MbrlCatalogueTitleDetail

Do you wish to reserve the book?
P026 Inflammatory Bowel Disease (IBD) Related Outcomes in Patients Diagnosed With COVID-19
P026 Inflammatory Bowel Disease (IBD) Related Outcomes in Patients Diagnosed With COVID-19
Hey, we have placed the reservation for you!
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
P026 Inflammatory Bowel Disease (IBD) Related Outcomes in Patients Diagnosed With COVID-19
Oops! Something went wrong.
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Title added to your shelf!
Title added to your shelf!
View what I already have on My Shelf.
Oops! Something went wrong.
Oops! Something went wrong.
While trying to add the title to your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
P026 Inflammatory Bowel Disease (IBD) Related Outcomes in Patients Diagnosed With COVID-19
P026 Inflammatory Bowel Disease (IBD) Related Outcomes in Patients Diagnosed With COVID-19

Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
How would you like to get it?
We have requested the book for you! Sorry the robot delivery is not available at the moment
We have requested the book for you!
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
P026 Inflammatory Bowel Disease (IBD) Related Outcomes in Patients Diagnosed With COVID-19
P026 Inflammatory Bowel Disease (IBD) Related Outcomes in Patients Diagnosed With COVID-19
Journal Article

P026 Inflammatory Bowel Disease (IBD) Related Outcomes in Patients Diagnosed With COVID-19

2021
Request Book From Autostore and Choose the Collection Method
Overview
BACKGROUND:Patients with IBD report increased gastrointestinal symptoms, including diarrhea, abdominal pain, and nausea following COVID-19 diagnosis. While there has been a great amount of research assessing outcomes of COVID-19 in patients with IBD, little is known about the effects of COVID-19 on IBD disease activity. We aimed to explore IBD related outcomes in a cohort of IBD patients affected by COVID-19.METHODS:We performed a retrospective case series of patients with IBD who were diagnosed with COVID-19 and seen in a single tertiary care referral center from March 2020 to March 2021 after IRB approval. We compared patients who were in stable remission up to 90 days prior to the COVID-19 diagnosis to those who were not in remission during the same time frame. COVID-19 diagnosis was made based on a combination of symptoms and positive rapid antigen and/or PCR test. Disease activity was estimated based on routinely measured clinical disease severity indices documented in office visit notes, including partial Mayo score for ulcerative colitis (UC) or Harvey-Bradshaw Index for Crohn's disease (CD) and/or endoscopic scoring documented in procedure notes including Mayo endoscopic subscore for UC or simple endoscopic score for CD documented in the procedure notes. For the primary outcome, we assessed IBD related outcomes by determining the need for escalation of immunosuppressive maintenance therapy, and/or need for IBD related hospitalization/surgery within 3 months after diagnosis of COVID-19. For the secondary outcome, COVID-19 related outcomes were assessed including need for hospitalization, ICU stay, use of COVID-19 related therapy such as monoclonal antibodies, and death. Continuous variables were compared between groups using student t test. Categorical variables were compared using Chi-square test.RESULTS:We identified 57 eligible patients. At the time of COVID-19 diagnosis, 30 (52.6%) were in remission, 0 (0%) had mild disease, 23 (40.3%) had moderate disease activity, and 4 (7.0%) had severe disease activity. No patients discontinued maintenance medications for more than 14 days due to COVID-19 diagnosis. No differences in age, gender, race, body max index, and combordities were noted between those not in remission versus those who were in remission (p>0.05). Patients who were not in remission were more likely to be on steroids at the time of COVID-19 diagnosis (47% vs 0%, p =0.00001) including budesonide and prednisone. Patients who were not in remission were more likely to be on biologics at the time of COVID-19 diagnosis (96.3%% vs 73.3%, p =0.03). Patients in remission had overall low rates of needing escalation in immunosuppressive maintenance therapy and IBD related hospitalization/surgery (6.7% and 0%, respectively). Patients who were not in remission were more likely to require escalation in immunosuppressive maintenance therapy (44.4% vs 6.7%, p 0.0015) and IBD related hospitalization/surgery compared to those in remission (18.5% vs 0.0%, p=0.02). No differences in COVID-19 related outcomes including need for hospitalization, ICU stay, use of COVID-19 related therapy such as monoclonal antibodies, and death were noted between the two groups (p>0.05).CONCLUSION:Our study suggests minimal impact of COVID-19 on IBD related outcomes in patients in remission. Patients who were not in remission did have worse IBD related outcomes compared to those in remission, however, the findings could reflect the natural history of IBD related disease rather than being related to COVID-19. COVID-19 related outcomes were no different in those who were not in remission versus those who were in remission. Future larger scale studies are warranted to study the findings further.
Publisher
Wolters Kluwer,Wolters Kluwer Health Medical Research, Lippincott Williams & Wilkins