Literature DB >> 19652186

Etiology, management, and outcome of the Budd-Chiari syndrome.

Sarwa Darwish Murad1, Aurelie Plessier, Manuel Hernandez-Guerra, Federica Fabris, Chundamannil E Eapen, Matthias J Bahr, Jonel Trebicka, Isabelle Morard, Luc Lasser, Joerg Heller, Antoine Hadengue, Philippe Langlet, Helena Miranda, Massimo Primignani, Elwyn Elias, Frank W Leebeek, Frits R Rosendaal, Juan-Carlos Garcia-Pagan, Dominique C Valla, Harry L A Janssen.   

Abstract

BACKGROUND: The Budd-Chiari syndrome (BCS) is hepatic venous outflow obstruction. What is known about the syndrome is based on small studies of prevalent cases.
OBJECTIVE: To characterize the causes and treatment of incident BCS.
DESIGN: Consecutive case series of patients with incident BCS, enrolled from October 2003 to October 2005 and followed until May 2006.
SETTING: Academic and nonacademic hospitals in France, Spain, Italy, Great Britain, Germany, Belgium, the Netherlands, Portugal, and Switzerland. PATIENTS: Persons older than 16 years with definite hepatic outflow obstruction diagnosed by imaging. Persons with hepatic outflow obstruction due to heart failure, sinusoidal obstruction syndrome, cancer, or liver transplantation were excluded. MEASUREMENTS: Signs and symptoms; laboratory and imaging findings; diagnosis; treatment; and overall, transplantation-free, and intervention-free survival.
RESULTS: 163 incident cases of BCS were identified. Median follow-up was 17 months (range, 0.1 to 31 months). Most patients (84%) had at least 1 thrombotic risk factor, and many (46%) had more than 1; the most common was myeloproliferative disorders (49% of 103 tested patients). Patients were mainly treated with anticoagulation (140 patients [86%]), transjugular intrahepatic portosystemic shunting (56 patients [34%]), or liver transplantation (20 patients [12%]), and 80 patients (49%) were managed noninvasively. Only 3 patients underwent surgical shunting. The survival rate was 87% (95% CI, 82% to 93%) at 1 year and 82% (CI, 75% to 88%) at 2 years. LIMITATION: Treatment was not standardized across all centers, and data on important clinical variables were missing for some patients.
CONCLUSION: Most patients with BCS have at least 1 thrombotic risk factor, and many have more than 1; myeloproliferative disorders are most common. One- and 2-year survival rates are good with contemporary management, which includes noninvasive therapies (anticoagulation and diuretics) and invasive techniques. Transjugular intrahepatic portosystemic shunting seems to have replaced surgical shunting as the most common invasive therapeutic procedure. PRIMARY FUNDING SOURCE: Fifth Framework Programme of the European Commission.

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Year:  2009        PMID: 19652186     DOI: 10.7326/0003-4819-151-3-200908040-00004

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  101 in total

1.  Treatment of Budd-Chiari syndrome with urokinase following predilation in patients with old inferior vena cava thrombosis.

Authors:  P-X Ding; Y-D Li; X-W Han; G Wu; S-F Shui; Y-L Wang
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Review 2.  Splanchnic vein thrombosis: clinical presentation, risk factors and treatment.

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3.  Budd-Chiari syndrome management: Lights and shadows.

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4.  Budd-Chiari syndrome revisited: 38 years' experience with surgical portal decompression.

Authors:  Marshall J Orloff; Jon I Isenberg; Henry O Wheeler; Pat O Daily; Barbara Girard
Journal:  J Gastrointest Surg       Date:  2011-11-08       Impact factor: 3.452

5.  Studies on Budd-chiari syndrome complicated with hepatocellular carcinoma: most patients without inferior vena cava obstruction.

Authors:  Xiaowei Dang; Luhao Li; Suxin Li; Yafei Wang; Hai Li; Shaokai Xu; Peiqin Xu
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6.  Antithrombotic therapy for VTE disease: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines.

Authors:  Clive Kearon; Elie A Akl; Anthony J Comerota; Paolo Prandoni; Henri Bounameaux; Samuel Z Goldhaber; Michael E Nelson; Philip S Wells; Michael K Gould; Francesco Dentali; Mark Crowther; Susan R Kahn
Journal:  Chest       Date:  2012-02       Impact factor: 9.410

7.  Aetiological factors of Budd-Chiari syndrome in Algeria.

Authors:  Nawel Afredj; Nawal Guessab; Abdelbasset Nani; Sid Ahmed Faraoun; Ibtissem Ouled Cheikh; Rafik Kerbouche; Djouhar Hannoun; Zine Charef Amir; Hayet Ait Kaci; Kamel Bentabak; Aurélie Plessier; Dominique-Charles Valla; Valerie Cazals-Hatem; Marie-Hélène Denninger; Tadjeddine Boucekkine; Nabil Debzi
Journal:  World J Hepatol       Date:  2015-04-28

8.  Treatment of Budd-Chiari syndrome with a focus on transjugular intrahepatic portosystemic shunt.

Authors:  Anders Bay Neumann; Stine Degn Andersen; Dennis Tønner Nielsen; Peter Holland-Fischer; Hendrik Vilstrup; Henning Grønbæk
Journal:  World J Hepatol       Date:  2013-01-27

9.  Thrombophilia differences in splanchnic vein thrombosis and lower extremity deep venous thrombosis in North America.

Authors:  Edyta Sutkowska; Robert D McBane; Alfonso J Tafur; Krzysztof Sutkowski; Diane E Grill; Joshua P Slusser; Waldemar E Wysokinski
Journal:  J Gastroenterol       Date:  2012-12-18       Impact factor: 7.527

10.  Endovascular stenting of the inferior vena cava in a patient with Budd-Chiari syndrome and main hepatic vein thrombosis: a case report.

Authors:  Young-In Yoon; Shin Hwang; Gi-Young Ko; Tae-Yong Ha; Gi-Won Song; Dong-Hwan Jung; Young-Sang Lee; Sung-Gyu Lee
Journal:  Korean J Hepatobiliary Pancreat Surg       Date:  2015-02-28
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