Role of ferritin in predicting mortality in decompensated liver cirrhosis

2013 ◽  
Vol 3 (1) ◽  
pp. S89-S90
Author(s):  
Rajiv Baijal ◽  
K.H.R. Praveen ◽  
Deepak Gupta ◽  
Nimish Shah ◽  
Sandeep Kulkarni
2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Esther Sastre ◽  
Laura Caracuel ◽  
Isabel Prieto ◽  
Pablo Llévenes ◽  
M. Ángeles Aller ◽  
...  

2020 ◽  
Vol 8 (3) ◽  
pp. 150-158
Author(s):  
Fabian Benz ◽  
Raphael Mohr ◽  
Frank Tacke ◽  
Christoph Roderburg

AbstractPatients with advanced chronic liver diseases, particularly with decompensated liver cirrhosis, can develop specific pulmonary complications independently of any pre-existing lung disease. Especially when dyspnea occurs in combination with liver cirrhosis, patients should be evaluated for hepato-pulmonary syndrome (HPS), porto-pulmonary hypertension (PPHT), hepatic hydrothorax and spontaneous bacterial empyema, which represent the clinically most relevant pulmonary complications of liver cirrhosis. Importantly, the pathophysiology, clinical features, diagnosis and the corresponding therapeutic options differ between these entities, highlighting the role of specific diagnostics in patients with liver cirrhosis who present with dyspnea. Liver transplantation may offer a curative therapy, including selected cases of HPS and PPHT. In this review article, we summarize the pathogenesis, clinical features, diagnostic algorithms and treatment options of the 4 specific pulmonary complications in patients with liver cirrhosis.


1980 ◽  
Vol 44 (03) ◽  
pp. 146-149 ◽  
Author(s):  
Nicole Ardaillou ◽  
Jeannine Yvart ◽  
Philippe Le Bras ◽  
Marie-José Larrieu

SummaryThe catabolism of human fragment D, (FgD), obtained by plasmin digestion of fibrinogen has been investigated in normal subjects and patients with liver cirrhosis and the results compared with those obtained for fibrinogen (Fg). Fg was labelled with I-125 and Fg D with I-131 using the chloramine T method. The plasma disappearance curves of both labelled proteins fitted a two exponential curve. In controls the plasma clearance rate of Fg D was greater than that of Fg as shown by the marked difference between the half-lives of these two tracers: 8,9 and 83,5 hours for Fg D and Fg respectively. The fractional catabolic rate of Fg D was 3.38 times the plasma pool per day. In nine patients with liver cirrhosis, catabolism of Fg was not modified. In contrast, catabolism of Fg D was significantly reduced with a half life of 13.0 hours and a low fractional catabolic rate. These results suggest the role of the liver in the catabolism of Fg D in man.


Author(s):  
A Giorgio ◽  
G De Stefano ◽  
S Iaquinta ◽  
U Scognamiglio ◽  
V Giorgio ◽  
...  

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