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一所聋哑人学校男生的听力损伤模式。

The pattern of hearing impairment among schoolboys in an Institute for deaf subjects.

作者信息

Abolfotouh M A, Al-Ghamdi S A

机构信息

Family & Community Medicine Department, College of Medicine and Medical Sciences, King Khalid University, PO Box 641, Abha, Kingdom of Saudi Arabia.

出版信息

Saudi Med J. 2000 Sep;21(9):873-6.

Abstract

OBJECTIVE

The aim of this study was to study the pattern of deafness among boys of Al-Amal Institutes for the Deaf in Abha, the capital city of Asir Region, Southwestern Saudi Arabia.

METHODS

All students (n=155) were subjected to full otoscopic and audiometric examinations, and the type and degree of deafness were graded according to the recommendation of the British Society of Audiology. Computerized tomography scan was carried out to exclude congenital inner ear deformity, and specific Igm antibodies assay for TORCHS was carried out when the history of intrauterine infection was positive or suggestive.

RESULTS

More than 97% of students had sensori-neural hearing loss of various grades (55% profound, 28% severe and 14.5% moderate), while congenital conductive deafness constituted 3% of all cases. Residual hearing was reported for 43% of cases. There was delayed identification of deafness with an inverse relation between the age of identification of deafness and its severity (F = 227.66, P < 0.001). Prematurity (30%), intrauterine infection (17%) and heredity (15.5%) were the most frequently encountered causes of deafness. Postnatal causes accounted for only 20%, mostly due to meningitis 12%, other childhood fevers 5% and trauma 2.5%. Deafness of unknown cause constituted 12% of all cases.

CONCLUSION

The preventable causes of deafness in the region has not yet been overcome, a finding that will necessitate more efforts to upgrade the prenatal and perinatal health care. Late identification of hearing impairment will make the improvement in the audiology screening for infants the priority need.

摘要

目的

本研究旨在调查沙特阿拉伯西南部阿西尔地区首府阿卜哈市阿玛尔聋人研究所男童的耳聋模式。

方法

对所有155名学生进行全面的耳镜检查和听力测定,并根据英国听力学学会的建议对耳聋的类型和程度进行分级。进行计算机断层扫描以排除先天性内耳畸形,当宫内感染史呈阳性或有提示时,进行TORCHS特异性IgM抗体检测。

结果

超过97%的学生患有不同程度的感音神经性听力损失(55%为重度,28%为重度,14.5%为中度),而先天性传导性耳聋占所有病例的3%。43%的病例报告有残余听力。耳聋的确诊存在延迟,耳聋确诊年龄与其严重程度呈负相关(F = 227.66,P < 0.001)。早产(30%)、宫内感染(17%)和遗传(15.5%)是最常见的耳聋原因。产后原因仅占20%,主要是脑膜炎12%、其他儿童发热5%和外伤2.5%。不明原因的耳聋占所有病例的12%。

结论

该地区可预防的耳聋原因尚未得到克服,这一发现需要加大力度提升产前和围产期保健水平。听力障碍的确诊延迟将使改善婴儿听力筛查成为当务之急。

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