van Rheenen Patrick F, Kolho Kaija-Leena, Russell Richard K, Aloi Marina, Deganello Annamaria, Hussey Séamus, Junge Norman, De Laffolie Jan, Deneau Mark R, Fitzpatrick Emer, Griffiths Anne M, Hojsak Iva, Nicastro Emanuele, Nita Andreia, Pakarinen Mikko, Ricciuto Amanda, de Ridder Lissy, Sonzogni Aurelio, Tenca Andrea, Samyn Marianne, Indolfi Giuseppe
Department of Paediatric Gastroenterology, Hepatology, and Nutrition, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Children's Hospital, University of Helsinki and HUS, Helsinki, Finland.
J Pediatr Gastroenterol Nutr. 2025 Feb;80(2):374-393. doi: 10.1002/jpn3.12378. Epub 2024 Dec 31.
We aimed to provide an evidence-supported approach to diagnose, monitor, and treat children with inflammatory bowel disease (IBD) and primary sclerosing cholangitis (PSC).
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.
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.
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.
我们旨在提供一种有循证依据的方法,用于诊断、监测和治疗患有炎症性肠病(IBD)和原发性硬化性胆管炎(PSC)的儿童。
核心小组拟定了七个采用PICO结构的临床问题。医学图书馆员使用MEDLINE和EMBASE对从创刊至2022年12月的文献进行了系统检索。文献中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、放射学及外科学领域的国际专家组成的咨询小组。达成至少80%共识的声明被视为最终声明。其他声明经过完善后进行第二轮在线投票或被否决。
定期筛查γ-谷氨酰转移酶(GGT)对于检测IBD患儿可能存在的胆道疾病至关重要。磁共振胰胆管造影是用于确立PSC诊断的首选影像学检查方法。肝活检对于评估小胆管PSC或自身免疫性肝炎具有重要意义。在PSC诊断时未患已知IBD的儿童应首先进行粪便钙卫蛋白筛查以排查无症状性结肠炎,此后至少每年筛查一次。胆汁淤积性肝酶谱异常的儿童可考虑使用熊去氧胆酸进行治疗,若GGT有显著降低或恢复正常则可继续用药。口服万古霉素可能对GGT和肠道炎症有有益作用,但鉴于缺乏长期研究,建议谨慎使用。合并有自身免疫性肝炎确凿特征的PSC-IBD患儿可能从皮质类固醇和抗代谢药物治疗中获益。
我们提出了关于诊断标准、随访策略和治疗策略的最新指南,并指出了PSC-IBD儿童和青少年中的研究空白。