Emmeline Centre for Hearing Implants.
Otology and Skull Base Unit, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Otol Neurotol. 2020 Jun;41(5):e556-e562. doi: 10.1097/MAO.0000000000002569.
To assess the complication rate of magnetic resonance imaging (MRI) using 1.5 T scanners on cochlear implant (CI) and auditory brainstem implant (ABI) recipients over 14.5 years.
Prospective study conducted in a tertiary referral center for cochlear and auditory brainstem implantation, including patients with neurofibromatosis 2. The primary outcome was complications related to MRI scanning in implant recipients, including failure to complete MRI sessions. The secondary outcome was magnet void size due to MRI scanning with magnet in situ.
Ninety-seven patients (21 ABI recipients, 76 CI recipients of whom 23 were bilateral) underwent a total of 428 MRI sessions consisting of 680 MRI procedures, which generated 2,601 MRI sequences (excluding localizers). Of these, 28/428 (6.5%) MRI sessions were performed with magnet removed, and the remaining 400/428 (93.4%) with the magnet in situ. The overall complication rate per session was 15/428 (3.5%). The majority of complications were accounted for by patient discomfort, in some cases requiring abandoning the scan session, but 5 magnet dislocations were also recorded. There were no cases of implant device failure or excessive demagnetization of the receiver stimulator magnet.For CI and ABI recipients, the implant caused large voids of around 110 mm × 60 mm with the magnet in situ which reduced to 60 mm × 30 mm when the magnet was removed. However, it was usually possible to visualize the internal acoustic meatus and cerebellopontine angle by positioning the implant package higher and further forward compared with conventional positioning.
MRI scanning in ABI and CI recipients is generally safe and well tolerated without magnet removal, and carries a low rate of complications. However, patients should be fully informed of the possibility of discomfort, and precautions such as local anesthetic injection and head bandaging may reduce the likelihood of adverse events.
评估在 14.5 年以上的时间里,1.5T 扫描仪对接受耳蜗植入(CI)和听觉脑干植入(ABI)的患者进行磁共振成像(MRI)的并发症发生率。
这是一项在三级转诊中心进行的前瞻性研究,包括神经纤维瘤病 2 型患者。主要结局是与 MRI 扫描相关的植入物受检者的并发症,包括未能完成 MRI 检查。次要结局是 MRI 扫描时原位磁铁的磁体空隙大小。
97 名患者(21 名 ABI 受检者,76 名 CI 受检者,其中 23 名双侧)共进行了 428 次 MRI 检查,共进行了 680 次 MRI 检查,共生成了 2601 次 MRI 序列(不包括定位器)。其中,28/428(6.5%)次 MRI 检查在移除磁铁后进行,其余 400/428(93.4%)次 MRI 检查在磁铁原位进行。每次检查的总体并发症发生率为 15/428(3.5%)。大多数并发症是由患者不适引起的,在某些情况下需要放弃扫描,但也记录了 5 例磁铁脱位。没有植入物设备故障或接收器刺激器磁铁过度退磁的情况。对于 CI 和 ABI 受检者,当磁铁在位时,植入物会产生大约 110mm×60mm 的大空隙,当磁铁移除时,空隙会缩小到 60mm×30mm。然而,通过将植入物包定位得更高、更靠前,通常可以观察到内听道和桥小脑角。
在不移除磁铁的情况下,ABI 和 CI 受检者的 MRI 扫描通常是安全且耐受良好的,并发症发生率较低。然而,应充分告知患者可能出现不适,并采取局部麻醉注射和头部包扎等预防措施,以降低不良事件的发生概率。