DASH Prediction Score for Recurrent VTE

DASH Prediction Score for Recurrent VTE online calculator

Predicts likelihood of recurrence of VTE.

The DASH Score is meant to be applied to stable patients. It should not be applied to patients with active hemorrhage or those with signs and symptoms of VTE.

Many patients diagnosed with VTE are put on long-term or even life-long anticoagulation. The DASH Score predicts which individuals may be low-risk enough to stop anticoagulation after an appropriate 3-6 month period.

D-dimer abnormal
Measured ~1 month after stopping anticoagulation:


Age ≤50 years:

Male patient:

Hormone use at VTE onset (if female)
If male patient, select “No”:


Patient’s score Points Annual Recurrence Rate of VTE Management
0 0 0 0

Addition of the selected points:

CriteriaWeighted Score
D-dimer abnormal+2
Age ≤50 years+1
Sex – Male+1
Hormone use at time of initial VTE (if female)-2

Clinical interpretation:

In a patient with previously diagnosed VTE who has completed a 3-6 month course of anticoagulation if the DASH score is:

PointsAnnual Recurrence Rate of VTEManagement
≤1Low RiskConsider discontinuing anticoagulation, as this group has an annual recurrence risk of 3.1%.
 ≥2High riskConsider continuing anticoagulation, as this group has an annual recurrence risk of 9.3%.    

In patients previously diagnosed with VTE who have completed a 3-6 month course of anticoagulation, DASH Scores ≤1 are associated with 3.1% annual recurrence, which may be low enough to consider discontinuing anticoagulation. Conversely, patients with DASH Scores ≥2 are at high risk for recurrent VTE and may require long-term anticoagulation.

Statistical interpretation:

DASH ScoreAnnual Recurrence Rate

The DASH prediction rule is a risk stratification tool which aids physicians in deciding whether a patient with their first unprovoked venous thromboembolism (VTE) is at risk for recurrence and could aid in deciding how long a patient should be on anticoagulation. Patients were excluded from this study if they had:

  • antiphospholipid antibodies or antithrombin deficiency;
  • Surgery;
  • Trauma;
  • Active cancer;
  •  Immobility;
  •  Pregnancy/peripartum status,

as these were thought to be “provoked” or “secondary” VTE.

The authors of the original study performed a meta-analysis of available individual patient data derived from prospective studies of patients with first VTE who received anticoagulation and followed up over 5 years.

Patients were excluded if they had known VTE risk factors such as surgery, trauma, active cancer, immobility, or pregnancy. Oral contraception use and hormone therapy, or a thrombophilic blood abnormality, were included.

Patients were followed up after anticoagulation was stopped, and documentation was kept for recurrence, death or restarting of anticoagulation.

The final variables included: D-dimer, age ≤50, patient sex, and hormone use at the time of initial VTE. After correction for optimism each was given a score: +2 for abnormal dimer, +1 for age ≤50, +1 for male sex, -2 for hormone use (in females).

In the study cohort the annualized recurrence of VTE was 3.1% for patients with a DASH ≤1 and 9.3% for a DASH >1. The authors concluded that in their cohort up to 51.6% of patients had a DASH ≤1 and could have avoided life-long anticoagulation.

Controversy exists regarding the length of time a patient should be anticoagulated after their first VTE. D-dimer is measured ~1 month after stopping anticoagulation. The cited 5-year recurrence rate of VTE is 25-30%. The recurrence risk of VTE decreases with time. The risk of bleeding complications due to anticoagulation increases with time of use.

The DASH Score has been externally validated; however, recurrence risk in patients >65 years old is still >5% even in patients with low DASH Scores (Tosetto 2017).

Anticoagulation in the original study was limited to vitamin K antagonists, and its use with other drug classes has yet to be established.

No decision rule should trump clinical assessment. Consider the clinical scenario before continuing or discontinuing anticoagulation for VTE.

Tosetto A, Iorio A, Marcucci M, Baglin T, Cushman M, Eichinger S, Palareti G, Poli D, Tait RC, Douketis J. Predicting disease recurrence in patients with previous unprovoked venous thromboembolism: a proposed prediction score (DASH).J Thromb Haemost. 2012 Jun;10(6):1019-25. doi: 10.1111/j.1538-7836.2012.04735.x. https://pubmed.ncbi.nlm.nih.gov/22489957/
Kearon C, Iorio A, Palareti G. Risk of recurrent venous thromboembolism after stopping treatment in cohort studies: recommendation for acceptable rates and standardized reporting. J Thromb Haemost 2010; 8: 2313–5. https://onlinelibrary.wiley.com/doi/full/10.1111/j.1538-7836.2010.03991.x
Tosetto A, Testa S, Martinelli I, et al. External validation of the DASH prediction rule: a retrospective cohort study. J Thromb Haemost. 2017;15(10):1963-1970. https://onlinelibrary.wiley.com/doi/full/10.1111/jth.13781
Kearon C, Kahn SR, Agnelli G, Goldhaber S, Raskob GE, Comerota AJ. Antithrombotic therapy for venous thromboembolic disease: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition). Chest 2008; 133: 454S–545S.

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Charlson Comorbidity Index (CCI) Online Calculator

Charlson Comorbidity Index predicts 10-year survival in patients with multiple comorbidities.


History of definite or probable MI (EKG changes and/or enzyme changes)

Exertional or paroxysmal nocturnal dyspnea and has responded to digitalis, diuretics, or afterload reducing agents

Intermittent claudication or past bypass for chronic arterial insufficiency, history of gangrene or acute arterial insufficiency, or untreated thoracic or abdominal aneurysm (≥6 cm)

History of a cerebrovascular accident with minor or no residua and transient ischemic attacks

Chronic cognitive deficit

Any history of treatment for ulcer disease or history of ulcer bleeding

Severe = cirrhosis and portal hypertension with variceal bleeding history, moderate = cirrhosis and portal hypertension but no variceal bleeding history, mild = chronic hepatitis (or cirrhosis without portal hypertension)

Severe = on dialysis, status post kidney transplant, uremia, moderate = creatinine >3 mg/dL (0.27 mmol/L)

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