Otoacoustic emissions - an approach for monitoring aminoglycoside induced ototoxicity in children

被引:39
作者
Stavroulaki, P
Apostolopoulos, N
Dinopoulou, D
Vossinakis, I
Tsakanikos, M
Douniadakis, D
机构
[1] Childrens Hosp P&A Kyriakou, Dept Otorhinolaryngol Head & Neck Surg, Athens, Greece
[2] Southmead Gen Hosp, Dept Otolaryngol Head & Neck Surg, Bristol BS10 5NB, Avon, England
关键词
otoacoustic emissions; auditory brainstem response; pure tone audiometry; ototoxicity; gentamicin;
D O I
10.1016/S0165-5876(99)00247-5
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objectives: the early detection of hearing impairment caused by ototoxic drugs, such as aminoglycosides, has been the aim of research world-wide. Histopathological studies have shown that the outer hair cells are the most susceptible cochlear components to injury from ototoxic drugs like aminoglycosides. Otoacoustic emissions reflect the functional status of the outer hair cells and constitute the only non-invasive means of objective cochlear investigation. The aim of this study was to evaluate the potential of otoacoustic emissions in early identification of aminoglycoside-induced cochlear dysfunction. In addition, a comparison with pure-tone audiometry or auditory brainstem responses was performed in order to determine if this test might provide a more reliable method of monitoring early ototoxic insults to the cochlea. Methods: twenty four children receiving gentamicin (4 mg/kg once daily) for 6-29 days were included in the study. Eleven children received gentamicin for up to 7 days (group A), while 13 underwent longer-term therapy lasting 8-29 days (group B). Hearing was seriary monitored using transient evoked otoacoustic emissions and pure-tone audiometry (0.25-12 kHz) or auditory brainstem responses for younger or uncooperative children. Transient evoked otoacoustic emissions data were analysed in terms of emission amplitude and response reproducibility as a function of frequency. Results: all patients yielded a normal baseline audiometric assessment upon hospital admission. For group A patients no significant changes in hearing levels were observed either by pure-tone audiometry (P = 0.2), auditory brainstem responses (P = 0.3) or transient evoked otoacoustic emissions (mean response: P = 0.06, reproducibility by frequency: P > 0.05). For group B patients no significant changes in hearing levels measured by pure-tone audiometry (P = 0.1) or auditory brainstem responses (P = 0.4) were observed. Transient evoked otoacoustic emissions however revealed a statistically significant decrease in the mean response level (P = 0.017) and in the reproducibility over the whole frequency spectrum (1 kHz: P = 0.0057, 2 kHz: P = 0.0247, 3 kHz: P = 0.0134, 4 kHz: P = 0.0049, 5 kHz: P = 0.0019). Conclusions: the findings suggest that transient evoked otoacoustic emissions are an extremely sensitive measure of the early effects of aminoglycoside-induced injury to the peripheral auditory system. Therefore, their use is recommended for regular monitoring of cochlear function, in the presence of potentially toxic factors, aiming at prevention of permanent damage. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:177 / 184
页数:8
相关论文
共 33 条
[1]  
*AM SPEECH HEAR AS, 1987, J AM SPEECH LANG HEA, V20, P297
[2]   QUANTITATIVE ASSESSMENT OF HUMAN COCHLEAR FUNCTION BY EVOKED OTOACOUSTIC EMISSIONS [J].
AVAN, P ;
BONFILS, P ;
LOTH, D ;
NARCY, P ;
TROTOUX, J .
HEARING RESEARCH, 1991, 52 (01) :99-112
[3]  
BENDUSH CL, 1982, AMINOGLYCOSIDES MICR, P453
[4]   A CORRELATIVE STUDY OF EVOKED OTOACOUSTIC EMISSION PROPERTIES AND AUDIOMETRIC THRESHOLDS [J].
BONFILS, P ;
PIRON, JP ;
UZIEL, A ;
PUJOL, R .
ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 1988, 245 (01) :53-56
[5]   ACOUSTIC DISTORTION PRODUCTS CAN BE USED TO MONITOR THE EFFECTS OF CHRONIC GENTAMICIN TREATMENT [J].
BROWN, AM ;
MCDOWELL, B ;
FORGE, A .
HEARING RESEARCH, 1989, 42 (2-3) :143-156
[6]   OTOTOXICITY OF AMINOGLUCOSIDE ANTIBIOTICS IN LONG-TERM TREATMENT FOR CYSTIC-FIBROSIS [J].
CRIFO, S ;
ANTONELLI, M ;
GAGLIARDI, M ;
LUCARELLI, N ;
MARCOLINI, P .
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 1980, 2 (03) :251-253
[7]   A CONTROLLED-STUDY OF THE RELIABILITY OF PURE-TONE AUDIOMETRY FOR THE DETECTION OF GENTAMICIN AUDITORY TOXICITY [J].
DAVEY, PG ;
JABEEN, FJ ;
HARPUR, ES ;
SHENOI, PM ;
GEDDES, AM .
JOURNAL OF LARYNGOLOGY AND OTOLOGY, 1983, 97 (01) :27-36
[8]   PROSPECTIVE CONTROLLED EVALUATION OF AUDITORY FUNCTION IN NEONATES GIVEN NETILMICIN OR AMIKACIN [J].
FINITZOHIEBER, T ;
MCCRACKEN, GH ;
BROWN, KC .
JOURNAL OF PEDIATRICS, 1985, 106 (01) :129-136
[9]   TEST RETEST RELIABILITY OF DISTORTION-PRODUCT AND TRANSIENTLY EVOKED OTOACOUSTIC EMISSIONS [J].
FRANKLIN, DJ ;
MCCOY, MJ ;
MARTIN, GK ;
LONSBURYMARTIN, BL .
EAR AND HEARING, 1992, 13 (06) :417-429
[10]  
HALL JW, 1988, SEMIN HEAR, V9, P15