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Diagnostic accuracy of a Sars-CoV-2 rapid test and optimal time for seropositivity according to the onset of symptoms

Dados Bibliográficos

ID5166248
AutoresCaroline Nespolo De David (0000-0002-6196-7501, Hospital Moinhos de Vento), Fernanda Hammes Varela (0000-0003-1947-5279, Hospital Moinhos de Vento, Brasil; Pontifícia Universidade Católica do Rio Grande do Sul, Brasil), Ivaine Tais Sauthier Sartor (0000-0002-8775-6622, Hospital Moinhos de Vento), Márcia Polese-Bonatto (0000-0001-6049-926X, Hospital Moinhos de Vento), Ingrid Rodrigues Fernandes (0000-0002-0895-0698, Hospital Moinhos de Vento), Gabriela Oliveira Zavaglia (0000-0001-5419-665X, Hospital Moinhos de Vento), Luciane Beatriz Kern (0000-0001-7521-8256, Hospital Moinhos de Vento), Charles Francisco Ferreira (0000-0001-9777-7382, Hospital Moinhos de Vento), Gisele Alsina Nader Bastos (0000-0001-9668-1434, Hospital Moinhos de Vento), Paulo Márcio Pitrez (0000-0001-7319-1133, Hospital Moinhos de Vento), Walquiria Aparecida Ferreira De Almeida (0000-0003-2082-6283, Ministério da Saúde, Brazil), Victor Bertollo Gomes Porto (0000-0002-3112-6154, Ministério da Saúde, Brazil), Alexandre Prehn Zavascki (0000-0001-5331-4837, Hospital Moinhos de Vento, Brasil; Universidade Federal do Rio Grande do Sul, Brazil), Renato Tetelbom Stein (0000-0003-0269-0757, Pontifícia Universidade Católica do Rio Grande do Sul), Marcelo Comerlato Scotta (0000-0001-5892-4052, Hospital Moinhos de Vento, Brasil; Pontifícia Universidade Católica do Rio Grande do Sul, Brasil)
Ano2022
Volume38
Fascículo1
Páginase00069921-e00069921
Data de publicação2022-01-01
Peer ReviewedSim
Open AccessSim
TipoARTICLE
PeriódicoCadernos de Saude Publica (JOURNAL)
Identificadores do periódicoISSN: 0102-311X • E-ISSN: 1678-4464
EditoraFapUNIFESP (SciELO) (PUBLISHER)
DOI10.1590/0102-311x00069921
PMID35043881
OpenAlexW4206385355
SCIELO_PIDS0102-311X2022000105007
IdiomaEN
Referências citadas24

Point-of-care serological tests for SARS-CoV-2 have been used for COVID-19 diagnosis. However, their accuracy over time regarding the onset of symptoms is not fully understood. We aimed to assess the accuracy of a point-of-care lateral flow immunoassay (LFI). Subjects, aged over 18 years, presenting clinical symptoms suggestive of acute SARS-CoV-2 infection were tested once by both nasopharyngeal and oropharyngeal RT-PCR and LFI. The accuracy of LFI was assessed in periodic intervals of three days in relation to the onset of symptoms. The optimal cut-off point was defined as the number of days required to achieve the best sensitivity and specificity. This cut-off point was also used to compare LFI accuracy according to participants' status: outpatient or hospitalized. In total, 959 patients were included, 379 (39.52%) tested positive for SARS-CoV-2 with RT-PCR, and 272 (28.36%) tested positive with LFI. LFI best performance was achieved after 10 days of the onset of symptoms, with sensitivity and specificity of 84.9% (95%CI: 79.8-89.1) and 94.4% (95%CI: 91.0-96.8), respectively. Although the specificity was similar (94.6% vs. 88.9%, p = 0.051), the sensitivity was higher in hospitalized patients than in outpatients (91.7% vs. 82.1%, p = 0.032) after 10 days of the onset of symptoms. Best sensitivity of point-of-care LFI was found 10 days after the onset of symptoms which may limit its use in acute care. Specificity remained high regardless of the number of days since the onset of symptoms

Cut-point · Diagnostic accuracy · Diagnostic test · Outpatient clinic · Predictive value of tests · Serology · Infection Control and Ventilation · Respiratory viral infections research · SARS-CoV-2 detection and testing

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  • A Novel Coronavirus from Patients with Pneumonia in China, 2019

    Na Zhu, 양승민 양승민 et al.•New England Journal of Medicine•2020

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