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Population pharmacokinetics and dosing optimization of azlocillin in neonates with early-onset sepsis: a real-world study.
Wu, Yue-E; Wang, Tao; Yang, Hua-Liang; Tang, Bo-Hao; Kong, Li; Li, Xin; Gao, Qi; Li, Xue; Yao, Bu-Fan; Shi, Hai-Yan; Huang, Xin; Wang, Wen-Qi; Jacqz-Aigrain, Evelyne; Allegaert, Karel; van den Anker, John; Tian, Xiu-Ying; Zhao, Wei.
Afiliación
  • Wu YE; Department of Clinical Pharmacy, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan 250012, China.
  • Wang T; Department of Pharmacy, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin 300100, China.
  • Yang HL; Department of Pharmacy, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin 300100, China.
  • Tang BH; Department of Clinical Pharmacy, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan 250012, China.
  • Kong L; Department of Neonatology, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin 300100, China.
  • Li X; Department of Neonatology, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin 300100, China.
  • Gao Q; Department of Neonatology, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin 300100, China.
  • Li X; Tianjin Key Laboratory of Human Development and Reproductive Regulation, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin 300100, China.
  • Yao BF; Department of Clinical Pharmacy, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan 250012, China.
  • Shi HY; Department of Clinical Pharmacy, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan 250012, China.
  • Huang X; Department of Pharmacy, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, China.
  • Wang WQ; Department of Pharmacy, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, China.
  • Jacqz-Aigrain E; Clinical Research Centre, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, China.
  • Allegaert K; Department of Paediatric Pharmacology and Pharmacogenetics, Hôpital Robert Debré, APHP, Paris, France.
  • van den Anker J; Clinical Investigation Centre CIC1426, Hôpital Robert Debré, Paris, France.
  • Tian XY; University of Paris, Paris, France.
  • Zhao W; Department of Development and Regeneration and Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
J Antimicrob Chemother ; 76(3): 699-709, 2021 02 11.
Article en En | MEDLINE | ID: mdl-33188385
OBJECTIVES: Nowadays, real-world data can be used to improve currently available dosing guidelines and to support regulatory approval of drugs for use in neonates by overcoming practical and ethical hurdles. This proof-of-concept study aimed to assess the population pharmacokinetics of azlocillin in neonates using real-world data, to make subsequent dose recommendations and to test these in neonates with early-onset sepsis (EOS). METHODS: This prospective, open-label, investigator-initiated study of azlocillin in neonates with EOS was conducted using an adaptive two-step design. First, a maturational pharmacokinetic-pharmacodynamic model of azlocillin was developed, using an empirical dosing regimen combined with opportunistic samples resulting from waste material. Second, a Phase II clinical trial (ClinicalTrials.gov: NCT03932123) of this newly developed model-based dosing regimen of azlocillin was conducted to assure optimized target attainment [free drug concentration above MIC during 70% of the dosing interval ('70% fT>MIC')] and to investigate the tolerance and safety in neonates. RESULTS: A one-compartment model with first-order elimination, using 167 azlocillin concentrations from 95 neonates (31.7-41.6 weeks postmenstrual age), incorporating current weight and renal maturation, fitted the data best. For the second step, 45 neonates (30.3-41.3 weeks postmenstrual age) were subsequently included to investigate target attainment, tolerance and safety of the pharmacokinetic-pharmacodynamic model-based dose regimen (100 mg/kg q8h). Forty-three (95.6%) neonates reached their pharmacokinetic target and only two neonates experienced adverse events (feeding intolerance and abnormal liver function), possibly related to azlocillin. CONCLUSIONS: Target attainment, tolerance and safety of azlocillin was shown in neonates with EOS using a pharmacokinetic-pharmacodynamic model developed with real-world data.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Azlocilina / Sepsis Tipo de estudio: Guideline / Observational_studies Límite: Humans / Newborn Idioma: En Revista: J Antimicrob Chemother Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Azlocilina / Sepsis Tipo de estudio: Guideline / Observational_studies Límite: Humans / Newborn Idioma: En Revista: J Antimicrob Chemother Año: 2021 Tipo del documento: Article País de afiliación: China