The Journal of Emergency Medicine
Volume 41, Issue 5 , Pages 524-530, November 2011

The Value of Procalcitonin, a Novel Inflammatory Marker, in the Diagnosis of Myocardial Infarction and Evaluation of Acute Coronary Syndrome Patients

  • Firat Bektas, MD

      Affiliations

    • Department of Emergency Medicine, Akdeniz University Faculty of Medicine, Antalya, Turkey
    • Corresponding Author InformationReprint Address: Firat Bektas, md, Department of Emergency Medicine, Akdeniz University Faculty of Medicine, Antalya 07059, Turkey
  • ,
  • Secgin Soyuncu, MD

      Affiliations

    • Department of Emergency Medicine, Akdeniz University Faculty of Medicine, Antalya, Turkey
  • ,
  • Ilker Gunduz, MD

      Affiliations

    • Department of Emergency Medicine, Akdeniz University Faculty of Medicine, Antalya, Turkey
  • ,
  • Ibrahim Basarici, MD

      Affiliations

    • Department of Cardiology, Akdeniz University Faculty of Medicine, Antalya, Turkey
  • ,
  • Halide Akbas, MD

      Affiliations

    • Department of Biochemistry, Akdeniz University Faculty of Medicine, Antalya, Turkey
  • ,
  • Cenker Eken, MD

      Affiliations

    • Department of Emergency Medicine, Akdeniz University Faculty of Medicine, Antalya, Turkey

Received 4 December 2009; received in revised form 22 February 2010; accepted 19 May 2010. published online 03 September 2010.

Abstract 

Background

Procalcitonin is a calcitonin precursor that is used as an inflammatory biomarker in the plasma of patients with sepsis.

Objective

The aim of this study was to determine the diagnostic accuracy of emergency department (ED) point-of-care blood procalcitonin testing in identifying myocardial infarction (MI) in patients with chest pain of presumed ischemic origin.

Methods

Patients over 18 years of age who presented to the ED with MI-typical chest pain of presumed ischemic origin were included in the study. An initial point-of-care blood sample was drawn from each study patient for testing procalcitonin, troponin T, myoglobin, and creatine kinase-MB levels. A second sample was taken 4h after admission for a procalcitonin test. Finally, a 6-h post-admission blood sample was taken to measure troponin T, myoglobin, and creatine kinase-MB levels in each study patient who had an initial negative cardiac marker test.

Results

A total of 1008 patients with chest pain were admitted to the ED during the study period, and a total of 141 patients met study criteria and were entered into the study. ED point-of-care blood procalcitonin testing to identify myocardial infarction in patients with chest pain of presumed ischemic origin had a sensitivity of 38.3% (95% confidence interval [CI] 28.8–47.3%) and a specificity of 77.8% (95% CI 70.0–84.4%), a positive likelihood ratio (LR+) of 1.725 and a negative likelihood ratio (LR−) of 0.792. The 4th hour diagnostic values (sensitivity, specificity, LR+ and LR−) of procalcitonin semi-quantitative (PCT-Q) testing were 90% (95% CI 80.9−95.7%), 59.3% (95% CI 52.5−63.5%), 2.2, and 0.16, respectively.

Conclusion

ED point-of-care testing for procalcitonin had poor diagnostic accuracy for predicting myocardial infarction.

Keywords: procalcitonin, myocardial infarction, acute coronary syndrome, emergency, point-of-care testing

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 This study was supported by Akdeniz University Research Foundation.

PII: S0736-4679(10)00522-6

doi:10.1016/j.jemermed.2010.05.073

The Journal of Emergency Medicine
Volume 41, Issue 5 , Pages 524-530, November 2011