Academic Journal

Single-Dose Pharmacokinetics of Meropenem during Continuous Venovenous Hemofiltration

Bibliographic Details
Title: Single-Dose Pharmacokinetics of Meropenem during Continuous Venovenous Hemofiltration
Authors: Thalhammer, Florian, Schenk, Peter, Burgmann, Heinz, El Menyawi, Ibrahim, Hollenstein, Ursula M., Rosenkranz, Alexander R., Sunder-Plassmann, Gere, Breyer, Stefan, Ratheiser, Klaus
Source: Antimicrobial Agents and Chemotherapy ; volume 42, issue 9, page 2417-2420 ; ISSN 0066-4804 1098-6596
Publisher Information: American Society for Microbiology
Publication Year: 1998
Description: The pharmacokinetic properties of meropenem were investigated in nine critically ill patients treated by continuous venovenous hemofiltration (CVVH). All patients received one dose of 1 g of meropenem intravenously. High-flux polysulfone membranes were used as dialyzers. Meropenem levels were measured in plasma and ultrafiltrate by high-performance liquid chromatography. The total body clearance and elimination half-life were 143.7 ± 18.6 ml/min and 2.46 ± 0.41 h, respectively. The post- to prehemofiltration ratio of meropenem was 0.24 ± 0.06. Peak plasma drug concentrations measured 60 min postinfusion were 28.1 ± 2.7 μg/ml, and trough levels after 6 h of CVVH were 6.6 ± 1.5 μg/ml. The calculated total daily meropenem requirement in these patients with acute renal failure and undergoing CVVH was 2,482 ± 321 mg. Based on these data, we conclude that patients with severe infections who are undergoing CVVH can be treated effectively with 1 g of meropenem every 8 h.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1128/aac.42.9.2417
DOI: 10.1128/AAC.42.9.2417
Availability: https://doi.org/10.1128/aac.42.9.2417
https://journals.asm.org/doi/pdf/10.1128/AAC.42.9.2417
Rights: https://journals.asm.org/non-commercial-tdm-license
Accession Number: edsbas.E15B8560
Database: BASE
Description
DOI:10.1128/aac.42.9.2417