2015
DOI: 10.1002/lary.25670
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Safety and effectiveness of the Vibrant Soundbridge in treating conductive and mixed hearing loss: A systematic review

Abstract: As demonstrated in the literature, the VSB as an active device offers an effective alternative for patients with various middle ear pathologies, particularly with mixed hearing loss and failed previous tympanoplasties when classical ossiculoplasty could not provide enough functional gain. This new strategy in hearing rehabilitation has led to an improved quality of hearing and life. Laryngoscope, 126:1451-1457, 2016.

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Cited by 55 publications
(46 citation statements)
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“…The surgical procedure is straight forward and nowadays considered to be a routine surgery procedure [Lenarz et al, 1998]. The safety and efficiency of the system have been proven many times over the last 2 decades [Fraysse et al, 2001;Hüttenbrink et al, 2010;Schwab et al, 2012;Maier et al, 2015;Ernst et al, 2016;Bruchhage et al, 2017].…”
Section: Introductionmentioning
confidence: 99%
“…The surgical procedure is straight forward and nowadays considered to be a routine surgery procedure [Lenarz et al, 1998]. The safety and efficiency of the system have been proven many times over the last 2 decades [Fraysse et al, 2001;Hüttenbrink et al, 2010;Schwab et al, 2012;Maier et al, 2015;Ernst et al, 2016;Bruchhage et al, 2017].…”
Section: Introductionmentioning
confidence: 99%
“…An active middle ear implant using the Vibrant Soundbridge (VSB; MED-EL, Innsbruck, Austria) is another option for auditory rehabilitation in patients with mixed hearing loss who failed with conventional modalities. 2) The floating mass transducer (FMT) of the VSB can be placed on various middle ear structures either directly or using different types of couplers in order to deliver vibratory mechanical energy to the cochlea. 3) It is challenging to achieve sufficient hearing gain in patients with mixed hearing loss.…”
Section: Introductionmentioning
confidence: 99%
“…Late complications, (1 year or more postoperative) including implant or wire extrusion, dislocation of transducer/coupler assembly and loss of coupling (e.g., increase in in situ thresholds) need to be reported, as well as technical complications and device failures. If a revision surgery was necessary, it must be stated whether it was due to medical/ surgical (procedure) or device-related reasons [Ernst et al, 2016;Gavilan et al, 2015;Hobson et al, 2010;Lassaletta et al, 2016;Mohamad et al, 2016;Van Rompaey et al, 2011;Wazen et al, 2011;Zwartenkot et al, 2016].…”
Section: Reporting Of Surgical and Medical Characteristicsmentioning
confidence: 99%