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Vibrant Soundbridge – Lessons Learnt Over Two Decades

Presenting Author: Jeyanthi Kulasegarah

Published online by Cambridge University Press:  03 June 2016

Jeyanthi Kulasegarah
Affiliation:
Queen Elizabeth Hospital Birmingham
Nina Mistry
Affiliation:
Queen Elizabeth Hospital Birmingham
Huw Cooper
Affiliation:
Queen Elizabeth Hospital Birmingham
Stuart Burrell
Affiliation:
Queen Elizabeth Hospital Birmingham
Christopher Coulson
Affiliation:
Queen Elizabeth Hospital Birmingham
Konstance Tzifa
Affiliation:
Queen Elizabeth Hospital Birmingham
Richard Irving
Affiliation:
Queen Elizabeth Hospital Birmingham
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Abstract

Type
Abstracts
Copyright
Copyright © JLO (1984) Limited 2016 

Learning Objectives: Appropriate patient selection for middle ear implant is important.

Introduction: The Vibrant Soundbridge (VSB) is an active middle ear implant that is currently used in patients with conductive, sensorineural, and mixed hearing loss. Initially it was intended for adults with moderate to severe sensorineural hearing loss with previous experience with conventional hearing aids. Since 2006, it was also used for conductive hearing loss and from 2009 onwards, the indication was extended to children. The first implantation in UK was performed in 1997 in our department.

Objective: Our experience of VSB over a period of almost two decades will be presented.

Method: A retrospective survey of two groups of patients: Group I (VSB inserted 1997–2002) and Group II (VSB inserted 2011–2015) were conducted. We looked at indications, surgical and audiological data between the two groups. Long-term follow-up data presented for Group I.

Results: In total 28 VSB were implanted between 1997 and 2015: 14 patients in Group I and 12 patients in Group II (2 patients with bilateral VSB implants). In Group I, all 14 patients had the VSB coupled to the incus for moderate to severe sensorineural hearing loss. Among them, 6 patients are still VSB users. One patient went on to have a cochlear implant 9 years after VSB surgery due to progressive hearing loss. In Group II, all apart from one patient is a VSB user 12 months post implantation. Two patients had round window placement and one patient had a stapes placement, the remaining 11 VSB were the conventional incus coupler. The indications included conductive and mixed hearing loss for chronic middle ear disease (4 patients) and obliterative otitis externa (2 patients).

Conclusion: The VSB implantable hearing technology has been proven to be safe, effective and highly desirable option for patients with conductive, mixed and sensorineural hearing loss. With improvements in patient selection and technology, patient outcomes have improved over time.