Brown C J, Abbas P J, Gantz B J
Department of Otolaryngology-Head and Neck Surgery, The University of Iowa, Iowa City, USA.
Am J Otol. 1998 May;19(3):320-7.
This study aimed to compare recordings of the electrically evoked whole nerve action potential (EAP) made using the reverse telemetry system of the Nucleus CI24M device with those recorded from individuals who use the Ineraid cochlear implant system.
Data were collected in a prospective fashion from Nucleus CI24M cochlear implant users and compared with retrospective data collected from patients who use the Ineraid device.
All data were collected at the Department of Otolaryngology-Head and Neck Surgery, University of Iowa Hospitals and Clinics.
Data are reported from 8 patients who use the Nucleus CI24M cochlear implant and 20 patients who use the Ineraid cochlear implant system.
The interventions described in this study were diagnostic in nature.
EAP growth and refractory recovery data are reported. EAP thresholds recorded from patients who use the Nucleus CI24M device also are compared with behavioral thresholds for the stimulus used to evoke the EAP as well as the stimulation levels needed to program the speech processor.
EAP morphology, growth, and refractory recovery functions recorded using the Nucleus CI24M reverse telemetry system compared favorably with similar measures recorded from Ineraid cochlear implant users.
Reasonable EAP responses can be recorded using the Nucleus CI24M device. More data are needed to determine whether the information about neural responsiveness available with this device will be clinically useful.
本研究旨在比较使用Nucleus CI24M设备的反向遥测系统记录的电诱发全神经动作电位(EAP)与使用Ineraid人工耳蜗系统的个体所记录的EAP。
以前瞻性方式收集Nucleus CI24M人工耳蜗使用者的数据,并与从使用Ineraid设备的患者收集的回顾性数据进行比较。
所有数据均在爱荷华大学医院和诊所的耳鼻咽喉 - 头颈外科收集。
报告了8名使用Nucleus CI24M人工耳蜗的患者和20名使用Ineraid人工耳蜗系统的患者的数据。
本研究中描述的干预措施本质上是诊断性的。
报告了EAP增长和不应期恢复数据。还将使用Nucleus CI24M设备的患者记录的EAP阈值与用于诱发EAP的刺激的行为阈值以及编程言语处理器所需的刺激水平进行了比较。
使用Nucleus CI24M反向遥测系统记录的EAP形态、增长和不应期恢复功能与Ineraid人工耳蜗使用者记录的类似测量结果相比具有优势。
使用Nucleus CI24M设备可以记录合理的EAP反应。需要更多数据来确定该设备提供的有关神经反应性的信息是否具有临床实用性。