abstract
Ototoxicity is a well-established toxicity associated with a subgroup of
antineoplastic therapies that includes platinum chemotherapy, radiation
or surgery involving the ear and auditory nerve, and supportive care
agents such as aminoglycoside antibiotics and loop diuretics. The
reported prevalence of ototoxicity in patients who have received
potentially ototoxic therapy ranges from 4% to 90% depending on factors
such as age of the patient population, agent(s) used, cumulative dose,
and administration techniques. The impact of ototoxicity on subsequent
health-related and psychosocial outcomes in these patients can be
substantial, and the burden of morbidity related to ototoxic agents is
particularly high in very young children. Considerable interindividual
variability in the prevalence and severity of ototoxicity has been
observed among patients receiving similar treatment, suggesting genetic
susceptibility as a risk factor. The development and testing of
otoprotective agents is ongoing; however, to the author's knowledge, no
US Food and Drug Administration-approved otoprotectants are currently
available. Prospective monitoring for ototoxicity allows for comparison
of auditory outcomes across clinical trials, as well as for early
detection, potential alterations in therapy, and auditory intervention
and rehabilitation to ameliorate the adverse consequences of hearing
loss.
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