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MR compatibility of Med EL cochlear implants: clinical testing at 1.0 T.

机译:Med EL人工耳蜗的MR兼容性:1.0 T下的临床测试。

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PURPOSE: Our aim was to evaluate the MR compatibility of Med EL cochlear implants by performing in vitro and in vivo tests. METHOD: All experiments were done on a 1.0 T machine. Potential movement of the cochlear electrode relative to a scale was recorded. Potential dislodgment of the magnetic receiver coil was evaluated with the coil fixed to the retroauricular skin of a volunteer. Temperature changes were measured with temperature sensors fixed to the electrode, performing standard MR sequences. In 11 patients, MRI of the brain was performed 1 day before explantation of the devices using standard MR sequences. Testing of the auditory abilities was done before and after the examination. All explanted devices were assessed for function. RESULTS: There was no detectable movement of the electrode or the receiver coil nor any temperature change. There were no adverse events for the patients. All 11 explanted cochlear implants retained their function. CONCLUSION: Med EL cochlear implants are not a firm contraindication for MRI.
机译:目的:我们的目的是通过进行体外和体内测试来评估Med EL人工耳蜗的MR兼容性。方法:所有实验均在1.0 T机器上进行。记录耳蜗电极相对于标尺的电位运动。在将线圈固定在志愿者的耳后皮肤上的情况下,评估了电磁接收器线圈的潜在位移。用固定在电极上的温度传感器测量温度变化,执行标准的MR序列。在11例患者中,在使用标准MR序列植入设备前1天进行了脑部MRI检查。在检查之前和之后进行听觉能力的测试。对所有植入的装置进行功能评估。结果:没有发现电极或接收线圈的运动,也没有任何温度变化。没有患者的不良事件。所有11种外植的人工耳蜗均保持其功能。结论:Med EL人工耳蜗不是MRI的严格禁忌症。

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