Labyrinthotomy or vestibulotomy in anatomic and congenital variations of the oval window and facial nerve.

IF 1.3
Khalid A Al-Mazrou, Yildirim A Bayazit
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引用次数: 3

Abstract

Objective: To present the results of our experience with labyrinthotomy or vestibulotomy in cases where the oval window is blocked by the facial nerve and in the presence of bilateral congenital agenesis of the oval window, respectively.

Study design: Retrospective analysis of the records of the patients operated in two different centers.

Methods: Between 2007 and 2012, 5 ears of 4 patients who were operated on in two different clinics with a presumptive diagnosis of otosclerosis were included in the study. There were 3 female patients and 1 male. The ages ranged from 10 to 26 (mean 19 years). All patients had unilateral conductive hearing loss except 1 (10-year-old girl or patient 1). Pure tone averages were calculated at the frequencies 0.5, 1, 2 and 4 kHz both pre- and postoperatively according to the Committee on Hearing and Equilibrium 1995 Guidelines for the Evaluation of Results of Treatment of Conductive Hearing Loss. All patients underwent a middle ear exploration and postoperatively the initial audiological examination was performed after 6 months.

Results: Retrospective analysis revealed that vestibulotomy or labyrinthotomy was performed in 5 ears of 4 patients. Postoperative dizziness was encountered in 2 patients who had vestibulotomy due to oval window agenesis, which ceased spontaneously at 1 month postoperatively. The perioperative period was otherwise uneventful. None of the patients had sensorineural hearing loss or deterioration of hearing. There was a significant improvement in hearing after the operation. A 28-dB improvement in the mean air conduction pure tone thresholds was achieved.

Conclusion: Vestibulotomy and labyrinthotomy are safe and effective procedures in terms of hearing restoration, which can be applied in cases of congenital agenesis of the oval window or obstruction of the oval window by the facial nerve.

迷宫术或前庭切开术在解剖及先天性卵形窗及面神经变异中的应用。
目的:介绍面神经阻断卵形窗和双侧先天性卵形窗发育不全分别行迷路切开和前庭切开的经验。研究设计:回顾性分析在两个不同中心手术的患者记录。方法:选取2007年至2012年在两家不同的诊所接受手术的4例患者的5耳,推测诊断为耳硬化。女性3例,男性1例。年龄10 ~ 26岁,平均19岁。除1例(10岁女孩或患者1)外,所有患者均为单侧传导性听力损失。根据听力与平衡委员会1995年《传导性听力损失治疗结果评估指南》,术前和术后在0.5、1、2和4 kHz频率处计算纯音平均值。所有患者均行中耳探查,术后6个月进行初次听力学检查。结果:回顾性分析4例患者5耳行前庭切除术或迷路切除术。2例因卵圆窗发育不全行前庭切开术患者术后出现头晕,术后1个月自行消失。围手术期其他方面平安无事。所有患者均无感觉神经性听力损失或听力恶化。术后听力有明显改善。平均空气传导纯音阈值提高了28 db。结论:前庭切开术和迷路切开术是一种安全有效的听力修复方法,可用于先天性卵圆窗发育不全或面神经阻塞卵圆窗的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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