Value of plasma fibrin D-dimers for detection of acute aortic dissection

Holger Eggebrecht1, Christoph K Naber, Christian Bruch

  • 1Department of Cardiology, West-German Heart Center Essen, University of Duisburg-Essen, Germany. holger.eggebrecht@uni-essen.de

Insights

Elevated D-dimer levels and white blood cell counts are key indicators for acute aortic dissection (AD). These biomarkers, alongside C-reactive protein, aid in diagnosing AD, distinguishing it from other chest pain causes.

Area of Science:

  • Cardiovascular Medicine
  • Diagnostic Biomarkers
  • Inflammatory Response

Background:

  • Acute aortic dissection (AD) requires rapid diagnosis and treatment.
  • Currently, no specific laboratory test aids in AD diagnosis.
  • Systemic inflammatory biomarkers are being investigated for diagnostic value.

Purpose of the Study:

  • To evaluate the utility of systemic inflammatory biomarkers in detecting acute aortic dissection (AD).
  • To assess the diagnostic value of D-dimers, white blood cell (WBC) count, C-reactive protein (CRP), and fibrinogen in AD.

Main Methods:

  • Compared plasma D-dimers, WBC count, CRP, and fibrinogen in 64 chest-pain patients.
  • Included groups: acute AD, pulmonary embolism (PE), acute myocardial infarction (AMI), and non-cardiac chest pain (CP).
  • Used 32 asymptomatic chronic AD patients as a control group.

Main Results:

  • Acute AD patients exhibited significantly elevated D-dimer levels, comparable to PE patients but higher than other groups.
  • White blood cell (WBC) count was significantly increased in acute AD compared to all other groups.
  • C-reactive protein (CRP) levels were elevated in acute AD, with no significant difference from PE patients. Fibrinogen levels showed no significant group differences.

Conclusions:

  • D-dimer levels are significantly elevated in both acute aortic dissection (AD) and pulmonary embolism (PE).
  • Acute AD is associated with notable systemic inflammatory reactions.
  • Measuring D-dimers can be a valuable adjunct to the diagnostic work-up for suspected AD.
Abstract

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