COVID‐19 outcomes in patients with inflammatory bowel diseases in Latin America: Results from SECURE‐IBD registry

Background and Aim One of the most impacted regions by the pandemic globally, Latin America is facing socioeconomic and health‐care challenges that can potentially affect disease outcomes. Recent data suggest that inflammatory bowel disease (IBD) patients do not have an increased risk of the develop...

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Published inJournal of Gastroenterology and Hepatology Vol. 36; no. 11; pp. 3033 - 3040
Main Authors Queiroz, Natália S F, Martins, Camilla de Almeida, Quaresma, Abel B, Hino, Adriano A F, Steinwurz, Flavio, Ungaro, Ryan C, Kotze, Paulo G
Format Journal Article Web Resource
LanguageEnglish
Published Australia John Wiley & Sons, Inc 01.11.2021
Wiley Subscription Services, Inc
John Wiley and Sons Inc
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Summary:Background and Aim One of the most impacted regions by the pandemic globally, Latin America is facing socioeconomic and health‐care challenges that can potentially affect disease outcomes. Recent data suggest that inflammatory bowel disease (IBD) patients do not have an increased risk of the development of COVID‐19 complications. However, the impact of COVID‐19 on IBD patients living in least developed areas remains to be fully elucidated. This study aims to describe the outcomes of IBD patients diagnosed with COVID‐19 in countries from Latin America based on data from the SECURE‐IBD registry. Methods Patients from Latin America enrolled in the SECURE‐IBD registry were included. Descriptive analyses were used to summarize clinical and sociodemographic characteristics. The studied outcomes were (i) a composite of need for intensive care unit admission, ventilator use, and/or death (primary outcome) and (ii) a composite of any hospitalization and/or death (secondary outcome). Multivariable regression was used to identify risk factors of severe COVID‐19. Results During the study period, 230 cases (Crohn's disease: n = 115, ulcerative colitis: n = 114, IBD‐unclassified [IBD‐U]: n = 1) were reported to the SECURE‐IBD database from 13 different countries. Primary outcome was observed in 17 (7.4%) patients, and the case fatality rate was 1.7%. In the adjusted multivariable model, the use of systemic corticosteroids (odds ratio [OR] 10.97; 95% confidence interval [CI]: 3.44–34.99) was significantly associated with the primary outcome. Older age (OR 1.03; 95% CI: 1.00–1.05), systemic corticosteroids (OR 9.33; 95% CI: 3.84–22.63), and the concomitant presence of one (OR 2.14; 95% CI: 0.89–5.15) or two (OR 10.67; 95% CI: 1.74–65.72) comorbidities were associated with the outcome of hospitalization or death. Conclusion Inflammatory bowel disease patients with COVID‐19 in Latin America appear to have similar outcomes to the overall global data. Risk factors of severe COVID‐19 are similar to prior reports.
Bibliography:Funding none for this specific study.
N. S. F. Q. has served as a speaker and advisory board member of Janssen, Takeda, and AbbVie. A. A. F. H. and C. A. M. have no conflict of interest. A. B. Q. has received fees for serving as a speaker for AbbVie and Janssen. He also does clinical research for Roche. P. G. K. is a speaker and consultant for AbbVie, Janssen, Pfizer, and Takeda. He also does clinical research for Lilly, Takeda, and Pfizer. R. C. U. has served as an advisory board member or consultant for Eli Lilly, Janssen, Pfizer, and Takeda; research support from AbbVie, Boehringer Ingelheim, and Pfizer. F. S. is a speaker, consultant, and researcher for AbbVie, Novartis, Ferring, Janssen, Pfizer, Sandoz, Takeda, and UCB.
There is a general funding for the creation and maintenance of the SECURE‐IBD database: the Helmsley Charitable Trust (2003‐04445), National Center for Advancing Translational Sciences (UL1TR002489), a T32DK007634 (EJB), and a K23KD111995‐01A1 (RCU). Additional funding provided by Pfizer, Takeda, Janssen, AbbVie, Lilly, Genentech, Boehringer Ingelheim, Bristol Myers Squibb, Celltrion, and Arenapharm.
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Declaration of conflict of interest N. S. F. Q. has served as a speaker and advisory board member of Janssen, Takeda, and AbbVie. A. A. F. H. and C. A. M. have no conflict of interest. A. B. Q. has received fees for serving as a speaker for AbbVie and Janssen. He also does clinical research for Roche. P. G. K. is a speaker and consultant for AbbVie, Janssen, Pfizer, and Takeda. He also does clinical research for Lilly, Takeda, and Pfizer. R. C. U. has served as an advisory board member or consultant for Eli Lilly, Janssen, Pfizer, and Takeda; research support from AbbVie, Boehringer Ingelheim, and Pfizer. F. S. is a speaker, consultant, and researcher for AbbVie, Novartis, Ferring, Janssen, Pfizer, Sandoz, Takeda, and UCB.
Funding none for this specific study. There is a general funding for the creation and maintenance of the SECURE‐IBD database: the Helmsley Charitable Trust (2003‐04445), National Center for Advancing Translational Sciences (UL1TR002489), a T32DK007634 (EJB), and a K23KD111995‐01A1 (RCU). Additional funding provided by Pfizer, Takeda, Janssen, AbbVie, Lilly, Genentech, Boehringer Ingelheim, Bristol Myers Squibb, Celltrion, and Arenapharm.
ISSN:0815-9319
1440-1746
DOI:10.1111/jgh.15588