Background: Transiently evoked otoacoustic emissions (TEOAEs) is an objective diagnostic method of assessing the cochlear status. The aim of this study was to present the results of hearing screening in children and to evaluate TEOAEs in the diagnosis of middle-ear pathology compared with tympanometry and pure-tone audiometry.
Material/methods: A group of school-aged children underwent otolaryngological evaluation, tympanometry, TEOAEs, and audiometry. We analyzed data from both ears with abnormal tympanograms and ears with normal tympanograms but abnormal otoscopic findings or positive otologic history. Included in our study were 497 ears.
Results: Two hundred ten (42%) ears had a tympanogram of type A, 102 (20.5%) of type B, and 185 (37.5%) of type C. Otoacoustic emissions were found in 200 (95%), 37 (36%), and 145 (78%) of these ears, respectively. In ears with a tympanogram of B type and present otoacoustic emissions, a pure-tone average (PTA) worse than 30 dB HL was found in 16 ears (43%), whereas in ears with a tympanogram of B type and absent otoacoustic emissions, PTA worse than 30 dB HL was found in 47 ears (72.3%). The respective numbers for ears with a tympanogram of C type were 18 (12.4%) and 19 (47.5%).
Conclusions: TEOAEs may be recorded in significant percentages of ears with abnormal tympanograms and middle-ear pathology. Although the sensitivity of this method is low, it may be used in conjunction with other methods of evaluating the middle ear and may give some information about the hearing status of the ear.
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Am J Otolaryngol
December 2024
Department of Clinical Laboratory, Wenzhou People's Hospital, Wenzhou Women and Children's Hospital, Zhejiang, China. Electronic address:
Background: The purpose of the research was to examine the prevalence rates of screening for genetics and hearing simultaneously in neonates and provide scientific evidence for the beneficial application of newborn screening in the Southeast China population.
Methods: Between June 2015 and March 2023, 27,843 newborns were enrolled in the study. All participants were screened by otoacoustic emissions at 2 days of age.
J Am Acad Audiol
July 2024
Department of Audiology, Monash Health Melbourne, Victoria, Australia.
Objective: The objectives of the study were to (i) evaluate the effectiveness of wideband absorbance (WBA) at ambient pressure (WBA), tympanic peak pressure (WBA), and 0 daPa (WBA) to identify conductive hearing loss (CHL) in infants and (ii) compare the sensitivity and specificity of the three WBA tests with that of high-frequency tympanometry (HFT) and transient-evoked otoacoustic emissions (TEOAE).
Method: A total of 31 ears with hearing thresholds no greater than 20 dB HL (reference group from 20 infants [mean age: 3.1 weeks]) and 47 ears with CHL from 31 infants (mean age: 3.
Isr Med Assoc J
December 2024
Department of Dermatology, Emek Medical Center, Afula, Israel.
Background: Little is known about audiovestibular function in psoriasis, a chronic systemic inflammatory disease that affects 2% of the world's population.
Objectives: To investigate audiovestibular function in patients with psoriasis.
Methods: In this prospective case-control trial, we enrolled 33 patients with psoriasis and 30 healthy controls.
Front Psychol
December 2024
Department of Speech, Language and Hearing Sciences, Indiana University, Bloomington, IN, United States.
The Test of Basic Auditory Capabilities (TBAC) consists of 19 discrimination and identification tasks selected to study individual differences in audition. In one TBAC study, performance was measured for 340 normal-hearing subjects, but no investigation into possible sex differences was undertaken. That dataset now has been re-analyzed by sex.
View Article and Find Full Text PDFInt J Mol Sci
November 2024
The Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Pirogov Russian National Research Medical University, 117513 Moscow, Russia.
Auditory neuropathy spectrum disorder (ANSD) is often missed by standard hearing tests, accounting for up to 10% of hearing impairments (HI) and commonly linked to variants in 23 genes. We assessed 122 children with HI, including 102 with sensorineural hearing loss (SNHL) and 20 with ANSD. SNHL patients were genotyped for common variants using qPCR, while ANSD patients underwent whole exome sequencing, with variants analyzed across 249 genes.
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