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Invasive pneumococcal disease in a pediatric population, Auckland, New Zealand

 

作者: LESLEY VOSS,   DIANA LENNON,   KARA OKESENE-GAFA,   SHANTHI AMERATUNGA,   DIANA MARTIN,  

 

期刊: The Pediatric Infectious Disease Journal  (OVID Available online 1994)
卷期: Volume 13, issue 10  

页码: 873-877

 

ISSN:0891-3668

 

年代: 1994

 

出版商: OVID

 

关键词: Streptococcus pneumoniae;meningitis;serotype;vaccine;surveillance

 

数据来源: OVID

 

摘要:

Streptococcus pneumoniaeis one of the major invasive pathogens in childhood. The increasing worldwide prevalence of penicillin-resistant strains makes management of invasive infections difficult and underscores the need for effective vaccines. Currently avaialable vaccines are of limited value in the pediatric age group. Trials are taking place to evaluate conjugated pneumococcal vaccines and in view of this it is important to establish local epidemiology of pneumococcal disease. The aims of this population-based study were to review all of the cases of invasive pneumococcal disease occurring during a 9-year period (1984 to 1992) in Auckland, New Zealand. Through the use of laboratory records and hospital discharge codes, 413 isolates from 407 patients were found. Age-specific incidence for all invasive disease was 22.0/100 000 for children less than 15 years old but 56.0/100 000 for children less than 5 years old (X2Yates corrected 18.20;P= 0.001). Two-thirds were less than 2 years old. The rates were higher in Maori and Pacific Island children than in Caucasian children. A total of 70 isolates from 68 patients with meningitis occurred. The majority were less than 5 years old (incidence of meningitis was 10.0/100 000) and 84% were less than 2 years old. The overall mortality from meningitis was 4.3%. Of the 129 isolates serogrouped or serotyped, 14, 6 and 19 accounted for 23%, 16% and 16%, respectively, of cases. Although 98% of serotypes identified would be covered by the currently available 23-valent vaccine, two-thirds of the children affected by these isolates would be unprotected because of poor immunogenicity of polysaccharide vaccines in children less than 2 years old.

 

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