当前的Espaghan小儿腹腔疾病指南,三级护理中心经验:进一步简化的建议。

IF 1.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Translational Medicine at UniSa Pub Date : 2019-01-12 eCollection Date: 2019-07-01
M Malamisura, R Colantuono, V M Salvati, R Croce, G D'Adamo, T Passaro, E D'Angelo, M Boffardi, A Garzi, B Malamisura
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引用次数: 0

摘要

根据2012年ESPGHAN乳糜泻(CD)诊断标准,患有明显吸收不良综合征、抗组织谷氨酰胺转胺酶IgA(tTG2)≥10倍截止值、抗肌内膜IgA(EMA)和HLA DQ2/DQ8基因的儿童可以避免十二指肠活检(DB)。本研究的目的是报告我们的经验,并评估实际指南的准确性。患者和方法:这是对我中心2012年至2018年所有诊断为CD的患者进行的回顾性研究。对所有入选患者的家族史、症状、血清学、遗传学、Marsh分级和随访数据进行分析。结果:共有481名儿童[平均年龄6.4岁;F:M=1.8:1]被纳入研究。未接受DB治疗的患者的平均年龄(4.51岁)低于接受DB治疗(6.48岁)。在256名抗tTG2≥10倍的患者中,121名患者因症状轻微(84/121)或无症状(37/121)而接受DB治疗。在所有病例中均发现Marsh 3型,HLA单倍型与CD诊断一致。结论:我们的研究证实,无论症状如何,血清学对CD的诊断都具有首要意义。这些数据表明,在抗tTG2 IgA≥10倍临界值的情况下,活检和HLA单倍型搜索对患者来说是浪费和无益的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Current Espghan Guidelines for Celiac Disease in Pediatric Age, Tertiary Care Center Experience: A Proposal for Further Simplification.

Current Espghan Guidelines for Celiac Disease in Pediatric Age, Tertiary Care Center Experience: A Proposal for Further Simplification.

Current Espghan Guidelines for Celiac Disease in Pediatric Age, Tertiary Care Center Experience: A Proposal for Further Simplification.

Current Espghan Guidelines for Celiac Disease in Pediatric Age, Tertiary Care Center Experience: A Proposal for Further Simplification.

According to the 2012 ESPGHAN criteria for diagnosis of celiac disease (CD), duodenal biopsy (DB) can be avoided in children with a clear malabsorption syndrome, anti-tissue transglutaminase IgA (tTG2) ≥ 10x the cut-off, anti-endomysium IgA (EMA) and HLA DQ2/DQ8 genes. The aim of this study is to report our experience and evaluate the accuracy of the actual guidelines.

Patients and methods: This is a retrospective study conducted on all patients diagnosed CD from 2012 to 2018 in our Center. For all patients enrolled were analyzed: data of family history, symptoms, serology, genetics, Marsh grade and follow-up.

Results: A total of 481 children [mean age 6,4 yrs; F:M= 1.8:1] were included in the study. The mean age of patients who were not subject to DB was lower (4.51 yrs) comparing with patients that received DB (6.48 yrs). Out of the 256 patients with anti-tTG2 ≥ 10 fold, 121 underwent DB because of mild symptoms (84/121) or no symptoms (37/121). In all cases Marsh type 3 was found and HLA haplotypes was compatible with CD diagnosis.

Conclusions: Our study confirms that the serology has a primary importance to diagnose CD, regardless of the symptoms. These data suggest that biopsy and HLA haplotypes search, in presence of anti-tTG2 IgA ≥ 10x the cut-off, are wasteful and unhelpful for the patients.

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Translational Medicine at UniSa
Translational Medicine at UniSa MEDICINE, RESEARCH & EXPERIMENTAL-
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