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Meta-Analysis
. 2016 Jun 12;2016(6):CD009163.
doi: 10.1002/14651858.CD009163.pub3.

Antibiotics for otitis media with effusion in children

Affiliations
Meta-Analysis

Antibiotics for otitis media with effusion in children

Roderick P Venekamp et al. Cochrane Database Syst Rev. .

Abstract

Background: Otitis media with effusion (OME) is characterised by an accumulation of fluid in the middle ear behind an intact tympanic membrane, without the symptoms or signs of acute infection. Since most cases of OME will resolve spontaneously, only children with persistent middle ear effusion and associated hearing loss potentially require treatment. Previous Cochrane reviews have focused on the effectiveness of ventilation tube insertion, adenoidectomy, nasal autoinflation, antihistamines, decongestants and corticosteroids in OME. This review, focusing on the effectiveness of antibiotics in children with OME, is an update of a Cochrane review published in 2012.

Objectives: To assess the benefits and harms of oral antibiotics in children up to 18 years with OME.

Search methods: The Cochrane ENT Information Specialist searched the ENT Trials Register; Central Register of Controlled Trials (CENTRAL 2016, Issue 3); PubMed; Ovid EMBASE; CINAHL; Web of Science; ClinicalTrials.gov; ICTRP and additional sources for published and unpublished trials. The date of the search was 14 April 2016.

Selection criteria: Randomised controlled trials comparing oral antibiotics with placebo, no treatment or therapy of unproven effectiveness in children with OME.

Data collection and analysis: We used the standard methodological procedures expected by Cochrane.

Main results: Twenty-five trials (3663 children) were eligible for inclusion. Two trials did not report on any of the outcomes of interest, leaving 23 trials (3258 children) covering a range of antibiotics, participants, outcome measures and time points for evaluation. Overall, we assessed most studies as being at low to moderate risk of bias.We found moderate quality evidence (six trials including 484 children) that children treated with oral antibiotics are more likely to have complete resolution at two to three months post-randomisation (primary outcome) than those allocated to the control treatment (risk ratio (RR) 2.00, 95% confidence interval (CI) 1.58 to 2.53; number needed to treat to benefit (NNTB) 5). However, there is evidence (albeit of low quality; five trials, 742 children) indicating that children treated with oral antibiotics are more likely to experience diarrhoea, vomiting or skin rash (primary outcome) than those allocated to control treatment (RR 2.15, 95% CI 1.29 to 3.60; number needed to treat to harm (NNTH) 20).In respect of the secondary outcome of complete resolution at any time point, we found low to moderate quality evidence from five meta-analyses, including between two and 14 trials, of a beneficial effect of antibiotics, with a NNTB ranging from 3 to 7. Time periods ranged from 10 to 14 days to six months.In terms of other secondary outcomes, only two trials (849 children) reported on hearing levels at two to four weeks and found conflicting results. None of the trials reported data on speech, language and cognitive development or quality of life. Low quality evidence did not show that oral antibiotics were associated with a decrease in the rate of ventilation tube insertion (two trials, 121 children) or in tympanic membrane sequelae (one trial, 103 children), while low quality evidence indicated that children treated with antibiotics were less likely to have acute otitis media episodes within four to eight weeks (five trials, 1086 children; NNTB 18) and within six months post-randomisation (two trials, 199 children; NNTB 5). It should, however, be noted that the beneficial effect of oral antibiotics on acute otitis media episodes within four to eight weeks was no longer significant when we excluded studies with high risk of bias.

Authors' conclusions: This review presents evidence of both benefits and harms associated with the use of oral antibiotics to treat children up to 16 years with OME. Although evidence indicates that oral antibiotics are associated with an increased chance of complete resolution of OME at various time points, we also found evidence that these children are more likely to experience diarrhoea, vomiting or skin rash. The impact of antibiotics on short-term hearing is uncertain and low quality evidence did not show that oral antibiotics were associated with fewer ventilation tube insertions. Furthermore, we found no data on the impact of antibiotics on other important outcomes such as speech, language and cognitive development or quality of life.Even in situations where clear and relevant benefits of oral antibiotics have been demonstrated, these must always be carefully balanced against adverse effects and the emergence of bacterial resistance. This has specifically been linked to the widespread use of antibiotics for common conditions such as otitis media.

PubMed Disclaimer

Conflict of interest statement

AGMS has received an honorarium from GlaxoSmithKline for participating in educational activities and workshops related to pneumococcal vaccination and otitis media. She has received funds from GlaxoSmithKline for research on microbial pathogens in acute tympanostomy tube otorrhoea.

AGMS and MJB are Co‐ordinating Editors of Cochrane ENT, but had no role in the editorial process for this review.

RPV is an Editor for the Cochrane Acute Respiratory Infections Group and Cochrane ENT, but had no role in the editorial process for this review.

TMAvD, AGMS and RPV were involved in research on microbial pathogens in acute tympanostomy tube otorrhoea, partly funded by GlaxoSmithKline.

Figures

1
1
Study flow diagram.
2
2
'Risk of bias' graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
3
3
'Risk of bias' summary: review authors' judgements about each risk of bias item for each included study.
4
4
Forest plot of comparison: 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, outcome: 1.1 Complete resolution of OME at 2 to 3 months.
5
5
Forest plot of comparison: 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, outcome: 1.2 Adverse effects.
1.1
1.1. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 1 Complete resolution of OME at 2 to 3 months.
1.2
1.2. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 2 Adverse effects.
1.3
1.3. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 3 Complete resolution of OME at 2 to 4 weeks.
1.4
1.4. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 4 Complete resolution of OME at more than 6 months.
1.5
1.5. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 5 Complete resolution of OME at end of treatment (10 to 14 days).
1.6
1.6. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 6 Complete resolution of OME at end of treatment (4 weeks).
1.7
1.7. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 7 Complete resolution of OME at end of treatment (3 months).
1.8
1.8. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 8 Complete resolution of OME at end of treatment (6 months).
1.9
1.9. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 9 Insertion of ventilation tubes.
1.10
1.10. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 10 Tympanic membrane sequelae.
1.11
1.11. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 11 AOM within 4 to 8 weeks.
1.12
1.12. Analysis
Comparison 1 Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 12 AOM within 6 months.
2.1
2.1. Analysis
Comparison 2 Sensitivity analysis ‐ Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 1 Complete resolution of OME at 2 to 3 months.
2.2
2.2. Analysis
Comparison 2 Sensitivity analysis ‐ Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 2 Adverse effects.
2.3
2.3. Analysis
Comparison 2 Sensitivity analysis ‐ Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 3 Complete resolution of OME at 2 to 4 weeks.
2.4
2.4. Analysis
Comparison 2 Sensitivity analysis ‐ Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 4 Complete resolution of OME at more than 6 months.
2.5
2.5. Analysis
Comparison 2 Sensitivity analysis ‐ Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 5 Complete resolution of OME at end of treatment (10 to 14 days).
2.6
2.6. Analysis
Comparison 2 Sensitivity analysis ‐ Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 6 Complete resolution of OME at end of treatment (4 weeks).
2.7
2.7. Analysis
Comparison 2 Sensitivity analysis ‐ Antibiotics versus placebo, no treatment or therapy of unproven effectiveness, Outcome 7 AOM within 4 to 8 weeks.

Update of

References

References to studies included in this review

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Thomsen 1989 {published data only}
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Balle 1998 {published data only}
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