TY - JOUR
T1 - Two-phase survey on the frequency of use and safety of MRI for hearing implant recipients
AU - van de Heyning, Paul
AU - Mertens, Griet
AU - Topsakal, Vedat
AU - de Brito, Ruben
AU - Wimmer, Wilhelm
AU - Caversaccio, Marco D.
AU - Dazert, Stefan
AU - Volkenstein, Stefan
AU - Zernotti, Mario
AU - Parnes, Lorne S.
AU - Staecker, Hinrich
AU - Bruce, Iain A.
AU - Rajan, Gunesh
AU - Atlas, Marcus
AU - Friedland, Peter
AU - Skarzynski, Piotr H.
AU - Sugarova, Serafima
AU - Kuzovkov, Vladislav
AU - Hagr, Abdulrahman
AU - Mlynski, Robert
AU - Schmutzhard, Joachim
AU - Usami, Shin Ichi
AU - Lassaletta, Luis
AU - Gavilán, Javier
AU - Godey, Benoit
AU - Raine, Christopher H.
AU - Hagen, Rudolf
AU - Sprinzl, Georg M.
AU - Brown, Kevin
AU - Baumgartner, Wolf Dieter
AU - Karltorp, Eva
N1 - Publisher Copyright:
© 2021, The Author(s).
PY - 2021/11
Y1 - 2021/11
N2 - 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.
AB - 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.
KW - Auditory brainstem implant
KW - Bone conduction
KW - Cochlear implant
KW - Magnetic resonance imaging
KW - Middle ear implant
KW - Safety
UR - http://www.scopus.com/inward/record.url?scp=85103373128&partnerID=8YFLogxK
U2 - 10.1007/s00405-020-06525-3
DO - 10.1007/s00405-020-06525-3
M3 - Journal article
C2 - 33788034
AN - SCOPUS:85103373128
SN - 0937-4477
VL - 278
SP - 4225
EP - 4233
JO - European Archives of Oto-Rhino-Laryngology
JF - European Archives of Oto-Rhino-Laryngology
IS - 11
ER -