Nasopharyngeal Carriage of Streptococcus pneumoniae in Healthy Children: Implications for the Use of Heptavalent Pneumococcal Conjugate Vaccine

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http://www.medscape.com/viewarticle/432528?srcmp=ped-052402

Nasopharyngeal Carriage of Streptococcus pneumoniae in Healthy Children: Implications for the Use of Heptavalent Pneumococcal Conjugate Vaccine


 

from Emerging Infectious Diseases

Paola Marchisio, Susanna Esposito, Gian Carlo Schito, Anna Marchese, Roberta Cavagna, Nicola Principi, and the Hercules Project Collaborative Group


 

Abstract and Introduction

Abstract

We assessed the prevalence of Streptococcus pneumoniae serotypes in the nasopharynx of healthy children, antimicrobial susceptibility patterns, risk factors for carriage, and the coverage of heptavalent pneumococcal conjugate vaccine. In 2,799 healthy infants and children, the S. pneumoniae carrier rate was 8.6% (serotypes 3, 19F, 23F, 19A, 6B, and 14 were most common). Most pneumococci (69.4%) were resistant to one or more antimicrobial classes. The rate of penicillin resistance was low (9.1%); macrolide resistance was high (52.1%). Overall, 63.2% of the isolates belonged to strains covered by the heptavalent pneumococcal vaccine. This percentage was higher in children <2 years old (73.1%) and in those ages 2-5 years (68.9%). Sinusitis in the previous 3 months was the only risk factor for carrier status; acute otitis media was the only risk factor for the carriage of penicillin-resistant S. pneumoniae. Most isolated strains are covered by the heptavalent conjugate vaccine, especially in the first years of life, suggesting that its use could reduce the incidence of pneumococcal disease.

 

Introduction

The nasopharynx of children has resident microbial flora that do not usually harm the child but, in some cases, constitute a reservoir of pathogens implicated in respiratory tract infections and invasive diseases[1,2]. The bacteria carried in the nasopharynx of healthy children reflect the infection-causing strains currently circulating in the community[3], and so studies of the prevalence of different pathogens and their resistance patterns can provide useful indications for more rational therapeutic and preventive strategies.

The asymptomatic nasopharyngeal carriage of Streptococcus pneumoniae is widely prevalent in young children and has been related to the development of disease and the spread of the pathogen[4,5]; furthermore, nasopharyngeal colonization by antibiotic-resistant S. pneumoniae has steadily increased over the last few years[6,7]. Antibiotic-resistant strains are more often carried by infants and young children than adults and belong to a limited number of serotypes that are also some of the most common causes of invasive pediatric diseases[8-10].

A heptavalent conjugate vaccine, which includes the most common serotypes involved in invasive diseases, effectively induces protection against pneumococcal nasopharyngeal carriage[11,12]. However, while the vaccine is statistically effective in preventing carriage of vaccine-related strains, a number of reports show an increase in the percentage of nonvaccine strains in immunized patients[13,14].

We assessed the prevalence of different S. pneumoniae serotypes in the nasopharynx of healthy children attending day-care centers and primary schools, determined their antimicrobial susceptibility to a wide range of therapeutic compounds, identified the risk factors for carrier status, and defined the possible coverage provided by the heptavalent pneumococcal conjugate vaccine during the first years of life.

 

 


 

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Paola Marchisio, Susanna Esposito, University of Milan, Milan, Italy; Gian Carlo Schito, Anna Marchese, University of Genoa, Genoa, Italy; Roberta Cavagna, Nicola Principi, University of Milan, Milan, Italy; and the Hercules Project Collaborative Group

Dr. Marchisio is associate professor of pediatrics at the University of Milan. Her main interests are antibiotic resistance, bacterial pathogenesis, and pediatric infectious diseases, particularly upper respiratory tract infections,.


 


Emerg Infect Dis 8(5), 2002. © 2002 Centers for Disease Control and Prevention (CDC)



 

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