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Prevalence of inducible clindamycin resistance in macrolide-resistant Staphylococcus spp

S Fokas1, S Fokas, M Tsironi

  • 1Sparta General Hospital, Microbiology, Sparta, Laconia, Greece. spifokas@yahoo.gr

Insights

Inducible clindamycin resistance is a significant concern in Staphylococcus aureus and coagulase-negative staphylococci (CoNS) in Greek hospitals. Routine screening is essential to identify these resistant strains and prevent treatment failures.

Area of Science:

  • Medical Microbiology
  • Infectious Diseases
  • Antimicrobial Resistance

Background:

  • Macrolide resistance is a growing problem in Staphylococcus aureus and coagulase-negative staphylococci (CoNS).
  • Inducible clindamycin resistance (ICR) can lead to treatment failures if not detected.
  • Phenotypic characterization is crucial for understanding resistance mechanisms.

Purpose of the Study:

  • To investigate the prevalence of inducible clindamycin resistance in Staphylococcus aureus and CoNS isolates.
  • To compare the frequency of inducible versus constitutive macrolide resistance phenotypes.
  • To emphasize the need for routine screening for ICR in staphylococcal infections.

Main Methods:

  • Phenotypic testing of macrolide-resistant Staphylococcus aureus (n=45) and CoNS (n=75) isolates.
  • Isolates collected from a Greek hospital between January 2002 and December 2003.
  • Assessment for inducible and constitutive clindamycin resistance patterns.

Main Results:

  • In Staphylococcus aureus, constitutive macrolide resistance (60%) was most common, followed by inducible resistance (35%).
  • In CoNS, the inducible resistance phenotype (50%) was more prevalent than the constitutive phenotype (41%).
  • A significant incidence of inducible clindamycin resistance was observed in both bacterial groups.

Conclusions:

  • Inducible clindamycin resistance is a significant finding in staphylococcal isolates from this Greek hospital.
  • Screening all staphylococcal isolates is necessary to distinguish ICR from true susceptibility.
  • Accurate identification of ICR is vital for appropriate antibiotic selection and patient management.

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