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. 2022 Oct;46(5):722-723.
doi: 10.1111/1753-6405.13285. Epub 2022 Aug 4.

Diagnostic accuracy of thirteen COVID-19 (SARS-CoV-2) rapid antigen self-tests with very high sensitivity approved for home use in Australia

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Diagnostic accuracy of thirteen COVID-19 (SARS-CoV-2) rapid antigen self-tests with very high sensitivity approved for home use in Australia

Edwin A Shores et al. Aust N Z J Public Health. 2022 Oct.
No abstract available

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Figures

Figure 1
Figure 1
Comparison of the positive predictive values of 13 rapid antigen tests approved by the Australian TGA under different prevalence rates. Notes: A=Rapid SARS‐CoV‐2 Antigen Test Card Self‐Test; B=Panbio™ Self‐Test COVID‐19 Antigen; C=OnSite® COVID‐19 Ag Self Test; D=Flowflex OnSite® COVID‐19 Ag Self‐Test; E=Cellife/Medriva COVID‐19 Antigen Test; F=Gardian T3 COVID‐19‐SARS‐CoV‐2 Antigen Saliva Self‐Test; G=All Test SARS‐CoV‐2 Antigen Rapid Test (Nasal Swab); H=Gmate® COVID‐19 Ag Saliva; I=V‐CHEK COVID‐19 Antigen Saliva Test; J=Novel/Sonictec Coronavirus (SARS‐CoV‐2) Antigen Rapid Test Device (Nasal Swab); K=Clungene COVID‐19 Antigen Rapid Test (For Self‐testing); L=LYHER® Novel Coronavirus (COVID‐19) Antigen Test Kit (Colloidal Gold) For self‐testing with nasal swab specimens; M=Orawell COVID‐19 Ag Rapid Saliva Test Device (Self‐test)

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References

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