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Antimicrobial Agents and Chemotherapy, September 1998, p. 2421-2424, Vol. 42, No. 9
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Pharmacokinetics of Meropenem in Critically Ill Patients with Acute Renal Failure Treated by Continuous Hemodiafiltration

W. A. Krueger,1,* T. H. Schroeder,1 M. Hutchison,2 E. Hoffmann,1 H.-J. Dieterich,1 A. Heininger,1 C. Erley,3 A. Wehrle,1 and K. Unertl1

Department of Anesthesiology1 and Department of Internal Medicine,3 Tübingen University Hospital, Tübingen, Germany, and ZENECA Pharmaceuticals,2 Mereside, Alderly Park, Macclesfield, Cheshire, United Kingdom

Received 29 December 1997/Returned for modification 6 April 1998/Accepted 22 June 1998

The pharmacokinetics of meropenem were studied in nine anuric critically ill patients treated by continuous venovenous hemodiafiltration. Peak levels after infusion of 1,000 mg over 30 min amounted to 103.2 ± 45.9 µg/ml, and trough levels at 12 h were 9.6 ± 3.8 µg/ml. A dosage of 1,000 mg of meropenem twice a day provides plasma drug levels covering intermediately susceptible microorganisms. Further reductions of the dosage might be appropriate for highly susceptible bacteria or when renal replacement therapies with lower clearances are applied.


* Corresponding author. Present address: Channing Laboratory, Brigham and Women's Hospital, Harvard Medical School, 181 Longwood Ave., Boston, MA 02115. Phone: (617) 525-2680. Fax: (617) 731-1541. E-mail: wkrueger{at}rics.bwh.harvard.edu.


Antimicrobial Agents and Chemotherapy, September 1998, p. 2421-2424, Vol. 42, No. 9
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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