Troponin I as a specific marker of myocardial injury: from theory to clinical practice in the diagnosis of acute coronary syndrome

Objective To assess the diagnostic accuracy of troponin I (Tril) elevation in patients with acute coronary syndrome (ACS) in the emergency department (ED). Methods We retrospectively studied 166 patients with elevated Tril and electrocardiographic (ECG) change consistent with non-ST-segment elevation myocardial infarction. They were transferred from the ED to our coronary care unit (CCU) to undergo coronary angiography. Results Significant coronary stenosis were identified in 101 (61%) of patients. The other 65 patients were found to have different cardiac diseases (n = 52) and in 13 patients diagnoses were not even related to the cardiovascular system. Wall motion abnormalities were assessed by echocardiographic wall motion score index (WMSI). Positive predictive value (PPV) of Tril varied from 53 to 65% for higher progressive values of the biomarker. The following PPVs were then calculated: PPV(Tnl + CK-MB) = 64%; PPV(Tnl + WMSI) = 72%, PPV(Tnl + CK-MB + WMSI) = 74%. Conclusions Abnormal values of Trill were detected in a variety of diseases not related to ACS. Even if troponin release indicates myocardial injury, it is not always synonymous with infarction or ischemia. A misinterpretation of Tril elevation may give rise to a diagnostic dilemma and cause unnecessary morbidity. An integration of biomarkers (Tril and CK-MB), ECG and WMSI will help identify false-positive ACS patients and avoid inappropriate admissions to CCU. (C) 2004 Lippincott Williams Wilkins.