2010
DOI: 10.1053/j.gastro.2010.05.001
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Oral Viscous Budesonide Is Effective in Children With Eosinophilic Esophagitis in a Randomized, Placebo-Controlled Trial

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Cited by 393 publications
(397 citation statements)
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“…Patients who had evidence of a pathological amount of distal oesophageal acid exposure (>4% of the total study time) were treated with an oral proton pump inhibitor (PPI), esomeprazole 40 mg twice daily; and those with normal 24-h pH studies were treated with an oral budesonide suspension [two budesonide 0.5 mg ⁄ 2 mL ampules and one, 1 g packet of Splenda (sucralose) mixed together] twice daily for a total of 2 mg of budesonide per day. 11 Response to treatment was assessed by histology and symptoms as measured by the MDQ-30. All subjects underwent a standard 24-h transnasal catheter-based ambulatory oesophageal pH monitoring study.…”
Section: Methodsmentioning
confidence: 99%
“…Patients who had evidence of a pathological amount of distal oesophageal acid exposure (>4% of the total study time) were treated with an oral proton pump inhibitor (PPI), esomeprazole 40 mg twice daily; and those with normal 24-h pH studies were treated with an oral budesonide suspension [two budesonide 0.5 mg ⁄ 2 mL ampules and one, 1 g packet of Splenda (sucralose) mixed together] twice daily for a total of 2 mg of budesonide per day. 11 Response to treatment was assessed by histology and symptoms as measured by the MDQ-30. All subjects underwent a standard 24-h transnasal catheter-based ambulatory oesophageal pH monitoring study.…”
Section: Methodsmentioning
confidence: 99%
“…While there is consensus among the members of scientific community and regulatory agencies that symptoms should be assessed by patients themselves [24,25], the extent of correlation between patient-reported outcomes and endoscopic and histologic findings has not yet been determined and needs to undergo further evaluation. [26][27][28][29] We addressed the potential issue of a referral bias by comparing the results of time-dependent stricture development in the group of 200 patients diagnosed by the senior author (AS) with the group of 460 externally diagnosed EoE patients. Although the assessment of endoscopic features at the time of EoE diagnosis was not standardized in this external cohort, we found, similarly to the results in the "core" cohort of 200 patients, that the prevalence of strictures at the time of EoE diagnosis significantly increased with ongoing duration of untreated disease.…”
Section: A C C E P T E D Accepted Manuscriptmentioning
confidence: 99%
“…Although there were no common criteria to define histological remission in the studies reviewed, a majority of the randomized controlled trial studies used more stringent values ranging from 0 to ≤5 eosinophils/hpf to define histological remission or resolution 22, 26, 66, 67, 68. Compared to dietary treatment studies (e.g.…”
Section: Discussionmentioning
confidence: 99%