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关于听力植入物接受者使用 MRI 的频率和安全性的两阶段调查。

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

机构信息

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

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

出版信息

Eur Arch Otorhinolaryngol. 2021 Nov;278(11):4225-4233. doi: 10.1007/s00405-020-06525-3. Epub 2021 Mar 31.

Abstract

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.

摘要

目的

磁共振成像(MRI)常用于可视化和诊断软组织。人工耳蜗(HI)植入者在其一生中可能至少需要进行一次 MRI 扫描。然而,MRI 扫描仪可能会与植入磁体相互作用,从而对 HI 植入者造成并发症。本研究分两个阶段进行,旨在评估奥地利 MED-EL 公司(MED-EL GmbH,因斯布鲁克)生产的 HI 患者进行 MRI 扫描的安全性和性能。

方法

设计了一项调查,并在两个阶段分发给 HEARRING 诊所,以获取有关 MED-EL 设备植入者 MRI 使用情况的信息。第 1 阶段侧重于 MRI 在 Cochlear 植入(CI)接受者头部区域的诊断成像中的使用频率。第 2 阶段收集了关于对 HI 接受者进行 MRI 扫描的安全性信息。

结果

本研究报告的 106 次 MRI 扫描中,有 126 次是在磁场强度为 1.5T 的情况下对佩戴 SYNCHRONY CI 或 SYNCHRONY ABI 的 HI 接受者进行的。头部和脊柱是最常成像的区域。126 次扫描中,有 123 次无任何并发症;2 名 HI 接受者感到不适/疼痛。在使用未经批准的扫描仪对植入物进行 MRI 后,一名植入者需要重新植入。只有 1 例需要手术取出植入物,以减少成像伪影。

结论

符合条件的 MED-EL 公司的 SYNCHRONY CI 或 SYNCHRONY ABI 植入者,在遵循制造商的安全政策和程序的情况下,可安全地进行 1.5T MRI 扫描。

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