Tuberculosis Drugs and Sensorineural Hearing Loss
Yes, several tuberculosis (TB) drugs, particularly aminoglycosides, can cause sensorineural hearing loss, with the risk being highest for amikacin (33.4%), followed by kanamycin, streptomycin, and lowest for capreomycin (2.0%). 1
Aminoglycoside Ototoxicity
Mechanism and Risk
- Aminoglycosides (streptomycin, amikacin, kanamycin) and polypeptides (capreomycin) can cause irreversible damage to the vestibular branch of the eighth cranial nerve, resulting in ototoxicity 2
- Ototoxicity can be vestibular (affecting balance) or cochlear (causing hearing loss) 2
- The risk of hearing loss increases with:
Drug-Specific Ototoxicity Profiles
Streptomycin
- Primarily causes vestibular dysfunction (vertigo, ataxia, nystagmus) but can also cause hearing loss 2
- Risk increases with cumulative doses above 100-120g 2
- Ototoxicity can progress even after discontinuation of the drug 2
- Contraindicated in pregnancy due to risk of fetal hearing loss 2
Amikacin and Kanamycin
- Higher risk of cochlear toxicity (hearing loss) compared to vestibular toxicity 2
- Amikacin has the highest reported incidence of hearing loss (33.4%) among TB injectable drugs 1, 5
- High-frequency hearing loss was observed in 24% of patients receiving amikacin in one study 2
- Kanamycin showed ototoxicity in 18% of patients after 6 weeks of therapy in one study 6
Capreomycin
- Has the lowest reported incidence of ototoxicity (2.0%) among injectable TB drugs 1, 5
- Still carries risks of nephrotoxicity and ototoxicity 2
Monitoring and Prevention
Recommended Monitoring
- Baseline audiogram, vestibular testing, Romberg testing, and serum creatinine measurement before starting treatment 2
- Monthly assessment of renal function and questioning about auditory or vestibular symptoms 2
- Regular high-quality audiometry, especially for high-frequency hearing loss which occurs early 2
- Repeat audiogram and vestibular testing if symptoms of eighth nerve toxicity develop 2
Risk Mitigation Strategies
- Dose adjustment in elderly patients and those with renal impairment 2
- Monitoring serum drug levels to avoid toxicity, especially with amikacin where measurements are readily available 2
- Consider alternative treatments in patients with known mitochondrial DNA variants or family history of aminoglycoside ototoxicity 3
- Early detection and discontinuation may prevent irreversible damage 3
Clinical Implications
Treatment Considerations
- In MDR-TB treatment, amikacin has shown better treatment success rates compared to kanamycin and capreomycin, despite higher ototoxicity risk 2
- The benefit of injectable agents must be weighed against the significant risk of permanent hearing loss 1, 5
- Recent guidelines recommend considering aminoglycoside-sparing regimens when possible, especially for patients at high risk of ototoxicity 4
- When aminoglycosides must be used, single daily dosing is preferred to divided doses to minimize toxicity while maintaining efficacy 2
High-Risk Populations
- Patients with pre-existing hearing loss have 1.71 times higher risk of developing additional hearing loss 4
- Risk increases by 16% for every 10 years of age 4
- Patients receiving high doses (≥75 mg/kg/week) have 1.33 times higher risk of requiring regimen modification due to ototoxicity 4
- Patients with diabetes, hypertension, and lower socioeconomic status may be at higher risk 6