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The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
D-dimer and fibrinogen indicate ischemic risk in patients with atrial fibrillation after percutaneous coronary
Diona Gjermeni1, Viktoria Anfang1, Sofia Szabó1
1Department of Cardiology and Angiology, University Heart Center Freiburg-Bad Krozingen, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Insights
Antiphospholipid antibodies (aPL) did not correlate with ischemic or bleeding risks in atrial fibrillation (AF) patients post-percutaneous coronary intervention (PCI). Elevated d-dimer and fibrinogen levels, however, significantly predicted adverse cardiovascular events and bleeding risk.
Area of Science:
- Cardiology
- Hematology
- Thrombosis Research
Background:
- Atrial fibrillation (AF) patients undergoing percutaneous coronary intervention (PCI) face risks of ischemic events and bleeding.
- Antiphospholipid antibodies (aPL) are implicated in thrombotic events, but their role in AF patients post-PCI is unclear.
- Conventional coagulation markers may offer insights into these risks.
Purpose of the Study:
- To investigate the association between antiphospholipid antibodies (aPL) and coagulation markers with ischemic and bleeding risks.
- To evaluate the predictive value of these markers in AF patients after PCI.
Main Methods:
- Prospective, two-center observational cohort study of 158 AF patients post-PCI.
- Assessed lupus anticoagulant (LA), anti-cardiolipin (aCL), and anti-β2-Glycoprotein 1 (aβ2GP1) antibodies.
- Measured fibrinogen (FIB), d-dimer, and prothrombin fragment 1+2 (PF1+2) levels.
- Primary outcomes: major adverse cardiovascular events (MACE) and major bleeding at 6 months.
Main Results:
- aPL presence was not significantly associated with MACE or bleeding.
- Elevated d-dimer strongly predicted higher risk for MACE (HR 5.06) and major bleeding (HR 7.04).
- Elevated d-dimer improved the predictive capacity of the HAS-BLED score for major bleeding (AUC 0.79).
- Increased FIB levels were linked to a higher MACE risk (HR 3.65).
Conclusions:
- Antiphospholipid antibodies (aPL) do not appear to be significant risk factors for ischemic or bleeding events in AF patients post-PCI.
- Coagulation biomarkers, particularly d-dimer and fibrinogen, show promise in assessing thrombotic and bleeding risks in this patient population.
- These findings suggest that conventional coagulation markers may be more clinically relevant than aPL for risk stratification in AF patients undergoing PCI.
Background:
This study aimed to evaluate the association of antiphospholipid antibodies (aPL) and conventional markers of coagulation with ischemic and bleeding risk in patients with atrial fibrillation (AF) undergoing percutaneous coronary intervention (PCI).
Methods:
In this prospective two-center observational cohort study, patients with AF and an indication for oral anticoagulation (OAC) were enrolled after PCI. Blood was drawn on day 1-3 after PCI. Dilute Russell's viper venom time was used to determine lupus anticoagulant (LA) in OAC-free plasma. Anti-cardiolipin (aCL) IgG, IgM, and anti-β2-Glycoprotein 1 (aβ2GP1) IgG were analyzed by enzyme-linked immunosorbent assay (ELISA). Fibrinogen (FIB), d-dimer, and prothrombin fragment 1 and 2 (PF 1 + 2) were measured in citrated plasma. The primary ischemic outcome was time to major adverse cardiovascular events (MACE; death, myocardial infarction, or stroke) assessed at 6 months. Bleeding was defined according to International Society on Thrombosis and Haemostasis.
Results:
158 patients were enrolled between May 2020 and May 2021 on day 1-3 after PCI. The median age was 78 years (interquartile range [IQR] 72-82), 111 (70%) were male, and 39 (25%) presented with acute coronary syndrome. D-dimer was elevated in 74 (47%) patients, FIB was increased in 40 (25%) and PF1 + 2 in 68 (43%) patients. 32 (20%) patients had ≥ 1 antiphospholipid antibody elevated (aPL; LA: 19 [12%], aCL: 14 [9%], aβ2GP1: 2 [1%]). The presence of aPL was neither significantly associated with MACE (HR 1.46, 95% CI [0.39-5.49], p = 0.579), nor bleeding (HR 1.07 [0.30-3.84], p = 0.917). Elevated d-dimer was significantly associated with higher risk for MACE (HR 5.06 [1.09-23.41], p = 0.038) and major bleeding (HR 7.04 [1.58-31.47], p = 0.011). Elevated D-dimer increased the predictive capacity of HAS-BLED for major bleedings (HAS-BLED: AUC 0.71 [0.60-0.83] vs. HAS-BLED + d-dimer: AUC 0.79 [0.70-0.88]; p = 0.025). Increased levels of FIB were associated with higher risk for MACE (HR 3.65 [1.11-11.96], p = 0.033).
Conclusion:
Biomarkers of coagulation might be suitable to assess ischemic and bleeding risk in patients with AF following PCI.
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