Pharmacokinetics and pharmacodynamics of polymyxin B and proposed dosing regimens in elderly patients with multi-drug-resistant Gram-negative bacterial infections

•There are very limited studies on the pharmacokinetics (PK) and pharmacodynamics (PD) of polymyxin B in elderly patients.•Population PK models and Monte Carlo simulations were performed with 23 patients (age ≥65 years).•Fixed regimens of 50 mg and 75 mg may be sufficient to reach the PK/PD target i...

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Veröffentlicht in:International journal of antimicrobial agents 2022-11, Vol.60 (5-6), p.106693, Article 106693
Hauptverfasser: Wang, Peile, Liu, Dongmei, Sun, Tongwen, Zhang, Xiaojian, Yang, Jing
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Sprache:eng
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Zusammenfassung:•There are very limited studies on the pharmacokinetics (PK) and pharmacodynamics (PD) of polymyxin B in elderly patients.•Population PK models and Monte Carlo simulations were performed with 23 patients (age ≥65 years).•Fixed regimens of 50 mg and 75 mg may be sufficient to reach the PK/PD target if the minimum inhibitory concentration is ≤0.5 mg/L. There are limited data on the pharmacokinetics (PK) and pharmacodynamics (PD) of polymyxin B in the elderly population. The objective of this study was to develop a population PK model of polymyxin B in elderly patients, determine factors that affect its PK parameters, and propose alternative dosing regimens. Critically ill elderly patients (age ≥65 years) who received intravenous polymyxin B for multi-drug-resistant Gram-negative bacterial infections were enrolled. A population PK model was developed using Phoenix NLME software. Monte Carlo simulations were performed to optimize regimens attaining the PK/PD target of AUC24h/MIC >50 and target exposure of 50–100 mg‧h/L. Clinical efficacy and nephrotoxicity of polymyxin B treatment were also assessed. A total of 142 polymyxin B concentrations from 23 patients were available. A two-compartment model with first-order elimination was developed, and albumin was the significant covariate of PK parameters. However, albumin had only a slight effect on polymyxin B exposure. Simulation results indicated that two fixed regimens of 50 mg and 75 mg would be sufficient to reach the PK/PD targets when the minimum inhibitory concentrations was ≤0.5 mg/L. With the exception of 1.25 mg/kg for 58 kg, other weight-based regimens (1.25–1.5 mg/kg for 70 kg and 80 kg; twice daily) may result in at least 40% of predicted AUCss,24h >100 mg‧h/L. In conclusion, fixed maintenance dosing of 50 mg and 75 mg for polymyxin B may maximize efficacy while balancing nephrotoxicity concerns for elderly patients.
ISSN:0924-8579
1872-7913
DOI:10.1016/j.ijantimicag.2022.106693