Your browser doesn't support javascript.
Higher SARS-CoV-2 detection of oropharyngeal compared with nasopharyngeal or saliva specimen for molecular testing: a multicentre randomised comparative accuracy study.
Todsen, Tobias; Tolsgaard, Martin G; Benfield, Thomas; Folke, Fredrik; Jakobsen, Kathrine K; Gredal, Niels Tobias; Ersbøll, Annette K; von Buchwald, Christian; Kirkby, Nikolai.
  • Todsen T; Department of Otorhinolaryngology, Head and Neck Surgery and Audiology, Rigshospitalet - Copenhagen University Hospital, Copenhagen, Denmark Tobias.Todsen@regionh.dk.
  • Tolsgaard MG; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Benfield T; Department of Otorhinolaryngology and Maxillofacial Surgery, Zealand University Hospital, Koege, Denmark.
  • Folke F; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Jakobsen KK; Copenhagen Academy for Medical Education and Simulation, Rigshospitalet, Copenhagen, Denmark.
  • Gredal NT; Department of Obstetrics, Rigshospitalet, Copenhagen, Denmark.
  • Ersbøll AK; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • von Buchwald C; Department of Infectious Diseases, Copenhagen University Hospital, Amager and Hvidovre, Hvidovre, Denmark.
  • Kirkby N; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Thorax ; 2023 May 19.
Article in English | MEDLINE | ID: covidwho-2326700
ABSTRACT

BACKGROUND:

Testing is critical for detecting SARS-CoV-2 infection, but the best sampling method remains unclear.

OBJECTIVES:

To determine whether nasopharyngeal swab (NPS), oropharyngeal swab (OPS) or saliva specimen collection has the highest detection rate for SARS-CoV-2 molecular testing.

METHODS:

We conducted a randomised clinical trial at two COVID-19 outpatient test centres where NPS, OPS and saliva specimens were collected by healthcare workers in different orders for reverse transcriptase PCR testing. The SARS-CoV-2 detection rate was calculated as the number positive by a specific sampling method divided by the number in which any of the three sampling methods was positive. As secondary outcomes, test-related discomfort was measured with an 11-point numeric scale and cost-effectiveness was calculated.

RESULTS:

Among 23 102 adults completing the trial, 381 (1.65%) were SARS-CoV-2 positive. The SARS-CoV-2 detection rate was higher for OPSs, 78.7% (95% CI 74.3 to 82.7), compared with NPSs, 72.7% (95% CI 67.9 to 77.1) (p=0.049) and compared with saliva sampling, 61.9% (95% CI 56.9 to 66.8) (p<0.001). The discomfort score was highest for NPSs, at 5.76 (SD, 2.52), followed by OPSs, at 3.16 (SD 3.16) and saliva samples, at 1.03 (SD 18.8), p<0.001 between all measurements. Saliva specimens were associated with the lowest cost, and the incremental costs per detected SARS-CoV-2 infection for NPSs and OPSs were US$3258 and US$1832, respectively.

CONCLUSIONS:

OPSs were associated with higher SARS-CoV-2 detection and lower test-related discomfort than NPSs for SARS-CoV-2 testing. Saliva sampling had the lowest SARS-CoV-2 detection but was the least costly strategy for mass testing. TRIAL REGISTRATION NUMBER NCT04715607.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Language: English Year: 2023 Document Type: Article Affiliation country: Thorax-2022-219599

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Language: English Year: 2023 Document Type: Article Affiliation country: Thorax-2022-219599