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. 2024 Jan 19;14(2):218. doi: 10.3390/diagnostics14020218

Table 2.

Clinical, endoscopic, and histological data in patients with EoE before and after a 6-week treatment with orodispersible budesonide tablets.

EoE Patients at
Baseline (n = 14)
EoE Patients Post
Treatment (n = 14)
p
Straumann Dysphagia Index; median (IQR) 9 (3–13) 1 (1–6) <0.001
Esophageal dilation; n 2 0 0.241
EEsAI-PRO score; mean ± SD (range) 49 ± 28 (15–80) 12 ± 25 (0–42) <0.001
EREFS score; median (IQR) 4 (2–8) 0 (0–4) <0.001
Edema; n <0.001
0: Distinct vascularity 1 13
1: Decreased 13 1
2: Absent 0 0
Rings; n 0.384
0: None 9 10
1: Mild 1 3
2: Moderate 3 1
3: Severe 1 0
Exudates; n <0.001
0: None 1 13
1: Mild 3 1
2: Severe 10 0
Furrows; n <0.001
0: None 0 13
1: Mild 14 1
2: Severe 0 0
Strictures; n 0.049
0: Absent 10 14
1: Present 4 0
Crêpe paper; n 0.241
0: Absent 12 14
1: Present 2 0
Peak eosinophil count at proximal esophagus, cells/high power field; median (IQR) 40 (17–120) 0 (0–5) <0.001
Peak eosinophilic count at distal esophagus, cells/high power field; median (IQR) 53 (28–100) 0 (0–16) <0.001
Discomfort after EndoFLIPTM; n 1 0 0.5

IQR, interquartile range; EesAI-PRO, eosinophilic esophagitis activity index—patient-reported outcome; EoE, eosinophilic esophagitis, EREFS, endoscopic reference score, EndoFLIPTM, endoscopic functional lumen imaging probe.