About: Abnormal Liver Function Test is a research topic. Over the lifetime, 833 publications have been published within this topic receiving 19686 citations.
TL;DR: A clinicobiological score combining age, BMI, triglycerides, and ALT had 100% negative predictive value for septal fibrosis when scoring 0 or 1 (100% sensitivity for a specificity of 47%).
TL;DR: A high prevalence of liver test abnormalities and liver injury was observed in 417 patients with COVID-19 admitted to the only referral hospital in Shenzhen, China and the prevalence increased substantially during hospitalization.
TL;DR: The interpretation of the routinely performed liver tests along with the indications and utility of quantitative tests are discussed, including the Model for End Stage Liver Disease rather than any single parameter.
Abstract: Interpretation of abnormalities in liver function tests is a common problem faced by clinicians. This has become more common with the introduction of automated routine laboratory testing. Not all persons with one or more abnormalities in these tests actually have liver disease. The various biochemical tests, their pathophysiology, and an approach to the interpretation of abnormal liver function tests are discussed in this review.
TL;DR: All CF patients with liver disease need annual follow-up to evaluate the development of cirrhosis, portal hypertension or liver failure, particularly in children with hepatic dysfunction or advanced portal hypertension.
TL;DR: A pragmatic approach to diagnosis and staging of NAFLD is discussed so that patients at the highest risk of liver-related complications can be identified.
Abstract: Non-alcoholic fatty liver disease (NAFLD) is now the commonest cause of abnormal liver function tests (LFTs) in the UK with approximately a third of the population being affected. The exact prevalence is not known, but population studies from the USA and China using magnetic resonance spectroscopy estimate that approximately 30% of the general population have steatosis. It is a spectrum of disease ranging from simple steatosis, to non-alcoholic steatohepatitis (NASH), through to advanced fibrosis and cirrhosis. The majority have simple steatosis, but approximately 10–30% develop NASH and the development of NASH cirrhosis is associated with a poor long-term prognosis. Patients with NASH have increased liver-related and cardiovascular mortality. Many patients with NAFLD remain undiagnosed, and recognising those at risk is the first step. Clinicians overly rely on abnormal liver enzymes to identify patients with NAFLD, so patients with significant liver disease can be overlooked, potentially missing opportunities for intervention. Although liver biopsy is the gold standard method for diagnosing and staging NAFLD, the majority of patients can be effectively diagnosed non-invasively with tests that are routinely available in the clinic today. This review discusses a pragmatic approach to diagnosis and staging of NAFLD so that patients at the highest risk of liver-related complications can be identified.