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

Auditory brainstem implant Bone conduction Cochlear implant Magnetic resonance imaging Middle ear implant Safety

Journal

European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
ISSN: 1434-4726
Titre abrégé: Eur Arch Otorhinolaryngol
Pays: Germany
ID NLM: 9002937

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 15 06 2020
accepted: 26 11 2020
pubmed: 1 4 2021
medline: 6 10 2021
entrez: 31 3 2021
Statut: ppublish

Résumé

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). 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. 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. 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.

Identifiants

pubmed: 33788034
doi: 10.1007/s00405-020-06525-3
pii: 10.1007/s00405-020-06525-3
pmc: PMC8486706
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4225-4233

Informations de copyright

© 2021. The Author(s).

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Auteurs

Paul van de Heyning (P)

ENT Department, Antwerp University Hospital (UZA), Edegem/Antwerp, Belgium. paul@vandeheyning.com.

Griet Mertens (G)

ENT Department, Antwerp University Hospital (UZA), Edegem/Antwerp, Belgium.

Vedat Topsakal (V)

ENT Department, Antwerp University Hospital (UZA), Edegem/Antwerp, Belgium.

Ruben de Brito (R)

Hospital for Rehabilitation of Cranio-Facial Anomalies, Bauru-Sao Paulo, Brazil.

Wilhelm Wimmer (W)

Department for ENT, Head and Neck Surgery, Bern University Hospital, Bern, Switzerland.

Marco D Caversaccio (MD)

Department for ENT, Head and Neck Surgery, Bern University Hospital, Bern, Switzerland.

Stefan Dazert (S)

Bochum St. Elisabeth University Hospital, Bochum, Germany.

Stefan Volkenstein (S)

Bochum St. Elisabeth University Hospital, Bochum, Germany.

Mario Zernotti (M)

Córdoba Sanatorium Allende, Servicio de Otorrinolaryingologia (Servicio ORL), Córdoba, Argentina.

Lorne S Parnes (LS)

London Health Sciences Center-University Hospital, London, Ontario, Canada.

Hinrich Staecker (H)

Department of Otorinolaryngology, Kansas University Center for Hearing and Balance Disorders, Kansas City, USA.

Iain A Bruce (IA)

Pediatric ENT Department, Royal Manchester Children's Hospital, Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.
Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

Gunesh Rajan (G)

University of Western Australia, Crawley, Perth, Australia.
Department of Otolaryngology, Head and Neck Surgery, Luzerner Kantonsspital, Luzern, Switzerland.

Marcus Atlas (M)

Ear Sciences Center, Lions Hearing Clinic, Subiaco, Australia.

Peter Friedland (P)

Ear Sciences Center, Lions Hearing Clinic, Subiaco, Australia.

Piotr H Skarzynski (PH)

Institute of Sensory Organs, Nadarzyn/Kajetany, Poland.
Department of Teleaudiology and Screening, World Hearing Center of the Institute of Physiology and Pathology of Hearing, Kajetany, Poland.

Serafima Sugarova (S)

St. Petersburg ENT and Speech Research Institute, St. Petersburg, Russia.

Vladislav Kuzovkov (V)

St. Petersburg ENT and Speech Research Institute, St. Petersburg, Russia.

Abdulrahman Hagr (A)

King Abdullah Ear Specialist Center, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.

Robert Mlynski (R)

Universität Rostock "Otto Körner", Klinik und Poliklinik für Hals-Nasen-Ohrenheilkunde, Rostock, Germany.

Joachim Schmutzhard (J)

ENT Department, Medical University of Innsbruck, Innsbruck, Austria.

Shin-Ichi Usami (SI)

Shinshu University School of Medicine, Matsumoto, Japan.

Luis Lassaletta (L)

Madrid Hospital La Paz, Madrid, Spain.

Javier Gavilán (J)

Madrid Hospital La Paz, Madrid, Spain.

Benoit Godey (B)

Centre Hospitalier Universitaire (CHU) de Rennes, Rennes, France.

Christopher H Raine (CH)

Bradford Royal Infirmary Yorkshire Auditory Implant Center, Bradford, UK.

Rudolf Hagen (R)

Würzburg ENT University Hospital, Würzburg, Germany.

Georg M Sprinzl (GM)

St. Pölten University Hospital, St. Pölten, Austria.

Kevin Brown (K)

UNC Ear and Hearing Center at Chapel Hill School of Medicine, Chapel Hill, NC, USA.

Wolf-Dieter Baumgartner (WD)

Vienna Medical University-General Hospital AKH, Vienna, Austria.

Eva Karltorp (E)

Karolinska University Hospital, Solna, Sweden.

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Classifications MeSH