» Articles » PMID: 34943771

Is Dosing of Ethambutol As Part of a Fixed-Dose Combination Product Optimal for Mechanically Ventilated ICU Patients with Tuberculosis? A Population Pharmacokinetic Study

Abstract

Background: Tuberculosis (TB) patients admitted to intensive care units (ICU) have high mortality rates. It is uncertain whether the pharmacokinetics of first-line TB drugs in ICU patients are different from outpatients. This study aims to compare the pharmacokinetics of oral ethambutol in TB patients in ICU versus TB outpatients and to determine whether contemporary dosing regimens achieve therapeutic exposures.

Methods: A prospective population pharmacokinetic study of ethambutol was performed in Amazonas State, Brazil. Probability of target attainment was determined using AUC/MIC > 11.9 and C/MIC > 0.48 values. Optimized dosing regimens were simulated at steady state.

Results: Ten ICU patients and 20 outpatients were recruited. Ethambutol pharmacokinetics were best described using a two-compartment model with first-order oral absorption. Neither ICU patients nor outpatients consistently achieved optimal ethambutol exposures. The absorption rate for ethambutol was 2-times higher in ICU patients ( < 0.05). Mean bioavailability for ICU patients was >5-times higher than outpatients ( < 0.0001). Clearance and volume of distribution were 93% ( < 0.0001) and 53% ( = 0.002) lower in ICU patients, respectively.

Conclusions: ICU patients displayed significantly different pharmacokinetics for an oral fixed-dose combination administration of ethambutol compared to outpatients, and neither patient group consistently achieved pre-defined therapeutic exposures.

Citing Articles

The impact of alcohol and illicit substance use on the pharmacokinetics of first-line TB drugs.

Wijk M, Gausi K, Malatesta S, Weber S, Court R, Myers B J Antimicrob Chemother. 2024; 79(8):2022-2030.

PMID: 38985541 PMC: 11290884. DOI: 10.1093/jac/dkae206.


Is the Pharmacokinetics of First-Line Anti-TB Drugs a Cause of High Mortality Rates in TB Patients Admitted to the ICU? A Non-Compartmental Pharmacokinetic Analysis.

Beraldi-Magalhaes F, Parker S, Sanches C, Garcia L, Souza Carvalho B, Costa A Trop Med Infect Dis. 2023; 8(6).

PMID: 37368730 PMC: 10303681. DOI: 10.3390/tropicalmed8060312.

References
1.
Ferreira M, Neves C, de Souza A, Beraldi-Magalhaes F, Migliori G, Kritski A . Predictors of mortality among intensive care unit patients coinfected with tuberculosis and HIV. J Bras Pneumol. 2018; 44(2):118-124. PMC: 6044649. DOI: 10.1590/s1806-37562017000000316. View

2.
Tweed C, Crook A, Amukoye E, Dawson R, Diacon A, Hanekom M . Toxicity associated with tuberculosis chemotherapy in the REMoxTB study. BMC Infect Dis. 2018; 18(1):317. PMC: 6042413. DOI: 10.1186/s12879-018-3230-6. View

3.
Hasenbosch R, Alffenaar J, Koopmans S, Kosterink J, van der Werf T, van Altena R . Ethambutol-induced optical neuropathy: risk of overdosing in obese subjects. Int J Tuberc Lung Dis. 2008; 12(8):967-71. View

4.
Horita Y, Alsultan A, Kwara A, Antwi S, Enimil A, Ortsin A . Evaluation of the Adequacy of WHO Revised Dosages of the First-Line Antituberculosis Drugs in Children with Tuberculosis Using Population Pharmacokinetic Modeling and Simulations. Antimicrob Agents Chemother. 2018; 62(9). PMC: 6125554. DOI: 10.1128/AAC.00008-18. View

5.
Ritschel W, Vachharajani N, Johnson R, Hussain A . The allometric approach for interspecies scaling of pharmacokinetic parameters. Comp Biochem Physiol C Comp Pharmacol Toxicol. 1992; 103(2):249-53. DOI: 10.1016/0742-8413(92)90003-p. View