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    Vaccines for preventing influenza in healthy children

    Tom Jefferson1, Alessandro Rivetti2, Anthony Harnden3, Carlo Di Pietrantonj2, Vittorio

    Demicheli4

    1

    Vaccines Field, The Cochrane Collaboration, Roma, Italy.2

    Servizio Regionale diRiferimento per l'Epidemiologia, SSEpi-SeREMI - Cochrane Vaccines Field, Azienda

    Sanitaria Locale ASL AL, Alessandria, Italy. 3Department of Primary Health Care, Institute

    of Health Sciences, Oxford, UK. 4Health Councillorship - Servizio Regionale di Riferimento

    per l'Epidemiologia, SSEpi-SeREMI - Cochrane Vaccines Field, Regione Piemonte -

    Azienda Sanitaria Locale ASL AL, Torino, Italy

    Contact address: Tom Jefferson, Vaccines Field, The Cochrane Collaboration, Via Adige

    28a, Anguillara Sabazia, Roma, 00061, [email protected]@assr.it;

    [email protected].(Editorial group:Cochrane Acute Respiratory Infections Group.)

    Cochrane Database of Systematic Reviews, Issue 4, 2008 (Status in this issue: Unchanged)Copyright 2008 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

    DOI: 10.1002/14651858.CD004879.pub3

    This version first published online: 23 April 2008 in Issue 2, 2008. Last assessed as up-to-

    date: 29 September 2007

    This record should be cited as: Jefferson T, Rivetti A, Harnden A, Di Pietrantonj C,

    Demicheli V. Vaccines for preventing influenza in healthy children. Cochrane Database of

    Systematic Reviews2008, Issue 2. Art. No.: CD004879. DOI:

    10.1002/14651858.CD004879.pub3.

    Abstract

    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 influenzavaccines.

    Search strategy

    We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane

    Library2007, issue 3); OLD MEDLINE (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.

    mailto:[email protected]:[email protected]:[email protected]:[email protected];%[email protected]:[email protected];%[email protected]:[email protected];%[email protected]:[email protected];%[email protected]://www.mrw.interscience.wiley.com/cochrane/clabout/articles/ARI/frame.htmlhttp://www.mrw.interscience.wiley.com/cochrane/clabout/articles/ARI/frame.htmlhttp://www.mrw.interscience.wiley.com/cochrane/clabout/articles/ARI/frame.htmlhttp://www.mrw.interscience.wiley.com/cochrane/clabout/articles/ARI/frame.htmlmailto:[email protected];%[email protected]:[email protected];%[email protected]:[email protected]
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    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, livevaccines 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 availablefor 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.

    Plain language summary

    Vaccines for preventing influenza in healthy children

    Children and the elderly are the two age groups that appear to have the most complications

    following an influenza infection. Influenza has a viral origin and often results in an acute

    respiratory illness affecting the lower or upper parts respiratory tract, or both. Viruses are

    mainly of two subtypes (A or B) and spread periodically during the autumn-winter months.

    Many other viruses however, can also cause illness of the respiratory tract.

    Diffusion and severity of the disease could be very different during different epidemics.

    Efforts to contain epidemic diffusion rely mainly on widespread vaccination. Recent policy

    from several internationally-recognised institutions, recommend immunisation of healthy

    children between 6 and 23 month of age (together with their contacts) as a public health

    measure.

    The review authors found that in children aged from two years, nasal spray vaccines made

    from weakened influenza viruses were better at preventing illness caused by the influenza

    virus (82% of illnesses were prevented) than injected vaccines made from the killed virus

    (59%). Neither type was particularly good at preventing 'flu-like illness' caused by other

    types of viruses (33% and 36% respectively). In children under the age of two, the efficacy of

    inactivated vaccine was similar to placebo. It was not possible to analyse the safety of

    vaccines from the studies due to the lack of standardisation in the information given but very

    little information was found on the safety of inactivated vaccines, the most commonly usedvaccine, in young children.

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