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Hepatitis C-related liver cirrhosis-strategies for the prevention of hepatic decompensation,hepatocarcinogenesis,and mortality 被引量:10
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作者 Nobuyuki Toshikuni Tomiyasu Arisawa Mikihiro Tsutsumi 《World Journal of Gastroenterology》 SCIE CAS 2014年第11期2876-2887,共12页
Liver cirrhosis (LC) is a critical stage of chronic liver disease, including that caused by hepatitis C virus (HCV). In the absence of antiviral therapy, 67%-91% of patients with HCV-related LC patients die of liver-r... Liver cirrhosis (LC) is a critical stage of chronic liver disease, including that caused by hepatitis C virus (HCV). In the absence of antiviral therapy, 67%-91% of patients with HCV-related LC patients die of liver-related causes, including hepatocellular carcinoma (HCC) and liver failure. Among the therapeutic strategies used to prevent liver-related complications in these patients is standard therapy with pegylated interferon and ribavirin, which induces a sustained virological response (SVR) in 25% of HCV genotype 1-infected patients and in 69% of patients infected with genotypes 2 and 3. SVR in patients with HCV-related LC has been associated with reduced rates of hepatic decompensation, HCC, and mortality. More recently developed direct-acting antiviral agents have shown excellent antiviral efficacy, with preliminary data demonstrating that an interferon-free regimen that includes these direct-acting antiviral agents achieved SVR in more than 50% of patients with HCV genotype 1 LC. Branched-chain amino acid supplementation, improvement of insulin resistance, and the use of &#x003b2;-blockers for portal hypertension may also reduce liver-related complications. Here, we review advances in antiviral and adjunctive therapies for improved outcomes in patients with HCV-associated LC. 展开更多
关键词 Hepatitis C virus Liver cirrhosis Hepatic decompensation Hepatocellular carcinoma MORTALITY PREVENTION INTERFERON Direct-acting antiviral agents
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Clinical efficacy of tolvaptan for treatment of refractory ascites in liver cirrhosis patients 被引量:37
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作者 Xin Zhang Shu-Zhen Wang +7 位作者 Jun-Fu Zheng Wen-Min Zhao Peng Li Chun-Lei Fan Bing Li Pei-Ling Dong Lei Li Hui-Guo Ding 《World Journal of Gastroenterology》 SCIE CAS 2014年第32期11400-11405,共6页
AIM: To evaluate the efficacy and safety of tolvaptan to treat refractory ascites in decompensated liver cirrhosis patients with or without further complications, such as hepatorenal syndrome and/or hepatocellular car... AIM: To evaluate the efficacy and safety of tolvaptan to treat refractory ascites in decompensated liver cirrhosis patients with or without further complications, such as hepatorenal syndrome and/or hepatocellular carcinoma. 展开更多
关键词 TOLVAPTAN Refractory ascites HYPONATREMIA decompenSATION Liver cirrhosis
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病毒性肝炎肝硬化失代偿期患者评分系统对短期预后的分析 被引量:8
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作者 吴吉圆 张冬琴 +3 位作者 刘菲菲 焦方舟 王鲁文 龚作炯 《中国肝脏病杂志(电子版)》 CAS 2017年第1期54-60,共7页
目的评估终末期肝病模型(MELD)评分、Child-Turcotte-Pugh(CTP)分级和终末期肝病模型钠(MELDNa)评分对肝硬化失代偿期患者出院后3个月病死率的预测价值。方法研究对象为2014年1月1日至2015年10月1日入住武汉大学人民医院的120例单纯病... 目的评估终末期肝病模型(MELD)评分、Child-Turcotte-Pugh(CTP)分级和终末期肝病模型钠(MELDNa)评分对肝硬化失代偿期患者出院后3个月病死率的预测价值。方法研究对象为2014年1月1日至2015年10月1日入住武汉大学人民医院的120例单纯病毒性肝炎肝硬化失代偿期患者。收集所有患者的临床资料,分别计算MELD评分、CTP评分和MELDNa评分,统计研究对象出院后3个月内病死率并评估上述评分系统预测肝硬化失代偿期患者短期预后的价值。结果 3个月病死与生存患者的MELD评分、CTP评分和MELDNa评分差异有统计学意义(z值分别为-6.532、-6.674、-6.399,P均<0.001),MELDNa评分模型预测效果最佳(AUROC=0.882,P<0.001)。结论 MELD评分、CTP评分和MELDNa评分都能准确评估病毒性肝炎肝硬化失代偿期患者的短期(3个月)预后,MELDNa评分模型能够改进预测效能,但仍需大规模临床研究予以证实。 展开更多
关键词 病毒性肝炎 肝硬化 短期预后 MELD评分 Child-Turcotte-Pugh分级 MELDNa评分
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