Department of Pediatrics.
Pediatric Gastroenterology, Kaplan Medical Center, Rehovot.
J Pediatr Gastroenterol Nutr. 2022 Apr 1;74(4):471-475. doi: 10.1097/MPG.0000000000003374. Epub 2021 Dec 28.
Identifying predictors of inflammatory bowel disease (IBD) outcome in order to optimize individual patient management in has become an important goal. We aimed to describe the long-term outcome of pediatric Crohn disease (CD) patients and identify risk factors for complicated behavior.
Pediatric CD patients diagnosed between 1998 and 2014, with long-term follow-up were included. Baseline data; age, gender, weight/height/BMI percentiles, and family history of IBD. Disease characteristics (Paris classification), laboratory testing, imaging and treatment were documented. Outcome data; evidence of stricturing or penetrating disease, hospitalizations, surgical intervention, malignancies, and mortality.
Of 93 patients included, mean age at diagnosis 13.5 (±3.2), 51 (55%) male, median follow-up 10.3 years (±4 SD(. Disease location at diagnosis: 29 (31.2%) distal ileum, 17 (18.3%) colonic, 40 (43.0%) ileo-colonic. Seven (7.5%) had upper gastrointestinal and 36 (38.7%) perianal involvement. Behavior at diagnosis, 68 (73.1%) inflammatory (B1), and 25 (26.9%) complicated [(B2 (stricturing) and/or B3 (penetrating)]. Twenty (23.2%) of B1 evolved to B2 and/or B3, thus by the end of follow-up 45 (48.4%) had complicated behavior. Sixty-seven (72%) were hospitalized, 20 (21.5%) underwent surgery, two developed malignancy with no mortalities. In a logistic regression model, growth delay (hazard ratio [HR], 5.02 [1.10-22.85], P = 0.037) and low albumin levels (HR, 3.97 [1.32-11.97], P = 0.014) at diagnosis were predictors of complicated disease in adulthood.
Over a quarter of pediatric Crohn disease patients present with complicated behavior. During follow-up another quarter progress to complicated disease behavior. Delayed growth and low albumin at diagnosis predict progression.
为了优化个体患者管理,确定炎症性肠病(IBD)结局的预测因素已成为一个重要目标。我们旨在描述儿科克罗恩病(CD)患者的长期结局,并确定复杂行为的危险因素。
纳入 1998 年至 2014 年间诊断的、具有长期随访的儿科 CD 患者。记录基线数据,包括年龄、性别、体重/身高/BMI 百分位数和 IBD 家族史。记录疾病特征(巴黎分类)、实验室检查、影像学和治疗情况。结局数据包括狭窄或穿透性疾病、住院、手术干预、恶性肿瘤和死亡。
93 例患者中,诊断时的平均年龄为 13.5(±3.2)岁,51 例(55%)为男性,中位随访时间为 10.3 年(±4 标准差)。诊断时的疾病部位:29 例(31.2%)为回肠末端,17 例(18.3%)为结肠,40 例(43.0%)为回结肠。7 例(7.5%)有上消化道受累,36 例(38.7%)有肛周受累。诊断时的行为表现,68 例(73.1%)为炎症性(B1),25 例(26.9%)为复杂性[(B2(狭窄)和/或 B3(穿透)]。20 例(23.2%)B1 进展为 B2 和/或 B3,因此,在随访结束时,45 例(48.4%)有复杂性行为。67 例(72%)住院,20 例(21.5%)接受手术,2 例发生恶性肿瘤,无死亡病例。在逻辑回归模型中,诊断时生长延迟(危险比 [HR],5.02 [1.10-22.85],P=0.037)和低白蛋白水平(HR,3.97 [1.32-11.97],P=0.014)是成年后发生复杂疾病的预测因素。
超过四分之一的儿科 CD 患者表现为复杂行为。在随访期间,又有四分之一的患者发展为复杂疾病行为。诊断时生长延迟和低白蛋白水平预示着病情进展。