Coronavirus disease 2019 outbreak: is liver disease a prognostic tool?

2021 ◽  
Vol 63 (4) ◽  
Author(s):  
Gianni TESTINO ◽  
Sharmila FAGOONEE
2008 ◽  
Vol 48 ◽  
pp. S81
Author(s):  
D. Duller ◽  
J. Haas ◽  
V. Stadlbauer ◽  
D. Kniepeiss ◽  
S.T. Palma ◽  
...  

2015 ◽  
Vol 6 (1) ◽  
pp. 38-41
Author(s):  
Rubayat Sheik Giasuddin ◽  
Mobin Khan ◽  
ASM Giasuddin ◽  
Md Mahmudur Rahman Siddiqui

Liver Fibrosis (LF) is a common outcome in chronic liver disease (CLD). Over a period of time, the process results in cirrhosis leading to disruption in functional capacity of liver. Further serious complications may occur including portal hypertension, liver failure and cancer. The magnitude of CLD has increased being recognized as a major cause for morbidity and mortality globally and it is increasing progressively in Bangladesh also. Question arises "Is the transabdominal needle biopsy of liver, the traditional reference standard method, sufficient and efficient enough for detecting and assessing liver fibrosis particularly in the early stages of significant liver disease?" More simpler, convenient and less expensive blood tests such as 'Enhanced Liver Fibrosis (ELF) immunoassay test', Fibrotest and Aspartate transaminase-platelet ratio index (APRI), have been developed and reported for identification of significant CLD and use as prognostic tool in clinical practice. Among them, the ELF test had been found to be statistically the best for diagnosing and predicting clinical outcomes in patients with CLD and may be a useful prognostic tool in clinical practice. This ELF immunoassay test has been briefly reviewed in this article. Short title: ELF immunoassay test for CLDAnwer Khan Modern Medical College Journal Vol. 6, No. 1: January 2015, Pages 38-41


2016 ◽  
Vol 64 (2) ◽  
pp. S284
Author(s):  
R.E. Stauber ◽  
J. Haas ◽  
D. Wagner ◽  
D. Kniepeiss ◽  
V. Stadlbauer ◽  
...  

Author(s):  
Odell T. Minick ◽  
Hidejiro Yokoo

Mitochondrial alterations were studied in 25 liver biopsies from patients with alcoholic liver disease. Of special interest were the morphologic resemblance of certain fine structural variations in mitochondria and crystalloid inclusions. Four types of alterations within mitochondria were found that seemed to relate to cytoplasmic crystalloids.Type 1 alteration consisted of localized groups of cristae, usually oriented in the long direction of the organelle (Fig. 1A). In this plane they appeared serrated at the periphery with blind endings in the matrix. Other sections revealed a system of equally-spaced diagonal lines lengthwise in the mitochondrion with cristae protruding from both ends (Fig. 1B). Profiles of this inclusion were not unlike tangential cuts of a crystalloid structure frequently seen in enlarged mitochondria described below.


2020 ◽  
Vol 134 (16) ◽  
pp. 2189-2201
Author(s):  
Jessica P.E. Davis ◽  
Stephen H. Caldwell

Abstract Fibrosis results from a disordered wound healing response within the liver with activated hepatic stellate cells laying down dense, collagen-rich extracellular matrix that eventually restricts liver hepatic synthetic function and causes increased sinusoidal resistance. The end result of progressive fibrosis, cirrhosis, is associated with significant morbidity and mortality as well as tremendous economic burden. Fibrosis can be conceptualized as an aberrant wound healing response analogous to a chronic ankle sprain that is driven by chronic liver injury commonly over decades. Two unique aspects of hepatic fibrosis – the chronic nature of insult required and the liver’s unique ability to regenerate – give an opportunity for pharmacologic intervention to stop or slow the pace of fibrosis in patients early in the course of their liver disease. Two potential biologic mechanisms link together hemostasis and fibrosis: focal parenchymal extinction and direct stellate cell activation by thrombin and Factor Xa. Available translational research further supports the role of thrombosis in fibrosis. In this review, we will summarize what is known about the convergence of hemostatic changes and hepatic fibrosis in chronic liver disease and present current preclinical and clinical data exploring the relationship between the two. We will also present clinical trial data that underscores the potential use of anticoagulant therapy as an antifibrotic factor in liver disease.


2001 ◽  
Vol 120 (5) ◽  
pp. A45-A45
Author(s):  
N KU ◽  
R GISH ◽  
T WRIGHT ◽  
M OMARY
Keyword(s):  

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