Nospes S, Brockmann M A, Läßig A
Schwerpunkt Kommunikationsstörungen/HNO-Klinik, Universitätsmedizin Mainz, Langenbeckstr. 1, 55131, Mainz, Deutschland.
Klinik und Poliklinik für Neuroradiologie, Universitätsmedizin Mainz, Mainz, Deutschland.
Radiologe. 2019 Jan;59(1):48-56. doi: 10.1007/s00117-018-0462-9.
More than 100,000 patients with cochlear implants live in Germany. In addition, numerous patients have auditory bone conducted, middle-ear conducted or brainstem conducted implants equipped with implanted magnets. At the same time, the number of patients being examined by magnetic resonance imaging (MRI) is increasing. Therefore, MRI compatibility of these implants is an essential quality feature.
This article provides information about technical innovations and new auditory devices since November 2013 that have medical-technical certification in the European Union and the USA. We communicate the restrictions of the manufacturers and a selective literature search in PubMed using the following keywords: MRI compatibility/MRI safety + cochlear implant/auditory brainstem implant/Bonebridge/Sophono alpha/Vibrand Soundbridge/BAHA attract. We included all publications of this search concerning MRI compatibility of hearing implants complemented by papers cited in the primary articles.
In rare cases, high electromagnetic field intensities as used in MRI can cause shearing movements up to dislocation of the implant or the magnet of the device. As a result the implant function could fail. Image artifacts in head MRIs can be reduced by using appropriate MRI sequences. Nevertheless, possible artifacts and the hereby reduced validity of the skull MRI results have to be considered when indicating the examination. Meanwhile, all innovations of these auditory devices are licensed to 1.5 T MRI examination, some implants up to 3.0 T MRI magnetic field intensity. For older devices, the necessary safety measures listed in the article published by Nospes, Mann and Keilmann in November 2013 should be used.
Respecting the manufacturer's instructions, MRI scans without removal of the magnet in patients with these auditory implants is safe. However, due to possible defects/dislocations of the implant that may occur and the reduced quality of the skull MRI images, the indication for MRI in devices with MRI certification should only be performed under close consultation between the investigating physicians, the implanting team supervising the patient and the radiologist. All other possible diagnostic procedures should be exhausted first.
德国有超过10万名人工耳蜗植入患者。此外,许多患者佩戴了配备植入式磁体的听觉骨传导、中耳传导或脑干传导植入物。与此同时,接受磁共振成像(MRI)检查的患者数量正在增加。因此,这些植入物的MRI兼容性是一项至关重要的质量特性。
本文提供了自2013年11月以来具有欧盟和美国医学技术认证的技术创新和新型听觉装置的信息。我们传达了制造商的限制,并在PubMed中使用以下关键词进行了选择性文献检索:MRI兼容性/MRI安全性+人工耳蜗/听觉脑干植入物/骨桥/Sophono alpha/振动声桥/BAHA attract。我们纳入了此次检索中所有关于听力植入物MRI兼容性的出版物,并补充了主要文章中引用的论文。
在极少数情况下,MRI中使用的高电磁场强度可能会导致剪切运动,直至植入物或设备磁体脱位。结果,植入物功能可能会失效。通过使用适当的MRI序列,可以减少头部MRI中的图像伪影。然而,在进行检查时,必须考虑可能的伪影以及由此降低的颅骨MRI结果的有效性。同时,这些听觉装置的所有创新产品都已获得1.5T MRI检查许可,一些植入物可达3.0T MRI磁场强度。对于较旧的设备,应采用Nospes、Mann和Keilmann在2013年11月发表的文章中列出的必要安全措施。
遵循制造商的说明,这些听觉植入患者在不取出磁体的情况下进行MRI扫描是安全的。然而,由于可能出现的植入物缺陷/脱位以及颅骨MRI图像质量下降,对于具有MRI认证的设备,MRI检查的指征应仅在调查医生、监督患者的植入团队和放射科医生密切协商后进行。所有其他可能的诊断程序应首先用尽。