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Utility of SARS-CoV-2 rapid antigen testing for patient triage in the emergency department: A clinical implementation study in Melbourne, Australia.
Bond, Katherine A; Smith, Ben; Gardiner, Emma; Liew, K C; Williams, Eloise; Walsham, Nicola; Putland, Mark; Williamson, Deborah A.
  • Bond KA; Department of Microbiology, Royal Melbourne Hospital, at The Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
  • Smith B; Department of Infectious Diseases, The University of Melbourne at The Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
  • Gardiner E; Victorian Infectious Diseases Reference Laboratory at The Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
  • Liew KC; Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
  • Williams E; Department of Emergency Medicine, Royal Melbourne Hospital, Melbourne, Australia.
  • Walsham N; Department of Emergency Medicine, Royal Melbourne Hospital, Melbourne, Australia.
  • Putland M; Department of Microbiology, Royal Melbourne Hospital, at The Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
  • Williamson DA; Victorian Infectious Diseases Reference Laboratory at The Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
Lancet Reg Health West Pac ; 25: 100486, 2022 Aug.
Article in English | MEDLINE | ID: covidwho-1867463
ABSTRACT

Background:

Early, rapid detection of SARS-CoV-2 is essential in healthcare settings in order to implement appropriate infection control precautions and rapidly assign patients to care pathways. Rapid testing methods, such as SARS-CoV-2 rapid antigen testing (RAT) may improve patient care, despite a lower sensitivity than real-time PCR (RT-PCR) testing.

Methods:

Patients presenting to an Emergency Department (ED) in Melbourne, Australia, were risk-stratified for their likelihood of active COVID-19 infection, and a non-randomised cohort of patients were tested by both Abbott Panbio™ COVID-19 Ag test (RAT) and SARS-CoV-2 RT-PCR. Patients with a positive RAT in the 'At or High Risk' COVID-19 group were moved immediately to a COVID-19 ward rather than waiting for a RT-PCR result. Clinical and laboratory data were assessed to determine test performance characteristics; and length of stay in the ED was compared for the different patient cohorts.

Findings:

Analysis of 1762 paired RAT/RT-PCR samples demonstrated an overall sensitivity of 75.5% (206/273; 95% CI 69·9-80·4) for the Abbott Panbio™ COVID-12 Ag test, with specificity of 100% (1489/1489; 95% CI 99·8-100). Sensitivity improved with increasing risk for COVID-19 infection, from 72·4% (95% CI 52·8-87·3) in the 'No Risk' cohort to 100% (95% CI 29·2-100) in the 'High Risk' group. Time in the ED for the 'At/High Risk' group decreased from 421 minutes (IQR 281, 525) for those with a positive RAT result to 274 minutes (IQR140, 425) for those with a negative RAT result, p = 0.02.

Interpretation:

The positive predictive value of a positive RAT in this setting was high, allowing more rapid instigation of COVID-19 care pathways and an improvement in patient flow within the ED.

Funding:

Royal Melbourne Hospital, Melbourne, Australia.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal: Lancet Reg Health West Pac Year: 2022 Document Type: Article Affiliation country: J.lanwpc.2022.100486

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal: Lancet Reg Health West Pac Year: 2022 Document Type: Article Affiliation country: J.lanwpc.2022.100486