key: cord-0696684-inakrtw0
authors: Creemers, Rob H.; Rezazadeh Ardabili, Ashkan; Jonkers, Daisy M.; Leers, Mathie P. G.; Romberg-Camps, Mariëlle J.; Pierik, Marie J.; van Bodegraven, Ad A.
title: Severe COVID-19 in inflammatory bowel disease patients in a population-based setting
date: 2021-10-05
journal: PLoS One
DOI: 10.1371/journal.pone.0258271
sha: 1b42baa0fec6beb48cd9a276dd1abec0e17052f6
doc_id: 696684
cord_uid: inakrtw0

OBJECTIVE: Data on the course of severe COVID-19 in inflammatory bowel disease (IBD) patients remains limited. We aimed to determine the incidence rate and clinical course of severe COVID-19 in the heavily affected South-Limburg region in the Netherlands. METHODS: All COVID-19 patients admitted to the only two hospitals covering the whole South-Limburg region between February 27, 2020 and January 4, 2021 were included. Incidence rates for hospitalization due to COVID-19 were determined for the IBD (n = 4980) and general population (n = 597,184) in South-Limburg. RESULTS: During a follow-up of 4254 and 510,120 person-years, 20 IBD patients (0.40%; 11 ulcerative colitis (UC), 9 Crohn’s disease (CD)) and 1425 (0.24%) patients from the general population were hospitalized due to proven COVID-19 corresponding to an incidence rate of 4.7 (95% Confidence interval (CI) 3.0–7.1) and 2.8 (95% CI 2.6–2.9) per 1000 patient years, respectively (Incidence rate ratio: 1.68, 95% CI 1.08–2.62, p = 0.019). Median age (IBD: 63.0 (IQR 58.0–75.8) years vs. general population: 72.0 (IQR 62.0–80.0) years, p = 0.10) and mean BMI (IBD: 24.4 (SD 3.3) kg/m(2) vs. general population 24.1 (SD 4.9) kg/m(2), p = 0.79) at admission were comparable in both populations. As for course of severe COVID-19, similar rates of ICU admission (IBD: 12.5% vs. general population: 15.7%, p = 1.00), mechanical ventilation (6.3% vs. 11.2%, p = 1.00) and death were observed (6.3% vs. 21.8%, p = 0.22). CONCLUSION: We found a statistically significant higher rate of hospitalization due to COVID-19 in IBD patients in a population-based setting in a heavily impacted Dutch region. This finding reflects previous research that showed IBD patients using systemic medication were at an increased risk of serious infection. However, although at an increased risk of hospitalization, clinical course of severe COVID-19 was comparable to hospitalized patients without IBD.

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Millions of people, including patients with Inflammatory Bowel Diseases (IBD), have been affected by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The broad use of immunosuppressants and biologicals in IBD patients increases susceptibility to opportunistic or severe infections [1] [2] [3] . Coronavirus disease 2019 (COVID- 19) is an infectious disease caused by SARS-CoV-2 [4] . Data on incidence and clinical course of severe COVID-19 compared to a general population remains relatively sparse [5] [6] [7] [8] [9] [10] [11] [12] . Especially data from population-based settings in heavily affected regions are underrepresented.

In a recent Swedish population-based study, IBD patients were at an increased risk of hospitalization for COVID-19 compared to the general population, even after adjusting for comorbidities [13] . Remarkably, the subsequent risk for intensive care unit (ICU) admission or death was comparable with a low absolute risk of severe COVID-19 in IBD patients [13] . To guide vaccination strategies against SARS-CoV-2, it is crucial to exactly delineate populations at risk for a severe course of COVID-19.

South-Limburg is a border region in the Southeast of the Netherlands with 597,184 inhabitants enclosed by Germany and Belgium [14] . All regional inpatient care is provided by two hospitals: Zuyderland Medical Centre, a large general district hospital, and Maastricht University Medical Centre+. During the COVID-19 pandemic, the second highest COVID-19 mortality rate (144.7 per 100,000) in the Netherlands (96.0 national average) has been reported for this region [15] .

This report aimed to expand the current knowledge on severe COVID-19 in the IBD population by calculating the incidence rate and examining the clinical course of severe COVID-19 compared to the regional population in a population-based setting in South-Limburg.

The IBD-cohort comprised all patients in the South-Limburg region with an IBD diagnosis at February 27 th 2020 in either one of the only two hospitals covering this region. Due to lockdown and travel limitations all regional COVID-19 patients were treated in these hospitals. The total IBD population in South-Limburg is currently estimated at 4980 patients.

As control population, the total number of inhabitants in the South-Limburg region on February 27 th , 2020 (n = 597,184) were included. Population data were obtained from the Dutch Central Bureau of Statistics (CBS) [14] .

Both populations were observed from February 27 th , 2020, date of first confirmed COVID-19 diagnosis in the Netherlands, until January 4 th , 2021, the start date of COVID-19 vaccinations in the Netherlands. 

This study had two main outcomes: (1) incidence rate of severe COVID-19 was calculated for both IBD patients and the regional population. All IBD patients from the South Limburg region who were admitted for COVID-19-related complaints were included. For the regional population, data on COVID-19 hospitalization were obtained from The Dutch National Institute for Public Health and Environment (RIVM) which publishes daily updated metadata.

(2) To compare clinical course of severe COVID-19 in IBD patients with comparators, baseline characteristics and data on the course of severe COVID-19 were collected for all severe COVID-19 cases in Zuyderland Medical Centre. For this outcome, severe COVID-19 was defined as a confirmed COVID-19 diagnosis (i.e., COVID-19 associated symptoms and either a positive SARS-CoV-2 polymerase chain reaction or CT-CORADS score (�4)) requiring hospitalization, and/or resulting in ICU admission or death. All patients admitted to Zuyderland Medical Centre were prospectively registered in the Zuyderland COVID-19 Registry (ELVIS). After inclusion, patients with IBD in their medical history were identified based on the ICD-10 codes.

This study was approved by the Ethics Committee of Zuyderland Medical Centre (Z2020171). All COVID-19 patients admitted to Zuyderland MC were registered in the ZuydErLand COVID-19 regiStry (ELVIS). All patients in the ELVIS registry received written information about the registry as well as an opt-out form in case they did not want to participate. None of the patients included in this study objected to participation. This opt-out mechanism was approved by the Ethics Committee of Zuyderland Medical Centre.

Incidence rates were calculated as the ratio between COVID-19 hospitalizations (events) and patient-years of follow-up (time). Difference between incidence rates was assessed by calculating the incidence rate ratio using the 'Exact Poisson Method' [16] . Baseline characteristics are presented as means with standard deviations (SD) or medians with interquartile range (IQR) for normal or non-normal distributed numerical variables respectively, and as number of patients with corresponding percentage for categorical variables. Independent samples t-test or Mann-Whitney U test was used for comparison of numerical variables and Chi-square test for categorical variables. Statistical analyses were conducted using SPSS (Version 26.0). A twosided P value �0.05 was considered statistically significant.

During a follow-up of 4254 person-years, 20 IBD patients (0.40%; 11UC, 9CD) were hospitalized in the South-Limburg region due to COVID-19 corresponding to an incidence rate of 4.7 (95% Confidence interval (CI) 3.0-7.1) per 1000 person-years. During the same period, in the general population 1425 patients (0.24%) were admitted to the hospital with COVID-19 during 510,120 person-years yielding an incidence rate of 2.8 (95% CI 2.6-2.9) per 1000 personyears and translating to an incidence rate ratio of 1.68 (95% CI 1.08-2.62, p = 0.019) for IBD versus the general population ( Table 1) .

Out of 870 patients hospitalized for severe COVID-19 in the Zuyderland MC, 16 patients had IBD (10 UC, 6 CD). Baseline characteristics for the study population are presented in Table 2 . Median age and BMI at admission were comparable between the IBD population and comparators. A lower, but statistically non-significant, burden of comorbidities (Charlson comorbidity index (CCI) �4 37.5% vs. 56.7%) was registered in the IBD population.

As for clinical course of severe COVID-19, rates of oxygen support, ICU admission, and mechanical ventilation did not differ between IBD patients versus matched time frame comparators without IBD. Furthermore, no statistically significant difference in death rate date was observed (Table 2 ).

In the present study, we aimed to investigate the incidence rate and clinical outcomes of severe COVID-19 for the IBD population. We observed a statistically significant increase in hospitalization rates due to COVID-19 in a population of 4980 IBD patients when compared to the general population in South-Limburg. This finding reflects previous research in a large population based nationwide cohort study that showed that IBD patients using systemic medication were at an increased risk of serious infections [1] . It is important to note that although we demonstrated an increased risk of hospitalization, the risk of a serious course of COVID-19 was not different in the IBD population compared to the matched time frame comparator population without IBD.

Epidemiological data and disease outcome data on severe COVID-19 in IBD patients from the Netherlands and Denmark have previously been reported [7, 8] . In these studies, SARS--CoV-2 testing data from the general population were compared with data on symptomatic COVID-19 in IBD patients, likely to overrepresent the number of cases in the general population. In another recent population-based study from Sweden, it was assessed whether IBD patients were at an increased risk of severe COVID-19 [13] . In the latter study, patients were identified at hospital admission, and IBD patients were matched with general population controls, therefore enabling more precise risk estimations. Reported incidence rates were 5.4 (95% CI 4.6-6.2), and 3.4 (95%CI 3.1-3.7) per 1000 patient years for COVID-19 hospital admissions in the IBD population and matched controls, respectively. In the present study, similar incidence rates for COVID-19 hospitalization (IBD: 4.7, 95%CI 3.0-7.1 vs. Comparators: 2.8, 95% CI 2.6-2.9) were observed.

Regarding the course of severe COVID-19, baseline patient characteristics of both groups did not differ. Interestingly, BMI, a well-established risk factor for worse disease outcome, was not different between the two groups and equal to the Dutch average [17, 18] . On post-hoc Table 2 . Baseline and severe COVID-19 course characteristics of the IBD population and regional matched time frame comparators. 

analysis, BMI of patients requiring ICU admission was significantly higher compared to non-ICU patients in both groups (mean BMI 25.8 (SD: 4.6) vs mean BMI 23.9 (SD: 4.8), p<0.001), confirming the importance of BMI as a risk factor for severe COVID-19. Additionally, the clinical course of severe COVID-19 was comparable between IBD patients and comparators, as reported before in different settings [19] [20] [21] [22] . Interestingly, none of the IBD patients with severe COVID-19 were on biologicals when in fact a substantial proportion of IBD patients in our population currently use biologicals, in particular anti-tumour necrosis factor (TNF) agents such as infliximab and adalimumab. Since TNF is recognized as an important component of the cytokine response during the inflammatory phase, also known as the cytokine release syndrome (CRS), several studies have described the rationale for anti-TNF therapy in COVID-19 [23, 24] . Moreover, accumulating observational clinical data in IBD and other immune mediated inflammatory diseases (IMIDs) have highlighted the potential benefit of anti-TNF therapies as treatment for COVID-19 and have also led to initiation of various clinical trials that are currently investigating use of anti-TNF in COVID-19 [25] . All in all, although cases were limited, the observation of no anti-TNF users among the IBD patients with severe COVID-19 in the current study further substantiates the potential protective role of anti-TNF agents in the pathophysiology of COVID-19.

Among the strengths of this study is the strict definition of severe COVID-19 applied to both the IBD population as well as the matched time frame comparators. Furthermore, the prospective ELVIS registry enabled detailed phenotyping of baseline and COVID-19 characteristics in both IBD patients and comparators, thus providing us with means to find signals that may be missed in larger retrospective cohorts based on selected cases. As therapeutic focus shifts from reducing symptoms of SARS-CoV-2 infection to preventing severe infection through vaccination, the presented data may be of help to identify most benefitting populations since IBD and treatment of it do not seem to worsen clinical course of severe COVID-19. Nevertheless, we recognize several limitations in this study, of which most important the limited number of severe COVID-19 cases. The limited number of cases prevented adjustment of incidence rates for demographic and clinical characteristics and sub-analyses to identify risk factors for severe COVID-19. Therefore, the statistical comparisons should be interpreted with care. In conclusion, we found a statistically significant higher rate of hospitalization due to COVID-19 in IBD patients in a population-based setting in a heavily impacted Dutch region. This finding reflects previous population-based reports in which was shown that IBD patients using systemic medication are at an increased risk of serious infection, as contrasted with casebased analyses in larger series in which IBD did not seem to be a risk factor for contracting SARS-CoV-2 infection. However, despite increased rates of hospitalization, clinical course of COVID-19 was comparable to hospitalized patients without IBD.

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The authors thank the Research Department (Bureau Wetenschappelijk Onderzoek, BWO), namely Anke Linssen, Esther Bergman, Christel Jacquot, Marijke Lemmens and Audrey Merry for data management of the ELVIS registry.