3.1 Randomised trial (102 weeks of follow‐up) |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
3.1.1 Clinical recurrence (CDAI >150) until week 102 |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
3.1.2 Endoscopic recurrence (Rutgeerts' score ≥i2) at week 102 |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
3.1.3 Endoscopic recurrence (Rutgeerts' score ≥i3) at week 102 |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
3.1.4 Adverse events at 102 weeks |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
3.2 Cohort studies |
2 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
3.2.1 Clinical recurrence (32 months of median follow‐up) |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
3.2.2 Surgical recurrence (50 months of median follow‐up) |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
3.2.3 Azathioprine withdrawal due to adverse event (50 months of median follow‐up) |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |