Newborn Hearing Screening Results in Patients with Enlarged Vestibular Aqueduct.

OBJECTIVES Enlarged vestibular aqueduct (EVA) is the most common anatomic abnormality contributing to permanent hearing loss (HL) in children. Although the association between EVA and HL is well-documented, the pass rate for the newborn hearing screening (NBHS) for patients with EVA-related HL is not. Our objective was to investigate the association between NBHS results and audiologic and clinical outcomes in a large cohort of pediatric patients with EVA. METHODS This was a retrospective chart review of patients seen in the Boston Children's Hospital (BCH) Department of Otolaryngology and Communication Enhancement with confirmed HL, known NBHS results, and confirmed EVA. Demographic, clinical, audiologic, and imaging data were collected from the medical record. Frequency-specific data points from pure-tone audiograms and/or automated auditory brainstem response tests were recorded, and four-frequency pure tone average was calculated using air conduction thresholds at 500, 1000, 2000, and 4000 Hz. RESULTS Of the 183 patients included in the study, 84 (45.9%) passed their NBHS, whereas 99 (54.1%) did not pass. Compared with patients who did not pass, patients who passed were more likely to have unilateral EVA and unilateral HL, whereas they were less likely to undergo cochlear implantation and to have causative SLC26A4 variants. CONCLUSIONS EVA-associated HL may be identified at birth or during childhood, with nearly half the patients in this cohort passing their NBHS. Our results provide prognostic information for patients with EVA who pass their NBHS and highlight the importance of regular hearing monitoring for children not initially suspected of having HL. LEVEL OF EVIDENCE Level IV Laryngoscope, 2023.

[1]  L. Bruschini,et al.  Enlarged vestibular aqueduct and Mondini Malformation: audiological, clinical, radiologic and genetic features , 2020, European Archives of Oto-Rhino-Laryngology.

[2]  K. Kawai,et al.  Torticollis in children with enlarged vestibular aqueducts. , 2020, International journal of pediatric otorhinolaryngology.

[3]  C. Morton,et al.  A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children , 2019, Genetics in Medicine.

[4]  X. Yi,et al.  Newborn hearing concurrent genetic screening for hearing impairment-a clinical practice in 58,397 neonates in Tianjin, China. , 2013, International journal of pediatric otorhinolaryngology.

[5]  J. Meinzen-Derr,et al.  Significance of unilateral enlarged vestibular aqueduct , 2013, The Laryngoscope.

[6]  Bo Gyung Kim,et al.  Limitations of hearing screening in newborns with PDS mutations. , 2013, International journal of pediatric otorhinolaryngology.

[7]  M. Kenna,et al.  Enlarged vestibular aqueduct: Review of controversial aspects , 2011, The Laryngoscope.

[8]  B. Qaqish,et al.  Large vestibular aqueduct syndrome , 2011, The Laryngoscope.

[9]  H. Rehm,et al.  Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss. , 2010, Archives of otolaryngology--head & neck surgery.

[10]  J. Hardin,et al.  Hearing screening at well-child visits. , 2005, Archives of pediatrics & adolescent medicine.

[11]  K. Arnos,et al.  SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities , 2005, Journal of Medical Genetics.

[12]  E. Arjmand,et al.  Audiometric findings in children with a large vestibular aqueduct. , 2004, Archives of otolaryngology--head & neck surgery.

[13]  M. Halsted,et al.  Enlarged Vestibular Aqueduct Syndrome in the Pediatric Population , 2003, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

[14]  E. Green,et al.  Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndrome. , 1998, Archives of otolaryngology--head & neck surgery.

[15]  V. Sheffield,et al.  Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS) , 1997, Nature Genetics.

[16]  D. Edelstein,et al.  The large vestibular aqueduct syndrome in children. A review of 12 cases and the description of a new clinical entity. , 1989, Archives of otolaryngology--head & neck surgery.

[17]  G. Valvassori,et al.  The Large Vestibular Aqueduct Syndrome , 1978 .