Optimal Dosage Regimen of Meropenem for Pediatric Patients Based on Pharmacokinetic/Pharmacodynamic Considerations

被引:31
|
作者
Ohata, Yuka [2 ]
Tomita, Yoshiko [2 ]
Nakayama, Mitsunobu [2 ]
Kozuki, Tsuneo [2 ,3 ]
Sunakawa, Keisuke [4 ,5 ]
Tanigawara, Yusuke [1 ]
机构
[1] Keio Univ, Sch Med, Dept Clin Pharmacokinet & Pharmacodynam, Tokyo 1608582, Japan
[2] Dainippon Sumitomo Pharma Co Ltd, Drug Dev Div, Osaka, Japan
[3] Dainippon Sumitomo Pharma Co Ltd, Sales & Mkt Div, Osaka, Japan
[4] Kitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
[5] Kitasato Univ, Grad Sch Infect Control Sci, Tokyo, Japan
关键词
meropenem; %T>MIC; PK/PD; pediatrics; Monte Carlo simulation; FEBRILE NEUTROPENIC PATIENTS; MONTE-CARLO-SIMULATION; POPULATION PHARMACOKINETICS; TARGET ATTAINMENT; PHARMACODYNAMICS;
D O I
10.2133/dmpk.DMPK-11-RG-027
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A population pharmacokinetic (PK) model for meropenem in Japanese pediatric patients with various infectious diseases was developed based on 116 plasma concentrations from 50 pediatric patients. The population PK parameters developed in this analysis are useful for calculation of the percent time above minimum inhibitory concentration (%T>MIC) and for optimal dosing of meropenem in pediatric patients. After dosing at 20 mg/kg t.i.d. by 0.5-h infusion (approved standard dose for pediatric patients in Japan), the target value of 50%T>MIC was achieved, indicating that 20 mg/kg t.i.d. by 0.5-h infusion is effective for susceptible bacteria. In contrast, for bacteria with higher MICs such as Pseudomonas aeruginosa (MIC >= 2 mu g/mL), the probability of target attainment of 50%T>MIC was 60.7% at a dose of 40 mg/kg t.i.d. by 0.5-h infusion (highest dose approved for pediatric patients in Japan). The simulations described in this article indicated that 40 mg/kg t.i.d. with a longer infusion duration (e.g., 4h) is more effective against bacteria with a MIC higher than 2 mu g/mL. The predicted probability of target attainment for 50%T>MIC (97.0%) was well correlated not only to the microbiological efficacy rate (97.0%) but also to the clinical efficacy rate (95.9%) in the present phase 3 study.
引用
收藏
页码:523 / 531
页数:9
相关论文
共 50 条
  • [1] Pancreatic Penetration of Meropenem and Dosage Considerations Based on Site-Specific Pharmacokinetic-Pharmacodynamic Analysis
    Kondo, Naru
    Ikawa, Kazuro
    Murakami, Yoshiaki
    Uemura, Kenichiro
    Sudo, Takeshi
    Hashimoto, Yasushi
    Ohge, Hiroki
    Morikawa, Norifumi
    Sueda, Taijiro
    [J]. GASTROENTEROLOGY, 2014, 146 (05) : S1098 - S1098
  • [2] Evaluation of pharmacokinetic pharmacodynamic target attainment of meropenem in pediatric patients
    Alsultan, Abdullah
    Aldawsari, Maram R.
    Alturaiq, Nujood Khaled
    Syed, Saeed Ali
    Alsubai, Abdulaziz
    Kurdee, Zeyad
    Alsubaie, Sarah
    Alqahtani, Saeed
    Abouelkheir, Manal
    [J]. PEDIATRICS AND NEONATOLOGY, 2024, 65 (04): : 386 - 390
  • [3] DOSAGE REGIMEN DESIGN - PHARMACODYNAMIC CONSIDERATIONS
    WILLIAMS, RL
    [J]. JOURNAL OF CLINICAL PHARMACOLOGY, 1992, 32 (07): : 597 - 602
  • [4] Prostatic penetration of meropenem in humans, and dosage considerations for prostatitis based on a site-specific pharmacokinetic/pharmacodynamic evaluation
    Nishikawa, Genya
    Ikawa, Kazuro
    Nakamura, Kogenta
    Yamada, Yoshiaki
    Zennami, Kenji
    Mitsui, Kenji
    Narushima, Masahiro
    Ikeda, Kayo
    Morikawa, Norifumi
    Sumitomo, Makoto
    [J]. INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2013, 41 (03) : 267 - 271
  • [5] Clarithromycin: Pharmacokinetic and pharmacodynamic interrelationships and dosage regimen
    Periti, P
    Mazzei, T
    [J]. JOURNAL OF CHEMOTHERAPY, 1999, 11 (01) : 11 - 27
  • [6] Prostatic Penetration of Meropenem in Humans, and Dosage Considerations for Prostatitis Based on Site-Specific Pharmacokinetic-Pharmacodynamic Evaluation
    Nishikawa, G.
    Ikawa, K.
    Nakamura, K.
    Yamada, Y.
    Zennami, K.
    Morikawa, N.
    Sumitomo, M.
    [J]. UROLOGY, 2012, 80 (03) : S154 - S154
  • [7] Individualized dosage regimen of immunosuppressive drugs based on pharmacokinetic and pharmacodynamic analysis
    Fukudo, Masahide
    [J]. YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 2007, 127 (07): : 1081 - 1089
  • [8] Pharmacokinetic Modeling of Bepotastine for Determination of Optimal Dosage Regimen in Pediatric Patients with Allergic Rhinitis or Urticaria
    Yoon, Sukyong
    Jin, Byung Hak
    Kim, Choon Ok
    Park, Kyungsoo
    Park, Min Soo
    Chae, Dongwoo
    [J]. PHARMACEUTICS, 2024, 16 (03)
  • [9] Optimal treatment schedule of meropenem for adult patients with febrile neutropenia based on pharmacokinetic-pharmacodynamic analysis
    Ohata, Yuka
    Tomita, Yoshiko
    Nakayama, Mitsunobu
    Tamura, Kazuo
    Tanigawara, Yusuke
    [J]. JOURNAL OF INFECTION AND CHEMOTHERAPY, 2011, 17 (06) : 831 - 841
  • [10] The pharmacokinetic-pharmacodynamic approach to a rational dosage regimen for antibiotics
    Toutain, PL
    Del Castillo, JRE
    Bousquet-Mélou, A
    [J]. RESEARCH IN VETERINARY SCIENCE, 2002, 73 (02) : 105 - 114