Table 1:
Baseline characteristics by final long-term PPI dose regimen in patients with endoscopic follow-up (n = 50)
Final dose unchanged (n = 14) |
Final dose increased (n = 3) |
Final dose lowered (n = 22) |
Final dose re-increased (n = 11) |
p* | |
---|---|---|---|---|---|
Age (mean years ± SD) | 47.7 ± 14.2 | 40.1 ± 9.0 | 46.5 ± 14.9 | 40.7 ± 12.5 | 0.55 |
Male (n, %) | 9 (64) | 2 (67) | 10 (45) | 8 (73) | 0.44 |
White (n, %) | 12 (86) | 3 (100) | 21 (95) | 10 (91) | 0.71 |
Symptoms (n, %) | |||||
Dysphagia | 14 (100) | 3 (100) | 22 (100) | 11 (100) | -- |
Heartburn | 7 (50) | 1 (33) | 4 (18) | 1 (9) | 0.09 |
Abdominal pain | 3 (21) | 1 (33) | 3 (14) | 0 (0) | 0.34 |
Nausea/vomiting | 3 (21) | 1 (33) | 2 (14) | 0 (0) | 0.34 |
Atopy (n, %) | |||||
Seasonal allergies | 7 (50) | 2 (67) | 16 (73) | 4 (36) | 0.21 |
Asthma | 5 (36) | 2 (67) | 7 (32) | 1 (9) | 0.22 |
Food allergies | 2 (14) | 2 (67) | 5 (23) | 1 (9) | 0.15 |
Eczema | |||||
Endoscopic findings (n, %) | |||||
Rings | 10 (71) | 0 (0) | 12 (55) | 10 (91) | 0.02 |
Stricture | 6 (43) | 1 (33) | 7 (32) | 4 (36) | 0.93 |
Narrowing | 1 (7) | 0 (0) | 3 (14) | 2 (18) | 0.76 |
Furrows | 7 (50) | 1 (33) | 15 (68) | 8 (72) | 0.42 |
Exudates | 7 (50) | 0 (0) | 8 (36) | 6 (55) | 0.32 |
Edema | 4 (29) | 0 (0) | 9 (41) | 4 (36) | 0.53 |
Dilation performed | 5 (34) | 2 (67) | 11 (50) | 4 (37) | 0.66 |
Peak eosinophil counts (mean eos/hpf ± SD) | |||||
Pre-PPI treatment | 65.2 ± 41.0 | 83.3 ± 93.6 | 61.1 ± 38.3 | 71.7 ± 72.8 | 0.88 |
Post-PPI treatment | 4.7 ± 5.1 | 9.8 ± 4.0 | 5.5 ± 4.4 | 4.1 ± 4.3 | 0.28 |
Mean follow-up time (years ± SD) | 2.4 ± 1.8 | 2.8 ± 3.1 | 2.8 ± 1.9 | 6.8 ± 3.6 | < 0.001 |
PPI medication type (n, %) | 0.12 | ||||
Dexlansoprazole | 0 (0) | 0 (0) | 0 (0) | 0 (0) | |
Mean daily dose† (mg ± SD) | -- | -- | -- | -- | |
Esomeprazole | 1 (7) | 0 (0) | 4 (18) | 2 (18) | |
Mean daily dose (mg ± SD) | 40 ± 0 | -- | 70 ± 20 | 80 ± 0 | |
Lansoprazole | 2 (14) | 0 (0) | 1 (5) | 2 (18) | |
Mean daily dose (mg ± SD) | 60 ± 0 | -- | 60 ± 0 | 60 ± 0 | |
Omeprazole | 7 (50) | 2 (67) | 17 (77) | 7 (64) | |
Mean daily dose (mg ± SD) | 40 ± 0 | 40 ± 0 | 44.7 ± 0 | 40 ± 0 | |
Pantoprazole | 4 (29) | 1 (33) | 0 (0) | 0 (0) | |
Mean daily dose (mg ± SD) | 60 ± 23.1 | 40 ± 0 | -- | -- | |
PPI dose category (n, %)‡ | 0.08 | ||||
Single/standard | 2 (14) | 1 (33) | 0 (0) | 0 (0) | |
Double | 12 (86) | 2(67) | 17 (77) | 9 (82) | |
Quadruple | 0 (0) | 0 (0) | 5 (23) | 2 (18) |
Means compared with means compared with ANOVA, proportions compared with Chi squared
There were no statistically significant differences between the mean doses for any of the PPIs
Categorization based one standard doses as follows: omeprazole 20 mg, pantoprazole 40mg, esomeprazole 20 mg, lansoprazole 30 mg, with double and quadruple calculated accordingly; no patients received rabeprazole.