• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Optimization of Antibiotic Chemotherapy Based on Pharmacokinetics and Phannacodynamics of Antibiotics in Patients with Severe Infections

Research Project

Project/Area Number 13672399
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field 応用薬理学・医療系薬学
Research InstitutionKeio University

Principal Investigator

MORITA Kunihiko  School of Medicine, Hospital Pharmacy, Associate Professor, 医学部, 助教授 (80327717)

Co-Investigator(Kenkyū-buntansha) KOBAYASHI Yoshio  School of Medicine, Clinical Laboratory , Assistant Professor, 医学部, 講師 (80118950)
TANIGAWARA Yusuke  School of Medicine, Hospital Pharmacy, Professor, 医学部, 教授 (30179832)
Project Period (FY) 2001 – 2002
Project Status Completed (Fiscal Year 2002)
Budget Amount *help
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 2002: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 2001: ¥2,700,000 (Direct Cost: ¥2,700,000)
Keywordscarbapenem / aminoglycoside / glycopeptide / therapeutic drug monitoring / peak serum concentration / trough serum concentration / CRP / clinical efficacy / メロペネム / アミカシン / トブラマイシン / 血液透析 / 薬物血中濃度モニタリング / 重症感染症 / アミノグリコシド系抗生物質 / 薬物体内動態 / 感受性試験 / MIC
Research Abstract

To optimization of antibiotic chemotherapy, we investigated the relationship between clinical efficacies and pharmacokinetics of carbapenem, aminoglycosides, and glycopeptides in patients with sivere infections such as P. aeruginosa and/or S. aureus. Firstly, we compared retrospectively the serum levels of meropenem (MEPM), a carbapenem antibiotic, and its efficacy observed under the four-times daily (injection of 500 mg at 6-h interval) regimen with those observed under twice-daily regimen in 22 patients (mean age±SE, 62.4±3.7) with severe infections. The clinical efficacy of MEPM was evaluated by the degrees of decreased CRP level, as a marker of inflammatory, during the treatment periods. The mean trough level of MEPM in the effective patient group (7.5mcg/mL) was higher than that of the non-effective patient group (2.2 mcg/mL). The mean trough level of MEPM in four-times daily regimen group (6.0 mcg/mL) was higher than that in two-times daily regimen group (2.0mcg/mL). No relationship between the mean peak levels in these regimens was found. These results indicated that the injection of 500 mg of MEPM at 6-h interval was more effective than the injection of 500-1000 mg at 12-h or more longer interval. We investigated retrospectively the relationship between clinical efficacies and serum levels of aminoglycosides such as arbekacin (ABK), amikacin (AMK) and tobramycin (TOB) in the patients with sivere infections. As for efficacy, serum peak levels (Cmax) was associated to the clinical cure rate. Monitoring of trough is important to prevent the occurrence of nephrotoxicity, whereas Cmax can be associated with efficacy. These findings will be useful for optimal use of this aminoglycoside for the treatment of MRSA-infected patients

Report

(3 results)
  • 2002 Annual Research Report   Final Research Report Summary
  • 2001 Annual Research Report
  • Research Products

    (17 results)

All Other

All Publications (17 results)

  • [Publications] H.Konishi, et al.: "Depression of phenytoin metabolic capacity by 5-fluorouracil and doxifluridine in rats"J. Pharm. Pharmacol.. 55. 143-149 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] H.Konishi, et al.: "Probable metabolic interaction of doxifluridine with phenytoin"Ann. Pharmacother.. 36. 831-834 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] T.Kakimoto, et al.: "Thalidomaide for the Treatment of Refractory Multiple Myeloma : Association of Plasma Concentrations o Thalidomaide and Angiogenic Growthfactors with Clinical Outcome"Jpn. J. Canser. Res.. 93. 1029-1036 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] H.Konishi, et al.: "Moricizine, an antiarrhythmic agent, as a potent inhibitor of hepatic microsomal CYP1A"Pharmacology. 66. 190-198 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] K.Morita, et al.: "Changes in serum albumin level and unbound fraction of valproate in patients with infections"Jpn. J. TDM. 18. 61-69 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] H,Konishi et al.: "Depression of phenytoin metabolic capacity by 5-fluorouracil and doxifluridine in rats."J. Pharm. Pharmacol.. 55. 143-149 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] H,Konlshi et al.: "Probable metabolic interaction of doxifluridine with phenytoin"Ann, Pharmacother. 36. 834-836 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] T,Kakimoto et al.: "Thalidomaide for the treatment of refractory multiple myeloma:Association of plasma concentrations o thalidomaide and angiogenic growthfactors with clinical outcome."Jpn. J. Canser. Res.. 93. 1029-1036 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] H,Konishi et al.: "Moricizine, an antiarrhythmic agent, as a potent inhibitor of heoatic microsomal CYP1A,"Pharmacology. 66. 190-198 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] K,Morita et al.: "Changes in serum albumin level and unbound fraction of valproate in patients with infections."Jpn. J. TDM. 18(1). 61-69 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] H.Konishi, et al.: "Depression of phenytoin metabolic capacity by 5-fluorouracil and doxifluridine in rats"J. Pharm. Pharmacol.. 55. 143-149 (2003)

    • Related Report
      2002 Annual Research Report
  • [Publications] H.Konishi, et al.: "Probable metabolic interaction of doxifluridine with phenytoin"Ann. Pharmacother.. 36. 831-834 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] T.Kakimoto, et al.: "Thalidomaide for the treatment of refractory multiple myeloma : Association of plasma concentrations o thalidomaide and angiogenic growth factors with clinical outcome"Jpn. J. Canser. Res.. 93. 1029-1036 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] H.Konishi, et al.: "Moricizine, an antiarrhythmic agent, as a potent inhibitor of hepatic microsomal CYPlA"Pharmacology. 66. 190-198 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] K.Morita, et al.: "Changes in serum albumin level and unbound fraction of valproate in patients with infections"Jpn. J. TDM. 18. 61-69 (2001)

    • Related Report
      2002 Annual Research Report
  • [Publications] K.Morita, et al.: "Marked changes in serum albumin level and unbound fraction of valproate in patients with infections"Jpn.J.TDM,. 18. 61-69 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] 森田邦彦 ほか: "MRSA感染症治療に用いられる抗生物質のTDM:そのピーク値とトラフ値の意義"化学療法の領域. 17. 241-247 (2001)

    • Related Report
      2001 Annual Research Report

URL: 

Published: 2001-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi