Is there randomized controlled trial evidence to support the use of grommets (ventilation tubes) in children with hearing loss associated with otitis media with effusion?

2014 ◽  
Author(s):  
Su-Ting T. Li
Keyword(s):  
Randomized Controlled Trial ◽  
Hearing Loss ◽  
Otitis Media ◽  
Otitis Media With Effusion ◽  
Controlled Trial ◽  
Randomized Controlled ◽  
Ventilation Tubes ◽  
Children With Hearing Loss ◽  
Trial Evidence

scholarly journals Effect of nasal balloon autoinflation in children with otitis media with effusion in primary care: an open randomized controlled trial

2015 ◽  
Vol 187 (13) ◽  
pp. 961-969 ◽  
Author(s):  
Ian Williamson ◽  
Jane Vennik ◽  
Anthony Harnden ◽  
Merryn Voysey ◽  
Rafael Perera ◽  
...  
Keyword(s):  
Primary Care ◽  
Randomized Controlled Trial ◽  
Otitis Media ◽  
Otitis Media With Effusion ◽  
Controlled Trial ◽  
Randomized Controlled

scholarly journals Preventing Ventilation Tube Otorrhea and Obstruction (PreVenTO2): A Randomized Controlled Trial

2021 ◽  
Author(s):  
Luke Wang ◽  
Debra Phyland ◽  
Charles Giddings
Keyword(s):  
Randomized Controlled Trial ◽  
Otitis Media ◽  
Otitis Media With Effusion ◽  
Controlled Trial ◽  
Acute Otitis Media ◽  
Trial Registration ◽  
Control Group ◽  
Ventilation Tube ◽  
Tube Obstruction ◽  
Randomized Controlled

Objectives: To determine the effectiveness of ciprofloxacin 0.3% antibiotic eardrops in preventing clinically significant postoperative otorrhea and tube obstruction following grommet insertion in children. Design: 3-arm double-blinded randomized controlled trial. Randomisation in 1:1:1 ratio into two interventional and one control arm. The interventional groups received either 5 drops of topical ciprofloxacin 0.3% eardrops in each ear intraoperatively or intraoperatively and for 5 days postoperatively. The control group received no drops. Patients were assessed by blinded assessors at 6 weeks postoperatively. Setting: The study was conducted in a large tertiary health network in Melbourne, Australia. Participants: All children, 17 years and under, undergoing bilateral MEVT surgery with or without concurrent upper airway surgery for recurrent acute otitis media and chronic otitis media with effusion were approached. Main Outcome Measures: Presence of postoperative otorrhea and ventilation tube obstruction at 6 weeks postoperatively. Results: 256 pediatric patients completed the study with a median age of 4.02 years. 153 participants were male. Intraoperative antibiotics were more effective than control in preventing otorrhea (RR=0.341, 95%CI 0.158–0.738, NNT= 11.25, p=.006). Postoperative antibiotics were more effective than control in preventing ventilation tube obstruction (RR=0.424, 95%CI 0.193 to 0.930, NNT=14.7 p=.032). Conclusion: Intraoperative topical ciprofloxacin was effective at preventing early postoperative otorrhea and a prolonged course was effective at preventing ventilation tube obstruction. Future studies on this topic should seek to clarify whether particular subgroups of patients benefit more from prophylactic topical antibiotics and model for cost-effectiveness. Trial Registration: This trial was registered prospectively on the Australian New Zealand Clinical Trials Registry (ACTRN12618001082291) on the 28th of June 2018. Available at URL: https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=375306

Lack of Efficacy of Middle-Ear Inflation: Treatment of Otitis Media with Effusion in Children

1989 ◽  
Vol 100 (4) ◽  
pp. 317-323 ◽  
Author(s):  
Kenny H. Chan ◽  
Charles D. Bluestone
Keyword(s):  
Randomized Controlled Trial ◽  
Treatment Group ◽  
Otitis Media ◽  
Middle Ear ◽  
Otitis Media With Effusion ◽  
Controlled Trial ◽  
Observation Group ◽  
Middle Ear Effusion ◽  
Randomized Controlled ◽  
Ear Effusion

A randomized controlled trial was conducted to evaluate the efficacy of autoinflation of the middle ear in the treatment of otitis media with effusion. Forty-one children with middle ear effusion not responsive to antimicrobial therapy enrolled in the study. Of these subjects, 75 percent had effusion duration over 3 months. A system consisting of a disposable anesthesia mask attached to a flowmeter was used to teach children to perform autoinflation based on a modified Valsalva technique. Subjects were stratified according to their ability to achieve tubal opening as assessed by tympanometry and tubosonometry. Subjects were randomly assigned to either treatment or observation group and were followed weekly for 2 weeks; subjects in the treatment group attempted inflation three times each day for 2 weeks. Of the 19 subjects who were in the autoinflation group, only one (5.3 percent) was effusion-free at the two-week endpoint and of the 21 subjects in the control, only two (9.5 percent) were without middle-ear effusion. Autoinflation was ineffective for treatment of children with otitis media with effusion in our study.

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