Parkinson Aaron J, Arcaroli Jennifer, Staller Steven J, Arndt Patti L, Cosgriff Anne, Ebinger Kiara
Cochlear Corporation, Englewood, Colorado 80112, USA.
Ear Hear. 2002 Feb;23(1 Suppl):41S-48S. doi: 10.1097/00003446-200202001-00005.
The purpose of this article is to present psychophysical data for 40 Nucleus 24 Contour adult patients with 1 mo of device experience and speech perception results for a group of 56 adult patients with 3 mo experience using the Nucleus 24 Contour cochlear implant system. Postoperative hearing thresholds (i.e., under headphones) in the implanted ear were also assessed in a group of 85 patients who had measurable hearing preoperatively. This was of interest because preservation of residual hearing, postoperatively, is consistent with atraumatic insertion of the electrode array. In addition, data will be presented that reflected feedback from 40 surgeons who participated in the trial.
Participants in this study were 18 yr of age or older, with bilateral severe to profound sensorineural hearing loss with no congenital component. Preoperatively, they scored < or = 50% open-set sentence recognition (HINT sentences) in the ear to be implanted and < or = 60% in the best-aided condition. The investigation was a repeated-measures single-subject experiment and took place at 46 different North American clinical sites. Preoperative performance was compared with postoperative performance 3 mo after device activation. Clinicians were able to program patients' processors with one, two, or all three speech-processing strategies. Testing took place using the participant's preferred speech-processing strategy (SPEAK, CIS, or ACE). Preoperative unaided hearing thresholds were compared with unaided thresholds in the implanted ear measured 1 mo after device activation. Surgeons were canvassed regarding surgical use and design of the device via a questionnaire after having completed at least one Nucleus 24 Contour surgery.
Average T- and C-levels for the Nucleus 24 Contour patients were considerably lower than those using the Nucleus 24 (CI24M). A total of 85 patients had measurable hearing preoperatively at two or more audiometric frequencies in the ear implanted. Of these patients 41 (48%) had measurable hearing at one or more frequencies and 32 (38%) had measurable hearing at two or more frequencies postoperatively. In general, surgeons found the Nucleus 24 Contour easy to insert and were pleased with the design features of the device. The downsized receiver/stimulator (of the Nucleus 24 Contour) required less drilling than the Nucleus 24, reducing surgical time, as well as making the Contour better suited for implantation in those with small skull sizes (e.g., small children and infants). After 3 mo of device use, mean open-set speech perception in quiet and in noise was significantly better than preoperative performance on all test measures. Patients using the ACE strategy had significantly better mean scores for all measures than patients using SPEAK. Only two patients preferred to use the CIS coding strategy. CONCLUSIONS The results presented in this article demonstrated that the design objectives of the Nucleus 24 Contour were met. Namely, results from this study, together with insertion studies, were consistent with perimodiolar placement using an implant design that the majority of surgeons found easy to insert with relatively minimal trauma. Reduced T- and C-levels were observed with Contour patients when compared with patients using the Nucleus 24 with the straight array, consistent with perimodiolar placement. A survey of surgeons participating in the clinical trial indicated easier, or equally easy, insertion of the Contour array, compared with previous Nucleus products as well as other manufacturers' devices, without the use of additional insertion tools or array positioners. Postoperatively, 46% of patients with preoperative residual hearing maintained some level of unaided hearing postoperatively, suggesting atraumatic insertion of the Nucleus 24 Contour electrode array. It is worth noting that all 216 patients implanted during this study had full insertions of their Contour electrode arrays. High levels of open-set speech perception in quiet and in noise were achieved and patients using the ACE strategy had significantly better mean scores for all measures than patients using SPEAK. Only two patients preferred to use the CIS coding strategy.
本文旨在呈现40名使用Nucleus 24 Contour成人耳蜗植入系统1个月的患者的心理物理学数据,以及56名使用该系统3个月的成人患者的言语感知结果。还对一组85名术前有可测量听力的患者植入耳的术后听力阈值(即头戴耳机时)进行了评估。这一点很重要,因为术后残余听力的保留与电极阵列的无创伤插入是一致的。此外,还将呈现来自参与该试验的40位外科医生的反馈数据。
本研究的参与者年龄在18岁及以上,患有双侧严重至极重度感音神经性听力损失且无先天性因素。术前,他们在拟植入耳中的开放式语句识别(HINT语句)得分≤50%,在最佳助听条件下得分≤60%。该研究是一项重复测量单受试者实验,在北美46个不同的临床地点进行。将术前表现与设备激活后3个月的术后表现进行比较。临床医生能够使用一种、两种或所有三种言语处理策略为患者的处理器进行编程。测试使用参与者首选的言语处理策略(SPEAK、CIS或ACE)进行。将术前未助听听力阈值与设备激活后1个月测量的植入耳未助听阈值进行比较。在完成至少一例Nucleus 24 Contour手术后,通过问卷调查向外科医生询问该设备的手术使用和设计情况。
Nucleus 24 Contour患者的平均T级和C级明显低于使用Nucleus 24(CI24M)的患者。共有85名患者在植入耳的两个或更多听力计频率上术前有可测量听力。在这些患者中,41名(48%)术后在一个或更多频率上有可测量听力,32名(38%)在两个或更多频率上有可测量听力。总体而言,外科医生发现Nucleus 24 Contour易于插入,并对该设备的设计特点感到满意。(Nucleus 24 Contour的)小型化接收器/刺激器比Nucleus 24需要更少的钻孔,减少了手术时间,也使Contour更适合植入颅骨尺寸较小的患者(如小儿和婴儿)。设备使用3个月后,在所有测试指标上,安静和噪声环境下的平均开放式言语感知明显优于术前表现。使用ACE策略的患者在所有指标上的平均得分显著高于使用SPEAK策略的患者。只有两名患者更喜欢使用CIS编码策略。结论本文呈现的结果表明,Nucleus 24 Contour的设计目标得以实现。也就是说,本研究结果与植入研究结果一致,即使用大多数外科医生认为易于插入且创伤相对较小的植入设计实现了蜗周植入。与使用直阵列的Nucleus 24患者相比,Contour患者的T级和C级降低,这与蜗周植入一致。对参与临床试验的外科医生的一项调查表明,与之前的Nucleus产品以及其他制造商的设备相比,Contour阵列更容易或同样容易插入,无需使用额外的插入工具或阵列定位器。术后,46%术前有残余听力的患者术后保持了一定程度的未助听听力,这表明Nucleus 24 Contour电极阵列的插入是无创伤的。值得注意的是,在本研究中植入的所有216名患者的Contour电极阵列均完全插入。在安静和噪声环境下均实现了高水平的开放式言语感知,使用ACE策略的患者在所有指标上的平均得分显著高于使用SPEAK策略的患者。只有两名患者更喜欢使用CIS编码策略。