2023年加拿大炎症性肠病的影响:COVID-19和IBD

Gilaad G Kaplan, M Ellen Kuenzig, Joseph W Windsor, Charles N Bernstein, Alain Bitton, Stephanie Coward, Jennifer L Jones, Kate Lee, Sanjay K Murthy, Laura E Targownik, Juan-Nicolás Peña-Sánchez, Sara Ghandeharian, Noelle Rohatinsky, Jake Weinstein, Tyrel Jones May, Mira Browne, Nazanin Jannati, Sahar Tabatabavakili, James H B Im, Saketh Meka, Sonya Vukovic, Tal Davis, Quinn Goddard, Julia Gorospe, Taylor Stocks, Léa Caplan, Najla Kanaan, Daniel Stuart, Tesa Ramsay, Kelly J Robinson, Diane Charron-Bishop, Eric I Benchimol
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引用次数: 0

摘要

2019冠状病毒病大流行对炎症性肠病(IBD)社区产生了巨大影响。在大流行开始时,人们缺乏关于SARS-CoV-2对IBD影响的知识,特别是在免疫系统受到药物抑制的人群中。在整个大流行期间,科学文献呈指数级增长,导致了针对IBD患者的临床指导和疫苗建议。加拿大克罗恩病和结肠炎部成立了COVID-19和IBD工作组,以处理和交流将知识迅速转化为IBD患者及其护理人员、医疗保健提供者和政策制定者的指导。大流行开始时的建议是基于对以往病毒的经验的推测,并考虑到预防原则。我们现在知道,IBD患者感染COVID-19的风险与一般人群相同。与健康人群一样,高龄和合并症会增加罹患严重COVID-19的风险。活跃发作和/或需要高剂量强的松治疗的IBD患者容易出现严重的COVID-19结局。因此,建议使用维持疗法(如生物制剂)。IBD患者的三剂量mRNA COVID-19疫苗方案产生了强大的抗体反应,其不良事件概况与一般人群相似。已观察到接种疫苗后出现突破性感染,特别是随着病毒继续进化,这支持接受二价疫苗增强剂。关于IBD及其治疗对COVID-19后长期预后影响的数据有限。有必要进行研究,以解决在不断演变的大流行期间IBD患者出现的新问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The 2023 Impact of Inflammatory Bowel Disease in Canada: COVID-19 and IBD.

The COVID-19 pandemic had a monumental impact on the inflammatory bowel disease (IBD) community. At the beginning of the pandemic, knowledge on the effect of SARS-CoV-2 on IBD was lacking, especially in those with medication-suppressed immune systems. Throughout the pandemic, scientific literature exponentially expanded, resulting in clinical guidance and vaccine recommendations for individuals with IBD. Crohn's and Colitis Canada established the COVID-19 and IBD Taskforce to process and communicate rapidly transforming knowledge into guidance for individuals with IBD and their caregivers, healthcare providers, and policy makers. Recommendations at the onset of the pandemic were based on conjecture from experience of prior viruses, with a precautionary principle in mind. We now know that the risk of acquiring COVID-19 in those with IBD is the same as the general population. As with healthy populations, advanced age and comorbidities increase the risk for severe COVID-19. Individuals with IBD who are actively flaring and/or who require high doses of prednisone are susceptible to severe COVID-19 outcomes. Consequently, sustaining maintenance therapies (e.g., biologics) is recommended. A three-dose mRNA COVID-19 vaccine regimen in those with IBD produces a robust antibody response with a similar adverse event profile as the general population. Breakthrough infections following vaccine have been observed, particularly as the virus continues to evolve, which supports receiving a bivalent vaccine booster. Limited data exist on the impact of IBD and its therapies on long-term outcomes following COVID-19. Ongoing research is necessary to address new concerns manifesting in those with IBD throughout the evolving pandemic.

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