Can Biomarkers Correctly Predict Ventilator-associated Pneumonia in Patients Treated With Targeted Temperature Management After Cardiac Arrest? An Exploratory Study of the Multicenter Randomized Antibiotic (ANTHARTIC) Study.


Journal

Critical care explorations
ISSN: 2639-8028
Titre abrégé: Crit Care Explor
Pays: United States
ID NLM: 101746347

Informations de publication

Date de publication:
Jul 2024
Historique:
medline: 3 7 2024
pubmed: 3 7 2024
entrez: 3 7 2024
Statut: epublish

Résumé

Ventilator-associated pneumonia (VAP) frequently occurs in patients with cardiac arrest. Diagnosis of VAP after cardiac arrest remains challenging, while the use of current biomarkers such as C-reactive protein (CRP) or procalcitonin (PCT) is debated. To evaluate biomarkers' impact in helping VAP diagnosis after cardiac arrest. This is a prospective ancillary study of the randomized, multicenter, double-blind placebo-controlled ANtibiotherapy during Therapeutic HypothermiA to pRevenT Infectious Complications (ANTHARTIC) trial evaluating the impact of antibiotic prophylaxis to prevent VAP in out-of-hospital patients with cardiac arrest secondary to shockable rhythm and treated with therapeutic hypothermia. An adjudication committee blindly evaluated VAP according to predefined clinical, radiologic, and microbiological criteria. All patients with available biomarker(s), sample(s), and consent approval were included. The main endpoint was to evaluate the ability of biomarkers to correctly diagnose and predict VAP within 48 hours after sampling. The secondary endpoint was to study the combination of two biomarkers in discriminating VAP. Blood samples were collected at baseline on day 3. Routine and exploratory panel of inflammatory biomarkers measurements were blindly performed. Analyses were adjusted on the randomization group. Among 161 patients of the ANTHARTIC trial with available biological sample(s), patients with VAP ( Our exploratory study shows that specific biomarkers, especially CRP combined with IL6, could help to better diagnose or predict early VAP occurrence in cardiac arrest patients.

Identifiants

pubmed: 38957212
doi: 10.1097/CCE.0000000000001104
pii: CCE-D-24-00032
pmc: PMC11219183
doi:

Substances chimiques

Biomarkers 0
Procalcitonin 0
Anti-Bacterial Agents 0
C-Reactive Protein 9007-41-4

Types de publication

Journal Article Randomized Controlled Trial Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1104

Informations de copyright

Copyright © 2024 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine.

Déclaration de conflit d'intérêts

The authors have disclosed that they do not have any potential conflicts of interest.

Auteurs

Nicolas Deye (N)

Medical ICU, Lariboisiere University Hospital, Inserm UMR-S 942, APHP, Paris, France.

Amelie Le Gouge (A)

Inserm CIC 1415, CHU de Tours, Tours, France.

Bruno François (B)

Réanimation Polyvalente, INSERM CIC 1435 and UMR 1092, CHU Limoges, Limoges, France.

Camille Chenevier-Gobeaux (C)

Biochemical Laboratory, Cochin University Hospital, APHP, Paris, France.

Thomas Daix (T)

Réanimation Polyvalente, INSERM CIC 1435 and UMR 1092, CHU Limoges, Limoges, France.

Hamid Merdji (H)

Service de Médecine Intensive-Réanimation, Nouvel Hôpital Civil, Hôpitaux Universitaires de Strasbourg, INSERM UMR 1260, Regenerative NanoMedicine, FMTS, Strasbourg, France.

Alain Cariou (A)

Medical ICU, Cochin University Hospital, AP-HP Centre Université Paris Cité, Paris, France.

Pierre-François Dequin (PF)

INSERM UMR 1100 and Médecine Intensive-Réanimation, Tours, France.

Christophe Guitton (C)

Medecine Intensive Réanimation, Center Hospitalier Universitaire, Nantes, France.

Bruno Mégarbane (B)

Department of Medical and Toxicological Critical Care, Paris Cité University, Lariboisiere University Hospital, Inserm UMR-S 1144, Paris, France.

Jacques Callebert (J)

Biochemical Laboratory, Lariboisiere University Hospital, Inserm UMR-S 1144, Paris, France.

Bruno Giraudeau (B)

Inserm CIC 1415, CHU de Tours, Tours, France.

Alexandre Mebazaa (A)

Université de Paris, Inserm UMR-S 942 MASCOT, Paris, France.
Department of Anaesthesiology and Intensive Care, Lariboisière University Hospital, APHP, Paris, France.

Nicolas Vodovar (N)

Université de Paris, Inserm UMR-S 942 MASCOT, Paris, France.

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Classifications MeSH