Table 13.
Study | Country | Intervention | Comparator | Study design | Follow-up | n | Clinical response |
Arts et al[36] | Belgium | Cyclosporine | - | Retrospective cohort | 9 d | 86 | 83.7%1 |
Prieux-Klotz et al[37] | France | AZA or 6-MP | - | Retrospective cohort | 38 mo | 80 | 70%2 |
Yamamoto et al[38] | Japan | Tacrolimus | Anti-TNF | Retrospective | 12 wk | 100 | 62% (tacrolimus); 64% (anti-TNF); P > 0.993 |
Ogata et al[39] | Japan | Tacrolimus | Placebo | RCT | 2 wk | 62 | 50% (tacrolimus); 13.3% (placebo); P = 0.0034 |
Van Assche et al[48] | Belgium | Cyclosporine 4 mg/kg | Cyclosporine 2 mg/kg | RCT | 2 wk | 73 | 84.2% (4 mg/kg); 85.7% (2 mg/kg)5 |
Oshitani et al[47] | Japan | Prednisolone | Methylprednisolone | Retrospective cohort | 7-14 d | 71 | 82% (prednisolone); 82% (methylprednisolone)6 |
Response defined as colectomy avoided;. 2Clinical response defined by a decrease in the partial Mayo score of at least 3 points and 30% with a rectal bleeding Mayo subscore ≤ 1;
Clinical response was defined as a decrease of at least 2 points in the clinical section (stool frequency and/or rectal bleeding);
Clinical response was defined as improvement in all Disease Activity Index subscores;
Clinical response was defined as a score of less than 10 at day 8 with a drop of ≥ 3 as compared with baseline;
Clinical response considered as at least one of: decreased blood in stools compared with previous findings; soft or normal stool; no nocturnal defecation. 6-MP: 6-mercaptopurine; AZA: Azathioprine; n: Number of patients; RCT: Randomized clinical trial; TNF: Tumor necrosis factor.