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Pharmacokinetic/pharmacodynamic modelling approaches in paediatric infectious diseases and immunology()
Pharmacokinetic/pharmacodynamic (PKPD) 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 t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Publishers, B.V
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076844/ https://www.ncbi.nlm.nih.gov/pubmed/24440429 http://dx.doi.org/10.1016/j.addr.2014.01.002 |
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author | Barker, Charlotte I.S. Germovsek, Eva Hoare, Rollo L. Lestner, Jodi M. Lewis, Joanna Standing, Joseph F. |
author_facet | Barker, Charlotte I.S. Germovsek, Eva Hoare, Rollo L. Lestner, Jodi M. Lewis, Joanna Standing, Joseph F. |
author_sort | Barker, Charlotte I.S. |
collection | PubMed |
description | Pharmacokinetic/pharmacodynamic (PKPD) 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. |
format | Online Article Text |
id | pubmed-4076844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier Science Publishers, B.V |
record_format | MEDLINE/PubMed |
spelling | pubmed-40768442014-07-07 Pharmacokinetic/pharmacodynamic modelling approaches in paediatric infectious diseases and immunology() Barker, Charlotte I.S. Germovsek, Eva Hoare, Rollo L. Lestner, Jodi M. Lewis, Joanna Standing, Joseph F. Adv Drug Deliv Rev Article Pharmacokinetic/pharmacodynamic (PKPD) 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. Elsevier Science Publishers, B.V 2014-06-30 /pmc/articles/PMC4076844/ /pubmed/24440429 http://dx.doi.org/10.1016/j.addr.2014.01.002 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Article Barker, Charlotte I.S. Germovsek, Eva Hoare, Rollo L. Lestner, Jodi M. Lewis, Joanna Standing, Joseph F. Pharmacokinetic/pharmacodynamic modelling approaches in paediatric infectious diseases and immunology() |
title | Pharmacokinetic/pharmacodynamic modelling approaches in paediatric infectious diseases and immunology() |
title_full | Pharmacokinetic/pharmacodynamic modelling approaches in paediatric infectious diseases and immunology() |
title_fullStr | Pharmacokinetic/pharmacodynamic modelling approaches in paediatric infectious diseases and immunology() |
title_full_unstemmed | Pharmacokinetic/pharmacodynamic modelling approaches in paediatric infectious diseases and immunology() |
title_short | Pharmacokinetic/pharmacodynamic modelling approaches in paediatric infectious diseases and immunology() |
title_sort | pharmacokinetic/pharmacodynamic modelling approaches in paediatric infectious diseases and immunology() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076844/ https://www.ncbi.nlm.nih.gov/pubmed/24440429 http://dx.doi.org/10.1016/j.addr.2014.01.002 |
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