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感音神经性听力损失患儿的眼科检查结果

Ophthalmologic findings in children with sensorineural hearing loss.

作者信息

Sharma Arun, Ruscetta Melissa N, Chi David H

机构信息

Department of Otolaryngology, University of Washington, Seattle, USA.

出版信息

Arch Otolaryngol Head Neck Surg. 2009 Feb;135(2):119-23. doi: 10.1001/archoto.2008.546.

Abstract

OBJECTIVES

To determine the prevalence of refractive and nonrefractive ophthalmologic abnormalities in children with sensorineural hearing loss (SNHL) and to evaluate the overall utility of routine ophthalmological examination in children with SNHL.

DESIGN

An institutional review board-approved retrospective analysis of ophthalmologic findings in children (18 years and younger) with SNHL seen between November 6, 2000, and June 4, 2007.

SETTING

Tertiary care university children's hospital.

PATIENTS

Children (18 years and younger) with SNHL.

MAIN OUTCOME MEASURES

Ophthalmologic findings and SNHL.

RESULTS

There were 226 patients with SNHL who underwent ophthalmologic examination. Of these patients, 49 (21.7%) had an ophthalmologic abnormality. Refractive errors were present in 23 patients (10.2%), whereas nonrefractive conditions were present in 29 patients (12.8%). The cause of SNHL was syndromic in 11 patients (4.9%), of whom 5 (2.2%) had syndromes with associated ophthalmologic abnormalities. No statistically significant differences were found in ophthalmologic findings based on severity or laterality of SNHL. The prevalence of ophthalmologic findings was not significantly different between patients whose conditions were diagnosed on the basis of newborn screening and other patients. Ophthalmologic abnormalities were found in 1 of 27 patients (3.7%) with biallelic GJB2 mutations and 22 of 106 patients (20.7%) without any GJB2 mutations (P = .04).

CONCLUSIONS

In this study, the overall prevalence of ophthalmologic findings in children with SNHL was 21.7%. Ophthalmologic anomalies were present in 3.7% of children with GJB2 mutations. Routine ophthalmologic examination can be beneficial in the evaluation of children with SNHL.

摘要

目的

确定感音神经性听力损失(SNHL)患儿屈光和非屈光性眼科异常的患病率,并评估常规眼科检查对SNHL患儿的整体效用。

设计

对2000年11月6日至2007年6月4日期间就诊的18岁及以下SNHL患儿的眼科检查结果进行机构审查委员会批准的回顾性分析。

地点

三级医疗大学儿童医院。

患者

18岁及以下的SNHL患儿。

主要观察指标

眼科检查结果和SNHL。

结果

226例SNHL患儿接受了眼科检查。其中,49例(21.7%)存在眼科异常。23例(10.2%)存在屈光不正,29例(12.8%)存在非屈光性疾病。11例(4.9%)SNHL患儿病因是综合征性的,其中5例(2.2%)患有伴有相关眼科异常的综合征。基于SNHL的严重程度或患侧性,眼科检查结果未发现统计学上的显著差异。基于新生儿筛查诊断病情的患者与其他患者之间,眼科检查结果的患病率无显著差异。27例双等位基因GJB2突变患者中有1例(3.7%)发现眼科异常,106例无任何GJB2突变的患者中有22例(20.7%)发现眼科异常(P = 0.04)。

结论

在本研究中,SNHL患儿眼科检查结果的总体患病率为21.7%。GJB2突变患儿中3.7%存在眼科异常。常规眼科检查对评估SNHL患儿可能有益。

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