Recognition and management of infections caused by vancomycin-intermediate Staphylococcus aureus (VISA) and

B P Howden1

  • 1Infectious Disease Department, Austin Health, Heidelberg, Australia. Benjamin.Howden@austin.org.au

Internal Medicine Journal
|November 8, 2005
PubMed

Insights

Vancomycin resistance in Staphylococcus aureus, including vancomycin-intermediate (VISA) and heterogeneous (hVISA) strains, is a growing clinical concern. Effective management involves aggressive surgery and non-glycopeptide antibiotics.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Clinical Medicine

Background:

  • Vancomycin resistance in Staphylococcus aureus presents a significant clinical challenge.
  • Low-level resistance, vancomycin-intermediate S. aureus (VISA) and heterogenous vancomycin-intermediate S. aureus (hVISA), is more prevalent than true vancomycin-resistant S. aureus (VRSA).

Purpose of the Study:

  • To review the epidemiology, clinical features, and management strategies for hVISA and VISA infections.
  • To highlight the clinical implications of vancomycin resistance in S. aureus for detection and treatment.

Main Methods:

  • Literature review of current knowledge on VISA and hVISA.
  • Analysis of epidemiological data, clinical manifestations, and treatment outcomes.

Main Results:

  • VISA and hVISA strains are reported globally, often in patients with comorbidities and prior antibiotic use.
  • These strains are increasingly linked to treatment failures with glycopeptide antibiotics.
  • Aggressive surgical intervention and non-glycopeptide antimicrobial therapy show improved patient outcomes.

Conclusions:

  • Clinicians and laboratories must recognize VISA and hVISA as critical clinical issues.
  • Suspected or confirmed infections warrant consideration of aggressive surgical debridement and alternative non-glycopeptide therapies.

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