The diagnostic value of platelet distribution width in patients with mild COVID‐19

COVID‐19 has a worldwide distribution; however, there is no effective diagnosis marker, especially for the mild‐type COVID‐19. The purpose of the current study was to identify parameters for mild‐type COVID‐19. We retrospectively analyzed a single‐center data of patients with mild COVID‐19. Forty pa...

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Detalles Bibliográficos
Autores principales: Wang, Yan, Fan, Zhe, Wang, Shuang, Zhuang, Chengjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8059752/
https://www.ncbi.nlm.nih.gov/pubmed/33772893
http://dx.doi.org/10.1002/jcla.23703
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author Wang, Yan
Fan, Zhe
Wang, Shuang
Zhuang, Chengjun
author_facet Wang, Yan
Fan, Zhe
Wang, Shuang
Zhuang, Chengjun
author_sort Wang, Yan
collection PubMed
description COVID‐19 has a worldwide distribution; however, there is no effective diagnosis marker, especially for the mild‐type COVID‐19. The purpose of the current study was to identify parameters for mild‐type COVID‐19. We retrospectively analyzed a single‐center data of patients with mild COVID‐19. Forty patients diagnosed with COVID‐19 were enrolled. Peripheral blood indices between the admission and discharge times were collected and analyzed. The platelet distribution width (PDW) was shown to be an indicator of significant change. The receiver operating characteristic curve for PDW was 0.7; the sensitivity and specificity for PDW were 82.5% and 55.0%, respectively. Therefore, a potential diagnostic value of PDW for mild‐type COVID‐19 was demonstrated.
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spelling pubmed-80597522021-04-23 The diagnostic value of platelet distribution width in patients with mild COVID‐19 Wang, Yan Fan, Zhe Wang, Shuang Zhuang, Chengjun J Clin Lab Anal Brief Report COVID‐19 has a worldwide distribution; however, there is no effective diagnosis marker, especially for the mild‐type COVID‐19. The purpose of the current study was to identify parameters for mild‐type COVID‐19. We retrospectively analyzed a single‐center data of patients with mild COVID‐19. Forty patients diagnosed with COVID‐19 were enrolled. Peripheral blood indices between the admission and discharge times were collected and analyzed. The platelet distribution width (PDW) was shown to be an indicator of significant change. The receiver operating characteristic curve for PDW was 0.7; the sensitivity and specificity for PDW were 82.5% and 55.0%, respectively. Therefore, a potential diagnostic value of PDW for mild‐type COVID‐19 was demonstrated. John Wiley and Sons Inc. 2021-03-27 /pmc/articles/PMC8059752/ /pubmed/33772893 http://dx.doi.org/10.1002/jcla.23703 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Brief Report
Wang, Yan
Fan, Zhe
Wang, Shuang
Zhuang, Chengjun
The diagnostic value of platelet distribution width in patients with mild COVID‐19
title The diagnostic value of platelet distribution width in patients with mild COVID‐19
title_full The diagnostic value of platelet distribution width in patients with mild COVID‐19
title_fullStr The diagnostic value of platelet distribution width in patients with mild COVID‐19
title_full_unstemmed The diagnostic value of platelet distribution width in patients with mild COVID‐19
title_short The diagnostic value of platelet distribution width in patients with mild COVID‐19
title_sort diagnostic value of platelet distribution width in patients with mild covid‐19
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8059752/
https://www.ncbi.nlm.nih.gov/pubmed/33772893
http://dx.doi.org/10.1002/jcla.23703
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