Literature DB >> 2141778

Efficacy of teicoplanin in two dosage regimens for experimental endocarditis caused by a beta-lactamase-producing strain of Enterococcus faecalis with high-level resistance to gentamicin.

J D Yao1, C Thauvin-Eliopoulos, G M Eliopoulos, R C Moellering.   

Abstract

Optimal therapy for the treatment of infections caused by strains of enterococci demonstrating high-level resistance to gentamicin and other aminoglycosides has not been established. The present study examined the efficacy of teicoplanin, a glycopeptide antibiotic active against gram-positive bacterial infections in various animal models, in the treatment of experimental endocarditis due to a beta-lactamase-producing strain of Enterococcus faecalis with high-level resistance to gentamicin. Vancomycin was used as a comparative antibiotic. In the first set of experiments, both antimicrobial agents were administered by continuous intravenous infusion for 5 days at dosages which yielded comparable mean levels in serum (plus or minus the standard deviation) of 14.6 +/- 4.3 micrograms/ml for teicoplanin and 14.3 +/- 2.2 micrograms/ml for vancomycin. These regimens proved similarly effective in sterilizing cardiac vegetations (38 versus 50% of treated animals, respectively; P greater than 0.05). Mean (plus or minus the standard deviation) residual bacterial titers within vegetations were reduced to 3.2 +/- 1.2 log10 CFU/g and 3.4 +/- 1.7 log10 CFU/g, respectively. In separate experiments, the potential of teicoplanin to cure endocarditis was assessed, using two dosage regimens: (i) 30 mg/kg per day (mean level in serum, 13 micrograms/ml) for 10 days or (ii) 150 mg/kg per day (mean level in serum, 84 micrograms/ml) for 5 days. Surviving animals were sacrificed 10 days after the discontinuation of therapy. Both teicoplanin regimens were more effective than the comparative vancomycin (150 mg/kg per day) regimen: 92 versus 43% cured (P =0.025) in the standard-dose group, and 82 versus 37% cured (P = 0.015) in the high-dose group. Results in this rat model of enterococcal endocarditis show that teicoplanin may prove useful in the treatment of serious infections due to high level-gentamicin-resistant enterococci in humans.

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Year:  1990        PMID: 2141778      PMCID: PMC171700          DOI: 10.1128/AAC.34.5.827

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  29 in total

1.  High-level, plasmid-borne resistance to gentamicin in Streptococcus faecalis subsp. zymogenes.

Authors:  T Horodniceanu; L Bougueleret; N El-Solh; G Bieth; F Delbos
Journal:  Antimicrob Agents Chemother       Date:  1979-11       Impact factor: 5.191

2.  In vitro activity of SK&F 104662, a new glycopeptide antibiotic.

Authors:  J D Yao; G M Eliopoulos; R C Moellering
Journal:  Antimicrob Agents Chemother       Date:  1989-06       Impact factor: 5.191

3.  Susceptibility and bactericidal activity studies of four beta-lactamase-producing enterococci.

Authors:  J E Patterson; M J Zervos
Journal:  Antimicrob Agents Chemother       Date:  1989-02       Impact factor: 5.191

4.  Serious infection due to beta-lactamase-producing Streptococcus faecalis with high-level resistance to gentamicin.

Authors:  J E Patterson; S M Colodny; M J Zervos
Journal:  J Infect Dis       Date:  1988-11       Impact factor: 5.226

5.  A multicentre open clinical trial of teicoplanin in infections caused by gram-positive bacteria.

Authors:  P Lewis; J J Garaud; F Parenti
Journal:  J Antimicrob Chemother       Date:  1988-01       Impact factor: 5.790

6.  Characterization and comparison of two penicillinase-producing strains of Streptococcus (Enterococcus) faecalis.

Authors:  J E Patterson; B L Masecar; M J Zervos
Journal:  Antimicrob Agents Chemother       Date:  1988-01       Impact factor: 5.191

7.  Comparative synergistic activity of nafcillin, oxacillin, and methicillin in combination with gentamicin against.

Authors:  R H Glew; R S Millering; C Wennersten
Journal:  Antimicrob Agents Chemother       Date:  1975-06       Impact factor: 5.191

8.  Treatment of experimental endocarditis caused by a beta-lactamase-producing strain of Enterococcus faecalis with high-level resistance to gentamicin.

Authors:  R G Hindes; S H Willey; G M Eliopoulos; L B Rice; C T Eliopoulos; B E Murray; R C Moellering
Journal:  Antimicrob Agents Chemother       Date:  1989-07       Impact factor: 5.191

9.  Rat model of experimental endocarditis.

Authors:  J Santoro; M E Levison
Journal:  Infect Immun       Date:  1978-03       Impact factor: 3.441

10.  Evaluation of teicoplanin for treatment of endocarditis caused by gram-positive cocci in 20 patients.

Authors:  C Leport; C Perronne; P Massip; P Canton; P Leclercq; E Bernard; P Lutun; J J Garaud; J L Vilde
Journal:  Antimicrob Agents Chemother       Date:  1989-06       Impact factor: 5.191

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  10 in total

1.  In vivo activity of evernimicin (SCH 27899) against methicillin-resistant Staphylococcus aureus in experimental infective endocarditis.

Authors:  H W Boucher; C Thauvin-Eliopoulos; D Loebenberg; G M Eliopoulos
Journal:  Antimicrob Agents Chemother       Date:  2001-01       Impact factor: 5.191

2.  In vivo activities of evernimicin (SCH 27899) against vancomycin-susceptible and vancomycin-resistant enterococci in experimental endocarditis.

Authors:  M Souli; C Thauvin-Eliopoulos; G M Eliopoulos
Journal:  Antimicrob Agents Chemother       Date:  2000-10       Impact factor: 5.191

Review 3.  Current perspectives on glycopeptide resistance.

Authors:  N Woodford; A P Johnson; D Morrison; D C Speller
Journal:  Clin Microbiol Rev       Date:  1995-10       Impact factor: 26.132

4.  Increasing problems in the therapy of enterococcal infections.

Authors:  G M Eliopoulos
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1993-06       Impact factor: 3.267

5.  Efficacy of daptomycin in experimental endocarditis due to methicillin-resistant Staphylococcus aureus.

Authors:  George Sakoulas; George M Eliopoulos; Jeff Alder; Claudie Thauvin Eliopoulos
Journal:  Antimicrob Agents Chemother       Date:  2003-05       Impact factor: 5.191

6.  Antimicrobial susceptibility and molecular epidemiology of beta-lactamase-producing, aminoglycoside-resistant isolates of Enterococcus faecalis.

Authors:  S M Markowitz; V D Wells; D S Williams; C G Stuart; P E Coudron; E S Wong
Journal:  Antimicrob Agents Chemother       Date:  1991-06       Impact factor: 5.191

7.  Comparison of ampicillin-sulbactam with vancomycin for treatment of experimental endocarditis due to a beta-lactamase-producing, highly gentamicin-resistant isolate of Enterococcus faecalis.

Authors:  S R Lavoie; E S Wong; P E Coudron; D S Williams; S M Markowitz
Journal:  Antimicrob Agents Chemother       Date:  1993-07       Impact factor: 5.191

8.  Double-blind comparison of teicoplanin versus vancomycin in febrile neutropenic patients receiving concomitant tobramycin and piperacillin: effect on cyclosporin A-associated nephrotoxicity.

Authors:  A Kureishi; P J Jewesson; M Rubinger; C D Cole; D E Reece; G L Phillips; J A Smith; A W Chow
Journal:  Antimicrob Agents Chemother       Date:  1991-11       Impact factor: 5.191

Review 9.  Teicoplanin. A reappraisal of its antimicrobial activity, pharmacokinetic properties and therapeutic efficacy.

Authors:  R N Brogden; D H Peters
Journal:  Drugs       Date:  1994-05       Impact factor: 9.546

10.  Influence of low-level resistance to vancomycin on efficacy of teicoplanin and vancomycin for treatment of experimental endocarditis due to Enterococcus faecium.

Authors:  B Fantin; R Leclercq; M Arthur; J Duval; C Carbon
Journal:  Antimicrob Agents Chemother       Date:  1991-08       Impact factor: 5.191

  10 in total

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