Journal
BMJ-BRITISH MEDICAL JOURNAL
Volume 339, Issue -, Pages -Publisher
BMJ PUBLISHING GROUP
DOI: 10.1136/bmj.b4984
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Funding
- Health Technology Assessment Programme
- MRC [MC_U122797165, MC_U122785828, G0501681] Funding Source: UKRI
- Medical Research Council [MC_U122785828, MC_U122797165, U1475000004, G0501681] Funding Source: researchfish
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Objective To determine the clinical effectiveness of topical intranasal corticosteroids in children with bilateral otitis media with effusion. Design Double blind randomised placebo controlled trial. Setting 76 Medical Research Council General Practice Research Framework practices throughout the United Kingdom, between 2004 and 2007. Participants 217 children aged 4-11 years who had at least one practice recorded episode of otitis media or a related ear problem in the previous 12 months, and with bilateral otitis media with effusion confirmed by a research nurse using otoscopy plus micro-tympanometry (B/B or B/C2, modified Jerger types). Intervention Mometasone furoate 50 mu g or placebo spray given once daily into each nostril for three months. Main outcome measures Proportions of children cured of bilateral otitis media with effusion assessed with tympanometry (C1 or A type) at one month (primary end point), three months, and nine months; adverse events; three month diary symptoms. Results 41% (39/96) of the topical steroid group and 45% (44/98) of the placebo group were cured in one or both ears at one month (difference favouring placebo 4.3% (95% confidence interval -9.3% to 18.1%). Poisson regression was done with adjustment for four pre-specified covariates (clinical severity, P=0.003; atopy, P=0.67; age, P=0.92; season, P=0.71). The adjusted relative risk at one month was 0.97 (95% confidence interval 0.74 to 1.26). At three months, 58% of the topical steroid group and 52% of the placebo group were cured (relative risk 1.23, 0.84 to 1.80). Diary symptoms did not differ between the two groups, and no significant harms were reported. Conclusions Topical steroids are unlikely to be an effective treatment for otitis media with effusion in general practice. High rates of natural resolution occurred by 1-3 months. Trial registration Current Controlled Trials ISRCTN38988331; National Research Register NO575123823; MREC 03/11/073.
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