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Pooling for SARS-CoV2 Surveillance: Validation and Strategy for Implementation in K-12 Schools.
Simas, Alexandra M; Crott, Jimmy W; Sedore, Chris; Rohrbach, Augusta; Monaco, Anthony P; Gabriel, Stacey B; Lennon, Niall; Blumenstiel, Brendan; Genco, Caroline A.
  • Simas AM; Department of Immunology, Tufts University School of Medicine, Boston, MA, United States.
  • Crott JW; Office of the Vice Provost of Research, Tufts University, Boston, MA, United States.
  • Sedore C; Jean Mayer United States Department of Agriculture (USDA) Human Nutrition Research on Aging at Tufts University, Boston, MA, United States.
  • Rohrbach A; Tufts Technology Services, Somerville, MA, United States.
  • Monaco AP; Office of the Vice Provost of Research, Tufts University, Boston, MA, United States.
  • Gabriel SB; Tufts University, Medford, MA, United States.
  • Lennon N; Broad Institute of MIT and Harvard, Cambridge, MA, United States.
  • Blumenstiel B; Broad Institute of MIT and Harvard, Cambridge, MA, United States.
  • Genco CA; Broad Institute of MIT and Harvard, Cambridge, MA, United States.
Front Public Health ; 9: 789402, 2021.
Article in English | MEDLINE | ID: covidwho-1607927
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ABSTRACT
Repeated testing of a population is critical for limiting the spread of the SARS-CoV-2 virus and for the safe reopening of educational institutions such as kindergarten-grade 12 (K-12) schools and colleges. Many screening efforts utilize the CDC RT-PCR based assay which targets two regions of the novel Coronavirus nucleocapsid gene. The standard approach of testing each person individually, however, poses a financial burden to these institutions and is therefore a barrier to using testing for re-opening. Pooling samples from multiple individuals into a single test is an attractive alternate approach that promises significant cost savings-however the specificity and sensitivity of such approaches needs to be assessed prior to deployment. To this end, we conducted a pilot study to evaluate the feasibility of analyzing samples in pools of eight by the established RT-PCR assay. Participants (1,576) were recruited from amongst the Tufts University community undergoing regular screening. Each volunteer provided two swabs, one analyzed separately and the other in a pool of eight. Because the positivity rate was very low, we spiked approximately half of the pools with laboratory-generated swabs produced from known positive cases outside the Tufts testing program. The results of pooled tests had 100% correspondence with those of their respective individual tests. We conclude that pooling eight samples does not negatively impact the specificity or sensitivity of the RT-PCR assay and suggest that this approach can be utilized by institutions seeking to reduce surveillance costs.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / COVID-19 Type of study: Experimental Studies / Prognostic study Limits: Humans Language: English Journal: Front Public Health Year: 2021 Document Type: Article Affiliation country: Fpubh.2021.789402

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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / COVID-19 Type of study: Experimental Studies / Prognostic study Limits: Humans Language: English Journal: Front Public Health Year: 2021 Document Type: Article Affiliation country: Fpubh.2021.789402