Publications by authors named "Yinyi Wei"

What Is Known And Objectives: Voriconazole has a complex pharmacokinetic profile and exhibits different pharmacokinetic characteristics in adults and children. Nevertheless, few studies have been conducted on the population pharmacokinetics (PPK) of voriconazole in children with haematological malignancies. This study aims to build a PPK model and propose a suitable voriconazole treatment scheme for children with haematological malignancies.

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Article Synopsis
  • This study aimed to explore how different factors affect the way mycophenolate mofetil (MMF) is processed in children's bodies after liver transplantation, and to develop a model that can help doctors adjust dosages accordingly.
  • Researchers performed a prospective study in one center, collecting blood samples from pediatric patients given MMF for at least four days post-transplant to analyze mycophenolic acid levels using advanced liquid chromatography.
  • A two-compartment pharmacokinetics model was created using data from 20 patients, revealing significant variability in drug clearance rates and showing that body weight and dosage significantly influenced how the drug was cleared and distributed in the body.
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The high variability and unpredictability of the plasma concentration of voriconazole (VRC) pose a major challenge for clinical administration. The aim of this study was to develop a population pharmacokinetics (PPK) model of VRC and identify the factors influencing VRC PPK in patients with talaromycosis. Medical records and VRC medication history of patients with talaromycosis who were treated with VRC as initial therapy were collected.

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Purpose: To analyze factors influencing tacrolimus (TAC) trough concentration (C) in β-thalassemia major (β-TM) pediatric patients after allogeneic hematopoietic stem cell transplantation (Allo-HSCT) and to investigate the effects of genotype polymorphism and drug-drug interactions on TAC trough concentration in children with β-TM. Furthermore, to analyze the correlation between TAC C and efficacy and adverse reactions.

Patients And Methods: Prospectively collection of demographic information and details of combined treatment of patients with β-TM receiving HSCT, and genotypes of CYP3A4, CYP3A5, and ABCB1 (rs1045642, rs1128503, rs2032582) were obtained for each patient.

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What Is Known And Objectives: Various population pharmacokinetic (PopPK) models for vancomycin in children and adolescents have been constructed to optimize the therapeutic regimen of vancomycin. However, little is known about their predictive performance when extrapolated to different clinical centres. Therefore, the aim of this study was to externally validate the predictability of vancomycin PopPK model when extrapolated to different clinical centres and verify its applicability in an independent data set.

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Background: Hematopoietic stem cell transplantation (HSCT) is an effective treatment for hematological disorders. Tacrolimus is widely used after HSCT, but it has highly interindividual variable pharmacokinetics. Population pharmacokinetics (PPK) researches of tacrolimus in children with β-thalassemia major (β-TM) undergoing HSCT are insufficient.

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