Pharmacokinetic/pharmacodynamic evaluation of linezolid in hospitalized paediatric patients: a step toward dose optimization by means of therapeutic drug monitoring and Monte Carlo simulation

被引:41
作者
Cojutti, Piergiorgio [1 ,2 ]
Maximova, Natalia [3 ]
Crichiutti, Giovanni [4 ]
Isola, Miriam [5 ]
Pea, Federico [1 ,2 ]
机构
[1] Univ Santa Maria della Misericordia, Azienda Osped, Inst Clin Pharmacol, Udine, Italy
[2] Univ Udine, Dept Expt & Clin Med Sci, I-33100 Udine, Italy
[3] IRCCS Burlo Garofolo, Inst Maternal & Child Hlth, Trieste, Italy
[4] Univ Santa Maria della Misericordia, Azienda Osped, Clin Pediat, Udine, Italy
[5] Univ Udine, Sect Stat, Dept Med & Biol Sci, I-33100 Udine, Italy
关键词
MDR staphylococci; oxazolidinones; drug interactions; drug underexposure; IMPAIRED RENAL-FUNCTION; LONG-TERM TREATMENT; PHARMACOKINETICS; INFECTIONS; CHILDREN; PLASMA; PHARMACODYNAMICS; INFANTS; RIFAMPIN; PROFILE;
D O I
10.1093/jac/dku337
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To report on linezolid exposure in a paediatric population who routinely underwent therapeutic drug monitoring (TDM) for dosage optimization and to assess the factors affecting interpatient variability. Methods: We performed a retrospective study of patients whose plasma C-min and C-max levels were measured during linezolid treatment. Adequate exposure was defined as a C-min of 2-7 mg/L and/or an estimated AUC(24) of 160-300 mg. h/L. Patients were divided into two subgroups (Group 1, 2-11 years; Group 2, 12-18 years). Monte Carlo simulation was performed to investigate whether or not the currently recommended dosages might enable a high probability of target attainment (PTA) of two thresholds for linezolid efficacy (AUC(24)/MIC >= 80 or >= 100). Data on demographic characteristics, disease, microbiology and haematochemical parameters and outcomes were collected. Results: A total of 23 patients were included. Standard dosages were suboptimal in 50.0% and 44.4% of patients in Group 1 and Group 2, respectively. Among those who underwent multiple instances of TDM, the dosages were increased in 33.3% of cases in both groups, and decreased in 6.6% and 9.5% of cases in Group 1 and Group 2, respectively. Co-treatment with phenobarbital, proton pump inhibitors and amiodarone accounted for most of the variability in C-min (adjusted R-2 of 0.692). Simulations showed a PTA of >= 90% with the current dosing regimens in both groups only for pathogens with an MIC <= 1 mg/L. Conclusions: Higher dosages of linezolid may be needed, especially in Group 1 when in the presence of pathogens with an MIC >1 mg/L. The role of TDM should be encouraged for optimization of linezolid exposure in the paediatric setting in the presence of infections caused by pathogens with borderline susceptibility and/or for patients co-treated with drugs that may alter linezolid exposure.
引用
收藏
页码:198 / 206
页数:9
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