An P, Ji M, Ren H, et al. Protection of 318 inflammatory bowel disease patients from the outbreak and rapid spread of COVID-19 infection in Wuhan, China. Lancet 2020 Feb 27 [Epub ahead of print]
A new beta-coronavirus, called severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was recently identified in Wuhan, China (N Engl J Med 2020;382:727–733). The virus proved to be transmitted from person to person and to be highly contagious, causing the onset of a pandemic in a short time (WHO Director-General’s opening remarks at the media briefing on COVID-19. March 11, 2020. Available at: www.who.int/dg/speeches/detail/who-director-general-s-opening-remarks-at-the-media-briefing-on-covid-19---11-march-2020). SARS-CoV-2 infection can be asymptomatic or cause coronavirus disease 2019 (COVID-19), which mainly includes respiratory and gastrointestinal symptoms and in severe cases it can be fatal (JAMA 2020;323:1061–1069). Several measures have been taken to prevent the further spread of the virus, including the use of masks, gloves, and disinfectants, and restrictions to avoid traveling to risk areas and having close contact with other people (Q&A on coronaviruses (COVID-19). Available at: www.who.int/news-room/q-a-detail/q-a-coronaviruses). Moreover, many countries have imposed quarantine and lockdown of schools and all nonessential activities (J Travel Med 2020 Mar 17 [Epub ahead of print]). In this context, particular attention should be paid to patients treated with immunosuppressive drugs or biologics, because they have a higher risk of infection (Clin Gastroenterol Hepatol 2020;18:69–81.e3). Other risk factors identified for the development of COVID-19 are advanced age, the presence of chronic diseases such as hypertension and diabetes, some professional categories (eg, health care personnel, policemen, and supermarket clerks) and exposure to infected people (Q&A on coronaviruses (COVID-19). Available at: www.who.int/news-room/q-a-detail/q-a-coronaviruses). In a recent work published in the Lancet (Lancet 2020 Feb 27 [Epub ahead of print]), precautions taken by a Wuhan center for inflammatory bowel diseases (IBD) were reported. All biological and immunosuppressive treatments were discontinued, visits in person were replaced by online consultations, and 318 patients were daily recommended to wash their hands frequently, to decrease the time spent outside the home, and to use masks outside the home (Lancet 2020 Feb 27 [Epub ahead of print]). It is important to underline that a relevant percentage of evaluated patients had risk factors of infection: chronic diseases (15.4%), immunosuppressive agent therapy (11.0%), elderly (10.4%), high-risk professional categories (7.5%), and biological therapy (6.3%) (Lancet 2020 Feb 27 [Epub ahead of print]). Recommendations were followed by 90% of patients and no cases of COVID-19 infection were detected after a period of approximately 2 months (Lancet 2020 Feb 27 [Epub ahead of print]). Finally, the authors stressed the importance of daily warnings and recommendations, which favored a wide adherence of patients and contributed to avoid viral contagion (Lancet 2020 Feb 27 [Epub ahead of print]).
Comment
The COVID-19 health emergency has forced physicians to deal with problems never before encountered and to take quick decisions in consideration of the urgent needs. In addition, the limited knowledge regarding transmission modalities, clinical symptoms, and natural history of the virus infection has made the management of patients with IBD and the adoption of preventive measures even more complex and difficult. Currently, the main source of transmission seems to be mediated by air droplets (Lancet 2020 Feb 27 [Epub ahead of print]), although ever-increasing evidence supports the possibility of a fecal–oral infection route (Gastroenterology 2020;158;1518–1519). As of March 29, 2020, the World Health Organization has reported 634,835 confirmed cases of infection worldwide and 29,957 deaths (Novel coronavirus (2019-nCoV) situation reports. Available at: www.who.int/emergencies/diseases/novel-coronavirus-2019/situation-reports). So far, epidemiologic data of COVID-19 in patients with IBD have not been published and it is unclear whether patients with IBD have an increased risk of infection. Interestingly, patients with active ulcerative colitis and Crohn’s disease have a greater tissue concentration of angiotensin-converting enzyme 2, the molecule that allows SARS-CoV-2 spike protein to bind the host cell and infect humans (Gut 2020;69:841–851). Similarly, the level of serine protease, an essential primer to activate the spike protein, is about 10 times higher in patients with IBD than in healthy subjects, suggesting an increased risk of infection in these patients (Front Cell Infect Microbiol 2020;10:21). These data justify concerns for patients with IBD and highlight the need to clarify whether there is an association between immunosuppressive/biological therapies and coronavirus infection. Importantly, a 3 times higher risk of serious viral infections (cytomegalovirus, Epstein-Barr virus, varicella zoster virus, and herpes simplex virus) was detected in patients with IBD compared with the general population (United European Gastroenterology Journal 2019:2050640619889763). Although the absolute risk of developing a viral infection was acceptable, the presence of an active disease and treatment with thiopurines were reported as the factors most influencing the infectious risk (United European Gastroenterology Journal 2019:2050640619889763). Recently, the International Organization of IBD stated that vedolizumab and ustekinumab are safe drugs and do not increase the risk of infection, although the risks of infection related to treatments with thiopurine, anti-tumor necrosis factor agents, and tofacitinib are uncertain (IOIBD update on COVID19 for patients with Crohn’s disease and ulcerative colitis | IOIBD. Available at: www.ioibd.org/ioibd-update-on-covid19-for-patients-with-crohns-disease-and-ulcerative-colitis/).
In the work from An et al (Lancet 2020 Feb 27 [Epub ahead of print) all patients discontinued therapy and no patient contracted the infection. This patient management should be discussed. First, some drugs such as thiopurines have a very high clearance time and therefore it would take a long time before decreasing the risk of infection (Nat Rev Gastroenterol Hepatol 2020;17:253–255). Second, therapy discontinuation is associated with an increased risk of disease recurrence/worsening and may lead to an increase of negative outcomes such as hospitalizations and surgeries (Cochrane Database Syst Rev 2018;5:CD012540; Am J Gastroenterol 2017;112:120–131; J Crohns Colitis 2018;12:17–31). Third, in this period many countries are lockdown and hospitals are overloaded with work and have changed their organization, minimizing nonessential outpatient activities and focusing on COVID-19 patients (N Engl J Med 2020 Mar 18 [Epub ahead of print]; N Engl J Med 2020 Mar 23 [Epub ahead of print]). All these factors result in greater difficulty in managing IBD recurrences and do not allow to guarantee the best management of patients with active diseases. For these reasons, IBD drug discontinuation should not be recommended in all patients not suspected of COVID-19 (IOIBD update on COVID19 for patients with Crohn’s disease and ulcerative colitis | IOIBD. Available at: www.ioibd.org/ioibd-update-on-covid19-for-patients-with-crohns-disease-and-ulcerative-colitis/; N Engl J Med 2020 Mar 18 [Epub ahead of print]). The therapeutic approach should be personalized and should be based on the balance between the risk of viral infection and the risk of disease recurrence. The ongoing therapies should be stopped only in clearly COVID-19 patients, while in positive SARS-CoV-2 cases (without disease) the decision should be based on the type of drug and the risk of COVID-19 occurrence (IOIBD update on COVID19 for patients with Crohn’s disease and ulcerative colitis | IOIBD. Available at: www.ioibd.org/ioibd-update-on-covid19-for-patients-with-crohns-disease-and-ulcerative-colitis/; N Engl J Med 2020 Mar 18 [Epub ahead of print]). Large national and international studies are needed to identify the best way to prevent COVID-19 in patients with IBD, to understand whether patients with IBD are at increased risk of being infected, and to clarify whether they should be considered as a high-risk population as well as the impact of IBD-related drugs on COVID-19.
Another aspect suggested by An et al (Lancet 2020 Feb 27 [Epub ahead of print]) is the relevance of the continuous assistance to patients with IBD also at home. Home patient management has been called telemedicine and it is a well-accepted approach by patients, as evidenced by the high adherence to home therapies or recommendations from physicians (Dig Dis Sci 2007;52:357–364; BMJ Evid Based Med 2019;24:37–38). Telemedicine has also been associated with a reduction in gastroenterological consultations and hospitalizations and could be a valid alternative to improve the quality of IBD patient care during the COVID-19 outbreak (BMJ Evid Based Med 2019;24:37–38). Chinese experience showed that telemedicine is possible and effective, although long-term follow-up of this cohort is essential to confirm the real impact of the preventive strategies. Furthermore, the biggest challenge for Western countries will be to extrapolate Chinese success and overcome cultural differences that could hinder adhesion rates. In conclusion, the coronavirus pandemic is straining the existing health systems and will leave an indelible mark on both patients and physicians, but it is providing new insights and could be a starting point for investing in new approaches and increasingly personalizing patient care.
Marcia Cruz-Correa, Section Editor
David A. Schwartz, Section Editor
Footnotes
Conflicts of interest The authors have made the following disclosures: F. D’Amico declares no conflict of interest. L. Peyrin-Biroulet has served as a speaker, consultant, and advisory board member for Merck, Abbvie, Janssen, Genentech, Mitsubishi, Ferring, Norgine, Tillots, Vifor, Hospira/Pfizer, Celltrion, Takeda, Biogaran, Boerhinger-Ingelheim, Lilly, HAC- Pharma, Index Pharmaceuticals, Amgen, Sandoz, Forward Pharma GmbH, Celgene, Biogen, Lycera, Samsung Bioepis, and Theravance. S. Danese has served as a speaker, consultant, and advisory board member for Schering-Plough, AbbVie, Actelion, Alphawasserman, AstraZeneca, Cellerix, Cosmo Pharmaceuticals, Ferring, Genentech, Grunenthal, Johnson and Johnson, Millenium Takeda, MSD, Nikkiso Europe GmbH, Novo Nordisk, Nycomed, Pfizer, Pharmacosmos, UCB Pharma, and Vifor.