AI Article Synopsis

  • Rapid antigen detection tests (RADTs) are a quick and cost-effective method for diagnosing COVID-19, with limited studies conducted in China despite promising results worldwide.
  • A study in Shanghai involved 716 COVID-19 patients and 203 non-infected individuals to evaluate the RADT performance against real-time reverse transcription-PCR (RT-PCR), showing high sensitivity in various scenarios, especially in symptomatic patients.
  • The RADT demonstrated excellent specificity and sensitivity (above 80%) for symptomatic individuals, particularly those with upper respiratory tract symptoms, making it effective for screening COVID-19 infections during the epidemic.

Article Abstract

Rapid and reliable diagnosis is important for the management of individuals infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The rapid antigen detection test (RADT) is a rapid, inexpensive, and easy method. Several studies have reported that RADTs performed well in many countries; however, very few studies have been reported in China. In this study, we assessed the performance of the RADT (Ediagnosis COVID-19 antigen test kit). This study was conducted in a centralized isolation site in Shanghai and enrolled 716 patients with COVID-19 and 203 noninfected participants. Nasopharyngeal swabs from all participants were collected on the same day and tested using the RADT and real-time reverse transcription-PCR (RT-PCR). The performance of the RADT was evaluated in different scenarios, such as threshold cycle () values, symptomatic phase, and symptoms on the day of testing. The results demonstrated that the sensitivity for patients with values lower than 20 was 96.55% (95% confidence interval [CI], 87.05 to 99.4). The sensitivities were 78.4% (95% CI, 69.96 to 85.05) for participants within 5 days after the first RT-PCR-positive result and 90.77% (95% CI, 80.34 to 96.19) within 5 days after symptom onset. Moreover, the sensitivity of the RADT was more than 80% for patients with symptoms on the day of testing, including fever (89.29%), cough (86.84%), stuffy nose (92.59%), runny nose (92%), sore throat (81.25%), and muscle pain (80.77%), especially for those with upper respiratory tract symptoms. The specificity of the RADT was good in all scenarios. During the SARS-CoV-2 epidemic, Ediagnosis performed excellently in individuals with a higher viral load (evidenced by lower values), individuals in the early symptomatic phase, and especially those with upper respiratory tract symptoms. RADTs have demonstrated excellent performance in many counties for screening SARS-CoV-2 infection, but very few studies have been conducted in China. The performance of RADTs is largely related to different real-life scenarios. In our study, the performance of the RADT was evaluated in different scenarios, such as values, symptomatic phase, and symptoms on the day of testing. The results demonstrated that Ediagnosis (an RADT made in China) performed excellently for individuals with a higher viral load (evidenced by lower values), individuals in the early symptomatic phase, and especially those with upper respiratory tract symptoms.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927082PMC
http://dx.doi.org/10.1128/spectrum.04542-22DOI Listing

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