Hepatitis C recurrence is not associated with allograft steatosis within the first year after liver transplantation

Victor I. Machicao, Murli Krishna, Hugo Bonatti, Bashar A. Aqel, Justin H. Nguyen, Stephen D. Weigand, Barry G. Rosser, Christopher Hughes, Rolland C. Dickson – 20 April 2004 – The natural history of allograft steatosis in hepatitis C (HCV)‐infected patients after liver transplantation (LT) is poorly understood. The aim of our study was to determine the relationship of allograft steatosis to HCV recurrence after LT. All patients undergoing LT at our center from March 1998 to December 2001 were included in the study.

The development of de novo hepatocellular carcinoma in patients on a liver transplant list: Frequency, size, and assessment of current screening methods

David H. Van Thiel, Sherri Yong, S. David Li, Marc Kennedy, John Brems – 20 April 2004 – Chronic end stage liver disease is the most frequent indication for liver transplantation. Individuals with end stage cirrhosis, and therefore individuals on liver transplant lists, are at increased risk of developing a hepatic cancer.

New national liver transplant allocation policy: Is the regional review board process fair?

Michael D. Voigt, Bridget Zimmerman, Daniel A. Katz, Stephen C. Rayhill – 20 April 2004 – Experienced transplant professionals may predict mortality better, in highly selected cirrhotic patients referred for accelerated listing to regional review boards, than the (Pediatric) Model for End‐Stage Liver Disease score. However, these requests are often denied. We wished to establish if (1) such denials increase mortality and (2) referring physicians predict mortality better than the score.

Hepatocellular carcinoma in HCV‐infected patients awaiting liver transplantation: Genes involved in tumor progression

Valeria R. Mas, Daniel G. Maluf, Richard Stravitz, Catherine I. Dumur, Bradly Clark, Cheryl Rodgers, Andrea Ferreira‐Gonzalez, Robert A. Fisher – 20 April 2004 – Hepatocellular carcinoma (HCC) is the fifth most common cancer and the third leading cause of cancer death in the world. The present study aimed to investigate the genes involved in viral carcinogenesis and tumor progression in liver transplant recipients with hepatitis C virus (HCV) and HCC.

Prediction of sustained virological response in liver transplant recipients with recurrent hepatitis C virus following combination pegylated interferon alfa‐2b and ribavirin therapy using tissue hepatitis C virus reverse transcriptase polymerase chain rea

Guy W. Neff, Christopher B. O'Brien, Robert Cirocco, Marzia Montalbano, Maria de Medina, Phillip Ruiz, Amr S. Khaled, Pablo A. Bejarano, Kamran Safdar, Mary A. Hill, Andreas G. Tzakis, Eugene R. Schiff – 20 April 2004 – The optimal duration of therapy for pegylated interferon combined with ribavirin in recurrent Hepatitis C virus (HCV) following liver transplantation is not known.

C2 monitoring of cyclosporine in de novo liver transplant recipients: The clinician's perspective

Federico Villamil, Stephen Pollard – 20 April 2004 – Adjusting cyclosporine (CsA) dose based on blood concentration at 2 hours after dose (C2) has been shown in prospective clinical trials to reduce the risk of rejection compared with conventional trough monitoring. In addition, it provides equivalent efficacy to tacrolimus in liver transplant patients, with a favorable safety profile. Target C2 should be defined on an individual basis depending on adjunctive therapy and the level of exposure required.

Prognostic value of altered oral glutamine challenge in patients with minimal hepatic encephalopathy

Manuel Romero‐Gómez, Lourdes Grande, Inés Camacho – 25 March 2004 – Oral glutamine challenge (OGC) has been found to be safe, and an altered response predicts elevated risk of overt hepatic encephalopathy (HE) in patients with minimal hepatic encephalopathy (MHE). We assessed the survival prognosis of patients with cirrhosis, but without current overt HE, who have an altered OGC and MHE. MHE was inferred using 3 neuropsychological tests. Venous ammonia concentrations were measured pre‐ and post‐60 minutes of a 10 g oral glutamine load.

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