Clinical features to distinguish meningitis among young infants at a rural Kenyan hospital.


Journal

Archives of disease in childhood
ISSN: 1468-2044
Titre abrégé: Arch Dis Child
Pays: England
ID NLM: 0372434

Informations de publication

Date de publication:
02 2021
Historique:
received: 24 01 2020
revised: 23 06 2020
accepted: 01 07 2020
pubmed: 21 8 2020
medline: 23 2 2021
entrez: 22 8 2020
Statut: ppublish

Résumé

Detection of meningitis is essential to optimise the duration and choice of antimicrobial agents to limit mortality and sequelae. In low and middle-income countries most health facilities lack laboratory capacity and rely on clinical features to empirically treat meningitis. We conducted a diagnostic validation study to investigate the performance of clinical features (fever, convulsions, irritability, bulging fontanel and temperature ≥39°C) and WHO-recommended signs (drowsiness, lethargy, unconsciousness, convulsions, bulging fontanel, irritability or a high-pitched cry) in discriminating meningitis in young infants. Retrospective cohort study. Kilifi County Hospital. Infants aged <60 days hospitalised between 2012 and 2016. Definite meningitis defined as positive cerebrospinal fluid (CSF) culture, microscopy or antigen test, or leucocytes ≥0.05 x 10∧9/L. Of 4809 infants aged <60 days included, 81 (1.7%) had definite meningitis. WHO-recommended signs had sensitivity of 58% (95% CI 47% to 69%) and specificity of 57% (95% CI 56% to 59%) for definite meningitis. Addition of history of fever improved sensitivity to 89% (95% CI 80% to 95%) but reduced specificity to 26% (95% CI 25% to 27%). Presence of ≥1 of 5 previously identified signs had sensitivity of 79% (95% CI 69% to 87%) and specificity of 51% (95% CI 50% to 53%). Despite a lower prevalence of definite meningitis, the performance of previously identified signs at admission in predicting meningitis was unchanged. Presence of history of fever improves the sensitivity of WHO-recommended signs but loses specificity. Careful evaluation, repeated assessment and capacity for lumbar puncture and CSF microscopy to exclude meningitis in most young infants with potential signs are essential to management in this age group.

Sections du résumé

BACKGROUND
Detection of meningitis is essential to optimise the duration and choice of antimicrobial agents to limit mortality and sequelae. In low and middle-income countries most health facilities lack laboratory capacity and rely on clinical features to empirically treat meningitis.
OBJECTIVE
We conducted a diagnostic validation study to investigate the performance of clinical features (fever, convulsions, irritability, bulging fontanel and temperature ≥39°C) and WHO-recommended signs (drowsiness, lethargy, unconsciousness, convulsions, bulging fontanel, irritability or a high-pitched cry) in discriminating meningitis in young infants.
DESIGN
Retrospective cohort study.
SETTING
Kilifi County Hospital.
PATIENTS
Infants aged <60 days hospitalised between 2012 and 2016.
MAIN OUTCOME MEASURE
Definite meningitis defined as positive cerebrospinal fluid (CSF) culture, microscopy or antigen test, or leucocytes ≥0.05 x 10∧9/L.
RESULTS
Of 4809 infants aged <60 days included, 81 (1.7%) had definite meningitis. WHO-recommended signs had sensitivity of 58% (95% CI 47% to 69%) and specificity of 57% (95% CI 56% to 59%) for definite meningitis. Addition of history of fever improved sensitivity to 89% (95% CI 80% to 95%) but reduced specificity to 26% (95% CI 25% to 27%). Presence of ≥1 of 5 previously identified signs had sensitivity of 79% (95% CI 69% to 87%) and specificity of 51% (95% CI 50% to 53%).
CONCLUSIONS
Despite a lower prevalence of definite meningitis, the performance of previously identified signs at admission in predicting meningitis was unchanged. Presence of history of fever improves the sensitivity of WHO-recommended signs but loses specificity. Careful evaluation, repeated assessment and capacity for lumbar puncture and CSF microscopy to exclude meningitis in most young infants with potential signs are essential to management in this age group.

Identifiants

pubmed: 32819909
pii: archdischild-2020-318913
doi: 10.1136/archdischild-2020-318913
pmc: PMC7841476
doi:

Types de publication

Evaluation Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

130-136

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Christina W Obiero (CW)

Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya cobiero@kemri-wellcome.org.
Department of Global Health, University of Amsterdam Faculty of Medicine, Amsterdam, Noord-Holland, The Netherlands.

Neema Mturi (N)

Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.

Salim Mwarumba (S)

Department of Microbiology, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.

Moses Ngari (M)

Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
The Childhood Acute Illness and Nutrition (CHAIN) Network, Nairobi, Kenya.

Charles Newton (C)

Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Department of Psychiatry, University of Oxford Centre for Tropical Medicine and Global Health, Oxford, Oxfordshire, UK.

Michael Boele van Hensbroek (M)

Department of Global Health, University of Amsterdam Faculty of Medicine, Amsterdam, Noord-Holland, The Netherlands.

James Alexander Berkley (JA)

Clinical Research Department, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
The Childhood Acute Illness and Nutrition (CHAIN) Network, Nairobi, Kenya.
Nuffield Department of Medicine, University of Oxford Centre for Tropical Medicine and Global Health, Oxford, Oxfordshire, UK.

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