Diagnosis and risk stratification of patients with anginal pain and non-diagnostic electrocardiograms
1Regional Medical Cardiology Centre, Royal Victoria Hospital, Belfast, UK.
Insights
Cardiac troponins, particularly troponin I (cTnI) at 12 hours, are highly sensitive for diagnosing acute coronary syndromes in patients with chest pain and normal ECGs. Elevated cTnI independently predicts a higher risk of future cardiac events within three months.
Area of Science:
- Cardiology
- Biochemistry
- Emergency Medicine
Background:
- Patients with acute chest pain and normal or non-diagnostic ECGs present diagnostic challenges.
- Early risk stratification is crucial for this subgroup to prevent adverse cardiac events.
Purpose of the Study:
- To evaluate the diagnostic and risk stratification roles of cardiac troponin T (cTnT), troponin I (cTnI), CKMB mass, and myoglobin.
- To assess these markers in patients with acute chest pain suggestive of myocardial ischemia but with non-diagnostic ECGs.
Main Methods:
- Prospective study of 214 patients with acute chest pain and normal/non-diagnostic ECGs.
- Blood samples analyzed for cTnT, cTnI, CKMB mass, and myoglobin at admission and 12 hours.
- 3-month follow-up for cardiac events including death, myocardial infarction, revascularization, and unstable angina.
Main Results:
- At 12 hours, cardiac troponins showed higher sensitivity for acute coronary syndromes than conventional markers (cTnI 48%, cTnT 38%).
- Elevated cTnI at 12 hours was the most statistically significant predictor of future cardiac events (p < 0.0001).
- cTnI at 12 hours and stress test response were independent predictors of 3-month cardiac events.
Conclusions:
- Cardiac troponins, especially cTnI at 12 hours, are superior for diagnosing acute coronary syndromes in this patient group.
- Elevated cTnI at 12 hours is independently associated with an increased risk of future cardiac events within 3 months.
Abstract:
Patients with acute chest pain suggestive of myocardial ischaemia, and normal or non-diagnostic electrocardiograms, form a difficult subgroup for diagnosis and early risk stratification. We prospectively evaluated the role of troponin T (cTnT), troponin I (cTnI), CKMB mass and myoglobin, in the diagnosis and risk stratification of 214 patients with acute chest pain of < or = 24 h and non-diagnostic or normal ECGs admitted directly to the Cardiac Unit of the Royal Victoria Hospital Belfast from the Mobile Coronary Care Unit or the Accident/Emergency Department. This was a single-centre prospective study, and follow-up (3 months) was complete for all patients. Blood was assessed for quantitative cTnT, cTnI, CKMB mass and myoglobin, and qualitative cTnT on admission and at 12 h. Diagnosis of index event and incidence of new cardiac events (death, non-fatal myocardial infarction, revascularization, or readmission for unstable angina) over 3 months were assessed. Based on standard criteria, myocardial infarction occurred in 37/214 (17%), and unstable angina in 72/214 (34%). At 12 h from admission, cardiac troponins had higher sensitivity for the diagnosis of acute coronary syndromes (myocardial infarction and unstable angina) than conventional markers (cTnI 48%, cTnT 38%, CKMB mass 30% or myoglobin 27%). At 3 months, a new cardiac event had occurred in 42/214 (20%). Significantly higher event rates occurred when any of the biochemical markers was elevated, but the statistical significance was highest for patients with elevated cTnI (p < 0.0001). Whilst gender, history of ischaemic heart disease (IHD), stress test response, cTnT, cTnI, CKMB mass and myoglobin were univariate predictors, cTnI at 12 h and stress test response were the only two independent significant predictors for a subsequent cardiac event at 3 months. Raised cTnI at 12 h after admission had the highest sensitivity for the diagnosis of acute coronary syndromes, and was independently associated with a 2-3 times increased risk of future cardiac events within 3 months among patients with acute chest pain suggestive of myocardial ischaemia but with normal or non-diagnostic ECGs.
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