Psychosocial assessment rather than severity of liver failure dominates selection for liver transplantation in patients with alcohol‐associated liver disease

2021 ◽  
Author(s):  
KE Daniel ◽  
LA Matthews ◽  
N Deiss‐Yehiely ◽  
J Myers ◽  
M Garvey ◽  
...  

2018 ◽  
Vol 94 (1112) ◽  
pp. 335.2-347 ◽  
Author(s):  
Claire Kelly ◽  
Marinos Pericleous

Wilson disease is a rare but important disorder of copper metabolism, with a failure to excrete copper appropriately into bile. It is a multisystem condition with presentations across all branches of medicine. Diagnosis can be difficult and requires a high index of suspicion. It should be considered in unexplained liver disease particularly where neuropsychiatric features are also present. Treatments are available for all stages of disease. A particularly important presentation not to overlook is acute liver failure which carries a high mortality risk and may require urgent liver transplantation. Here, we provide an overview of this complex condition.



2020 ◽  
pp. 3089-3100
Author(s):  
Jane Macnaughtan ◽  
Rajiv Jalan

Liver failure occurs when loss of hepatic parenchymal function exceeds the capacity of hepatocytes to regenerate or repair liver injury. Acute liver failure is characterized by jaundice and prolongation of the prothrombin time in the context of recent acute liver injury, with hepatic encephalopathy occurring within 8 weeks of the first onset of liver disease. Acute-on-chronic liver failure is characterized by hepatic and/or extrahepatic organ failure in patients with cirrhosis associated with an identified or unidentified precipitating event. The commonest causes of acute liver failure are acute viral hepatitis and drugs. Acute-on-chronic liver failure is most commonly precipitated by infection, alcohol abuse, and superimposed viral infection. The main clinical manifestations are hepatic encephalopathy, coagulopathy, jaundice, renal dysfunction, and haemodynamic instability. Infection and systemic inflammation contribute to pathogenesis and critically contribute to prognosis. Specific therapy for the underlying liver disease is administered when available, but this is not possible for most causes of liver failure. Treatment is predominantly supportive, with particular emphasis on (1) correction or removal of precipitating factors; (2) if encephalopathy is present, using phosphate enemata, nonhydrolysed disaccharide laxatives, and/or rifaximin; (3) early detection and prompt treatment of complications such as hypoglycaemia, hypokalaemia, cerebral oedema, infection, and bleeding. The onset of organ failure should prompt discussion with a liver transplantation centre. The mortality of acute liver failure (without liver transplantation) is about 40%. Patients with acute liver failure who do not develop encephalopathy can be expected to recover completely. Those who recover from an episode of acute-on-chronic liver failure should be considered for liver transplantation because otherwise their subsequent mortality remains high.



2019 ◽  
Vol 28 (9-10) ◽  
pp. 1116-1122 ◽  
Author(s):  
Wei Zhou ◽  
Erek D. Nelson ◽  
Anan A. Abu Rmilah ◽  
Bruce P. Amiot ◽  
Scott L. Nyberg

Owing to the increasing worldwide burden of liver diseases, the crucial need for safe and effective interventions for treating end-stage liver failure has been a very productive line of inquiry in the discipline of hepatology for many years. Liver transplantation is recognized as the most effective treatment for end-stage liver disease; however, the shortage of donor organs, high medical costs, and lifelong use of immunosuppressive agents represent major drawbacks and demand exploration for alternative treatments. Stem cell-based therapies have been widely studied in the field of liver diseases and are considered to be among the most promising therapies. Herein, we review recent advances in the application of stem cell-related therapies in liver disease with the aim of providing readers with relevant knowledge in this field and inspiration to spur further inquiry.







2021 ◽  
Author(s):  
Adem Tuncer ◽  
Mehmet Zeki Öğüt ◽  
Sertac Usta ◽  
Sami Akbulut ◽  
Tevfik Tolga Sahin ◽  
...  

Abstract Aim: The treatment of end-stage liver disease is liver transplantation. There are studies regarding liver transplantation in patients with colorectal cancer and neuroendocrine tumor liver metastasis indicating comparable results with patients who were transplanted for hepatocellular carcinoma. The aim of the present study is to present a case of a patient with Hepatitis B virus related chronic liver disease and rectal neuroendocrine tumor who underwent concomitant living donor liver transplantation and low anterior resection. Case report: The patients was a 62 years old male patient with hepatitis B virus related end-stage liver failure and a rectal neuroendocrine tumor determined during colonoscopy surveillance. Model for end stage liver disease score was 21 and had two episodes of life-threatening variceal bleeding. We performed living donor liver transplantation and low anterior resection to the patient. Currently patient is doing well 2 years after the operation. Conclusion: Our case is the first in literature showing concomitant liver transplantation for hepatitis B virus related liver failure and rectal resection for neuroendocrine tumor. These procedures can be performed synchronously provided that the etiology of liver failure is unrelated to neuroendocrine tumor and the primary tumor has favorable tumor biologic characteristics. We reviewed the English literature, we did not find any case who underwent rectal NET surgery and HBV-related liver transplantation in the same operation. We wanted to present this first case in the literature.



2021 ◽  
Vol 2 (3) ◽  
pp. 294-295
Author(s):  
Alessandro Parente ◽  
Vincenzo Ronca

Liver transplantation (LT) is the only recognized effective treatment for end-stage liver disease (ESLD) and acute fulminant liver failure [...]



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