Evidence map›Paper›PMID 39332842›Full record

Observational studyArchives of disease in childhood2025

The value of white blood cell count in predicting serious bacterial infections in children presenting to the emergency department: a multicentre observational study.

Naomi Kemps, Clementien Vermont, Chantal D Tan, Ulrich von Both, Enitan Carrol, Marieke Emonts, Michiel van der Flier, Jethro Adam Herberg, Benno Kohlmaier, Michael Levin and 13 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Archives of disease in childhood, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. Role of biomarkers in pediatric sepsis: What evidence says?World journal of clinical pediatrics · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Naomi KempsDepartment of General Paediatrics, Erasmus MC Sophia Children Hospital, Rotterdam, The Netherlands.ORCID http://orcid.org/0009-0008-4156-7050
Clementien VermontDepartment of Paediatric Infectious Diseases and Immunology, Erasmus MC Sophia Children Hospital, Rotterdam, The Netherlands.
Chantal D TanDepartment of General Paediatrics, Erasmus MC Sophia Children Hospital, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-1148-9716
Ulrich von BothDivision of Paediatric Infectious Diseases, Dr. von Hauner Children's Hospital, Munchen, Germany.ORCID http://orcid.org/0000-0001-8411-1071
Enitan CarrolInstitute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
Marieke EmontsPaediatric Immunology, Infectious Diseases & Allergy, Great North Children's Hospital, Newcastle upon Tyne, UK.
Michiel van der FlierPediatric Infectious Diseases and Immunology, Amalia Children's Hospital, Nijmegen, The Netherlands.
Jethro Adam HerbergSection of Paediatric Infectious Diseases, Imperial College London, London, UK.ORCID http://orcid.org/0000-0001-6941-6491
Benno KohlmaierDepartment of General Paediatrics, Medical University of Graz, Graz, Austria.ORCID http://orcid.org/0000-0003-0685-689X
Michael LevinSection of Paediatric Infectious Diseases, Imperial College London, London, UK.
Emma LimPaediatric Immunology, Infectious Diseases & Allergy, Great North Children's Hospital, Newcastle upon Tyne, UK.
Ian MaconochieDepartment of Paediatric Emergency Medicine, Imperial College London, London, UK.
Federico Martinón-TorresGenetics, Vaccines, Infections and Paediatrics Research Group, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0002-9023-581X
Ruud Gerard NijmanSection of Paediatric Infectious Diseases, Imperial College London, London, UK.ORCID http://orcid.org/0000-0001-9671-8161
Marko PokornDepartment of Infectious Diseases, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Irene Rivero-CalleGenetics, Vaccines, Infections and Paediatrics Research Group, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain.
Aleksandra RudzāteDepartment of Paediatrics, Children Clinical University Hospital, Riga, Latvia.
Maria TsoliaDepartment of Paediatrics, P. and A. Kyriakou Children's Hospital, Athens, Greece.
Dace ZavadskaDepartment of Paediatrics, Children Clinical University Hospital, Riga, Latvia.
Werner ZenzDepartment of General Paediatrics, Medical University of Graz, Graz, Austria.
Henriette A MollDepartment of General Paediatrics, Erasmus MC Sophia Children Hospital, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0001-9304-3322
Joany M ZachariasseDepartment of General Paediatrics, Erasmus MC Sophia Children Hospital, Rotterdam, The Netherlands j.zachariasse@erasmusmc.nl.ORCID http://orcid.org/0000-0002-4093-8509
PERFORM consortium (Personalised Risk assessment in febrile children to optimise Real-life Management across the European Union)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhite blood cell count (WBC) is a widely used marker for the prediction of serious bacterial infection (SBI); however, previous research has shown poor performance. This study aims to assess the value of WBC in the prediction of SBI in children at the emergency department (ED) and compare its value with C reactive protein (CRP) and absolute neutrophil count (ANC).

methodsThis study is an observational multicentre study including febrile children aged 0-18 years attending 1 of 12 EDs in 8 European countries. The association between WBC and SBI was assessed by multivariable logistic regression, adjusting for age, CRP and duration of fever. Additionally, diagnostic performance was assessed by sensitivity and specificity. Results were compared with CRP and ANC.

resultsWe included 17 082 children with WBC measurements, of which 1854 (10.9%) had an SBI. WBC >15 had an adjusted OR of 1.9 (95% CI 1.7 to 2.1) for prediction of SBI, after adjusting for confounders. Sensitivity and specificity were 0.56 (95% CI 0.54 to 0.58) and 0.74 (0.73 to 0.75) for WBC >15, and 0.32 (0.30 to 0.34) and 0.91 (0.91 to 0.91) for WBC >20, respectively. In comparison, CRP >20 mg/L had a sensitivity of 0.87 (95% CI 0.85 to 0.88) and a specificity of 0.59 (0.58 to 059). For CRP >80 mg/L, the sensitivity was 0.55 (95% CI 0.52 to 057) and the specificity was 0.91 (0.90 to 0.91). Additionally, for ANC >10, the sensitivity was 0.55 (95% CI 0.53 to 0.58) and the specificity was 0.75 (0.75 to 0.76). The combination of WBC and CRP did not improve performance compared with CRP alone.

conclusionWBC does not have diagnostic benefit in identifying children with an SBI compared with CRP and should only be measured for specific indications.

Indexed as

Bacterial InfectionsEmergency Service, HospitalAdolescentBiomarkersChildChild, PreschoolC-Reactive ProteinEuropeFemaleHumansInfantInfant, NewbornLeukocyte CountMaleNeutrophilsPredictive Value of TestsBiomarkersC-Reactive Proteinepidemiologyinfectious disease medicinepaediatric emergency medicinepaediatrics

Identifiers

PMID39332842
PMCPMC11866293

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.