4.1 Article

Clinical Considerations for Routine Auditory and Vestibular Monitoring in Patients With Cystic Fibrosis

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AMERICAN JOURNAL OF AUDIOLOGY
卷 30, 期 3S, 页码 800-809

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AMER SPEECH-LANGUAGE-HEARING ASSOC
DOI: 10.1044/2021_AJA-21-00031

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资金

  1. National Institute on Deafness and Other Communication Disorders [ZIA-DC000064, 1R21DC016128-01A1, DC004555, DC016680, 1R01DC017867, 1R01DC017425]
  2. Cystic Fibrosis Foundation [GARINI1A90]
  3. UK National Institute for Health Research (NIHR)
  4. National Center for Rehabilitative Auditory Research at the Portland VA Health Care System [C2361C]

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The consensus statement outlines four clinical recommendations for implementing routine and guideline adherent ototoxicity management in CF patients, including asking questions during routine CF case history, utilizing timely measures, establishing baselines and conducting evaluations, and repeating annual evaluations for patients with ototoxic antibiotic exposure. Efforts to implement an ototoxicity management program are crucial for improving identification of ototoxicity signs and symptoms, ensuring timely follow-up, and enabling informed decision-making for treatment modifications.
Purpose: Specific classes of antibiotics, such as amiloglycosides have well-established adverse events producing permanent hearing loss, tinnitus, and balance and/or vestibular problems (i.e., ototoxicity). Although these antibiotics are frequently used to treat pseudomonas and other bacterial infections in patients with cystic fibrosis (CF), there are no formalized recommendations describing approaches to implementation of guideline adherent ototoxicity monitoring as part of CF clinical care. Method: This consensus statement was developed by the International Ototoxicity Management Working Group (IOMG) Ad Hoc Committee on Aminoglycoside Antibiotics to address the clinical need for ototoxicity management in CF patients treated with known ototoxic medications. These clinical protocol considerations were created using consensus opinion from a community of international experts and available evidence specific to patients with CF, as well as published national and international guidelines on ototoxicity monitoring. Results: The IOMG advocates four clinical recommendations for implementing routine and guideline adherent ototoxicity management in patients with CF. These are (a) including questions about hearing, tinnitus, and balance/vestibular problems as part of the routine CF case history for all patients; (b) utilizing timely point-of-care measures; (c) establishing a baseline and conducting posttreatment evaluations for each course of intravenous ototoxic drug treatment; and (d) repeating annual hearing and vestibular evaluations for all patients with a history of ototoxic antibiotic exposure. Conclusion: Increased efforts for implementation of an ototoxicity management program in the CF care team model will improve identification of ototoxicity signs and symptoms, allow for timely therapeutic follow-up, and provide the clinician and patient an opportunity to make an informed decision about potential treatment modifications to minimize adverse events.

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