Department of Otolaryngology-Head and Neck Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Department of Hearing and Speech Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Otolaryngol Head Neck Surg. 2024 May;170(5):1411-1420. doi: 10.1002/ohn.677. Epub 2024 Feb 14.
To assess patient factors, audiometric performance, and patient-reported outcomes in cochlear implant (CI) patients who would not have qualified with in-quiet testing alone.
Retrospective chart review.
Tertiary referral center.
Adult CI recipients implanted between 2012 and 2022 were identified. Patients with preoperative AzBio Quiet > 60% in the implanted ear, requiring multitalker babble to qualify, comprised the in-noise qualifying (NQ) group. NQ postoperative performance was compared with the in-quiet qualifying (QQ) group using CNC, AzBio Quiet, and AzBio +5 dB signal-to-noise ratio. Speech, Spatial and Qualities of Hearing Scale (SSQ), Cochlear Implant Quality of Life scale (CIQOL-10), and daily device usage were also compared between the groups.
The QQ group (n = 771) and NQ group (n = 67) were similar in age and hearing loss duration. NQ had higher average preoperative and postoperative speech recognition scores. A larger proportion of QQ saw significant improvement in CNC and AzBio Quiet scores in the CI-only listening condition (eg, CI-only AzBio Quiet: 88% QQ vs 51% NQ, P < .001). Improvement in CI-only AzBio +5 dB and in all open set testing in the best-aided binaural listening condition was similar between groups (eg, Binaural AzBio Quiet 73% QQ vs 59% NQ, P = .345). Postoperative SSQ ratings, CIQOL scores, and device usage were also equivalent between both groups.
Patients who require in-noise testing to meet CI candidacy demonstrate similar improvements in best-aided speech perception and patient-reported outcomes as in-QQ, supporting the use of in-noise testing to determine CI qualification for borderline CI candidates.
评估不符合安静测试标准但通过噪声测试而有资格植入人工耳蜗的患者的患者因素、听力表现和患者报告的结果。
回顾性图表审查。
三级转诊中心。
确定了 2012 年至 2022 年间植入人工耳蜗的成年人工耳蜗植入患者。术前在植入耳中 AzBio Quiet > 60%,需要多说话者杂音才能合格的患者构成噪声测试合格(NQ)组。使用 CNC、AzBio Quiet 和 AzBio +5 dB 信噪比比较 NQ 术后表现与安静测试合格(QQ)组。比较两组间的言语、空间和听力量表(SSQ)、人工耳蜗生活质量量表(CIQOL-10)和日常设备使用率。
QQ 组(n = 771)和 NQ 组(n = 67)在年龄和听力损失持续时间方面相似。NQ 患者的术前和术后言语识别评分更高。在仅使用人工耳蜗的听力条件下,QQ 组有更大比例的患者 CNC 和 AzBio Quiet 评分显著改善(例如,仅使用人工耳蜗的 AzBio Quiet:88% QQ 比 51% NQ,P <.001)。在最佳辅助双耳听力条件下,仅使用人工耳蜗的 AzBio +5 dB 和所有开放式测试的改善在两组之间相似(例如,双耳 AzBio Quiet:73% QQ 比 59% NQ,P =.345)。术后 SSQ 评分、CIQOL 评分和设备使用率在两组之间也相当。
需要噪声测试才能符合人工耳蜗候选资格的患者在最佳辅助言语感知和患者报告的结果方面表现出相似的改善,支持使用噪声测试来确定边缘性人工耳蜗候选者的人工耳蜗资格。