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A SARS-CoV-2 Prediction Model from Standard Laboratory Tests.

Identifieur interne : 000851 ( Main/Exploration ); précédent : 000850; suivant : 000852

A SARS-CoV-2 Prediction Model from Standard Laboratory Tests.

Auteurs : Vafa Bayat [États-Unis] ; Steven Phelps [États-Unis] ; Russell Ryono [États-Unis] ; Chong Lee [États-Unis] ; Hemal Parekh [États-Unis] ; Joel Mewton [États-Unis] ; Farshid Sedghi [États-Unis] ; Payam Etminani [États-Unis] ; Mark Holodniy [États-Unis]

Source :

RBID : pubmed:32785701

Abstract

BACKGROUND

With the limited availability of testing for the presence of the SARS-CoV-2 virus and concerns surrounding the accuracy of existing methods, other means of identifying patients are urgently needed. Previous studies showing a correlation between certain laboratory tests and diagnosis suggest an alternative method based on an ensemble of tests.

METHODS

We have trained a machine learning model to analyze the correlation between SARS-CoV-2 test results and 20 routine laboratory tests collected within a 2-day period around the SARS-CoV-2 test date. We used the model to compare SARS-CoV-2 positive and negative patients.

RESULTS

In a cohort of 75,991 veteran inpatients and outpatients who tested for SARS-CoV-2 in the months of March through July, 2020, 7,335 of whom were positive by RT-PCR or antigen testing, and who had at least 15 of 20 lab results within the window period, our model predicted the results of the SARS-CoV-2 test with a specificity of 86.8%, a sensitivity of 82.4%, and an overall accuracy of 86.4% (with a 95% confidence interval of [86.0%, 86.9%]).

CONCLUSIONS

While molecular-based and antibody tests remain the reference standard method for confirming a SARS-CoV-2 diagnosis, their clinical sensitivity is not well known. The model described herein may provide a complementary method of determining SARS-CoV-2 infection status, based on a fully independent set of indicators, that can help confirm results from other tests as well as identify positive cases missed by molecular testing.


DOI: 10.1093/cid/ciaa1175
PubMed: 32785701
PubMed Central: PMC7454351


Affiliations:


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<b>BACKGROUND</b>
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<p>With the limited availability of testing for the presence of the SARS-CoV-2 virus and concerns surrounding the accuracy of existing methods, other means of identifying patients are urgently needed. Previous studies showing a correlation between certain laboratory tests and diagnosis suggest an alternative method based on an ensemble of tests.</p>
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<b>METHODS</b>
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<p>We have trained a machine learning model to analyze the correlation between SARS-CoV-2 test results and 20 routine laboratory tests collected within a 2-day period around the SARS-CoV-2 test date. We used the model to compare SARS-CoV-2 positive and negative patients.</p>
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<b>RESULTS</b>
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<p>In a cohort of 75,991 veteran inpatients and outpatients who tested for SARS-CoV-2 in the months of March through July, 2020, 7,335 of whom were positive by RT-PCR or antigen testing, and who had at least 15 of 20 lab results within the window period, our model predicted the results of the SARS-CoV-2 test with a specificity of 86.8%, a sensitivity of 82.4%, and an overall accuracy of 86.4% (with a 95% confidence interval of [86.0%, 86.9%]).</p>
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<p>While molecular-based and antibody tests remain the reference standard method for confirming a SARS-CoV-2 diagnosis, their clinical sensitivity is not well known. The model described herein may provide a complementary method of determining SARS-CoV-2 infection status, based on a fully independent set of indicators, that can help confirm results from other tests as well as identify positive cases missed by molecular testing.</p>
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<name sortKey="Holodniy, Mark" sort="Holodniy, Mark" uniqKey="Holodniy M" first="Mark" last="Holodniy">Mark Holodniy</name>
<name sortKey="Lee, Chong" sort="Lee, Chong" uniqKey="Lee C" first="Chong" last="Lee">Chong Lee</name>
<name sortKey="Mewton, Joel" sort="Mewton, Joel" uniqKey="Mewton J" first="Joel" last="Mewton">Joel Mewton</name>
<name sortKey="Parekh, Hemal" sort="Parekh, Hemal" uniqKey="Parekh H" first="Hemal" last="Parekh">Hemal Parekh</name>
<name sortKey="Phelps, Steven" sort="Phelps, Steven" uniqKey="Phelps S" first="Steven" last="Phelps">Steven Phelps</name>
<name sortKey="Ryono, Russell" sort="Ryono, Russell" uniqKey="Ryono R" first="Russell" last="Ryono">Russell Ryono</name>
<name sortKey="Sedghi, Farshid" sort="Sedghi, Farshid" uniqKey="Sedghi F" first="Farshid" last="Sedghi">Farshid Sedghi</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/CovidStanfordV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000851 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000851 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    CovidStanfordV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     pubmed:32785701
   |texte=   A SARS-CoV-2 Prediction Model from Standard Laboratory Tests.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:32785701" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a CovidStanfordV1 

Wicri

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Data generation: Tue Feb 2 21:24:25 2021. Site generation: Tue Feb 2 21:26:08 2021