Candida auris Screening Recommendations in Healthcare Settings
Screening for Candida auris is strongly recommended for high-risk patients, with axilla and groin composite swabs being the preferred sampling method using specialized culture media or PCR-based detection. 1, 2
Screening Indications
Screening should be implemented for patients at high risk of C. auris colonization, including:
The positivity rate for C. auris screening in high-risk patients is approximately 3-4%, justifying targeted surveillance 5
Preferred Screening Methods
Composite swabs of the axilla and groin are the recommended sampling sites for C. auris screening 1
Laboratory testing options include:
Conventional identification systems often misidentify C. auris as other Candida species (C. famata, C. sake) or even as Rhodotorula or Saccharomyces, necessitating specialized testing 4
Screening Protocol Implementation
For newly admitted high-risk patients:
For contact tracing:
Infection Control Considerations
C. auris can persist in the healthcare environment and on patient skin for prolonged periods (up to a year or more) 6
Patients who develop C. auris infections typically remain colonized even after treatment, requiring continued infection control measures 2
Environmental cleaning requires sporicidal disinfectants (hydrogen peroxide, peracetic acid-based, or chlorine-based) as quaternary ammonium compounds have poor activity against Candida species 1
Common Pitfalls and Caveats
Relying solely on standard identification methods may lead to misidentification of C. auris 4
Standard culture techniques have limited sensitivity; specialized media and molecular methods improve detection 3
Screening only a single anatomical site may miss colonization, as C. auris can colonize multiple body sites 3, 6
Failure to implement proper infection control measures after identifying colonized patients can lead to outbreaks 2
The current evidence base for C. auris screening is primarily from outbreak settings rather than prospective studies, suggesting that screening protocols should be informed by both available evidence and fungal microbiology principles 6