Pneumococcal serogroups and serotypes in severe pneumococcal pneumonia in Belgian children:: Theoretical coverage of the 7-valent and 9-valent pneumococcal conjugate vaccines

被引:12
作者
De Schutter, Iris
Malfroot, Anne
Pierard, Denis
Lauwers, Sabine
机构
[1] Vrije Univ Brussels, Acad Ziekenhuis, Dept Pediat, Pediat Resp Med & Cyst Fibrosis Clin, B-1090 Brussels, Belgium
[2] Cyst Fibrosis Clin & Infectiol, Brussels, Belgium
[3] Vrije Univ Brussels, Acad Ziekenhuis, Dept Microbiol, B-1090 Brussels, Belgium
关键词
community acquired pneumonia; Streptococcus pneumoniae; pneumococcal pneumonia; childhood; vaccine preventable disease; pneumococcal conjugate vaccine coverage;
D O I
10.1002/ppul.20437
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
Background: Although the causative pneumococcal serotypes of invasive diseases are already extensively studied, few data are available about the pneumococcal serotypes additionally isolated from broncho-alveolar lavage samples in childhood pneumonia. Study aim: To identify the causative pneumococcal serotypes in culture proven childhood community acquired pneumonia (CAP) and to calculate the effectiveness of the heptavalent and nonavalent pneumococcal vaccine (7- and 9-valent PnV) in severe pneumococcal pneumonia. Methods: All pneumococcal isolates stored from broncho-alveolar lavage, blood culture and pleural fluid in healthy children with CAP were characterized. Results: Seventy children (median age 2 years 3.5 months) could be included. The most prevalent serotypes were: SGT1 (21.4%), SGT6 (20.0%), SGT19 (12.8%), SGT23 (10.0%), and SGT14 (7.1%). SGT1 was especially prevalent in complicated cases and children >5 years. This first ranking of SGT1 is not reported in invasive pneumococcal disease studies. The overall theoretical coverage of the 7-valent PnV and the 9-valent PnV for pneumococcal pneumonia was 45.7% and 72.8%. The theoretical coverage of both vaccines was equal for non-invasive pneumonia (64%) but the theoretical coverage of the 9-valent PnV for invasive pneumonia was much higher (79% vs. 37.2%). Antibiotic susceptibility to penicillin was 84%, 70% to tetracycline and 61% to erythromycin; however only one strain (MIC = 4 mg/L) was highly resistant to penicillin. Conclusions: Based on this serotyping, the theoretical coverage of the 7-valent PnV for proven pneumococcal pneumonia is good but decreases with age. A 9-valent PnV containing SGT1 could significantly increase the coverage, especially for invasive pneumonia. According to these data, penicillin remains the first choice antibiotic treatment for childhood CAP in Belgium.
引用
收藏
页码:765 / 770
页数:6
相关论文
共 22 条
[1]
Postlicensure surveillance for pneumococcal invasive disease after use of heptavalent pneumococcal conjugate vaccine in Northern California Kaiser Permanente [J].
Black, S ;
Shinefield, H ;
Baxter, R ;
Austrian, R ;
Bracken, L ;
Hansen, J ;
Lewis, E ;
Fireman, B .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2004, 23 (06) :485-489
[2]
Effectiveness of heptavalent pneumococcal conjugate vaccine in children younger than five years of age for prevention of pneumonia [J].
Black, SB ;
Shinefield, HR ;
Ling, S ;
Hansen, J ;
Fireman, B ;
Spring, D ;
Noyes, J ;
Lewis, E ;
Ray, P ;
Lee, J ;
Hackell, J .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2002, 21 (09) :810-815
[3]
Geographic distribution and clonal diversity of Streptococcus pneumoniae serotype 1 isolates [J].
Brueggemann, AB ;
Spratt, BG .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (11) :4966-4970
[4]
An epidemiological investigation of a sustained high rate of pediatric parapneumonic empyema: Risk factors and microbiological associations [J].
Byington, CL ;
Spencer, LY ;
Johnson, TA ;
Pavia, AT ;
Allen, D ;
Mason, EO ;
Kaplan, S ;
Carroll, KC ;
Daly, JA ;
Christenson, JC ;
Samore, MH .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (04) :434-440
[5]
Serotypes and sequence types of pneumococci causing invasive disease in Scotland prior to the introduction of pneumococcal conjugate polysaccharide vaccines [J].
Clarke, SC ;
Scott, KJ ;
McChlery, SM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (10) :4449-4452
[6]
Efficacy of nine-valent pneumococcal conjugate vaccine against pneumonia and invasive pneumococcal disease in The Gambia: randomised, double-blind, placebo-controlled trial [J].
Cutts, FT ;
Zaman, SMA ;
Enwere, G ;
Jaffar, S ;
Levine, OS ;
Okoko, JB ;
Oluwalana, C ;
Vaughan, A ;
Obaro, SK ;
Leach, A ;
McAdam, KP ;
Biney, E ;
Saaka, M ;
Onwuchekwa, U ;
Yallop, F ;
Pierce, NF ;
Greenwood, BM ;
Adegbola, RA .
LANCET, 2005, 365 (9465) :1139-1146
[7]
de Blic J, 2000, EUR RESPIR J, V15, P217
[8]
Efficacy of a pneumococcal conjugate vaccine against acute otitis media [J].
Eskola, J ;
Kilpi, T ;
Palmu, A ;
Jokinen, J ;
Haapakoski, J ;
Herva, E ;
Takala, A ;
Käyhty, H ;
Karma, P ;
Kohberger, R ;
Siber, G ;
Mäkela, PH ;
Lockhart, S ;
Ecrola, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (06) :403-409
[9]
Theoretic coverage of heptavalent pneumococcal conjugate vaccine in the prevention of community-acquired pneumonia in children in Italy [J].
Esposito, S ;
Madore, DV ;
Gironi, S ;
Bosis, S ;
Tosi, S ;
Bianchi, C ;
Cimino, C ;
Principi, N .
VACCINE, 2003, 21 (21-22) :2704-2707
[10]
Streptococcus pneumoniae bacteraemia in Belgium:: differential characteristics in children and the elderly population and implications for vaccine use [J].
Flamaing, J ;
Verhaegen, J ;
Peetermans, WE .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 50 (01) :43-50