Extracorporal liver support with molecular adsorbents recirculating system in patients with hepatitis B-associated fulminant hepatic failure

被引:13
作者
Tsai, MH
Chen, YC
Wu, CS
Ho, YP
Fang, JT
Lien, JM
Yang, C
Chu, YY
Liu, NJ
Lin, CH
Chiu, CT
Chen, PC
机构
[1] Chang Gung Mem Hosp, Div Gastroenterol, Taipei 10591, Taiwan
[2] Chang Gung Mem Hosp, Div Crit Care Nephrol, Taipei 10591, Taiwan
[3] Chang Gung Mem Hosp, Div Gastroenterol, Chiayi, Taiwan
关键词
MARS; HBV; fulminant hepatic failure;
D O I
10.1111/j.1742-1241.2005.00604.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hepatitis B virus (HBV) infection is the most prevalent cause of fulminant hepatic failure (FHF) in the Far East. HBV-associated FHF is characterised by rapidly progressive end organ dysfunction/failure and a very poor prognosis. To investigate how molecular adsorbent recirculating system (MARS) treatment impacts multiple organ system function in HBV-associated FHF. Ten consecutive patients were treated with MARS in a period of 12 months. Clinical, biochemical and haemodynamic parameters were assessed before and after MARS. Various disease severity scoring systems including model for end-stage liver disease, APACHE II, APACHE III, sequential organ failure assessment and organ system failure scores were also assessed. There were significant improvements in hepatic encephalopathy grading (p < 0.001), mean arterial pressure (p < 0.001), plasma renin activity (p = 0.027), bilirubin (p < 0.001), ammonia (p = 0.001) and creatinine levels (p < 0.001). There were also significant improvements in all the scoring systems evaluated. Meanwhile, platelet count was significantly decreased (p < 0.001). One patient was successfully bridged to liver transplantation. Three patients were alive at 3 months of follow-up. MARS can improve multiple organ functions in HBV-associated FHF. On the basis of these findings, randomised controlled studies are indicated and justified.
引用
收藏
页码:1289 / 1294
页数:6
相关论文
共 31 条
[1]   The importance of proteins in defense against oxidation [J].
Bourdon, E ;
Blache, D .
ANTIOXIDANTS & REDOX SIGNALING, 2001, 3 (02) :293-311
[2]   Renal failure after upper gastrointestinal bleeding in cirrhosis:: Incidence, clinical course, predictive factors, and short-term prognosis [J].
Cárdenas, A ;
Ginès, P ;
Uriz, J ;
Bessa, X ;
Salmerón, JM ;
Mas, A ;
Ortega, R ;
Calahorra, B ;
De las Heras, D ;
Bosch, J ;
Arroyo, V ;
Rodes, J .
HEPATOLOGY, 2001, 34 (04) :671-676
[3]  
Cheng VCC, 2003, SEMIN LIVER DIS, V23, P239
[4]   THE ROLE OF HEPATITIS-C VIRUS IN FULMINANT VIRAL-HEPATITIS IN AN AREA WITH ENDEMIC HEPATITIS-A AND HEPATITIS-B [J].
CHU, CM ;
SHEEN, IS ;
LIAW, YF .
GASTROENTEROLOGY, 1994, 107 (01) :189-195
[5]  
CONN HO, 1977, GASTROENTEROLOGY, V72, P573
[6]   Circulatory, respiratory, cerebral, and renal derangements in acute liver failure: Pathophysiology and management [J].
Ellis, A ;
Wendon, J .
SEMINARS IN LIVER DISEASE, 1996, 16 (04) :379-388
[7]  
FIORE LD, 2003, HEPATOLOGY TXB LIVER, P549
[8]   Application of Molecular Adsorbents Recirculating System to remove NO and cytokines in severe liver failure patients with multiple organ dysfunction syndrome [J].
Guo, LM ;
Liu, JY ;
Xu, DZ ;
Li, BS ;
Han, H ;
Wang, LH ;
Zhang, WY ;
Lu, LH ;
Guo, X ;
Sun, FX ;
Zhang, HY ;
Liu, XD ;
Zhang, JP ;
Yao, Y ;
He, ZP ;
Wang, MM .
LIVER INTERNATIONAL, 2003, 23 :16-20
[9]   The sympathetic nervous system in liver disease [J].
Henriksen, JH ;
Moller, S ;
Ring-Larsen, H ;
Christensen, NJ .
JOURNAL OF HEPATOLOGY, 1998, 29 (02) :328-341
[10]  
Henriksen JH, 1998, ITAL J GASTROENTEROL, V30, P320