Literature DB >> 9027956

Use of bioartificial and artificial liver support devices.

R D Hughes1, R Williams.   

Abstract

With all the new work and current interest in extracorporeal liver support systems incorporating hepatocytes, the findings with earlier artificial systems need to be reconsidered, particularly as they may constitute a component of some bioartificial devices. Furthermore, new and more effective artificial systems are currently under development. Essential hepatic functions need to be replaced, including excretory (the capability of adsorbents and dialysis) and synthetic and biotransformatory function, but the relative importance of these three functions in terms of promoting recovery of the native liver is as yet unclear. Two bioartificial devices have already been used clinically in the treatment of acute liver failure (ALF): the bioartificial liver (BAL) based on pig hepatocytes attached to microcarriers, and the extracorporeal liver assist device (ELAD) which contains a human liver-derived tumor cell line. As with earlier completely artificial systems, the results so far obtained in man are less impressive than in animal models of ALF. An important question not yet answered relates to quantity of cells and specific function in the new hybrid bioreactor devices required for clinical benefit, as well as the duration of support needed. A better understanding of the effects of these devices on the metabolic function of the damaged liver and the recovery process will be essential in the further development and design of effective systems. Controlled clinical trials on a multicenter basis will be needed for proper evaluation of these new approaches to treatment of ALF. From our own initial experience, the design of these protocols and the selection of biochemical tests will be difficult.

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Year:  1996        PMID: 9027956     DOI: 10.1055/s-2007-1007256

Source DB:  PubMed          Journal:  Semin Liver Dis        ISSN: 0272-8087            Impact factor:   6.115


  6 in total

1.  Liver support in acute liver failure.

Authors:  Robin D Hughes
Journal:  Wien Klin Wochenschr       Date:  2003-09-15       Impact factor: 1.704

Review 2.  Artificial and bioartificial support systems for liver failure.

Authors:  J P Liu; L L Gluud; B Als-Nielsen; C Gluud
Journal:  Cochrane Database Syst Rev       Date:  2004

3.  Effect of extracorporeal bioartificial liver support system on fulminant hepatic failure rabbits.

Authors:  Ying-Jie Wang; Meng-Dong Li; Yu-Ming Wang; Guo-Zheng Chen; Guo-Dong Lu; Zao-Xia Tan
Journal:  World J Gastroenterol       Date:  2000-04       Impact factor: 5.742

4.  Experimental study of bioartificial liver with cultured human liver cells.

Authors:  Ying-Jie Wang; Meng-Dong Li; Yu-Ming Wang; Qing-He Nie; Guo-Zheng Chen
Journal:  World J Gastroenterol       Date:  1999-04       Impact factor: 5.742

5.  Analysis of substrate specificity of pig CYP2B22 and CYP2C49 towards herbicides by transgenic rice plants.

Authors:  Hiroyuki Kawahigashi; Sakiko Hirose; Kenjirou Ozawa; Yoshiko Ido; Misaki Kojima; Hideo Ohkawa; Yasunobu Ohkawa
Journal:  Transgenic Res       Date:  2005-12       Impact factor: 2.788

6.  Successful treatment of refractory cerebral oedema in ecstasy/cocaine-induced fulminant hepatic failure using a new high-efficacy liver detoxification device (FPSA-Prometheus).

Authors:  Ludwig Kramer; Edith Bauer; Peter Schenk; Rudolf Steininger; Marion Vigl; Reinhold Mallek
Journal:  Wien Klin Wochenschr       Date:  2003-09-15       Impact factor: 1.704

  6 in total

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