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Effect of viral suppression on hepatic venous pressure gradient in hepatitis C with cirrhosis and portal hypertension.
Afdhal, N; Everson, G T; Calleja, J L; McCaughan, G W; Bosch, J; Brainard, D M; McHutchison, J G; De-Oertel, S; An, D; Charlton, M; Reddy, K R; Asselah, T; Gane, E; Curry, M P; Forns, X.
Affiliation
  • Afdhal N; Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
  • Everson GT; University of Colorado Denver, Aurora, Colorado, USA.
  • Calleja JL; Hospital U. Puerta de Hierro, CIBEREHD, Universidad Autonoma, Madrid, Spain.
  • McCaughan GW; Royal Prince Alfred Hospital, Centenary Research Institute, University of Sydney, Sydney, NSW, Australia.
  • Bosch J; Liver Unit, Hospital Clinic, IDIBAPS, CIBEREHD, Barcelona, Spain.
  • Brainard DM; Swiss Liver Center, Inselspital, Bern University, Bern, Switzerland.
  • McHutchison JG; Gilead Sciences, Inc., Foster City, California, USA.
  • De-Oertel S; Gilead Sciences, Inc., Foster City, California, USA.
  • An D; Gilead Sciences, Inc., Foster City, California, USA.
  • Charlton M; Gilead Sciences, Inc., Foster City, California, USA.
  • Reddy KR; Intermountain Medical Center, Murray, Utah, USA.
  • Asselah T; University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
  • Gane E; Hôpital Beaujon, Department of Hepatology, AP-HP, INSERM UMR1149 and University Paris-Diderot, Clichy, France.
  • Curry MP; University of Auckland, Auckland, New Zealand.
  • Forns X; Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
J Viral Hepat ; 24(10): 823-831, 2017 10.
Article in En | MEDLINE | ID: mdl-28295923
ABSTRACT
Portal hypertension is a predictor of liver-related clinical events and mortality in patients with hepatitis C and cirrhosis. The effect of interferon-free hepatitis C treatment on portal pressure is unknown. Fifty patients with Child-Pugh-Turcotte (CPT) A and B cirrhosis and portal hypertension (hepatic venous pressure gradient [HVPG] >6 mm Hg) were randomized to receive 48 weeks of open-label sofosbuvir plus ribavirin at Day 1 or after a 24-week observation period. The primary endpoint was sustained virologic response 12 weeks after therapy (SVR12) in patients who received ≥1 dose of treatment. Secondary endpoints included changes in HVPG, laboratory parameters, and MELD and CPT scores. A subset of patients was followed 48 weeks posttreatment to determine late changes in HVPG. SVR12 occurred in 72% of patients (33/46). In the 37 patients with paired HVPG measurements at baseline and the end of treatment, mean HVPG decreased by -1.0 (SD 3.97) mm Hg. Nine patients (24%) had ≥20% decreases in HVPG during treatment. Among 39 patients with pretreatment HVPG ≥12 mm Hg, 27 (69%) achieved SVR12. Four of the 33 (12%) patients with baseline HVPG ≥12 mm Hg had HVPG <12 mm Hg at the end of treatment. Of nine patients with pretreatment HVPG ≥12 mm Hg who achieved SVR12 and completed 48 weeks of follow-up, eight (89%) had a ≥20% reduction in HVPG, and three reduced their pressure to <12 mm Hg. Patients with chronic HCV and compensated or decompensated cirrhosis who achieve SVR can have clinically meaningful reductions in HVPG at long-term follow-up. (EudraCT 2012-002457-29).
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis C / Portal Pressure / Hepacivirus / Hepatic Veins / Hypertension, Portal / Liver Cirrhosis Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Viral Hepat Journal subject: GASTROENTEROLOGIA Year: 2017 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis C / Portal Pressure / Hepacivirus / Hepatic Veins / Hypertension, Portal / Liver Cirrhosis Type of study: Clinical_trials / Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Viral Hepat Journal subject: GASTROENTEROLOGIA Year: 2017 Type: Article Affiliation country: United States