Literature DB >> 8226432

Bactericidal effect of gentamicin peak concentration provides a rationale for administration of bolus doses.

A J McLean1, L L IoannidesDemos, S C Li, E B Bastone, W J Spicer.   

Abstract

A study was made of the influence of peak gentamicin concentration (Cmax) independent of the area under the antibiotic concentration-time curve (AUC) on the bactericidal effect of gentamicin against Escherichia coli NCTC 10418. Bacteria in the lag phase were exposed to in-vitro gentamicin concentration-time profiles which modelled complete profiles determined in vivo in patients after an intravenous bolus (1 min) or infusion (30 min) regimen. An additional in-vitro profile reflected antibiotic removal 30 min after bolus dosing. Bacterial viable cell counts and gentamicin concentrations were measured before and during antibiotic exposure. Both Cmax and AUC were shown to be factors determining antibacterial activity; however Cmax independently represented some 35% of total exposure effect. These findings indicate grounds for preferring bolus intravenous gentamicin dosing with appropriate attention to potential toxicity.

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Year:  1993        PMID: 8226432     DOI: 10.1093/jac/32.2.301

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  6 in total

1.  Relationships between antimicrobial effect and area under the concentration-time curve as a basis for comparison of modes of antibiotic administration: meropenem bolus injections versus continuous infusions.

Authors:  A A Firsov; H Mattie
Journal:  Antimicrob Agents Chemother       Date:  1997-02       Impact factor: 5.191

2.  Initial concentration-time profile of gentamicin determines efficacy against Enterobacter cloacae ATCC 13047.

Authors:  C R Rayner; L L Ioannides-Demos; J A Brien; L L Liolios; W J Spicer
Journal:  Antimicrob Agents Chemother       Date:  1998-06       Impact factor: 5.191

3.  Changes in MIC alter responses of Pseudomonas aeruginosa to tobramycin exposure.

Authors:  L L Ioannides-Demos; L Liolios; P Wood; W J Spicer; A J McLean
Journal:  Antimicrob Agents Chemother       Date:  1998-06       Impact factor: 5.191

4.  Optimal aminoglycoside therapy following the sepsis: how much is too much?

Authors:  Laleh Mahmoudi; Ramin Niknam; Sarah Mousavi; Arezoo Ahmadi; Hooshyar Honarmand; Shadi Ziaie; Mojtaba Mojtahedzadeh
Journal:  Iran J Pharm Res       Date:  2013       Impact factor: 1.696

5.  Intraosseous and intravenous administration of antibiotics yields comparable plasma concentrations during experimental septic shock.

Authors:  G Strandberg; A Larsson; M Lipcsey; J Michalek; M Eriksson
Journal:  Acta Anaesthesiol Scand       Date:  2015-01-05       Impact factor: 2.105

6.  Elution of gentamicin and vancomycin from polymethylmethacrylate beads and hip spacers in vivo.

Authors:  Konstantinos Anagnostakos; Philippe Wilmes; Eduard Schmitt; Jens Kelm
Journal:  Acta Orthop       Date:  2009-04       Impact factor: 3.717

  6 in total

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