Brückner Annecarin, Werkstetter Katharina J, de Laffolie Jan, Wendt Claudia, Prell Christine, Weidenhausen Tanja, Zimmer Klaus P, Koletzko Sibylle
Division of Pediatric Gastroenterology, Dr. von Hauner Children's Hospital, Ludwig Maximilians University, Munich.
Department of Pediatrics, University Hospital Gießen and Marburg, Justus-Liebig-University, Gießen, Germany.
J Pediatr Gastroenterol Nutr. 2018 Jan;66(1):73-78. doi: 10.1097/MPG.0000000000001649.
Perianal disease (PD) with fistula and/or abscess formation is a severe complication in Crohn disease (CD). We examined prevalence, incidence, and risk factors for PD development in a pediatric CD cohort.
Patients with CD from the prospective, multicenter registry for inflammatory bowel disease from Germany and Austria (CEDATA-GPGE) were included if diagnosed at the age of 18 years or younger, registered within 3 months after diagnosis, and having at least 2 follow-up visits within the first year of registration. We examined potential risk factors for PD with Kaplan-Meier analysis and a final Cox model considering sex, family history of inflammatory bowel disease, extraintestinal manifestations, disease location, and induction therapy (corticosteroids or nutritional therapy).
Of 2406 patients with CD, 742 fulfilled inclusion criteria (59% boys, mean age at diagnosis 12.4 ± 3.4 years). PD was present at diagnosis in 41 patients (5.5%; 80.9% boys), whereas 32 patients (4.3%, 81.3% male) developed PD during follow-up (mean 2.0 ± 1.6 years). The cumulative incidence of PD at 12 and 36 months after diagnosis was 3.5% and 7.5%, respectively. Potential risk factors for PD development during follow-up were male sex (hazard ratio = 3.2, [95%; confidence interval 1.2-7.8]) and induction therapy with corticosteroids (hazard ratio = 2.5 [1.1-5.5]). Diagnostic evaluation at PD diagnosis was incomplete in 40% of affected subjects. PD resolved within 1 year in 50% of cases.
Approximately 10% of CD patients in our cohort suffered from PD within the first 3 years of their disease. Male sex and initial corticosteroid therapy were associated with an increased risk to develop PD after diagnosis.
伴有肛瘘和/或脓肿形成的肛周疾病(PD)是克罗恩病(CD)的一种严重并发症。我们研究了儿童CD队列中PD发生的患病率、发病率及危险因素。
纳入来自德国和奥地利炎症性肠病前瞻性多中心注册研究(CEDATA - GPGE)的CD患者,这些患者年龄在18岁及以下,诊断后3个月内登记,且在登记的第一年内至少有2次随访。我们采用Kaplan - Meier分析及最终的Cox模型研究PD的潜在危险因素,该模型考虑了性别、炎症性肠病家族史、肠外表现、疾病部位及诱导治疗(皮质类固醇或营养治疗)。
2406例CD患者中,742例符合纳入标准(59%为男孩,诊断时平均年龄12.4±3.4岁)。41例患者(5.5%;80.9%为男孩)诊断时即有PD,而32例患者(4.3%,81.3%为男性)在随访期间(平均2.0±1.6年)发生PD。诊断后12个月和36个月时PD的累积发病率分别为3.5%和7.5%。随访期间发生PD的潜在危险因素为男性(风险比=3.2,[95%置信区间1.2 - 7.8])及皮质类固醇诱导治疗(风险比=2.5 [1.1 - 5.5])。40%的PD患者诊断评估不完整。50%的病例中PD在1年内缓解。
我们队列中约10%的CD患者在疾病的前3年内患有PD。男性及初始皮质类固醇治疗与诊断后发生PD的风险增加相关。