Department of Otorhinolaryngology - Head and Neck Surgery, Medical Center, Faculty of Medicine, Albert Ludwig University Freiburg, Killianstr. 5, 79106, Freiburg, Germany.
Klinik für Hals‑, Nasen- und Ohrenheilkunde, Universitätsklinikum Freiburg, Medizinische, Fakultät, Albert-Ludwigs-Universität Freiburg, Killianstr. 5, 79106, Freiburg, Germany.
HNO. 2024 Jan;72(Suppl 1):1-9. doi: 10.1007/s00106-023-01337-3. Epub 2023 Oct 9.
The active transcutaneous, partially implantable osseointegrated bone conduction system Cochlear™ Osia® (Cochlear, Sydney, Australia) has been approved for use in German-speaking countries since April 2021. The Osia is indicated for patients either having conductive (CHL) or mixed hearing loss (MHL) with an average bone conduction (BC) hearing loss of 55 dB HL or less, or having single-sided deafness (SSD).
The aim of this retrospective study was to investigate the prediction of postoperative speech recognition with Osia® and to evaluate the speech recognition of patients with MHL and in particular an aided dynamic range of less than 30 dB with Osia®.
Between 2017 and 2022, 29 adult patients were fitted with the Osia®, 10 patients (11 ears) with CHL and 19 patients (25 ears) with MHL. MHL was subdivided into two groups: MHL‑I with four-frequency pure-tone average in BC (BC-4PTA) ≥ 20 dB HL and < 40 dB HL (n = 15 patients; 20 ears) vs. MHL-II with BC-4PTA ≥ 40 dB HL (n = 4 patients; 5 ears). All patients tested a bone conduction hearing device on a softband preoperatively. Speech intelligibility in quiet was assessed preoperatively using the Freiburg monosyllabic test in unaided condition, with the trial BCHD preoperatively and with Osia® postoperatively with Osia®. The maximum word recognition score (mWRS) unaided and the word recognition score (WRS) with the test system at 65 dB SPL were correlated with the postoperative WRS with Osia® at 65 dB SPL.
Preoperative prediction of postoperative outcome with Osia® was better using the mWRS than by the WRS at 65 dB SPL with the test device on the softband. Postoperative WRS was most predictive for patients with CHL and less predictable for patients with mixed hearing loss with BC-4PTA ≥ 40 dB HL. For the test device on a softband, the achievable outcome tended to a minimum, with the mWRS tending to predict the realistically achievable outcome.
Osia® can be used for the treatment of CHL and MHL within the indication limits. The average preoperative bone conduction hearing threshold also provides an approximate estimate of the postoperative WRS with Osia®, for which the most accurate prediction is obtained using the preoperative mWRS. Prediction accuracy decreases from a BC-4PTA of ≥ 40 dB HL.
自 2021 年 4 月以来,可穿透皮肤的部分植入式骨整合 Cochlear™ Osia®(科利尔,悉尼,澳大利亚)已在德语国家获得批准使用。Ossia 适用于患有传导性听力损失(CHL)或混合性听力损失(MHL)、平均骨导听力损失(BC)为 55dB HL 或更低、或患有单侧听力损失(SSD)的患者。
本回顾性研究旨在探讨 Osia®术后言语识别的预测,并评估 MHL 患者,特别是骨导助听听阈小于 30dB 的患者使用 Osia®的言语识别情况。
2017 年至 2022 年期间,29 例成人患者植入了 Osia®,其中 10 例(11 耳)为 CHL,19 例(25 耳)为 MHL。MHL 分为两组:BC-4PTA≥20dB HL 且<40dB HL 的 MHL-I 组(n=15 例;20 耳)和 BC-4PTA≥40dB HL 的 MHL-II 组(n=4 例;5 耳)。所有患者在术前均通过软带测试了骨导听力设备。术前使用未助听的 Freiburg 单音节测试评估言语清晰度,术前使用试验性 BCHD 测试和 Osia®测试,术后使用 Osia®测试。未助听时最大言语识别得分(mWRS)和测试系统在 65dB SPL 时的言语识别得分(WRS)与 Osia®在 65dB SPL 时的术后 WRS 相关。
使用软带测试时,与测试设备在 65dB SPL 时的 WRS 相比,mWRS 对 Osia®术后结果的预测更好。对于 CHL 患者,术后 WRS 预测性最强,而对于 BC-4PTA≥40dB HL 的混合性听力损失患者,预测性较差。对于软带测试设备,可实现的结果趋于最小值,mWRS 趋于预测实际可实现的结果。
Ossia®可用于治疗 CHL 和 MHL 的适应证范围内的听力损失。平均术前骨导听力阈值也可大致估计 Osia®术后的 WRS,其中使用术前 mWRS 可获得最准确的预测。预测准确性从 BC-4PTA≥40dB HL 开始下降。