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Can patients at elevated risk of stroke treated with anticoagulants be further risk stratified?
Lawrence Baruch1, Brian F Gage, Jay Horrow
1Bronx VA Hospital, Bronx, NY 10468, USA. baruchlarry@att.net
Insights
Stroke risk in atrial fibrillation patients varies. The CHADS(2), SPAF, and Framingham schemes accurately predicted ischemic stroke in patients on anticoagulant therapy, aiding in identifying high-risk individuals.
Area of Science:
- Cardiology
- Neurology
- Clinical Trials
Background:
- Atrial fibrillation (AF) patients exhibit diverse stroke risks influenced by age and comorbidities.
- Accurate stroke risk stratification is crucial for effective prevention in AF patients.
Purpose of the Study:
- To evaluate the predictive performance of established stroke risk classification schemes in AF patients.
- To identify AF patients at significant stroke risk despite optimal anticoagulant treatment.
Main Methods:
- Compared seven stroke risk schemes: ACCP 2001, ACCP 2004, SPAF, AF Investigators, Framingham, van Walraven, and CHADS(2).
- Utilized data from 7329 AF patients in the SPORTIF III and V trials, treated with warfarin or ximelagatran.
- Primary outcome was ischemic stroke, adjudicated centrally.
Main Results:
- Over 11,245 patient-years, 159 ischemic strokes occurred (1.4%/year).
- Framingham (c=0.64), CHADS(2) (c=0.65), and SPAF (c=0.61) demonstrated significant stroke prediction.
- These three schemes outperformed chance in predicting ischemic stroke.
Conclusions:
- CHADS(2), SPAF, and Framingham schemes showed superior predictive accuracy for ischemic stroke in AF patients on anticoagulants.
- These validated schemes can help clinicians identify high-risk individuals for targeted interventions.
- Improved risk stratification may enhance stroke prevention strategies in atrial fibrillation.
Background And Purpose:
Patients with atrial fibrillation have a varied risk of stroke, depending on age and comorbid conditions. The objective of this study was to assess the predictive value of stroke risk classification schemes and to identify patients with atrial fibrillation who are at substantial risk of stroke despite optimal anticoagulant therapy.
Methods:
Seven recognized classification schemes-the American College of Chest Physicians 2001, American College of Chest Physicians 2004, Stroke Prevention in Atrial Fibrillation (SPAF), Atrial Fibrillation Investigators, Framingham, van Walraven, and CHADS(2)-were compared for their ability to predict ischemic stroke in patients receiving anticoagulant therapy. Data came from the Stroke Prevention using an ORal Thrombin Inhibitor in atrial Fibrillation III and V trials, which compared the efficacy of adjusted-dose warfarin and the direct thrombin inhibitor ximelagatran (36 mg twice daily) in preventing thromboembolic events in 7329 patients with chronic or paroxysmal nonvalvular atrial fibrillation who were at moderate or high risk of ischemic stroke. The main outcome measure was ischemic stroke, as determined by a central event adjudication committee.
Results:
During 11 245 patient-years of follow-up, 159 patients had an ischemic stroke (1.4%/year). As indicated by c statistics and hazard ratios, 3 of the classification schemes predicted stroke significantly better than chance: Framingham (c=0.64), CHADS(2) (c=0.65), and SPAF (c=0.61).
Conclusions:
In a large cohort of atrial fibrillation patients at moderate or high risk of ischemic stroke treated with warfarin or ximelagatran, the CHADS(2), SPAF, and Framingham schemes had greater predictive accuracy than chance. This predictive ability may allow clinicians to target high-risk patients for more aggressive intervention.
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