Changes in the Nature and Severity of Invasive Pneumococcal Disease in Children Before and After the Seven-valent and Thirteen-valent Pneumococcal Conjugate Vaccine Programs in Calgary, Canada

被引:17
|
作者
Ricketson, Leah J. [1 ]
Conradi, Nicholas G. [6 ]
Vanderkooi, Otto G. [1 ,2 ,3 ,4 ]
Kellner, James D. [1 ,5 ]
机构
[1] Univ Calgary, Alberta Childrens Hosp Res Inst, Dept Pediat, Calgary, AB, Canada
[2] Univ Calgary, Alberta Childrens Hosp Res Inst, Dept Community Hlth Sci Microbiol, Calgary, AB, Canada
[3] Univ Calgary, Alberta Childrens Hosp Res Inst, Dept Immunol & Infect Dis, Calgary, AB, Canada
[4] Univ Calgary, Alberta Childrens Hosp Res Inst, Dept Pathol & Lab Med, Calgary, AB, Canada
[5] Univ Calgary, Alberta Childrens Hosp Res Inst, Dept Community Hlth Sci, Calgary, AB, Canada
[6] Univ Limerick, Grad Entry Med Sch, Limerick, Ireland
关键词
Streptococcus pneumoniae; pneumococcus; pediatric; invasive pneumococcal disease; pneumococcal conjugate vaccine; STREPTOCOCCUS-PNEUMONIAE; EMERGENCY-DEPARTMENT; INFECTIONS; CARRIAGE; TRENDS; ERA; EPIDEMIOLOGY; SURVEILLANCE; POPULATION; MENINGITIS;
D O I
10.1097/INF.0000000000001709
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Since the introduction of childhood pneumococcal conjugate vaccines, invasive pneumococcal disease (IPD) incidence has decreased in children and the predominant serotypes causing disease have changed. This study describes changes in the clinical features of IPD in children (<18 years) before and after the conjugate vaccine introduction. Methods: The Calgary Area Streptococcus pneumoniae Epidemiology Research study collects information on all IPD cases in Calgary, Alberta, Canada. Descriptive and regression analyses were used to compare IPD in the pre-vaccine (January 2000 to August 2002), post-7-valent protein-polysaccharide conjugate vaccine (September 2002 to June 2010) and post-13-valent protein-polysaccharide conjugate vaccine (PCV13) (July 2010 to December 2015) periods; intensive care unit and inpatient admissions were outcome measures. Results: The incidence of IPD in children (<18 years) decreased from an average of 17 cases/100,000/yr in 2000-2001 to 4 cases/100,000/yr in 2015. The median age of children presenting with IPD shifted from 2.0 years (interquartile range: 2.5) in the pre-vaccine period to 3.9 years (interquartile range: 6.2) in the post-PCV13 period. The proportion of children with a comorbidity that is an indication for pneumococcal vaccination did not change. Invasive disease with focus (meningitis, pneumonia, empyema, peritonitis) compared with invasive disease with bacteremia only increased from 44.6% in pre-vaccine to 64.0% and 61.4% in the post-7-valent protein-polysaccharide conjugate vaccine and post-PCV13 periods, respectively (P = 0.017). Having IPD in the post-PCV13 period compared with the pre-vaccine period was associated with an increased odds of hospitalization [Odds ratio (OR): 2.9; 95% Confidence Interval (CI): 1.4-6.2]. Conclusions: Clinical features of IPD have changed since pneumococcal conjugate vaccines were introduced, with a shift toward more focal infections requiring hospitalization. Although overall IPD cases have declined, disease that does occur appears to be more severe.
引用
收藏
页码:22 / 27
页数:6
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