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发育不良或先天性缺失卵圆窗的手术治疗。

Surgical Management for Dysplastic or Congenitally Absent Oval Window.

机构信息

Otologic/Neurotologic Surgery and Wellness, AdventHealth System Celebration.

Otolaryngology-Head and Neck Surgery, University of Central Florida.

出版信息

Otol Neurotol. 2018 Dec;39(10):e1039-e1046. doi: 10.1097/MAO.0000000000002001.

Abstract

OBJECTIVE

To evaluate surgical findings and hearing results for patient's undergoing the described surgical approach for congenitally absent or dysplastic oval window (OW).

STUDY DESIGN

The Institutional Review Board approved retrospective review of patients with conductive hearing loss (CHL) operated on from 1992 to 2016.

SETTING

Academic tertiary center.

PATIENTS

Patients with CHL, an intact tympanic membrane (TM), and without history of chronic infection underwent middle ear exploration. Eleven patients and 13 ears underwent an oval window drill-out (OWD) procedure.

INTERVENTION

Eleven patients presented, all with dysplastic or congenitally absent oval window (CAOW). CHL was identified using audiometry and tuning forks, many patients also had preoperative computed tomography temporal bones. A transcanal approach was used and an OWD was performed with a variety of prostheses placed.

MAIN OUTCOME MEASURE

Audiometric studies before and after intervention were compared with 12 month and long-term follow-up (1-22 yr).

RESULTS

Preoperative air-bone gaps ranged from 40 to 60 dB and averaged 55.1 dB. Postoperative air-bone gaps ranged from 0 to 60 dB and averaged 24.1 dB. The preoperative pure-tone average (PTA) ranged from 55 to 99 dB and averaged 71.3 dB. Postoperative PTA ranged from 21 to 108 dB and averaged 49.6 dB.

CONCLUSION

Dysplastic and CAOW are uncommon congenital major ear anomalies. OWD is a viable treatment option, though careful counseling is critical, as significant complications are possible, especially with facial nerve (FN) abnormalities. This series demonstrates successful closure of the air-bone gap for many patients with this technique.

摘要

目的

评估接受描述性手术方法治疗先天性或发育不良的卵圆窗(OW)缺失患者的手术发现和听力结果。

研究设计

机构审查委员会批准了对 1992 年至 2016 年期间因传导性听力损失(CHL)接受手术的患者进行回顾性研究。

设置

学术三级中心。

患者

患有 CHL、完整鼓膜(TM)且无慢性感染史的患者接受中耳探查。11 名患者和 13 只耳朵接受了卵圆窗钻开(OWD)手术。

干预措施

11 名患者出现,均为发育不良或先天性缺乏卵圆窗(CAOW)。使用听力计和音叉确定 CHL,许多患者还进行了术前颞骨计算机断层扫描。采用经耳道入路,使用各种假体进行 OWD。

主要观察指标

比较干预前后的听力研究,并进行 12 个月和长期随访(1-22 年)。

结果

术前气骨间隙范围为 40 至 60dB,平均为 55.1dB。术后气骨间隙范围为 0 至 60dB,平均为 24.1dB。术前纯音平均(PTA)范围为 55 至 99dB,平均为 71.3dB。术后 PTA 范围为 21 至 108dB,平均为 49.6dB。

结论

发育不良和 CAOW 是罕见的先天性大耳畸形。OWD 是一种可行的治疗选择,尽管需要谨慎咨询,因为可能会出现严重并发症,特别是面神经(FN)异常。本系列通过该技术为许多患者成功封闭了气骨间隙。

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