Related Experiment Video
Updated: May 20, 2026

Endaural Endoscopic Atticoantrotomy (Retrograde Mastoidectomy) using a Constant Suction Bone-drilling Technique
Published on: May 23, 2021
Persistent conductive or mixed hearing loss after the placement of tympanostomy tubes
Kenneth R Whittemore1, Briana K Dornan, Tara Lally
1Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, MA 02115, United States. Kenneth.whittemore@childrens.harvard.edu
Insights
Persistent hearing loss in children after tympanostomy tube placement can stem from various causes, including anatomical issues and genetic syndromes. Early diagnosis and tailored investigations are key for effective management of pediatric hearing loss.
Area of Science:
- Pediatric Otolaryngology
- Audiology
- Medical Genetics
Background:
- Serous otitis media is common in children, often treated with tympanostomy tubes.
- Persistent conductive or mixed hearing loss can occur after tympanostomy tube placement.
- Understanding the etiology of post-tympanostomy tube hearing loss is crucial for appropriate management.
Purpose of the Study:
- To describe the clinical findings in children with persistent hearing loss after tympanostomy tube placement.
- To identify potential causes and diagnostic approaches for this specific patient group.
Main Methods:
- Retrospective chart review of 39 children with conductive or mixed hearing loss post-tympanostomy tube placement.
- Review included clinical histories, physical examinations, audiological evaluations, diagnostic studies, and surgical findings.
- Institutional Review Board approval was obtained from Boston Children's Hospital.
Main Results:
- Identified causes of hearing loss: ossicular and cochlear abnormalities, 'third window' effects, cholesteatomas, genetic syndromes, and unknown factors.
- Functional tubes caused isolated mild low-frequency conductive hearing loss in four patients.
- Bilateral hearing loss was associated with genetic syndromes; mixed hearing loss with cochlear abnormalities, 'third window' effects, or genetic syndromes.
- Computed tomography (CT) aided diagnosis in 16/25 patients; vestibular-evoked myogenic potential (VEMP) testing suggested diagnosis in 3/4 patients.
Conclusions:
- Laterality and type of hearing loss are important diagnostic indicators in children with persistent hearing loss post-tympanostomy tube placement.
- Genetic testing is recommended for patients with bilateral hearing loss due to potential underlying syndromes.
- Inner ear anomalies should be evaluated in patients with mixed hearing loss; mild, low-frequency hearing loss requires monitoring and further investigation if it progresses.
Objective:
Described is a case series of clinical findings in children with persistent conductive or mixed hearing loss following tympanostomy tube placement for serous otitis media.
Study Design:
Retrospective chart review.
Setting:
Tertiary pediatric hospital.
Subjects/Methods:
Medical records of thirty-nine children who were referred for either conductive or mixed hearing loss post-tympanostomy tube placement were reviewed for clinical histories, physical examinations, audiological evaluations, diagnostic studies, consultations, and surgical findings. Approval was obtained from the Boston Children's Hospital Institutional Review Board.
Results:
Causes of hearing loss included ossicular abnormalities, cochlear abnormalities, 'third window' effects, cholesteatomas, genetic syndromes, and unknown causes. In four patients with isolated mild low-frequency conductive hearing loss, the cause was the presence of functional tubes. All patients diagnosed with a genetic syndrome had bilateral hearing loss. Patients with mixed hearing loss were diagnosed with cochlear abnormalities, 'third window' effects, or genetic syndromes. Computed tomography led to diagnosis in sixteen of twenty-five patients. Vestibular-evoked myogenic potential testing suggested a diagnosis in three of four patients.
Conclusion:
In children with persistent hearing loss following tympanostomy tube placement, identifying the laterality and type of hearing loss appears to be of importance in diagnosis. Patients with bilateral hearing loss should be considered for genetic testing, given the possibility of a syndrome. Patients identified with a mixed hearing loss should be evaluated for inner ear anomalies. Patients with mild, low-frequency hearing losses should be monitored audiologically and investigated further only if the hearing loss progresses and/or there is no resolution following tube extrusion.
More Related Videos
Related Concept Videos
Anatomy of the Ear
Tracheostomy: Procedure and Tubes
Tracheostomy tubes can be made of semiflexible plastic (polyurethane or silicone), rigid plastic, or metal, and they come in...
Auditory Pathway
When viewed cross-sectionally, the cochlea reveals the scala vestibuli and scala tympani flanking the...
Hearing

