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儿童单侧及不对称性听力损失

Unilateral and asymmetric hearing loss in childhood.

作者信息

Gouveia Fernanda Navarro, Jacob-Corteletti Lilian Cássia Bórnia, Silva Bárbara Cristiane Sordi, Araújo Eliene Silva, Amantini Regina Célia Bortoleto, Oliveira Eduardo Boaventura, Alvarenga Kátia de Freitas

机构信息

Faculdade de Odontologia de Bauru - FOB, Universidade de São Paulo - USP - Bauru (SP), Brasil.

Universidade Federal do Rio Grande do Norte - UFRN - Natal (RN), Brasil.

出版信息

Codas. 2020 Jan 27;32(1):e20180280. doi: 10.1590/2317-1782/20192018280. eCollection 2020.

Abstract

PURPOSE

To describe unilateral and bilateral asymmetric sensorineural hearing loss in children and its etiological, audiological and demographic characteristics.

METHODS

Retrospective cross-sectional study developed in the Seção de Implante Coclear of Hospital de Reabilitação de Anomalias Craniofaciais, through the analysis of medical records.

RESULTS

Data from 1152 patients were analyzed: 424 (37%) adolescents, adults or elderly, and 728 (63%) children, of whom 691 (95%) had bilateral symmetrical hearing loss, and 37 (5%) had unilateral hearing loss (n=10) or bilateral asymmetric (n=27) sensorineural hearing loss. The mean age at diagnosis of unilateral sensorineural hearing loss was 33.58±21.69 months, and for asymmetric bilateral it was 33.12±21.69 months, with a prevalence of 1.4% and 3.7%, respectively. The highest risk indicator for hearing loss for both groups was the family history of permanent deafness, which began in childhood. The majority of the relatives of children with unilateral sensorineural hearing loss presented the highest low socioeconomic classification (50%), while children with bilateral asymmetric sensorineural hearing loss were also be subdivided into upper (37%) and lower (37%).

CONCLUSION

We observed a greater occurrence of asymmetric bilateral sensorineural hearing loss compared to unilateral hearing loss, as well as the hereditary risk indicator, with a predominance of the deep ear and female preponderance in both groups. Although neonatal hearing screening provides early identification of unilateral sensorineural hearing loss, the age at the audiological diagnosis is still above the recommended level. In addition, the majority of the children's family members presented a low level of income.

摘要

目的

描述儿童单侧和双侧不对称感音神经性听力损失及其病因、听力学和人口统计学特征。

方法

在颅面畸形康复医院人工耳蜗植入科开展回顾性横断面研究,通过分析病历进行。

结果

分析了1152例患者的数据:424例(37%)为青少年、成年人或老年人,728例(63%)为儿童,其中691例(95%)有双侧对称性听力损失,37例(5%)有单侧听力损失(n = 10)或双侧不对称(n = 27)感音神经性听力损失。单侧感音神经性听力损失诊断时的平均年龄为33.58±21.69个月,双侧不对称者为33.12±21.69个月,患病率分别为1.4%和3.7%。两组听力损失的最高风险指标均为始于儿童期的永久性耳聋家族史。单侧感音神经性听力损失儿童的大多数亲属社会经济分类最低(50%),而双侧不对称感音神经性听力损失儿童也可细分为高(37%)低(37%)两类。

结论

我们观察到双侧不对称感音神经性听力损失比单侧听力损失更常见,以及遗传风险指标,两组均以深部耳为主且女性占优势。尽管新生儿听力筛查能早期发现单侧感音神经性听力损失,但听力学诊断年龄仍高于推荐水平。此外,大多数儿童家庭成员收入水平较低。

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