ORIGINAL ARTICLE |
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Year : 2020 | Volume
: 4
| Issue : 4 | Page : 346-348 |
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Saliva as an alternate specimen source for the diagnosis of coronavirus disease 2019 in symptomatic patients using cepheid xpert xpress SARS-CoV-2
Maya Habous1, Rania Medhat Seliem1, Laila AlDabal2, Firas Al-Najjar3, Maimona Elimam1, Meera Jainmboo1, Bayan Abdalla1, Zahra Abdullahi1, Ayesha Nasser1
1 Department of Pathology, Rashid Hospital, Dubai, United Arab Emirates 2 Department of Medical Affairs, Infectious Diseases Unit, Rashid Hospital, Dubai, United Arab Emirates 3 Department of Emergency, Rashid Hospital, Dubai, United Arab Emirates
Correspondence Address:
Dr. Maya Habous Microbiology & Infection Control Unit, Pathology and Genetics Department, Rashid Hospital, Dubai United Arab Emirates
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/bbrj.bbrj_170_20
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Background: Rapid and accurate SARS-CoV-2 diagnostic testing is essential for controlling the ongoing coronavirus disease 2019 (COVID-19) pandemic. The current gold standard for COVID-19 diagnosis is real-time reverse transcription-polymerase chain reaction (RT-PCR) detection of SARS-CoV-2 from nasopharyngeal swab (NPS) specimens. The objective of this study is to assess saliva specimens for the diagnosis of COVID-19 using the GeneXpert® Xpress SARS-CoV-2 assay. Materials and Methods: In June 2020, we prospectively simultaneously collected saliva samples and a standard NPS from 60 patients meeting case definition of COVID-19 in the Emergency Department and from inpatients in Rashid Hospital at Dubai Health Authority during the outbreak of COVID-19. Real-time RT-PCR using the Cepheid Xpert Xpress SARS-CoV-2 was performed, and the results of the two specimens were compared. Results: A total of 60 paired NPS and saliva specimens were tested. An analysis of the agreement between the two specimens demonstrated a 97% observed agreement. 30/28 samples were positive in saliva when compared to the NPS, resulting in a positive percent agreement of 93%. 30/32 samples had a negative saliva and NPS. Two samples demonstrated detectable levels of SARS-CoV-2 nucleic acid in the saliva, but the NPS was negative, resulting in a negative percent agreement of 94%. Conclusion: Our data showed that saliva is an acceptable sensitive and specific alternative source for detecting SARS-CoV-2 nucleic acid and the use of saliva samples is safer and more convenient for the patient. NPS sampling inconsistency may be one of the potential issues for false-negative results.
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