เภสัชจลนศาสตร์ประชากรของยาแวนโคมัยซินในผู้ป่วยเด็กชาวไทย

This retrospective study aimed to estimate vancomycin pharmacokinetic (PK) parameters, investigate factors influencing PK parameters. A total of 348 serum vancomycin concentrations were obtained in 212 pediatric patients, aged 1 month to 18 years, who were admitted at King Chulalongkorn Memorial Hos...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: ชนิกา ชูพันธ์
مؤلفون آخرون: ธิติมา วัฒนวิจิตรกุล
التنسيق: Theses and Dissertations
اللغة:Thai
منشور في: จุฬาลงกรณ์มหาวิทยาลัย 2018
الموضوعات:
الوصول للمادة أونلاين:https://digiverse.chula.ac.th/Info/item/dc:31428
الوسوم: إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
المؤسسة: Chulalongkorn University
اللغة: Thai
الوصف
الملخص:This retrospective study aimed to estimate vancomycin pharmacokinetic (PK) parameters, investigate factors influencing PK parameters. A total of 348 serum vancomycin concentrations were obtained in 212 pediatric patients, aged 1 month to 18 years, who were admitted at King Chulalongkorn Memorial Hospital between 2012 to 2017. In total, this study enrolled 212 pediatric patients with 348 serum vancomycin concentrations. Median of age was 3.5 years (range 1 month – 17.9 years). Population pharmacokinetic analysis was performed using NONMEM® program with first-order conditional estimation with interaction method. Vancomycin pharmacokinetics was adequately explained by one-compartment model with first-order elimination. Mean vancomycin clearance (CL) and volume of distribution (Vd) were 0.13±0.06 L/h/kg and 0.88±0.15 L/kg, respectively. Factors influencing PK parameters were weight (kg) and estimated glomerular filtration rate (eGFR; ml/min/1.73m[superscript 2]) as shown in the following equations: CL (L/h) = 1.66*(weight/14)[superscript 0.75]*(eGFR/108.9) and Vd (L) = 12.7*(weight/14). Interindividual variability of CL was 34.8% and Vd was 39.6%. The final model was validated using bootstrap and visual predictive check (VPC). The final PK estimates were close to PK parameters from 1,000-bootstrap replicates and within 95% confidence interval of bootstrap results. VPC (1,000 replicates) showed only 6% of vancomycin concentrations distributed outside 90% confidence interval. These results suggest that the model is appropriate to describe vancomycin pharmacokinetics.