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Preliminary audiologic and peri-operative outcomes of the Sophono™ transcutaneous bone conduction device: A systematic review. | LitMetric

AI Article Synopsis

  • The study focused on the effectiveness and safety of the Sophono™ transcutaneous bone conduction device for improving hearing in patients.
  • Eight studies involving 86 patients, mostly children with ear atresia, reported a significant average auditory improvement of 31.10 decibels.
  • While 29% of patients experienced post-operative complications, the overall results indicate that the device has potential benefits for hearing rehabilitation, particularly in children, with a need for careful management to mitigate skin issues related to its use.

Article Abstract

Objective: To delineate the auditory functional improvement and peri-operative outcomes of the Sophono™ transcutaneous bone conduction device.

Methods: Eligible articles presenting patients implanted with the Sophono™ were identified through a comprehensive search of PubMed and Embase electronic databases. All relevant articles were reviewed to justify inclusion independently by 2 authors. Studies that successfully passed critical appraisal for directness of evidence and risk of bias were included.

Results: From a total of 125 articles, 8 studies encompassing 86 patients using 99 implants were selected. Most patients (79.1%) were children. Ear atresia (67.5%) was the most frequently reported indication for Sophono™ implantation. Overall pure tone average auditory improvement was 31.10 (±8.29) decibel. During a mean follow-up time of 12.48 months, 25 patients (29%) presented with post-operative complications from which 3 were deemed as serious implant-related adverse events (3.5%).

Conclusions: The Sophono™ transcutaneous bone conduction device shows promising functional improvement, no intra-operative complications and minor post-operative skin related complications. If suitable, the device could be a proposed solution for the rehabilitation of hearing in children meeting eligibility criteria. A wearing schedule must be implemented in order to reduce magnet-related skin complications.

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Source
http://dx.doi.org/10.1016/j.ijporl.2017.08.014DOI Listing

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