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Biosensor for Detection of Antibiotic Resistant Staphylococcus Bacteria
Published on: May 8, 2013
Recognition and management of infections caused by vancomycin-intermediate Staphylococcus aureus (VISA) and
1Infectious Disease Department, Austin Health, Heidelberg, Australia. Benjamin.Howden@austin.org.au
Abstract:
Vancomycin resistance in Staphylococcus aureus has recently emerged as an important clinical problem with implications for laboratory detection and clinical management of patients infected with resistant strains. To date, low-level vancomycin resistance in the form of vancomycin-intermediate S. aureus (VISA) and heterogenous vancomycin-intermediate S. aureus (hVISA) have been more common, with only four cases of true vancomycin resistant S. aureus (VRSA) reported. This article reviews current knowledge about the epidemiology, clinical manifestations and optimal management of hVISA and VISA infections. VISA and hVISA have now been reported from many countries, and these strains tend to occur in patients with significant comorbidities and previous antibiotic exposure. Despite the difficulties in laboratory detection, there are increasing data linking VISA and hVISA to failure of glycopeptide antimicrobial therapy. Aggressive surgical intervention and non-glycopeptide-based antimicrobial therapy appears to improve outcomes for patients infected with these low-level vancomycin-resistant strains. Clinicians and diagnostic laboratories need to be aware of VISA and hVISA as a clinical problem, and consider aggressive surgical debridement and non-glycopeptide-based therapy where infections with such strains are suspected or proven.
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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