Celiac disease diagnosis in clinical practice: ESPGHAN quality of care survey from 129 pediatric hospitals across 28 countries.

IF 2.6 3区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Anna Litwin, Thu Giang Le Thi, Nabil El-Lababidi, Angelika Kindermann, Rouzha Pancheva, Konstantinos Gerasimidis, Cristina Campos Goncalves, Paula Crespo Escobar, Tena Niseteo, Katharina Ikrath, Sibylle Koletzko
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引用次数: 0

Abstract

Objectives: European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) guidelines recommend first-line serology for suspected celiac disease (CeD), measuring only transglutaminase antibodies (TGA-immunoglobulin A [IgA]) plus total IgA. If TGA-IgA is ≥10 times the normal value, pediatric gastroenterologists (pedGI) may diagnose CeD without biopsies if autoantibodies against endomysial antibodies (EMA-IgA) are positive in a 2nd blood sample. This Quality-of-Care (QoC) project benchmarked diagnostic workup in clinical practice using ESPGHAN CeD guidelines as reference.

Methods: A pseudonymized survey on CeD practices was sent to 141 hospitals within the ESPGHAN QoC-network in 28 countries.

Results: Questionnaires were completed by 129/141 (91.5%) hospitals, with 121 (94%) having pedGI staff. As reasons conflicting with good QoC for CeD in their setting, responders assumed knowledge deficits among the public (57%), primary care providers (64%), non-GI physicians (16%), and pedGIs (0%). For initial testing, 66% of physicians ordered only total IgA and TGA-IgA, 7% did not use this combination, and 29% ordered additional serology (TGA-IgG, EMA, antibodies against deaminated gliadin peptide, or native gliadin). Regarding conflicting results for TGA-IgA and histopathology in IgA-sufficient children, 61% incorrectly classified negative TGA-IgA with Marsh 2 and 57% with Marsh 3 lesions as "potential CeD," while 49% excluded CeD in the case of villous atrophy and negative TGA-IgA. Routine practice did not align with the ESPGHAN recommendations regarding performance of duodenal biopsies (27%), EMA-testing (34%), and diagnosis of CeD in IgA-deficient children (32%).

Conclusions: We identified areas for improving QoC regarding both effectiveness and efficacy, in pediatric patients with suspected CeD, and consequently developed easy-to-use tools to improve guideline implementation.

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临床实践中的乳糜泻诊断:来自28个国家129家儿科医院的ESPGHAN护理质量调查
目的:欧洲儿科胃肠病学、肝病学和营养学会(ESPGHAN)指南推荐疑似乳糜泻(CeD)的一线血清学,仅测量转谷氨酰胺酶抗体(tga -免疫球蛋白A [IgA])加总IgA。如果TGA-IgA≥正常值的10倍,儿科胃肠病学家(pedGI)如果在第二次血液样本中发现针对肌内膜抗体的自身抗体(EMA-IgA)阳性,则可以诊断为CeD而无需活检。这个医疗质量(QoC)项目使用ESPGHAN CeD指南作为参考,在临床实践中对诊断工作进行基准测试。方法:向28个国家ESPGHAN qoc网络内的141家医院发送了一份关于CeD实践的匿名调查。结果:141家医院中有129家(91.5%)完成了问卷调查,其中121家(94%)有pedGI工作人员。在他们的环境中,与良好的质量质量相冲突的原因是,应答者认为公众(57%)、初级保健提供者(64%)、非胃肠道医生(16%)和儿科患儿(0%)存在知识缺陷。在初始测试中,66%的医生只要求总IgA和TGA-IgA, 7%的医生不使用这种组合,29%的医生要求额外的血清学(TGA-IgG, EMA,抗脱氨麦胶蛋白肽抗体,或天然麦胶蛋白)。关于iga充足儿童中TGA-IgA和组织病理学的相互矛盾的结果,61%的儿童错误地将Marsh 2和Marsh 3病变的TGA-IgA阴性归为“潜在的CeD”,而49%的儿童在绒毛萎缩和TGA-IgA阴性的情况下排除了CeD。常规实践与ESPGHAN关于十二指肠活检(27%)、ema检测(34%)和iga缺乏儿童CeD诊断(32%)的建议不一致。结论:我们确定了在怀疑患有CeD的儿科患者中提高有效性和疗效的QoC的领域,并因此开发了易于使用的工具来改进指南的实施。
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来源期刊
CiteScore
5.30
自引率
13.80%
发文量
467
审稿时长
3-6 weeks
期刊介绍: ​The Journal of Pediatric Gastroenterology and Nutrition (JPGN) provides a forum for original papers and reviews dealing with pediatric gastroenterology and nutrition, including normal and abnormal functions of the alimentary tract and its associated organs, including the salivary glands, pancreas, gallbladder, and liver. Particular emphasis is on development and its relation to infant and childhood nutrition.
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