Morzaria Sanjay, Westerberg Brian D, Kozak Frederick K
Division of Otolaryngology, University of British Columbia.
J Otolaryngol. 2005 Oct;34(5):297-303. doi: 10.2310/7070.2005.34501.
To develop an evidence-based algorithm for determining the etiology of bilateral sensorineural hearing loss (SNHL) in a child.
The frequency of different etiologies was previously determined. A systematic review of the literature for articles published between 1940 and January 2003 was performed for studies providing information on the diagnosis of each etiology relevant to their clinical presentation.
Connexin mutation testing is highly sensitive and specific. CT scanning of the temporal bones is frequently valuable in detecting inner ear malformations. Routine laboratory studies are rarely helpful. ECG is particularly valuable when a history of syncope or arrhythmias or a family history of sudden death in a young child is elicited. There is no literature to support routine urinalysis for the diagnosis of Alport syndrome and thyroid studies lack specificity in the absence of physical findings (goiter).
An evidence-based algorithm was developed that included: history, physical and audiological evaluation, and ophthalmological evaluation. Further directed investigations may include genetic testing for the Cx26 mutation, CT scan of the temporal bones, ECG and urinalysis.
制定一种基于证据的算法,用于确定儿童双侧感音神经性听力损失(SNHL)的病因。
先前已确定不同病因的发生频率。对1940年至2003年1月发表的文献进行系统综述,以查找提供与每种病因临床表现相关诊断信息的研究。
连接蛋白突变检测具有高度敏感性和特异性。颞骨CT扫描在检测内耳畸形方面通常很有价值。常规实验室检查很少有帮助。当出现晕厥或心律失常病史或幼儿猝死家族史时,心电图特别有价值。没有文献支持将常规尿液分析用于诊断阿尔波特综合征,并且在没有体格检查发现(甲状腺肿)的情况下,甲状腺检查缺乏特异性。
制定了一种基于证据的算法,包括:病史、体格检查和听力学评估以及眼科评估。进一步的针对性检查可能包括Cx26突变的基因检测、颞骨CT扫描、心电图和尿液分析。