Fat depletion in liver transplant candidates with autoimmune hepatitis as compared to alcohol-related liver disease

Endoscopy ◽  
2006 ◽  
Vol 37 (12) ◽  
Author(s):  
A Qasim ◽  
O O'Conor ◽  
J Sultan ◽  
D Brady ◽  
J Hegarty ◽  
...  
2017 ◽  
Vol 30 (11) ◽  
pp. 1140-1149 ◽  
Author(s):  
Aloysious D. Aravinthan ◽  
Andrew S. Barbas ◽  
Adam C. Doyle ◽  
Mahmood Tazari ◽  
Gonzalo Sapisochin ◽  
...  

Author(s):  
Narendra S. Choudhary ◽  
Neeraj Saraf ◽  
Saurabh Mehrotra ◽  
Sanjiv Saigal ◽  
Arvinder S. Soin

2013 ◽  
Vol 27 (6) ◽  
pp. 829-837 ◽  
Author(s):  
Jeffrey Campsen ◽  
Michael Zimmerman ◽  
James Trotter ◽  
Johnny Hong ◽  
Chris Freise ◽  
...  

2019 ◽  
Vol 2019 ◽  
pp. 1-5
Author(s):  
Mahmood Alawainati ◽  
Jawad Khamis ◽  
Muneer Abdulla ◽  
Saeed Alsaeed

Background. There are multiple aetiologies for dyspnea in patients with liver disease, including pneumonia, pulmonary embolism, hepatic hydrothorax, portopulmonary syndrome, and hepatopulmonary syndrome. The aim of this paper is to emphasize the importance of early diagnosis and management of hepatopulmonary syndrome. Case Presentation. We report a case of a 65-year-old male who was known to have chronic hepatitis C presented with one-year history of shortness of breath and cyanosis. The initial impression of pulmonary embolism was excluded by comprehensive diagnostic investigations. The correlation between the clinical picture and investigations raised the possibility of hepatopulmonary syndrome which was confirmed by contrast-enhanced transthoracic echocardiography. Conclusions. High suspicion is required to diagnose hepatopulmonary syndrome in patients with liver disease and hypoxemia. Screening for this complication is appropriate in liver transplant candidates, and diagnosed patients should be evaluated extensively for liver transplant.


2020 ◽  
Vol 9 (2) ◽  
pp. 319
Author(s):  
Jaspreet S. Suri ◽  
Christopher J. Danford ◽  
Vilas Patwardhan ◽  
Alan Bonder

Background: Outcomes on the liver transplant waitlist can vary by etiology. Our aim is to investigate differences in waitlist mortality of autoimmune hepatitis (AIH), primary biliary cholangitis (PBC), and primary sclerosing cholangitis (PSC) using the United Network for Organ Sharing (UNOS) database. Methods: We identified patients who were listed for liver transplantation from 1987 to 2016 with a primary diagnosis of AIH, PBC, or PSC. We excluded patients with overlap syndromes, acute hepatic necrosis, missing data, and those who were children. The primary outcome was death or removal from the waitlist due to clinical deterioration. We compared waitlist survival using competing risk analysis. Results: Between 1987 and 2016, there were 7412 patients listed for liver transplant due to AIH, 8119 for PBC, and 10,901 for PSC. Patients with AIH were younger, more likely to be diabetic, and had higher listing model for end-stage liver disease (MELD) scores compared to PBC and PSC patients. Patients with PBC and AIH were more likely to be removed from the waitlist due to death or clinical deterioration. On competing risk analysis, AIH patients had a similar risk of being removed from the waitlist compared to those with PBC (subdistribution hazard ratio (SHR) 0.94, 95% CI 0.85–1.03) and higher risk of removal compared to those with PSC (SHR 0.8, 95% CI 0.72 to 0.89). Conclusion: Autoimmune hepatitis carries a similar risk of waitlist removal to PBC and a higher risk than PSC. The etiology of this disparity is not entirely clear and deserves further investigation.


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