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原发性纤毛运动障碍患儿的听力转归——一项纵向研究

Hearing outcomes in children with primary ciliary dyskinesia--a longitudinal study.

作者信息

Majithia A, Fong J, Hariri M, Harcourt J

机构信息

Flat 9 Skillen Lodge, 552 Uxbridge Road, Pinner, Middlesex HA5 3PR, UK.

出版信息

Int J Pediatr Otorhinolaryngol. 2005 Aug;69(8):1061-4. doi: 10.1016/j.ijporl.2005.02.013. Epub 2005 Mar 16.

Abstract

Primary ciliary dyskinesia (PCD) is a congenital abnormality of ciliary structure or function. The otological manifestations of the disease include otitis media with effusion (OME). To date, the severity of hearing loss and natural progression of OME in this select group of patients has not been documented. In this retrospective observational study, we looked at the tympanograms and audiograms of all children with PCD attending the Royal Brompton Hospital multidisciplinary clinic. Our results show an improvement in both hearing thresholds and tympanograms with age (p<0.001). Most cases resolve by the age of 12. This supports the current practice of conservative management in these patients. The problems of persistent otorrhoea and residual tympanic membrane perforation are thereby avoided with the reassurance that hearing loss will spontaneously resolve with time.

摘要

原发性纤毛运动障碍(PCD)是一种纤毛结构或功能的先天性异常。该疾病的耳科表现包括分泌性中耳炎(OME)。迄今为止,这一特定患者群体中听力损失的严重程度和OME的自然病程尚未有文献记载。在这项回顾性观察研究中,我们查看了在皇家布朗普顿医院多学科诊所就诊的所有PCD患儿的鼓室图和听力图。我们的结果显示,听力阈值和鼓室图均随年龄改善(p<0.001)。大多数病例在12岁时得到缓解。这支持了目前对这些患者进行保守治疗的做法。从而避免了持续性耳漏和鼓膜残余穿孔的问题,并让患者放心听力损失会随时间自行缓解。

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