Literature DB >> 2816859

Aminoglycoside ototoxicity in cystic fibrosis. Evaluation by high-frequency audiometry.

T I McRorie1, J Bosso, L Randolph.   

Abstract

In this study, we sought to determine the clinical usefulness of high-frequency audiometry (8000 to 20,000 Hz) in detecting aminoglycoside-induced increases in pure-tone hearing thresholds before they are noticed in conventionally tested frequencies. We measured hearing thresholds from 250 to 20,000 Hz in 22 patients with cystic fibrosis who were treated with aminoglycosides. The audiograms were age-matched and were compared with those from 13 patients with cystic fibrosis and 38 subjects without cystic fibrosis, all of whom had never received aminoglycoside therapy. In patients with cystic fibrosis who were treated with aminoglycosides (younger than 20 years), there were statistically significant elevations only in frequencies higher than 16,000 Hz. Patients with cystic fibrosis who were treated with aminoglycosides who were 20 years and older had elevated thresholds in all frequencies tested. Patients with cystic fibrosis who were not treated with aminoglycosides did not differ statistically from controls. High-frequency audiometry may serve as a useful measure of elevation in pure-tone hearing thresholds that precede noticeable loss of auditory acuity in patients with cystic fibrosis who are receiving long-term aminoglycoside therapy.

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Year:  1989        PMID: 2816859     DOI: 10.1001/archpedi.1989.02150230086028

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  11 in total

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Review 8.  Optimisation of antibiotic therapy in cystic fibrosis patients. Pharmacokinetic considerations.

Authors:  C A Lindsay; J A Bosso
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9.  Functional Impacts of Aminoglycoside Treatment on Speech Perception and Extended High-Frequency Hearing Loss in a Pediatric Cystic Fibrosis Cohort.

Authors:  Chelsea M Blankenship; Lisa L Hunter; M Patrick Feeney; Madison Cox; Lindsey Bittinger; Angela C Garinis; Li Lin; Gary McPhail; John P Clancy
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Review 10.  Hearing thresholds at high frequency in patients with cystic fibrosis: a systematic review.

Authors:  Debora T M Caumo; Lúcia B Geyer; Adriane R Teixeira; Sérgio S M Barreto
Journal:  Braz J Otorhinolaryngol       Date:  2016-11-09
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