4.8 Review

Recent advances in clinical practice: management of inflammatory bowel disease during the COVID-19 pandemic

期刊

GUT
卷 71, 期 7, 页码 1426-1439

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/gutjnl-2021-326784

关键词

COVID-19; ulcerative colitis; Crohn's disease; immune response; inflammatory bowel disease; SARS-CoV-2; vaccine; antibody

资金

  1. Wellcome GW4-CAT fellowship
  2. Crohn's Colitis UK
  3. InnoHK, The Government of Hong Kong, Special Administrative Region of the People's Republic of China

向作者/读者索取更多资源

This review summarizes the risk and outcomes of COVID-19 in patients with IBD, as well as the latest guidance on SARS-CoV-2 vaccines. Certain medications may be associated with adverse outcomes to COVID-19, while a decrease in endoscopy procedures has led to missed cancer cases.
The COVID-19 pandemic has raised considerable concerns that patients with inflammatory bowel disease (IBD), particularly those treated with immunosuppressive therapies, may have an increased risk of SARS-CoV-2 acquisition, develop worse outcomes following COVID-19, and have suboptimal vaccine response compared with the general population. In this review, we summarise data on the risk of COVID-19 and associated outcomes, and latest guidance on SARS-CoV-2 vaccines in patients with IBD. Emerging evidence suggests that commonly used medications for IBD, such as corticosteroids but not biologicals, were associated with adverse outcomes to COVID-19. There has been no increased risk of de novo, or delayed, IBD diagnoses, however, an overall decrease in endoscopy procedures has led to a rise in the number of missed endoscopic-detected cancers during the pandemic. The impact of IBD medication on vaccine response has been a research priority recently. Data suggest that patients with IBD treated with antitumour necrosis factor (TNF) medications had attenuated humoral responses to SARS-CoV-2 vaccines, and more rapid antibody decay, compared with non-anti-TNF-treated patients. Reassuringly, rates of breakthrough infections and hospitalisations in all patients who received vaccines, irrespective of IBD treatment, remained low. International guidelines recommend that all patients with IBD treated with immunosuppressive therapies should receive, at any point during their treatment cycle, three primary doses of SARS-CoV-2 vaccines with a further booster dose as soon as possible. Future research should focus on our understanding of the rate of antibody decay in biological-treated patients, which patients require additional doses of SARS-CoV-2 vaccine, the long-term risks of COVID-19 on IBD disease course and activity, and the potential risk of long COVID-19 in patients with IBD.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据