Table 1.
Patient demographics.
| Sex | Age (years) | F-calpro (μg/g) | UC/CD | Endoscopic diagnosis | Medication | Severity of the disease during the 3-year follow-up |
|---|---|---|---|---|---|---|
| F | 39 | > 2000 | UC | proctitis | prednisolone + azathioprine 150 mg | severe |
| F | 19 | 1400 | UC | pancolitis | methylprednisolone + azathioprine 25 mg × 2 + 5-ASA 1600 mg × 2 | severe |
| F | 28 | > 2000 | UC | pancolitis | prednisolone + 5-ASA 1600 mg × 2 | mild/moderate |
| M | 27 | > 2000 | CD | jejunitis, ileitis | methylprednisolone | severe |
| F | 19 | > 2000 | UC | pancolitis | prednisolone + 5-ASA 1600 mg × 2 | severe |
| F | 19 | > 2000 | I | pancolitis | methylprednisolone + 5-ASA 2 g + 1 g | severe |
| F | 31 | > 2000 | UC | pancolitis | methylprednisolone + azathioprine 150 mg + 5-ASA 1600 mg × 2 | severe |
| F | 30 | 1294 | CD | ileitis, sigmoiditis | methylprednisolone + azathioprine 25 mg × 2 | mild/moderate |
| F | 36 | 393 | CD | ileitis | prednisolone + mercaptopurine 50 mg × 1 | mild/moderate |
| F | 54 | 557 | CD | ileitis | budesonide 9 mg × 1 + azathioprine 25 mg × 1 | mild/moderate |
| M | 37 | 5860 | UC | pancolitis | prednisolone + azathioprine 25 mg × 2 | severe |
| F | 19 | 3178 | CD | ileitis, segmental colitis | methylprednisolone | mild/moderate |
| F | 85 | 45 | CD | Segmental colitis | budesonide 9 mg × 1 | mild/moderate |
| M | 79 | 607 | CD | jejunitis, ileitis | budesonide 9 mg × 1 | mild/moderate |
F, Female, M, Male, F-calpro, Fecal calprotectin, UC, Ulcerative colitis, CD, Crohn’s disease, I, Intermediate colitis. The medication is described at beginning the of the diagnosed relapse. The dose of intravenous methylprednisolone was 40 + 20 mg per day (for the hospitalized patients), and the dose of per oral prednisolone (for the patients at outpatient clinic) was 40 mg per day and the cut down of prednisolone was − 5 mg per week consecutively. The dose of oral budesonide was 9 mg per day at the time of relapse and the cut down of the dose was − 3 mg per month consecutively. 5-ASA = 5-aminosalicylic acid. All the parameters besides the severity of the disease are described at the time of enrollment. The severity of the disease is described during the 3-year follow up.