| Literature DB >> 33063927 |
Thomas M Goodsall1,2, Sangwoo Han1, Robert V Bryant1,2.
Abstract
BACKGROUND AND AIM: The coronavirus disease 2019 (COVID-19) pandemic has led to a rapid shift in care delivery models for patients with inflammatory bowel disease (IBD); however, little is known about patient perceptions during this period. We aimed to prospectively evaluate the attitudes, concerns, and health behavior of IBD patients during COVID-19.Entities:
Keywords: COVID-19; Crohn's disease; Inflammatory bowel disease; Patient perceptions; Ulcerative colitis
Mesh:
Year: 2020 PMID: 33063927 PMCID: PMC7675463 DOI: 10.1111/jgh.15299
Source DB: PubMed Journal: J Gastroenterol Hepatol ISSN: 0815-9319 Impact factor: 4.369
Demographic and clinical characteristics of 97 respondents
| Age (median, range) | 49, 17–77 |
| Current smokers | 14 (14%) |
| IBD phenotype | |
| Crohn's disease | 57 (59%) |
| Ulcerative colitis | 38 (39%) |
| Unsure/indeterminate | 2 (2%) |
| Current medications | |
| Prednisolone | 8 (13%) |
| Budesonide | 3 (5%) |
| 5‐Aminosalacylates | 35 (49%) |
| Rectal therapy | 10 (17%) |
| Thiopurines | 35 (51%) |
| Methotrexate | 5 (9%) |
| Infliximab | 19 (30%) |
| Adalimumab | 6 (10%) |
| Golimumab | 2 (4%) |
| Vedolizumab | 14 (23%) |
| Ustekinumab | 9 (15%) |
| Tofacitinib | 1 (2%) |
| Combination medication use | |
| Thiopurine and biologic agent | 18 (19%) |
| Methotrexate and biologic agent | 4 (4%) |
| Prednisolone and biologic agent | 2 (2%) |
| Prednisolone, thiopurine, and vedolizumab | 1 (1%) |
IBD, inflammatory bowel disease.
Perceived risks ranked 1 (no increase in risk) to 4 (great increase in risk) of inflammatory bowel disease medications for catching coronavirus disease 2019
| Medication | No or small increase in risk (1–2) | Moderate or great increase in risk (3–4) | Mean value |
| 5‐ASAs | 31 (79%) | 8 (21%) | 1.66 (1.03) |
| Budesonide | 8 (67%) | 4 (33%) | 2.08 (1.16) |
| Tofacitinib | 6 (60%) | 4 (40%) | 2.1 (1.1) |
| Vedolizumab | 12 (57%) | 9 (43%) | 2.15 (1.14) |
| Steroids | 19 (54%) | 16 (46%) | 2.19 (1.24) |
| Ustekinumab | 10 (56%) | 8 (44%) | 2.56 (1.10) |
| Thiopurines | 16 (34%) | 31 (66%) | 2.66 (1.04) |
| Methotrexate | 8 (40%) | 12 (60%) | 2.8 (1.20) |
| Anti‐TNFα | 12 (35%) | 22 (65%) | 2.85 (1.01) |
5‐ASA; 5‐aminosalicylates, anti‐TNFα; anti‐tumor necrosis factor‐α medications.
Perceived risks ranked 1 (no increase in risk) to 4 (Great increase in risk) of IBD medications for developing severe illness or death from coronavirus disease 2019
| Medication | No or small increase in risk (1–2) | Moderate or great increase in risk (3–4) | Mean value |
| 5‐ASAs | 23 (74%) | 8 (26%) | 1.74 (0.93) |
| Tofacitinib | 3 (43%) | 4 (57%) | 2.15 (1.07 |
| Budesonide | 6 (46%) | 7 (54%) | 2.31 (1.32) |
| Vedolizumab | 9 (47%) | 10 (53%) | 2.4 (1.07) |
| Steroids | 17 (49%) | 18 (51%) | 2.51 (1.09) |
| Thiopurines | 14 (36%) | 25 (64%) | 2.77 (0.93) |
| Methotrexate | 6 (33%) | 12 (67%) | 2.78 (1.06) |
| Anti‐TNFα | 9 (21%) | 22 (79%) | 2.87 (0.92) |
| Ustekinumab | 5 (31%) | 11 (69%) | 2.88 (1.02) |
5‐ASA; 5‐aminosalicylates, anti‐TNFα; anti‐tumor necrosis factor‐α medications.