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Identification of Perinatal Risk Factors for Auditory Neuropathy Spectrum Disorder

Objectives/Hypothesis To identify medical risk factors associated with auditory neuropathy spectrum disorder (ANSD). Study Design Retrospective case–control study. Methods During a 2‐year period (2013–2014) patients with newly diagnosed ANSD were identified at a tertiary care facility. Twenty‐two pa...

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Published in:The Laryngoscope 2021-03, Vol.131 (3), p.671-674
Main Authors: West, Alisha N., Kuan, Edward C., Peng, Kevin A.
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Kuan, Edward C.
Peng, Kevin A.
description Objectives/Hypothesis To identify medical risk factors associated with auditory neuropathy spectrum disorder (ANSD). Study Design Retrospective case–control study. Methods During a 2‐year period (2013–2014) patients with newly diagnosed ANSD were identified at a tertiary care facility. Twenty‐two patients (n = 22) were identified aged 0.5 to 8.1 years. There were 15 males and seven females. Sixteen had bilateral, four had left‐sided, and two had right‐sided ANSD. Two age‐matched, side‐matched, and gender‐matched control groups were then collected. The first group was 22 normal‐hearing children (n = 22). The second was 22 children with sensorineural hearing loss (SNHL) (n = 22) who did not meet the criteria for ANSD. The chart of each subject was reviewed for the following five‐predictor variables: prematurity, low birth weight, jaundice, use of mechanical ventilation, and administration of ototoxic medications. Analysis of variance was performed to analyze the prevalence of perinatal risk factors among the three groups. Multivariate linear regression was then applied. Results When comparing the ANSD group to both the normal‐hearing and SNHL groups, the subjects with ANSD had statistically significant higher rates of prematurity, low birth weight, jaundice, and mechanical ventilation. Multiple regression analysis was performed to identify predictors of ANSD compared to each control group individually. Jaundice in the first month of life approached significance when comparing the ANSD group to the normal‐hearing group, and was the only medical risk factor found to be statistically significant when comparing the ANSD group to the SNHL group. Conclusions A history of neonatal hyperbilirubinemia was significantly more common in children with ANSD compared to children with severe SNHL. Level of Evidence 3 Laryngoscope, 131:671–674, 2021
doi_str_mv 10.1002/lary.28904
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Study Design Retrospective case–control study. Methods During a 2‐year period (2013–2014) patients with newly diagnosed ANSD were identified at a tertiary care facility. Twenty‐two patients (n = 22) were identified aged 0.5 to 8.1 years. There were 15 males and seven females. Sixteen had bilateral, four had left‐sided, and two had right‐sided ANSD. Two age‐matched, side‐matched, and gender‐matched control groups were then collected. The first group was 22 normal‐hearing children (n = 22). The second was 22 children with sensorineural hearing loss (SNHL) (n = 22) who did not meet the criteria for ANSD. The chart of each subject was reviewed for the following five‐predictor variables: prematurity, low birth weight, jaundice, use of mechanical ventilation, and administration of ototoxic medications. Analysis of variance was performed to analyze the prevalence of perinatal risk factors among the three groups. Multivariate linear regression was then applied. Results When comparing the ANSD group to both the normal‐hearing and SNHL groups, the subjects with ANSD had statistically significant higher rates of prematurity, low birth weight, jaundice, and mechanical ventilation. Multiple regression analysis was performed to identify predictors of ANSD compared to each control group individually. Jaundice in the first month of life approached significance when comparing the ANSD group to the normal‐hearing group, and was the only medical risk factor found to be statistically significant when comparing the ANSD group to the SNHL group. Conclusions A history of neonatal hyperbilirubinemia was significantly more common in children with ANSD compared to children with severe SNHL. Level of Evidence 3 Laryngoscope, 131:671–674, 2021</description><identifier>ISSN: 0023-852X</identifier><identifier>EISSN: 1531-4995</identifier><identifier>DOI: 10.1002/lary.28904</identifier><identifier>PMID: 32609896</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Auditory neuropathy ; Case-Control Studies ; Child ; Child, Preschool ; Female ; hearing loss ; Hearing Loss, Central - etiology ; Hearing Loss, Sensorineural - complications ; Humans ; hyperbilirubinemia ; Hyperbilirubinemia - complications ; Infant ; Infant, Low Birth Weight ; Infant, Newborn ; Infant, Premature ; Jaundice, Neonatal - complications ; Linear Models ; Male ; neonatal ; Ototoxicity - complications ; Respiration, Artificial - adverse effects ; Retrospective Studies ; Risk Assessment ; Risk Factors</subject><ispartof>The Laryngoscope, 2021-03, Vol.131 (3), p.671-674</ispartof><rights>2020 The American Laryngological, Rhinological and Otological Society, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3294-c69ce0770b182ae10272cd4a391aa3ee484ec8b717ae8a7ed2019d477e10b92c3</citedby><cites>FETCH-LOGICAL-c3294-c69ce0770b182ae10272cd4a391aa3ee484ec8b717ae8a7ed2019d477e10b92c3</cites><orcidid>0000-0003-3475-0718 ; 0000-0003-1661-769X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32609896$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>West, Alisha N.</creatorcontrib><creatorcontrib>Kuan, Edward C.</creatorcontrib><creatorcontrib>Peng, Kevin A.</creatorcontrib><title>Identification of Perinatal Risk Factors for Auditory Neuropathy Spectrum Disorder</title><title>The Laryngoscope</title><addtitle>Laryngoscope</addtitle><description>Objectives/Hypothesis To identify medical risk factors associated with auditory neuropathy spectrum disorder (ANSD). Study Design Retrospective case–control study. Methods During a 2‐year period (2013–2014) patients with newly diagnosed ANSD were identified at a tertiary care facility. Twenty‐two patients (n = 22) were identified aged 0.5 to 8.1 years. There were 15 males and seven females. Sixteen had bilateral, four had left‐sided, and two had right‐sided ANSD. Two age‐matched, side‐matched, and gender‐matched control groups were then collected. The first group was 22 normal‐hearing children (n = 22). The second was 22 children with sensorineural hearing loss (SNHL) (n = 22) who did not meet the criteria for ANSD. The chart of each subject was reviewed for the following five‐predictor variables: prematurity, low birth weight, jaundice, use of mechanical ventilation, and administration of ototoxic medications. Analysis of variance was performed to analyze the prevalence of perinatal risk factors among the three groups. Multivariate linear regression was then applied. Results When comparing the ANSD group to both the normal‐hearing and SNHL groups, the subjects with ANSD had statistically significant higher rates of prematurity, low birth weight, jaundice, and mechanical ventilation. Multiple regression analysis was performed to identify predictors of ANSD compared to each control group individually. Jaundice in the first month of life approached significance when comparing the ANSD group to the normal‐hearing group, and was the only medical risk factor found to be statistically significant when comparing the ANSD group to the SNHL group. Conclusions A history of neonatal hyperbilirubinemia was significantly more common in children with ANSD compared to children with severe SNHL. 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Study Design Retrospective case–control study. Methods During a 2‐year period (2013–2014) patients with newly diagnosed ANSD were identified at a tertiary care facility. Twenty‐two patients (n = 22) were identified aged 0.5 to 8.1 years. There were 15 males and seven females. Sixteen had bilateral, four had left‐sided, and two had right‐sided ANSD. Two age‐matched, side‐matched, and gender‐matched control groups were then collected. The first group was 22 normal‐hearing children (n = 22). The second was 22 children with sensorineural hearing loss (SNHL) (n = 22) who did not meet the criteria for ANSD. The chart of each subject was reviewed for the following five‐predictor variables: prematurity, low birth weight, jaundice, use of mechanical ventilation, and administration of ototoxic medications. Analysis of variance was performed to analyze the prevalence of perinatal risk factors among the three groups. Multivariate linear regression was then applied. Results When comparing the ANSD group to both the normal‐hearing and SNHL groups, the subjects with ANSD had statistically significant higher rates of prematurity, low birth weight, jaundice, and mechanical ventilation. Multiple regression analysis was performed to identify predictors of ANSD compared to each control group individually. Jaundice in the first month of life approached significance when comparing the ANSD group to the normal‐hearing group, and was the only medical risk factor found to be statistically significant when comparing the ANSD group to the SNHL group. Conclusions A history of neonatal hyperbilirubinemia was significantly more common in children with ANSD compared to children with severe SNHL. 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subjects Auditory neuropathy
Case-Control Studies
Child
Child, Preschool
Female
hearing loss
Hearing Loss, Central - etiology
Hearing Loss, Sensorineural - complications
Humans
hyperbilirubinemia
Hyperbilirubinemia - complications
Infant
Infant, Low Birth Weight
Infant, Newborn
Infant, Premature
Jaundice, Neonatal - complications
Linear Models
Male
neonatal
Ototoxicity - complications
Respiration, Artificial - adverse effects
Retrospective Studies
Risk Assessment
Risk Factors
title Identification of Perinatal Risk Factors for Auditory Neuropathy Spectrum Disorder
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