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Pearson
Acute coronary syndrome (ACS, formerly called ischemic heart disease) refers to a large spectrum of clinical conditions including unstable angina, myocardial injury, and myocardial infarction (MI). ACS is caused by a sudden onset of cardiac tissue ischemia secondary to impaired blood flow. The precipitating event is blockage in the coronary arteries or a mismatch between the demand and supply of blood to cardiac tissue. The resulting tissue ischemia can cause changes on an electrocardiogram (ECG), as well as symptoms such as substernal chest pressure and radiation of pain to the left arm, shoulder, or jaw. Patients who present with symptoms of ACS, including chest pain, should be immediately evaluated. The recommended evaluation includes a clinical assessment, ECG, and laboratory testing. Laboratory testing for ACS includes diagnostic testing for markers of damage to heart tissue such as cardiac troponins (cTns), as well as prognostic testing (eg, B-type natriuretic peptide).
Quick Answers for Clinicians
Although cardiac troponin (cTn) I (cTnI) is more specific to myocardial injury than is cardiac troponin T (cTnT), serial measurements of either cTnI or cTnT can be used in the evaluation of acute coronary syndrome (ACS). Compared with conventional cTn assays, high-sensitivity cTn (hs-cTn) testing can detect elevated levels sooner after symptom onset, which allows for more frequent measurements and increases the likelihood of detecting a rising/falling pattern. It is important to use the same test when performing serial measurements and to ensure the use of the appropriate upper reference limit for the particular test being used.
Cardiac troponin (cTn) testing is best performed as close to patients as possible in cases of suspected acute coronary syndrome (ACS); however, point-of-care (POC) tests are not currently preferred over automated assays due to the limited availability of high-sensitivity POC tests. As the use of high-sensitivity POC assays is an emerging area of testing, guidance is likely to be reevaluated when more of these assays have been validated.
Indications for Testing
Laboratory testing for ACS is used to:
- Screen and assess risk for future ACS in adults
- Diagnose ACS in patients with signs, symptoms, and clinical findings consistent with ACS
- Determine prognosis in patients diagnosed with or being evaluated for ACS ,
Laboratory Testing
Diagnosis
Cardiac troponin I and T (cTnI and cTnT, respectively) are the preferred biomarkers for the evaluation of myocardial injury and MI , , ; high-sensitivity cTn (hs-cTn) assays are recommended if available. cTn levels are generally elevated within 2-4 hours of symptom onset but may not become abnormal for up to 12 hours. cTn elevations may persist for >14 days. Although cTns are generally only released in response to cardiac injury, recent evidence suggests that cTnT may be detected in response to skeletal muscle injury. A variety of cardiac conditions besides MI can produce elevated cTns. Therefore, serial measurements that demonstrate a rise or fall in cTn levels are required to distinguish between myocardial injury and MI. Current guidelines recommend a first cTn test on presentation with chest pain, and a second test 3-6 hours later (or sooner if using hs-cTn). Patients who present very early or very late after symptom onset may require additional testing to detect an increase or decrease in cTn values.
Prognosis
The presence and magnitude of cTn elevations at presentation are useful for prognosis of short- and long-term mortality in ACS. In addition to measurements at presentation, it may be reasonable to remeasure troponin on day 3 or 4 in patients with MI to assess infarct size and the dynamics of necrosis. Several additional biomarkers, including natriuretic peptides, have also been associated with mortality and comorbidities that confer added risk of mortality (such as heart failure) in ACS.
Risk Assessment for Future Events
Multiple organizations recommend laboratory testing, such as high-sensitivity C-reactive protein (hsCRP) screening, to guide risk assessment for and implementation of preventive measures against future ACS. , Refer to the Atherosclerotic Cardiovascular Disease Risk Markers topic for information on ACS screening and risk assessment.
ARUP Laboratory Tests
Quantitative Immunoturbidimetry
Electrochemiluminescent Immunoassay (ECLIA)
Quantitative Chemiluminescent Immunoassay
Quantitative Electrochemiluminescent Immunoassay
Quantitative Chemiluminescent Immunoassay
Chemiluminescent Immunoassay/Quantitative Enzymatic Assay
Quantitative Electrochemiluminescent Immunoassay
References
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Amsterdam EA, Wenger NK, Brindis RG, et al. 2014 AHA/ACC guideline for the management of patients with non-ST-elevation acute coronary syndromes: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2014;64(24):e139-e228.
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