2005
DOI: 10.1016/j.transproceed.2005.03.124
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Peginterferon and Ribavirin in Patients With HCV Cirrhosis After Liver Transplantation

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Cited by 25 publications
(12 citation statements)
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“…Pegylated IFNs appear to increase the risk of non-respiratory infections independently from neutropenia [17], which may be explained by their distinctive pharmacokinetic differences from standard IFN [23]. A sustained virological response was achieved in three (33.3%) patients, which is similar to previous series with IFN-based therapies in patients with cirrhosis, where HCV eradication rates were between 10% and 30%, especially in HCV genotype non-1 patients (up to 50%) [6,7,15,19,[24][25][26]. However, in view of the low response rates (20%) to antiviral therapy in patients with recurrent disease after liver transplantation or with preemptive antiviral therapy in patients undergoing liver transplantation [21,27], a pre-transplant approach seems to be reasonable.…”
Section: Discussionsupporting
confidence: 75%
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“…Pegylated IFNs appear to increase the risk of non-respiratory infections independently from neutropenia [17], which may be explained by their distinctive pharmacokinetic differences from standard IFN [23]. A sustained virological response was achieved in three (33.3%) patients, which is similar to previous series with IFN-based therapies in patients with cirrhosis, where HCV eradication rates were between 10% and 30%, especially in HCV genotype non-1 patients (up to 50%) [6,7,15,19,[24][25][26]. However, in view of the low response rates (20%) to antiviral therapy in patients with recurrent disease after liver transplantation or with preemptive antiviral therapy in patients undergoing liver transplantation [21,27], a pre-transplant approach seems to be reasonable.…”
Section: Discussionsupporting
confidence: 75%
“…The pretreatment CTP grade was A in six patients and B in three. The MELD score was 11 [6][7][8][9][10][11][12][13][14][15][16][17] (median [range]). Three patients were infected with HCV genotype 1b, four with genotype 3a and two with genotype 4.…”
Section: Resultsmentioning
confidence: 99%
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“…[93][94][95][96]98,99,102,105,106,109,110,127,145,146 Most published studies are uncontrolled trials with a high variability in patient selection, and type and timing of antiviral therapy. Rates of SVR have been less than those achieved in the nontransplant setting.…”
Section: Peg-ifn Plus Ribavirinmentioning
confidence: 99%
“…Pegylated IFNa in combination with RBV significantly improved the antiviral response rates in the treatment of naive patients with chronic HCV infection [12] and have been shown to be safe and effective in liver transplant recipients, reaching sustained virological response (SVR) rates of up to 40% for all genotypes [13][14][15][16][17][18][19][20][21][22]. Antiviral therapies can be conducted pre-OLT, preemptively in the early posttransplant period, and when HCV recurrence has developed.…”
Section: Introductionmentioning
confidence: 99%