Celiac Disease Center, Columbia University, New York.
Cedars-Sinai Medical Center, Los Angeles, California.
Gastroenterology. 2022 Nov;163(5):1461-1469. doi: 10.1053/j.gastro.2022.07.086. Epub 2022 Sep 19.
DESCRIPTION: The purpose of this expert review is to summarize the diagnosis and management of refractory celiac disease. It will review evaluation of patients with celiac disease who have persistent or recurrent symptoms, differential diagnosis, nutritional support, potential therapeutic options, and surveillance for complications of this condition. METHODS: This expert review was commissioned and approved by the American Gastroenterological Association (AGA) Institute Clinical Practice Updates Committee (CPUC) and the AGA Governing Board to provide timely guidance on a topic of high clinical importance to the AGA membership and underwent internal peer review by the CPUC and external peer review through standard procedures of Gastroenterology. These Best Practice Advice (BPA) statements were drawn from a review of the published literature and from expert opinion. Since systematic reviews were not performed, these BPA statements do not carry formal ratings of the quality of evidence or strength of the presented considerations. Best Practice Advice Statements BEST PRACTICE ADVICE 1: In patients believed to have celiac disease who have persistent or recurrent symptoms or signs, the initial diagnosis of celiac disease should be confirmed by review of prior diagnostic testing, including serologies, endoscopies, and histologic findings. BEST PRACTICE ADVICE 2: In patients with confirmed celiac disease with persistent or recurrent symptoms or signs (nonresponsive celiac disease), ongoing gluten ingestion should be excluded as a cause of these symptoms with serologic testing, dietitian review, and detection of immunogenic peptides in stool or urine. Esophagogastroduodenoscopy with small bowel biopsies should be performed to look for villous atrophy. If villous atrophy persists or the initial diagnosis of celiac disease was not confirmed, consider other causes of villous atrophy, including common variable immunodeficiency, autoimmune enteropathy, tropical sprue, and medication-induced enteropathy. BEST PRACTICE ADVICE 3: For patients with nonresponsive celiac disease, after exclusion of gluten ingestion, perform a systematic evaluation for other potential causes of symptoms, including functional bowel disorders, microscopic colitis, pancreatic insufficiency, inflammatory bowel disease, lactose or fructose intolerance, and small intestinal bacterial overgrowth. BEST PRACTICE ADVICE 4: Use flow cytometry, immunohistochemistry, and T-cell receptor rearrangement studies to distinguish between subtypes of refractory celiac disease and to exclude enteropathy-associated T-cell lymphoma. Type 1 refractory celiac disease is characterized by a normal intraepithelial lymphocyte population and type 2 is defined by the presence of an aberrant, clonal intraepithelial lymphocyte population. Consultation with an expert hematopathologist is necessary to interpret these studies. BEST PRACTICE ADVICE 5: Perform small bowel imaging with capsule endoscopy and computed tomography or magnetic resonance enterography to exclude enteropathy-associated T-cell lymphoma and ulcerative jejunoileitis at initial diagnosis of type 2 refractory celiac disease. BEST PRACTICE ADVICE 6: Complete a detailed nutritional assessment with investigation of micronutrient and macronutrient deficiencies in patients diagnosed with refractory celiac disease. Check albumin as an independent prognostic factor. BEST PRACTICE ADVICE 7: Correct deficiencies in macro- and micronutrients using oral supplements and/or enteral support. Consider parenteral nutrition for patients with severe malnutrition due to malabsorption. BEST PRACTICE ADVICE 8: Corticosteroids, most commonly open-capsule budesonide or, if unavailable, prednisone, are the medication of choice and should be used as first-line therapy in either type 1 or type 2 refractory celiac disease. BEST PRACTICE ADVICE 9: Patients with refractory celiac disease require regular follow-up by a multidisciplinary team, including gastroenterologists and dietitians, to assess clinical and histologic response to therapy. Identify local experts with expertise in celiac disease to assist with management. BEST PRACTICE ADVICE 10: Patients with refractory celiac disease without response to steroids may benefit from referral to a center with expertise for management or evaluation for inclusion in clinical trials.
描述:本专家综述的目的是总结难治性乳糜泻的诊断和管理。它将回顾患有持续性或复发性症状的乳糜泻患者的评估、鉴别诊断、营养支持、潜在的治疗选择以及这种疾病并发症的监测。
方法:本专家综述由美国胃肠病学协会(AGA)研究所临床实践更新委员会(CPUC)和 AGA 理事会委托和批准,旨在就 AGA 成员高度重视的一个重要临床主题提供及时的指导,并通过 CPUC 的内部同行评审和胃肠病学的标准同行评审程序进行外部同行评审。这些最佳实践建议(BPA)陈述是从对已发表文献的审查和专家意见中得出的。由于没有进行系统评价,因此这些 BPA 陈述不具有证据质量或提出考虑因素强度的正式评级。
最佳实践建议 1:对于被认为患有乳糜泻且有持续性或复发性症状或体征的患者,应通过回顾先前的诊断性检测,包括血清学、内窥镜检查和组织学发现,来确认乳糜泻的初始诊断。
最佳实践建议 2:对于患有持续性或复发性症状或体征(无反应性乳糜泻)的确诊乳糜泻患者,应通过血清学检测、营养师审查和粪便或尿液中免疫原性肽的检测,排除这些症状是由于持续摄入麸质引起的。应进行食管胃十二指肠镜检查和小肠活检,以寻找绒毛萎缩。如果绒毛萎缩持续存在或最初的乳糜泻诊断未得到确认,则应考虑其他引起绒毛萎缩的原因,包括常见可变免疫缺陷、自身免疫性肠病、热带口炎性腹泻和药物诱导的肠病。
最佳实践建议 3:对于无反应性乳糜泻患者,在排除麸质摄入后,应进行系统评估以确定其他潜在的症状原因,包括功能性肠病、显微镜结肠炎、胰腺功能不全、炎症性肠病、乳糖或果糖不耐受和小肠细菌过度生长。
最佳实践建议 4:使用流式细胞术、免疫组织化学和 T 细胞受体重排研究来区分难治性乳糜泻的亚型,并排除肠病相关 T 细胞淋巴瘤。1 型难治性乳糜泻的特征是正常的上皮内淋巴细胞群,2 型定义为存在异常的、克隆性的上皮内淋巴细胞群。有必要咨询血液病理学专家来解释这些研究。
最佳实践建议 5:在 2 型难治性乳糜泻的初始诊断时,通过胶囊内镜和计算机断层扫描或磁共振肠造影术进行小肠成像,以排除肠病相关 T 细胞淋巴瘤和溃疡性空肠回肠炎。
最佳实践建议 6:对诊断为难治性乳糜泻的患者进行详细的营养评估,并调查微量营养素和宏量营养素的缺乏情况。检查白蛋白作为一个独立的预后因素。
最佳实践建议 7:使用口服补充剂和/或肠内支持来纠正宏量和微量营养素的缺乏。对于因吸收不良而严重营养不良的患者,考虑使用肠外营养。
最佳实践建议 8:皮质类固醇,最常见的是开放胶囊布地奈德,或者如果不可用,则是泼尼松,是首选药物,应作为 1 型或 2 型难治性乳糜泻的一线治疗药物。
最佳实践建议 9:难治性乳糜泻患者需要由包括胃肠病学家和营养师在内的多学科团队定期随访,以评估治疗的临床和组织学反应。确定具有乳糜泻管理专业知识的当地专家来协助管理。
最佳实践建议 10:对类固醇无反应的难治性乳糜泻患者可能受益于转介到具有专业知识的中心进行管理或评估是否纳入临床试验。
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