Startseite Pharmacokinetics of ceftriaxone in patients undergoing continuous renal replacement therapy
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Pharmacokinetics of ceftriaxone in patients undergoing continuous renal replacement therapy

  • Koji Goto , Yuhki Sato EMAIL logo , Norihisa Yasuda , Seigo Hidaka , Yosuke Suzuki , Ryota Tanaka , Tetsuya Kaneko , Ko Nonoshita und Hiroki Itoh
Veröffentlicht/Copyright: 6. August 2016

Abstract

Background:

The duration of time for which the serum levels exceed the minimum inhibitory concentration (MIC) is an important pharmacokinetics (PK)/pharmacodynamics (PD) parameter correlating with efficacy for the antibiotic, ceftriaxone (CTRX). However, no reports exist regarding the PK or PD in patients undergoing continuous renal replacement therapy (CRRT). The purpose of this study was to examine the PK and safety of CTRX in patients undergoing CRRT in order to establish safer and more effective regimens.

Methods:

CTRX (1 g once a day) was intravenously administered four or more times to nine patients undergoing CRRT. Blood was collected after administration to measure CTRX concentrations in serum and the filtration fraction of CRRT by high-performance liquid chromatography. In addition to calculating PK parameters from serum CTRX, we (a) estimated by simulation CTRX concentrations when the dose interval was extended to once every 2 or 3 days, (b) calculated CTRX clearance via CRRT from CTRX concentrations in the filtration fraction, and (c) assessed the safety of CTRX use.

Results:

Total body clearance and the half-life of CTRX were 7.46 mL/min (mean) and 26.5 h, respectively, in patients undergoing CRRT. CTRX was found in the filtration fraction, and the estimated clearance by CRRT was about 70% of total body clearance. Simulations revealed that even when the dose interval is increased to 2 or 3 days, CTRX would retain its efficacy.

Conclusions:

Our findings suggest that, depending on the condition of patients undergoing CRRT, CTRX could be used safely against pathogens with a CTRX MIC ≤2 µg/mL, even when extending the dose interval.

Acknowledgments

We would like to thank all staff and patients who were willing to participate in this study. This study was supported by the Intensive Care Unit, Oita University Hospital. We are grateful to the ICU staff for their understanding and cooperation. We would also like to thank the biomedical equipment technicians in our hospital for providing excellent safety and technical support.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission. YS and NY designed the research study, carried out the research, and drafted the manuscript. YS designed the research study. RT, TK, and FT performed the statistical analysis. HI conceived the study, coordination and helped to draft the manuscript.

  2. Research funding: None declared.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in thestudy design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2016-2-22
Accepted: 2016-7-2
Published Online: 2016-8-6
Published in Print: 2016-11-1

©2016 Walter de Gruyter GmbH, Berlin/Boston

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