Literature DB >> 8787887

Ampicillin-sulbactam is effective in prevention and therapy of experimental endocarditis caused by beta-lactamase-producing coagulase-negative staphylococci.

M C Ramos1, M Ing, E Kim, M D Witt, A S Bayer.   

Abstract

Optimal strategies for the prophylaxis and therapy of endocarditis caused by oxacillin-resistant, coagulase-negative staphylococci in patients with native or prosthetic valvular heart disease are not well defined. We compared the in vivo efficacies of ampicillin-sulbactam-based regimens with those of vancomycin-based oxacillin-resistant, beta-lactamase-producing coagulase-negative staphylococcal isolate (Staphylococcus haemolyticus SE220). Ampicillin-sulbactam (100 and 20 mg/kg of body weight, respectively, given intramuscularly in a two-dose regimen) was equivalent to vancomycin (30 mg/kg given intravenously in a two-dose regimen) in its prophylactic efficacy against the coagulase-negative staphylococcal strain (93 and 80%, respectively). The combination of ampicillin-sulbactam plus either rifampin or vancomycin did not enhance the prophylactic efficacy compared with that of ampicillin-sulbactam or vancomycin alone. In the therapy of established aortic valve endocarditis in rabbits caused by this same coagulase-negative staphylococcal strain, animals received 7-day ampicillin-sulbactam-based or vancomycin-based regimens with or without rifampin. All treatment regimens were effective at lowering intravegetation coagulase-negative staphylococcal densities and rendering vegetations culture negative compared with the coagulase-negative staphylococcal densities and vegetations of untreated controls, with ampicillin-sulbactam in combination with rifampin or vancomycin being the most active regimen. However, only the regimen of ampicillin-sulbactam in combination with vancomycin effectively prevented relapse of endocarditis posttherapy after a 5-day antibiotic-free period. For animals receiving rifampin-containing regimens, relapses of endocarditis were associated with the in vivo development of rifampin resistance among coagulase-negative staphylococcal isolates in the vegetation. Ampicillin-sulbactam was highly effective in the prevention of experimental endocarditis caused by a beta-lactamase-producing, oxacillin-resistant coagulase-negative staphylococcal strain. Ampicillin-sulbactam was also efficacious for the therapy of coagulase-negative staphylococcal endocarditis, especially when it was combined with vancomycin to prevent posttherapeutic relapses.

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Year:  1996        PMID: 8787887      PMCID: PMC163064     

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


  27 in total

1.  Fifteen-year experience with bloodstream isolates of coagulase-negative staphylococci in neonatal intensive care.

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Journal:  J Clin Microbiol       Date:  1988-04       Impact factor: 5.948

2.  Plasmid-mediated resistance to vancomycin and teicoplanin in Enterococcus faecium.

Authors:  R Leclercq; E Derlot; J Duval; P Courvalin
Journal:  N Engl J Med       Date:  1988-07-21       Impact factor: 91.245

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Journal:  Infect Immun       Date:  1982-02       Impact factor: 3.441

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Authors:  B Farr; G L Mandell
Journal:  Med Clin North Am       Date:  1982-01       Impact factor: 5.456

5.  An outbreak of infections caused by strains of Staphylococcus aureus resistant to methicillin and aminoglycosides. I. Clinical studies.

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Journal:  J Infect Dis       Date:  1979-03       Impact factor: 5.226

6.  Ampicillin, sulbactam, and rifampin combination treatment of experimental methicillin-resistant Staphylococcus aureus endocarditis in rabbits.

Authors:  H F Chambers; M Kartalija; M Sande
Journal:  J Infect Dis       Date:  1995-04       Impact factor: 5.226

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Authors:  T T Ward; R E Winn; A I Hartstein; D L Sewell
Journal:  Infect Control       Date:  1981 Nov-Dec

8.  Risk factors for the development of prosthetic valve endocarditis.

Authors:  S B Calderwood; L A Swinski; C M Waternaux; A W Karchmer; M J Buckley
Journal:  Circulation       Date:  1985-07       Impact factor: 29.690

9.  Novel method for detection of beta-lactamases by using a chromogenic cephalosporin substrate.

Authors:  C H O'Callaghan; A Morris; S M Kirby; A H Shingler
Journal:  Antimicrob Agents Chemother       Date:  1972-04       Impact factor: 5.191

10.  Coagulase-negative staphylococci resistant to beta-lactam antibiotics in vivo produce penicillin-binding protein 2a.

Authors:  H F Chambers
Journal:  Antimicrob Agents Chemother       Date:  1987-12       Impact factor: 5.191

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  4 in total

1.  Treatment of experimental staphylococcal endocarditis due to a strain with reduced susceptibility in vitro to vancomycin: efficacy of ampicillin-sulbactam.

Authors:  M Backo; E Gaenger; A Burkart; Y L Chai; A S Bayer
Journal:  Antimicrob Agents Chemother       Date:  1999-10       Impact factor: 5.191

2.  Phenotypic resistance to thrombin-induced platelet microbicidal protein in vitro is correlated with enhanced virulence in experimental endocarditis due to Staphylococcus aureus.

Authors:  V K Dhawan; M R Yeaman; A L Cheung; E Kim; P M Sullam; A S Bayer
Journal:  Infect Immun       Date:  1997-08       Impact factor: 3.441

3.  LB11058, a new cephalosporin with high penicillin-binding protein 2a affinity and activity in experimental endocarditis due to homogeneously methicillin-resistant Staphylococcus aureus.

Authors:  Jacques Vouillamoz; José M Entenza; Peter Hohl; Philippe Moreillon
Journal:  Antimicrob Agents Chemother       Date:  2004-11       Impact factor: 5.191

4.  Efficacy of trovafloxacin, a new quinolone antibiotic, in experimental staphylococcal endocarditis due to oxacillin-resistant strains.

Authors:  A S Bayer; C Li; M Ing
Journal:  Antimicrob Agents Chemother       Date:  1998-07       Impact factor: 5.191

  4 in total

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