R. Pandey, R. Pathak, Arun Gnawali, P. Khadga, Sashi Sharma, A. Jha, R. Hamal, D. Koirala, P. Parajuli
{"title":"Diagnostic Accuracy of Non-invasive Laboratory-Based Fibrosis Scores in Predicting the Presence of Esophageal Varices in Liver Cirrhosis","authors":"R. Pandey, R. Pathak, Arun Gnawali, P. Khadga, Sashi Sharma, A. Jha, R. Hamal, D. Koirala, P. Parajuli","doi":"10.3126/jaim.v9i2.32814","DOIUrl":null,"url":null,"abstract":"Cirrhosis is the end-stage for chronic liver disease and is the leading cause of liver-related death globally.1 Cirrhosis is frequently compensated. The development of complications of portal hypertension and/or liver dysfunction is decompensated cirrhosis. It is defined by the presence of variceal hemorrhage, ascites, encephalopathy, hepatorenal syndrome, jaundice or hepatocellular carcinoma. The transition from a compensated to a decompensated stage occurs at a rate of 5 to 7% per year.2 Esophageal variceal bleeding is a life-threatening portal hypertension-related complication in liver cirrhosis.3 Esophageal varices are present at diagnosis in approximately 50% of cirrhotic patients and the rate of development of new varices and increase in grades of varices is 8% per year.4 The mortality is 3.4% per year in patients with non-bleeding varices. By comparison, the mortality rises to 57% per year in patients with variceal bleeding. Thus, early diagnosis of varices and primary prophylaxis of variceal bleeding in high-risk patients with liver cirrhosis is important in improving survival.5","PeriodicalId":75443,"journal":{"name":"Advances in internal medicine","volume":"9 1","pages":"54-59"},"PeriodicalIF":0.0000,"publicationDate":"2020-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in internal medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3126/jaim.v9i2.32814","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Cirrhosis is the end-stage for chronic liver disease and is the leading cause of liver-related death globally.1 Cirrhosis is frequently compensated. The development of complications of portal hypertension and/or liver dysfunction is decompensated cirrhosis. It is defined by the presence of variceal hemorrhage, ascites, encephalopathy, hepatorenal syndrome, jaundice or hepatocellular carcinoma. The transition from a compensated to a decompensated stage occurs at a rate of 5 to 7% per year.2 Esophageal variceal bleeding is a life-threatening portal hypertension-related complication in liver cirrhosis.3 Esophageal varices are present at diagnosis in approximately 50% of cirrhotic patients and the rate of development of new varices and increase in grades of varices is 8% per year.4 The mortality is 3.4% per year in patients with non-bleeding varices. By comparison, the mortality rises to 57% per year in patients with variceal bleeding. Thus, early diagnosis of varices and primary prophylaxis of variceal bleeding in high-risk patients with liver cirrhosis is important in improving survival.5