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.

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.

Related Concept Videos

Pulmonary Tuberculosis V01:28

Pulmonary Tuberculosis V

Medical management of tuberculosis (TB) patients involves a comprehensive approach that includes diagnosis, treatment, and monitoring. The specific strategies can vary depending on the type of tuberculosis (latent or active), the patient's overall health status, and other considerations.
Latent tuberculosis infection occurs when TB bacteria are present in a person's body, but are not causing illness or symptoms. It is not contagious, and preventive treatment is crucial to avoid the...
1.0K
Estimation of k and VD of Aminoglycosides01:20

Estimation of k and VD of Aminoglycosides

Aminoglycosides are a class of antibiotics used to treat various bacterial infections. Clinicians must determine the elimination rate constant (k) and volume of distribution (VD) to optimize therapeutic efficacy and minimize toxicity. The k value represents the rate at which the drug is removed from the body, and the VD reflects the degree to which the drug distributes into body tissues. Accurately estimating these parameters allows healthcare professionals to tailor drug dosing to individual...
336
Pulmonary Tuberculosis I01:29

Pulmonary Tuberculosis I

Tuberculosis, often called TB, is a contagious illness primarily caused by Mycobacterium tuberculosis. It mainly affects the lung parenchyma but can also impact other body parts.
Causative Organism
The primary infectious agent causing tuberculosis is Mycobacterium tuberculosis, a slow-growing, acid-fast, aerobic rod that exhibits sensitivity to heat and ultraviolet light. Instances of Mycobacterium bovis and Mycobacterium avium contributing to the development of TB infection are rare.
Mode of...
1.7K
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations01:15

Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations

Gentamicin, an aminoglycoside antibiotic, is commonly administered via intermittent intravenous infusion to treat severe infections. An intermittent one-hour infusion of gentamicin, administered at eight-hour intervals, allows for precise control of plasma drug concentrations, minimizing toxicity while ensuring therapeutic efficacy. Pharmacokinetic principles govern the dynamics of plasma concentrations and can be mathematically described using specific equations.The plasma drug concentration...
386
Drug Accumulation During Multiple Dosing: Intermittent IV Infusions01:24

Drug Accumulation During Multiple Dosing: Intermittent IV Infusions

Intermittent intravenous (IV) infusion is a method of drug administration where medications are delivered over short infusion periods followed by intervals of no drug delivery. This approach helps to prevent sustained high drug concentrations in the bloodstream, reducing the risk of adverse effects associated with prolonged exposure. Unlike continuous infusion, steady-state concentrations may not be achieved during a single dosing cycle but can be reached through repeated...
428
Mechanism of Antibiotic Resistance in MRSA01:25

Mechanism of Antibiotic Resistance in MRSA

Antibiotic resistance in bacteria arises when microorganisms evolve the ability to withstand drugs designed to kill them or inhibit their growth, rendering once-effective treatments useless. This phenomenon, driven by genetic change and selection under antibiotic exposure, poses a profound threat to modern medicine. Mechanisms include drug-inactivating enzymes (e.g., β-lactamases), efflux pumps that eject antibiotics, mutations altering antibiotic targets, decreased drug uptake, and...
245