炎性肠病儿童原发性硬化性胆管炎:来自肝病委员会和IBD波尔图组的ESPGHAN立场文件

IF 2.4 3区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Journal of Pediatric Gastroenterology and Nutrition Pub Date : 2025-02-01 Epub Date: 2024-12-31 DOI:10.1002/jpn3.12378
Patrick F van Rheenen, Kaija-Leena Kolho, Richard K Russell, Marina Aloi, Annamaria Deganello, Séamus Hussey, Norman Junge, Jan De Laffolie, Mark R Deneau, Emer Fitzpatrick, Anne M Griffiths, Iva Hojsak, Emanuele Nicastro, Andreia Nita, Mikko Pakarinen, Amanda Ricciuto, Lissy de Ridder, Aurelio Sonzogni, Andrea Tenca, Marianne Samyn, Giuseppe Indolfi
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引用次数: 0

摘要

目的:我们旨在提供一种有证据支持的方法来诊断、监测和治疗儿童炎症性肠病(IBD)和原发性硬化性胆管炎(PSC)。方法:核心组制定7个pico结构的临床问题。一位医学图书管理员使用MEDLINE和EMBASE进行了从成立到2022年12月的系统文献检索。来自文献的核心信息被表述为立场声明,然后分发给由儿科胃肠病学和肝病学、组织病理学、成人胃肠病学和肝病学、放射学和外科等国际专家组成的声音委员会。达到至少80%一致的陈述被认为是最终的。其他陈述经过修改,然后进行第二次在线投票或否决。结果:定期筛查γ -谷氨酰转移酶(GGT)对发现IBD患儿可能的胆道疾病至关重要。MR胰胆管造影是确定PSC诊断的放射学方式的选择。肝活检与小管PSC或自身免疫性肝炎的评估相关。在PSC诊断时不知道IBD的儿童应接受粪便钙保护蛋白的无症状结肠炎初步筛查,此后每年至少进行一次筛查。有胆汁淤积性肝酶谱的儿童可以考虑用熊去氧胆酸治疗,如果GGT有意义的降低或正常化,可以继续治疗。口服万古霉素可能对GGT和肠道炎症有有益作用,但由于缺乏长期研究,建议谨慎使用。PSC-IBD合并自身免疫性肝炎的儿童可能受益于皮质类固醇和抗代谢物。结论:我们在诊断标准、随访策略和治疗策略方面提供了最新的指导,并指出了儿童和青少年PSC-IBD的研究空白。
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Primary sclerosing cholangitis in children with inflammatory bowel disease: An ESPGHAN position paper from the Hepatology Committee and the IBD Porto group.

Objective: We aimed to provide an evidence-supported approach to diagnose, monitor, and treat children with inflammatory bowel disease (IBD) and primary sclerosing cholangitis (PSC).

Methods: The core group formulated seven PICO-structured clinical questions. A systematic literature search from inception to December 2022 was conducted by a medical librarian using MEDLINE and EMBASE. Core messages from the literature were phrased as position statements and then circulated to a sounding board composed of international experts in pediatric gastroenterology and hepatology, histopathology, adult gastroenterology and hepatology, radiology, and surgery. Statements reaching at least 80% agreement were considered as final. The other statements were refined and then subjected to a second online vote or rejection.

Results: Regular screening for gamma-glutamyltransferase (GGT) is essential for detecting possible biliary disease in children with IBD. MR cholangiopancreatography is the radiological modality of choice for establishing the diagnosis of PSC. Liver biopsy is relevant in the evaluation of small duct PSC or autoimmune hepatitis. Children who do not have known IBD at the time of PSC diagnosis should undergo initial screening with fecal calprotectin for asymptomatic colitis, and then at least once yearly thereafter. Children with a cholestatic liver enzyme profile can be considered for treatment with ursodeoxycholic acid and can continue if there is a meaningful reduction or normalization in GGT. Oral vancomycin may have a beneficial effect on GGT and intestinal inflammation, but judicious use is recommended due to the lack of long-term studies. Children with PSC-IBD combined with convincing features of autoimmune hepatitis may benefit from corticosteroids and antimetabolites.

Conclusions: We present state-of-the-art guidance on the diagnostic criteria, follow-up strategies, and therapeutic strategies and point out research gaps in children and adolescents with PSC-IBD.

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来源期刊
CiteScore
5.30
自引率
13.80%
发文量
467
审稿时长
3-6 weeks
期刊介绍: ​The Journal of Pediatric Gastroenterology and Nutrition (JPGN) provides a forum for original papers and reviews dealing with pediatric gastroenterology and nutrition, including normal and abnormal functions of the alimentary tract and its associated organs, including the salivary glands, pancreas, gallbladder, and liver. Particular emphasis is on development and its relation to infant and childhood nutrition.
期刊最新文献
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