Al-Malky Ghada, Dawson Sally J, Sirimanna Tony, Bagkeris Emmanouil, Suri Ranjan
University College London Ear Institute, 332 Gray's Inn Road, London WC1X 8EE, UK.
University College London Ear Institute, 332 Gray's Inn Road, London WC1X 8EE, UK.
J Cyst Fibros. 2015 Mar;14(2):248-54. doi: 10.1016/j.jcf.2014.07.009. Epub 2014 Aug 13.
Intravenous aminoglycoside (IV AG) antibiotics, widely used in patients with cystic fibrosis (CF), are known to have ototoxic complications. Despite this, audiological monitoring is not commonly performed and if performed, uses only standard pure-tone audiometry (PTA). The aim of this study was to investigate ototoxicity in CF children, to determine the most appropriate audiological tests and to identify possible risk factors.
Auditory assessment was performed in CF children using standard pure tone audiometry (PTA), extended high-frequency (EHF) audiometry and distortion-product otoacoustic emissions (DPOAE).
70 CF children, mean (SD) age 10.7 (3.5) years, were recruited. Of the 63 children who received IV AG, 15 (24%) children had ototoxicity detected by EHF audiometry and DPOAE. Standard PTA only detected ototoxicity in 13 children. Eleven of these children had received at least 10 courses of IV AG courses. A 25 to 85 dBHL hearing loss (mean±SD: 57.5±25.7 dBHL) across all EHF frequencies and a significant drop in DPOAE amplitudes at frequencies 4 to 8 kHz were detected. However, standard PTA detected a significant hearing loss (>20 dBHL) only at 8 kHz in 5 of these 15 children and none in 2 subjects who had significantly elevated EHF thresholds. The number of courses of IV AG received, age and lower lung function were shown to be risk factors for ototoxicity.
CF children who had received at least 10 courses of IV AG had a higher risk of ototoxicity. EHF audiometry identified 2 more children with ototoxicity than standard PTA and depending on facilities available, should be the test of choice for detecting ototoxicity in children with CF receiving IV AG.
静脉注射氨基糖苷类(IV AG)抗生素广泛用于囊性纤维化(CF)患者,已知其具有耳毒性并发症。尽管如此,听力监测并不常用,即便进行监测,也仅采用标准纯音听力测定法(PTA)。本研究的目的是调查CF儿童的耳毒性,确定最合适的听力测试方法,并识别可能的风险因素。
对CF儿童进行听觉评估,采用标准纯音听力测定法(PTA)、扩展高频(EHF)听力测定法和畸变产物耳声发射(DPOAE)。
招募了70名CF儿童,平均(标准差)年龄为10.7(3.5)岁。在63名接受IV AG治疗的儿童中,15名(24%)儿童通过EHF听力测定法和DPOAE检测出耳毒性。标准PTA仅在13名儿童中检测出耳毒性。这些儿童中有11名接受了至少10个疗程的IV AG治疗。在所有EHF频率上检测到25至85 dBHL的听力损失(平均±标准差:57.5±25.7 dBHL),在4至8 kHz频率处DPOAE振幅显著下降。然而,标准PTA仅在这15名儿童中的5名儿童的8 kHz频率处检测到显著听力损失(>20 dBHL),在2名EHF阈值显著升高的受试者中未检测到。接受IV AG的疗程数、年龄和较低的肺功能被证明是耳毒性的风险因素。
接受至少10个疗程IV AG治疗的CF儿童耳毒性风险更高。EHF听力测定法比标准PTA多识别出2名耳毒性儿童,根据现有设备情况,EHF听力测定法应作为检测接受IV AG治疗的CF儿童耳毒性的首选测试方法。