THE VALUE OF PROCALCITONIN, A NOVEL INFLAMMATORY MARKER, IN THE DIAGNOSIS OF MYOCARDIAL INFARCTION AND EVALUATION OF ACUTE CORONARY SYNDROME PATIENTS

被引:10
作者
Bektas, Firat [1 ]
Soyuncu, Secgin [1 ]
Gunduz, Ilker [1 ]
Basarici, Ibrahim [2 ]
Akbas, Halide [3 ]
Eken, Cenker [1 ]
机构
[1] Akdeniz Univ, Fac Med, Dept Emergency Med, TR-07059 Antalya, Turkey
[2] Akdeniz Univ, Fac Med, Dept Cardiol, TR-07059 Antalya, Turkey
[3] Akdeniz Univ, Fac Med, Dept Biochem, TR-07059 Antalya, Turkey
关键词
procalcitonin; myocardial infarction; acute coronary syndrome; emergency; point-of-care testing; C-REACTIVE PROTEIN; CARDIOVASCULAR-DISEASE; SERUM PROCALCITONIN; ACUTE-PANCREATITIS; RISK-ASSESSMENT; METAANALYSIS; PREVENTION; GUIDELINES; MANAGEMENT; PROGNOSIS;
D O I
10.1016/j.jemermed.2010.05.073
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
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 4 h 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. (C) 2011 Elsevier Inc.
引用
收藏
页码:524 / 530
页数:7
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