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The exploration of population pharmacokinetic model for meropenem in augmented renal clearance and investigation of optimum setting of dose.
Tamatsukuri, Tatsuro; Ohbayashi, Masayuki; Kohyama, Noriko; Kobayashi, Yasuna; Yamamoto, Toshinori; Fukuda, Kenichiro; Nakamura, Shunsuke; Miyake, Yasufumi; Dohi, Kenji; Kogo, Mari.
  • Tamatsukuri T; Division of Pharmacotherapeutics, Department of Clinical Pharmacy, Showa University School of Pharmacy, Tokyo, Japan. Electronic address: t.tamatsukuri@gmail.com.
  • Ohbayashi M; Division of Pharmacotherapeutics, Department of Clinical Pharmacy, Showa University School of Pharmacy, Tokyo, Japan.
  • Kohyama N; Division of Pharmacotherapeutics, Department of Clinical Pharmacy, Showa University School of Pharmacy, Tokyo, Japan.
  • Kobayashi Y; Department of Pharmacology and Therapeutics, Faculty of Pharmaceutical Sciences, Niigata University of Pharmacy and Applied Life Sciences, Niigata, Japan.
  • Yamamoto T; Showa University Medical Foundation, Tokyo, Japan.
  • Fukuda K; Department of Emergency, Disaster and Critical Care Medicine, Showa University, Tokyo, Japan.
  • Nakamura S; Department of Emergency Medicine, Wakayama Rosai Hospital, Wakayama, Japan.
  • Miyake Y; Department of Emergency Medicine, Teikyo University School of Medicine, Tokyo, Japan.
  • Dohi K; Department of Emergency, Disaster and Critical Care Medicine, Showa University, Tokyo, Japan.
  • Kogo M; Division of Pharmacotherapeutics, Department of Clinical Pharmacy, Showa University School of Pharmacy, Tokyo, Japan.
J Infect Chemother ; 24(10): 834-840, 2018 Oct.
Article en En | MEDLINE | ID: mdl-30087007
ABSTRACT
In recent years, augmented renal clearance (ARC), in which renal function is excessively enhanced, has been reported, and its influence on ß-lactam antibiotics has been investigated. In this study, we aimed to determine the optimum population pharmacokinetic model of meropenem in patients with sepsis with ARC, and evaluated dosing regimens based on renal function. Seventeen subjects (6 with ARC and 11 without) were enrolled in this study. Predicted meropenem concentrations were evaluated for bias and precision using the Bland-Altman method. To examine the dosing regimen, Monte Carlo simulation was performed to calculate the cumulative fraction of response (CFR). In patients with ARC, the bias (average of the predicted value and measured value residuals) of models constructed by Crandon et al. (2011), Roberts et al. (2009), and Jaruratanasirikul et al. (2015) were 5.96 µg/mL, 10.91 µg/mL, and 4.41 µg/mL, respectively. Following 2 g meropenem every 8 h (180 min infusion), CFR ≥ 90%, a criterion of success for empirical therapy, was achieved, even with creatinine clearance of 130-250 mL/min. For patients with sepsis and ARC, the model of Jaruratanasirikul et al. showed the highest degree of accuracy and precision and confirmed the efficacy of the meropenem dosing regimen in this patient population.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sepsis / Meropenem / Riñón / Antibacterianos Tipo de estudio: Health_economic_evaluation / Prognostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sepsis / Meropenem / Riñón / Antibacterianos Tipo de estudio: Health_economic_evaluation / Prognostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2018 Tipo del documento: Article