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10.1038/s41598-021-83723-x

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suck abstract from ncbi


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pmid33619321      Sci+Rep 2021 ; 11 (1): 4310
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  • Digital PCR for high sensitivity viral detection in false-negative SARS-CoV-2 patients #MMPMID33619321
  • Poggio P; Songia P; Vavassori C; Ricci V; Banfi C; Barbieri SS; Garoffolo G; Myasoedova VA; Piacentini L; Raucci A; Scopece A; Sommariva E; Vinci MC; Carcione D; Biondi ML; Mancini ME; Formenti A; Andreini D; Assanelli EM; Agostoni P; Camera M; Colombo GI; Pesce M
  • Sci Rep 2021[Feb]; 11 (1): 4310 PMID33619321show ga
  • Patients requiring diagnostic testing for coronavirus disease 2019 (COVID-19) are routinely assessed by reverse-transcription quantitative polymerase chain reaction (RT-qPCR) amplification of Sars-CoV-2 virus RNA extracted from oro/nasopharyngeal swabs. Despite the good specificity of the assays certified for SARS-CoV-2 molecular detection, and a theoretical sensitivity of few viral gene copies per reaction, a relatively high rate of false negatives continues to be reported. This is an important challenge in the management of patients on hospital admission and for correct monitoring of the infectivity after the acute phase. In the present report, we show that the use of digital PCR, a high sensitivity method to detect low amplicon numbers, allowed us to correctly detecting infection in swab material in a significant number of false negatives. We show that the implementation of digital PCR methods in the diagnostic assessment of COVID-19 could resolve, at least in part, this timely issue.
  • |*False Negative Reactions[MESH]
  • |Adult[MESH]
  • |Aged[MESH]
  • |COVID-19/*diagnosis/diagnostic imaging/genetics[MESH]
  • |Diagnostic Tests, Routine/methods[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Real-Time Polymerase Chain Reaction/*methods[MESH]
  • |SARS-CoV-2/genetics/*pathogenicity[MESH]
  • |Sensitivity and Specificity[MESH]


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