The Medical Management of Paediatric Crohn’s Disease: an ECCO-ESPGHAN Guideline Update

Patrick F. van Rheenen(University Medical Center Groningen), Marina Aloi(Sapienza University of Rome), Amit Assa(Tel Aviv University), Jiří Bronský(University Hospital in Motol), Johanna C. Escher(Erasmus MC - Sophia Children’s Hospital), Ulrika L. Fagerberg(Karolinska Institutet), Marco Gasparetto(Barts Health NHS Trust), Konstantinos Gerasimidis(University of Glasgow), Anne M. Griffiths(University of Toronto), Paul Henderson(University of Edinburgh), Sibylle Koletzko(University of Warmia and Mazury in Olsztyn), Kaija‐Leena Kolho(University of Helsinki), Arie Levine(Tel Aviv University), Johan Van Limbergen(Amsterdam University Medical Centers), Francisco Javier Martín Carpi(Hospital Sant Joan de Déu Barcelona), Víctor Manuel Navas‐López(Hospital Regional Universitario de Málaga), Salvatore Oliva(Sapienza University of Rome), Lissy de Ridder(Erasmus MC - Sophia Children’s Hospital), Richard K. Russell(Royal Hospital for Sick Children), Dror S. Shouval(Tel Aviv University), Antonino Spinelli(Humanitas University), Dan Turner(Hebrew University of Jerusalem), David C. Wilson(University of Edinburgh), Eytan Wine(University of Alberta), Frank M. Ruemmele(Délégation Paris 5)
Journal of Crohn s and Colitis
July 31, 2020
Cited by 680Open Access
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Abstract

OBJECTIVE: We aimed to provide an evidence-supported update of the ECCO-ESPGHAN guideline on the medical management of paediatric Crohn's disease [CD]. METHODS: We formed 10 working groups and formulated 17 PICO-structured clinical questions [Patients, Intervention, Comparator, and Outcome]. A systematic literature search from January 1, 1991 to March 19, 2019 was conducted by a medical librarian using MEDLINE, EMBASE, and Cochrane Central databases. A shortlist of 30 provisional statements were further refined during a consensus meeting in Barcelona in October 2019 and subjected to a vote. In total 22 statements reached ≥ 80% agreement and were retained. RESULTS: We established that it was key to identify patients at high risk of a complicated disease course at the earliest opportunity, to reduce bowel damage. Patients with perianal disease, stricturing or penetrating behaviour, or severe growth retardation should be considered for up-front anti-tumour necrosis factor [TNF] agents in combination with an immunomodulator. Therapeutic drug monitoring to guide treatment changes is recommended over empirically escalating anti-TNF dose or switching therapies. Patients with low-risk luminal CD should be induced with exclusive enteral nutrition [EEN], or with corticosteroids when EEN is not an option, and require immunomodulator-based maintenance therapy. Favourable outcomes rely on close monitoring of treatment response, with timely adjustments in therapy when treatment targets are not met. Serial faecal calprotectin measurements or small bowel imaging [ultrasound or magnetic resonance enterography] are more reliable markers of treatment response than clinical scores alone. CONCLUSIONS: We present state-of-the-art guidance on the medical treatment and long-term management of children and adolescents with CD.


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