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  3. Two-phase survey on the frequency of use and safety of MRI for hearing implant recipients.
 

Two-phase survey on the frequency of use and safety of MRI for hearing implant recipients.

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BORIS DOI
10.48350/155432
Date of Publication
March 31, 2021
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
van de Heyning, Paul
Mertens, Griet
Topsakal, Vedat
de Brito, Ruben
Wimmer, Wilhelmorcid-logo
Universitätsklinik für Hals-, Nasen- und Ohrenkrankheiten, Kopf- und Halschirurgie (HNOK)
Caversaccio, Marco
Universitätsklinik für Hals-, Nasen- und Ohrenkrankheiten, Kopf- und Halschirurgie (HNOK)
Dazert, Stefan
Volkenstein, Stefan
Zernotti, Mario
Parnes, Lorne S
Staecker, Hinrich
Bruce, Iain A
Rajan, Gunesh
Atlas, Marcus
Friedland, Peter
Skarzynski, Piotr H
Sugarova, Serafima
Kuzovkov, Vladislav
Hagr, Abdulrahman
Mlynski, Robert
Schmutzhard, Joachim
Usami, Shin-Ichi
Lassaletta, Luis
Gavilán, Javier
Godey, Benoit
Raine, Christopher H
Hagen, Rudolf
Sprinzl, Georg M
Brown, Kevin
Baumgartner, Wolf-Dieter
Karltorp, Eva
Subject(s)

600 - Technology::610...

Series
European archives of oto-rhino-laryngology
ISSN or ISBN (if monograph)
0937-4477
Publisher
Springer
Language
English
Publisher DOI
10.1007/s00405-020-06525-3
PubMed ID
33788034
Uncontrolled Keywords

Auditory brainstem im...

Description
PURPOSE

Magnetic resonance imaging (MRI) is often used to visualize and diagnose soft tissues. Hearing implant (HI) recipients are likely to require at least one MRI scan during their lifetime. However, the MRI scanner can interact with the implant magnet, resulting in complications for the HI recipient. This survey, which was conducted in two phases, aimed to evaluate the safety and performance of MRI scans for individuals with a HI manufactured by MED-EL (MED-EL GmbH, Innsbruck, Austria).

METHODS

A survey was developed and distributed in two phases to HEARRING clinics to obtain information about the use of MRI for recipients of MED-EL devices. Phase 1 focused on how often MRI is used in diagnostic imaging of the head region of the cochlear implant (CI) recipients. Phase 2 collected safety information about MRI scans performed on HI recipients.

RESULTS

106 of the 126 MRI scans reported in this survey were performed at a field strength of 1.5 T, on HI recipients who wore the SYNCHRONY CI or SYNCHRONY ABI. The head and spine were the most frequently imaged regions. 123 of the 126 scans were performed without any complications; two HI recipients experienced discomfort/pain. One recipient required reimplantation after an MRI was performed using a scanner that had not been approved for that implant. There was only one case that required surgical removal of the implant to reduce the imaging artefact.

CONCLUSION

Individuals with either a SYNCHRONY CI or SYNCHRONY ABI from MED-EL can safely undergo a 1.5 T MRI when it is performed according to the manufacturer's safety policies and procedures.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/41718
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Van-de-heyning-2021-Two-phase-survey-on-the-frequency-o.pdfAdobe PDF461.6 KBpublishedOpen
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