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作者信息

Müller Alexander, Kropp Miriam H, Mir-Salim Parwis, Aristeidou Aristotelis, Dziemba Oliver C

机构信息

Hörzentrum Berlin (HZB), Klinik für HNO, Vivantes Klinikum im Friedrichshain, Berlin, Deutschland.

Hörzentrum Berlin (HZB), Klinik für HNO, Vivantes Klinikum im Friedrichshain, Berlin, Deutschland.

出版信息

Z Med Phys. 2021 Aug;31(3):276-288. doi: 10.1016/j.zemedi.2020.07.002. Epub 2020 Sep 6.

Abstract

BACKGROUND

In rare cases, a cochlear implantation can lead to a so-called tip fold-over during insertion of the electrode array. In order to detect or exclude such a misalignment a radiological check of the cochlear implant (CI) electrode array is carried out intra- or often post-operatively (gold standard), thereby exposing the patient to additional radiation. Alternatively, successful electrode insertion can be verified by measuring the spread of excitation (SOE). However, interpretation of the test results requires considerable expertise, and standardized measurement protocols and reference values are also essential. Therefore, the aim of the study is to evaluate an automated screening procedure in order to obtain a reliable statement about the normal tonotopic position of the implanted CI electrode array intraoperatively and with as little effort as possible.

METHODS

For CI surgery with Cochlear™ Nucleus® implants, an intraoperative tip-fold-over (TFO) screening was performed in a bi-centric study in over 100 adult patients: Firstly, threshold measurements for electrically evoked compound action potential (ECAP) using AutoNRT™ were recorded. Subsequently, SOE measurements were carried out on electrodes 13 and 22. The automated evaluation of the SOE data sets then made it possible to make a dichotomous decision about a normal or abnormal test result. The position of the electrode array was checked intra- or post-operatively using conventional transorbital X-ray (reference method).

RESULTS

The intraoperative TFO screening procedure is applicable in around 80% of cases. The accuracy of the screening for measurements via the active stimulation electrodes 13 / 22 is 63.9% / 95.4%. The classification error is 36.1% / 4.6% and the phi coefficient is 0.27 / 0.69. All radiologically proven tip-fold-overs were reliably identified with the intraoperative screening (sensitivity = 100%). A higher specificity (>95%) can be achieved only with measurements via electrode 22.

CONCLUSIONS

The TFO Screening via measurement at electrode 22 can successfully distinguish between a correct and incorrect position of the electrode array due to a tip-fold-over, and the remaining cases would require further imaging.

摘要

背景

在极少数情况下,人工耳蜗植入过程中电极阵列插入时可能会导致所谓的尖端折叠。为了检测或排除这种错位,通常在手术中或术后对人工耳蜗(CI)电极阵列进行放射学检查(金标准),这会使患者受到额外的辐射。另外,可通过测量兴奋扩散(SOE)来验证电极是否成功插入。然而,测试结果的解读需要相当专业的知识,标准化的测量方案和参考值也至关重要。因此,本研究的目的是评估一种自动化筛查程序,以便在术中尽可能轻松地获得关于植入的CI电极阵列正常音调定位的可靠结论。

方法

对于使用科利耳公司(Cochlear™)的 Nucleus® 植入体进行的CI手术,在一项双中心研究中,对100多名成年患者进行了术中尖端折叠(TFO)筛查:首先,使用AutoNRT™记录电诱发复合动作电位(ECAP)的阈值测量值。随后,对电极13和22进行SOE测量。然后,对SOE数据集进行自动评估,从而能够对测试结果正常或异常做出二分决策。使用传统的经眶X射线(参考方法)在术中或术后检查电极阵列的位置。

结果

术中TFO筛查程序在约80%的病例中适用。通过有源刺激电极13/22进行测量的筛查准确率分别为63.9%/95.4%。分类错误率分别为36.1%/4.6%,phi系数分别为0.27/0.69。所有经放射学证实的尖端折叠均通过术中筛查可靠识别(敏感性 = 100%)。仅通过电极22进行测量才能实现更高的特异性(>95%)。

结论

通过在电极22处进行测量的TFO筛查能够成功区分由于尖端折叠导致的电极阵列位置正确与否,其余病例则需要进一步成像检查。

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