External validation of a high-sensitive troponin I algorithm for rapid evaluation of acute myocardial infarction in a Danish cohort

Author:

Andersen Camilla Fuchs1234ORCID,Bang Camilla123,Lauridsen Kasper Glerup123ORCID,Frederiksen Christian Alcaraz5ORCID,Schmidt Morten67ORCID,Jensen Tage3,Hornung Nete8,Løfgren Bo139

Affiliation:

1. Research Center for Emergency Medicine, Aarhus University, Palle Juul-Jensens Boulevard 99, J103, Aarhus N 8200, Denmark

2. Clinical Research Unit, Randers Regional Hospital, Skovlyvej 15, Randers 8930, Denmark

3. Department of Internal Medicine, Randers Regional Hospital, Skovlyvej 15, 8930 Randers, Denmark

4. Department of Cardiology, Herlev and Gentofte University Hospital, Borgmester Ib Juuls Vej, 1, Herlev, Hellerup 2730, Denmark

5. Department of Cardiology, Aarhus University Hospital, Palle Juul-Jensens Boulevard 99, Aarhus N 8200, Denmark

6. Department of Cardiology, Regional Hospital West Jutland, Gl Landevej 61, Herning 7400, Denmark

7. Department of Clinical Epidemiology, Aarhus University Hospital, Olof Palmes Allé 43-45, Aarhus N 8200, Denmark

8. Department of Clinical Biochemistry, Regional Hospital West Jutland, Gl Landevej 61, Herning 7400, Denmark

9. Department of Clinical Medicine, Aarhus University Hospital, Incuba Skejby, building 2, Palle Juul-Jensens Boulevard 82, Aarhus N 8200, Denmark

Abstract

Abstract Aims An accelerated diagnostic algorithm for ruling-in or ruling-out myocardial infarction (MI) after 1 hour (1 h) has recently been derived and internally validated for the Siemens ADVIA Centaur TNIH assay. We aimed to validate the diagnostic performance of the TNIH 0 h/1 h algorithm ad modum Boeddinghaus in a Danish cohort. Methods and results Patients with chest pain suggestive of MI were prospectively enrolled. High-sensitive troponin I (TNIH) was measured at admission (0 h) and after 30 minutes (30 m), 1 h, and 3 hours (3 h). We externally validated the TNIH 0 h/1 h algorithm ad modum Boeddinghaus in Danish patients. Moreover, we applied the algorithm using the second TNIH measurement at 30 m instead of 1 h. We enrolled 1003 patients: median (Q1–Q3) age 64 (52–74) years, 42% female, and 23% with previous MI. Myocardial infarction was the final diagnosis in 9% of patients. Median (Q1–Q3) times from admission to 30 m and 1 h blood draw were 35 min (30–37 min) and 67 min (62–75 min), respectively. Using the 0 h and 1 h results, 468 (47%) patients were assigned to rule-out, 104 (10%) to rule-in, and 431 (43%) to the observational zone. This resulted in a negative predictive value of 100% (95% confidence interval: 99.2–100%), sensitivity of 100% (95.9–100%), positive predictive value of 79.8 (70.8–87.0%), and specificity of 97.7% (96.5–98.6%). The diagnostic performance after 30 m was similar. Conclusions The TNIH 0 h/1 h algorithm ad modum Boeddinghaus performed excellently for rule-out of MI in a Danish cohort. The Boeddinghaus algorithm also performed excellently after only 30 m. Trial registration number NCT03634384. Trial registry name and URL Rapid Use of High-Sensitive Cardiac Troponin I for Ruling-in and Ruling-out Acute Myocardial Infarction (RACING-MI), https://clinicaltrials.gov/ct2/show/NCT03634384.

Funder

Grosserer L. F. Foghts Foundation

Boserup Foundation

Helga and Peter Korning Foundation

Holger and Ruth Hesse’s Memorial Foundation

Henry and Astrid Møller Foundation

Højmosegård Grant

Oda and Hans Svenningsen’s Foundation

The Foundation of 1870

AP Møller Foundation

Randers Regional Hospital and Aarhus University

TNIH

Siemens Healthcare A/S

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Critical Care and Intensive Care Medicine,General Medicine

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