The Cardiovascular
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VTE-BLEED Score

Estimates the risk of major bleeding during stable (extended) anticoagulation after venous thromboembolism.

VTE-BLEED Score
Active cancer
Male with uncontrolled hypertension (systolic BP ≥140 mmHg)
Only applies to male patients; scores 0 in women regardless of blood pressure.
Anaemia (Hb <13 g/dL in men, <12 g/dL in women)
History of major or clinically relevant non-major bleeding
Age ≥60 years
Renal dysfunction (creatinine clearance/eGFR <60 mL/min)
Result0 points

Low risk of major bleeding during stable anticoagulation (derivation cohort incidence approximately 2.8%).

Risk category
Low (<2 points)
Expected major bleeding incidence
~2.8%

When to use

  • Estimating major bleeding risk to help decide on extending anticoagulation beyond the initial 3–6 months after a first VTE.
  • Weighing bleeding risk against recurrence risk once the acute (first 30 days) treatment phase has passed.

Formula

Sum of: active cancer (2 points), male with uncontrolled hypertension i.e. systolic BP ≥140 mmHg (1 point), anaemia i.e. Hb <13 g/dL men or <12 g/dL women (1.5 points), history of major or clinically relevant non-major bleeding (1.5 points), age ≥60 years (1.5 points), renal dysfunction i.e. creatinine clearance/eGFR <60 mL/min (1.5 points). Range 0–9; a threshold of 2 points optimally separates low- from high-risk patients.

Pearls and pitfalls

  • Derived and validated for patients on stable anticoagulation after the first 30 days of treatment following acute VTE, not for the early/acute treatment phase.
  • Derived from the dabigatran arms of the pooled RE-COVER trials using logistic regression; 'male with uncontrolled hypertension' is the only time-varying component.
  • None of its variables overlap with VTE-recurrence prediction scores, which avoids the ambiguity of trading off two scores that share predictors.

References

  1. Klok FA, Hösel V, Clemens A, et al. Prediction of bleeding events in patients with venous thromboembolism on stable anticoagulation treatment. Eur Respir J. 2016;48(5):1369-1376.