Berg A L, Spitzer J B, Garvin J H
Department of Speech Communication Sciences, Pace University, New York Presbyterian Hospital, and Columbia University College of Physicians and Surgeons, New York 10038-1598, USA.
Laryngoscope. 1999 Nov;109(11):1806-14. doi: 10.1097/00005537-199911000-00016.
To describe hearing changes in a group of 28 children (age range, 8-180 mo) undergoing protocol-based cisplatin therapy.
Conventional, play audiometry, visual reinforcement audiometry (VRA), immittance audiometry, transient click evoked otoacoustic emissions (OAEs), and auditory brainstem response (ABR) evoked potentials were used to assess peripheral sensitivity and for threshold determination.
Bilateral symmetrical high-frequency sensorineural hearing loss was noted in 9 of the 28 children (26%). Hearing loss was evident as early as 1 month after chemotherapy and as late as 50 months and was not dependent on individual or cumulative dosage of cisplatin.
描述一组28名儿童(年龄范围8 - 180个月)在接受基于方案的顺铂治疗过程中的听力变化。
采用传统纯音听力测试、游戏测听法、视觉强化测听法(VRA)、声导抗测听法、瞬态短声诱发耳声发射(OAEs)和听觉脑干反应(ABR)诱发电位来评估外周敏感性并确定阈值。
28名儿童中有9名(26%)出现双侧对称性高频感音神经性听力损失。听力损失最早在化疗后1个月出现,最晚在50个月出现,且不依赖于顺铂的单次或累积剂量。
1)感音神经性听力损失的出现与顺铂的单次和/或累积剂量无关;2)化疗后儿童的定期医学评估应纳入听力评估,因为感音神经性听力损失的发作无法预测;3)对于听力损失影响低频至中频的儿童,可能需要佩戴个人助听器;对于高于3000 Hz的听力损失,个人辅助听力设备(调频系统)可能更合适;4)可能需要言语语言病理学家进行评估和干预,以解决因听力损失导致的可能的发音或语言发育问题。