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Assessment of Coagulation and Hemostasis Biomarkers in a Subset of Patients With Chronic Cardiovascular Disease
Maureen J Miller1, Cheryl L Maier1, Alexander Duncan1
1Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Insights
A comprehensive coagulation panel is crucial for understanding hemostasis in cardiovascular disease. Prothrombin fragment 1.2 (PF1.2) elevations suggest thrombin generation in cardiomyopathy, while D-dimers in heart assist device patients may indicate device presence.
Area of Science:
- Cardiovascular Medicine
- Hematology
- Clinical Diagnostics
Background:
- Single coagulation markers may not fully represent hemostasis and fibrinolysis in chronic cardiovascular diseases.
- Patients with cardiovascular conditions often present complex hemostatic profiles.
Purpose of the Study:
- To evaluate the utility of a comprehensive coagulation panel in patients with cardiovascular diseases.
- To differentiate hemostatic activation patterns in patients with heart assist devices versus cardiomyopathies.
Main Methods:
- Retrospective analysis of coagulation panels including prothrombin fragment 1.2 (PF1.2), thrombin: antithrombin complexes, fibrin monomers, and D-dimers.
- Patient cohort included individuals with heart assist devices, cardiomyopathies, atrial fibrillation, and intracardiac thrombosis.
- Statistical comparison of marker elevations between patient groups.
Main Results:
- PF1.2 was significantly more elevated in cardiomyopathy patients (61.1%) compared to those with cardiac assist devices (15.7%).
- D-dimer elevation was more frequent in cardiac assist device patients (98.8%) versus cardiomyopathy patients (83.3%).
- Elevated D-dimers without other marker increases in cardiac assist device patients likely reflect the device itself.
Conclusions:
- Comprehensive coagulation panels provide a more complete picture of hemostasis than single markers in cardiovascular disease.
- Cardiomyopathy is associated with increased thrombin generation (indicated by PF1.2), while cardiac assist devices may lead to elevated D-dimers independent of significant hemostatic activation.
Abstract:
Measurement of a single marker of coagulation may not provide a complete picture of hemostasis activation and fibrinolysis in patients with chronic cardiovascular diseases. We assessed retrospective orders of a panel which included prothrombin fragment 1.2 (PF1.2), thrombin: antithrombin complexes, fibrin monomers, and D-dimers in patients with heart assist devices, cardiomyopathies, atrial fibrillation and intracardiac thrombosis (based on ordering ICD-10 codes). During 1 year there were 117 panels from 81 patients. Fifty-six (69%) patients had heart assist devices, cardiomyopathy was present in 17 patients (21%) and 29 patients (36%) had more than 1 condition. PF1.2 was most frequently elevated in patients with cardiomyopathy (61.1%) compared to those with cardiac assist devices (15.7%; P = 0.0002). D-dimer elevation was more frequent in patients with cardiac assist devices (98.8%) compared to those patients with cardiomyopathy (83.3%; P = 0.014). Patients with cardiomyopathy show increases of PF1.2 suggesting thrombin generation. In contrast, elevations of D-dimers without increase in other coagulation markers in patients with cardiac assist devices likely reflect the presence of the intravascular device and not necessarily evidence of hemostatic activation.
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