Mesalamine enemas for induction of remission in oral mesalamine-refractory pediatric ulcerative colitis: A prospective cohort study

Arie Levine, Baruch Yerushalmi, Michal Kori, Efrat Broide, Yael Mozer-Glassberg, Ron Shaoul, Kaija Leena Kolho, Eyal Shteyer, Hussein Shamaly, Oren Ledder, Shlomi Cohen, Sarit Peleg, Chen Sarbagili Shabat, Gili Focht, Ebby Shachmon, Mona Boaz, Avi On, Dan Turner

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Background: Paediatric ulcerative colitis [UC] is more extensive than adult disease, and more often refractory to mesalamine. However, no prospective trials have evaluated mesalamine enemas for inducing remission in children. Our goal was to evaluate the ability of mesalamine enemas to induce remission in mild to moderate paediatric UC refractory to oral mesalamine. Methods: This was an open-label arm of a previously reported randomised controlled trial of once-daily mesalamine in active paediatric UC [MUPPIT trial]. Children aged 4-18 years, with a Paediatric Ulcerative Colitis Activity Index [PUCAI] score of 10-55, were enrolled after failing at least 3 weeks of full-dose oral mesalamine. Patients treated with steroids or enemas in the previous month and those with isolated proctitis were excluded. Children received Pentasa® enemas 25 mg/kg [up to 1g] daily for 3 weeks with the previous oral dose. The primary endpoint was clinical remission by Week 3. Results: A total of 38 children were enrolled (mean age 14.6 ± 2.3 years; 17/38 [45%] with extensive colitis). Clinical remission was obtained in 16 [42%] and response was obtained in 27 [71%] at Week 3. Eight children deteriorated and required steroids. There were no differences in baseline parameters between those who entered or failed to enter remission, including disease extent [43% in left-sided and 41% in extensive colitis] and disease activity [44% in mild and 41% in moderate activity]. Conclusion: Clinical remission can be markedly increased in children who are refractory to oral mesalamaine by adding mesalamine enemas for 3 weeks, before commencing steroids.

Original languageEnglish
Pages (from-to)970-974
Number of pages5
JournalJournal of Crohn's and Colitis
Volume11
Issue number8
DOIs
StatePublished - 1 Aug 2017

Bibliographical note

Publisher Copyright:
Copyright © 2017 European Crohn's and Colitis Organisation (ECCO). Published by Oxford University Press. All rights reserved.

Funding

This investigator-initiated trial was partially funded by an educational grant from Ferring who also provided the study medication and monitoring service; however, Ferring were not involved in any part of the trial design, management, analyses or manuscript preparation. No professional writing assistance has been provided. DT received in the past 3 year consultation fee, research grant, royalties, or honorarium from Janssen, Pfizer, Hospital for Sick Children, Ferring, MegaPharm, AstraZeneca, Abbvie, Takeda, Rafa, Boehringer Ingelheim, Biogen, Atlantic Health. AL has received travel grants or speaker’s honoraria, participated in advisory boards, or received research grants from Nestle, Jannsen, Abbvie, Takeda. OL received travel grant from Ferring. KLK received study support from the Finnish Paediatric Research Foundation and Helsinki University Hospital Research Fund, membership of Advisory Board Abbvie and MSD [Finland], consultant fees from Ferring and Tillotts Pharma. RS received Nestle research dupport, Jannsen research support, Megapharm research support, Golden Heart consulting, Enzymotec consulting, Wissotzki consulting, Materna speaking, Teva speaking, Mead Johnsson speaking, and Lapidot consulting fees.

FundersFunder number
Finnish Paediatric Research Foundation
Helsinki University Hospital
Meso Scale Diagnostics
Ferring
Ferring Pharmaceuticals
Tillotts Pharma

    Keywords

    • Child
    • Drugs
    • Ulcerative colitis

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