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. 2015 Jan;94(2):e320.
doi: 10.1097/MD.0000000000000320.

Etiology and antimicrobial susceptibility of middle ear fluid pathogens in Costa Rican children with otitis media before and after the introduction of the 7-valent pneumococcal conjugate vaccine in the National Immunization Program: acute otitis media microbiology in Costa Rican children

Affiliations

Etiology and antimicrobial susceptibility of middle ear fluid pathogens in Costa Rican children with otitis media before and after the introduction of the 7-valent pneumococcal conjugate vaccine in the National Immunization Program: acute otitis media microbiology in Costa Rican children

Arturo Abdelnour et al. Medicine (Baltimore). 2015 Jan.

Abstract

Acute otitis media (AOM) microbiology was evaluated in children after 7-valent pneumococcal conjugate vaccine (PCV7) introduction in Costa Rica (private sector, 2004; National Immunization Program, 2009). This was a combined prospective and retrospective study conducted in a routine clinical setting in San José, Costa Rica. In the prospective part of the study, which was conducted post-PCV7 introduction (2010-2012), standard bacteriological procedures were used to evaluate the etiology and serotype distribution of middle ear fluid samples collected by tympanocentesis or otorrhea from children aged 3-59 months diagnosed with AOM. E-tests were used to evaluate antimicrobial susceptibility in culture-positive samples. Retrospective data recorded between 1999 and 2004 were used for comparison of bacterial etiology and serotype distribution before and after PCV7 introduction. Statistical significance was evaluated in bivariate analyses at the P-value < 0.05 level (without multiplicity correction). Post-PCV7 introduction, Haemophilus influenzae was detected in 118/456 and Streptococcus pneumoniae in 87/456 AOM episodes. Most H. influenzae isolates (113/118) were non-typeable. H. influenzae was more (27.4% vs 20.8%) and S. pneumoniae less (17.1% vs 25.5%) frequently observed in vaccinated (≥ 2 PCV7 doses or ≥ 1 PCV7 dose at >1 year of age) versus unvaccinated children. S. pneumoniae non-susceptibility rates were 1.1%, 34.5%, 31.7%, and 50.6% for penicillin, erythromycin, azithromycin, and trimethoprim/sulfamethoxazole (TMP-SMX), respectively. H. influenzae non-susceptibility rate was 66.9% for TMP-SMX. Between pre- and post-PCV7 introduction, H. influenzae became more (20.5% vs 25.9%; P-value < 0.001) and S. pneumoniae less (27.7% vs 19.1%; P-value = 0.002) prevalent, and PCV7 serotype proportions decreased among pneumococcal isolates (65.8% vs 43.7%; P-value = 0.0005). Frequently identified pneumococcal serotypes were 19F (34.2%), 3 (9.7%), 6B (9.7%), and 14 (9.7%) pre-PCV7 introduction, and 19F (27.6%), 14 (8.0%), and 35B (8.0%) post-PCV7 introduction. Following PCV7 introduction, a change in the distribution of AOM episodes caused by H. influenzae and pneumococcal serotypes included in PCV7 was observed in Costa Rican children. Pneumococcal vaccines impact should be further evaluated following broader vaccination coverage.

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Conflict of interest statement

AAb, CS, and NP have no conflict of interest to declare. AAr declares his institution having received grants, consulting fees or honorarium, provision of writing assistance, medical equipment or administrative support during the conduct of the study. Outside the submitted work, his institution has received board membership and consultancy fees, grants and payments for lectures, including service on speaker's bureau. AAr is currently an employee of Pfizer Inc. RD reports his institution having received grants from Crucell, MSD, and Pfizer, and having received consulting fee and honorarium from Crucell, MSD, Novartis, Pfizer, and the GlaxoSmithKline Group of companies. During the conduct of the study, he was also a speaker for Crucell, GlaxoSmithKline Group of companies, and Pfizer. Outside the submitted work, his institution has received grants from Crucell, GlaxoSmithKline Group of companies, MSD, Novartis, Pfizer, and he received payments for lectures including service on speakers bureau from Crucell, the GlaxoSmithKline Group of companies, and Pfizer. EO-B, J-YP, MMC, RC, RDA, MVD are employees of the GlaxoSmithKline Group of companies. At the time of study conduct and analysis, MVD was an employee of the GlaxoSmithKline group of companies. EO-B, MMC, MVD, RC, and RDA also own stock/stock options or shares/restricted shares. J-YP declares receiving fees for participation in review activities, such as data monitoring boards, statistical analysis, end point committees, and MMC receiving consulting fee and honorarium during the conduct of the study.

Figures

FIGURE 1
FIGURE 1
Bacterial etiology by type of episode (final study analysis). N = number of episodes; Where co-infections occurred, both bacteria were reported independently in the relevant category.
FIGURE 2
FIGURE 2
Bacterial etiology by vaccination status (final study analysis). N = number of episodes; Where co-infections occurred, both bacteria were reported independently in the relevant category; Children were classified as vaccinated against pneumococcal diseases if they had received ≥2 PCV7 doses at any age or ≥1 PCV7 dose at >1 year of age.

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