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Cochlear Implant Receiver Location and Migration: Experimental Validation Pilot Study of a Clinically Applicable Screening Method

机译:耳蜗植入接收器位置和迁移:临床应用筛选方法的实验验证试验研究

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Objectives: Postoperative follow-up after cochlear implantation lacks a reliable screening method to detect cochlear implant receiver device migration. This study aims to validate a clinically applicable method to assess the position and migration of the cochlear implant receiver device. Study design: Validation study. Setting: Tertiary university medical center. Participants and method: To assess the cochlear implant receiver device location, round markers representing the external magnet were placed on both sides of the head of volunteers. Four independent clinicians took measurements of the distances between reference points on the head and the center of the marker. The reference points were: the lateral canthus (LC), tragus tip (TT), the mastoid angle (MA), and the mandibular angle (AM). Main outcome measures: The inter-clinician reliability was determined by calculating the intraclass correlation coefficient (ICC) and confidence interval (CI) with a two-way mixed model and both consistency and absolute agreement types for each distance. Results: Eight volunteers were included resulting in 16 individual cases. The consistency type ICC's for each reference point were: LC 0.90 (CI = 0.80, 0.96), TT 0.83 (CI = 0.69, 0.93), MA 0.75 (CI = 0.56, 0.89), and AM 0.29 (CI = 0.05, 0.59). The absolute agreement ICC's were: LC 0.87 (CI = 0.73, 0.95), TT 0.83 (CI = 0.68, 0.93), MA 0.68 (CI = 0.42, 0.86), and AM 0.18 (CI = 0.01, 0.46). The inter-clinician reliability was good to excellent for the lateral canthus and tragus tip reference points. Conclusions: The cochlear receiver device location can be assessed reliably by measuring the distance between the LC, TT, and the external magnet. This method can be used to registrate implant receiver location after implantation and detect implant migration postoperatively.
机译:目的:耳蜗植入后的术后随访缺乏可靠的筛选方法来检测耳蜗植入接收器装置迁移。本研究旨在验证临床适用的方法,以评估耳蜗植入机器设备的位置和迁移。研究设计:验证研究。环境:第三大学医学中心。参与者和方法:评估耳蜗植入机器设备的位置,将代表外部磁铁的圆形标记放置在志愿者头部的两侧。四名独立临床医生对头部和标记中心之间的参考点之间的距离进行了测量。参考点是:横向角膜(LC),曲子尖端(TT),乳突角(MA)和下颌角(AM)。主要结果措施:通过使用双向混合模型和每个距离的双向混合模型计算脑内相关系数(ICC)和置信区间(CI)来确定临床医生可靠性。结果:包括八名志愿者,导致16个个别案件。每个参考点的一致性ICC为:LC 0.90(CI = 0.80,0.96),TT 0.83(CI = 0.69,0.93),MA 0.75(CI = 0.56,0.89),AM 0.29(CI = 0.05,0.59) 。绝对协议ICC是:LC 0.87(CI = 0.73,0.95),TT 0.83(CI = 0.68,0.93),MA 0.68(CI = 0.42,0.86),AM 0.18(CI = 0.01,0.46)。临床医生可靠性良好至于横向骑族和曲折尖端参考点。结论:通过测量LC,TT和外部磁体之间的距离,可以可靠地评估耳蜗接收器设备位置。该方法可用于在植入后注册植入接收器位置并术后检测植入物迁移。

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