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Published on: September 9, 2012
[Measurement of d-dimers in non-valvular atrial fibrillation. First prospective Tunisian study]
W El Borgi1, S Romdhane1, W Sdiri2
1Laboratoire d'hématologie biologique, hôpital Aziza Othmana, Tunis, Tunisie.
Insights
D-dimer testing can help identify atrial fibrillation patients with higher clotting risk. Elevated D-dimer levels, above 300 ng/ml, indicate increased thrombo-embolic risk and may complement INR monitoring.
Area of Science:
- Cardiology
- Biomarkers
- Thrombosis
Context:
- Atrial fibrillation (AF) poses a significant risk of thrombo-embolic complications.
- Accurate risk stratification is crucial for effective AF management.
- Existing biomarkers for thrombo-embolic risk in AF require further validation.
Purpose:
- To evaluate the clinical utility of D-dimer testing in assessing thrombo-embolic risk in patients with atrial fibrillation.
- To determine if D-dimer levels correlate with clinical, echocardiographic, or biological data in AF patients.
- To identify a potential D-dimer threshold for distinguishing AF patients with increased risk.
Summary:
- A prospective study of 50 AF cases and 19 controls found significantly higher D-dimer levels in patients (590±506 ng/ml) versus controls (225.26±112.95 ng/ml), P=0.02.
- No significant correlation was observed between D-dimer levels and age, sex, AF type/etiology, CHA2DS2-VASc score, or left atrial size.
- D-dimer levels were higher in patients with an INR < 2 (P=0.004) and a threshold of 300 ng/ml significantly differentiated patients from controls (P<0.001).
Impact:
- D-dimer measurement can aid clinicians in identifying AF patients with heightened coagulability and thrombo-embolic risk.
- D-dimer testing may serve as a valuable adjunct to INR monitoring, refining risk assessment alongside anticoagulation and bleeding risk evaluation.
- This study supports the integration of D-dimer testing into AF management protocols for improved risk stratification.
Abstract:
Atrial fibrillation can expose to thrombo-embolic complications. Many biomarkers have been tested to refine the stratification of thrombo-embolic risk. The study aim was to assess the interest of the d-dimer testing in this pathology. We conducted a prospective observational study including 50 cases and 19 controls, enrolled at the cardiology department of the Mongi Slim Hospital, from July to November 2012. The d-dimer assay was performed on mini-VIDAS(®) and analyzed according to clinical, echocardiographic and biological data. The mean age of patients was 61.8±10.6years. The mean CHA2DS2-VASc score was 2.58±1.31. The average of D-dimer levels was 590±506ng/ml in patients and 225.26±112.95ng/ml in controls (P=0.02). No significant difference has been found between the d-dimer level and age, sex, type and etiology of atrial fibrillation, the CHA2DS2-VASc score, the left atrial surface. Among patients on acenocoumarol, d-dimer levels was significantly higher in patients with an INR<2 compared to those with an INR≥2 (P=0.004). We identified a positive d-dimer threshold (300ng/ml) in patients distinguishing them significantly with controls (P<0.001). In conclusion, the measurement of d-dimers could help clinicians to identify patients with atrial fibrillation having an increased coagulability and, therefore, an increased thrombo-embolic risk. It could be complementary to the determination of INR in monitoring anticoagulation therapy: d-dimers level refines the thrombo-embolic risk and INR measurement assesses the level of anticoagulation and the bleeding risk.
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