Levine B A, Shelton C, Berliner K I, Sheehy J L
Department of Otolaryngology, University of Southern California School of Medicine, Los Angeles.
Arch Otolaryngol Head Neck Surg. 1989 Jul;115(7):814-6. doi: 10.1001/archotol.1989.01860310052021.
Charts of 161 patients with unilateral chronic otitis media were reviewed for evidence of sensorineural hearing loss, defined as the difference in preoperative bone conduction thresholds between diseased and normal contralateral ears. Mean bone conduction differences were small but statistically significant, ranging from 5.6 to 12.8 dB across the frequencies. Approximately 45% of the subjects had differences greater than 10 dB for high frequencies, but less than 12% had a difference greater than 20 dB for the pure-tone average. Significant relationships were found between sensorineural hearing loss and the presence of acquired cholesteatoma in the middle ear, diseased mucosa of the promontory and hypotympanum, and diseased ossicles. These findings suggest that more severe middle ear disease may result in sensorineural hearing loss. However, for the majority of subjects, the amount of sensorineural hearing loss was judged not to be clinically significant.
回顾了161例单侧慢性中耳炎患者的病历,以寻找感音神经性听力损失的证据,感音神经性听力损失定义为患侧与对侧正常耳术前骨导阈值的差异。平均骨导差异较小,但具有统计学意义,各频率范围为5.6至12.8分贝。约45%的受试者高频差异大于10分贝,但纯音平均差异大于20分贝的不到12%。发现感音神经性听力损失与中耳后天性胆脂瘤、鼓岬和下鼓室病变黏膜以及病变听小骨之间存在显著相关性。这些发现表明,更严重的中耳疾病可能导致感音神经性听力损失。然而,对于大多数受试者,感音神经性听力损失的程度被判定为无临床意义。