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Re-analysis of clinical features of 89 patients with autoimmune hepatitis using the revised scoring system proposed by the International Autoimmune Hepatitis Group.

机译:使用国际自身免疫性肝炎小组提出的修订评分系统,对89例自身免疫性肝炎患者的临床特征进行重新分析。

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OBJECTIVE: The diagnostic criteria of autoimmune hepatitis (AIH) were recently modified by the International Autoimmune Hepatitis Group. This study was performed to assess the impact of the revised scoring system on the diagnosis of AIH. PATIENTS AND METHODS: We re-analyzed the clinical features of 89 patients diagnosed as AIH in Nagasaki Prefecture, Japan, using the revised scoring system, and compared the scores and final diagnosis with our previously published results using the original system. RESULTS: Of the 89 patients with AIH, 40 (45%) were classified using the new system as "definite" AIH, 41 (46%) as "probable" AIH, and 8 (9%) patients were categorized as "others". Of these, 37 (42%), 35 (39%), and 4 (4%) patients who were classified as "definite", "probable", and "others" by the original system remained in the same category by the revised system, respectively. However, 3, 4, and 6 patients were re-categorized as "definite" from "probable", "others" from "probable", and "probable" from "definite", respectively. The difference in aggregate scores between the above two systems ranged from -5 to +2. The main contributing factors to the changes in aggregate AIH score were "other autoimmune disease(s)" and "interface hepatitis without lobular involvement and bridging necrosis on liver histology". However, the main contributing factors to the demotions from "definite" to "probable" and form "probable" to "others" were those related to the characteristics of biliary diseases, i.e., antimitochondrial antibody positive, biliary changes in liver histology, and alkaline phosphatase: aspartate aminotransferase ratio between 1.5 and 3.0. Moreover, two patients who had no histological evidence of AIH were both re-categorized as "others" from "probable" AIH. CONCLUSION: Our results indicated that the diagnosis, whether based on the revised or original system, was the same in the majority of AIH patients, but the revised scoring system excluded cases who had features suggestive of biliary diseases from "definite" AIH, and also confirmed that a diagnosis of "definite" AIH should not be made without liver histology.
机译:目的:国际自身免疫性肝炎小组最近修改了自身免疫性肝炎(AIH)的诊断标准。进行这项研究是为了评估修订评分系统对AIH诊断的影响。患者和方法:我们使用修订的评分系统重新分析了日本长崎县诊断为AIH的89例患者的临床特征,并将评分和最终诊断与我们先前使用原始系统发表的结果进行了比较。结果:在89例AIH患者中,有40例(45%)被使用新系统分类为“确定” AIH,41例(46%)被归为“可能” AIH,8例(9%)被分类为“其他”。 。在这些患者中,被原始系统分类为“确定”,“可能”和“其他”的37(42%),35(39%)和4(4%)患者在修订后仍属于同一类别系统。但是,分别将3、4和6位患者从“可能”重新分类为“确定”,将“其他”重新划分为“可能”,将“其他”重新划分为“确定”。上述两个系统之间的总得分差异在-5到+2之间。导致总AIH评分改变的主要因素是“其他自身免疫性疾病”和“无小叶侵犯和桥接肝组织学坏死的界面肝炎”。但是,引起胆汁疾病从“确定”到“可能”降级以及从“可能”到“其他”降级的主要因素是与胆道疾病特征相关的因素,即抗线粒体抗体阳性,肝组织学中的胆道变化和碱性磷酸酶:天冬氨酸转氨酶的比率在1.5和3.0之间。此外,没有组织学证据的AIH的两名患者都被从“可能的” AIH中重新分类为“其他”。结论:我们的结果表明,无论是基于修订版系统还是原始系统,大多数AIH患者的诊断都是相同的,但修订的评分系统从“确定的” AIH中排除了具有胆道疾病特征的病例,并且证实没有肝脏组织学就不能诊断为“确定的” AIH。

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