Pharmacokinetics and Pharmacodynamics of Antifungal Agents in Neonates and Children

被引:2
|
作者
Antachopoulos, Charalampos [1 ]
Roilides, Emmanuel [1 ]
机构
[1] Aristotle Univ Thessaloniki, Hippokration Gen Hosp, Fac Med, Dept Pediat 3,Sch Hlth Sci, Konstantinoupoleos 49, GR-54642 Thessaloniki, Greece
关键词
Pharmacokinetics; Pharmacodynamics; Pediatric patients; Amphotericin B; Azoles; Echinocandins; LIPOSOMAL AMPHOTERICIN-B; INVASIVE PULMONARY ASPERGILLOSIS; POSACONAZOLE PLASMA-CONCENTRATIONS; PEDIATRIC CANCER-PATIENTS; POPULATION PHARMACOKINETICS; ORAL SUSPENSION; LIPID COMPLEX; MURINE MODEL; SAFETY; VORICONAZOLE;
D O I
10.1007/s12281-020-00402-6
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose of Review This review summarizes current knowledge on pharmacokinctics (PK) and pharmacodynamics (PD) of various formulations of amphotericin B, triazoles (fluconazole, itraconazole, voriconazole, posaconazole, isavuconazole), and echinocandins (caspofungin, micafungin, anidulafungin) in the pediatric population. Recent Findings The PD indices associated with in vivo outcome have been defined for all antifungal agents. PK parameters have been studied across all range of ages; however, data often originate from small patient series, particularly regarding neonates and young infants. Dose-exposure simulations in population PK studies provide the probability of PD target attainment using various dosage regimens. Therapeutic drug monitoring (TDM) has been recognized as a valuable tool to individualize dosing for azoles due to significant inter-patient variability. Summary Our understanding of PK/PD of antifungal agents in pediatric patients has significantly advanced over the last years allowing age-specific dosing recommendations. Yet, however, several PK questions regarding specific patient groups remain to be addressed.
引用
收藏
页码:317 / 328
页数:12
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