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Published on: February 29, 2020
Otitis media with effusion: an underestimated cause of hearing loss in infants
An Boudewyns1, Frank Declau, Jenneke Van den Ende
1Department of Otorhinolaryngology, Head and Neck Surgery, Antwerp University Hospital, University of Antwerp, Antwerp, Belgium. an.boudewyns@uza.be
Insights
Otitis media with effusion (OME) causes temporary hearing loss in infants, impacting early development. Prompt treatment is recommended if it doesn't resolve spontaneously to ensure normal hearing.
Area of Science:
- Pediatric Audiology
- Otolaryngology
- Neonatal Health
Background:
- Otitis media with effusion (OME) is a primary cause of failed neonatal hearing screenings.
- The impact of OME on infant hearing in early life remains poorly understood.
Purpose of the Study:
- To evaluate the impact of OME on hearing status in infants during their first months.
- To assess the degree of hearing loss and disease progression in infants with OME.
Main Methods:
- Prospective evaluation of infants who failed universal newborn hearing screening.
- Assessment included OME presence, hearing loss degree, and disease evolution using auditory brainstem response (ABR).
Main Results:
- Of 152 infants referred, 84 (55.3%) had OME; 64 were analyzed after exclusions.
- Infants presented with moderate-to-severe hearing loss (50 dB nHL); spontaneous resolution occurred in 15.
- All infants achieved normal hearing by a median age of 4.8 months, with no permanent hearing loss detected.
Conclusions:
- OME causes significant, yet transient, hearing loss in early infancy, a critical developmental period.
- Active intervention for persistent OME is crucial to prevent language delays.
- Early detection and management of OME are essential to rule out underlying sensorineural hearing loss.
Objective:
Otitis media with effusion (OME) is the major reason for failure of neonatal hearing screening. However, little is known about the impact on hearing status of OME in infants during the first months of life.
Patients:
Infants who failed universal newborn hearing screening.
Methods:
Prospective evaluation for the presence of OME, the degree of hearing loss and the disease evolution.
Results:
Between 2007 and 2008, approximately 152 infants were referred because of unilateral or bilateral failure on universal newborn hearing screening with an automated auditory brainstem response device. Eighty-four (55.3%) had OME, 20 of them were lost to follow-up. The remainder 64 infants comprised 37 boys and 27 girls, with a median age of 49 days (range, 40-65 d) at admission. Auditory brainstem response thresholds were 50 dB nHL (range, 40-60) in both ears. A spontaneous resolution of OME was documented in 15 infants. In the remaining, hearing normalized after tympanocentesis or placement of ventilation tubes. Normal hearing could be ascertained in all children at a median age of 4.8 months (range, 3.3-7.8 mo). In the group of infants analyzed, no permanent hearing loss could be detected.
Conclusion:
OME is an important cause of transient, moderately severe hearing loss during the first months of life--a critical period for development of the auditory system. Active treatment should be considered if spontaneous resolution does not occur to prevent any delay in language acquisition and to exclude an underlying sensorineural hearing loss.
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