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First experience of implementing Candida auris real-time PCR for surveillance in the UK: detection of multiple introductions with two international clades and improved patient outcomes.
Taori, S K; Rhodes, J; Khonyongwa, K; Szendroi, A; Smith, M; Borman, A M; Kumarage, J; Brown, C S; Moore, G; Desai, N.
Affiliation
  • Taori SK; Department of Medical Microbiology, NHS Lothian, Edinburgh, UK. Electronic address: surabhi.taori@nhslothian.scot.nhs.uk.
  • Rhodes J; Imperial College London, London, UK.
  • Khonyongwa K; Information Services, UK Health Security Agency, London, UK.
  • Szendroi A; Department of Infection Sciences, King's College Hospital NHS Foundation Trust, London, UK.
  • Smith M; Department of Infection Sciences, King's College Hospital NHS Foundation Trust, London, UK.
  • Borman AM; UK National Mycology Reference Laboratory, National Infection Service, UK Health Security Agency and Medical Research Council Centre for Medical Mycology at the University of Exeter, Exeter, UK.
  • Kumarage J; Department of Infection Sciences, King's College Hospital NHS Foundation Trust, London, UK.
  • Brown CS; HCAI/AMR, National Infection Service, UK Health Security Agency, London, UK.
  • Moore G; Biosafety, Air and Water Microbiology Group, National Infection Service, UK Health Security Agency, London, UK.
  • Desai N; Department of Infection Sciences, King's College Hospital NHS Foundation Trust, London, UK.
J Hosp Infect ; 127: 111-120, 2022 Sep.
Article in En | MEDLINE | ID: mdl-35753522
ABSTRACT

BACKGROUND:

Candida auris has been associated with rapid transmission and high mortality. A novel PCR-based surveillance programme was initiated at a London teaching hospital from January 2018. The results of this implementation until March 2019 are presented along with the clinical, transmission and phylogenetic characteristics encountered in that setting.

METHODS:

A real-time PCR assay for C. auris was developed, validated, and implemented for direct use on skin swabs and urine. Environmental swabs were also tested by PCR as an emergency outbreak-control measure. Clinical risk factors and outcomes of patients were determined. Environmental dispersal was assessed using 24 h settle plate cultures around nine colonized patients followed by air sampling around one colonized patient during high- and low-turbulence activities. Sequencing was performed using Illumina HiSeq and maximum likelihood phylogenies were constructed using rapid bootstrap analysis.

RESULTS:

Twenty-one C. auris colonized patients were identified. Median turnaround time of colonization detection reduced from 141 h (5.8 days) to approximately 24 h enabling rapid infection-control precautions. Settle plates detected 70-600 cfu/m2 around colonized patients over 24 h and air sampling suggested dispersal during turbulent activities. C. auris DNA was detected from 35.7% environmental swabs. Despite being in a high-risk setting, no patients developed invasive infection. Sequencing analysis of isolates from this centre identified two introductions of the South Asian (Clade I) and one of the South African (Clade III) strain.

CONCLUSION:

The PCR offers a rapid, scalable method of screening and supports clinical risk reduction in settings likely to encounter multiple introductions.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Candidiasis Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: J Hosp Infect Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Candidiasis Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: J Hosp Infect Year: 2022 Document type: Article
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