Retrospective Evaluation of Two Fast-track Strategies to Rule Out Acute Coronary Syndrome in a Real-life Chest Pain
Martin Schønemann-Lund1, Mikkel Malby Schoos2, Kasper Iversen3
1Department of Internal Medicine, Hudiksvalls Sjukhus, Hudiksvall, Sweden.
Insights
A new European Society of Cardiology (ESC) guideline protocol for ruling out non-ST-elevation acute coronary syndrome (N-STE ACS) was evaluated. A simpler protocol using undetectable high-sensitivity troponin T (hs-TnT) levels showed similar or superior sensitivity for diagnosing N-STE ACS.
Area of Science:
- Cardiology
- Emergency Medicine
- Diagnostic Testing
Background:
- The European Society of Cardiology (ESC) introduced a new protocol for ruling out non-ST-elevation acute coronary syndrome (N-STE ACS).
- This protocol involves diagnostic levels of high-sensitivity troponin T (hs-TnT).
Purpose of the Study:
- To evaluate a modified ESC rule-out protocol (Protocol 1) using hs-TnT.
- To compare Protocol 1 with a simpler approach (Protocol 2) using undetectable hs-TnT levels for ruling out patients.
- To assess diagnostic accuracy, re-admission rates, and mortality.
Main Methods:
- 534 patients with suspected ACS were included.
- Protocol 1: symptom duration, hs-TnT at 0 and 6-9h, GRACE score, symptom status at 6-9h.
- Protocol 2: single hs-TnT blood sample.
Main Results:
- Protocol 1 ruled out 27.9% of patients, with 87.3% sensitivity and 87.6% negative predictive value for ACS.
- Protocol 2 ruled out 17.5% of patients, achieving 94.1% sensitivity and 90.8% negative predictive value.
- Both protocols demonstrated effectiveness in identifying patients with adverse outcomes.
Conclusions:
- The modified ESC rule-out protocol (Protocol 1) is diagnostically valuable for N-STE ACS.
- A simpler protocol (Protocol 2) using undetectable hs-TnT levels may offer similar or superior sensitivity.
- Further validation of Protocol 2 is suggested for efficient N-STE ACS rule-out.
Background:
The European Society of Cardiology (ESC) guideline on non-ST-elevation acute coronary syndrome (N-STE ACS) proposed a new ACS rule-out protocol.
Objectives:
To evaluate this new tool, which uses diagnostic levels of high-sensitivity troponin T (hs-TnT; > 14 ng/L) in a slightly modified version and compare this to a recently proposed approach using undetectable levels of hs-TnT to rule out patients.
Methods:
There were 534 consecutive patients with suspected ACS included. Protocol 1: symptom duration, hs-TnT at 0 and 6-9 h, Global Registry of Acute Coronary Events (GRACE) score, and symptom status at 6-9 h. Protocol 2: a single blood sample of hs-TnT. The primary endpoint was a discharge diagnosis of ACS by blinded adjudication. Secondary endpoints were ACS re-admission < 30 days and 1-year mortality.
Results:
Protocol 1 classified 434/534 (81%) patients, with 27.9% being ruled out. All myocardial infarctions were correctly ruled in, but 15 cases of unstable angina were missed, resulting in a sensitivity and negative predictive value of 87.3% (79.6-92.5%) and 87.6% (80.4-92.9%), respectively. Protocol 2 ruled out 17.5% of the population, yielding a sensitivity and negative predictive value of 94.1% (88.2-97.6%) and 90.8% (81.9-96.2%), respectively. Both protocols correctly ruled in 2/3 patients with ACS re-admission < 30 days and 55/56 1-year fatalities.
Conclusion:
The present study confirms the diagnostic value of a modified version of the ESC rule-out protocol (Protocol 1) in N-STE ACS patients, but also suggests that a simpler protocol using undetectable levels of hs-TnT (Protocol 2) could provide a similar or even superior sensitivity.
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