Congenital aural atresia surgery: Long-term results

被引:112
作者
De la Cruz, A
Teufert, KB
机构
[1] House Ear Res Inst, Dept Clin Studies, Los Angeles, CA 90057 USA
[2] Univ So Calif, Sch Med, Los Angeles, CA 90089 USA
关键词
D O I
10.1016/S0194-5998(03)00531-X
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 [耳鼻咽喉科学];
摘要
OBJECTIVES: The study goal was to evaluate the stability of hearing results from short- to long-term follow-up in patients who underwent surgery for congenital aural atresia. We also reviewed complications such as external auditory canal stenosis, lateralization and perforation of the tympanic membrane, sensorineural hearing loss, and facial palsy. METHODS: We conducted a retrospective chart review of 116 patients who underwent congenital aural atresiaplasty between 1985 and 2002 at the House Ear Clinic. There were 116 atretic ears. Complication rates and short- and long-term (up to 13.6 years) hearing results were evaluated for primary and revision cases. RESULTS. Closure of the air-bone-gap (ABG) to 30 dB or less at short-term follow-up occurred in 58.5% of primary surgeries and 56% of revisions. The longterm postoperative ABG was 30 dB or less in 50.8% of the primary cases and 39.1% of the revisions. Paired comparison analysis found no significant change in ABG from short- to long-term follow-up for either primary or revision cases. Soft tissue stenosis was seen in 8% of primary surgeries and 3.4% of revisions. Ossicular chain refixation was seen in 11.5% and 6.9% of primary and revision surgeries, respectively. There were no dead ears. CONCLUSION. Atresiaplasty surgery in individuals with congenital aural. atresia can yield reliable, lasting hearing results with a low incidence of complications.
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页码:121 / 127
页数:7
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