Mansbach A L
Service d'O.R.L., H.U.D.E.R.F, Bruxelles.
Rev Med Brux. 2006 Sep;27(4):S250-7.
Considerable progress has been achieved these last years in the field of hearing screening, diagnosis of hearing loss in children and rehabilitation methods. It is now generally accepted that every child with hearing impairment must receive intervention before six months of age. This is only possible thanks to early and systematic hearing screening. The objective screening methods--transient evoked otoacoustic emissions and automated auditory brainstem responses--have excellent specificity and sensitivity and are non invasive. They have replaced the subjective techniques which resulted in a high percentage of false negative cases. The performance of etiologic assessments has dramatically improved, thanks to advancements in genetics and imagery. The identification of deafness-causing genes has provided an insight into inner ear physiology and has permitted to clarify a great number of recessive deafness cases. Computed tomographic and magnetic resonance imaging allow much more precise information gathering about the integrity of the auditory pathway. Finally, cochlear implantation has deeply modified the social and educational prognosis of the severe or profound deaf child. In the vast majority of cases, children implanted early and who do not present associated handicaps, will succeed in communicating within the hearing world and will attend mainstream schools.
近年来,听力筛查、儿童听力损失诊断及康复方法领域取得了显著进展。现在人们普遍认为,每个听力受损儿童都必须在6个月大之前接受干预。这只有通过早期和系统的听力筛查才有可能实现。客观筛查方法——瞬态诱发耳声发射和自动听性脑干反应——具有出色的特异性和敏感性,且是非侵入性的。它们已经取代了那些导致高比例假阴性病例的主观技术。由于遗传学和影像学的进步,病因评估的表现有了显著改善。致聋基因的识别为内耳生理学提供了见解,并有助于阐明大量隐性耳聋病例。计算机断层扫描和磁共振成像能够收集关于听觉通路完整性的更精确信息。最后,人工耳蜗植入深刻改变了重度或极重度聋儿的社会和教育预后。在绝大多数情况下,早期植入且没有相关障碍的儿童将能够在听力世界中成功交流并进入主流学校就读。