Objective: To document that commercially available topical gentamicin-conta
ining eardrops carry a risk of ototoxicity if they reach the middle ear thr
ough a tympanic membrane defect, Study Design: Clinical study, retrospectiv
e case-note review. Setting: Department of Otolaryngology, The Toronto Hosp
ital, University of Toronto. Patients: Sixteen patients were identified wit
h well-documented histories, physical findings and laboratory investigation
s consistent with topical gentamicin-induced ototoxicity. One patient with
incapacitating unilateral Meniere's disease underwent successful intentiona
l vestibular ablation using topical gentamicin/steroid drops. Results: In a
ll eases of inadvertent ototoxicity, patients had used the drops for longer
than 7 days (average 20.7 d) prior to symptoms developing. All patients de
veloped 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 Me
niere's disease confirms the vestibulotoxic nature of commercially availabl
e topical gentamicin preparations, Conclusions: Physicians should consider
the potential for ototoxicity if gentamicin-containing eardrops (and by ext
rapolation all topical aminoglycoside drops) are used for longer than 7 day
s in patients with a tympanic membrane defect. These preparations should no
t be used in the presence of healthy middle ear mucosa and should be discon
tinued shortly after the discharge has stopped. It is important to recogniz
e that toxicity is primarily vestibular rather than cochlear.