Declines in Pediatric Bacterial Meningitis in the Republic of Benin Following Introduction of Pneumococcal Conjugate Vaccine: Epidemiological and Etiological Findings, 2011-2016.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
05 09 2019
Historique:
entrez: 11 9 2019
pubmed: 11 9 2019
medline: 29 9 2020
Statut: ppublish

Résumé

Pediatric bacterial meningitis (PBM) remains an important cause of disease in children in Africa. We describe findings from sentinel site bacterial meningitis surveillance in children <5 years of age in the Republic of Benin, 2011-2016. Cerebrospinal fluid (CSF) was collected from children admitted to Parakou, Natitingou, and Tanguieta sentinel hospitals with suspected meningitis. Identification of Streptococcus pneumoniae (pneumococcus), Haemophilus influenzae, and Neisseria meningitidis (meningococcus) was performed by rapid diagnostic tests, microbiological culture, and/or polymerase chain reaction; where possible, serotyping/grouping was performed. A total of 10 919 suspected cases of meningitis were admitted to the sentinel hospitals. Most patients were 0-11 months old (4863 [44.5%]) and there were 542 (5.0%) in-hospital deaths. Overall, 4168 CSF samples were screened for pathogens and a total of 194 (4.7%) PBM cases were confirmed, predominantly caused by pneumococcus (98 [50.5%]). Following pneumococcal conjugate vaccine (PCV) introduction in 2011, annual suspected meningitis cases and deaths (case fatality rate) progressively declined from 2534 to 1359 and from 164 (6.5%) to 14 (1.0%) in 2012 and 2016, respectively (P < .001). Additionally, there was a gradual decline in the proportion of meningitis cases caused by pneumococcus, from 77.3% (17/22) in 2011 to 32.4% (11/34) in 2016 (odds ratio, 7.11 [95% confidence interval, 2.08-24.30]). Haemophilus influenzae meningitis fluctuated over the surveillance period and was the predominant pathogen (16/34 [47.1%]) by 2016. The observed decrease in pneumococcal meningitis after PCV introduction may be indicative of changing patterns of PBM etiology in Benin. Maintaining vigilant and effective surveillance is critical for understanding these changes and their wider public health implications.

Sections du résumé

BACKGROUND
Pediatric bacterial meningitis (PBM) remains an important cause of disease in children in Africa. We describe findings from sentinel site bacterial meningitis surveillance in children <5 years of age in the Republic of Benin, 2011-2016.
METHODS
Cerebrospinal fluid (CSF) was collected from children admitted to Parakou, Natitingou, and Tanguieta sentinel hospitals with suspected meningitis. Identification of Streptococcus pneumoniae (pneumococcus), Haemophilus influenzae, and Neisseria meningitidis (meningococcus) was performed by rapid diagnostic tests, microbiological culture, and/or polymerase chain reaction; where possible, serotyping/grouping was performed.
RESULTS
A total of 10 919 suspected cases of meningitis were admitted to the sentinel hospitals. Most patients were 0-11 months old (4863 [44.5%]) and there were 542 (5.0%) in-hospital deaths. Overall, 4168 CSF samples were screened for pathogens and a total of 194 (4.7%) PBM cases were confirmed, predominantly caused by pneumococcus (98 [50.5%]). Following pneumococcal conjugate vaccine (PCV) introduction in 2011, annual suspected meningitis cases and deaths (case fatality rate) progressively declined from 2534 to 1359 and from 164 (6.5%) to 14 (1.0%) in 2012 and 2016, respectively (P < .001). Additionally, there was a gradual decline in the proportion of meningitis cases caused by pneumococcus, from 77.3% (17/22) in 2011 to 32.4% (11/34) in 2016 (odds ratio, 7.11 [95% confidence interval, 2.08-24.30]). Haemophilus influenzae meningitis fluctuated over the surveillance period and was the predominant pathogen (16/34 [47.1%]) by 2016.
CONCLUSIONS
The observed decrease in pneumococcal meningitis after PCV introduction may be indicative of changing patterns of PBM etiology in Benin. Maintaining vigilant and effective surveillance is critical for understanding these changes and their wider public health implications.

Identifiants

pubmed: 31505630
pii: 5561331
doi: 10.1093/cid/ciz478
pmc: PMC6761314
doi:

Substances chimiques

Pneumococcal Vaccines 0
Vaccines, Conjugate 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

S140-S147

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America.

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Auteurs

Joseph Agossou (J)

Department of Mother and Child, Faculty of Medicine, University of Parakou, Parakou, Benin.
Borgou Regional University Teaching Hospital, Parakou, Benin.

Chinelo Ebruke (C)

World Health Organization (WHO) Collaborating Centre for New Vaccines Surveillance, Medical Research Council Unit The Gambia at London School of Hygiene and Tropical Medicine, Fajara, Banjul.

Alphonse Noudamadjo (A)

Department of Mother and Child, Faculty of Medicine, University of Parakou, Parakou, Benin.
Borgou Regional University Teaching Hospital, Parakou, Benin.

Julien D Adédémy (JD)

Department of Mother and Child, Faculty of Medicine, University of Parakou, Parakou, Benin.
Borgou Regional University Teaching Hospital, Parakou, Benin.

Eric Y Dènon (EY)

Service National de Laboratoire Sante Publique, Cotonou.

Honoré S Bankolé (HS)

Service National de Laboratoire Sante Publique, Cotonou.

Mariam A Dogo (MA)

Service National de Laboratoire Sante Publique, Cotonou.

Rolande Assogba (R)

Saint Jean de Dieu Hospital of Tanguieta, Benin.

Moussa Alassane (M)

Saint Jean de Dieu Hospital of Tanguieta, Benin.

Abdoullah Condé (A)

Department of Mother and Child, Faculty of Medicine, University of Parakou, Parakou, Benin.
Borgou Regional University Teaching Hospital, Parakou, Benin.

Falilatou Agbeille Mohamed (FA)

Department of Mother and Child, Faculty of Medicine, University of Parakou, Parakou, Benin.
Borgou Regional University Teaching Hospital, Parakou, Benin.

Gérard Kpanidja (G)

Department of Mother and Child, Faculty of Medicine, University of Parakou, Parakou, Benin.
Borgou Regional University Teaching Hospital, Parakou, Benin.

Moutawakilou Gomina (M)

Borgou Regional University Teaching Hospital, Parakou, Benin.

François Hounsou (F)

Service National de Laboratoire Sante Publique, Cotonou.

Basile G Aouanou (BG)

Service National de Laboratoire Sante Publique, Cotonou.
Saint Jean de Dieu Hospital of Tanguieta, Benin.

Catherine Okoi (C)

World Health Organization (WHO) Collaborating Centre for New Vaccines Surveillance, Medical Research Council Unit The Gambia at London School of Hygiene and Tropical Medicine, Fajara, Banjul.

Claire Oluwalana (C)

World Health Organization (WHO) Collaborating Centre for New Vaccines Surveillance, Medical Research Council Unit The Gambia at London School of Hygiene and Tropical Medicine, Fajara, Banjul.

Archibald Worwui (A)

World Health Organization (WHO) Collaborating Centre for New Vaccines Surveillance, Medical Research Council Unit The Gambia at London School of Hygiene and Tropical Medicine, Fajara, Banjul.

Peter S Ndow (PS)

World Health Organization (WHO) Collaborating Centre for New Vaccines Surveillance, Medical Research Council Unit The Gambia at London School of Hygiene and Tropical Medicine, Fajara, Banjul.

Jean Nounagnon (J)

Saint Jean de Dieu Hospital of Tanguieta, Benin.

Jason M Mwenda (JM)

WHO Regional Office for Africa, Brazzaville, Republic of Congo.

Rock A Sossou (RA)

WHO Country Office, Cotonou, Benin.

Brenda A Kwambana-Adams (BA)

World Health Organization (WHO) Collaborating Centre for New Vaccines Surveillance, Medical Research Council Unit The Gambia at London School of Hygiene and Tropical Medicine, Fajara, Banjul.

Martin Antonio (M)

World Health Organization (WHO) Collaborating Centre for New Vaccines Surveillance, Medical Research Council Unit The Gambia at London School of Hygiene and Tropical Medicine, Fajara, Banjul.
Microbiology and Infection Unit, Warwick Medical School, University of Warwick, Coventry, United Kingdom.

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