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Published on: October 11, 2024
Identification of oral clefts as a risk factor for hearing loss during newborn hearing screening
Patricia L Purcell1, Kathleen Cy Sie1,2, Todd C Edwards3
1Department of Otolaryngology - Head & Neck Surgery, University of Washington, Seattle WA.
Insights
Many children with oral clefts are misclassified as not at-risk for hearing loss. This impacts timely hearing screening and diagnosis for these vulnerable infants.
Area of Science:
- Pediatric Audiology
- Craniofacial Anomalies
- Public Health Surveillance
Background:
- Children with oral clefts have an increased risk of hearing loss.
- Newborn hearing screening aims to identify infants at risk early.
- Accurate classification of risk factors is crucial for appropriate follow-up.
Purpose of the Study:
- To evaluate the accuracy of hearing loss risk classification for infants with oral clefts.
- To describe hearing screening and diagnostic outcomes in this population.
- To identify factors associated with misclassification.
Main Methods:
- Identified infants with cleft lip and palate or isolated cleft palate using Washington State birth certificates (2008-2013).
- Cross-referenced birth records with the Early Hearing Detection, Diagnosis and Intervention (EHDDI) database.
- Employed multivariate logistic regression to analyze associations between classification status and screening outcomes.
Main Results:
- A significant proportion of infants with oral clefts were not classified as having a craniofacial anomaly in the EHDDI database (only 39%).
- Misclassification was associated with lower rates of initial hearing screening referral (OR 0.3) and delayed screening (OR 4.4).
- Of 50 infants with diagnostic results, 50% had hearing loss.
Conclusions:
- The majority of infants with oral clefts are misclassified regarding hearing loss risk in the EHDDI database.
- This misclassification can lead to delayed or missed hearing interventions.
- Improved data accuracy in EHDDI is needed to ensure timely audiological care for infants with oral clefts.
Objective:
This study assessed whether children with oral clefts are appropriately classified as at-risk for hearing loss at the time of newborn hearing screening and describes their screening and diagnostic results.
Design:
Birth certificates were used to identify children with cleft lip and palate or isolated cleft palate born in Washington State from 2008-2013. These were cross-referenced with the state's Early Hearing Detection, Diagnosis and Intervention (EHDDI) database. Multivariate logistic regression was used to examine associations.
Results:
Birth records identified 235 children with cleft lip and palate and 116 with isolated cleft palate. Six children were listed as having both diagnoses. Only 138 (39%) of these children were designated as having a craniofacial anomaly in the EHDDI database. Children who were misclassified were less likely to have referred on initial hearing screening, OR 0.3, 95% CI [0.2, 0.5]. Misclassification of risk factor status was also associated with delayed hearing screening past 30 days of age or unknown age at screening, OR 4.4, 95% CI [1.5, 13.3], p-value 0.008. Of 50 children with diagnostic results; 25 (50%) had hearing loss: 18 conductive, 2 mixed, and 5 unspecified.
Conclusion:
A majority of children with oral clefts were misclassified regarding risk factor for hearing loss in the EHDDI database.
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