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Clinical features of bacterial meningitis among hospitalised children in Kenya

BACKGROUND: Diagnosing bacterial meningitis is essential to optimise the type and duration of antimicrobial therapy to limit mortality and sequelae. In sub-Saharan Africa, many public hospitals lack laboratory capacity, relying on clinical features to empirically treat or not treat meningitis. We in...

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Autores principales: Obiero, Christina W., Mturi, Neema, Mwarumba, Salim, Ngari, Moses, Newton, Charles R., van Hensbroek, Michaël Boele, Berkley, James A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8176744/
https://www.ncbi.nlm.nih.gov/pubmed/34082778
http://dx.doi.org/10.1186/s12916-021-01998-3
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author Obiero, Christina W.
Mturi, Neema
Mwarumba, Salim
Ngari, Moses
Newton, Charles R.
van Hensbroek, Michaël Boele
Berkley, James A.
author_facet Obiero, Christina W.
Mturi, Neema
Mwarumba, Salim
Ngari, Moses
Newton, Charles R.
van Hensbroek, Michaël Boele
Berkley, James A.
author_sort Obiero, Christina W.
collection PubMed
description BACKGROUND: Diagnosing bacterial meningitis is essential to optimise the type and duration of antimicrobial therapy to limit mortality and sequelae. In sub-Saharan Africa, many public hospitals lack laboratory capacity, relying on clinical features to empirically treat or not treat meningitis. We investigated whether clinical features of bacterial meningitis identified prior to the introduction of conjugate vaccines still discriminate meningitis in children aged ≥60 days. METHODS: We conducted a retrospective cohort study to validate seven clinical features identified in 2002 (KCH-2002): bulging fontanel, neck stiffness, cyanosis, seizures outside the febrile convulsion age range, focal seizures, impaired consciousness, or fever without malaria parasitaemia and Integrated Management of Childhood Illness (IMCI) signs: neck stiffness, lethargy, impaired consciousness or seizures, and assessed at admission in discriminating bacterial meningitis after the introduction of conjugate vaccines. Children aged ≥60 days hospitalised between 2012 and 2016 at Kilifi County Hospital were included in this analysis. Meningitis was defined as positive cerebrospinal fluid (CSF) culture, organism observed on CSF microscopy, positive CSF antigen test, leukocytes ≥50/μL, or CSF to blood glucose ratio <0.1. RESULTS: Among 12,837 admissions, 98 (0.8%) had meningitis. The presence of KCH-2002 signs had a sensitivity of 86% (95% CI 77–92) and specificity of 38% (95% CI 37–38). Exclusion of ‘fever without malaria parasitaemia’ reduced sensitivity to 58% (95% CI 48–68) and increased specificity to 80% (95% CI 79–80). IMCI signs had a sensitivity of 80% (95% CI 70–87) and specificity of 62% (95% CI 61–63). CONCLUSIONS: A lower prevalence of bacterial meningitis and less typical signs than in 2002 meant the lower performance of KCH-2002 signs. Clinicians and policymakers should be aware of the number of lumbar punctures (LPs) or empirical treatments needed for each case of meningitis. Establishing basic capacity for CSF analysis is essential to exclude bacterial meningitis in children with potential signs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-021-01998-3.
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spelling pubmed-81767442021-06-04 Clinical features of bacterial meningitis among hospitalised children in Kenya Obiero, Christina W. Mturi, Neema Mwarumba, Salim Ngari, Moses Newton, Charles R. van Hensbroek, Michaël Boele Berkley, James A. BMC Med Research Article BACKGROUND: Diagnosing bacterial meningitis is essential to optimise the type and duration of antimicrobial therapy to limit mortality and sequelae. In sub-Saharan Africa, many public hospitals lack laboratory capacity, relying on clinical features to empirically treat or not treat meningitis. We investigated whether clinical features of bacterial meningitis identified prior to the introduction of conjugate vaccines still discriminate meningitis in children aged ≥60 days. METHODS: We conducted a retrospective cohort study to validate seven clinical features identified in 2002 (KCH-2002): bulging fontanel, neck stiffness, cyanosis, seizures outside the febrile convulsion age range, focal seizures, impaired consciousness, or fever without malaria parasitaemia and Integrated Management of Childhood Illness (IMCI) signs: neck stiffness, lethargy, impaired consciousness or seizures, and assessed at admission in discriminating bacterial meningitis after the introduction of conjugate vaccines. Children aged ≥60 days hospitalised between 2012 and 2016 at Kilifi County Hospital were included in this analysis. Meningitis was defined as positive cerebrospinal fluid (CSF) culture, organism observed on CSF microscopy, positive CSF antigen test, leukocytes ≥50/μL, or CSF to blood glucose ratio <0.1. RESULTS: Among 12,837 admissions, 98 (0.8%) had meningitis. The presence of KCH-2002 signs had a sensitivity of 86% (95% CI 77–92) and specificity of 38% (95% CI 37–38). Exclusion of ‘fever without malaria parasitaemia’ reduced sensitivity to 58% (95% CI 48–68) and increased specificity to 80% (95% CI 79–80). IMCI signs had a sensitivity of 80% (95% CI 70–87) and specificity of 62% (95% CI 61–63). CONCLUSIONS: A lower prevalence of bacterial meningitis and less typical signs than in 2002 meant the lower performance of KCH-2002 signs. Clinicians and policymakers should be aware of the number of lumbar punctures (LPs) or empirical treatments needed for each case of meningitis. Establishing basic capacity for CSF analysis is essential to exclude bacterial meningitis in children with potential signs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-021-01998-3. BioMed Central 2021-06-04 /pmc/articles/PMC8176744/ /pubmed/34082778 http://dx.doi.org/10.1186/s12916-021-01998-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Obiero, Christina W.
Mturi, Neema
Mwarumba, Salim
Ngari, Moses
Newton, Charles R.
van Hensbroek, Michaël Boele
Berkley, James A.
Clinical features of bacterial meningitis among hospitalised children in Kenya
title Clinical features of bacterial meningitis among hospitalised children in Kenya
title_full Clinical features of bacterial meningitis among hospitalised children in Kenya
title_fullStr Clinical features of bacterial meningitis among hospitalised children in Kenya
title_full_unstemmed Clinical features of bacterial meningitis among hospitalised children in Kenya
title_short Clinical features of bacterial meningitis among hospitalised children in Kenya
title_sort clinical features of bacterial meningitis among hospitalised children in kenya
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8176744/
https://www.ncbi.nlm.nih.gov/pubmed/34082778
http://dx.doi.org/10.1186/s12916-021-01998-3
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