Literature DB >> 21705096

Screening for delayed-onset hearing loss in preschool children who previously passed the newborn hearing screening.

Jingrong Lü1, Zhiwu Huang, Tao Yang, Yun Li, Ling Mei, Mingliang Xiang, Yongchuan Chai, Xiaohua Li, Lei Li, Guoyin Yao, Yu Wang, Xiaoming Shen, Hao Wu.   

Abstract

OBJECTIVE: The goal of this study was to investigate the prevalence of delayed-onset hearing loss in preschool children who previously passed newborn hearing screening in Shanghai, China.
METHODS: Between October 2009 and September 2010, 21,427 preschool children were enrolled from five areas of Shanghai, who had passed newborn hearing screening. Children were screened for delayed-onset hearing loss with pediatric audiometers. Children with positive results in initial and re-screening tests were assessed audiologically and for risk indicators according to the Year 2007 Statement of the American Joint Committee on Infant Hearing (JCIH).
RESULTS: During the study period, 445 children (2.08%) were referred for audiologic assessment; 16 (0.75/1000, 95% CI 0.38-1.12) had permanent delayed-onset hearing loss. Of these, five (0.23/1000) had bilateral moderate hearing loss; seven (0.33/1000) had mild bilateral hearing loss; and four (0.19/1000) had unilateral moderate or mild hearing loss. JCIH risk indicators were established for six children (6/16, 37.5%), including parental concern regarding speech and language developmental delay, neonatal intensive care unit with assisted ventilation or hyperbilirubinemia, recurrent otitis media with effusion, craniofacial malformation, and family history (n=1 for each). The remaining ten (62.5%) had no related risk factors.
CONCLUSIONS: A significant proportion of preschool children have undiagnosed delayed-onset hearing loss. Hearing screening in preschool is recommended for an early detection.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

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Year:  2011        PMID: 21705096     DOI: 10.1016/j.ijporl.2011.05.022

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  10 in total

1.  Childhood hearing surveillance activity in Italy: preliminary recommendations.

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2.  Auditory processing remains sensitive to environmental experience during adolescence in a rodent model.

Authors:  Kelsey L Anbuhl; Justin D Yao; Robert A Hotz; Todd M Mowery; Dan H Sanes
Journal:  Nat Commun       Date:  2022-05-24       Impact factor: 17.694

3.  Delayed-onset hearing loss in pediatric candidates for cochlear implantation.

Authors:  Sung-Wook Jeong; Min-Young Kang; Jae-Ryong Kim; Lee-Suk Kim
Journal:  Eur Arch Otorhinolaryngol       Date:  2015-05-09       Impact factor: 2.503

4.  Service Delivery to Children With Mild Hearing Loss: Current Practice Patterns and Parent Perceptions.

Authors:  Elizabeth A Walker; Meredith Spratford; Sophie E Ambrose; Lenore Holte; Jacob Oleson
Journal:  Am J Audiol       Date:  2017-03-01       Impact factor: 1.493

Review 5.  Language disorders in children with unilateral hearing loss: a systematic review.

Authors:  Maria Renata José; Maria Fernanda Capoani Garcia Mondelli; Mariza Ribeiro Feniman; Simone Aparecida Lopes-Herrera
Journal:  Int Arch Otorhinolaryngol       Date:  2013-12-03

Review 6.  Hearing impairment and language delay in infants: Diagnostics and genetics.

Authors:  Ruth Lang-Roth
Journal:  GMS Curr Top Otorhinolaryngol Head Neck Surg       Date:  2014-12-01

7.  Alteration of Cortical and Subcortical Structures in Children With Profound Sensorineural Hearing Loss.

Authors:  Hang Qu; Hui Tang; Jiahao Pan; Yi Zhao; Wei Wang
Journal:  Front Hum Neurosci       Date:  2020-12-09       Impact factor: 3.169

8.  Hearing thresholds elevation and potential association with emotional problems among 1,914 children in Beijing, China.

Authors:  Huidi Xiao; Nubiya Amaerjiang; Weiwei Wang; Menglong Li; Jiawulan Zunong; Hui En; Xuelei Zhao; Cheng Wen; Yiding Yu; Lihui Huang; Yifei Hu
Journal:  Front Public Health       Date:  2022-08-04

9.  The p.V37I exclusive genotype of GJB2: a genetic risk-indicator of postnatal permanent childhood hearing impairment.

Authors:  Lei Li; Jingrong Lu; Zheng Tao; Qi Huang; Yongchuan Chai; Xiaohua Li; Zhiwu Huang; Yun Li; Mingliang Xiang; Jun Yang; Guoyin Yao; Yu Wang; Tao Yang; Hao Wu
Journal:  PLoS One       Date:  2012-05-04       Impact factor: 3.240

10.  Large scale newborn deafness genetic screening of 142,417 neonates in Wuhan, China.

Authors:  Zongjie Hao; Denggang Fu; Yang Ming; Jinlong Yang; Qi Huang; Weilong Lin; Huan Zhang; Bin Zhang; Aifen Zhou; Xijiang Hu; Cong Yao; Yunping Dong; Huijun Z Ring; Brian Z Ring
Journal:  PLoS One       Date:  2018-04-10       Impact factor: 3.240

  10 in total

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