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局部用庆大霉素制剂的耳毒性。

Ototoxicity of topical gentamicin preparations.

作者信息

Bath A P, Walsh R M, Bance M L, Rutka J A

机构信息

Department of Otolaryngology, The Toronto Hospital, University of Toronto, Ontario, Canada.

出版信息

Laryngoscope. 1999 Jul;109(7 Pt 1):1088-93. doi: 10.1097/00005537-199907000-00015.

DOI:10.1097/00005537-199907000-00015
PMID:10401847
Abstract

OBJECTIVE

To document that commercially available topical gentamicin-containing eardrops carry a risk of ototoxicity if they reach the middle ear through a tympanic membrane defect.

STUDY DESIGN

Clinical study, retrospective case-note review.

SETTING

Department of Otolaryngology, The Toronto Hospital, University of Toronto.

PATIENTS

Sixteen patients were identified with well-documented histories, physical findings and laboratory investigations consistent with topical gentamicin-induced ototoxicity. One patient with incapacitating unilateral Meniere's disease underwent successful intentional vestibular ablation using topical gentamicin/steroid drops.

RESULTS

In all cases of inadvertent ototoxicity, patients had used the drops for longer than 7 days (average 20.7 d) prior to symptoms developing. All patients developed vestibulotoxicity that was confirmed on ENG testing. Only 1 patient had a noticeable worsening of cochlear reserve. Deliberate and successful therapeutic ablation of vestibular function in a patient with unilateral Meniere's disease confirms the vestibulotoxic nature of commercially available topical gentamicin preparations.

CONCLUSIONS

Physicians should consider the potential for ototoxicity if gentamicin-containing eardrops (and by extrapolation all topical aminoglycoside drops) are used for longer than 7 days in patients with a tympanic membrane defect. These preparations should not be used in the presence of healthy middle ear mucosa and should be discontinued shortly after the discharge has stopped. It is important to recognize that toxicity is primarily vestibular rather than cochlear.

摘要

目的

证明市售含庆大霉素的滴耳剂如果通过鼓膜穿孔进入中耳会有耳毒性风险。

研究设计

临床研究,回顾性病例笔记审查。

研究地点

多伦多大学多伦多医院耳鼻喉科。

患者

确定了16例患者,其病史、体格检查结果和实验室检查结果充分证明与局部使用庆大霉素引起的耳毒性一致。一名患有严重单侧梅尼埃病的患者使用局部庆大霉素/类固醇滴耳剂成功进行了意向性前庭消融。

结果

在所有意外耳毒性病例中,患者在症状出现前使用滴耳剂的时间超过7天(平均20.7天)。所有患者均出现前庭毒性,经眼震电图测试证实。只有1例患者的耳蜗储备有明显恶化。一名单侧梅尼埃病患者的前庭功能经有意治疗性消融成功,证实了市售局部庆大霉素制剂的前庭毒性性质。

结论

如果鼓膜穿孔患者使用含庆大霉素的滴耳剂(由此推断所有局部用氨基糖苷类滴耳剂)超过7天,医生应考虑耳毒性的可能性。这些制剂在中耳黏膜健康时不应使用,且在引流停止后应尽快停药。认识到毒性主要是前庭性而非耳蜗性很重要。

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Laryngoscope. 1999 Jul;109(7 Pt 1):1088-93. doi: 10.1097/00005537-199907000-00015.
2
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