Department of Otolaryngology Head and Neck Surgery, Hacettepe University School of Medicine, Ankara, Turkey.
Audiology Unit, Department of Otolaryngology Head and Neck Surgery, Hacettepe University School of Medicine, Ankara, Turkey.
J Int Adv Otol. 2021 May;17(3):228-233. doi: 10.5152/iao.2021.8457.
To introduce the concept of stapedotomy as a new treatment alternative in cochlear hypoplasia (CH) and propose a new guideline for its management.
Forty-two primary cases out of 355 presented with congenital stapes fixation between January 2003 and September 2015 were included in the study. Computed tomography scans of all cases with congenital stapes fixation were reviewed, and cases with inner ear anomalies were taken into account. Eleven cases had various inner ear anomalies, and 9 cases had various types of CH. In the present paper, only the CH cases with stapes fixation, all of whom underwent stapedotomy, are reviewed regarding preoperative audiological and radiological characteristics as well as surgical findings and postoperative audiological results.
The patients were aged between 4 and 22. There were 2 males (3 ears) and 4 females (6 ears). Three cases had bilateral stapedotomy. The remaining 3 cases had unilateral surgery. The average preoperative air-bone gap (ABG) was 50.3 dB. Postoperative hearing: preoperative ABG was 50.3 dB. Postoperative ABG was calculated as 20.1 dB hearing.
Hearing loss (HL) in hypoplastic cochlea demonstrates the full spectrum of HL types. CH is a unique inner ear anomaly that can be treated with all of the available rehabilitation modalities. As a result of current findings, a new treatment algorithm for CH is proposed.
介绍镫骨切开术作为一种治疗先天性镫骨固定的新方法,并提出新的管理指南。
回顾 2003 年 1 月至 2015 年 9 月期间因先天性镫骨固定而就诊的 355 例原发性病例,其中 42 例符合研究标准。所有先天性镫骨固定病例均行 CT 扫描,考虑到内耳畸形。11 例存在各种内耳畸形,9 例存在各种类型的先天性耳蜗发育不全。在本研究中,仅回顾了镫骨固定且均行镫骨切开术的先天性耳蜗发育不全病例,评估术前听力学和影像学特征、手术发现和术后听力学结果。
患者年龄 4 至 22 岁,男 2 例(3 耳),女 4 例(6 耳)。3 例双侧镫骨切开术,3 例单侧手术。术前平均气骨导差(ABG)为 50.3dB。术后听力:术前 ABG 为 50.3dB,术后 ABG 计算为 20.1dB。
先天性耳蜗发育不全患者的听力损失(HL)表现为各种 HL 类型。先天性耳蜗发育不全是一种独特的内耳畸形,可以通过所有现有的康复方式进行治疗。基于目前的研究结果,提出了一种新的先天性耳蜗发育不全治疗方案。