Literature DB >> 7977422

Extended dosage intervals for aminoglycosides.

D P Rodman1, A J Maxwell, J T McKnight.   

Abstract

The rationale for and effectiveness of extended dosage intervals for aminoglycosides are discussed. Aminoglycosides can be given once daily despite an elimination half-life of two to three hours because of the postantibiotic effect (PAE) of these agents. Aminoglycosides have a prolonged PAE against a variety of common gram-negative and gram-positive organisms. Higher serum aminoglycoside concentrations are associated with longer PAEs and increased bactericidal activity. Once-daily administration may reduce the potential for adaptive postexposure resistance by allowing less contact time between organism and drug. A major concern with aminoglycosides is the risk of nephrotoxicity and ototoxicity. The uptake of specific aminoglycosides by renal cortical cells is saturable; a longer dosage interval may decrease the risk of nephrotoxicity because higher transient serum aminoglycoside levels appear to be less nephrotoxic than lower but more persistent serum concentrations. Once-daily administration may reduce the risk of ototoxicity through a similar mechanism. An increasing number of clinical trials suggest tht once-daily administration of aminoglycosides and regimens involving shorter dosage intervals are equally effective in patients with normal renal function and gram-negative infections and that once-daily administration may reduce the frequency of toxicity or delay it. Patients with renal dysfunction or neutropenia may also benefit from once-daily administration. Most trials have been small, and in some of them other antimicrobials were given concurrently. Although more study is needed, the evidence to date suggests that once-daily administration of aminoglycosides is as effective as traditional regimens entailing shorter dosage intervals and may reduce the potential for toxicity.

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Year:  1994        PMID: 7977422

Source DB:  PubMed          Journal:  Am J Hosp Pharm        ISSN: 0002-9289


  2 in total

1.  Pharmacokinetics of aerosolized tobramycin in adult patients with cystic fibrosis.

Authors:  D J Touw; F A Jacobs; R W Brimicombe; H G Heijerman; W Bakker; D D Briemer
Journal:  Antimicrob Agents Chemother       Date:  1997-01       Impact factor: 5.191

2.  Pharmacokinetics and safety of tobramycin nebulization with the I-neb and PARI-LC Plus in children with cystic fibrosis: A randomized, crossover study.

Authors:  Annelies J van Velzen; Joris W F Uges; Harry G M Heijerman; Bert G M Arets; Marianne Nuijsink; Els C van der Wiel-Kooij; Erik M van Maarseveen; Gijsbert A van Zanten; Bas Pullens; Daan J Touw; Hettie M Janssens
Journal:  Br J Clin Pharmacol       Date:  2019-07-10       Impact factor: 4.335

  2 in total

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