Diagnostic Utility of Cerebrospinal Fluid White Blood Cell Components for the Identification of Bacterial Meningitis in Infants.

bacterial meningitis cerebrospinal fluid diagnostic utility infant white blood cell

Journal

Journal of the Pediatric Infectious Diseases Society
ISSN: 2048-7207
Titre abrégé: J Pediatric Infect Dis Soc
Pays: England
ID NLM: 101586049

Informations de publication

Date de publication:
26 Dec 2023
Historique:
received: 20 06 2023
accepted: 10 10 2023
medline: 26 12 2023
pubmed: 26 12 2023
entrez: 26 12 2023
Statut: ppublish

Résumé

To evaluate the diagnostic and predictive utility of cerebrospinal fluid (CSF) white blood cell (WBC) components in the diagnosis of bacterial meningitis in infants discharged from the neonatal intensive care unit (NICU). We identified a cohort of infants discharged from a Pediatrix NICU between 1997 and 2020 who did not have an immunodeficiency, had at least 1 CSF culture collected within the first 120 days of life, and at least 1 CSF laboratory specimen obtained on the day of culture collection. We only included an infant's first CSF culture and excluded cultures from CSF reservoirs and those growing contaminants or nonbacterial organisms. We examined the utility of CSF WBC components to diagnose or predict bacterial meningitis by calculating sensitivity, specificity, positive and negative predictive values, likelihood ratios, and area under the receiver operating curve (AUC) at different cutoff values for each parameter. We performed subgroup analysis excluding infants treated with antibiotics the day before CSF culture collection. Of the 20 756 infants that met the study inclusion criteria, 320 (2%) were diagnosed with bacterial meningitis. We found (AUC [95% CI]) CSF WBC count (0.76 [0.73-0.79]), CSF neutrophil count (0.74 [0.70-0.78]), and CSF neutrophil percent (0.71 [0.67-0.75]) had the highest predictive values for bacterial meningitis, even when excluding infants with early antibiotic administration. No single clinical prediction rule had the optimal discriminatory power for predicting culture-proven bacterial meningitis, and clinicians should be cautious when interpreting CSF WBC parameters in infants with suspected meningitis.

Sections du résumé

BACKGROUND BACKGROUND
To evaluate the diagnostic and predictive utility of cerebrospinal fluid (CSF) white blood cell (WBC) components in the diagnosis of bacterial meningitis in infants discharged from the neonatal intensive care unit (NICU).
METHODS METHODS
We identified a cohort of infants discharged from a Pediatrix NICU between 1997 and 2020 who did not have an immunodeficiency, had at least 1 CSF culture collected within the first 120 days of life, and at least 1 CSF laboratory specimen obtained on the day of culture collection. We only included an infant's first CSF culture and excluded cultures from CSF reservoirs and those growing contaminants or nonbacterial organisms. We examined the utility of CSF WBC components to diagnose or predict bacterial meningitis by calculating sensitivity, specificity, positive and negative predictive values, likelihood ratios, and area under the receiver operating curve (AUC) at different cutoff values for each parameter. We performed subgroup analysis excluding infants treated with antibiotics the day before CSF culture collection.
RESULTS RESULTS
Of the 20 756 infants that met the study inclusion criteria, 320 (2%) were diagnosed with bacterial meningitis. We found (AUC [95% CI]) CSF WBC count (0.76 [0.73-0.79]), CSF neutrophil count (0.74 [0.70-0.78]), and CSF neutrophil percent (0.71 [0.67-0.75]) had the highest predictive values for bacterial meningitis, even when excluding infants with early antibiotic administration.
CONCLUSIONS CONCLUSIONS
No single clinical prediction rule had the optimal discriminatory power for predicting culture-proven bacterial meningitis, and clinicians should be cautious when interpreting CSF WBC parameters in infants with suspected meningitis.

Identifiants

pubmed: 38146862
pii: 7499146
doi: 10.1093/jpids/piad087
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

S44-S52

Subventions

Organisme : National Institute of Child Health and Human Development
ID : 5R25HD076475-05

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of The Journal of the Pediatric Infectious Diseases Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Ashley E Lamb (AE)

Duke Clinical Research Institute, Durham, North Carolina, USA.

Sharla Rent (S)

Department of Pediatrics, Duke University, Durham, North Carolina, USA.

Asia J Brannon (AJ)

Duke Clinical Research Institute, Durham, North Carolina, USA.

Jonathan L Greer (JL)

Duke Clinical Research Institute, Durham, North Carolina, USA.

Nyssa P Ndey-Bongo (NP)

Duke Clinical Research Institute, Durham, North Carolina, USA.

Stephen H Cho (SH)

Duke Clinical Research Institute, Durham, North Carolina, USA.

Rachel G Greenberg (RG)

Duke Clinical Research Institute, Durham, North Carolina, USA.
Department of Pediatrics, Duke University, Durham, North Carolina, USA.

Daniel K Benjamin (DK)

Duke Clinical Research Institute, Durham, North Carolina, USA.
Department of Pediatrics, Duke University, Durham, North Carolina, USA.

Reese H Clark (RH)

Pediatrix-Obstetrix Center for Research and Education, Sunrise, Florida, USA.

Karan R Kumar (KR)

Duke Clinical Research Institute, Durham, North Carolina, USA.
Department of Pediatrics, Duke University, Durham, North Carolina, USA.

Classifications MeSH