囊性纤维化患者的上呼吸道。50名儿童的耳鼻喉检查
Upper respiratory tract in cystic fibrosis. Ear-nose-throat survey of 50 children.
作者信息
Taylor B, Evans J N, Hope G A
出版信息
Arch Dis Child. 1974 Feb;49(2):133-6. doi: 10.1136/adc.49.2.133.
Abstract
An ear-nose-throat survey was carried out on 50 children aged 4 to 10 years with cystic fibrosis. 10% were shown to be transiently deaf, associated with eustachian tube dysfunction. There were no confirmed cases of secretory otitis media. 10 children (20%) were found to have nasal polyps or gave a history of polypectomy. Though a high incidence of middle ear problems in children with cystic fibrosis has been reported from the U.S.A., neither deafness nor secretory otitis media was found to be a problem in the group studied.
摘要
对50名4至10岁的囊性纤维化患儿进行了耳鼻喉检查。结果显示，10%的患儿有短暂性耳聋，与咽鼓管功能障碍有关。没有确诊的分泌性中耳炎病例。10名儿童（20%）被发现患有鼻息肉或有息肉切除史。尽管美国有报道称囊性纤维化患儿中耳问题的发生率很高，但在所研究的群体中，耳聋和分泌性中耳炎都未被发现是问题。
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本文引用的文献
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Nasal polyposis in patients with cystic fibrosis.囊性纤维化患者的鼻息肉病
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Audiometric testing.听力测试。
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Cystic fibrosis and hearing. Integrity of the upper respiratory tract as related to hearing sensitivity.囊性纤维化与听力。上呼吸道完整性与听力敏感度的关系。
Clin Pediatr (Phila). 1970 Jul;9(7):390-402. doi: 10.1177/000992287000900707.
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