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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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