Skip to main navigation Skip to search Skip to main content

Clinical pharmacokinetics of aztreonam in cancer patients

P. G. Jones, G. P. Bodey, E. A. Swabb, D. H. Ho, V. Fainstein, J. Pasternak

Research output: Contribution to journalArticlepeer-review

Abstract

The pharmacokinetics of aztreonam were studied in 25 adult patients with hematological malignancies. Two groups of 9 patients each received aztreonam (1 or 2 g every 8 h) prophylactically, and 7 infected patients received a therapeutic regimen of aztreonam (1.5 g every 4 h). The mean peak serum concentration after a 1-g dose of aztreonam (given over 0.5 h on day 1) was 75.5 μg/ml; after a 2-g dose it was 177.2 μg/ml. The mean peak serum concentration after a 1.5-g dose of aztreonam (given over 2 h on day 1) was 68.5 μg/ml. The serum half-life ranged between 1.7 and 2.0 h for all regimens studied. The urinary concentration of the metabolite of aztreonam, SQ 26,992, increased during 1 week of administration of the drug; however, serum levels of the metabolite were barely detectable.

Original languageEnglish (US)
Pages (from-to)455-461
Number of pages7
JournalAntimicrobial Agents and Chemotherapy
Volume26
Issue number4
DOIs
StatePublished - 1984

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)
  • Infectious Diseases

Divisions

  • Infectious Disease

Fingerprint

Dive into the research topics of 'Clinical pharmacokinetics of aztreonam in cancer patients'. Together they form a unique fingerprint.

Cite this