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Prevalence and Risk Factors of Congenital Hearing Loss in Turkey: A Systematic Review
Yasemin Sökmen1, Resmiye Kaya Odabaş2, Ayten Taşpinar3
1Department of Midwifery, Faculty of Health Sciences, Ondokuz Mayıs University, Samsun, Türkiye yasemin.sokmen@omu.edu.tr ysmn0006@outlook.com.
Insights
Congenital hearing loss affects child development. This review identified key risk factors and prevalence rates in Turkey, aiding health service planning for newborn hearing screening.
Area of Science:
- Pediatrics
- Public Health
- Otolaryngology
Background:
- Congenital hearing loss significantly impacts a child's social, emotional, and intellectual development.
- Early identification and intervention are crucial for mitigating long-term effects.
- Understanding prevalence and risk factors is essential for effective health service planning.
Purpose of the Study:
- To systematically review and determine the prevalence of congenital hearing loss in newborns in Turkey.
- To identify the most common risk factors associated with congenital hearing loss in the Turkish newborn population.
Main Methods:
- A systematic review was conducted between November 2020 and February 2021.
- Searched major electronic databases (Google Scholar, PubMed, ScienceDirect, EBSCOhost, Springer) using keywords: "newborn hearing screening" and "congenital hearing loss."
- Analyzed 13 studies (1 prospective, 12 retrospective) from Turkey.
Main Results:
- The prevalence of congenital hearing loss was 0.5% in the general newborn population and 1.1% in newborns with identified risk factors.
- Common risk factors identified include: intensive care/mechanical ventilation >5 days, ototoxic drug use, hyperbilirubinemia requiring transfusion/phototherapy, prematurity, consanguineous marriage, and family history of hearing loss.
- Average timelines: screening within 1 month, diagnosis within 2 months, and intervention between 3-14 months of age.
Conclusions:
- The prevalence rates highlight the importance of robust newborn hearing screening programs in Turkey.
- Identifying and addressing key risk factors can improve early detection and intervention outcomes.
- Timely screening, diagnosis, and intervention are critical for children with congenital hearing loss.
Abstract:
Congenital hearing loss hinders the child's social, emotional, and intellectual development. This systematic review was planned because the determination of congenital hearing loss and risk factors will guide health service planning. This systematic review was conducted based on previous studies in Turkey to determine the prevalence and the risk factors of newborn congenital hearing loss. This systematic review was conducted between November 2020 and February 2021; Google Scholar, PubMed, ScienceDirect, EBSCOhost, and Springer electronic databases were screened with the keywords "newborn hearing screening" and "congenital hearing loss." According to the results of the systematic review of 13 studies, 1 prospective and 12 retrospective, the prevalence of congenital hearing loss is 0.5% and 1.1% in those with risk factors; newborns are screened within 1 month, diagnosed within 2 months on average, and intervened with between the 3rd and 14th months; and the most common risk factors for hearing loss are admission in intensive care/mechanical ventilation for more than 5 days/history of ototoxic drug use, hyperbilirubinemia requiring an exchange transfusion/phototherapy, prematurity, consanguineous marriage, and family history of hearing loss, respectively.
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