𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Eighteen years of liver transplantation experience in patients with advanced Budd-Chiari syndrome

✍ Scribed by Frank Ulrich; Johann Pratschke; Ulf Neumann; Andreas Pascher; Gero Puhl; Peter Fellmer; Sascha Weiss; Sven Jonas; Peter Neuhaus


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
217 KB
Volume
14
Category
Article
ISSN
1527-6465

No coin nor oath required. For personal study only.

✦ Synopsis


The long-term results of liver transplantation for Budd-Chiari syndrome (BCS) and timely indication for the procedure are still under debate. Innovations in interventional therapy and better understanding of underlying diseases have improved therapy strategies. The aim of this study was the analysis of patient and disease characteristics, outcome, and specific complications. Between September 1988 and December 2006 we performed 42 orthotopic liver transplantations (OLTs) in 39 patients with BCS. A total of 29 (74%) women and 10 men (26%) had a median age of 35 years; the median follow-up period was 96 months. Etiologically, 27 patients had a preoperative diagnosis of hematologic disease, including myeloproliferative disorders (MPD), followed by factor V Leiden mutation and antiphospholipid syndrome. The actuarial 5-year and 10-year survival rates were 89.4% and 83.5%, respectively, compared to 80.7% and 71.4%, respectively, for other indications (n Ο­ 1742). Retransplantation was necessary in 3 patients (7.1%) with portal vein thrombosis or recurrent BCS. Although the number of bleeding events was similar, incidence of vascular complications was significantly higher in patients with BCS. Thrombosis of the portal vein was observed in 4.8% versus 0.8% of the patients, whereas liver veins were affected in 7.1% versus 0.2%. Our data shows that severe acute or chronic forms of BCS with liver failure can be successfully treated by OLT. Despite higher rates of vascular complications, patient and graft survival are similar or even better compared to other indication groups. In conclusion, patients with reversible hepatic damage should be treated by combined strategies, including medical therapy and surgical or interventional shunting.


πŸ“œ SIMILAR VOLUMES


Twenty years of liver transplantation fo
✍ Dorry L. Segev; Geoffrey C. Nguyen; Jayme E. Locke; Christopher E. Simpkins; Rob πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 312 KB πŸ‘ 1 views

Several treatment options exist for the management of Budd-Chiari syndrome (BCS), yet the relative role and timing of liver transplantation (LT) remain poorly defined. Small case series published to date have not been able to delineate the impact of comorbidities and thromboembolic complications of

Timing of liver transplantation followin
✍ James D. Perkins πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 86 KB

The authors correctly caution that their prognostic score must be externally validated before use in a clinical setting. Hopefully, with further studies and validation, a recommendation can be made on which patients with BCS should proceed beyond TIPS in a timely manner to liver transplantation.

Successful liver transplantation for Bud
✍ Andrew L. Singer; Jamye E. Locke; Zoe A. Stewart; Bonnie E. Lonze; James P. Hami πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 173 KB

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired hemolytic anemia caused by somatic mutations in the phosphatidylinositol glycan-complementation class A gene and the resulting absence of a key complement regulatory protein, CD59. Affected red blood cells in patients with PNH undergo int

Determinants of survival and the effect
✍ Sarwa Darwish Murad; Dominique-Charles Valla; Piet C. de Groen; Guy Zeitoun; Jud πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 134 KB

Budd-Chiari syndrome (BCS) is a rare disorder that is characterized by hepatic venous outflow obstruction. The aim of this study was to assess determinants of survival and to evaluate the effect of portosystemic shunting. In this international multicenter study, 237 patients with BCS, diagnosed betw

Use of thromboelastography PlateletMappi
✍ Katherine James; Elisa Bertoja; James O'Beirne; Susan Mallett πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 311 KB

Budd-Chiari syndrome (BCS) is the end result of a number of disease states resulting in hepatic venous outflow obstruction. We report a Janus kinase 2-homozygous patient with BCS who thrombosed a transjugular intrahepatic portosystemic shunt (TIPS) despite treatment with warfarin (international norm