Automated measurement of neutrophil CD64 expression for diagnosing sepsis in critically ill patients.


Journal

Minerva anestesiologica
ISSN: 1827-1596
Titre abrégé: Minerva Anestesiol
Pays: Italy
ID NLM: 0375272

Informations de publication

Date de publication:
Sep 2019
Historique:
pubmed: 16 3 2019
medline: 28 7 2020
entrez: 16 3 2019
Statut: ppublish

Résumé

Although early identification of sepsis improves outcome, prompt and correct diagnostic remains often challenging. The expression of the high affinity immunoglobulin-Fc fragment receptor I CD64 on neutrophils is upregulated during acute inflammation. We here aimed at determining the usefulness of its rapid measurement in diagnosing sepsis. Seventy-two consecutive patients were enrolled upon admission to Intensive Care Unit within a two-month period. Sequential determination of serum C-reactive protein (CRP) and procalcitonin (PCT) concentrations was obtained. The neutrophil CD64 index was measured using Accellix-CD64® device, an in vitro diagnosis system allowing for an automatic and standardized measure. Serum concentrations of CRP and PCT as well as the neutrophil CD64 index were higher in septic patients compared to all others (P<0.05 for the three markers). Only CD64 index was an independent predictor of sepsis, though with modest sensitivity and specificity (78% and 70%, respectively). Repeat determination of CD64 index at day 2 correctly classified 85% of patients. This prospective study demonstrates the moderate performance of the neutrophil CD64 index, assessed through the Accellix-CD64® device, in diagnosing sepsis in the critically ill patient. However, repeat measurements improve its accuracy and may help to predict ICU-acquired infections.

Sections du résumé

BACKGROUND BACKGROUND
Although early identification of sepsis improves outcome, prompt and correct diagnostic remains often challenging. The expression of the high affinity immunoglobulin-Fc fragment receptor I CD64 on neutrophils is upregulated during acute inflammation. We here aimed at determining the usefulness of its rapid measurement in diagnosing sepsis.
METHODS METHODS
Seventy-two consecutive patients were enrolled upon admission to Intensive Care Unit within a two-month period. Sequential determination of serum C-reactive protein (CRP) and procalcitonin (PCT) concentrations was obtained. The neutrophil CD64 index was measured using Accellix-CD64® device, an in vitro diagnosis system allowing for an automatic and standardized measure.
RESULTS RESULTS
Serum concentrations of CRP and PCT as well as the neutrophil CD64 index were higher in septic patients compared to all others (P<0.05 for the three markers). Only CD64 index was an independent predictor of sepsis, though with modest sensitivity and specificity (78% and 70%, respectively). Repeat determination of CD64 index at day 2 correctly classified 85% of patients.
CONCLUSIONS CONCLUSIONS
This prospective study demonstrates the moderate performance of the neutrophil CD64 index, assessed through the Accellix-CD64® device, in diagnosing sepsis in the critically ill patient. However, repeat measurements improve its accuracy and may help to predict ICU-acquired infections.

Identifiants

pubmed: 30871305
pii: S0375-9393.19.13420-7
doi: 10.23736/S0375-9393.19.13420-7
doi:

Substances chimiques

Biomarkers 0
Procalcitonin 0
Receptors, IgG 0
C-Reactive Protein 9007-41-4

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

943-950

Commentaires et corrections

Type : CommentIn

Auteurs

Claire Thiriet (C)

Service of Reanimation, Central Hospital, Nancy, France.
Inserm U1116, Faculty of Medicine, University of Lorraine, Nancy, France.

Khaoula Mahjoub (K)

Service of Reanimation, Central Hospital, Nancy, France.
Inserm U1116, Faculty of Medicine, University of Lorraine, Nancy, France.

Guilhem Courte (G)

Service of Reanimation, Central Hospital, Nancy, France.
Inserm U1116, Faculty of Medicine, University of Lorraine, Nancy, France.

Pierre Labroca (P)

Service of Reanimation, Central Hospital, Nancy, France.
Inserm U1116, Faculty of Medicine, University of Lorraine, Nancy, France.

Aurélie Cravoisy (A)

Service of Reanimation, Central Hospital, Nancy, France.
Inserm U1116, Faculty of Medicine, University of Lorraine, Nancy, France.

Jérémie Lemarie (J)

Service of Reanimation, Central Hospital, Nancy, France.
Inserm U1116, Faculty of Medicine, University of Lorraine, Nancy, France.

Marie Conrad (M)

Service of Reanimation, Central Hospital, Nancy, France.
Inserm U1116, Faculty of Medicine, University of Lorraine, Nancy, France.

Lionel Nace (L)

Service of Reanimation, Central Hospital, Nancy, France.
Inserm U1116, Faculty of Medicine, University of Lorraine, Nancy, France.

Pierre-Edouard Bollaert (PE)

Service of Reanimation, Central Hospital, Nancy, France.
Inserm U1116, Faculty of Medicine, University of Lorraine, Nancy, France.

Sébastien Gibot (S)

Service of Reanimation, Central Hospital, Nancy, France - s.gibot@chu-nancy.fr.
Inserm U1116, Faculty of Medicine, University of Lorraine, Nancy, France.

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Classifications MeSH