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Population Pharmacokinetics and Individualized Medication of Azithromycin for Injection in Children Under 6 Years Old.
Zhang, Yuwen; Wang, Yinghui; Li, Jiangshuo; Wang, Honghong; Hou, Mengyu; Dong, Ruihua; Li, Xingang.
Afiliación
  • Zhang Y; Department of Pharmacy, Beijing Friendship Hospital, Capital Medical University, 100050, Beijing China.
  • Wang Y; Department of Pediatrics, Beijing Friendship Hospital, Capital Medical University, 100050, Beijing, China.
  • Li J; Department of Research Ward, Beijing Friendship Hospital, Capital Medical University, 101100, Beijing, China.
  • Wang H; Department of Pharmacy, Liuzhou Maternity and Child Healthcare Hospital, Affiliated Maternity Hospital and Affiliated Children's Hospital of Guangxi University of Science and Technology, 545001, Liuzhou, Guangxi, China.
  • Hou M; Department of Research Ward, Beijing Friendship Hospital, Capital Medical University, 101100, Beijing, China.
  • Dong R; Department of Research Ward, Beijing Friendship Hospital, Capital Medical University, 101100, Beijing, China. Electronic address: ruihua_dong_rw@163.com.
  • Li X; Department of Pharmacy, Beijing Friendship Hospital, Capital Medical University, 100050, Beijing China. Electronic address: lxg198320022003@163.com.
J Pharm Sci ; 113(5): 1351-1358, 2024 May.
Article en En | MEDLINE | ID: mdl-38253224
ABSTRACT
Pharmacokinetic data for injectable azithromycin in children remain limited. This study aims to develop and validate a population pharmacokinetic model of azithromycin for injection in children under 6 years old and optimize its dosage regimen in this population. We prospectively enrolled patients under 6 years old who received azithromycin for injection at Beijing Friendship Hospital, Capital Medical University. Demographic information, clinical characteristics, and venous blood samples were collected in accordance with the research protocol. Azithromycin concentrations were determined using a validated UPLC-MS/MS method. The population pharmacokinetic model was structured using Phoenix NLME. The adequacy and robustness of the model was evaluated using VPC and bootstrap. We optimized azithromycin's dosing regimen for injection through Monte Carlo simulations. We included 254 plasma concentration data from 148 patients to establish the model. The clearance and volume were 1.27 L/h/kg and 45.6 L/kg, respectively. The covariates included were weight and age. VPC plots and nonparametric bootstrap showed that the final PPK model was reliable and robust. Based on Monte Carlo simulation, we derived a simple and practical dosing scheme. The results provided reference for individualized dosing in this population. The individualized dosing scheme based on Monte Carlo simulation can optimize clinical decision-making and guide personalized therapy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Azitromicina / Espectrometría de Masas en Tándem Tipo de estudio: Guideline / Prognostic_studies Límite: Child / Child, preschool / Humans Idioma: En Revista: J Pharm Sci Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Azitromicina / Espectrometría de Masas en Tándem Tipo de estudio: Guideline / Prognostic_studies Límite: Child / Child, preschool / Humans Idioma: En Revista: J Pharm Sci Año: 2024 Tipo del documento: Article
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