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

• Published in: Antibiotics (Basel) Vol. 10; no. 12; p. 1559
• Main Authors: Beraldi-Magalhaes, Francisco, Parker, Suzanne L, Sanches, Cristina, Sousa Garcia, Leandro, Souza Carvalho, Brenda Karoline, Fachi, Mariana Millan, de Liz, Marcus Vinicius, Pontarolo, Roberto, Lipman, Jeffrey, Cordeiro-Santos, Marcelo, Roberts, Jason A
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 20-12-2021; MDPI
• Subjects: Absorption; Bioavailability; biological availability; Creatinine; critical care; Dosage; Drug dosages; Ethambutol; Exposure; HIV; Hospitals; Human immunodeficiency virus; Intensive care; Intensive care units; Minimum inhibitory concentration; Mortality; Oral administration; Patients; Pharmacokinetics; Pharmacology; Population studies; Tuberculosis; Ventilation; critical care; pharmacokinetics; biological availability; intensive care; ethambutol; tuberculosis
• ISSN: 2079-6382; 2079-6382
• DOI: 10.3390/antibiotics10121559

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.
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.
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.
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.