Original research articles |




* Barts Sexual Health Centre, Barts and The London NHS Trust, London EC1A 7BE;
Department of Sexual Health, Homerton University Hospital NHS Foundation Trust, London E9 6SR;
Greenway Centre, Newham University Hospital NHS Trust, London E13 8SL;
Joint Research Office, Bart's and The London NHS Trust, Queen Mary's School of Medicine and Dentistry, London E1 2AN;
** Centre For Infectious Disease, Institute For Cell And Molecular Science, Barts and the London School of Medicine and Dentistry, London E1 2AT, UK
Correspondence to: Dr Jill Zelin Email: Jill.Zelin{at}bartsandthelondon.nhs.uk
To date, no data have been published on the use of OraQuick® ADVANCE Rapid HIV-1/2 Test (OraQuick) in the UK. We report preliminary findings of an ongoing evaluation of OraQuick in UK genitourinary (GU) medicine clinics. A total of 820 samples from patients in high-risk groups for HIV were tested with OraQuick and results were compared with standard HIV antibody testing. HIV prevalence (enzyme immunoassay [EIA]) was 5.73%, sensitivity of OraQuick was 93.64% (95% CI 82.46–98.66%), specificity 99.87% (99.28–100%), positive predictive value 97.78% (88.27–99.94%) and negative predictive value 99.61% (98.87–99.92%). This includes three false-negatives considered to be due to observer error and now rectified by further training. This has increased test sensitivity to 100%. Our observed test performance of OraQuick compares well with EIA and with other rapid tests. We believe that simple, non-invasive antibody detection tests such as OraQuick can increase HIV testing and diagnosis in UK GU medicine and community settings.
Key Words: point-of-care oral fluid HIV rapid, tests
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