Tixagevimab and Cilgavimab (Evusheld) as Pre-exposure Prophylaxis for COVID-19 in Patients With Inflammatory Bowel Disease: A Propensity Matched Cohort Study.
COVID-19
cilgavimab
inflammatory bowel disease
tixagevimab
Journal
Crohn's & colitis 360
ISSN: 2631-827X
Titre abrégé: Crohns Colitis 360
Pays: England
ID NLM: 101752188
Informations de publication
Date de publication:
Jul 2023
Jul 2023
Historique:
medline:
8
9
2023
pubmed:
8
9
2023
entrez:
8
9
2023
Statut:
epublish
Résumé
Tixagevimab and cilgavimab (Evusheld) are 2 fully human monoclonal antibodies that received emergency-use authorization on December 21, 2021, for pre-exposure prophylaxis of coronavirus disease 2019 (COVID-19) in patients who are moderate-severely immunocompromised. The real-world efficacy of Evusheld in patients with inflammatory bowel disease (IBD) is not known. We conducted a retrospective cohort study using TriNetX, a multi-institutional database in patients with IBD who received Evusheld compared to patients with IBD who did not receive Evusheld (12.1.2021-10.28.2022). The primary outcome was to assess the risk of COVID-19 within 6 months. One-to-one propensity score matching (PSM) was performed for demographic parameters, comorbid conditions, IBD medications, and history of COVID-19. Risk was expressed as adjusted odds ratio (aOR) with 95% confidence interval (CI). Four hundred and eight patients (0.19%) with IBD received Evusheld (mean age 58.6 ± 15.4 years old, female 47.7%) during the study period. After PSM, there was no difference in the risk (aOR 0.88, 95% CI, 0.33-2.35) of COVID-19 in the Evusheld cohort compared to the IBD control cohort. No patients required ICU care or intubation/respiratory support or were deceased in the Evusheld cohort. Our study did not show that Evusheld decreases the risk of COVID-19 in patients with IBD. Prevention of moderate-severe COVID-19 in these patients should focus on vaccination strategies and early COVID-19 therapies.
Sections du résumé
Background
UNASSIGNED
Tixagevimab and cilgavimab (Evusheld) are 2 fully human monoclonal antibodies that received emergency-use authorization on December 21, 2021, for pre-exposure prophylaxis of coronavirus disease 2019 (COVID-19) in patients who are moderate-severely immunocompromised. The real-world efficacy of Evusheld in patients with inflammatory bowel disease (IBD) is not known.
Methods
UNASSIGNED
We conducted a retrospective cohort study using TriNetX, a multi-institutional database in patients with IBD who received Evusheld compared to patients with IBD who did not receive Evusheld (12.1.2021-10.28.2022). The primary outcome was to assess the risk of COVID-19 within 6 months. One-to-one propensity score matching (PSM) was performed for demographic parameters, comorbid conditions, IBD medications, and history of COVID-19. Risk was expressed as adjusted odds ratio (aOR) with 95% confidence interval (CI).
Results
UNASSIGNED
Four hundred and eight patients (0.19%) with IBD received Evusheld (mean age 58.6 ± 15.4 years old, female 47.7%) during the study period. After PSM, there was no difference in the risk (aOR 0.88, 95% CI, 0.33-2.35) of COVID-19 in the Evusheld cohort compared to the IBD control cohort. No patients required ICU care or intubation/respiratory support or were deceased in the Evusheld cohort.
Conclusions
UNASSIGNED
Our study did not show that Evusheld decreases the risk of COVID-19 in patients with IBD. Prevention of moderate-severe COVID-19 in these patients should focus on vaccination strategies and early COVID-19 therapies.
Identifiants
pubmed: 37680248
doi: 10.1093/crocol/otad047
pii: otad047
pmc: PMC10482141
doi:
Types de publication
Journal Article
Langues
eng
Pagination
otad047Informations de copyright
© The Author(s) 2023. Published by Oxford University Press on behalf of Crohn's & Colitis Foundation.
Déclaration de conflit d'intérêts
A.D.: None exists. J.G.H. holds the position of Associate Editor for Crohn’s & Colitis 360 and has been recused from reviewing or making decisions for the manuscript. G.S.K.: Advisor Board: Corvetas Research Foundation, Lilly Pharmaceuticals, GIE medical; Stock options: Digbi Health. F.A.F. is a consultant for BMS, Braintree Labs, GSK, IBD Educational Group, Innovation Pharmaceuticals, Janssen, Pfizer and Sebela. He sits on a DSMB for Adiso Therapeutics and Lilly.
Références
Viruses. 2022 Sep 09;14(9):
pubmed: 36146805
Am J Med. 2023 Jan;136(1):96-99
pubmed: 36181789
Sci Transl Med. 2022 Mar 9;14(635):eabl8124
pubmed: 35076282
Clin Gastroenterol Hepatol. 2023 Mar;21(3):841-843.e4
pubmed: 36152898
Am J Transplant. 2022 Dec;22(12):3130-3136
pubmed: 35727916
Kidney Int Rep. 2022 Nov;7(11):2537-2538
pubmed: 36060620
Inflamm Bowel Dis. 2023 May 2;29(5):705-715
pubmed: 35857336
Inflamm Bowel Dis. 2022 Dec 28;:
pubmed: 36576102
J Clin Rheumatol. 2023 Mar 1;29(2):109-111
pubmed: 36126256
N Engl J Med. 2022 Jun 9;386(23):2188-2200
pubmed: 35443106
Clin Microbiol Infect. 2022 Dec;28(12):1654.e1-1654.e4
pubmed: 35926762