Treatment adaptations and outcomes of patients experiencing inflammatory bowel disease flares during the early COVID-19 pandemic: the PREPARE-IBD multicentre cohort study

Aamir Saifuddin*, Alexandra J. Kent, Shameer J. Mehta, Lucy C. Hicks, Haidee A. Gonzalez, Jonathan P. Segal, Matthew J. Brookes, Sreedhar Subramanian, Neeraj Bhala, Thomas E. Conley, Kamal V. Patel, Christopher A. Lamb, Gareth J. Walker, Nicholas A. Kennedy, Shaji Sebastian, Shukri Abdale, Abdulla Abbesi, Anwar Abusrewil, Precious Aghimien, Saeed AhmedAkram Ali, Amjad Ali, Jad Alkhouri, Patrick Allen, Ammar Al-Rifaie, Richard Appleby, Ramesh Arasaradnam, Naila Arebi, Bradley Arms-Williams, Muteeb Ashraf, Au Andrea, Tamar Avades, Homira Ayubi, Samantha Baillie, Sharmili Balarajah, Aaron Bancil, Abdul Basit, Murad Bayati, Andrew Bell, Alexander Berry, Neeraj Bhala, Shivaram Bhat, Deborah Britton, Rachel Campbell, Paul Flanagan, Emma Johnston, Gary Morrison, Kirsty Nixon, Tony Tham, Bo Wang, PREPARE-IBD Collaborators, Andrew Spence

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)

Abstract

Background
The COVID-19 pandemic offered a unique opportunity to understand inflammatory bowel disease (IBD) management during unexpected disruption. This could help to guide practice overall.

Aims
To compare prescribing behaviour for IBD flares and outcomes during the early pandemic with pre-pandemic findings

Methods
We performed an observational cohort study comprising patients who contacted IBD teams for symptomatic flares between March and June 2020 in 60 National Health Service trusts in the United Kingdom. Data were compared with a pre-pandemic cohort after propensity-matching for age and physician global assessment of disease activity.

Results
We included 1864 patients in each of the pandemic and pre-pandemic cohorts. The principal findings were reduced systemic corticosteroid prescription during the pandemic in Crohn's disease (prednisolone: pandemic 26.5% vs. 37.1%; p 
Conclusions
Despite treatment adaptations during the pandemic, steroid-free outcomes were comparable with pre-pandemic levels, although concurrent flare and suspected COVID-19 caused worse outcomes. These findings have implications for IBD management during future pandemics and for standard practice.
Original languageEnglish
Pages (from-to)1460-1474
Number of pages15
JournalAlimentary Pharmacology and Therapeutics
Volume56
Issue number10
Early online date05 Oct 2022
DOIs
Publication statusPublished - 01 Nov 2022

Bibliographical note

Funding Information:
The study was funded by Hull University Teaching Hospitals NHS Trust.

Funding Information:
We are grateful to the clinical and research teams in the participating sites for identification of patients, data collection and data entry. UK gastroenterology trainees and trainee networks (MaGNET: Mersey Gastroenterology Network, GLINT: Gastro London Investigative Network for Trainees, WMRIG: West Midlands Research in Gastroenterology, GasTRIN NoW: Gastroenterology Trainee Research and Improvement Network North-West, OxYGEN: The Oxford and Thames Valley Young Gastroenterologists Network, TReNDD NI: Trainee Research Network in Digestive Diseases Northern Ireland) were integral in data collection for this study. We appreciate support from Crohn's & Colitis UK and the British Society of Gastroenterology for promotion of this study.

Funding Information:
SS holds research grants from Biogen, Takeda, AbbVie, Tillotts Pharma, Ferring and Biohit; served on the advisory boards of Takeda, AbbVie, Merck, Ferring, Pharmacocosmos, Warner Chilcott, Janssen, Falk Pharma, Biohit, TriGenix, Celgene and Tillots Pharma; and has received speaker fees from AbbVie, Biogen, AbbVie, Janssen, Merck, Warner Chilcott and Falk Pharma. GJW has served as a speaker and/or advisory board member for AbbVie, Falk and Janssen. He has had support to attend meetings from AbbVie, Falk, Janssen and Norgine. His department has received research funding from Tillotts. NAK has served as a speaker and/or advisory board member for Allergan, Falk, Janssen, Mylan, Pharmacosmos, Takeda and Tillotts. He has had support to attend meetings from AbbVie, Falk, Janssen and Norgine. His department has received research funding from AbbVie, Celgene, Celtrion, MSD, Napp, Pfizer, Pharmacosmos and Takeda. SrS has received speaker fees from MSD, Actavis, Abbvie, Dr Falk pharmaceuticals, Shire and received educational grants from MSD, Abbvie, Actavis and is an advisory board member for Celltrion, Dr Falk pharmaceuticals and Vifor pharmaceuticals. CAL has received research support and/or has received fees for delivery of non‐promotional education from: Genentech, Janssen, Takeda, Abbvie, Dr Falk, AstraZeneca, Eli Lilly, Orion, Pfizer, Roche, Sanofi Aventis, Ferring, UCB and Biogen. MJB has received research grants from Vifor International, Pharmacosmos and Tillots Pharma; has received speaker fee from Abbvie and Vifor International; has been an advisory board member for Tillots Pharma, Vifor International; and received travel/conference expenses from Vifor International, Abbvie and Tillots Pharma. AJK has served on the advisory boards for Abbvie, Janssen and BMS Celgene and has received speaker fees from Takeda, Pfizer and Janssen; and received travel/conference expenses from Tillotts, Janssen, Abbvie and Shield Therapeutics. KP has received honoraria for educational meetings and speaker fees from Abbvie, Janssen, Takeda, DrFalk and Ferring. KP has received Advisory Board fees from Abbvie and Janssen. TEC has received speaker fees from Celltrion. LCH, HAG, SJM, AS have no conflicts of interest to declare.

Publisher Copyright:
© 2022 John Wiley & Sons Ltd.

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology
  • Pharmacology (medical)

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