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Single High-Sensitivity Cardiac Troponin I to Rule Out Acute Myocardial Infarction
Yader Sandoval1, Stephen W Smith2, Sara A Love3
1Division of Cardiology, Hennepin County Medical Center and Minneapolis Heart Institute, Abbott Northwestern Hospital, Minn.
Insights
Single high-sensitivity cardiac troponin I (hs-cTnI) measurements effectively rule out acute myocardial infarction. These strategies identify patients with a very low risk of adverse events within 30 days.
Area of Science:
- Cardiology
- Biomarkers
- Emergency Medicine
Background:
- Acute myocardial infarction (AMI) diagnosis relies on sensitive biomarkers.
- High-sensitivity cardiac troponin I (hs-cTnI) assays offer improved diagnostic performance.
- Evaluating single hs-cTnI measurement strategies is crucial for efficient emergency department workflows.
Purpose of the Study:
- To assess the performance of single hs-cTnI measurement strategies for ruling out AMI.
- To determine the negative predictive value (NPV) and sensitivity of hs-cTnI for Type 1 and Type 2 AMI.
- To evaluate the safety outcome (AMI or cardiac death at 30 days) associated with hs-cTnI thresholds.
Main Methods:
- Prospective, observational study of 1631 emergency department patients.
- Utilized an investigational hs-cTnI assay for serial measurements.
- Analyzed hs-cTnI levels below the limit of detection (<1.9 ng/L) and a 5 ng/L threshold, with and without normal ECG.
Main Results:
- hs-cTnI < Limit of Detection (LoD) showed 99.6% NPV and 98.8% sensitivity for AMI.
- hs-cTnI < 5 ng/L demonstrated 98.9% NPV and 94.7% sensitivity for AMI.
- Combining hs-cTnI thresholds with normal ECG yielded high NPV and sensitivity for both AMI and safety outcomes.
Conclusions:
- Single hs-cTnI measurements, alone or with normal ECG, can rapidly identify low-risk patients for AMI.
- These strategies facilitate early identification of patients unlikely to experience adverse cardiac events.
- The findings support the use of hs-cTnI in streamlined protocols for ruling out AMI.
Background:
This study examined the performance of single high-sensitivity cardiac troponin I (hs-cTnI) measurement strategies to rule out acute myocardial infarction.
Methods:
This was a prospective, observational study of consecutive patients presenting to the emergency department (n = 1631) in whom cTnI measurements were obtained using an investigational hs-cTnI assay. The goals of the study were to determine 1) negative predictive value (NPV) and sensitivity for the diagnosis of acute myocardial infarction, type 1 myocardial infarction, and type 2 myocardial infarction; and 2) safety outcome of acute myocardial infarction or cardiac death at 30 days using hs-cTnI less than the limit of detection (LoD) (<1.9 ng/L) or the High-STEACS threshold (<5 ng/L) alone and in combination with normal electrocardiogram (ECG).
Results:
Acute myocardial infarction occurred in 170 patients (10.4%), including 68 (4.2%) type 1 myocardial infarction and 102 (6.3%) type 2 myocardial infarction. For hs-cTnI
Conclusion:
Strategies using a single hs-cTnI alone or in combination with a normal ECG allow the immediate identification of patients unlikely to have acute myocardial infarction and who are at very low risk for adverse events at 30 days.
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