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...
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Series: | The Scientific World Journal |
Online Access: | http://dx.doi.org/10.1100/2012/762649 |
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doaj-d7c5ed26b34c4bd3bc43c9a525b184172020-11-25T01:18:05ZengHindawi LimitedThe Scientific World Journal1537-744X2012-01-01201210.1100/2012/762649762649Population Pharmacokinetics of Vancomycin in Thai PatientsTunggul Adi Purwonugroho0Suvatna Chulavatnatol1Yupaporn Preechagoon2Busba Chindavijak3Kumthorn Malathum4Pakwan Bunuparadah5Faculty of Pharmacy, Mahidol University, Rajathevi, Bangkok 10400, ThailandFaculty of Pharmacy, Mahidol University, Rajathevi, Bangkok 10400, ThailandFaculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, ThailandFaculty of Pharmacy, Mahidol University, Rajathevi, Bangkok 10400, ThailandFaculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, ThailandFaculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok 10400, ThailandPopulation 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, CLCr (mL/min): CL=0.044×CLCr. Meanwhile, volume of central compartment, 𝑉1 (L), was linearly related with the age (years old): 𝑉1=0.542× Age. Intercompartment clearance (𝑄) and volume of peripheral compartment (𝑉2) was 6.95 L/h and 44.2 L, respectively. The interindividual variability for CL, 𝑉1, 𝑄, and 𝑉2 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.http://dx.doi.org/10.1100/2012/762649 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tunggul Adi Purwonugroho Suvatna Chulavatnatol Yupaporn Preechagoon Busba Chindavijak Kumthorn Malathum Pakwan Bunuparadah |
spellingShingle |
Tunggul Adi Purwonugroho Suvatna Chulavatnatol Yupaporn Preechagoon Busba Chindavijak Kumthorn Malathum Pakwan Bunuparadah Population Pharmacokinetics of Vancomycin in Thai Patients The Scientific World Journal |
author_facet |
Tunggul Adi Purwonugroho Suvatna Chulavatnatol Yupaporn Preechagoon Busba Chindavijak Kumthorn Malathum Pakwan Bunuparadah |
author_sort |
Tunggul Adi Purwonugroho |
title |
Population Pharmacokinetics of Vancomycin in Thai Patients |
title_short |
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_sort |
population pharmacokinetics of vancomycin in thai patients |
publisher |
Hindawi Limited |
series |
The Scientific World Journal |
issn |
1537-744X |
publishDate |
2012-01-01 |
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, CLCr (mL/min): CL=0.044×CLCr. Meanwhile, volume of central compartment, 𝑉1 (L), was linearly related with the age (years old): 𝑉1=0.542× Age. Intercompartment clearance (𝑄) and volume of peripheral compartment (𝑉2) was 6.95 L/h and 44.2 L, respectively. The interindividual variability for CL, 𝑉1, 𝑄, and 𝑉2 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. |
url |
http://dx.doi.org/10.1100/2012/762649 |
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