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Updated: Jun 13, 2026

Heterotopic Auxiliary Rat Liver Transplantation With Flow-regulated Portal Vein Arterialization in Acute Hepatic Failure
Published on: September 13, 2014
[Artificial liver support. Literature review]
Sarah Lafuente1, M Jesús Bertran, Angeles Escorsell
1Unitat d'Avaluació, Suport i Prevenció (UASP), Servei de Medicina Preventiva i Epidemiologia, Hospital Clínic de Barcelona, Institut d'Investigacions Biomédiques Agustí PÍ i Sunyer (IDIBAPS), Barcelona, España. slafuent@clinic.ub.es
Extracorporeal albumin dialysis systems effectively reduce toxic substances in liver failure patients. While showing clinical benefits, further research is needed to confirm survival advantages and safety profiles.
Area of Science:
- Hepatology and Nephrology
- Artificial Organ Support Systems
Background:
- Liver failure leads to the accumulation of toxic substances, necessitating advanced treatment modalities.
- Current treatments for liver failure have limitations, driving the need for innovative supportive therapies.
Purpose of the Study:
- To systematically review the efficacy and safety of extracorporeal albumin dialysis (EAD) systems in patients with liver failure.
- To evaluate specific EAD systems, including Molecular Adsorbent Recirculation System (MARS), Prometheus, and Biologic-DT.
Main Methods:
- Systematic review of controlled trials.
- Screening of 436 references to identify 10 relevant controlled trials.
- Analysis of interventions focusing on biochemical and clinical outcomes, and safety assessments.
Main Results:
- EAD systems demonstrated significant reduction in key toxic parameters such as bilirubin and creatinine.
- Some studies indicated clinical benefits, including improvements in hepatic encephalopathy and patient survival.
- Adverse events were reported in a limited number of studies, with coagulation disorders being the most frequent concern.
Conclusions:
- Albumin dialysis-based systems show promise in reducing toxic load and improving clinical outcomes in liver failure.
- Further rigorous studies are essential to comprehensively evaluate long-term survival benefits and standardize the reporting of adverse events.
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