Vaccines for preventing influenza in healthy children

被引:186
作者
Jefferson, T.
Rivetti, A.
Harnden, A.
Di Pietrantonj, C.
Demicheli, V
机构
[1] Vaccines Field, Cochrane Collaboration, Roma
[2] Servizio Regionale di Riferimento Per l'Epidemiologia, SSEpi-SeREMI - Cochrane Vaccines Field, Azienda Sanitaria Locale ASL AL, Alessandria
[3] Department of Primary Health Care, Institute of Health Sciences, Oxford
[4] Health Councillorship - Servizio Regionale di Riferimento Per l'Epidemiologia, SSEpi-SeREMI - Cochrane Vaccines Field, Regione Piemonte - Azienda Sanitaria Locale ASL AL, Torino
[5] Vaccines Field, Cochrane Collaboration, Anguillara Sabazia, Roma, 00061
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2008年 / 02期
关键词
D O I
10.1002/14651858.CD004879.pub3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The consequences of influenza in children and adults are mainly absenteeism from school and work. However, the risk of complications is greatest in children and people over 65 years old. Objectives To appraise all comparative studies evaluating the effects of influenza vaccines in healthy children; assess vaccine efficacy (prevention of confirmed influenza) and effectiveness (prevention of influenza-like illness) and document adverse events associated with influenza vaccines. Search strategy We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (T h e Cochrane Library 2007, issue 3); OLDMEDLINE (1950 to 1965); MEDLINE (1966 to September 2007); EMBASE (1974 to September 2007); Biological Abstracts (1969 to September 2007); and Science Citation Index (1974 to September 2007). Selection criteria Randomised controlled trials (RCTs), cohort and case-control studies of any influenza vaccine in healthy children under 16 years of age. Data collection and analysis Two review authors independently assessed trial quality and extracted data. Main results Fifty-one studies with 294,159 observations were included. Sixteen RCTs and 18 cohort studies were included in the analysis of vaccine efficacy and effectiveness. From RCTs, live vaccines showed an efficacy of 82% (95% confidence interval (CI) 71% to 89%) and an effectiveness of 33%( 95% CI 28% to 38%) in children older than two compared with placebo or no intervention. Inactivated vaccines had a lower efficacy of 59%( 95% CI 41% to 71%) than live vaccines but similar effectiveness: 36%( 95% CI 24% to 46%). In children under two, the efficacy of inactivated vaccine was similar to placebo. Variability in study design and presentation of data was such that a meta-analysis of safety outcome data was not feasible. Extensive evidence of reporting bias of safety outcomes from trials of live attenuated vaccines impeded meaningful analysis. Authors' conclusions Influenza vaccines are efficacious in children older than two but little evidence is available for children under two. There was a marked difference between vaccine efficacy and effectiveness. No safety comparisons could be carried out, emphasizing the need for standardisation of methods and presentation of vaccine safety data in future studies. It was surprising to find only one study of inactivated vaccine in children under two years, given current recommendations to vaccinate healthy children from six months old in the USA and Canada. If immunisation in children is to be recommended as a public health policy, large-scale studies assessing important outcomes and directly comparing vaccine types are urgently required.
引用
收藏
页数:252
相关论文
共 167 条
[41]   Direct and total effectiveness of the intranasal, live-attenuated, trivalent cold-adapted influenza virus vaccine against the 2000-2001 influenza A(H1N1) and B epidemic in healthy children [J].
Gaglani, MJ ;
Piedra, PA ;
Herschler, GB ;
Griffith, ME ;
Kozinetz, CA ;
Riggs, MW ;
Fewlass, C ;
Halloran, ME ;
Longini, IM ;
Glezen, WP .
ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE, 2004, 158 (01) :65-73
[42]  
Gendon Iu Z, 2004, Zh Mikrobiol Epidemiol Immunobiol, P62
[43]   The safety of trivalent influenza vaccine among healthy children 6 to 24 months of age [J].
Goodman, MJ ;
Nordin, JD ;
Harper, P ;
DeFor, T ;
Zhou, XZ .
PEDIATRICS, 2006, 117 (05) :E821-E826
[44]  
GRIGORIEVA EP, 1994, VOP VIRUSOL+, V39, P26
[45]   Safety and immunogenicity of a purified F protein respiratory syncytial virus (PFP-2) vaccine in seropositive children with bronchopulmonary dysplasia [J].
Groothuis, JR ;
King, SJ ;
Hogerman, DA ;
Paradiso, PR ;
Simoes, EAF .
JOURNAL OF INFECTIOUS DISEASES, 1998, 177 (02) :467-469
[46]   SAFETY AND IMMUNOGENICITY OF A PURIFIED HEMAGGLUTININ ANTIGEN IN VERY YOUNG HIGH-RISK CHILDREN [J].
GROOTHUIS, JR ;
LEHR, MV ;
LEVIN, MJ .
VACCINE, 1994, 12 (02) :139-141
[47]   CONTROLLED DOUBLE-BLIND COMPARISON OF REACTOGENICITY, IMMUNOGENICITY, AND PROTECTIVE EFFICACY OF WHOLE-VIRUS AND SPLIT-PRODUCT INFLUENZA VACCINES IN CHILDREN [J].
GROSS, PA ;
ENNIS, FA ;
GAERLAN, PF ;
DENSON, LJ ;
DENNING, CR ;
SCHIFFMAN, D .
JOURNAL OF INFECTIOUS DISEASES, 1977, 136 (05) :623-632
[48]  
GROSS PA, 1982, PEDIATRICS, V70, P982
[49]   REACTOGENICITY AND IMMUNOGENICITY OF BIVALENT INFLUENZA VACCINE IN ONE-DOSE AND 2-DOSE TRIALS IN CHILDREN - SUMMARY [J].
GROSS, PA .
JOURNAL OF INFECTIOUS DISEASES, 1977, 136 :S616-S625
[50]   LIVE ATTENUATED AND INACTIVATED INFLUENZA VACCINE IN SCHOOL-AGE-CHILDREN [J].
GRUBER, WC ;
TABER, LH ;
GLEZEN, WP ;
CLOVER, RD ;
ABELL, TD ;
DEMMLER, RW ;
COUCH, RB .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1990, 144 (05) :595-600