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The Model for Early COvid-19 Recognition (MECOR) Score: A Proof-of-Concept for a Simple and Low-Cost Tool to Recognize a Possible Viral Etiology in Community-Acquired Pneumonia Patients during COVID-19 Outbreak

Academic Article
Publication Date:
2020
abstract:
This study aims to assess the peripheral blood cell count “signature” of Severe Acute Respiratory Syndrome-Coronavirus 2 (SARS-CoV-2) to discriminate promptly between COronaVIrus Disease 19 (COVID-19) and community-acquired pneumonia (CAP). We designed a retrospective case-control study, enrolling 525 patients (283 COVID-19 and 242 with CAP). All patients had a fever and at least one of the following signs: cough, chest pain, or dyspnea. We excluded patients treated with immunosuppressants, steroids, or affected by diseases known to modify blood cell count. COVID-19 patients showed a significant reduction in white blood cells (neutrophils, lymphocytes, monocytes, eosinophils) and platelets. We studied these parameters univariately, combined the significant ones in a multivariate model (AUROC 0.86, Nagelkerke PSEUDO-R2 0.5, Hosmer–Lemeshow p-value 0.9) and examined its discriminative performance in an internally-randomized validation cohort (AUROC 0.84). The cut-off selected according to Youden’s Index (−0.13) showed a sensitivity of 84% and a specificity of 72% in the training cohort, and a sensitivity of 88% and a specificity of 73% in the validation cohort. In addition, we determined the probability of having COVID-19 pneumonia for each Model for possible Early COvid-19 Recognition (MECOR) Score value. In conclusion, our model could provide a simple, rapid, and cheap tool for prompt COVID-19 diagnostic triage in patients with CAP. The actual effectiveness should be evaluated in further, prospective studies also involving COVID-19 patients with negative nasopharyngeal swabs.
Iris type:
1.1 Articolo in rivista
Keywords:
Blood cell count; Coronavirus; COVID-19; Diagnosis; Interstitial lung disease; Neutrophils; Platelets; Pneumonia; SARS-CoV-2; Triage
List of contributors:
Sambataro, G.; Giuffre, M.; Sambataro, D.; Palermo, A.; Vignigni, G.; Cesareo, R.; Crimi, N.; Torrisi, S. E.; Vancheri, C.; Malatino, L.; Colaci, M.; Del Papa, N.; Pignataro, F.; Roman-Pognuz, E.; Fabbiani, M.; Montagnani, F.; Cassol, C.; Cavagna, L.; Zuccaro, V.; Zerbato, V.; Maurel, C.; Luzzati, R.; Di Bella, S.
Authors of the University:
CAVAGNA LORENZO
Handle:
https://iris.unipv.it/handle/11571/1438908
Published in:
DIAGNOSTICS
Journal
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https://watermark.silverchair.com/keaa793.pdf?token=AQECAHi208BE49Ooan9kkhW_Ercy7Dm3ZL_9Cf3qfKAc485ysgAAAwkwggMFBgkqhkiG9w0BBwagggL2MIIC8gIBADCCAusGCSqGSIb3DQEHATAeBglghkgBZQMEAS4wEQQMDCcvKQ29G2RyzPIRAgEQgIICvA80xbIpHjQOGIous8sj9vH2K77ah5LhpShhuqRNXWSDuiCHRF9iyv7SazS6v5nEJUMflaKrtl8k1D9cPcvSMzUsjZnMHTYhpHESCBndQSLdoFhVC7OTca98chC8oLq8FAlREbjuo2hWsSU3ZGJp3uuuR5PR0cmIB05TDvbMgsSysDkMqhuD_i0vIJa98V4XAkeJRjIYiquWIzd_bezASUBuJxtud7Tju9DB2WTdWpZQpYiOMTOvkWxEmlJbfI64iSkwwVib8O9UiIm7_eCs7aHz7cnK34QavmY305U0axjjIjLUb81BdZOemWJdnN8Z_od3xSyZmZcshCdU-Pml4O_mckFcgWRb264rZK0pSCcBODKxMXLvm0RZPZM3ah9vI9FE4lP3BcFdcOYglzXsX9gpQWYkSpQ0e0QI3Vcr0NpEJrYFcQ7DI2QxnkHL17t3m5Jsq1sf2v6x8ozE7OA0EiyJp_MFBy9cVJYwub6Hs4GEl-EzMLvyP11QPkNoeanau6IYC_tbnQH4i4VvFmB1ZPcy8ImCEbNLNtgB2bVwpeV88Yrn_Cvth4vqZ9EGXwv2s38MVoto-ro5A9kLISwi3_dEfiN7xTuWEjRNGLJ-tcRkZzUHiUP8P83tVdWmpUI_FgmEowMEgDzk6kcEmvl6Psz4WneSYGZduG7mvEIOUYxMxNC4p1OLWpDU-RLDOkEB1htjWnB7-WmPOlcPs_cu3O4cmK8oRE6LKZ4VEL3_FKdPsOOqPgG25EgOC46CUuHGZtYaSVjJKWqnlZU8_cETKf-Cb_JSdGFUaiT_3juUtL2DywkMIUHfRdDopMj53CZVxak79u_rpVUAG9lv3zIme8hmQLZaA95IgFuIOOOR4mlWs2JCDzGhsgMkmGTiHsvcykapo9d8QmbZWwxGzr5Z8tmdkYArV7Q7v8PRz0o
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