目的 研究柴芍四金汤预防ERCP术后胆总管结石复发的临床疗效。方法 选取昆山市中医医院脾胃肝胆科2014年1月至2016年12月因胆总管结石行ERCP取石病例120例,按随机数字表法将120例病例随机分为治疗组和对照组,每组各60例,治疗组口服自拟柴芍四金汤,每日1剂,水煎400 mL,分早晚两次温服,随证加减;对照组口服熊去氧胆酸250 mg/次,3次/d,2组均连续药物治疗6月,观察术后2周血清中总胆红素(Tbil)、直接胆红素(Dbil)、碱性磷酸酶(ALP)、谷氨酰转肽酶(GGT)指标、术后半年临床症状(包括腹痛、腹胀、恶心、纳差)及术后6月、12月、18月胆总管结石复发情况。结果 治疗组术后6月、12月及18月结石复发率略低于对照组,但两者差异无统计学意义( P >0.05);治疗组在改善腹痛、腹胀、恶心、纳差症状方面优于对照组( P <0.05);治疗组在改善血清Tbil、Dbil、ALP、GGT水平方面优于对照组( P <0.01)。结论 柴芍四金汤能有效预防ERCP术后胆总管结石的复发,且能改善胆总管结石引起的临床症状及血清生化指标。 相似文献
1. To investigate Genkwa Flos hepatotoxicity, a cell metabolomics strategy combined with serum pharmacology was performed on human HL-7702 liver cells in this study.
2. Firstly, cell viability and biochemical indicators were determined and the cell morphology was observed to confirm the cell injury and develop a cell hepatotoxicity model. Then, with the help of cell metabolomics based on UPLC-MS, the Genkwa Flos group samples were completely separated from the blank group samples in the score plots and seven upregulated as well as two down-regulated putative biomarkers in the loading plot were identified and confirmed. Besides, two signal molecules and four enzymes involved in biosynthesis pathway of lysophosphatidylcholine and the sphingosine kinase/sphingosine-1-phosphate pathway were determined to investigate the relationship between Genkwa Flos hepatotoxicity and these two classic pathways. Finally, the metabolic pathways related to specific biomarkers and two classic metabolic pathways were analyzed to explain the possible mechanism of Genkwa Flos hepatotoxicity.
3. Based on the results, lipid peroxidation and oxidative stress, phospholipase A2/lysophosphatidylcholine pathway, the disturbance of sphingosine-1-phosphate metabolic profile centered on sphingosine kinase/sphingosine-1-phosphate pathway and fatty acid metabolism might be critical participators in the progression of liver injury induced by Genkwa Flos. 相似文献