To the Editors,

We read with great interest the manuscript by Axelrad et al1 summarizing the characteristics of patients with inflammatory bowel disease (IBD) and coronavirus 2019 (COVID-19). We share with the authors the concern with IBD patients. Thus, our department established strategies to prioritize the care of these individuals, which were implemented on our practice by March 18, 2020, and were in course until the end of the state of emergency. Herein, we briefly describe the measures implemented and the obtained outcomes.

Most medical appointments were made by phone, and we ensured that patients had essential medications. To prevent disease flares, their usual therapy was maintained. The exception was for those who were under high-dose steroids (>20 mg/day), whose tapering was made as quickly as possible. In the case of IBD flare, the therapies commonly used in these circumstances were initiated.2 We modified our day care unit to ensure that patients kept their usual biologic medication safely; systematic screening for symptoms and fever was performed before treatments. We postponed all elective procedures, and endoscopy was performed only in urgent cases.3 All patients who were proposed for endoscopic procedures were previously tested for SARS-CoV-2, and health professionals always used protective equipment during procedures. Individuals who were admitted had been tested for SARS-CoV-2, allowing the creation of COVID-19 and COVID-19-free wards. A set of measures to prevent SARS-CoV-2 infection during hospitalizations were implemented, namely forbidding visits and reducing the number of patients per ward.

Over the period of the state of emergency, we achieved a rate of almost 95% of medical appointments by telemedicine and therapeutic compliance in 90% of cases. Our patients did not self-medicate and sought information about their IBD care by contacting our medical services or attending the emergency department. There was no significant increase in the rate of hospital admissions due to IBD decompensation compared with the same period last year. There were 1990 SARS-CoV-2 infections diagnosticated in our hospital, and 11 patients had IBD (Table 1). None of these patients had acute decompensation of IBD, and no deaths were reported. Thiopurines and biological therapies were suspended during the viral illness and restarted after complete symptoms resolution or when SARS-CoV-2 retesting was negative.

TABLE 1.

Characteristics of IBD Patients with Infection by COVID-19

PatientAge (years)SexIBDCD
Montreal phenotype
UC extensionDisease activityTherapyComorbiditiesSymptomsCT findingsTherapies for
COVID-19
HospitalizationICU admissionDeath
150FCDA2L2B3RemissionAzathioprineHypertension, dyslipidemia, asthmaFever, cough, myalgia, fatigueNDNDNoNoNo
241MCDA2L1B3RemissionNoneNoFever, sore throat, headacheNDNDNoNoNo
365MCDA3L1B1RemissionNoneHypertension, dyslipidemia, diabetesCough, headache,
myalgia
NDNDNoNoNo
421MCDA2L2B1RemissionInfliximabNoHeadache,
anosmia, dysgeusia
NDNDNoNoNo
544FCDA2L1B3ActiveAzathioprineCV disease, AsthmaFatigue, anosmia, dysgeusiaNDNDNoNoNo
624FUCLeft-sidedActiveMercaptopurineNoFever, sore throat, rhinorrhea, myalgia, fatigue, headacheNDNDNoNoNo
761MCDA1L3B2RemissionInfliximabNoFever, cough, headache, nausea/vomiting, anosmiaBilateral pneumonia5-day HCQYesNoNo
846MCDA3L1B1RemissionAdalimumabNoCoughNDNDNoNoNo
954FCDA2L1B2ActiveAzathioprineHypertensionCough, fever, fatigueNDNDNoNoNo
1049FUCExtensiveRemissionInfliximab, MesalazinePorphyria cutanea tardaSore throat, fatigue, diarrheaNDNDNoNoNo
1130FCDA2L3B1ActiveAdalimumabNoCough, fever, fatigueNDNDNoNoNo
PatientAge (years)SexIBDCD
Montreal phenotype
UC extensionDisease activityTherapyComorbiditiesSymptomsCT findingsTherapies for
COVID-19
HospitalizationICU admissionDeath
150FCDA2L2B3RemissionAzathioprineHypertension, dyslipidemia, asthmaFever, cough, myalgia, fatigueNDNDNoNoNo
241MCDA2L1B3RemissionNoneNoFever, sore throat, headacheNDNDNoNoNo
365MCDA3L1B1RemissionNoneHypertension, dyslipidemia, diabetesCough, headache,
myalgia
NDNDNoNoNo
421MCDA2L2B1RemissionInfliximabNoHeadache,
anosmia, dysgeusia
NDNDNoNoNo
544FCDA2L1B3ActiveAzathioprineCV disease, AsthmaFatigue, anosmia, dysgeusiaNDNDNoNoNo
624FUCLeft-sidedActiveMercaptopurineNoFever, sore throat, rhinorrhea, myalgia, fatigue, headacheNDNDNoNoNo
761MCDA1L3B2RemissionInfliximabNoFever, cough, headache, nausea/vomiting, anosmiaBilateral pneumonia5-day HCQYesNoNo
846MCDA3L1B1RemissionAdalimumabNoCoughNDNDNoNoNo
954FCDA2L1B2ActiveAzathioprineHypertensionCough, fever, fatigueNDNDNoNoNo
1049FUCExtensiveRemissionInfliximab, MesalazinePorphyria cutanea tardaSore throat, fatigue, diarrheaNDNDNoNoNo
1130FCDA2L3B1ActiveAdalimumabNoCough, fever, fatigueNDNDNoNoNo

Abbreviations: CD, Crohn’s disease; UC, ulcerative colitis; CT, computed tomography; ICU, intensive care unit; F, female; M, male; Montreal classification: age of onset (A): A1, 16 years or younger; A2, 17–40 years; A3, above 40 years; disease location (L): L1, terminal ileum; L2, colon; L3, ileocolon; L4, upper gastrointestinal tract; disease behaviour (B): B1, nonstricturing nonpenetrating; B2, structuring; B3, penetrating; CV, cardiovascular; ND, not done; HCQ, hydroxychloroquine. Note: Active disease was determined by a partial Mayo score >1 for UC and Harvey-Bradshaw index >4 for CD.2

TABLE 1.

Characteristics of IBD Patients with Infection by COVID-19

PatientAge (years)SexIBDCD
Montreal phenotype
UC extensionDisease activityTherapyComorbiditiesSymptomsCT findingsTherapies for
COVID-19
HospitalizationICU admissionDeath
150FCDA2L2B3RemissionAzathioprineHypertension, dyslipidemia, asthmaFever, cough, myalgia, fatigueNDNDNoNoNo
241MCDA2L1B3RemissionNoneNoFever, sore throat, headacheNDNDNoNoNo
365MCDA3L1B1RemissionNoneHypertension, dyslipidemia, diabetesCough, headache,
myalgia
NDNDNoNoNo
421MCDA2L2B1RemissionInfliximabNoHeadache,
anosmia, dysgeusia
NDNDNoNoNo
544FCDA2L1B3ActiveAzathioprineCV disease, AsthmaFatigue, anosmia, dysgeusiaNDNDNoNoNo
624FUCLeft-sidedActiveMercaptopurineNoFever, sore throat, rhinorrhea, myalgia, fatigue, headacheNDNDNoNoNo
761MCDA1L3B2RemissionInfliximabNoFever, cough, headache, nausea/vomiting, anosmiaBilateral pneumonia5-day HCQYesNoNo
846MCDA3L1B1RemissionAdalimumabNoCoughNDNDNoNoNo
954FCDA2L1B2ActiveAzathioprineHypertensionCough, fever, fatigueNDNDNoNoNo
1049FUCExtensiveRemissionInfliximab, MesalazinePorphyria cutanea tardaSore throat, fatigue, diarrheaNDNDNoNoNo
1130FCDA2L3B1ActiveAdalimumabNoCough, fever, fatigueNDNDNoNoNo
PatientAge (years)SexIBDCD
Montreal phenotype
UC extensionDisease activityTherapyComorbiditiesSymptomsCT findingsTherapies for
COVID-19
HospitalizationICU admissionDeath
150FCDA2L2B3RemissionAzathioprineHypertension, dyslipidemia, asthmaFever, cough, myalgia, fatigueNDNDNoNoNo
241MCDA2L1B3RemissionNoneNoFever, sore throat, headacheNDNDNoNoNo
365MCDA3L1B1RemissionNoneHypertension, dyslipidemia, diabetesCough, headache,
myalgia
NDNDNoNoNo
421MCDA2L2B1RemissionInfliximabNoHeadache,
anosmia, dysgeusia
NDNDNoNoNo
544FCDA2L1B3ActiveAzathioprineCV disease, AsthmaFatigue, anosmia, dysgeusiaNDNDNoNoNo
624FUCLeft-sidedActiveMercaptopurineNoFever, sore throat, rhinorrhea, myalgia, fatigue, headacheNDNDNoNoNo
761MCDA1L3B2RemissionInfliximabNoFever, cough, headache, nausea/vomiting, anosmiaBilateral pneumonia5-day HCQYesNoNo
846MCDA3L1B1RemissionAdalimumabNoCoughNDNDNoNoNo
954FCDA2L1B2ActiveAzathioprineHypertensionCough, fever, fatigueNDNDNoNoNo
1049FUCExtensiveRemissionInfliximab, MesalazinePorphyria cutanea tardaSore throat, fatigue, diarrheaNDNDNoNoNo
1130FCDA2L3B1ActiveAdalimumabNoCough, fever, fatigueNDNDNoNoNo

Abbreviations: CD, Crohn’s disease; UC, ulcerative colitis; CT, computed tomography; ICU, intensive care unit; F, female; M, male; Montreal classification: age of onset (A): A1, 16 years or younger; A2, 17–40 years; A3, above 40 years; disease location (L): L1, terminal ileum; L2, colon; L3, ileocolon; L4, upper gastrointestinal tract; disease behaviour (B): B1, nonstricturing nonpenetrating; B2, structuring; B3, penetrating; CV, cardiovascular; ND, not done; HCQ, hydroxychloroquine. Note: Active disease was determined by a partial Mayo score >1 for UC and Harvey-Bradshaw index >4 for CD.2

Our protocol showed that the level of care for IBD patients could be maintained during the pandemic. The risk of developing severe COVID-19 seems to be similar to the general population; however, it is suggested to keep close surveillance of these patients.

Author Contribution: IG drafted the manuscript. IG, SL, and GM critically revised and finalized the manuscript. All authors approved the final version of the manuscript.

REFERENCES

1.

Axelrad
JE
,
Malter
L
,
Hong
S
, et al.
From the American Epicenter: Coronavirus Disease 2019 in Patients with Inflammatory Bowel Disease in the New York City Metropolitan Area
.
Inflamm Bowel Dis
.
2020
;
izaa162
. [Epub ahead of print]

2.

Lamb
CA
,
Kennedy
NA
,
Raine
T
, et al. ;
IBD guidelines eDelphi consensus group
.
British Society of Gastroenterology consensus guidelines on the management of inflammatory bowel disease in adults
.
Gut.
2019
;
68
:
s1
s106
.

3.

British Society of Gastroenterology (BSG)
.
Endoscopy activity and COVID-19: BSG and JAG guidance – update 22.03.20
,
2020
. Accessed June 29, 2020. https://www.bsg.org.uk/covid-19-advice/endoscopy-activity-and-covid-19-bsg-and-jag-guidance/.

This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://dbpia.nl.go.kr/pages/standard-publication-reuse-rights)