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Dive into the research topics where Pierre Henri Bernard is active.

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Featured researches published by Pierre Henri Bernard.


Gastroenterology | 1999

European collaborative study on factors influencing outcome after liver transplantation for hepatitis C

Cyrille Feray; L. Caccamo; Graeme J. M. Alexander; Béatrice Ducot; Jean Gugenheim; Teresa Casanovas; Carmelo Loinaz; Michele Gigou; Patrizia Burra; Lisbeth Barkholt; Raffael Esteban; Thierry Bizollon; Jan Lerut; Anne Minello–Franza; Pierre Henri Bernard; Karl Nachbaur; Danielle Botta–Fridlund; Henri Bismuth; Solko W. Schalm; Didier Samuel

BACKGROUND & AIMS Liver transplantation for hepatitis C virus (HCV)-related liver disease is characterized by frequent graft infection by HCV. The prognosis and risk factors for morbidity and mortality in this condition were determined. METHODS A retrospective study of 652 consecutive anti-HCV-positive patients undergoing liver transplantation between 1984 and 1995 in 15 European centers was conducted; 102 patients coinfected with hepatitis B virus (HBV) received immunoglobulin prophylaxis for antibody to hepatitis B surface antigen. RESULTS Overall, 5-year survival was 72%. Five-year actuarial rates of hepatitis and cirrhosis were 80% and 10%. Genotypes 1b, 1a, and 2 were detected in 214 (80%), 24 (9%), and 24 (9%) of 268 patients analyzed. The only discriminant factor for patient or graft survival was hepatocellular carcinoma as primary indication. Independent risk factors for recurrent hepatitis included the absence of HBV coinfection before transplantation (relative risk [RR], 1.7; 95% confidence interval [CI], 1.2-2.6; P = 0.005), genotype 1b (RR, 2; 95% CI, 1.3-2.9; P = 0.01), and age > 49 years (RR, 1.4; 95% CI, 1.1-1.8; P = 0.01). CONCLUSIONS The results of transplantation for HCV-related disease are compromised by a significant risk of cirrhosis, although 5-year survival is satisfactory. Genotype 1b, age, and absence of pretransplantation coinfection by HBV are risk factors for recurrent HCV.


Gastroenterology | 2011

Noninvasive Tests for Fibrosis and Liver Stiffness Predict 5-Year Outcomes of Patients With Chronic Hepatitis C

Julien Vergniol; Juliette Foucher; Eric Terrebonne; Pierre Henri Bernard; Brigitte Le Bail; Wassil Merrouche; Patrice Couzigou; Victor de Ledinghen

BACKGROUND & AIMS Liver stiffness can be measured noninvasively to assess liver fibrosis in patients with chronic hepatitis C. In patients with chronic liver diseases, level of fibrosis predicts liver-related complications and survival. We evaluated the abilities of liver stiffness, results from noninvasive tests for fibrosis, and liver biopsy analyses to predict overall survival or survival without liver-related death with a 5-year period. METHODS In a consecutive cohort of 1457 patients with chronic hepatitis C, we assessed fibrosis and, on the same day, liver stiffness, performed noninvasive tests of fibrosis (FibroTest, the aspartate aminotransferase to platelet ratio index, FIB-4), and analyzed liver biopsy samples. We analyzed data on death, liver-related death, and liver transplantation collected during a 5-year follow-up period. RESULTS At 5 years, 77 patients had died (39 liver-related deaths) and 16 patients had undergone liver transplantation. Overall survival was 91.7% and survival without liver-related death was 94.4%. Survival was significantly decreased among patients diagnosed with severe fibrosis, regardless of the noninvasive method of analysis. All methods were able to predict shorter survival times in this large population; liver stiffness and results of FibroTest had higher predictive values. Patient outcomes worsened as liver stiffness and FibroTest values increased. Prognostic values of stiffness (P<.0001) and FibroTest results (P<.0001) remained after they were adjusted for treatment response, patient age, and estimates of necroinflammatory grade. CONCLUSIONS Noninvasive tests for liver fibrosis (measurement of liver stiffness or FibroTest) can predict 5-year survival of patients with chronic hepatitis C. These tools might help physicians determine prognosis at earlier stages and discuss specific treatments, such as liver transplantation.


Journal of Hepatology | 2014

Covered vs. uncovered stents for transjugular intrahepatic portosystemic shunt: a randomized controlled trial.

Jean Marc Perarnau; Amélie Le Gouge; Charlotte Nicolas; L. D’Alteroche; Patrick Borentain; Faouzi Saliba; Anne Minello; Rodolphe Anty; Carine Chagneau-Derrode; Pierre Henri Bernard; Armand Abergel; Isabelle Ollivier-Hourmand; J. Gournay; Jean Ayoub; Christophe Gaborit; Emmanuel Rusch; Bruno Giraudeau

BACKGROUND & AIMS The first studies comparing covered stents (CS) and bare stents (BS) to achieve Transjugular Intrahepatic Portosystemic Shunt (TIPS) were in favor of CS, but only one randomized study has been performed. Our aim was to compare the primary patency of TIPS performed with CS and BS. METHODS The study was planned as a multicenter, pragmatic (with centers different in size and experience), randomized, single-blinded (with blinding of patients only), parallel group trial. The primary endpoint was TIPS dysfunction defined as either a portocaval gradient ⩾12mmHg, or a stent lumen stenosis ⩾50%. A transjugular angiography with portosystemic pressure gradient measurement was scheduled every 6months after TIPS insertion. RESULTS 137 patients were randomized: 66 to receive CS, and 71 BS. Patients who were found to have a hepato-cellular carcinoma, or whose procedure was cancelled were excluded, giving a sample of 129 patients (62 vs. 67). Median follow-up for CS and BS were 23.6 and 21.8months, respectively. Compared to BS, the risk of TIPS dysfunction with CS was 0.60 95% CI [0.38-0.96], (p=0.032). The 2-year rate of shunt dysfunction was 44.0% for CS vs. 63.6% for BS. Early post TIPS complications (22.4% vs. 34.9%), risk of hepatic encephalopathy (0.89 [0.53-1.49]) and 2-year survival (70% vs. 67.5%) did not differ in the two groups. The 2-year cost/patient was 20k€ [15.9-27.5] for CS vs. 23.4k€ [18-37] for BS (p=0.52). CONCLUSIONS CS provided a significant 39% reduction in dysfunction compared to BS. We did not observe any significant difference with regard to hepatic encephalopathy or death.


Journal of Hepatology | 2014

Long term results of liver transplantation for Wilson’s disease: Experience in France

Olivier Guillaud; Jérôme Dumortier; Rodolphe Sobesky; Dominique Debray; Philippe Wolf; Claire Vanlemmens; François Durand; Yvon Calmus; Christophe Duvoux; Sébastien Dharancy; Nassim Kamar; Karim Boudjema; Pierre Henri Bernard; Georges-Philippe Pageaux; Ephrem Salamé; Jean Gugenheim; Alain Lachaux; Dalila Habes; Sylvie Radenne; Jean Hardwigsen; Olivier Chazouillères; Jean-Marc Trocello; Philippe Ichai; Sophie Branchereau; Olivier Soubrane; Denis Castaing; Emmanuel Jacquemin; Didier Samuel; Jean-Charles Duclos-Vallée

BACKGROUND & AIMS Liver transplantation (LT) is the therapeutic option for severe complications of Wilsons disease (WD). We aimed to report on the long-term outcome of WD patients following LT. METHODS The medical records of 121 French patients transplanted for WD between 1985 and 2009 were reviewed retrospectively. Seventy-five patients were adults (median age: 29 years, (18-66)) and 46 were children (median age: 14 years, (7-17)). The indication for LT was (1) fulminant/subfulminant hepatitis (n = 64, 53%), median age = 16 years (7-53), (2) decompensated cirrhosis (n = 50, 41%), median age = 31.5 years (12-66) or (3) severe neurological disease (n = 7, 6%), median age = 21.5 years (14.5-42). Median post-transplant follow-up was 72 months (0-23.5). RESULTS Actuarial patient survival rates were 87% at 5, 10, and 15 years. Male gender, pre-transplant renal insufficiency, non elective procedure, and neurological indication were significantly associated with poorer survival rate. None of these factors remained statistically significant under multivariate analysis. In patients transplanted for hepatic indications, the prognosis was poorer in case of fulminant or subfulminant course, non elective procedure, pretransplant renal insufficiency and in patients transplanted before 2000. Multivariate analysis disclosed that only recent period of LT was associated with better prognosis. At last visit, the median calculated glomerular filtration rate was 93 ml/min (33-180); 11/93 patients (12%) had stage II renal insufficiency and none had stage III. CONCLUSIONS Liver failure associated with WD is a rare indication for LT (<1%), which achieves an excellent long-term outcome, including renal function.


Gastroenterology | 1993

Functional characterization of liver-associated lymphocytes in patients with liver metastasis

Maria Winnock; Maria Garcia-Barcina; Sylvie Huet; Pierre Henri Bernard; Jean Saric; Paulette Bioulac-Sage; Norbert Gualde; Charles Balabaud

BACKGROUND The liver-associated lymphocytes (LAL) population is mainly composed of cells with natural killer (NK) activity expressing the CD3+/-CD56+ phenotype. No evident difference has been found in the phenotypic data between patients with benign or malignant liver disease. In this study, the cytotoxic pattern of this population has been characterized from patients who underwent an operation for benign or metastatic liver disease. METHODS LAL were isolated by sinusoidal high-pressure lavage from partial hepatectomies. Phenotype was characterized by flow cytometry, and cytotoxicity was evaluated by standard 4-hour 51Cr release assays against NK and lymphokine-activated killer (LAK)-sensitive targets. RESULTS In patients with benign liver disease, LAL showed spontaneous high levels of NK activity and LAK activity compared with peripheral blood lymphocytes. In patients with metastatic liver disease, no difference was observed in the levels of NK activity between LAL and peripheral blood, and the level of LAK activity was far lower than that expressed in patients with benign liver disease. CONCLUSIONS These results show that the cytotoxic pattern of peripheral blood lymphocytes does not mirror that of LAL. In patients with benign liver disease, LAL are in a state of activation, whereas the decreased level of LAL cytotoxicity in patients with metastatic liver disease suggests that the cytotoxic activity of these cells could be inhibited by the presence of suppressive factors.


Gastroenterologie Clinique Et Biologique | 2007

Management practices for gastrointestinal hemorrhage related to portal hypertention in cirrhotic patients: evaluation of the impact of the Paris consensus workshop

Claire Charpignon; Frédéric Oberti; Pierre Henri Bernard; Eric Bartoli; Arnault Pauwels; Philippe Renard; Jean-François Cadranel; Brigitte Bernard-Chabert; Jean-Claude Barbare; Isabelle Ingrand; Pierre Ingrand; Michel Beauchant

OBJECTIVES The purpose of this before-after observational survey was to evaluate compliance with good clinical practice guidelines for gastrointestinal hemorrhage related to portal hypertension and the impact of the French Consensus Workshop held in Paris in 2003. METHODS Data were recorded concerning episodes of gastrointestinal hemorrhage occurring in cirrhotic patients using a survey questionnaire in 2003 before the workshop and again in 2004. RESULTS Seventy-six index episodes were included in 2003 and 84 in 2004 in patients attending French hospitals. Before hospital admission, primary prophylaxis was similar in 2003 and 2004, but beta blockers were used alone more often in 2004 for secondary prophylaxis (42% vs 19%, P=0.018). The time from onset of bleeding to hospital admission was greater than 12 hours for 43 and 42% of patients and was not shorter in the event of recurrent hemorrhage. At admission, vasoactive drugs were given earlier in 2004 (<2h: 68% vs 35%, P<0.001). Use of antibiotic prophylaxis was similar in 2003 and 2004 (70% vs 61%, P=0.098), and was more common for Child-Pugh B or C patients (P=0.044). CONCLUSION The Paris Consensus Workshop enabled improved clinical practices. Weak points were insufficient screening for cirrhosis, long delay before admission, insufficient use of antibiotic prophylaxis which should be systematic.


Gastroenterology | 2014

Effectiveness of telaprevir or boceprevir in treatment-experienced patients with HCV genotype 1 infection and cirrhosis.

Christophe Hézode; Hélène Fontaine; C. Dorival; Fabien Zoulim; Dominique Larrey; V. Canva; Victor de Ledinghen; T. Poynard; Didier Samuel; Marc Bourlière; Laurent Alric; Jean Jacques Raabe; J.-P. Zarski; Patrick Marcellin; G. Riachi; Pierre Henri Bernard; Véronique Loustaud–Ratti; Olivier Chazouillères; Armand Abergel; Dominique Guyader; S. Metivier; A. Tran; Vincent Di Martino; X. Causse; Thong Dao; Damien Lucidarme; Isabelle Portal; Patrice Cacoub; J. Gournay; Véronique Grando–Lemaire


Journal of Hepatology | 1999

Evaluation of efficacy of liver transplantation in alcoholic cirrhosis using matched and simulated controls: 5-year survival

Thierry Poynard; Sylvie Naveau; Michel Doffoel; Karim Boudjema; Claire Vanlemmens; Georges Mantion; Michel Messner; Bernard Launois; Didier Samuel; Daniel Cherqui; G.-P. Pageaux; Pierre Henri Bernard; Yvon Calmus; J.-P. Zarski; Jean Philippe Miguet


Nephrology Dialysis Transplantation | 2001

The tolerance and efficacy of interferon‐α in haemodialysis patients with HCV infection: a multicentre, prospective study

Françoise Degos; Stanislas Pol; Marie Laure Chaix; Valérie Laffitte; Catherine Buffet; Pierre Henri Bernard; Claude Degott; Françoise Carnot; Philippe Chaumet Riffaud; Sylvie Chevret


World Journal of Gastroenterology | 2006

Management of digestive bleeding related to portal hypertension in cirrhotic patients: A French multicenter cross-sectional practice survey

Pierre Ingrand; J. Gournay; Pierre Henri Bernard; Frédéric Oberti; Brigitte Bernard-Chabert; Arnault Pauwels; Philippe Renard; Eric Bartoli; Jean-François Cadranel; Jean-Claude Barbare; Isabelle Ingrand; Michel Beauchant

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Didier Samuel

Université Paris-Saclay

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Jean Saric

University of Bordeaux

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Michel Beauchant

Institut national de la recherche agronomique

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Claire Vanlemmens

University of Franche-Comté

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Jean Gugenheim

University of Nice Sophia Antipolis

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Jean-Claude Barbare

University of Picardie Jules Verne

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