Outcomes of oral vancomycin therapy in children with atypical ulcerative colitis with or without confirmed primary sclerosing cholangitis: a real-world observational study.

IF 2.9 Q2 GASTROENTEROLOGY & HEPATOLOGY BMJ Open Gastroenterology Pub Date : 2025-02-12 DOI:10.1136/bmjgast-2024-001605
Laura Räisänen, Fariha Balouch, Annette McLaren-Kennedy, Julia Elizabeth Clark, Peter Lewindon
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Abstract

Objectives: Atypical ulcerative colitis (UC) presenting reverse gradient colitis, backwash ileitis, or rectal sparing and/or positive atypical antineutrophil cytoplasmic antibody serology is often associated with primary sclerosing cholangitis (PSC) and can be resistant to conventional medical therapies (CMT) for inflammatory bowel diseases. We report short-term and long-term outcomes of oral vancomycin therapy (OVT) in children with atypical UC and confirmed PSC in imaging/biopsy (PSC-UC) or treatment-resistant atypical UC without detectable PSC (aUC-non-PSC).

Methods: In this retrospective real-world observational study from a tertiary paediatric centre in Brisbane, Australia, 44 children with aUC (29 PSC-UC, 15 aUC-non-PSC) received 79 OVT courses between 2014 and 2023. Pre-post-OVT characteristics were compared and relapses/repeated courses were recorded.

Results: Pre-OVT, all had active colitis by Paediatric Ulcerative Colitis Activity Index (PUCAI), Feacal Calprotectin (FC) and/or colonoscopy. Post-OVT, PUCAI reduced from 15 (IQR 5-33) to 0 (IQR 0-5); 85% of children with pre-OVT PUCAI ≥10 achieved clinical remission (100% PSC-UC vs 64% aUC-non-PSC, p=0.019). FC reduced from 995 (IQR 319-1825) to 44 (IQR 16-79) µg/g; 83% of children with pre-OVT FC ≥100 µg/g achieved biochemical remission (92% PSC-UC vs 64% aUC-non-PSC, p=0.063). Colonoscopy confirmed Mayo 0 healing in 62% (67% PSC-UC vs 54% aUC-non-PSC, p=0.443) and 46% achieved pan-colonic histological remission (54% PSC-UC vs 31% aUC-non-PSC, p=0.173). All pre-post-OVT changes in these four markers were significant in both groups. After ceasing first OVT, 25/44 relapsed within 8.2 (IQR 1.9-14.5) months. Recommencing OVT regained biomarker remission in 13/25. During 3.8 (IQR 2.0-5.3) years of follow-up, 79 OVT courses in conjunction with CMT maintained deep remission in 67%. Routine stool testing (n=138) detected no vancomycin-resistant Enterococcus (VRE).

Conclusions: OVT induced and reinduced remission in children with atypical UC. Relapse often followed ceasing vancomycin, half responded to reinduction. No VRE was developed.

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口服万古霉素治疗伴有或未伴有原发性硬化性胆管炎的非典型溃疡性结肠炎患儿的疗效:一项真实世界的观察性研究
目的:非典型溃疡性结肠炎(UC)表现为反向梯度结肠炎、反冲洗性回肠炎或直肠保留和/或非典型抗中性粒细胞细胞质抗体阳性,通常与原发性硬化性胆管炎(PSC)相关,并且对炎性肠病的常规药物治疗(CMT)具有耐药性。我们报告了口服万古霉素治疗(OVT)治疗非典型UC和经影像学/活检证实的PSC (PSC-UC)或无PSC (aUC-non-PSC)的治疗抵抗性非典型UC的短期和长期结果。方法:在这项来自澳大利亚布里斯班一所三级儿科中心的回顾性现实世界观察性研究中,44名aUC儿童(29名PSC-UC, 15名aUC-非psc)在2014年至2023年间接受了79次OVT课程。比较ovt前后的特征并记录复发/重复病程。结果:ovt前,通过儿科溃疡性结肠炎活动指数(PUCAI)、粪钙保护蛋白(FC)和/或结肠镜检查,所有患者均有活动性结肠炎。ovt后,PUCAI由15 (IQR 5-33)降至0 (IQR 0-5);ovt前PUCAI≥10的患儿中有85%达到临床缓解(PSC-UC 100% vs auc -非psc 64%, p=0.019)。FC从995 (IQR 319-1825)降至44 (IQR 16-79)µg/g;ovt前FC≥100µg/g的儿童中,83%达到生化缓解(PSC-UC vs aUC-non-PSC, 92%, p=0.063)。结肠镜检查证实62%的患者Mayo 0愈合(67% PSC-UC vs 54% auc -非psc, p=0.443), 46%的患者实现了全结肠组织学缓解(54% PSC-UC vs 31% auc -非psc, p=0.173)。两组患者ovt前后这四项指标的变化均显著。第一次OVT停止后,25/44在8.2个月内(IQR 1.9-14.5)复发。重新开始OVT在2013 /25恢复了生物标志物缓解。在3.8年(IQR 2.0-5.3)的随访期间,79个OVT联合CMT疗程中67%的患者保持了深度缓解。常规粪便检查(138例)未检出万古霉素耐药肠球菌(VRE)。结论:OVT可诱导和再诱导非典型UC患儿缓解。复发常在停止万古霉素后发生,半数对再诱导有反应。未开发VRE。
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来源期刊
BMJ Open Gastroenterology
BMJ Open Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
5.90
自引率
3.20%
发文量
68
审稿时长
2 weeks
期刊介绍: BMJ Open Gastroenterology is an online-only, peer-reviewed, open access gastroenterology journal, dedicated to publishing high-quality medical research from all disciplines and therapeutic areas of gastroenterology. It is the open access companion journal of Gut and is co-owned by the British Society of Gastroenterology. The journal publishes all research study types, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Publishing procedures are built around continuous publication, publishing research online as soon as the article is ready.
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