An Assessment of the Clinical Acceptability of Direct Acoustic Cochlear Implantation for Adults With Advanced Otosclerosis in the United Kingdom.

Otol Neurotol

*National Institute for Health Research Nottingham Biomedical Research Centre, Ropewalk House †Otology and Hearing Group, Division of Clinical Neuroscience, School of Medicine, University of Nottingham, Nottingham ‡Royal United Hospitals Bath NHS Foundation Trust, Bath §Department of Otolaryngology, The Royal National Throat Nose and Ear Hospital, London ||Department of Otolaryngology, University Hospitals Birmingham, Birmingham ¶Department of Otolaryngology, Royal Hallamshire Hospital, Sheffield Teaching Hospitals, Sheffield, UK **Department of Otorhinolaryngology, Radboud University Medical Center, Nijmegen, The Netherlands ††Nottingham University Hospitals NHS Trust, Queen's Medical Centre, Nottingham, UK.

Published: August 2017

Hypothesis: Assess the clinical acceptability of direct acoustic cochlear implantation for patients with advanced otosclerosis and the support for conducting a controlled trial of its effectiveness in the United Kingdom.

Background: Emerging evidence supports the efficacy of direct acoustic cochlear implantation in patients with advanced otosclerosis whose needs cannot be managed using the combination of stapes surgery and hearing aids. A controlled trial would provide evidence for its effectiveness and cost-effectiveness to healthcare commissioners.

Methods: An online survey of clinical professionals was constructed to characterize current standard of care for patients with advanced otosclerosis and to assess whether clinicians would be willing to refer patients into a trial to evaluate direct acoustic cochlear implantation. A consensus process was conducted to define inclusion criteria for the future trial.

Results: No survey respondent considered direct acoustic cochlear implantation to be inappropriate with a majority indicating that they would refer patients into a future trial. The consensus was that there is a lack of available treatment options for those patients with bone conduction thresholds worse than 55 dB HL and who did not meet current criteria for cochlear implantation.

Conclusion: The present study confirms that a controlled trial to evaluate the effectiveness of direct acoustic cochlear implantation would have the support of clinicians in the United Kingdom. A feasibility study would be required to determine whether patients who meet the inclusion criteria could be recruited in a timely manner and in sufficient numbers to conduct a formal evaluation of effectiveness.

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Source
http://dx.doi.org/10.1097/MAO.0000000000001450DOI Listing

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