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婴儿期肝病临床特点分析 被引量:1

Clinical characteristics of infantile liver disease
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摘要 目的分析婴儿期胆汁淤积性和非胆汁淤积性肝病的临床特点。方法回顾分析肝病婴儿的临床资料,比较胆汁淤积和非胆汁淤积肝病婴儿的临床差异。结果1985例肝病婴儿中,男性866例、女性1119例,入院月龄为(2.88±3.08)月。胆汁淤积症婴儿477例(24.0%),非胆汁淤积症婴儿1508例(76.0%)。单因素分析示,胆汁淤积婴儿的月龄小于非胆汁淤积婴儿,总胆红素、直接胆红素、γ-谷氨酰转肽酶、碱性磷酸酶、总胆汁酸水平高于非胆汁淤积婴儿,差异均有统计学意义(P<0.05)。多元logistic回归分析示,γ-谷氨酰转肽酶、碱性磷酸酶和总胆汁酸水平越高,月龄、白蛋白水平越低,发生胆汁淤积的可能性越高。结论在婴儿期,相比非胆汁淤积性肝病,胆汁淤积性肝病起病早,γ-谷氨酰转肽酶、碱性磷酸酶和总胆汁酸水平高。 Objective To explore the clinical characteristics of infantile cholestatic liver diseases and non-cholestatic liver diseases.Methods The clinical data of liver disease in infants were retrospectively analyzed,and the clinical differences between cholestatic and non-cholestatic liver disease in infants were compared.Results Among 1985 children(866 males and 1119 females)aged(2.88±3.088)months at admission,there were 477 cases(24.0%)of cholestasis,and 1508 cases(76.0%)of non-cholestasis.Univariate analysis showed that the age of cholestasis infants was younger than that in non-cholestasis infants,and the levels of total bilirubin,direct bilirubin,γ-glutamyltranspeptidase,alkaline phosphatase and total bile acid were higher than those in non-cholestasis infants.The differences were statistically significant(all P<0.05).Multivariate logistic regression analysis showed that with the higher levels ofγ-glutamyltranspeptidase,alkaline phosphatase and total bile acid,the age and albumin level were lower and the possibility of cholestasis was higher.Conclusions Compared with non-cholestatic liver disease in childhood,cholestatic liver disease has earlier onset and higher levels of gamma glutamyltranspeptidase,alkaline phosphatase and total bile acid,which may help the differentiation in clinic.
作者 余荣华 王怡仲 张婷 YU Ronghua;WANG Yizhong;ZHANG Ting(Department of Gastroenterology,Hepatology,and Nutrition,Shanghai Children’s Hospital,Shanghai Jiao Tong University,Shanghai 200062,China)
出处 《临床儿科杂志》 CAS CSCD 北大核心 2021年第1期1-5,共5页 Journal of Clinical Pediatrics
基金 国家自然科学基金面上项目(No.81870373)。
关键词 胆汁淤积症 先天性胆道闭锁 婴儿 cholestasis congenital biliary atresia infant
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