Dear Editor:
We read the recent article by Ungaro et al1 with great interest. As the coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) continues to spread, gastroenterologists managing patients with inflammatory bowel disease (IBD) face uncertainty amid growing patient concerns regarding risks associated with immunosuppressive medications. Descriptions of initial patient cohorts from China did not include details about concomitant immunosuppressive therapy because immune-mediated diseases did not feature prominently among the reported comorbidities.2 On the basis of these cohorts, the most important factors associated with poorer outcomes were older age, diabetes, hypertension, and other cardiovascular disease.
An international registry of IBD patients with COVID-19 (Surveillance Epidemiology of Coronavirus [COVID-19] under Research Exclusion) was established.3 As of April 8, 2020, 382 cases were reported to the registry, of whom 106 had required hospitalization, and 13 had died. In the absence of data to inform decision making, several societies have proposed empiric guidelines for management of IBD patients. These recommendations should be considered in parallel with national/regional guidance from public health authorities, which include instructions for self-isolation that may substantially impact patient livelihoods and thus extend beyond the typical remit of guidelines for disease management. In the context of the rapidly evolving data, we summarize available recommendations from different gastroenterological societies.
To date, public guidance on the management of IBD patients during the COVID-19 pandemic has been issued by the British Society of Gastroenterology (BSG),4 Crohn’s and Colitis Canada (CCC),5 European Crohn’s and Colitis Organization (ECCO),6 , 7 and the International Organization for the Study of Inflammatory Bowel Disease (IOIBD)8 (Table 1 ).
Table 1.
British Society of Gastroenterology | European Crohn’s and Colitis Organization | International Organization for the Study of Inflammatory Bowel Disease | |
---|---|---|---|
Mesalamine |
|
|
|
Corticosteroids |
|
|
|
Immunomodulators (thiopurines, methotrexate) |
|
|
|
Biologics (TNF antagonists, anti-integrins, anti-interleukin 12/23) |
|
|
|
TNF antagonists |
|
|
|
JAK inhibitors |
|
|
|
Endoscopy |
|
|
|
Clinical trials |
|
|
|
COVID-19, coronavirus disease 2019; TNF, tumor necrosis factor.
All aforementioned societies recommend continuing IBD-specific treatment because risk of active disease was perceived to be higher than the uncertain risks of immunosuppression predisposing to higher risk of infection with SARS-CoV-2. Minimizing corticosteroid exposure by rapid tapering whenever possible is universally recommended, with the BSG also suggesting topical corticosteroids or exclusive enteral nutrition as alternatives for patients experiencing a flare. Thiopurine initiation is discouraged by both the BSG and ECCO because of increased perceived risk of viral infection and need for concomitant induction corticosteroid. Both BSG and ECCO advise caution with initiating combination therapy; the former also suggests considering stopping thiopurine treatment in patients ≥65 years and those with significant comorbidities in stable remission. For patients commencing biological therapy, subcutaneously administered drug may be preferred on the basis of local circumstances to maximize social distancing efforts. Forced switching to subcutaneous biologics should only be used in centers unable to provide infusions. There are no data to favor one class of biologics over another in the context of COVID-19. There is some indication that lower T-helper lymphocyte counts are associated with delayed clearance of viral RNA, which led ECCO to recommend against initiation of tofacitinib if therapeutic alternatives are available, in contrast to BSG and IOIBD.
In case an infection develops, ECCO suggests postponing biologic treatment until resolution and considering stopping thiopurines and tofacitinib for the duration of the infection. On the basis of experience with other coronaviruses and early experience with SARS-CoV-2, the benefits and harms of continuing corticosteroid treatment during infection should be weighed carefully. IOIBD suggests withholding all IBD-related medication, except for mesalamine, topical steroids, and possibly vedolizumab until resolution of symptoms in case COVID-19 develops. Alternatively, medication can be restarted after 2 negative nasopharyngeal polymerase chain reaction tests. For general measures to prevent viral transmission, ECCO and IOIBD emphasize hand hygiene and avoiding contact with infected people; CCC also advocates workplace modifications to enable physical distancing for patients using immunosuppressants. Guidance from the BSG is more stringent in suggesting that patients with a comorbidity or >70 years being treated with drugs other than mesalamine/topical corticosteroids should undergo “shielding,” a strict form of social distancing mandating the avoidance of face-to-face contact for at least 12 weeks. This recommendation extends to patients taking daily prednisolone equivalent of ≥20 mg, those during combination therapy induction, those with moderately-to-severely active disease despite treatment, and those with short bowel syndrome or requiring parenteral nutrition. This stricter guidance from the BSG is an outlier with major implications for individual patients and should be taken in the context of the individual case. Patients treated with biologics or immunomodulators, including stable patients on combination therapy, should practice stringent social distancing, whereas patients treated with mesalamine or topical corticosteroids should adhere to standard social distancing. Surveillance endoscopies should be deferred, and disease assessment endoscopies should be carefully assessed for priority, considering the possibility of alternative methods (biomarkers, radiology, and capsule endoscopy).
Footnotes
Conflicts of interest JH has received speaker’s fees from Biogen, Janssen, and Takeda. CM has received consulting fees from Robarts Clinical Trials Inc, Janssen, and AbbVie and speaker’s fees from Janssen and Pfizer. JKM is a scientific advisory board member, speaker, and/or consultant for AbbVie, Allergan, Celgene, Celltrion, Ferring, Hoffman-La Roche, Hospira, Janssen, Lilly, Merck, Pfizer, Procter & Gamble, Shire, and Takeda. BGF is a scientific advisory board member for AbbVie, Allergan, Amgen, AstraZeneca, Avaxia Biologics Inc, Boehringer-Ingelheim, Bristol-Myers Squibb, Celgene, Elan, Biogen, Ferring, Genentech–Roche, Janssen–Johnson & Johnson, Merck, Millennium, Nestlé, Novo Nordisk, Novartis, Pfizer, Prometheus, Protagonist, Receptos, Salix, Sigmoid Pharma, Takeda, Teva, TiGenix, Tillotts Pharma, and UCB Pharma; has received consulting fees from AbbVie, Actogenix, Akros, Albireo Pharma, Allergan, Amgen, AstraZeneca, Avaxia Biologics, Avir Pharma, Axcan, Baxter Healthcare, Biogen Idec, Boehringer Ingelheim, Bristol-Myers Squibb, Calypso Biotech, Celgene, Elan–Biogen, EnGene, Ferring, Genentech–Roche, GiCare Pharma, Gilead Sciences, Given Imaging, GlaxoSmithKline, Ironwood, Janssen Biotech–Centocor, Janssen–Johnson & Johnson, Kyowa Hakko Kirin, Eli Lilly, Merck, Mesoblast Pharma, Millennium, Nestlé, Novo Nordisk, Novartis, Pfizer, Prometheus, Protagonist, Receptos Salix, Sanofi, Shire, Sigmoid Pharma, Synergy Pharma, Takeda, Teva, TiGenix, Tillotts Pharma, UCB Pharma, Vertex, VHsquared, Wyeth, Zealand, and Zygenia; lecture fees from AbbVie, Janssen–Johnson & Johnson, Takeda, and UCB Pharma; and grant support from AbbVie, Amgen, AstraZeneca, Bristol-Myers Squibb, Janssen Biotech–Centocor, Janssen–Johnson & Johnson, Pfizer, Receptos, Sanofi, and Takeda; and is the Senior Scientific Officer of Robarts Clinical Trials Inc. VJ has received consulting fees from AbbVie, Eli Lilly, GlaxoSmithKline, Arena Pharmaceuticals, Genetech, Pendopharm, Sandoz, Merck, Takeda, Janssen, Robarts Clinical Trials Inc, Topivert, and Celltrion; and speaker’s fees from Takeda, Janssen, Shire, Ferring, AbbVie and Pfizer.
References
- 1.Ungaro RC, et al. Clin Gastroenterol Hepatol [Epub ahead of print]. Mar 22, 2020; 10.1016/j.cgh.2020.03.020. [DOI]
- 2.Guan WJ, et al. N Engl J Med [Epub ahead of print]. Feb 28, 2020; https://www.nejm.org/doi/10.1056/NEJMoa2002032.
- 3.SECURE-IBD Registry Surveillance Epidemiology of Coronavirus (COVID-19) Under Research Exclusion. https://covidibd.org/ Available from: Accessed April 8, 2020.
- 4.British Society of Gastroenterology. https://www.bsg.org.uk/wp-content/uploads/2020/03/BSG-plan-for-IBD-patients-during-COVID19-pandemic-v1.5.pdf Available from: Accessed March 23, 2020.
- 5.Crohn's and Colitis Canada. https://crohnsandcolitis.ca/Living-with-Crohn-s-Colitis/COVID-19-and-IBD Available from: Accessed March 30, 2020.
- 6.COVID-19 ECCO Task Force. https://ecco-ibd.eu/images/6_Publication/6_8_Surveys/1st_interview_COVID-19%20ECCOTaskforce_published.pdf Available from: Accessed March 23, 2020.
- 7.COVID-19 ECCO Task Force. https://ecco-ibd.eu/images/6_Publication/6_8_Surveys/2nd_Interview_COVID-19_ECCO_Taskforce_published.pdf Available from: Accessed March 23, 2020.
- 8.Rubin DT, et al. Gastroenterology [Epub ahead of print]. April 6, 2020; 10.1053/j.gastro.2020.04.012. [DOI]