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Featured researches published by F. Gauthier.


Journal of Pediatric Surgery | 1989

H-type shunt with an autologous venous graft for treatment of portal hypertension in children.

F. Gauthier; O. De Dreuzy; J. Valayer; Ph. Montupet

From 1981 to 1987, 86 children aged 16 months to 16 years underwent a portosystemic shunt procedure using an autologous venous graft (internal jugular vein in 80 cases). Fifty-five mesocaval, 20 splenorenal, 4 portacaval, and 7 makeshift shunts were constructed. The indication for shunting was an extrahepatic portal obstruction in 59 cases, intrahepatic portal obstruction in 23 cases (including 6 cases of congenital hepatic fibrosis), and Budd-Chiari syndrome in 4 cases. One patient of the latter group died early from intractable ascites with a nonfunctioning shunt, and a second child died 2 months after operation from unknown reasons with a patent shunt. With a follow-up over 1 year for 58 of the 84 survivors, 78 successes and 6 failures were recorded according to the clinical outcome and the findings of ultrasonic and endoscopic examinations. Three of the six children with a failed shunt have been submitted to a second successful H-type shunt operation. No case of encephalopathy was recorded in this series. Thus, with an approximate success rate of 95%, the H-type shunt with a venous graft should be recommended for treatment of portal hypertension of extrahepatic origin, especially in young children.


Journal of Pediatric Surgery | 1995

Liver retransplantation in children

H Hamada; J. Valayer; F. Gauthier; Thierry Yandza; H Takahashi

Between January 1988 and December 1993, 132 children received 154 orthotopic liver transplantation (OLT) at Bicêtre Hospital (France). Among them, 18 children underwent two and 2 children underwent three transplants (retransplant rate; 15.2%). Retransplantations were classified into three groups according to the interval between both OLTs: 1 (< 7 days, n = 8), 2 (8 days to 6 months, n = 10) and 3 (> 6 months, n = 4). Each group was compared with a control group whose grafts survived more than 1 week. There were no significant differences regarding age (35 +/- 49, 23 +/- 13, and 33 +/- 15 versus 49 +/- 41 months), cold ischemic time (566 +/- 105, 470 +/- 144, and 476 +/- 58 versus 455 +/- 110 minutes) and reduced size graft ratio (62.5%, 60%, and 75%, versus 58.3%). The causes of graft failure included primary nonfunctioning liver (PNF, n = 8) all in group 1 cases, biliary complications associated with hepatic artery thrombosis (HAT, n = 10; group 2, 6; group 3, 4), chronic rejection (n = 3; group 2, 1; group 3, 2) and three others (uncontrollable acute rejection, fulminant hepatitis, and secondary dysfunction, all in the group 2). The authors were unable to detect the cause of PNF. The overall survival rate after retransplantation was 62.5%, 60.0% and 75%, respectively. To reduce the rate of retransplants and improve the prognosis after OLT, further investigation into the cause of PNF, refinements in the anastomotic technique of the hepatic artery, and also early treatment of HAT are some of the goals to be achieved.


Pediatric Surgery International | 1992

Embolization of traumatic hemobilia in a child

P. de Lagausie; D. Pariente; F. Gauthier; O. de Dreuzy; J. Valayer

The management of a case of hemobilia in a child after abdominal trauma is described. Two intrahepatic false aneurysms and an arterioportal fistula in the right lobe of the liver were diagnosed by ultrasound and Doppler and successfully embolized during the diagnostic angiogram. Selective angiographic embolization may save the patient an operative procedure and appears to be an acceptable method for primary treatment of this condition in children.


Liver Transplantation | 1997

Portal vein complications after liver transplantation for biliary atresia.

C Chardot; J M Herrera; Dominique Debray; S. Branchereau; O De Dreuzy; Denis Devictor; B Dartayet; P Norwood; T. Lambert; D. Pariente; F. Gauthier; J. Valayer


European Journal of Pediatric Surgery | 1996

Spontaneous perforation of the biliary tract in infancy : A series of 11 cases

C Chardot; F. Iskandarani; O. De Dreuzy; B. Duquesne; D. Pariente; Olivier Bernard; F. Gauthier; J. Valayer


European Journal of Pediatric Surgery | 1999

Paediatric liver transplantation with a split graft : Experience at Bicêtre

C Chardot; S. Branchereau; O. De Dreuzy; C. Dubuisson; C. Le Pommelet; J. Waguet; G. Vellutini; F. Gauthier; J. Valayer


Pediatric transplantation. International congress | 1994

Pediatric liver transplantation: effect of the site of arterial inflow on the incidence of hepatic artery thrombosis according to recipient weight.

T. Yandza; H. Hamada; F. Gauthier; D. Pariente; A. Lababidi; O. De Dreuzy; J. Valayer


Society for Organ Sharing. International Congress | 1993

Biliary atresia : results of long-term conservative treatment and of liver transplantation

J. Valayer; F. Gauthier; T. Yandza; A. Lababidi; O. De Dreuzy; H. Hamada


Annales De Pediatrie | 1990

De la nécessité du diagnostic précoce des cholestases chirurgicales du nourrisson.

F. Gauthier; Laurent J; Pariente D; J. Valayer


Archives De Pediatrie | 1996

Role of the surgeon in the treatment of neuroblastoma in children

F. Gauthier; C Chardot; Sophie Branchereau

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D. Pariente

University of Paris-Sud

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O. de Dreuzy

University of Paris-Sud

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