Turner D, Walsh C M, Benchimol E I, Mann E H, Thomas K E, Chow C, McLernon R A, Walters T D, Swales J, Steinhart A H, Griffiths A M
Division of Pediatric Gastroenterology, Hepatology, and Nutrition, The Hospital for Sick Children, 555 University Avenue, Toronto, M5G 1X8, Canada.
Gut. 2008 Mar;57(3):331-8. doi: 10.1136/gut.2007.136481. Epub 2007 Nov 2.
Despite the predominance of extensive disease in children with ulcerative colitis, data concerning severe paediatric ulcerative colitis are sparse. We reviewed rates and predictors of response to intravenous-corticosteroid therapy in a single-centre cohort with long-term follow-up.
99 children (49% males; age 2-17 years) were hospitalised (1991-2000) for treatment of severe ulcerative colitis (90% extensive; 49% new onset ulcerative colitis). Clinical, laboratory and radiographic data were reviewed. A population-based subset was used to assess incidence. Predictors of corticosteroid response were analysed using univariate and multivariate analyses at days 3 and 5 of therapy. Colectomy rates were calculated using Kaplan-Meier survival analyses.
28% (95% CI, 23 to 34%) of children with ulcerative colitis resident in the Greater Toronto Area required admission for intravenous corticosteroid therapy, of whom 53 (53%; 95% CI, 44 to 63%) responded. Several predictors were associated with corticosteroid failure, but in multivariable modelling only C-reactive protein [OR = 3.5 (1.4 to 8.4)] and number of nocturnal stools [OR = 3.2 (1.6 to 6.6)] remained significant at both days 3 and 5. The Pediatric Ulcerative Colitis Activity Index (PUCAI), Travis and Lindgren's indices strongly predicted non-response. Radiographically, the upper range of colonic luminal width was 40 mm in children younger than 11 years versus 60 mm in older patients. Cumulative colectomy rates at discharge, 1 year and 6 years were 42%, 58% and 61%, respectively.
Children with ulcerative colitis commonly experience at least one severe exacerbation. Response to intravenous corticosteroids is poor. The PUCAI, determined at day 3 (>45 points) should be used to screen for patients likely to fail corticosteroids and at day 5 (>70 points) to dictate the introduction of second-line therapies.
尽管溃疡性结肠炎患儿中广泛性疾病占主导,但有关重度小儿溃疡性结肠炎的数据却很稀少。我们回顾了一个进行长期随访的单中心队列中静脉注射皮质类固醇治疗的反应率及预测因素。
99名儿童(49%为男性;年龄2至17岁)于1991年至2000年因重度溃疡性结肠炎住院治疗(90%为广泛性;49%为新发溃疡性结肠炎)。对临床、实验室和影像学数据进行了回顾。以人群为基础的亚组用于评估发病率。在治疗第3天和第5天,使用单因素和多因素分析来分析皮质类固醇反应的预测因素。使用Kaplan-Meier生存分析计算结肠切除术率。
大多伦多地区患有溃疡性结肠炎的儿童中有28%(95%可信区间,23%至34%)需要住院接受静脉注射皮质类固醇治疗,其中53名(53%;95%可信区间,44%至63%)有反应。几个预测因素与皮质类固醇治疗失败有关,但在多变量模型中,只有C反应蛋白[比值比 = 3.5(1.4至8.4)]和夜间排便次数[比值比 = 3.2(1.6至6.6)]在第3天和第5天都仍然具有显著性。小儿溃疡性结肠炎活动指数(PUCAI)、特拉维斯指数和林德格伦指数强烈预测无反应。影像学上,11岁以下儿童结肠腔宽度上限为40毫米,而年龄较大患者为60毫米。出院时、1年和6年的累积结肠切除术率分别为42%、58%和61%。
溃疡性结肠炎患儿通常至少经历一次严重发作。静脉注射皮质类固醇的反应较差。第3天(>45分)测定的PUCAI应用于筛查可能对皮质类固醇治疗无效的患者,第5天(>70分)则用于决定是否引入二线治疗。