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Published on: October 11, 2024
Analysis of risk factors associated with unilateral hearing loss in children who initially passed newborn hearing
Eric N Appelbaum1, Jessica B Howell1, Derek Chapman2
1Department of Otolaryngology-HNS, Virginia Commonwealth University, 401 North 11th Street, PO Box 980146, Richmond, VA, 23298, United States.
Insights
Neonatal indicators and craniofacial anomalies are key risk factors for unilateral hearing loss (UHL) in infants who pass initial newborn hearing screening. Early identification of these factors is crucial for timely intervention.
Area of Science:
- Pediatric audiology
- Neonatal screening
- Genetics and hearing loss
Background:
- Newborn hearing screening aims to identify infants with hearing loss early.
- The Joint Committee on Infant Hearing (JCIH) established risk factors to guide follow-up.
- Some infants passing initial screening may develop hearing loss later.
Purpose of the Study:
- To analyze the 2007 Joint Committee on Infant Hearing (JCIH) risk factors in children with confirmed unilateral hearing loss (UHL).
- To identify infants who initially passed newborn hearing screening but later developed UHL.
Main Methods:
- Retrospective record review of 16,108 infants from Virginia (2010-2012).
- Infants included had passed universal newborn hearing screening (UNHS) and possessed one or more JCIH risk factors.
- Study data was deemed exempt by relevant Institutional Review Boards.
Main Results:
- 4.9% of infants passed UNHS but had JCIH risk factors.
- 0.7% of this group were identified with confirmed hearing loss, including 0.2% with UHL (48 babies).
- Common risk factors for UHL included neonatal indicators, craniofacial anomalies, family history, and stigmata of syndrome.
Conclusions:
- Neonatal indicators and craniofacial anomalies were most prevalent in children with confirmed UHL post-screening.
- Craniofacial abnormalities were relatively more common in UHL cases compared to all hearing loss categories.
- Further research into the etiology and specific risk factor associations for hearing loss is recommended.
Objective:
To analyze 2007 Joint Committee on Infant Hearing (JCIH) risk factors in children with confirmed unilateral hearing loss (UHL) who initially passed newborn hearing screening.
Methods:
Retrospective record review of 16,108 infants who passed newborn hearing screening but had one or more JCIH risk factors prompting subsequent follow-up through the universal newborn hearing screening (UNHS) program in Virginia from 2010 to 2012. The study was reviewed and qualified as exempt by the Virginia Commonwealth University Institutional Review Board (IRB) and the Virginia Department of Health.
Results:
Over the 2-year study period, 14896 (4.9% of total births) children passed UNHS but had the presence of one or more JCIH risk factor. Ultimately, we identified 121 babies from this group with confirmed hearing loss (0.7%), with 48 babies (0.2%) showing UHL. The most common risk factors associated with the development of confirmed UHL after passing the initial screen were neonatal indicators, craniofacial anomalies, family history, and stigmata of syndrome associated with hearing loss.
Conclusion:
Neonatal indicators and craniofacial anomalies were the categories most often found in children with confirmed unilateral hearing loss who initially passed their newborn hearing screen. While neonatal indicators were also the most common associated risk factor in all hearing loss, craniofacial abnormalities are relatively more common in children with UHL who initially passed newborn hearing screening. Further studies assessing the etiology underlying the hearing loss and risk factor associations are warranted.
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