Pharmacokinetic/pharmacodynamic modelling approaches in paediatric infectious diseases and immunology

被引:32
作者
Barker, Charlotte I. S. [1 ,2 ]
Germovsek, Eva [2 ]
Hoare, Rollo L. [2 ,3 ]
Lestner, Jodi M. [1 ,4 ]
Lewis, Joanna [2 ,3 ]
Standing, Joseph F. [2 ,3 ]
机构
[1] Univ London, Div Clin Sci, Paediat Infect Dis Res Grp, London SW17 0RE, England
[2] UCL, Inst Child Hlth, Infect Dis & Microbiol Unit, London WC1N 1EH, England
[3] UCL, CoMPLEX, London WC1E 6BT, England
[4] Univ London Imperial Coll Sci Technol & Med, Fac Med, London, England
基金
英国医学研究理事会; 英国工程与自然科学研究理事会;
关键词
Pharmacokinetics/pharmacodynamics (PKPD); Non-linear mixed effects (NLME); Paediatrics; Antimicrobial; Antibacterial; Antifungal; Antiviral (and antiretrovirals); HIV viral and T-cell dynamics; Immune reconstitution; POPULATION PHARMACOKINETIC ANALYSIS; SINGLE-DOSE PHARMACOKINETICS; BONE-MARROW-TRANSPLANTATION; STEM-CELL TRANSPLANTATION; ITRACONAZOLE ORAL SOLUTION; UNRELATED CORD BLOOD; VERSUS-HOST-DISEASE; AMPHOTERICIN-B; IMMUNE RECONSTITUTION; CYSTIC-FIBROSIS;
D O I
10.1016/j.addr.2014.01.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pharmacokinetic/pharmacodynamic (PMPD) modelling is used to describe and quantify dose-concentration-effect relationships. Within paediatric studies in infectious diseases and immunology these methods are often applied to developing guidance on appropriate dosing. In this paper, an introduction to the field of PKPD modelling is given, followed by a review of the PKPD studies that have been undertaken in paediatric infectious diseases and immunology. The main focus is on identifying the methodological approaches used to define the PKPD relationship in these studies. The major findings were that most studies of infectious diseases have developed a PK model and then used simulations to define a dose recommendation based on a pre-defined PD target, which may have been defined in adults or in vitro. For immunological studies much of the modelling has focused on either PK or PD, and since multiple drugs are usually used, delineating the relative contributions of each is challenging. The use of dynamical modelling of in vitro antibacterial studies, and paediatric HIV mechanistic PD models linked with the PK of all drugs, are emerging methods that should enhance PKPD-based recommendations in the future. (C) 2014 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
引用
收藏
页码:127 / 139
页数:13
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