van Rheenen Patrick F, Aloi Marina, Assa Amit, Bronsky Jiri, Escher Johanna C, Fagerberg Ulrika L, Gasparetto Marco, Gerasimidis Konstantinos, Griffiths Anne, Henderson Paul, Koletzko Sibylle, Kolho Kaija-Leena, Levine Arie, van Limbergen Johan, Martin de Carpi Francisco Javier, Navas-López Víctor Manuel, Oliva Salvatore, de Ridder Lissy, Russell Richard K, Shouval Dror, Spinelli Antonino, Turner Dan, Wilson David, Wine Eytan, Ruemmele Frank M
Department of Paediatric Gastroenterology, University of Groningen, University Medical Centre Groningen, Beatrix Children's Hospital, Groningen, The Netherlands.
Pediatric Gastroenterology and Liver Unit, Maternal and Child Health Department, Sapienza - University of Rome, Rome, Italy.
J Crohns Colitis. 2020 Oct 7. doi: 10.1093/ecco-jcc/jjaa161.
We aimed to provide an evidence-supported update of the ECCO-ESPGHAN guideline on the medical management of paediatric Crohn's disease [CD].
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.
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.
We present state-of-the-art guidance on the medical treatment and long-term management of children and adolescents with CD.
我们旨在对欧洲克罗恩病和结肠炎组织(ECCO)与欧洲儿科胃肠病、肝病和营养学会(ESPGHAN)关于儿童克罗恩病(CD)药物治疗的指南进行循证更新。
我们组建了10个工作组,并制定了17个PICO结构的临床问题[患者、干预措施、对照措施和结局]。一名医学图书馆员使用MEDLINE、EMBASE和Cochrane中心数据库,对1991年1月1日至2019年3月19日的文献进行了系统检索。2019年10月在巴塞罗那举行的一次共识会议上,对30条临时声明的入围名单进行了进一步完善,并进行了投票。共有22条声明达成≥80%的共识并被保留。
我们确定,尽早识别疾病进程复杂的高危患者以减少肠道损伤是关键。患有肛周疾病、狭窄或穿透性病变或严重生长发育迟缓的患者,应考虑一开始就使用抗肿瘤坏死因子(TNF)药物并联合免疫调节剂。推荐进行治疗药物监测以指导治疗调整,而不是凭经验增加抗TNF剂量或更换治疗方案。低风险的腔内CD患者,应采用全肠内营养(EEN)诱导治疗,若无法采用EEN,则使用皮质类固醇,且需要基于免疫调节剂的维持治疗。良好的结局依赖于对治疗反应的密切监测,当未达到治疗目标时及时调整治疗方案。连续检测粪便钙卫蛋白或小肠成像[超声或磁共振小肠造影]比单纯的临床评分更能可靠地反映治疗反应。
我们提出了关于儿童和青少年CD药物治疗及长期管理的最新指南。