfarin NOT DOAC When:
  • Mechanical prosthetic heart valve
  • Moderate-severe rheumatic mitral stenosis
  • CrCl <15 mL/min (DOAC data limited)
  • Antiphospholipid syndrome (triple positive)

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References

  1. Van Gelder IC, Rienstra M, Bunting KV et al. 2024 ESC Guidelines for the management of atrial fibrillation. Eur Heart J. 2024;45(36):3314-3414. doi:10.1093/eurheartj/ehae176
  2. Yoshimura H, Providencia R, Finan C et al. Refining the CHA₂DS₂VASc risk stratification scheme: shall we drop the sex category criterion? Europace. 2024. PMC11574618.
  3. Teppo K, Lip GYH, Airaksinen KEJ et al. Comparing CHA₂DS₂-VA and CHA₂DS₂-VASc scores for stroke risk stratification. Lancet Reg Health Eur. 2024;43:100967.
  4. Lip GYH, Nieuwlaat R, Pisters R et al. Refining clinical risk stratification for predicting stroke and thromboembolism in atrial fibrillation. Chest. 2010;137(2):263-272.
  5. Camm AJ, Kirchhof P, Lip GYH et al. ESC Guidelines for the management of atrial fibrillation. Eur Heart J. 2010;31:2369-2429.
  6. January CT, Wann LS, Calkins H et al. 2019 AHA/ACC/HRS focused update of the 2014 guideline for management of patients with atrial fibrillation. J Am Coll Cardiol. 2019;74(1):104-132.
  7. Lip GYH, Teppo K, Nielsen PB. CHA₂DS₂-VASc or a non-sex score (CHA₂DS₂-VA) for stroke risk prediction in AF. Eur Heart J. 2024;45:3718-20.
  8. NICE guideline NG196. Atrial fibrillation: diagnosis and management. Updated June 2024.

⚠️ Medical Disclaimer: This calculator is for clinical decision support and educational purposes only. Anticoagulation decisions must be made by a qualified clinician taking into account the full clinical picture, individual bleeding risk, patient preferences, and current local guidelines. This tool does not replace clinical assessment.

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