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J Pediatr Gastroenterol Nutr. 2017 Jul;65(1):75-79. doi: 10.1097/MPG.0000000000001420.
2
Delay in Diagnosis of Celiac Disease in Patients Without Gastrointestinal Complaints.非胃肠道症状患者的乳糜泻诊断延迟。
Am J Med. 2017 Nov;130(11):1318-1323. doi: 10.1016/j.amjmed.2017.05.027. Epub 2017 Jun 13.
3
Evidence-Informed Expert Recommendations for the Management of Celiac Disease in Children.儿童乳糜泻管理的循证专家建议
Pediatrics. 2016 Sep;138(3). doi: 10.1542/peds.2015-3147. Epub 2016 Aug 26.
4
Addressing overuse starts with physicians: Choosing Wisely Canada.解决医疗过度使用问题要从医生做起:加拿大明智选择组织。
Can Fam Physician. 2016 Mar;62(3):199-200, 207-9.
5
Extraintestinal manifestations of coeliac disease.肠外麸质疾病相关性表现。
Nat Rev Gastroenterol Hepatol. 2015 Oct;12(10):561-71. doi: 10.1038/nrgastro.2015.131. Epub 2015 Aug 11.
6
Evaluation of the ESPGHAN Celiac Guidelines in a North American Pediatric Population.北美儿科人群中欧洲儿科胃肠病、肝病和营养学会乳糜泻指南的评估。
Am J Gastroenterol. 2015 May;110(5):760-7. doi: 10.1038/ajg.2015.87. Epub 2015 Mar 31.
7
ACG clinical guidelines: diagnosis and management of celiac disease.ACG 临床指南:乳糜泻的诊断和管理。
Am J Gastroenterol. 2013 May;108(5):656-76; quiz 677. doi: 10.1038/ajg.2013.79. Epub 2013 Apr 23.
8
Evaluation and management of skeletal health in celiac disease: position statement.乳糜泻骨骼健康的评估与管理:立场声明
Can J Gastroenterol. 2012 Nov;26(11):819-29. doi: 10.1155/2012/823648.
9
Meta-analysis: coeliac disease and the risk of all-cause mortality, any malignancy and lymphoid malignancy.荟萃分析:乳糜泻与全因死亡率、任何恶性肿瘤和淋巴恶性肿瘤的风险。
Aliment Pharmacol Ther. 2012 Mar;35(5):540-51. doi: 10.1111/j.1365-2036.2011.04972.x. Epub 2012 Jan 13.
10
European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease.欧洲儿科胃肠病学、肝病学和营养学学会关于乳糜泻诊断的指南。
J Pediatr Gastroenterol Nutr. 2012 Jan;54(1):136-60. doi: 10.1097/MPG.0b013e31821a23d0.

对开具乳糜泻抗体检测医嘱的医生进行初始管理情况的调查。

Survey of the initial management of celiac disease antibody tests by ordering physicians.

作者信息

Potter Kathryn, de Koning Lawrence, Butzner J Decker, Gidrewicz Dominica

机构信息

Department of Pediatrics, Cumming School of Medicine, University of Calgary, Calgary, Canada.

Department of Pathology and Laboratory Medicine, Cumming School of Medicine, University of Calgary, Calgary, Canada.

出版信息

BMC Pediatr. 2019 Jul 19;19(1):243. doi: 10.1186/s12887-019-1621-5.

DOI:10.1186/s12887-019-1621-5
PMID:31324159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6639898/
Abstract

BACKGROUND

Appropriate interpretation of a positive celiac antibody test by an ordering physician is important in order to institute proper management. We evaluated why children with an initial positive celiac serology were not referred for diagnostic biopsy or followed with serial testing by the ordering physician.

METHODS

Consecutive celiac serologies in all patients less than 18 years of age were evaluated over 3.5 years and 775 children with a positive tissue transglutaminase antibody (TTG) were identified. If no management of a positive TTG could be identified, a survey was sent to the ordering physician. Responses were categorized as appropriate or inappropriate management.

RESULTS

Of the 775 patients with a positive TTG, 193 (24.9%, 95% CI 21.9-28.1%) received no follow-up management. We contacted 173 ordering physicians and 120 (69%) responded. Of the 120 responses, 55 patients (45.8%, 95% CI 36.8-55.1%) were managed appropriately and 46 (38.3%, 95% CI 29.7-47.7%) were considered to be inappropriately managed when no repeat TTG was obtained within 18 months. Reasons for inappropriate management included: screen considered to be false positive (44.7%), patient was not experiencing symptoms of celiac disease (31.6%), symptoms had resolved (15.8%), results were not indicative of celiac disease (26.3%) and patients started a gluten-free diet with no evaluation of response (15.8%). In 19 patients the TTG was not acted upon for technical reasons.

CONCLUSIONS

Positive TTGs require appropriate interventions. These include: subspecialist referral for further evaluation and/or repeat testing to evaluate: 1) treatment response or 2) patients with minimal or no symptoms.

摘要

背景

为了进行恰当的管理,开单医生对乳糜泻抗体检测呈阳性结果进行恰当解读很重要。我们评估了为何初次乳糜泻血清学检测呈阳性的儿童未被转介进行诊断性活检,或未接受开单医生的系列检测随访。

方法

在3.5年的时间里,对所有18岁以下患者的连续乳糜泻血清学检测结果进行评估,共识别出775名组织转谷氨酰胺酶抗体(TTG)呈阳性的儿童。如果无法确定对TTG阳性结果的管理措施,则向开单医生发送一份调查问卷。回复被分类为恰当管理或不恰当管理。

结果

在775名TTG呈阳性的患者中,193名(24.9%,95%置信区间21.9 - 28.1%)未接受后续管理。我们联系了173名开单医生,120名(69%)回复。在这120份回复中,55名患者(45.8%,95%置信区间36.8 - 55.1%)得到了恰当管理,46名(38.3%,95%置信区间29.7 - 47.7%)在未在18个月内复查TTG时被认为管理不恰当。管理不恰当的原因包括:筛查结果被认为是假阳性(44.7%)、患者未出现乳糜泻症状(31.6%)、症状已缓解(15.8%)、结果不提示乳糜泻(26.3%)以及患者在未评估反应的情况下开始了无麸质饮食(15.8%)。有19名患者因技术原因未对TTG采取行动。

结论

TTG阳性需要采取恰当的干预措施。这些措施包括:转介给专科医生进行进一步评估和/或重复检测,以评估:1)治疗反应;2)症状轻微或无症状的患者。