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Aspects of inflammatory bowel disease during the COVID-19 pandemic and general considerations()

So far, available evidence suggests that patients with inflammatory bowel disease (IBD) are not at greater risk for developing COVID-19 infection. In regard to patients with IBD remission: 5-aminosalycylates (5-ASAs) do not increase the risk for infection and should be continued. There is no need to...

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Autores principales: de León-Rendón, J.L., Hurtado-Salazar, C., Yamamoto-Furusho, J.K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asociación Mexicana de Gastroenterología. Published by Masson Doyma México S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321053/
http://dx.doi.org/10.1016/j.rgmxen.2020.05.001
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author de León-Rendón, J.L.
Hurtado-Salazar, C.
Yamamoto-Furusho, J.K.
author_facet de León-Rendón, J.L.
Hurtado-Salazar, C.
Yamamoto-Furusho, J.K.
author_sort de León-Rendón, J.L.
collection PubMed
description So far, available evidence suggests that patients with inflammatory bowel disease (IBD) are not at greater risk for developing COVID-19 infection. In regard to patients with IBD remission: 5-aminosalycylates (5-ASAs) do not increase the risk for infection and should be continued. There is no need to suspend them or lower the dose. Immunomodulating drugs, such as thiopurines and methotrexate, should be continued, without modifying doses (even in patients with positive SARS-CoV-2 infection). No type of biologic therapy should be suspended, unless there are signs of COVID-19. Regarding patients with IBD activity: the oral and/or topical 5-ASA dose should be optimized in cases of disease relapse. Budesonide MMX should be considered in cases of mild-to-moderate activity, to avoid systemic steroid use. Systemic steroids should be avoided whenever possible because doses above 20 mg per day have an immunosuppressive effect, which could increase susceptibility to any type of infection, including COVID-19. The combined use of thiopurines with steroids and/or tumor necrosis factor (TNF) monoclonal antibodies should also be avoided because those combinations can increase the risk for infections, including COVID-19. Finally, biologic treatment with anti-TNF-alpha agents or any other mechanism of action, such as anti-integrins or anti-interleukins, should be suspended if patients become infected with SARS-CoV-2. The drugs can be restarted once the infectious process is resolved.
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spelling pubmed-73210532020-06-29 Aspects of inflammatory bowel disease during the COVID-19 pandemic and general considerations() de León-Rendón, J.L. Hurtado-Salazar, C. Yamamoto-Furusho, J.K. Revista de Gastroenterología de México (English Edition) Article So far, available evidence suggests that patients with inflammatory bowel disease (IBD) are not at greater risk for developing COVID-19 infection. In regard to patients with IBD remission: 5-aminosalycylates (5-ASAs) do not increase the risk for infection and should be continued. There is no need to suspend them or lower the dose. Immunomodulating drugs, such as thiopurines and methotrexate, should be continued, without modifying doses (even in patients with positive SARS-CoV-2 infection). No type of biologic therapy should be suspended, unless there are signs of COVID-19. Regarding patients with IBD activity: the oral and/or topical 5-ASA dose should be optimized in cases of disease relapse. Budesonide MMX should be considered in cases of mild-to-moderate activity, to avoid systemic steroid use. Systemic steroids should be avoided whenever possible because doses above 20 mg per day have an immunosuppressive effect, which could increase susceptibility to any type of infection, including COVID-19. The combined use of thiopurines with steroids and/or tumor necrosis factor (TNF) monoclonal antibodies should also be avoided because those combinations can increase the risk for infections, including COVID-19. Finally, biologic treatment with anti-TNF-alpha agents or any other mechanism of action, such as anti-integrins or anti-interleukins, should be suspended if patients become infected with SARS-CoV-2. The drugs can be restarted once the infectious process is resolved. Asociación Mexicana de Gastroenterología. Published by Masson Doyma México S.A. 2020 2020-06-28 /pmc/articles/PMC7321053/ http://dx.doi.org/10.1016/j.rgmxen.2020.05.001 Text en © 2020 Asociación Mexicana de Gastroenterología. Published by Masson Doyma México S.A. 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
de León-Rendón, J.L.
Hurtado-Salazar, C.
Yamamoto-Furusho, J.K.
Aspects of inflammatory bowel disease during the COVID-19 pandemic and general considerations()
title Aspects of inflammatory bowel disease during the COVID-19 pandemic and general considerations()
title_full Aspects of inflammatory bowel disease during the COVID-19 pandemic and general considerations()
title_fullStr Aspects of inflammatory bowel disease during the COVID-19 pandemic and general considerations()
title_full_unstemmed Aspects of inflammatory bowel disease during the COVID-19 pandemic and general considerations()
title_short Aspects of inflammatory bowel disease during the COVID-19 pandemic and general considerations()
title_sort aspects of inflammatory bowel disease during the covid-19 pandemic and general considerations()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321053/
http://dx.doi.org/10.1016/j.rgmxen.2020.05.001
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