Startseite Medizin Diagnostic performance of a point of care high-sensitivity cardiac troponin I assay and single measurement evaluation to rule out and rule in acute coronary syndrome
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Diagnostic performance of a point of care high-sensitivity cardiac troponin I assay and single measurement evaluation to rule out and rule in acute coronary syndrome

  • Vincenzo De Iuliis ORCID logo EMAIL logo , Anna Rita Gabriele , Francesca De Santis , Roberta De Rugeriis , Luigi Di Quinzio , Steeve Aloisi , Anna Carla Rosati , Manuela Benvenuto , Donatello Fabiani und Sofia Chiatamone Ranieri
Veröffentlicht/Copyright: 29. April 2024

Abstract

Objectives

About 10 million individuals in USA presented annually in the emergency department (ED) with chest pain or with signs and symptoms of acute coronary syndrome (ACS). The advent of point of care (POC) devices, able to measure high sensitivity troponin, are a very interesting tool in the ED setting for its rapid turnaround time (<10 min).

Methods

The present study evaluates the diagnostic performance of the Atellica VTLi (Siemens) in real life setting using the clinical data derived from integrated diagnoses of emergency room staff and cardiologist and in comparison with standard laboratory hs-cTnT assay (Cobas 8000, Elecsys, Roche). 966 patients admitted to the emergency department of “G. Mazzini Hospital” in Teramo, Italy, from July 27, 2022, through June 09, 2023, were enrolled.

Results

The diagnostic performance of POC hs-cTnI was evaluated. An appropriate POC hs-cTnI threshold values <4 ng/L supplied a sensitivity and an NPV of 100 % (95 % CI: 99.5–100) in order to achieve rapid rule out for MI through a single measurement at patient presentation in the ED. Furthermore, a derivation POC hs-cTnI concentration >54 ng/L provided a specificity of 97.2 % (95 % CI: 95.9–98.1) and a PPV of 43.5 % (95 % CI: 40.3–46.7) for ruling in MI.

Conclusions

This platform showed comparable diagnostic performance for myocardial infarction to the central laboratory. Our data suggest the possible use of the Atellica VTLi hs-cTnI POC assay either in emergency department of urban medical centre, either in rural hospital for triage and patient management.


Corresponding author: Vincenzo De Iuliis, MD, Department of Clinical Pathology, G. Mazzini Civil Hospital, Teramo, Italy, Phone: +39 0861429324, E-mail:

  1. Research ethics: The study was conducted in accordance with the Declaration of Helsinki.

  2. Informed consent: Not applicable.

  3. Author contributions: The authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  4. Competing interests: The authors state no conflict of interest.

  5. Research funding: None declared.

  6. Data availability: The raw data can be obtained on request from the corresponding author.

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Supplementary Material

This article contains supplementary material (https://doi.org/10.1515/cclm-2024-0225).


Received: 2024-02-17
Accepted: 2024-04-16
Published Online: 2024-04-29
Published in Print: 2024-10-28

© 2024 Walter de Gruyter GmbH, Berlin/Boston

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