Artificial and bioartificial liver devices: present and future

被引:143
作者
Carpentier, B. [1 ]
Gautier, A. [1 ]
Legallais, C. [1 ]
机构
[1] Univ Technol Compiegne, CNRS, UMR Biomech & Bioengn 6600, F-60205 Compiegne, France
关键词
ADSORBENT RECIRCULATING SYSTEM; EXTRACORPOREAL ALBUMIN DIALYSIS; ACUTE HEPATIC-FAILURE; SUPPORT-SYSTEM; ASSIST DEVICE; PHASE-I; CLINICAL-EXPERIENCE; BLOOD PURIFICATION; CONTROLLED-TRIAL; MARS;
D O I
10.1136/gut.2008.175380
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Liver failure is associated with high morbidity and mortality without transplantation. There are two types of device for temporary support: artificial and bioartificial livers. Artificial livers essentially use non-living components to remove the toxins accumulated during liver failure. Bioartificial livers have bioreactors containing hepatocytes to provide both biotransformation and synthetic liver functions. We review here the operating principles, chemical effects, clinical effects and complications of both types, with specific attention paid to bioartificial systems. Several artificial support systems have FDA marketing authorisation or are CE labelled, but the improvement they provide in terms of patient clinical outcome has not yet been fully demonstrated. At present, different bioartifical systems are being investigated clinically on the basis of their promises and capacity to provide and replace most liver functions. However, important issues such as cost, cell availability, maintenance of cell viability and functionality throughout treatment, and regulatory issues, as well as difficult challenges, including implementing cell-housing devices at the patient's bedside on an emergency basis, have delayed their appearance in intensive care units and on the market. Bioreactors are, nevertheless, when combined with artificial components, a pragmatic approach for future treatment of liver failure.
引用
收藏
页码:1690 / 1702
页数:13
相关论文
共 68 条
[1]  
ABRAHAM RB, 2001, TRANSPL P, V33, P2897
[2]  
[Anonymous], 2003, NUTRIENT REQUIREMENT, V2nd, P1
[3]  
Ash S R, 1991, ASAIO Trans, V37, pM332
[4]  
ASH SR, 1992, INT J ARTIF ORGANS, V15, P151
[5]   Powdered sorbent liver dialysis and pheresis in treatment of hepatic failure [J].
Ash, SR .
THERAPEUTIC APHERESIS, 2001, 5 (05) :404-416
[6]   HEMODIABSORPTION IN TREATMENT OF ACUTE HEPATIC-FAILURE AND CHRONIC CIRRHOSIS WITH ASCITES [J].
ASH, SR .
ARTIFICIAL ORGANS, 1994, 18 (05) :355-362
[7]  
ASH SR, 2006, ASAIO J, V52, pA11
[8]   Predictive value of arterial ammonia for complications and outcome in acute liver failure [J].
Bhatia, V ;
Singh, R ;
Acharya, SK .
GUT, 2006, 55 (01) :98-104
[9]   Sorbent-based artificial liver devices: principles of operation, chemical effects and clinical results [J].
Carpentier, Benoit ;
Ash, Stephen R. .
EXPERT REVIEW OF MEDICAL DEVICES, 2007, 4 (06) :839-861
[10]   In vitro assessment of encapsulated C3A hepatocytes functions in a fluidized bed bioreactor [J].
David, B ;
Dufresne, M ;
Nagel, MD ;
Legallais, C .
BIOTECHNOLOGY PROGRESS, 2004, 20 (04) :1204-1212