# Evaluation of COVID-19 rapid antigen test against polymerase chain reaction test in immunocompromised patients

**Authors:** Ali Sabateen, Dana Sadaqa, Taleen Nino, Ghayd Zaghal, George Qumsieh, Reena Fakhori, Hammam Rjoub, Tahreer Taha, Rami Zghari, Sari Abu Hanieh, Duaa Al-Basha, Marwan Qabaja, Hamza Alsaid, Musa Y. Hindiyeh

PMC · DOI: 10.1371/journal.pone.0306396 · PLOS ONE · 2024-08-02

## TL;DR

This study compares the accuracy of a rapid antigen test and a PCR test for detecting COVID-19 in immunocompromised patients, finding that the PCR test is more sensitive.

## Contribution

The study evaluates the performance of the Panbio rapid antigen test in a specific high-risk patient group, highlighting its limitations compared to PCR.

## Key findings

- The Panbio rapid antigen test had a sensitivity of 69.9% and a specificity of 100%.
- Patients with a Ct value less than 20 had the highest detection rate.
- Ct value was directly related to false-negative results, with a statistically significant p-value of 0.007.

## Abstract

On the 11th of March 2020, the world faced a new global pandemic, COVID-19 which is a disease caused by the novel coronavirus, it had multiple devastating outcomes on multiple sectors along with significant rates of mortality. These challenges encouraged the development of multiple testing methods, as well as anti-viral medications such as Molnupiravir, as well as evaluating the efficacy of available medications against it, like; Azithromycin, Ritonavir and Hydroxychloroquine. Vaccination against COVID-19 forged into a significant challenge, few months ensuing the first case of SARS-CoV-2, which was diagnosed in December 2019, in Wuhan-China, thus, multiple vaccines were approved for use around the world to combat this pandemic. Our study includes a sample of 556 oncology patients at Augusta Victoria Hospital in Jerusalem, all patients were tested using Panbio rapid antigen test and Allplex PCR Assay. The main objective was to study the sensitivity and specificity of Rapid antigen test, which contributes to a faster isolation call and management of infected patients, thus decreasing the risk on spread to other patients and health care. Patients were categorized based on two factors: Ct range and age group and studying their possible effect on false-negative results. Patients with Ct value less than 20, had the highest detection rate which is consistent with other studies in the literature. The sensitivity and specificity of Panbio Rapid Antigen testing were of 69.9% and 100%, respectively. A correlation between age group and false negative results could not be made, but a correlation between Ct value and false negative result was noticed, Ct value was directly related to false negative results. P-value of 0.007 indicated that results were statistically significant where PCR test is considered more sensitive compared to rapid antigen test.

## Linked entities

- **Chemicals:** Molnupiravir (PubChem CID 145996610), Azithromycin (PubChem CID 447043), Ritonavir (PubChem CID 5076), Hydroxychloroquine (PubChem CID 3652)
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Diseases:** COVID-19 (MESH:D000086382), infected (MESH:D007239)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Gammacoronavirus (genus) [taxon 694013]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11296623/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC11296623/full.md

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Source: https://tomesphere.com/paper/PMC11296623