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The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
Difference in left atrial D-dimer level in patients with atrial fibrillation treated with direct oral anticoagulant
Tetsuya Watanabe1, Koichi Tachibana2, Yukinori Shinoda2
1Division of Cardiology, Osaka General Medical Center, 3-1-56 Bandai-Higashi, Sumiyoshi-ku, Osaka, 558-8558, Japan. t.watanabe252@gmail.com.
Insights
Apixaban showed a better anticoagulant effect in the left atrium than edoxaban in atrial fibrillation (AF) patients. This study compared D-dimer levels in AF patients on different anticoagulants before ablation.
Area of Science:
- Cardiology
- Hematology
- Pharmacology
Background:
- Atrial fibrillation (AF) increases the risk of embolism.
- Elevated D-dimer levels indicate hyperactive fibrinolysis and thrombosis risk.
- Understanding differential anticoagulant effects is crucial for managing AF patients.
Purpose of the Study:
- To compare D-dimer levels in peripheral and left atrial (LA) blood of AF patients undergoing ablation.
- To evaluate the differential effects of anticoagulation therapies (dabigatran, apixaban, edoxaban) on D-dimer levels.
Main Methods:
- Analysis of 141 non-valvular AF patients (dabigatran, apixaban, edoxaban).
- Collection of peripheral venous and LA blood samples before pulmonary vein isolation.
- Examination of laboratory and echocardiographic parameters.
Main Results:
- LA D-dimer levels were significantly higher in edoxaban-treated patients compared to apixaban-treated patients (P=0.047).
- No significant differences in peripheral D-dimer levels were observed.
- Peripheral prothrombin fragment F1+2 and LVEF were predictors of high LA D-dimer levels.
Conclusions:
- Apixaban demonstrated a superior anticoagulant effect in the left atrium compared to edoxaban in AF patients.
- LA D-dimer levels were lower in apixaban-treated patients on the day of ablation.
Background:
Atrial fibrillation (AF) may cause cerebral and systemic embolism. An increased D-dimer level indicates hyperactivation of secondary fibrinolysis, resulting in predilection for thrombosis. To clarify the differential effects of anticoagulation therapy, we compared the D-dimer levels in peripheral and left atrial (LA) blood of atrial fibrillation patients scheduled for ablation.
Methods:
We analyzed 141 patients with non-valvular AF (dabigatran, n = 30; apixaban, n = 47; edoxaban, n = 64; mean age: 68 years, male: 60%). Peripheral venous blood and LA blood was collected before pulmonary vein isolation. We examined the laboratory and echocardiographic parameters.
Results:
After adjusting for baseline characteristics, D-dimer level in the LA was significantly higher in patients treated with edoxaban than that in those on apixaban (0.77 ± 0.05 vs. 0.60 ± 0.05 μg/mL, P = 0.047), although there were no significant differences in peripheral D-dimer levels. We classified the D-dimer value of the LA into a normal group (< 0.9) and a high value group (≥ 1.0); the peripheral prothrombin fragment F1 + 2 level (odds ratio [OR] 1.012; 95% confidence interval [CI]: 1.003-1.022; P = 0.008) and left ventricular ejection fraction (LVEF) (OR, 0.947; 95% CI, 0.910-0.986; P = 0.008) were potential predictors of high LA D-dimer levels.
Conclusions:
In apixaban-treated patients, the D-dimer level in the left atrium was lower than in edoxaban-treated patients on the day of ablation, suggesting that the anticoagulant effect of apixaban on the left atrium is better than that of edoxaban in patients with AF.
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