A blinded in‐vitro study to compare the efficacy of five topical ear drops in clearing grommets blocked with thick middle ear effusion fluid1

Objective:  To compare the efficacy of 5% NaHCO3, 3% H2O2, Sofradex (dexamethasone sodium metasulphobenzoate 0.05%, framycetin sulphate 0.5%, gramicidin 0.005%), 0.33% acetic acid and 0.9% NaCl eardrops in clearing grommets blocked with harvested thick middle ear effusion fluid. Study design:  A bli...

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Veröffentlicht in:Clinical otolaryngology 2005-02, Vol.30 (1), p.29-34
Hauptverfasser: Uppal, S., Sharma, R., Nadig, S.K., Back, G., England, R.J.A., Coatesworth, A.P.
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Sprache:eng
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Zusammenfassung:Objective:  To compare the efficacy of 5% NaHCO3, 3% H2O2, Sofradex (dexamethasone sodium metasulphobenzoate 0.05%, framycetin sulphate 0.5%, gramicidin 0.005%), 0.33% acetic acid and 0.9% NaCl eardrops in clearing grommets blocked with harvested thick middle ear effusion fluid. Study design:  A blinded in‐vitro study. Setting:  District general hospital. Participants:  A total of 473 grommets were blocked with freshly harvested unpooled thick middle ear effusion fluid obtained from 68 patients. Main outcome measures:  Patency of the grommets before and 7 days after intervention was ascertained by tympanometry and close visual inspection. Results:  Instillation of eardrops leads to a statistically significant increase in the clearance of grommets as compared with not using any drops (χ2 = 14.3, d.f. = 5, P = 0.006). The numbers needed to treat were 2.8 for NaHCO3, 3.2 for 0.9% NaCl, 3.9 for 0.33% acetic Acid, 4.4 for Sofradex and 9.5 for H2O2 eardrops. Pair‐wise comparison was only significant for comparison between 5% NaHCO3 and 3% H2O2 eardrops (Bonferroni corrected P = 0.01, odds ratio = 4.3, CI = 1.9–9.9). Conclusions:  Use of eardrops leads to a clinically and statistically significant increase in the clearance of blocked grommets. Of the five drops used, 5% NaHCO3 was the most efficacious and 3% H2O2 the least efficacious. Limitations of this in‐vitro study are recognized and a prospective in‐vivo double blind randomized controlled trial is planned.
ISSN:1749-4478
1749-4486
DOI:10.1111/j.1365-2273.2004.00920.x