Vancomycin-gentamicin synergism revisited: Effect of gentamicin susceptibility of methicillin-resistant Staphylococcus aureus


Mulazimoglu L., Drenning S., Muder R.

ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, cilt.40, sa.6, ss.1534-1535, 1996 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 40 Sayı: 6
  • Basım Tarihi: 1996
  • Doi Numarası: 10.1128/aac.40.6.1534
  • Dergi Adı: ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1534-1535
  • Marmara Üniversitesi Adresli: Hayır

Özet

Vancomycin monotherapy of deep-seated staphylococcal infection may be associated with poor bacteriological response, We evaluated 24 unique patient isolates of methicillin-resistant Staphylococcus aureus (MRSA) for vancomycin-gentamicin synergism by determining time-kill curves for vancomycin at 10 mu g/ml and gentamicin at 1 mu g/ml. Nine MRSA strains showed high-level gentamicin resistance (HLGR) (MIC, >500 mu g/ml), acid 15 did not, Vancomycin-gentamicin demonstrated synergism against none of the HLGR strains. For the non-HLGR strains, gentamicin agar dilution MICs ranged from 0.5 to >128 mu g/ml. Vancomycin-gentamicin demonstrated synergism against six of these strains and indifference against nine of them. There was no relationship between the agar dilution MIC of gentamicin and the occurrence of synergism against non-HLGR strains. We conclude that a gentamicin MIC of >500 mu g/ml predicts a lack of vancomycin-gentamicin synergism for strains of MRSA. For non-HLGR strains, synergism is not predictable from the gentamicin MIG.