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The Incidence of Amikacin Ototoxicity in Multidrug-ResistantTuberculosis Patients
Mohammad Reza Javadi1, Bahareh Abtahi, Kheirollah Gholami
1Department of Clinical Pharmacy, School of Pharmacy,Tehran University of Medical Sciences, Tehran, Iran.
Abstract:
Amikacin has been shown to irreversibly suppressCochlear activity.The aim of this study is to assess the incidence of amikacinototoxicity in multidrug-resistant tuberculosis patients and riskfactors associated withthis ototoxicity.In this cross-sectional study, 41 patientswith multidrug-resistant tuberculosis (MDR-TB) were included.All patients received fixed dose of intravenous amikacin(500 mg/day) and anti-TB medications for six months. Baseline Pure-Tone Audiometry (PTA) was performed on all patients,before and during the drug treatment with the frequency range between 250 Hz and 8000 Hz. Patients were closely observed for the occurrence of symptomatic ototoxicity using a questionnaire .To find an association between the incidence of cochlear damage and patients' demographics, all patients' data were recorded. A total of 29 patients suffered from hearing loss (70.1%) (Male: n = 18; Female: n = 20).Using logistic regression, the incidence ofamikacinototoxicity was higher in men than in women. There was a negative correlation between the duration of the amikacin treatment and the difference in hearing thresholds(r = -0.34, p = 0.03). The mean of hearing threshold was significantly increased before and after the amikacin treatment((23.68 ± 19.26 vs. 38.93 ± 22.80) (p < 0.0001)). The incidence of hearing loss was remarkable in MDR-TB patients treating with amikacin. However, risk factors' determination and monitoring of audiometric result variations could haveinfluenced the incidence of the amikacin ototoxicity.
Insights
Amikacin treatment for multidrug-resistant tuberculosis (MDR-TB) caused hearing loss in 70.1% of patients. Men were more affected, and longer treatment correlated with less hearing damage, suggesting careful monitoring is crucial.
Area of Science:
- Ototoxicology
- Pharmacology
- Infectious Diseases
Background:
- Amikacin is a critical antibiotic for multidrug-resistant tuberculosis (MDR-TB).
- Amikacin is known to cause irreversible cochlear damage (ototoxicity).
- Assessing amikacin ototoxicity incidence and risk factors in MDR-TB patients is essential.
Purpose of the Study:
- To determine the incidence of amikacin-induced ototoxicity in MDR-TB patients.
- To identify demographic and treatment-related risk factors for amikacin ototoxicity.
- To evaluate the impact of amikacin on hearing thresholds in MDR-TB patients.
Main Methods:
- A cross-sectional study included 41 MDR-TB patients receiving intravenous amikacin (500 mg/day) for six months.
- Pure-Tone Audiometry (PTA) was conducted before and during amikacin treatment (250 Hz–8000 Hz).
- Patients were monitored for symptomatic ototoxicity using questionnaires, and demographic data were collected.
Main Results:
- Hearing loss occurred in 70.1% of patients (29 out of 41).
- Amikacin ototoxicity incidence was higher in men than women.
- A negative correlation was found between amikacin treatment duration and hearing threshold changes (r = -0.34, p = 0.03).
- Mean hearing thresholds significantly increased post-treatment (23.68 ± 19.26 to 38.93 ± 22.80, p < 0.0001).
Conclusions:
- Amikacin treatment leads to a high incidence of hearing loss in MDR-TB patients.
- Gender and treatment duration may influence amikacin ototoxicity.
- Monitoring audiometric results and identifying risk factors are vital for managing amikacin ototoxicity.
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