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Venous Thromboembolism, Corticosteroids and COVID-19: A Systematic Review and Meta-Analysis

The novel coronavirus disease 2019 (COVID-19) predisposes patients to venous thromboembolism (VTE) due to risk factors, severe infection, and severe inflammatory responses. The objective is to determine the risk of developing VTE after corticosteroid administration during COVID-19 treatment. Using P...

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Autores principales: Sarfraz, Azza, Sarfraz, Zouina, Razzack, Aminah Abdul, Patel, Gaurav, Sarfraz, Muzna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883150/
https://www.ncbi.nlm.nih.gov/pubmed/33571009
http://dx.doi.org/10.1177/1076029621993573
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author Sarfraz, Azza
Sarfraz, Zouina
Razzack, Aminah Abdul
Patel, Gaurav
Sarfraz, Muzna
author_facet Sarfraz, Azza
Sarfraz, Zouina
Razzack, Aminah Abdul
Patel, Gaurav
Sarfraz, Muzna
author_sort Sarfraz, Azza
collection PubMed
description The novel coronavirus disease 2019 (COVID-19) predisposes patients to venous thromboembolism (VTE) due to risk factors, severe infection, and severe inflammatory responses. The objective is to determine the risk of developing VTE after corticosteroid administration during COVID-19 treatment. Using PRISMA reporting guidelines, a review was conducted from inception until 20 September 2020 with MESH terms including “venous thromboembolism” and “covid-19,” using MEDLINE, Scopus, CINAHL Plus, and WHO Global Database. The inclusion criteria included studies with COVID-19 patients aged 18 years and older with VTE diagnosed by duplex ultrasonography or computed tomography pulmonary angiography (CTPA). Exclusion criteria were studies with non COVID-19 patients and non-VTE patients aged less than 18 years. Quality appraisal was conducted of included studies using the Newcastle-Ottawa Scale (NOS). A random-effect model using 95% confidence intervals, and significance of findings was assessed using Review Manager V5.4.We included 12 observational studies with 2801 patients (VTE n = 434; non-VTE; n = 2367). Patients had a higher risk of presenting with VTE when being administered corticosteroids during treatment of COVID-19 (RR = 1.39, 95% CI = 1.10 to 1.77, I(2) = 0%). A positive effect size was found (SMD = 1.00, 95% CI = 0.67 to 1.32, I(2) = 85%) for D-dimer laboratory values (µg/mL) in the VTE group. While critically ill COVID-19 patients are more likely to require corticosteroid treatment, it may be associated with increased risk of VTE, and poor clinical prognosis. Risk assessment is warranted to further evaluate patients as case-by-case in reducing VTE and worsening clinical outcomes.
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spelling pubmed-78831502021-02-23 Venous Thromboembolism, Corticosteroids and COVID-19: A Systematic Review and Meta-Analysis Sarfraz, Azza Sarfraz, Zouina Razzack, Aminah Abdul Patel, Gaurav Sarfraz, Muzna Clin Appl Thromb Hemost Review The novel coronavirus disease 2019 (COVID-19) predisposes patients to venous thromboembolism (VTE) due to risk factors, severe infection, and severe inflammatory responses. The objective is to determine the risk of developing VTE after corticosteroid administration during COVID-19 treatment. Using PRISMA reporting guidelines, a review was conducted from inception until 20 September 2020 with MESH terms including “venous thromboembolism” and “covid-19,” using MEDLINE, Scopus, CINAHL Plus, and WHO Global Database. The inclusion criteria included studies with COVID-19 patients aged 18 years and older with VTE diagnosed by duplex ultrasonography or computed tomography pulmonary angiography (CTPA). Exclusion criteria were studies with non COVID-19 patients and non-VTE patients aged less than 18 years. Quality appraisal was conducted of included studies using the Newcastle-Ottawa Scale (NOS). A random-effect model using 95% confidence intervals, and significance of findings was assessed using Review Manager V5.4.We included 12 observational studies with 2801 patients (VTE n = 434; non-VTE; n = 2367). Patients had a higher risk of presenting with VTE when being administered corticosteroids during treatment of COVID-19 (RR = 1.39, 95% CI = 1.10 to 1.77, I(2) = 0%). A positive effect size was found (SMD = 1.00, 95% CI = 0.67 to 1.32, I(2) = 85%) for D-dimer laboratory values (µg/mL) in the VTE group. While critically ill COVID-19 patients are more likely to require corticosteroid treatment, it may be associated with increased risk of VTE, and poor clinical prognosis. Risk assessment is warranted to further evaluate patients as case-by-case in reducing VTE and worsening clinical outcomes. SAGE Publications 2021-02-11 /pmc/articles/PMC7883150/ /pubmed/33571009 http://dx.doi.org/10.1177/1076029621993573 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review
Sarfraz, Azza
Sarfraz, Zouina
Razzack, Aminah Abdul
Patel, Gaurav
Sarfraz, Muzna
Venous Thromboembolism, Corticosteroids and COVID-19: A Systematic Review and Meta-Analysis
title Venous Thromboembolism, Corticosteroids and COVID-19: A Systematic Review and Meta-Analysis
title_full Venous Thromboembolism, Corticosteroids and COVID-19: A Systematic Review and Meta-Analysis
title_fullStr Venous Thromboembolism, Corticosteroids and COVID-19: A Systematic Review and Meta-Analysis
title_full_unstemmed Venous Thromboembolism, Corticosteroids and COVID-19: A Systematic Review and Meta-Analysis
title_short Venous Thromboembolism, Corticosteroids and COVID-19: A Systematic Review and Meta-Analysis
title_sort venous thromboembolism, corticosteroids and covid-19: a systematic review and meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883150/
https://www.ncbi.nlm.nih.gov/pubmed/33571009
http://dx.doi.org/10.1177/1076029621993573
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