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Population Pharmacokinetics of Vancomycin in Thai Patients
Population pharmacokinetics of vancomycin in Thai adult patients was determined by non-linear mixed-effects approach using 319 vancomycin serum concentrations from 212 patients. The data were best fitted by a two-compartment model and it was used to examine the effect of patient characteristics on t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Scientific World Journal
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322481/ https://www.ncbi.nlm.nih.gov/pubmed/22547995 http://dx.doi.org/10.1100/2012/762649 |
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author | Purwonugroho, Tunggul Adi Chulavatnatol, Suvatna Preechagoon, Yupaporn Chindavijak, Busba Malathum, Kumthorn Bunuparadah, Pakwan |
author_facet | Purwonugroho, Tunggul Adi Chulavatnatol, Suvatna Preechagoon, Yupaporn Chindavijak, Busba Malathum, Kumthorn Bunuparadah, Pakwan |
author_sort | Purwonugroho, Tunggul Adi |
collection | PubMed |
description | Population pharmacokinetics of vancomycin in Thai adult patients was determined by non-linear mixed-effects approach using 319 vancomycin serum concentrations from 212 patients. The data were best fitted by a two-compartment model and it was used to examine the effect of patient characteristics on the vancomycin pharmacokinetics. In the final model, there was a linear relationship between vancomycin clearance, CL (L/h), and creatinine clearance calculated by Cockcroft-Gault equation, CL(Cr) (mL/min): CL =0.044 × CL(Cr). Meanwhile, volume of central compartment, V (1) (L), was linearly related with the age (years old): V (1) = 0.542 × Age. Intercompartment clearance (Q) and volume of peripheral compartment (V (2)) was 6.95 L/h and 44.2 L, respectively. The interindividual variability for CL, V (1), Q, and V (2) was 35.78, 20.93, 39.50, and 57.27%, respectively. Whereas, the intraindividual variability was 4.51 mg/L. Final model then was applied to predict serum vancomycin concentrations on validation group. Predictive performance revealed a bias of −1.43 mg/L (95% CI: −5.82–2.99) and a precision of 12.2 mg/L (95% CI: −1.60–26.16). In conclusion, population pharmacokinetic of vancomycin in Thai adult patients was developed. The model could be used to create vancomycin dosage regimen in the type of patient similar with the present study. |
format | Online Article Text |
id | pubmed-3322481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Scientific World Journal |
record_format | MEDLINE/PubMed |
spelling | pubmed-33224812012-04-30 Population Pharmacokinetics of Vancomycin in Thai Patients Purwonugroho, Tunggul Adi Chulavatnatol, Suvatna Preechagoon, Yupaporn Chindavijak, Busba Malathum, Kumthorn Bunuparadah, Pakwan ScientificWorldJournal Research Article Population pharmacokinetics of vancomycin in Thai adult patients was determined by non-linear mixed-effects approach using 319 vancomycin serum concentrations from 212 patients. The data were best fitted by a two-compartment model and it was used to examine the effect of patient characteristics on the vancomycin pharmacokinetics. In the final model, there was a linear relationship between vancomycin clearance, CL (L/h), and creatinine clearance calculated by Cockcroft-Gault equation, CL(Cr) (mL/min): CL =0.044 × CL(Cr). Meanwhile, volume of central compartment, V (1) (L), was linearly related with the age (years old): V (1) = 0.542 × Age. Intercompartment clearance (Q) and volume of peripheral compartment (V (2)) was 6.95 L/h and 44.2 L, respectively. The interindividual variability for CL, V (1), Q, and V (2) was 35.78, 20.93, 39.50, and 57.27%, respectively. Whereas, the intraindividual variability was 4.51 mg/L. Final model then was applied to predict serum vancomycin concentrations on validation group. Predictive performance revealed a bias of −1.43 mg/L (95% CI: −5.82–2.99) and a precision of 12.2 mg/L (95% CI: −1.60–26.16). In conclusion, population pharmacokinetic of vancomycin in Thai adult patients was developed. The model could be used to create vancomycin dosage regimen in the type of patient similar with the present study. The Scientific World Journal 2012-04-01 /pmc/articles/PMC3322481/ /pubmed/22547995 http://dx.doi.org/10.1100/2012/762649 Text en Copyright © 2012 Tunggul Adi Purwonugroho et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Purwonugroho, Tunggul Adi Chulavatnatol, Suvatna Preechagoon, Yupaporn Chindavijak, Busba Malathum, Kumthorn Bunuparadah, Pakwan Population Pharmacokinetics of Vancomycin in Thai Patients |
title | Population Pharmacokinetics of Vancomycin in Thai Patients |
title_full | Population Pharmacokinetics of Vancomycin in Thai Patients |
title_fullStr | Population Pharmacokinetics of Vancomycin in Thai Patients |
title_full_unstemmed | Population Pharmacokinetics of Vancomycin in Thai Patients |
title_short | Population Pharmacokinetics of Vancomycin in Thai Patients |
title_sort | population pharmacokinetics of vancomycin in thai patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322481/ https://www.ncbi.nlm.nih.gov/pubmed/22547995 http://dx.doi.org/10.1100/2012/762649 |
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