Predict 1-year major bleeding risk in atrial fibrillation patients on oral anticoagulation. Always paired with CHA₂DS₂-VASc to balance stroke vs bleeding risk.
HAS-BLED Score
0/9
Estimated 1-year major bleeding risk: 0.9%
Recommendation
Low bleeding risk. Anticoagulation is safe — proceed if CHA₂DS₂-VASc indicates it. Re-evaluate score annually.
EasyClinic surfaces patient BP trends, prescribed NSAIDs/antiplatelets, and INR control history right next to the HAS-BLED score — so you never miss a fixable risk factor.
The HAS-BLED score is the most widely validated tool to estimate 1-year risk of major bleeding in atrial fibrillation patients on oral anticoagulation. It was derived from the Euro Heart Survey (Pisters 2010) and is endorsed by ESC, AHA/ACC and CSI guidelines.
The score ranges 0–9. A score ≥3 indicates "high bleeding risk" — but critically, this is a signal to address modifiable bleeding factors and increase monitoring, NOT to withhold anticoagulation.
The real value of HAS-BLED is identifying modifiable factors to fix:
If only non-modifiable factors are present, do not withhold anticoagulation — net clinical benefit usually still favours OAC.
No. Net clinical benefit still favours OAC in nearly every such case. Address modifiable factors (BP, NSAIDs, alcohol, INR control), prefer a DOAC over warfarin, and document the risk-benefit discussion with the patient.
Apixaban (Eliquis, Apixaban-various generics) has the most favourable bleeding profile in head-to-head trials, particularly for major and intracranial bleeding. Dabigatran (Pradaxa) has higher GI bleeding risk. Rivaroxaban (Xarelto) is in between. All have lower ICH risk than warfarin.
Use the Rosendaal linear interpolation method — most lab/EMR systems automate this. A TTR < 60% over the prior 6 months scores 1 point. If unavailable, ≥ 2 INRs out of range in the past 6 months is a reasonable surrogate.
No. After the source is identified and treated (e.g., H. pylori eradication, endoscopic clipping, PPI), restart OAC — preferably apixaban — typically within 7–14 days. Indefinite OAC avoidance carries higher mortality than restart.
It was validated on warfarin cohorts but is widely applied to DOAC patients as a general bleeding risk signal. The Labile INR criterion does not apply to DOACs — but uncontrolled BP, NSAIDs, alcohol, and renal function are equally relevant.
EasyClinic auto-runs CHA₂DS₂-VASc and HAS-BLED on every AF patient, flags modifiable bleeding factors like uncontrolled BP and NSAID co-prescription, and tracks TTR for warfarin patients.
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