Literature DB >> 20209594

Long-term outcome of patients with hereditary hemorrhagic telangiectasia and severe hepatic involvement after orthotopic liver transplantation: a single-center study.

Sophie Dupuis-Girod1, Anne-Laure Chesnais, Isabelle Ginon, Jérôme Dumortier, Jean-Christophe Saurin, Gérard Finet, Evelyne Decullier, Denis Marion, Henri Plauchu, Olivier Boillot.   

Abstract

Hepatic involvement occurs in up to 74% of patients with hereditary hemorrhagic telangiectasia (HHT) and is characterized by a spectrum of arteriovenous malformations. Three different types of intrahepatic shunting may be present: hepatic artery to hepatic veins, hepatic artery to portal vein, and portal vein to hepatic vein. Hepatic involvement in HHT may lead to biliary ischemia, portal hypertension, or high-output cardiac failure (HOCF). Orthotopic liver transplantation (OLT) has been proposed as the only definitive curative treatment. The aim of this study was to evaluate the long-term outcome of patients with hepatic involvement due to HHT after OLT with respect to mortality, cardiac and hepatic status, epistaxis, and quality of life. Patients with HHT and severe hepatic vascular malformations who underwent OLT in the Lyon Liver Transplant Unit (LLTU) from 1993 to 2007 were followed at the LLTU and the French Reference Center for HHT. Quality of life was evaluated with the Short Form 36 questionnaire. There were 13 patients who fulfilled the entry criteria of the study (12 women and 1 man). The mean age at the time of OLT was 51.8 years (range = 33-65 years). Indications for OLT were cardiac failure (n = 9), biliary necrosis (n = 2), both cardiac failure and biliary necrosis (n = 1), and hemobilia (n = 1). The mean duration of follow-up was 109 months (range = 1-200 months). Twelve patients (92.3%) are still alive. For the 9 patients with HOCF, the mean cardiac index decreased from 5.4 L/minute/m(2) before OLT to 3.0 L/minute/m(2) after OLT. No severe hepatic complications were observed after OLT. Nine of the surviving patients (75%) experienced dramatic improvements in epistaxis and quality of life, including an ability to undertake more physical activity. In conclusion, OLT is an important therapeutic option for patients with HHT who have severe hepatic involvement. In the reported cohort, the mortality after OLT for this indication was low.

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Year:  2010        PMID: 20209594     DOI: 10.1002/lt.21990

Source DB:  PubMed          Journal:  Liver Transpl        ISSN: 1527-6465            Impact factor:   5.799


  18 in total

Review 1.  Differential diagnosis of hepatopulmonary syndrome (HPS): Portopulmonary hypertension (PPH) and hereditary hemorrhagic telangiectasia (HHT).

Authors:  Inna Krynytska; Mariya Marushchak; Anna Mikolenko; Anzhela Bob; Iryna Smachylo; Ludmyla Radetska; Olga Sopel
Journal:  Bosn J Basic Med Sci       Date:  2017-11-20       Impact factor: 3.363

2.  The Subjective Experience of Patients Diagnosed with Hereditary Hemorrhagic Telangiectasia: a Qualitative Study.

Authors:  Laura Geerts; Carole Fantini-Hauwel; Elodie Brugallé; Odile Boute; Frédéric Frénois; Lydie Defrance; Sylvie Manouvrier-Hanu; Florence Petit; Pascal Antoine
Journal:  J Genet Couns       Date:  2016-10-28       Impact factor: 2.537

Review 3.  Cardiac and Hemodynamic Manifestations of Hereditary Hemorrhagic Telangiectasia.

Authors:  Ahmed Farhan; Muhammad A Latif; Anum Minhas; Clifford R Weiss
Journal:  Int J Angiol       Date:  2022-07-09

4.  Natural history and outcome of hepatic vascular malformations in a large cohort of patients with hereditary hemorrhagic teleangiectasia.

Authors:  Elisabetta Buscarini; Gioacchino Leandro; Dario Conte; Cesare Danesino; Erica Daina; Guido Manfredi; Guido Lupinacci; Gianfranco Brambilla; Fernanda Menozzi; Federico De Grazia; Pietro Gazzaniga; Giuseppe Inama; Roberto Bonardi; Pasquale Blotta; Pierangelo Forner; Carla Olivieri; Annalisa Perna; Maurizio Grosso; Giacomo Pongiglione; Edoardo Boccardi; Fabio Pagella; Giorgio Rossi; Alessandro Zambelli
Journal:  Dig Dis Sci       Date:  2011-02-03       Impact factor: 3.199

5.  Raloxifene and Bevacizumab for severe complications of hereditary haemorrhagic telangiectasia in a haemodialysis patient.

Authors:  Enrique Morales; Rafael Morales; Eduardo Gutiérrez; Jorge Rojas-Rivera; Manuel Praga
Journal:  Clin Kidney J       Date:  2012-12

6.  Hereditary Hemorrhagic Telangiectasia with Hepatic Vascular Malformations.

Authors:  Yujiro Nishioka; Nobuhisa Akamatsu; Yasuhiko Sugawara; Junichi Kaneko; Junichi Arita; Yoshihiro Sakamoto; Kiyoshi Hasegawa; Norihiro Kokudo
Journal:  Case Rep Med       Date:  2015-05-21

Review 7.  Optimal management of hereditary hemorrhagic telangiectasia.

Authors:  Neetika Garg; Monica Khunger; Arjun Gupta; Nilay Kumar
Journal:  J Blood Med       Date:  2014-10-15

8.  Embolisation of PAVMs reported to improve nosebleeds by a subgroup of patients with hereditary haemorrhagic telangiectasia.

Authors:  Claire L Shovlin; Trishan Patel; James E Jackson
Journal:  ERJ Open Res       Date:  2016-04-29

9.  Complications and clinical outcome of hepatic artery embolisation in patients with hereditary haemorrhagic telangiectasia.

Authors:  Ajay Chavan; Lars Luthe; Michael Gebel; Hannelore Barg-Hock; Hans Seifert; Rudolph Raab; Timm Kirchhoff; B Schmuck
Journal:  Eur Radiol       Date:  2012-10-31       Impact factor: 5.315

10.  Circulatory contributors to the phenotype in hereditary hemorrhagic telangiectasia.

Authors:  Claire L Shovlin
Journal:  Front Genet       Date:  2015-04-09       Impact factor: 4.599

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