Liver insufficiency is a dramatic syndrome, with multiple organ involvement. A multiplicity of toxic substances (hydrophilic like ammonia and lipophylic like bilirubin or bile acids or mercaptans) are released into the systemic circulation, thus altering many enzymatic cellular processes. The patient’s death while on the transplantation waiting list is frequent, because of organ scarcity. Systems to support liver function may be useful to avoid further complications due to the typical toxic state, “bridging” the patients to the transplantation, or, in the event of an acute decompensation of a chronic liver disease, sustain liver function long enough to permit organ’s regeneration and functional recovery. An ideal liver support system should substitute the main functions of the liver (detoxification, synthesis and regulation). Extracorporeal systems now available may be totally artificial or bio-artificial. While the first are only able to perform detoxification, the second may add the functions of synthesis (plasma proteins, coagulation factors …) and regulation (neurotransmitters). Bioartificial liver working with isolated hepatocytes and a synthetic membrane in an extracorporeal system, are however still far from being ready for clinical use. At present, liver insufficiency may be treated with an extracorporeal support technology aimed either to detoxification alone or to a real purification. Charcoal hemoperfusion or exchange/absorption resins may be used for blood detoxification. Blood or plasma-exchange, from a theoretical point of view, could be suited for a polyvalent intoxication, as liver failure is; however, the multi-compartmental distribution of some solutes largely endangers the efficacy of these procedures. Selective plasmapheresis techniques are now available for some solutes (e.g. styrene for bilirubin) and may progressively reduce the plasma levels and presumably the deposits of the solute. Novel treatments introduced to improve detoxification, mainly of the protein-bound substances, are the molecular adsorbent recirculation system system (MARS) and Prometheus systems. MARS performs an albumin dialysis, where albumin is the exogenous carrier for the toxic substances, and different experiences have proved its efficacy mainly in the treatment of hepatic encephalopathy, while data on survival are still limited to small case series. With Prometheus, the most recent system developed for a wide detoxification, albumin-bound toxins are directly removed in two separate cartridges with different solute affinity, without the need for exogenous albumin; plasmadsorption is then coupled with a real dialysis process. After initial, promising results, the efficacy of Prometheus in the patients hard end-points will be evaluated in a large international trial. On the whole, liver support systems may offer, in many cases, a survival benefit. Stem cells are however, even in this filed, the real, great hope for the future of patients with end-stage liver disease.

Liver Support Systems / Santoro A.; Mancini E.; Ferramosca E.; Faenza S.. - STAMPA. - (2007), pp. 396-404.

Liver Support Systems

SANTORO, ANTONIO;FAENZA, STEFANO
2007

Abstract

Liver insufficiency is a dramatic syndrome, with multiple organ involvement. A multiplicity of toxic substances (hydrophilic like ammonia and lipophylic like bilirubin or bile acids or mercaptans) are released into the systemic circulation, thus altering many enzymatic cellular processes. The patient’s death while on the transplantation waiting list is frequent, because of organ scarcity. Systems to support liver function may be useful to avoid further complications due to the typical toxic state, “bridging” the patients to the transplantation, or, in the event of an acute decompensation of a chronic liver disease, sustain liver function long enough to permit organ’s regeneration and functional recovery. An ideal liver support system should substitute the main functions of the liver (detoxification, synthesis and regulation). Extracorporeal systems now available may be totally artificial or bio-artificial. While the first are only able to perform detoxification, the second may add the functions of synthesis (plasma proteins, coagulation factors …) and regulation (neurotransmitters). Bioartificial liver working with isolated hepatocytes and a synthetic membrane in an extracorporeal system, are however still far from being ready for clinical use. At present, liver insufficiency may be treated with an extracorporeal support technology aimed either to detoxification alone or to a real purification. Charcoal hemoperfusion or exchange/absorption resins may be used for blood detoxification. Blood or plasma-exchange, from a theoretical point of view, could be suited for a polyvalent intoxication, as liver failure is; however, the multi-compartmental distribution of some solutes largely endangers the efficacy of these procedures. Selective plasmapheresis techniques are now available for some solutes (e.g. styrene for bilirubin) and may progressively reduce the plasma levels and presumably the deposits of the solute. Novel treatments introduced to improve detoxification, mainly of the protein-bound substances, are the molecular adsorbent recirculation system system (MARS) and Prometheus systems. MARS performs an albumin dialysis, where albumin is the exogenous carrier for the toxic substances, and different experiences have proved its efficacy mainly in the treatment of hepatic encephalopathy, while data on survival are still limited to small case series. With Prometheus, the most recent system developed for a wide detoxification, albumin-bound toxins are directly removed in two separate cartridges with different solute affinity, without the need for exogenous albumin; plasmadsorption is then coupled with a real dialysis process. After initial, promising results, the efficacy of Prometheus in the patients hard end-points will be evaluated in a large international trial. On the whole, liver support systems may offer, in many cases, a survival benefit. Stem cells are however, even in this filed, the real, great hope for the future of patients with end-stage liver disease.
2007
Acute Kidney Injury
396
404
Liver Support Systems / Santoro A.; Mancini E.; Ferramosca E.; Faenza S.. - STAMPA. - (2007), pp. 396-404.
Santoro A.; Mancini E.; Ferramosca E.; Faenza S.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/130250
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