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  1. Article ; Online: Clinical evaluation of serological IgG antibody response on the Abbott Architect for established SARS-CoV-2 infection.

    Chew, K L / Tan, S S / Saw, S / Pajarillaga, A / Zaine, S / Khoo, C / Wang, W / Tambyah, P / Jureen, R / Sethi, S K

    Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases

    2020  Volume 26, Issue 9, Page(s) 1256.e9–1256.e11

    Abstract: ... 57; 71.6-92.1%).: Conclusion: The Abbott SARS-CoV-2 IgG test has high specificity. Clinical ... positive patients and 163 non-COVID-19 patients were tested for antibody with the Abbott SARS-CoV-2 IgG ... CoV-2 IgG assay in COVID-19 patients.: Methods: Residual sera from 177 symptomatic SARS-CoV-2 ...

    Abstract Objective: This study aimed to evaluate the diagnostic performance of the Abbott Architect SARS-CoV-2 IgG assay in COVID-19 patients.
    Methods: Residual sera from 177 symptomatic SARS-CoV-2-positive patients and 163 non-COVID-19 patients were tested for antibody with the Abbott SARS-CoV-2 IgG assay (Abbott Diagnostics, Chicago, USA). Clinical records for COVID-19 patients were reviewed to determine the time from onset of clinical illness to testing.
    Results: Specificity of the assay was 100.0% (95%CI: 97.1-100.0%). The clinical sensitivity of the assay varied depending on time from onset of symptoms, increasing with longer periods from the onset of clinical illness. The clinical sensitivity at ≤6 days was 8.6% (7/81; 95%CI: 3.8-17.5%), at 7-13 days 43.6% (17/39; 95%CI: 28.2-60.2%), at 14-20 days 84.0% (21/25; 95%CI: 63.1-94.7%), and at ≥21 days 84.4% (27/32; 95%CI: 66.5-94.1%). Clinical sensitivity was higher in the ≥14-day group compared to <14 days. There were no differences between the 14-20-day and ≥21-days groups; the combined clinical sensitivity for these groups (≥14 days) was 84.2% (49/57; 71.6-92.1%).
    Conclusion: The Abbott SARS-CoV-2 IgG test has high specificity. Clinical sensitivity was limited in the early stages of disease but improved from 14 days after the onset of clinical symptoms.
    MeSH term(s) Antibodies, Viral/blood ; Antibody Formation ; COVID-19/diagnosis ; COVID-19 Serological Testing/methods ; Humans ; Immunoglobulin G/blood ; Sensitivity and Specificity ; Singapore ; Time Factors
    Chemical Substances Antibodies, Viral ; Immunoglobulin G
    Keywords covid19
    Language English
    Publishing date 2020-06-09
    Publishing country England
    Document type Evaluation Study ; Journal Article
    ZDB-ID 1328418-6
    ISSN 1469-0691 ; 1470-9465 ; 1198-743X
    ISSN (online) 1469-0691
    ISSN 1470-9465 ; 1198-743X
    DOI 10.1016/j.cmi.2020.05.036
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Clinical evaluation of serological IgG antibody response on the Abbott Architect for established SARS-CoV-2 infection

    Chew, K.L. / Tan, S.S. / Saw, S. / Pajarillaga, A. / Zaine, S. / Khoo, C. / Wang, W. / Tambyah, P. / Jureen, R. / Sethi, S.K.

    Clinical Microbiology and Infection

    2020  Volume 26, Issue 9, Page(s) 1256.e9–1256.e11

    Keywords Microbiology (medical) ; Infectious Diseases ; General Medicine ; covid19
    Language English
    Publisher Elsevier BV
    Publishing country us
    Document type Article ; Online
    ZDB-ID 1328418-6
    ISSN 1469-0691 ; 1470-9465 ; 1198-743X
    ISSN (online) 1469-0691
    ISSN 1470-9465 ; 1198-743X
    DOI 10.1016/j.cmi.2020.05.036
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article: Clinical evaluation of serological IgG antibody response on the Abbott Architect for established SARS-CoV-2 infection

    Chew, K L / Tan, S S / Saw, S / Pajarillaga, A / Zaine, S / Khoo, C / Wang, W / Tambyah, P / Jureen, R / Sethi, S K

    Clin. microbiol. infect

    Abstract: ... patients and 163 non-COVID-19 patients were tested for antibody with the Abbott SARS-CoV-2 IgG assay ... days) was 84.2% (49/57; 71.6-92.1%). CONCLUSION: The Abbott SARS-CoV-2 IgG test has high specificity ... OBJECTIVE: This study aimed to evaluate the diagnostic performance of the Abbott Architect SARS-CoV ...

    Abstract OBJECTIVE: This study aimed to evaluate the diagnostic performance of the Abbott Architect SARS-CoV-2 IgG assay in COVID-19 patients. METHODS: Residual sera from 177 symptomatic SARS-CoV-2-positive patients and 163 non-COVID-19 patients were tested for antibody with the Abbott SARS-CoV-2 IgG assay (Abbott Diagnostics, Chicago, USA). Clinical records for COVID-19 patients were reviewed to determine the time from onset of clinical illness to testing. RESULTS: Specificity of the assay was 100.0% (95%CI: 97.1-100.0%). The clinical sensitivity of the assay varied depending on time from onset of symptoms, increasing with longer periods from the onset of clinical illness. The clinical sensitivity at ≤6 days was 8.6% (7/81; 95%CI: 3.8-17.5%), at 7-13 days 43.6% (17/39; 95%CI: 28.2-60.2%), at 14-20 days 84.0% (21/25; 95%CI: 63.1-94.7%), and at ≥21 days 84.4% (27/32; 95%CI: 66.5-94.1%). Clinical sensitivity was higher in the ≥14-day group compared to <14 days. There were no differences between the 14-20-day and ≥21-days groups; the combined clinical sensitivity for these groups (≥14 days) was 84.2% (49/57; 71.6-92.1%). CONCLUSION: The Abbott SARS-CoV-2 IgG test has high specificity. Clinical sensitivity was limited in the early stages of disease but improved from 14 days after the onset of clinical symptoms.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #591567
    Database COVID19

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