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High frequency hearing thresholds and product distortion otoacoustic emissions in cystic fibrosis patients()()

INTRODUCTION: The treatment of patients with cystic fibrosis involves the use of ototoxic drugs, mainly aminoglycoside antibiotics. Due to the use of these drugs, fibrocystic patients are at risk of developing hearing loss. OBJECTIVE: To evaluate the hearing of patients with cystic fibrosis by High...

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Autores principales: Geyer, Lucia Bencke, Menna Barreto, Sergio Saldanha, Weigert, Liese Loureiro, Teixeira, Adriane Ribeiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442703/
https://www.ncbi.nlm.nih.gov/pubmed/26480907
http://dx.doi.org/10.1016/j.bjorl.2015.08.011
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author Geyer, Lucia Bencke
Menna Barreto, Sergio Saldanha
Weigert, Liese Loureiro
Teixeira, Adriane Ribeiro
author_facet Geyer, Lucia Bencke
Menna Barreto, Sergio Saldanha
Weigert, Liese Loureiro
Teixeira, Adriane Ribeiro
author_sort Geyer, Lucia Bencke
collection PubMed
description INTRODUCTION: The treatment of patients with cystic fibrosis involves the use of ototoxic drugs, mainly aminoglycoside antibiotics. Due to the use of these drugs, fibrocystic patients are at risk of developing hearing loss. OBJECTIVE: To evaluate the hearing of patients with cystic fibrosis by High Frequency Audiometry and Distortion Product Otoacoustic Emissions. METHODS: Cross-sectional study. The study group consisted of 39 patients (7–20 years of age) with cystic fibrosis and a control group of 36 individuals in the same age group without otologic complaints, with normal audiometric thresholds and type A tympanometric curves. High Frequency Audiometry and Distortion Product Otoacoustic Emissions tests were conducted. RESULTS: The study group had significantly higher thresholds at 250, 1000, 8000, 9000, 10,000, 12,500, and 16,000 Hz (p = 0.004) as well as higher prevalence of otoacoustic emission alterations at 1000 and 6000 Hz (p = 0.001), with significantly lower amplitudes at 1000, 1400, and 6000 Hz. There was a significant association between alterations in hearing thresholds in High Frequency Audiometry with the number of courses of aminoglycosides administered (p = 0.005). Eighty-three percent of patients who completed more than ten courses of aminoglycosides had hearing loss in High Frequency Audiometry. CONCLUSION: A significant number of patients with cystic fibrosis who received repeated courses of aminoglycosides showed alterations in High Frequency Audiometry and Distortion Product Otoacoustic Emissions. The implementation of ten or more aminoglycoside cycles was associated with alterations in High Frequency Audiometry.
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spelling pubmed-94427032022-09-09 High frequency hearing thresholds and product distortion otoacoustic emissions in cystic fibrosis patients()() Geyer, Lucia Bencke Menna Barreto, Sergio Saldanha Weigert, Liese Loureiro Teixeira, Adriane Ribeiro Braz J Otorhinolaryngol Original Article INTRODUCTION: The treatment of patients with cystic fibrosis involves the use of ototoxic drugs, mainly aminoglycoside antibiotics. Due to the use of these drugs, fibrocystic patients are at risk of developing hearing loss. OBJECTIVE: To evaluate the hearing of patients with cystic fibrosis by High Frequency Audiometry and Distortion Product Otoacoustic Emissions. METHODS: Cross-sectional study. The study group consisted of 39 patients (7–20 years of age) with cystic fibrosis and a control group of 36 individuals in the same age group without otologic complaints, with normal audiometric thresholds and type A tympanometric curves. High Frequency Audiometry and Distortion Product Otoacoustic Emissions tests were conducted. RESULTS: The study group had significantly higher thresholds at 250, 1000, 8000, 9000, 10,000, 12,500, and 16,000 Hz (p = 0.004) as well as higher prevalence of otoacoustic emission alterations at 1000 and 6000 Hz (p = 0.001), with significantly lower amplitudes at 1000, 1400, and 6000 Hz. There was a significant association between alterations in hearing thresholds in High Frequency Audiometry with the number of courses of aminoglycosides administered (p = 0.005). Eighty-three percent of patients who completed more than ten courses of aminoglycosides had hearing loss in High Frequency Audiometry. CONCLUSION: A significant number of patients with cystic fibrosis who received repeated courses of aminoglycosides showed alterations in High Frequency Audiometry and Distortion Product Otoacoustic Emissions. The implementation of ten or more aminoglycoside cycles was associated with alterations in High Frequency Audiometry. Elsevier 2015-09-08 /pmc/articles/PMC9442703/ /pubmed/26480907 http://dx.doi.org/10.1016/j.bjorl.2015.08.011 Text en © 2015 Associac¸ão Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial. Published by Elsevier Editora Ltda. All rights. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Geyer, Lucia Bencke
Menna Barreto, Sergio Saldanha
Weigert, Liese Loureiro
Teixeira, Adriane Ribeiro
High frequency hearing thresholds and product distortion otoacoustic emissions in cystic fibrosis patients()()
title High frequency hearing thresholds and product distortion otoacoustic emissions in cystic fibrosis patients()()
title_full High frequency hearing thresholds and product distortion otoacoustic emissions in cystic fibrosis patients()()
title_fullStr High frequency hearing thresholds and product distortion otoacoustic emissions in cystic fibrosis patients()()
title_full_unstemmed High frequency hearing thresholds and product distortion otoacoustic emissions in cystic fibrosis patients()()
title_short High frequency hearing thresholds and product distortion otoacoustic emissions in cystic fibrosis patients()()
title_sort high frequency hearing thresholds and product distortion otoacoustic emissions in cystic fibrosis patients()()
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442703/
https://www.ncbi.nlm.nih.gov/pubmed/26480907
http://dx.doi.org/10.1016/j.bjorl.2015.08.011
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