Implementation of the cobas Liat influenza point-of-care test into an emergency department during a high-incidence season: a retrospective evaluation following real-world implementation

J Hosp Infect. 2019 Mar;101(3):285-288. doi: 10.1016/j.jhin.2018.12.008. Epub 2018 Dec 16.

Abstract

The cobas Liat influenza A/B and respiratory syncytial virus (RSV) assay (Liat) was used in the adult emergency department of a large London hospital from 21st January 2018 to 14th April 2018. Influenza was detected in 308 of 1027 (30%) samples tested; influenza A in 157 (15.3%), influenza B in 149 (14.5%) and RSV in 28 (2.7%). When compared against Fast Track Diagnostics Respiratory Pathogens 21 multiplex polymerase chain reaction and Cepheid Xpert Xpress Flu/RSV assay, Liat performance for the detection of influenza A or B was: sensitivity 85% [95% confidence interval (CI) 76-92)], specificity 98% (95% CI 97-99), negative predictive value 94% (95% CI 92-96) and positive predictive value 95% (95% CI 91-97).

Keywords: Infection control; Influenza virus A; Influenza virus B; Point-of-care technology; Polymerase chain reaction; Rapid diagnostic tests.

Publication types

  • Comparative Study
  • Evaluation Study

MeSH terms

  • Adult
  • Diagnostic Tests, Routine / methods*
  • Emergency Service, Hospital*
  • Humans
  • Incidence
  • Influenza A virus / isolation & purification
  • Influenza B virus / isolation & purification
  • Influenza, Human / diagnosis*
  • London
  • Point-of-Care Systems*
  • Predictive Value of Tests
  • Respiratory Syncytial Virus Infections / diagnosis*
  • Respiratory Syncytial Viruses / isolation & purification
  • Retrospective Studies
  • Sensitivity and Specificity