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COVID-19 outcomes in patients with Dermatomyositis: A registry-based cohort analysis

Background: Patients with rheumatic diseases (RDs) like DM are known to be vulnerable towards various types of infections due to aggressive disease activity mandating high dose immunosuppressive therapy. The severity of COVID-19 in RDs is limited in literature due to the heterogeneous nature of the...

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Autores principales: Pakhchanian, Haig, Khan, Hiba, Raiker, Rahul, Ahmed, Sakir, Kavadichanda, Chengappa, Abbasi, Maryam, Kardeş, Sinan, Agarwal, Vikas, Aggarwal, Rohit, Gupta, Latika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142211/
https://www.ncbi.nlm.nih.gov/pubmed/35750526
http://dx.doi.org/10.1016/j.semarthrit.2022.152034
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author Pakhchanian, Haig
Khan, Hiba
Raiker, Rahul
Ahmed, Sakir
Kavadichanda, Chengappa
Abbasi, Maryam
Kardeş, Sinan
Agarwal, Vikas
Aggarwal, Rohit
Gupta, Latika
author_facet Pakhchanian, Haig
Khan, Hiba
Raiker, Rahul
Ahmed, Sakir
Kavadichanda, Chengappa
Abbasi, Maryam
Kardeş, Sinan
Agarwal, Vikas
Aggarwal, Rohit
Gupta, Latika
author_sort Pakhchanian, Haig
collection PubMed
description Background: Patients with rheumatic diseases (RDs) like DM are known to be vulnerable towards various types of infections due to aggressive disease activity mandating high dose immunosuppressive therapy. The severity of COVID-19 in RDs is limited in literature due to the heterogeneous nature of the condition. Therefore, specific details on mortality is essential to navigate any precautions required in the treatment. Objectives: To determine outcomes of COVID-19 in DM as compared to controls, and identify the risk association of gender, race, interstitial lung disease, neoplasms, and use of immunosuppressant. Methods: Retrospective data of individuals with DM and COVID-19 and the general population with COVID-19 between January 2020 to August 2021 was retrieved from the TriNetX database. 1:1 Propensity Score matching was used to adjust for confounders. We assessed COVID-19 outcomes such as mortality, hospitalisation, ICU admission, severe COVID-19, mechanical ventilation (MV), acute kidney injury (AKI), venous thromboembolism (VTE), ischemic stroke, acute respiratory distress syndrome (ARDS), renal replacement therapy (RRT) and sepsis. Subgroup analyses included gender, race, ILD, cancer patients, disease-modifying rheumatic drugs (DMARDs) use, and glucocorticoids (GC) use. Results: We identified 5,574 DM patients with COVID-19, and 5,574 general population with COVID-19 (controls). DM with COVID-19 had a lower risk of mortality in comparison to controls [RR 0.76], hospitalisation [RR 0.8], severe COVID-19 [RR 0.76], AKI [RR 0.83], and sepsis [RR 0.73]. Males and African Americans were more likely to develop AKI [RR 1.35, 1.65], while African Americans had higher odds for severe COVID-19 [RR 1.62] and VTE [RR 1.54]. DM with ILD group also experienced higher odds for severe COVID-19 infection [RR 1.64], and VTE [RR 2.06]. DM patients receiving DMARDs and glucocorticoids had higher odds for hospitalisation [RR 1.46, 2.12], and sepsis [RR 3.25, 2.4] Subgroup analysis of 5-year neoplasm history amongst DM patients with COVID-19 was inadequate for meaningful comparison. Conclusion: Dermatomyositis patients without comorbities have reasonable COVID-19 outcomes including mortality and hospitalisation. Black race, male gender, ILD, DMARDS and glucocorticoid users, are associated with poor outcomes.
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spelling pubmed-91422112022-05-31 COVID-19 outcomes in patients with Dermatomyositis: A registry-based cohort analysis Pakhchanian, Haig Khan, Hiba Raiker, Rahul Ahmed, Sakir Kavadichanda, Chengappa Abbasi, Maryam Kardeş, Sinan Agarwal, Vikas Aggarwal, Rohit Gupta, Latika Semin Arthritis Rheum Article Background: Patients with rheumatic diseases (RDs) like DM are known to be vulnerable towards various types of infections due to aggressive disease activity mandating high dose immunosuppressive therapy. The severity of COVID-19 in RDs is limited in literature due to the heterogeneous nature of the condition. Therefore, specific details on mortality is essential to navigate any precautions required in the treatment. Objectives: To determine outcomes of COVID-19 in DM as compared to controls, and identify the risk association of gender, race, interstitial lung disease, neoplasms, and use of immunosuppressant. Methods: Retrospective data of individuals with DM and COVID-19 and the general population with COVID-19 between January 2020 to August 2021 was retrieved from the TriNetX database. 1:1 Propensity Score matching was used to adjust for confounders. We assessed COVID-19 outcomes such as mortality, hospitalisation, ICU admission, severe COVID-19, mechanical ventilation (MV), acute kidney injury (AKI), venous thromboembolism (VTE), ischemic stroke, acute respiratory distress syndrome (ARDS), renal replacement therapy (RRT) and sepsis. Subgroup analyses included gender, race, ILD, cancer patients, disease-modifying rheumatic drugs (DMARDs) use, and glucocorticoids (GC) use. Results: We identified 5,574 DM patients with COVID-19, and 5,574 general population with COVID-19 (controls). DM with COVID-19 had a lower risk of mortality in comparison to controls [RR 0.76], hospitalisation [RR 0.8], severe COVID-19 [RR 0.76], AKI [RR 0.83], and sepsis [RR 0.73]. Males and African Americans were more likely to develop AKI [RR 1.35, 1.65], while African Americans had higher odds for severe COVID-19 [RR 1.62] and VTE [RR 1.54]. DM with ILD group also experienced higher odds for severe COVID-19 infection [RR 1.64], and VTE [RR 2.06]. DM patients receiving DMARDs and glucocorticoids had higher odds for hospitalisation [RR 1.46, 2.12], and sepsis [RR 3.25, 2.4] Subgroup analysis of 5-year neoplasm history amongst DM patients with COVID-19 was inadequate for meaningful comparison. Conclusion: Dermatomyositis patients without comorbities have reasonable COVID-19 outcomes including mortality and hospitalisation. Black race, male gender, ILD, DMARDS and glucocorticoid users, are associated with poor outcomes. The Authors. Published by Elsevier Inc. 2022-10 2022-05-28 /pmc/articles/PMC9142211/ /pubmed/35750526 http://dx.doi.org/10.1016/j.semarthrit.2022.152034 Text en © 2022 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Pakhchanian, Haig
Khan, Hiba
Raiker, Rahul
Ahmed, Sakir
Kavadichanda, Chengappa
Abbasi, Maryam
Kardeş, Sinan
Agarwal, Vikas
Aggarwal, Rohit
Gupta, Latika
COVID-19 outcomes in patients with Dermatomyositis: A registry-based cohort analysis
title COVID-19 outcomes in patients with Dermatomyositis: A registry-based cohort analysis
title_full COVID-19 outcomes in patients with Dermatomyositis: A registry-based cohort analysis
title_fullStr COVID-19 outcomes in patients with Dermatomyositis: A registry-based cohort analysis
title_full_unstemmed COVID-19 outcomes in patients with Dermatomyositis: A registry-based cohort analysis
title_short COVID-19 outcomes in patients with Dermatomyositis: A registry-based cohort analysis
title_sort covid-19 outcomes in patients with dermatomyositis: a registry-based cohort analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142211/
https://www.ncbi.nlm.nih.gov/pubmed/35750526
http://dx.doi.org/10.1016/j.semarthrit.2022.152034
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