High-sensitivity troponin I with or without ultra-sensitive copeptin for the instant rule-out of acute myocardial infarction.

copeptin coronary artery disease emergency department high-sensitivity cardiac troponin myocardial infarction

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2022
Historique:
received: 13 03 2022
accepted: 26 07 2022
entrez: 26 8 2022
pubmed: 27 8 2022
medline: 27 8 2022
Statut: epublish

Résumé

The instant, single-sampling rule-out of acute myocardial infarction (AMI) is still an unmet clinical need. We aimed at testing and comparing diagnostic performance and prognostic value of two different single-sampling biomarker strategies for the instant rule-out of AMI. From the Biomarkers in Acute Cardiac Care (BACC) cohort, we recruited consecutive patients with acute chest pain and suspected AMI presenting to the Emergency Department of the University Medical Center Hamburg-Eppendorf, Hamburg, Germany. We compared safety, effectiveness and 12-month incidence of the composite endpoint of all-cause death and myocardial infarction between (i) a single-sampling, dual-marker pathway combining high-sensitivity cardiac troponin I (hs-cTnI) and ultra-sensitive copeptin (us-Cop) at presentation (hs-cTnI ≤ 27 ng/L, us-Cop < 10 pmol/L and low-risk ECG) and (ii) a single-sampling pathway based on one-off hs-cTnI determination at presentation (hs-cTnI < 5 ng/L and low-risk ECG). As a comparator, we used the European Society of Cardiology (ESC) 0/1-h dual-sampling algorithm. We enrolled 1,136 patients (male gender 65%) with median age of 64 years (interquartile range, 51-75). Overall, 228 (20%) patients received a final diagnosis of AMI. The two single-sampling instant rule-out pathways yielded similar negative predictive value (NPV): 97.4% (95%CI: 95.4-98.7) and 98.7% (95%CI: 96.9-99.6) for dual-marker and single hs-cTnI algorithms, respectively ( Instant rule-out pathways based on one-off determination of hs-cTnI alone or in combination with us-Cop are comparably safe as the ESC 0/1 h algorithm for the instant rule-out of AMI, yielding similar prognostic information. Instant rule-out strategies are safe alternatives to the ESC 0/1 h algorithm and allow the rapid and effective triage of suspected AMI in patients with low-risk ECG. However, adding copeptin to hs-cTn does not improve the safety of instant rule-out compared with the single rule-out hs-cTn at very low cut-off concentrations.

Sections du résumé

Background UNASSIGNED
The instant, single-sampling rule-out of acute myocardial infarction (AMI) is still an unmet clinical need. We aimed at testing and comparing diagnostic performance and prognostic value of two different single-sampling biomarker strategies for the instant rule-out of AMI.
Methods UNASSIGNED
From the Biomarkers in Acute Cardiac Care (BACC) cohort, we recruited consecutive patients with acute chest pain and suspected AMI presenting to the Emergency Department of the University Medical Center Hamburg-Eppendorf, Hamburg, Germany. We compared safety, effectiveness and 12-month incidence of the composite endpoint of all-cause death and myocardial infarction between (i) a single-sampling, dual-marker pathway combining high-sensitivity cardiac troponin I (hs-cTnI) and ultra-sensitive copeptin (us-Cop) at presentation (hs-cTnI ≤ 27 ng/L, us-Cop < 10 pmol/L and low-risk ECG) and (ii) a single-sampling pathway based on one-off hs-cTnI determination at presentation (hs-cTnI < 5 ng/L and low-risk ECG). As a comparator, we used the European Society of Cardiology (ESC) 0/1-h dual-sampling algorithm.
Results UNASSIGNED
We enrolled 1,136 patients (male gender 65%) with median age of 64 years (interquartile range, 51-75). Overall, 228 (20%) patients received a final diagnosis of AMI. The two single-sampling instant rule-out pathways yielded similar negative predictive value (NPV): 97.4% (95%CI: 95.4-98.7) and 98.7% (95%CI: 96.9-99.6) for dual-marker and single hs-cTnI algorithms, respectively (
Conclusions UNASSIGNED
Instant rule-out pathways based on one-off determination of hs-cTnI alone or in combination with us-Cop are comparably safe as the ESC 0/1 h algorithm for the instant rule-out of AMI, yielding similar prognostic information. Instant rule-out strategies are safe alternatives to the ESC 0/1 h algorithm and allow the rapid and effective triage of suspected AMI in patients with low-risk ECG. However, adding copeptin to hs-cTn does not improve the safety of instant rule-out compared with the single rule-out hs-cTn at very low cut-off concentrations.

Identifiants

pubmed: 36017085
doi: 10.3389/fcvm.2022.895421
pmc: PMC9395923
doi:

Types de publication

Journal Article

Langues

eng

Pagination

895421

Informations de copyright

Copyright © 2022 Ricci, Neumann, Rübsamen, Sörensen, Ojeda, Cataldo, Zeller, Schäfer, Hartikainen, Golato, Palermi, Zimarino, Blankenberg, Westermann and De Caterina.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Fabrizio Ricci (F)

Department of Neuroscience, Imaging and Clinical Sciences, "G. d'Annunzio" University, Chieti-Pescara, Italy.
Department of Clinical Sciences, Lund University, Malmö, Sweden.
Casa di Cura Villa Serena, Città Sant'Angelo, Pescara, Italy.

Johannes T Neumann (JT)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Hamburg, Germany.

Nicole Rübsamen (N)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.

Nils A Sörensen (NA)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Hamburg, Germany.

Francisco Ojeda (F)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.

Ivana Cataldo (I)

Unit of Clinical Pathology, SS. Annunziata University Hospital, Chieti, Italy.

Tanja Zeller (T)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Hamburg, Germany.

Sarina Schäfer (S)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.

Tau S Hartikainen (TS)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.

Maria Golato (M)

Unit of Clinical Pathology, SS. Annunziata University Hospital, Chieti, Italy.

Stefano Palermi (S)

Public Health Department, University of Naples Federico II, Naples, Italy.

Marco Zimarino (M)

Department of Neuroscience, Imaging and Clinical Sciences, "G. d'Annunzio" University, Chieti-Pescara, Italy.

Stefan Blankenberg (S)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Hamburg, Germany.

Dirk Westermann (D)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Hamburg, Germany.

Raffaele De Caterina (R)

Casa di Cura Villa Serena, Città Sant'Angelo, Pescara, Italy.
Cardiology Division, Pisa University Hospital and University of Pisa, Pisa, Italy.

Classifications MeSH