Streptococcus pneumoniae carriage among febrile children at the time of PCV-10 immunization in pediatric emergencies at Mohammed VI University Hospital Centre in Marrakesh (Morocco).


Journal

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
ISSN: 1769-664X
Titre abrégé: Arch Pediatr
Pays: France
ID NLM: 9421356

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 22 12 2017
revised: 17 07 2019
accepted: 26 08 2019
pubmed: 28 10 2019
medline: 1 5 2020
entrez: 25 10 2019
Statut: ppublish

Résumé

In Morocco, 13-valent pneumococcal conjugated vaccine (PCV) was introduced in the childhood immunization program in October 2010 and changed to PCV-10 in July 2012. The purpose of this study was firstly to determine the prevalence of pneumococcus carriage in a population of febrile infants in Marrakesh and secondly, to investigate the risk factors for carriage and the distribution of circulating serotypes. This prospective study was conducted from February to June 2017, in the pediatric emergency department of the Mother and Child Hospital of Mohammed VI University Hospital Centre (UHC) in Marrakesh. At total of 183febrile infants, aged 2-18months, were enrolled in this study and were swabbed for nasopharyngeal carriage. Pneumococci were cultured, identified, serotyped, and tested for penicillin susceptibility. Demographic data and risk factors for carriage were collected. The statistical analyses performed were the following: the analysis of the risk factors using logistic regression, the estimation of serotype diversity with the Simpson index, and the Chi The prevalence of Streptococcus pneumoniae carriage was 68.3%. Of the 183infants enrolled in this study, 111 had received at least one dose of PCV-10. Colonization by vaccine serotype among febrile children was related to incomplete vaccination status. In total, vaccine serotypes accounted for 6.4% (n=8): 19F (n=2), 1 (n=2) and one strain for each of the following serotypes: 14, 23F, 6B, and 9V. Non-vaccine and nontypeable strains presented 63.2% and 23.2%, respectively, with dominance of serotypes 6A (6.4%), 15A/15F (5.6%), 20, 22F/22A, 23B, and 11A/11D with a prevalence of 3.2%. The rate of pneumococcus strains with reduced susceptibility to penicillin was 33.6%, of which 90.2% were non-vaccine serotypes and nontypeable strains. Serotype diversity increased in the postvaccination period and the effectiveness of PCV-10 against vaccine serotypes was estimated at 89.6%. An important change in the distribution of vaccine and non-vaccine serotypes was observed after the introduction of the PCVs. In fact, the prevalence of vaccine serotypes decreased significantly while non-vaccine serotypes emerged. These results underscore the importance of maintaining close and prolonged surveillance of serotype distribution to monitor the dynamics of nasopharyngeal pneumococcal carriage.

Identifiants

pubmed: 31645292
pii: S0929-693X(19)30137-X
doi: 10.1016/j.arcped.2019.08.008
pii:
doi:

Substances chimiques

10-valent pneumococcal conjugate vaccine 0
Pneumococcal Vaccines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

453-458

Informations de copyright

Copyright © 2019 French Society of Pediatrics. Published by Elsevier Masson SAS. All rights reserved.

Auteurs

I Dilagui (I)

Microbiology Laboratory, University Hospital Centre Mohammed VI, Avenue Ibn Sina Amerchich, BP 2360, Marrakesh, Morocco; Faculty of Medicine and Pharmacy - Cadi Ayyad University- Sidi Abbad, B.P. 7010, Marrakesh, Morocco. Electronic address: ilhamdilagui@gmail.com.

F Z Moussair (FZ)

Microbiology Laboratory, University Hospital Centre Mohammed VI, Avenue Ibn Sina Amerchich, BP 2360, Marrakesh, Morocco; Faculty of Medicine and Pharmacy - Cadi Ayyad University- Sidi Abbad, B.P. 7010, Marrakesh, Morocco.

S Loqman (S)

Microbiology Laboratory, University Hospital Centre Mohammed VI, Avenue Ibn Sina Amerchich, BP 2360, Marrakesh, Morocco; Faculty of Medicine and Pharmacy - Cadi Ayyad University- Sidi Abbad, B.P. 7010, Marrakesh, Morocco.

I Diawara (I)

Microbiology Laboratory, Faculty of Medicine and Pharmacy, Hassan II University of Casablanca, BP 5696, Casablanca, Morocco; Faculty of Health Sciences and Techniques, Mohammed VI University of Health Sciences (UM6SS), Casablanca, Morocco.

K Zerouali (K)

Microbiology Laboratory, Faculty of Medicine and Pharmacy, Hassan II University of Casablanca, BP 5696, Casablanca, Morocco; Microbiology Laboratory, Ibn Rochd University Hospital Centre, 1, rue des hôpitaux, Casablanca, Morocco.

H Belabbes (H)

Microbiology Laboratory, Faculty of Medicine and Pharmacy, Hassan II University of Casablanca, BP 5696, Casablanca, Morocco; Microbiology Laboratory, Ibn Rochd University Hospital Centre, 1, rue des hôpitaux, Casablanca, Morocco.

S Zouhair (S)

Microbiology-Virology Laboratory, Avicenna Military Hospital, Gueliz, Avenue Al Mouqaouama, 40000, Marrakesh, Morocco; Faculty of Medicine and Pharmacy - Cadi Ayyad University- Sidi Abbad, B.P. 7010, Marrakesh, Morocco.

M Bourouss (M)

Pediatric Emergency Department, Mohammed VI University Hospital Centre, Avenue Ibn Sina Amerchich, BP 2360, Marrakesh, Morocco; Faculty of Medicine and Pharmacy - Cadi Ayyad University- Sidi Abbad, B.P. 7010, Marrakesh, Morocco.

M Bouskraoui (M)

Pediatric Department A, Mohammed VI University Hospital Centre Marrakesh, Avenue Ibn Sina Amerchich, BP 2360, Morocco; Faculty of Medicine and Pharmacy - Cadi Ayyad University- Sidi Abbad, B.P. 7010, Marrakesh, Morocco.

N Soraa (N)

Microbiology Laboratory, University Hospital Centre Mohammed VI, Avenue Ibn Sina Amerchich, BP 2360, Marrakesh, Morocco; Faculty of Medicine and Pharmacy - Cadi Ayyad University- Sidi Abbad, B.P. 7010, Marrakesh, Morocco.

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