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Hematological characteristics of patients in coronavirus 19 infection: a systematic review and meta-analysis

Background COVID-19 infection has become a pandemic and a global health issue since its origin in Wuhan, China in December 2019. The present systematic review and meta-analysis aim to assess hematological changes seen in COVID-19 infection and their association with the severity of the disease. Meth...

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Autores principales: Asghar, Muhammad, Hussain, Nooreen, Shoaib, Hasan, Kim, Minchul, Lynch, Teresa J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7598996/
https://www.ncbi.nlm.nih.gov/pubmed/33194119
http://dx.doi.org/10.1080/20009666.2020.1808360
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author Asghar, Muhammad
Hussain, Nooreen
Shoaib, Hasan
Kim, Minchul
Lynch, Teresa J.
author_facet Asghar, Muhammad
Hussain, Nooreen
Shoaib, Hasan
Kim, Minchul
Lynch, Teresa J.
author_sort Asghar, Muhammad
collection PubMed
description Background COVID-19 infection has become a pandemic and a global health issue since its origin in Wuhan, China in December 2019. The present systematic review and meta-analysis aim to assess hematological changes seen in COVID-19 infection and their association with the severity of the disease. Methods Pooled proportions were calculated using both fixed effects model and random effects model. Weighted mean difference and 95% CI were calculated and reported. Results Initial search identified 84 reference articles, 23 relevant articles were selected and reviewed. Compared to general population, the weighted mean difference of WBC count in all COVID-19 patients was lower by 0.97 × 10(9 )mm(3 )(95% CI = –1.29 to –0.66). In severe COVID-19 patients, the weighted mean difference of platelet count was lower by 23.85 × 10(9)/liter (95% CI = –35.18 to –9.53), as compared to general population. The weighted mean difference of prothrombin time, D-Dimer, and fibrinogen in severe COVID-19 patients was higher by 1.92 seconds (95% CI = 0.01 to 3.84), 6.23 mg/liter (95% CI = 0.11 to 12.36) and 1.88 g/liter (95% CI = 1.18 to 2.48) respectively, as compared to general population. Pooled proportion showed D-Dimer to be elevated in 80.00% (95 % CI = 50.00 to 99.00) of severe patients. Conclusions Our meta-analysis shows that patients with COVID-19 have significant thrombocytopenia, leukopenia along with elevated D-dimer, fibrinogen and prothrombin time. These laboratory findings are marked in severe COVID–19 infections and could be helpful in early recognition of severe infection.
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spelling pubmed-75989962020-11-12 Hematological characteristics of patients in coronavirus 19 infection: a systematic review and meta-analysis Asghar, Muhammad Hussain, Nooreen Shoaib, Hasan Kim, Minchul Lynch, Teresa J. J Community Hosp Intern Med Perspect Research Article Background COVID-19 infection has become a pandemic and a global health issue since its origin in Wuhan, China in December 2019. The present systematic review and meta-analysis aim to assess hematological changes seen in COVID-19 infection and their association with the severity of the disease. Methods Pooled proportions were calculated using both fixed effects model and random effects model. Weighted mean difference and 95% CI were calculated and reported. Results Initial search identified 84 reference articles, 23 relevant articles were selected and reviewed. Compared to general population, the weighted mean difference of WBC count in all COVID-19 patients was lower by 0.97 × 10(9 )mm(3 )(95% CI = –1.29 to –0.66). In severe COVID-19 patients, the weighted mean difference of platelet count was lower by 23.85 × 10(9)/liter (95% CI = –35.18 to –9.53), as compared to general population. The weighted mean difference of prothrombin time, D-Dimer, and fibrinogen in severe COVID-19 patients was higher by 1.92 seconds (95% CI = 0.01 to 3.84), 6.23 mg/liter (95% CI = 0.11 to 12.36) and 1.88 g/liter (95% CI = 1.18 to 2.48) respectively, as compared to general population. Pooled proportion showed D-Dimer to be elevated in 80.00% (95 % CI = 50.00 to 99.00) of severe patients. Conclusions Our meta-analysis shows that patients with COVID-19 have significant thrombocytopenia, leukopenia along with elevated D-dimer, fibrinogen and prothrombin time. These laboratory findings are marked in severe COVID–19 infections and could be helpful in early recognition of severe infection. Taylor & Francis 2020-10-29 /pmc/articles/PMC7598996/ /pubmed/33194119 http://dx.doi.org/10.1080/20009666.2020.1808360 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Asghar, Muhammad
Hussain, Nooreen
Shoaib, Hasan
Kim, Minchul
Lynch, Teresa J.
Hematological characteristics of patients in coronavirus 19 infection: a systematic review and meta-analysis
title Hematological characteristics of patients in coronavirus 19 infection: a systematic review and meta-analysis
title_full Hematological characteristics of patients in coronavirus 19 infection: a systematic review and meta-analysis
title_fullStr Hematological characteristics of patients in coronavirus 19 infection: a systematic review and meta-analysis
title_full_unstemmed Hematological characteristics of patients in coronavirus 19 infection: a systematic review and meta-analysis
title_short Hematological characteristics of patients in coronavirus 19 infection: a systematic review and meta-analysis
title_sort hematological characteristics of patients in coronavirus 19 infection: a systematic review and meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7598996/
https://www.ncbi.nlm.nih.gov/pubmed/33194119
http://dx.doi.org/10.1080/20009666.2020.1808360
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