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10.17235/reed.2020.7434/2020

http://scihub22266oqcxt.onion/10.17235/reed.2020.7434/2020
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33261503!�!33261503

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suck abstract from ncbi


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pmid33261503      Rev+Esp+Enferm+Dig 2021 ; 113 (2): 116-118
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  • Pre-procedural antibody testing for SARS-CoV-2 in the routine endoscopic practice #MMPMID33261503
  • Hernandez Camba A; Marcelino Reyes R; Hernandez-Guerra M; Blasco Amato OA; Bennemann P; De La Riva N; Diaz Machin S; Medina JA
  • Rev Esp Enferm Dig 2021[Feb]; 113 (2): 116-118 PMID33261503show ga
  • METHODS: a retrospective multicenter cohort study was performed of all endoscopic procedures performed between April 27 and June 15, 2020. A screening questionnaire (SQ) was performed with patients three days prior to the procedure and 14 days after. Furthermore, a serologic SARS-CoV-2 test was performed 48 hours before. RESULTS: two hundred and eleven consecutive patients with endoscopic procedures were included. No patients had a positive SQ, either on entry to the study or 14 days later. Only four patients (1.9 % [95 % CI: 0.07-4.8 %]) were positive for antibodies. CONCLUSION: the pre-endoscopy seroprevalence of SARS-CoV-2 is low in this cohort. Pre-procedural SARS-CoV-2 antibody testing does not add any benefit over clinical SQ to identify active COVID-19 patients.
  • |*COVID-19 Serological Testing[MESH]
  • |*Endoscopy, Gastrointestinal[MESH]
  • |COVID-19/*diagnosis/epidemiology[MESH]
  • |Cohort Studies[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Preoperative Period[MESH]
  • |Retrospective Studies[MESH]


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