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吕贝克耳畸形功能和美学重建流程图

The Lübeck flowchart for functional and aesthetic rehabilitation of aural atresia and microtia.

机构信息

Department of Otorhinolaryngology and Facial Plastic Operations, University Hospital Schleswig-Holstein, Lübeck, Germany.

出版信息

Otol Neurotol. 2012 Oct;33(8):1363-7. doi: 10.1097/MAO.0b013e3182659adf.

Abstract

OBJECTIVE

Current strategies for functional rehabilitation of microtia-atresia patients with bone-anchored implants or surgical atresia repair have been extended by the feasibility of active middle ear implants. The aim of the present research is to evaluate a new flowchart of the treatment of these patients that considers active middle ear implants.

PATIENTS

Congenital aural atresia and microtia.

INTERVENTION(S): Bilateral cases are provided with a conductive hearing aid after birth and implanted with an active middle ear implant within the second year. Unilateral cases are provided with a conductive hearing aid and implanted with a middle ear or bone-conduction device in early childhood. Unilateral cases without amplification in the vulnerable time after birth are carefully selected for late implantation. At age 8 to 10, the auricular reconstruction is completed.

MAIN OUTCOME MEASURE(S): Feasibility of implantation irrespective of age, functional gain in audiometry.

RESULTS

The results of early implantation are as good as those previously published for adolescents. Mean reaction threshold with the Vibrant Soundbridge was 21 dB. Mean functional gain was 48 dB. The local tissues are unaltered and ready for auricular reconstruction.

CONCLUSION

Active middle ear implants allow early and selective stimulation of the auditory pathway in children with congenital conductive hearing loss and are expected to lead to the normal development of the binaural hearing functions. To date, it is the only option if the stimulation is to be started at the age of 12 to 18 months. This was implemented into a new flowchart for aural atresia-microtia.

摘要

目的

当前,通过骨锚式植入物或手术闭锁修复来为小耳畸形伴闭锁患者进行功能康复的策略已得到扩展,这得益于可植入式中耳有源植入物的可行性。本研究旨在评估一种新的治疗流程,该流程考虑了可植入式中耳有源植入物的应用。

患者

先天性耳闭锁和小耳畸形。

干预措施

双侧患者在出生后配备传导性助听器,并在 2 年内植入可植入式中耳有源植入物;单侧患者在幼儿期配备传导性助听器并植入中耳或骨导设备;出生后在脆弱时期未进行放大的单侧患者被仔细挑选进行后期植入。8 至 10 岁时完成耳廓重建。

主要观察指标

无论年龄大小,植入的可行性,听力学功能增益。

结果

早期植入的结果与以前发表的青少年结果一样好。Vibrant Soundbridge 的平均反应阈值为 21dB,平均功能增益为 48dB。局部组织保持不变,为耳廓重建做好准备。

结论

可植入式中耳有源植入物可使患有先天性传导性听力损失的儿童早期、有选择地刺激听觉通路,并有望使双耳听力功能正常发育。到目前为止,如果要在 12 至 18 个月大的时候开始刺激,这是唯一的选择。这被纳入了新的耳闭锁-小耳畸形流程图。

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