Diagnostic Performance of High Sensitivity Compared with Contemporary Cardiac Troponin I for the Diagnosis of Acute Myocardial Infarction

Author:

Sandoval Yader1,Smith Stephen W23,Thordsen Sarah E1,Bruen Charles A24,Carlson Michelle D1,Dodd Kenneth W24,Driver Brian E2,Jacoby Katherine24,Johnson Benjamin K1,Love Sara A56,Moore Johanna C2,Sexter Anne7,Schulz Karen7,Scott Nathaniel L24,Nicholson Jennifer5,Apple Fred S56

Affiliation:

1. Division of Cardiology, Hennepin County Medical Center and Minneapolis Heart Institute, Abbott Northwestern Hospital, Minneapolis, MN

2. Department of Emergency Medicine, Hennepin County Medical Center, Minneapolis, MN

3. Department of Emergency Medicine, University of Minnesota, Minneapolis, MN

4. Department of Medicine, Hennepin County Medical Center, Minneapolis, MN

5. Department of Laboratory Medicine and Pathology, Hennepin County Medical, Minneapolis, MN

6. Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN

7. Minneapolis Medical Research Foundation, Minneapolis, MN

Abstract

Abstract BACKGROUND We examined the diagnostic performance of high-sensitivity cardiac troponin I (hs-cTnI) vs contemporary cTnI with use of the 99th percentile alone and with a normal electrocardiogram (ECG) to rule out acute myocardial infarction (MI) and serial changes (deltas) to rule in MI. METHODS We included consecutive patients presenting to a US emergency department with serial cTnI onclinical indication. Diagnostic performance for acute MI, including MI subtypes, and 30-day outcomes were examined. RESULTS Among 1631 patients, MI was diagnosed in 12.9% using the contemporary cTnI assay and in 10.4% using the hs-cTnI assay. For ruling out MI, contemporary cTnI ≤99th percentile at 0, 3, and 6 h and a normal ECG had a negative predictive value (NPV) of 99.5% (95% CI, 98.6–100) and a sensitivity of 99.1% (95% CI, 97.4–100) for diagnostic and safety outcomes. Serial hs-cTnI measurements ≤99th percentile at 0 and 3 h and a normal ECG had an NPV and sensitivity of 100% (95% CI, 100–100) for diagnostic and safety outcomes. For ruling in MI, contemporary cTnI measurements had specificities of 84.4% (95% CI, 82.5–86.3) at presentation and 78.7% (95% CI, 75.4–82.0) with serial testing at 0, 3, and 6 h, improving to 89.2% (95% CI, 87.1–91.3) by using serial cTnI changes (delta, 0 and 6 h) >150%. hs-cTnI had specificities of 86.9% (95% CI, 85.1–88.6) at presentation and 85.7% (95% CI, 83.5–87.9) with serial testing at 0 and 3 h, improving to 89.3% (95% CI, 87.3–91.2) using a delta hs-cTnI (0 and 3 h) >5 ng/L. CONCLUSIONS hs-cTnI and contemporary cTnI assays are excellent in ruling out MI following recommendations predicated on serial testing and the 99th percentile with a normal ECG. For ruling in MI, deltas improve the specificity. ClinicalTrials.gov Identifier: NCT02060760

Funder

Abbott Laboratories

Minneapolis Medical Research Foundation

Biokit

Hytest Ltd.

Instrumentation Laboratory

Research PI through Minneapolis Medical Research Foundation

Roche Diagnostics

Siemens Healthcare

Alere

Ortho-Clinical Diagnostics

Nanomix

Becton Dickinson

Singulex

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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