Otology & Neurotology

Home Current Issue Previous Issues Published Ahead-of-Print For Authors Journal Info
Skip Navigation LinksHome > February 2008 - Volume 29 - Issue 2 > Initial Clinical Experience With a Totally Implantable Cochl...
Otology & Neurotology:
February 2008 - Volume 29 - Issue 2 - pp 114-119
doi: 10.1097/MAO.0b013e31814b242f
Original Articles

Initial Clinical Experience With a Totally Implantable Cochlear Implant Research Device

Briggs, Robert J. S.; Eder, Helmut C.; Seligman, Peter M.; Cowan, Robert S. C.; Plant, Kerrie L.; Dalton, James; Money, David K.; Patrick, James F.

Collapse Box

Abstract

Objective: To evaluate the effectiveness and issues associated with a research totally implantable cochlear implant (TIKI).

Study Design: Limited patient trial.

Setting: Tertiary referral center.

Patients: Three adult human subjects with severe-to-profound sensorineural hearing loss.

Interventions: Subjects were implanted with a research TIKI developed by Cochlear Limited and the Co-operative Research Centre for Cochlear Implant and Hearing Aid Innovation. The TIKI has a lithium ion rechargeable battery, a package-mounted internal microphone, and sound-processing electronics that enable the use of "invisible hearing" without the use of an external device. The TIKI also functions with an external ESPrit 3G sound processor as a conventional cochlear implant. The standard surgical technique was modified to accommodate the larger device package. Postoperatively, subjects used TIKI in both invisible hearing and the conventional ESPrit 3G modes.

Main Outcome Measures: Device use was recorded in both invisible hearing and ESPrit 3G listening modes. Performance of the internal battery and microphone was assessed over time. Psychophysical MAP data were collected, and speech perception was measured at 1, 3, 6, and 12 months postoperatively in both listening modes.

Results: There were no surgical or postoperative complications. All subjects use both invisible hearing and conventional ESPrit 3G modes. Speech perception outcomes for all patients showed improvement from preoperative scores. As a consequence of the reduced sensitivity of the implanted microphone, speech perception results using the invisible hearing mode were significantly lower than the ESPrit 3G mode. Subjects reported some body noise interference that limited use of the invisible hearing mode; however, all continue to use the invisible hearing mode on a limited daily basis. The rechargeable battery functioned well, with a cycle time indicating the low-power implant design is effective and will deliver long battery life.

Conclusion: This study demonstrates that the challenges in developing a safe and effective TIKI can be overcome. Three subjects implanted with the research TIKI all reported benefit from routine use. For each subject, hearing outcomes using invisible hearing mode were not as good as when using the external ESPrit 3G sound processor in the conventional mode.

© 2008 Otology & Neurotology, Inc.

You currently do not have access to this article.

You may need to:

Note: If your society membership provides for full-access to this article, you may need to login on your society’s web site first.

Article Tools

You currently do not have access to this article.

You may need to:

Note: If your society membership provides for full-access to this article, you may need to login on your society’s web site first.

Search for Similar Articles
You may search for similar articles that contain these same keywords or you may modify the keyword list to augment your search.