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Updated: Jun 18, 2026

Neonatal Murine Cochlear Explant Technique as an In Vitro Screening Tool in Hearing Research
Published on: June 8, 2017
Newborn hearing screening: outcomes and management of infants
Hatice Kübra Bozkurt1,2, Fatma Ceyda Akın Öçal2, Ercan Karababa1,2
1University of Health Science, Gülhane Faculty of Health Science, Department of Audiology - Ankara, Türkiye.
Objective:
The aim of this study was to evaluate the prevalence and characteristics of hearing loss among infants referred after newborn hearing screening in a tertiary referral center in Türkiye and to examine its association with demographic and clinical risk factors.
Methods:
A retrospective study was conducted at SBÜ Gülhane Training and Research Hospital between January 2021 and December 2024, including 1,322 infants referred after newborn hearing screening due to either a "refer" result or the presence of risk factors despite passing automated auditory brainstem response. Relevant risk factors were analyzed.
Results:
Hearing loss was detected in 92 infants (7.0%), including 3.3% with unilateral and 3.7% with bilateral loss. By severity, the distribution was mild (2.8%), moderate (0.8%), moderately severe (0.3%), and profound (1.5%). While most infants with unilateral loss did not receive amplification, bilateral cases showed higher rates of hearing aid (28.6%) and cochlear implant (14.3%) use. Family history of hearing loss was the only factor significantly associated with device adoption (p<0.05).
Conclusion:
The prevalence of hearing loss in referred infants was higher than in population-based studies and aligned with findings in high-risk groups. Differences in device use between unilateral and bilateral cases highlight the importance of parental counseling. Strengthening follow-up and family awareness is crucial to improving early intervention outcomes, particularly in infants without a family history.
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