Failure of thrombin generation markers to triage patients presenting with chest pain

Marcus E. McKenzie, Anitha Pothula, Paul A. Gurbel, Sergei Y. Fuzaylov, Christopher M. O'Connor, Wendy A. Gattis, Victor L. Serebruany

Research output: Contribution to journalArticlepeer-review

Abstract

Thrombin generation (TG) is an important pathogenic factor in acute coronary syndromes including acute myocard ial infarction (AMI). Since the diagnostic utility of TG remains uncertain we sought to determine whether markers of TG may triage patients presenting to the Emergency Department with chest pain. Soluble plasma levels of prothrombin fragment 1 + 2 (F1+2), and thrombin/antithrombin III complexes (TAT) were determined by ELISA in 80 patients presenting with chest pain to the Emergency Department and compared with 20 controls. There were no differences in TG markers between patients with non-cardiac chest pain and healthy controls. Patients with unstable angina (UA), and congestive heart failure (CHF) did not differ from controls with respect to F1+2, and TAT was elevated in UA patients (6.05 ± 1.15 ng/ml, p = 0.033) when compared with controls (3.34 ± 0.20 ng/ml). Contrary to expectations, TAT levels at presentation with AMI were well below the concentrations observed in patiens with UA and CHF. Moreover, plasma F1+2 levels were significantly lower than in healthy controls (0.84 ± 0.10 ng/ml versus 1.22 ± 0.11, p = 0.026). At the time of presentation to the Emergency Department, F1+2 and TAT failed to suitably triage patients with chest pain. The surprisingly low levels of TG markers in AMI patients before applying intensive therapy and reperfusion strategies deserves further investigation. Copyright (C) 2000 S. Karger AG, Basel.

Original languageEnglish (US)
Pages (from-to)53-58
Number of pages6
JournalCardiology
Volume92
Issue number1
DOIs
StatePublished - Jan 1 1999

Keywords

  • Chest pain
  • ELISA
  • Emergency
  • Medicine
  • Thrombin generation

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Pharmacology (medical)

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