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.

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