Volume 8, Issue 8 pp. 701-707
Original Article
Free Access

Auxiliary liver transplantation for fulminant hepatitis B: Results from a series of six patients with special emphasis on regeneration and recurrence of hepatitis B

François Durand MD

Corresponding Author

François Durand MD

Service d'Hépatologie and INSERM U481, Hôpital Beaujon, Clichy, France

Service d'Hépatologie, Hôpital Beaujon, 100 Boulevard du Général Leclerc, 92110 Clichy, France. Telephone: (33) 14-087-5091; FAX: (33) 14-730-9440Search for more papers by this author
Jacques Belghiti

Jacques Belghiti

Service de Chirurgie Digestive, Hôpital Beaujon, Clichy, France

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Adriana Handra-Luca

Adriana Handra-Luca

Service d'Anatomie-Pathologique, Hôpital Beaujon, Clichy, France

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Claire Francoz

Claire Francoz

Service d'Hépatologie and INSERM U481, Hôpital Beaujon, Clichy, France

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Alain Sauvanet

Alain Sauvanet

Service de Chirurgie Digestive, Hôpital Beaujon, Clichy, France

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Patrick Marcellin

Patrick Marcellin

Service d'Hépatologie and INSERM U481, Hôpital Beaujon, Clichy, France

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Olivier Farges

Olivier Farges

Service de Chirurgie Digestive, Hôpital Beaujon, Clichy, France

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Jacques Bernuau

Jacques Bernuau

Service d'Hépatologie and INSERM U481, Hôpital Beaujon, Clichy, France

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Dominique Valla

Dominique Valla

Service d'Hépatologie and INSERM U481, Hôpital Beaujon, Clichy, France

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First published: 30 December 2003
Citations: 32

Abstract

Emergency liver transplantation is the treatment of choice for the most severe forms of fulminant hepatitis B. Auxiliary liver transplantation is an attractive alternative, offering the possibility of regeneration and discontinuation of immunosuppression. However, the use of auxiliary transplantation for fulminant hepatitis B is controversial because the remnant part of the native liver could be the source of recurrence of HBV infection. We report the results of auxiliary liver transplantation in six patients with fulminant hepatitis B. Postoperatively, all patients received gancyclovir and anti-hepatitis B surface immune globulins. Graft function has been satisfactory in all cases and all patients had rapid neurologic improvement. One patient died with a functional graft because of disseminated aspergillosis on postoperative day 17. The remaining 5 patients are currently alive. The 4 patients with more than 1-year follow-up had complete regeneration of the native liver and are free of immunosuppression. None of these patients had recurrence of hepatitis B. These results suggest that the use of an auxiliary graft is a safe alternative in selected patients with fulminant hepatitis B. Regeneration of the native liver, even if slow, seems to occur in most cases, allowing discontinuation of immunosuppression, which is a major advantage over conventional transplantation. Finally, the remnant part of the native liver does not compromise immunization against HBV.

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