Population Pharmacokinetics and Dosing Optimization of Ceftazidime in Infants [Pharmacology]
Shi, Z.-R., Chen, X.-K., Tian, L.-Y., Wang, Y.-K., Zhang, G.-Y., Dong, L., Jirasomprasert, T., Jacqz-Aigrain, E., Zhao, W.
The American Society for Microbiology (ASM)
Published 2018
The American Society for Microbiology (ASM)
Published 2018
| Publication Date: |
2018-03-28
|
|---|---|
| Publisher: |
The American Society for Microbiology (ASM)
|
| Print ISSN: |
0066-4804
|
| Electronic ISSN: |
1098-6596
|
| Topics: |
Biology
Medicine
|
| Published by: |
| _version_ | 1836398868094255105 |
|---|---|
| autor | Shi, Z.-R., Chen, X.-K., Tian, L.-Y., Wang, Y.-K., Zhang, G.-Y., Dong, L., Jirasomprasert, T., Jacqz-Aigrain, E., Zhao, W. |
| beschreibung | Ceftazidime, a third-generation cephalosporin, can be used for the treatment of adults and children with infections due to susceptible bacteria. To date, the pediatric pharmacokinetic data are limited in infants, and therefore we aimed to evaluate the population pharmacokinetics of ceftazidime in infants and to define the appropriate dose to optimize ceftazidime treatment. Blood samples were collected from children treated with ceftazidime, and concentrations of the drug were quantified by high-performance liquid chromatography with UV detection (HPLC-UV). A population pharmacokinetic analysis was performed using NONMEM software ( version 7.2.0). Fifty-one infants ( age range, 0.1 to 2.0 years ) were included. Sparse pharmacokinetic samples ( n = 90 ) were available for analysis. A one-compartment model with first-order elimination showed the best fit with the data. A covariate analysis identified that body weight and creatinine clearance (CL CR ) were significant covariates influencing ceftazidime clearance. Monte Carlo simulation demonstrated that the currently used dosing regimen of 50 mg / kg twice daily was associated with a high risk of underdosing in infants. In order to reach the target of 70% of the time that the free antimicrobial drug concentration exceeds the MIC ( fT 〉MIC ), 25 mg/kg every 8 h (q8h) and 50 mg/kg q8h were required for MICs of 4 and 8 mg/liter, respectively. The population pharmacokinetic characteristics of ceftazidime were evaluated in infants. An evidence-based dosing regimen was established based on simulation. |
| citation_standardnr | 6218917 |
| datenlieferant | ipn_articles |
| feed_id | 515 |
| feed_publisher | The American Society for Microbiology (ASM) |
| feed_publisher_url | http://www.asm.org/ |
| insertion_date | 2018-03-28 |
| journaleissn | 1098-6596 |
| journalissn | 0066-4804 |
| publikationsjahr_anzeige | 2018 |
| publikationsjahr_facette | 2018 |
| publikationsjahr_intervall | 7984:2015-2019 |
| publikationsjahr_sort | 2018 |
| publisher | The American Society for Microbiology (ASM) |
| quelle | Antimicrobial Agents and Chemotherapy |
| relation | http://aac.asm.org/cgi/content/short/62/4/e02486-17?rss=1 |
| search_space | articles |
| shingle_author_1 | Shi, Z.-R., Chen, X.-K., Tian, L.-Y., Wang, Y.-K., Zhang, G.-Y., Dong, L., Jirasomprasert, T., Jacqz-Aigrain, E., Zhao, W. |
| shingle_author_2 | Shi, Z.-R., Chen, X.-K., Tian, L.-Y., Wang, Y.-K., Zhang, G.-Y., Dong, L., Jirasomprasert, T., Jacqz-Aigrain, E., Zhao, W. |
| shingle_author_3 | Shi, Z.-R., Chen, X.-K., Tian, L.-Y., Wang, Y.-K., Zhang, G.-Y., Dong, L., Jirasomprasert, T., Jacqz-Aigrain, E., Zhao, W. |
| shingle_author_4 | Shi, Z.-R., Chen, X.-K., Tian, L.-Y., Wang, Y.-K., Zhang, G.-Y., Dong, L., Jirasomprasert, T., Jacqz-Aigrain, E., Zhao, W. |
| shingle_catch_all_1 | Population Pharmacokinetics and Dosing Optimization of Ceftazidime in Infants [Pharmacology] Ceftazidime, a third-generation cephalosporin, can be used for the treatment of adults and children with infections due to susceptible bacteria. To date, the pediatric pharmacokinetic data are limited in infants, and therefore we aimed to evaluate the population pharmacokinetics of ceftazidime in infants and to define the appropriate dose to optimize ceftazidime treatment. Blood samples were collected from children treated with ceftazidime, and concentrations of the drug were quantified by high-performance liquid chromatography with UV detection (HPLC-UV). A population pharmacokinetic analysis was performed using NONMEM software ( version 7.2.0). Fifty-one infants ( age range, 0.1 to 2.0 years ) were included. Sparse pharmacokinetic samples ( n = 90 ) were available for analysis. A one-compartment model with first-order elimination showed the best fit with the data. A covariate analysis identified that body weight and creatinine clearance (CL CR ) were significant covariates influencing ceftazidime clearance. Monte Carlo simulation demonstrated that the currently used dosing regimen of 50 mg / kg twice daily was associated with a high risk of underdosing in infants. In order to reach the target of 70% of the time that the free antimicrobial drug concentration exceeds the MIC ( fT >MIC ), 25 mg/kg every 8 h (q8h) and 50 mg/kg q8h were required for MICs of 4 and 8 mg/liter, respectively. The population pharmacokinetic characteristics of ceftazidime were evaluated in infants. An evidence-based dosing regimen was established based on simulation. Shi, Z.-R., Chen, X.-K., Tian, L.-Y., Wang, Y.-K., Zhang, G.-Y., Dong, L., Jirasomprasert, T., Jacqz-Aigrain, E., Zhao, W. The American Society for Microbiology (ASM) 0066-4804 00664804 1098-6596 10986596 |
| shingle_catch_all_2 | Population Pharmacokinetics and Dosing Optimization of Ceftazidime in Infants [Pharmacology] Ceftazidime, a third-generation cephalosporin, can be used for the treatment of adults and children with infections due to susceptible bacteria. To date, the pediatric pharmacokinetic data are limited in infants, and therefore we aimed to evaluate the population pharmacokinetics of ceftazidime in infants and to define the appropriate dose to optimize ceftazidime treatment. Blood samples were collected from children treated with ceftazidime, and concentrations of the drug were quantified by high-performance liquid chromatography with UV detection (HPLC-UV). A population pharmacokinetic analysis was performed using NONMEM software ( version 7.2.0). Fifty-one infants ( age range, 0.1 to 2.0 years ) were included. Sparse pharmacokinetic samples ( n = 90 ) were available for analysis. A one-compartment model with first-order elimination showed the best fit with the data. A covariate analysis identified that body weight and creatinine clearance (CL CR ) were significant covariates influencing ceftazidime clearance. Monte Carlo simulation demonstrated that the currently used dosing regimen of 50 mg / kg twice daily was associated with a high risk of underdosing in infants. In order to reach the target of 70% of the time that the free antimicrobial drug concentration exceeds the MIC ( fT >MIC ), 25 mg/kg every 8 h (q8h) and 50 mg/kg q8h were required for MICs of 4 and 8 mg/liter, respectively. The population pharmacokinetic characteristics of ceftazidime were evaluated in infants. An evidence-based dosing regimen was established based on simulation. Shi, Z.-R., Chen, X.-K., Tian, L.-Y., Wang, Y.-K., Zhang, G.-Y., Dong, L., Jirasomprasert, T., Jacqz-Aigrain, E., Zhao, W. The American Society for Microbiology (ASM) 0066-4804 00664804 1098-6596 10986596 |
| shingle_catch_all_3 | Population Pharmacokinetics and Dosing Optimization of Ceftazidime in Infants [Pharmacology] Ceftazidime, a third-generation cephalosporin, can be used for the treatment of adults and children with infections due to susceptible bacteria. To date, the pediatric pharmacokinetic data are limited in infants, and therefore we aimed to evaluate the population pharmacokinetics of ceftazidime in infants and to define the appropriate dose to optimize ceftazidime treatment. Blood samples were collected from children treated with ceftazidime, and concentrations of the drug were quantified by high-performance liquid chromatography with UV detection (HPLC-UV). A population pharmacokinetic analysis was performed using NONMEM software ( version 7.2.0). Fifty-one infants ( age range, 0.1 to 2.0 years ) were included. Sparse pharmacokinetic samples ( n = 90 ) were available for analysis. A one-compartment model with first-order elimination showed the best fit with the data. A covariate analysis identified that body weight and creatinine clearance (CL CR ) were significant covariates influencing ceftazidime clearance. Monte Carlo simulation demonstrated that the currently used dosing regimen of 50 mg / kg twice daily was associated with a high risk of underdosing in infants. In order to reach the target of 70% of the time that the free antimicrobial drug concentration exceeds the MIC ( fT >MIC ), 25 mg/kg every 8 h (q8h) and 50 mg/kg q8h were required for MICs of 4 and 8 mg/liter, respectively. The population pharmacokinetic characteristics of ceftazidime were evaluated in infants. An evidence-based dosing regimen was established based on simulation. Shi, Z.-R., Chen, X.-K., Tian, L.-Y., Wang, Y.-K., Zhang, G.-Y., Dong, L., Jirasomprasert, T., Jacqz-Aigrain, E., Zhao, W. The American Society for Microbiology (ASM) 0066-4804 00664804 1098-6596 10986596 |
| shingle_catch_all_4 | Population Pharmacokinetics and Dosing Optimization of Ceftazidime in Infants [Pharmacology] Ceftazidime, a third-generation cephalosporin, can be used for the treatment of adults and children with infections due to susceptible bacteria. To date, the pediatric pharmacokinetic data are limited in infants, and therefore we aimed to evaluate the population pharmacokinetics of ceftazidime in infants and to define the appropriate dose to optimize ceftazidime treatment. Blood samples were collected from children treated with ceftazidime, and concentrations of the drug were quantified by high-performance liquid chromatography with UV detection (HPLC-UV). A population pharmacokinetic analysis was performed using NONMEM software ( version 7.2.0). Fifty-one infants ( age range, 0.1 to 2.0 years ) were included. Sparse pharmacokinetic samples ( n = 90 ) were available for analysis. A one-compartment model with first-order elimination showed the best fit with the data. A covariate analysis identified that body weight and creatinine clearance (CL CR ) were significant covariates influencing ceftazidime clearance. Monte Carlo simulation demonstrated that the currently used dosing regimen of 50 mg / kg twice daily was associated with a high risk of underdosing in infants. In order to reach the target of 70% of the time that the free antimicrobial drug concentration exceeds the MIC ( fT >MIC ), 25 mg/kg every 8 h (q8h) and 50 mg/kg q8h were required for MICs of 4 and 8 mg/liter, respectively. The population pharmacokinetic characteristics of ceftazidime were evaluated in infants. An evidence-based dosing regimen was established based on simulation. Shi, Z.-R., Chen, X.-K., Tian, L.-Y., Wang, Y.-K., Zhang, G.-Y., Dong, L., Jirasomprasert, T., Jacqz-Aigrain, E., Zhao, W. The American Society for Microbiology (ASM) 0066-4804 00664804 1098-6596 10986596 |
| shingle_title_1 | Population Pharmacokinetics and Dosing Optimization of Ceftazidime in Infants [Pharmacology] |
| shingle_title_2 | Population Pharmacokinetics and Dosing Optimization of Ceftazidime in Infants [Pharmacology] |
| shingle_title_3 | Population Pharmacokinetics and Dosing Optimization of Ceftazidime in Infants [Pharmacology] |
| shingle_title_4 | Population Pharmacokinetics and Dosing Optimization of Ceftazidime in Infants [Pharmacology] |
| timestamp | 2025-06-30T23:33:52.711Z |
| titel | Population Pharmacokinetics and Dosing Optimization of Ceftazidime in Infants [Pharmacology] |
| titel_suche | Population Pharmacokinetics and Dosing Optimization of Ceftazidime in Infants [Pharmacology] |
| topic | W WW-YZ |
| uid | ipn_articles_6218917 |