Fragile neutrophils in surgical patients: A phenomenon associated with critical illness.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 30 03 2020
accepted: 08 07 2020
entrez: 5 8 2020
pubmed: 5 8 2020
medline: 9 10 2020
Statut: epublish

Résumé

Leukocyte viability (determined by e.g. propidium iodide [PI] staining) is automatically measured by hematology analyzers to check for delayed bench time. Incidental findings in fresh blood samples revealed the existence of leukocytes with decreased viability in critically ill surgical patients. Not much is known about these cells and their functional and/or clinical implications. Therefore, we investigated the incidence of decreased leukocyte viability, the implications for leukocyte functioning and its relation with clinical outcomes. An automated alarm was set in a routine hematology analyzer (Cell-Dyn Sapphire) for the presence of non-viable leukocytes characterized by increased fluorescence in the PI-channel (FL3:630±30nm). Patients with non-viable leukocytes were prospectively included and blood samples were drawn to investigate leukocyte viability in detail and to investigate leukocyte functioning (phagocytosis and responsiveness to a bacterial stimulus). Then, a retrospective analysis was conducted to investigate the incidence of fragile neutrophils in the circulation and clinical outcomes of surgical patients with fragile neutrophils hospitalized between 2013-2017. A high FL3 signal was either caused by 1) neutrophil autofluorescence which was considered false positive, or by 2) actual non-viable PI-positive neutrophils in the blood sample. These two causes could be distinguished using automatically generated data from the hematology analyzer. The non-viable (PI-positive) neutrophils proved to be viable (PI-negative) in non-lysed blood samples, and were therefore referred to as 'fragile neutrophils'. Overall leukocyte functioning was not impaired in patients with fragile neutrophils. Of the 11 872 retrospectively included surgical patients, 75 (0.63%) were identified to have fragile neutrophils during hospitalization. Of all patients with fragile neutrophils, 75.7% developed an infection, 70.3% were admitted to the ICU and 31.3% died during hospitalization. In conclusion, fragile neutrophils occur in the circulation of critically ill surgical patients. These cells can be automatically detected during routine blood analyses and are an indicator of critical illness.

Identifiants

pubmed: 32750099
doi: 10.1371/journal.pone.0236596
pii: PONE-D-20-09054
pmc: PMC7402494
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0236596

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Lillian Hesselink (L)

Department of trauma surgery, University Medical Center Utrecht, Utrecht, the Netherlands.
Center for Translational Immunology, Wilhelmina Children's Hospital, Utrecht, the Netherlands.

Roy Spijkerman (R)

Department of trauma surgery, University Medical Center Utrecht, Utrecht, the Netherlands.
Center for Translational Immunology, Wilhelmina Children's Hospital, Utrecht, the Netherlands.

Pien Hellebrekers (P)

Department of trauma surgery, University Medical Center Utrecht, Utrecht, the Netherlands.
Center for Translational Immunology, Wilhelmina Children's Hospital, Utrecht, the Netherlands.

Robert J van Bourgondiën (RJ)

Department of trauma surgery, University Medical Center Utrecht, Utrecht, the Netherlands.

Enja Blasse (E)

Department of Clinical Chemistry and Hematology, Utrecht, the Netherlands.

Saskia Haitjema (S)

Department of Clinical Chemistry and Hematology, Utrecht, the Netherlands.

Albert Huisman (A)

Department of Clinical Chemistry and Hematology, Utrecht, the Netherlands.

Wouter W van Solinge (WW)

Department of Clinical Chemistry and Hematology, Utrecht, the Netherlands.

Karlijn J P Van Wessem (KJP)

Department of trauma surgery, University Medical Center Utrecht, Utrecht, the Netherlands.

Leo Koenderman (L)

Center for Translational Immunology, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
Department of Respiratory Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.

Luke P H Leenen (LPH)

Department of trauma surgery, University Medical Center Utrecht, Utrecht, the Netherlands.

Falco Hietbrink (F)

Department of trauma surgery, University Medical Center Utrecht, Utrecht, the Netherlands.

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