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先天性耳道闭锁:经乳突入路;一项效果良好的古老技术。

Congenital aural atresia: transmastoid approach; an old technique with good results.

作者信息

El-Hoshy Zoheir, Abdel-Aziz Mosaad, Shabana Mohamed

机构信息

Department of Otolaryngology, Faculty of Medicine, Cairo University, Egypt.

出版信息

Int J Pediatr Otorhinolaryngol. 2008 Jul;72(7):1047-52. doi: 10.1016/j.ijporl.2008.03.011. Epub 2008 May 5.

Abstract

OBJECTIVE

Congenital aural atresia prevents sound conduction to the inner ear, so the child may suffer learning problems. Transmastoid approach is a safe method to create functional pathway by which sound can reach the cochlear fluids but it leaves mastoid cavity which may be problematic. The purpose of this study is to assess the feasibility of improving hearing in those patients on the expense of mastoid cavity.

METHODS

Forty children with congenital aural atresia were included in this study. All had functioning cochlea on evoked response audiometry and normal cochlear morphology with pneumatized mastoid on CT scan. Transmastoid approach was used for reconstruction of the external auditory canal with covering of the newly created canal using split thickness skin graft. Reconstruction of the tympanic membrane was carried out by temporalis fascia graft. Follow-up of the patients for 3 years was carried out.

RESULTS

Surgical success is considered on restoration of hearing and maintenance of a patent, infection-free ear canal. This study showed a successful hearing result in 85% of patients at 3 months postoperatively, this result diminished to 65% after 3 years. The incidence of canal restenosis was 17.5%; the narrowing was in the outer cartilaginous part. No cases developed facial nerve paralysis or sensorineural hearing loss postoperatively.

CONCLUSIONS

Congenital aural atresia is one of the most difficult and challenging surgeries for the otologic surgeon. However, in the hands of experienced otologists, repair of this deformity can be performed safely and with predictable results using transmastoid approach.

摘要

目的

先天性耳道闭锁会阻碍声音传导至内耳,因此患儿可能会出现学习问题。经乳突入路是一种创建功能性通路的安全方法,通过该通路声音能够到达耳蜗内淋巴液,但会留下可能存在问题的乳突腔。本研究的目的是评估以牺牲乳突腔为代价改善这些患者听力的可行性。

方法

本研究纳入了40例先天性耳道闭锁患儿。所有患儿在诱发反应测听中耳蜗功能正常,CT扫描显示耳蜗形态正常且乳突气化良好。采用经乳突入路重建外耳道,并用中厚皮片覆盖新形成的耳道。用颞肌筋膜移植片进行鼓膜重建。对患者进行了3年的随访。

结果

手术成功的标准是听力恢复以及保持外耳道通畅且无感染。本研究显示,术后3个月时85%的患者听力恢复良好,3年后这一比例降至65%。耳道再狭窄的发生率为17.5%;狭窄发生在外耳道软骨部。术后无患者出现面神经麻痹或感音神经性听力损失。

结论

先天性耳道闭锁是耳科医生最困难且最具挑战性的手术之一。然而,在经验丰富的耳科医生手中,使用经乳突入路可以安全地修复这种畸形,且结果可预测。

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