Supplementary Table 1.
Antiviral therapy (n=17) | Non-antiviral therapy (n=31) | P | |
---|---|---|---|
Post - admission treatment, n (%) | |||
GS | 10 (58.8%) | 16 (51.6%) | 0.632 |
AZA/6-MP | 5 (29.4%) | 11 (35.4%) | 0.670 |
IFX | 2 (11.8%) | 2 (6.5%) | 0.524 |
IFX+AZA | 0 | 2 (6.5%) | 0.285 |
EBV-DNA was negative in duplicates after 2 weeks | 14 (82.4%) | 26 (83.9%) | 0.893 |
EBV-DNA was negative in duplicates after 4 weeks | 17 (100.0%) | 31 (100.0%) | - |
Clinical remission within 3 months | |||
UC n (n) (%) | 8 (12) (66.7%) | 12 (16) (75.0%) | 0.629 |
CD n (n) (%) | 3 (5) (60.0%) | 10 (15) (66.7%) | 0.787 |
Surgery within 3 months, n (%) | 4 (23.6%) | 5 (16.1%) | 0.530 |
Lymphoma was observed during the follow-up, n (%) | 1 (5.9%) | 0 (0.0%) | 0.172 |
CAEBV was observed during the follow-up, n (%) | 0 (0.0%) | 0 (0.0%) | - |
IBD, Inflammatory bowel disease; UC, ulcerative colitis; CD, Crohn’s disease; CAEBV: chronic activity Epstein-Barr virus; EBV, Epstein-Barr virus; EBER-1, Epstein-Barr virus-encoded small-RNA 1; 5-ASA, 5-aminosalicylates; CS, corticosteroids; AZA, azathioprine; IFX, infliximab; IFX + AZA, infliximab in combination with azathioprine, all patients