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Evaluation of the Hepa Wash(®) treatment in pigs with acute liver failure

BACKGROUND: Mortality of patients with acute liver failure (ALF) is still unacceptably high. Available liver support systems are still of limited success at improving survival. A new type of albumin dialysis, the Hepa Wash(®) system, was newly introduced. We evaluated the new liver support system as...

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Autores principales: Al-Chalabi, Ahmed, Matevossian, Edouard, v Thaden, Anne-K, Luppa, Peter, Neiss, Albrecht, Schuster, Tibor, Yang, Zejian, Schreiber, Catherine, Schimmel, Patrick, Nairz, Ewald, Perren, Aurel, Radermacher, Peter, Huber, Wolfgang, Schmid, Roland M, Kreymann, Bernhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659067/
https://www.ncbi.nlm.nih.gov/pubmed/23668774
http://dx.doi.org/10.1186/1471-230X-13-83
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author Al-Chalabi, Ahmed
Matevossian, Edouard
v Thaden, Anne-K
Luppa, Peter
Neiss, Albrecht
Schuster, Tibor
Yang, Zejian
Schreiber, Catherine
Schimmel, Patrick
Nairz, Ewald
Perren, Aurel
Radermacher, Peter
Huber, Wolfgang
Schmid, Roland M
Kreymann, Bernhard
author_facet Al-Chalabi, Ahmed
Matevossian, Edouard
v Thaden, Anne-K
Luppa, Peter
Neiss, Albrecht
Schuster, Tibor
Yang, Zejian
Schreiber, Catherine
Schimmel, Patrick
Nairz, Ewald
Perren, Aurel
Radermacher, Peter
Huber, Wolfgang
Schmid, Roland M
Kreymann, Bernhard
author_sort Al-Chalabi, Ahmed
collection PubMed
description BACKGROUND: Mortality of patients with acute liver failure (ALF) is still unacceptably high. Available liver support systems are still of limited success at improving survival. A new type of albumin dialysis, the Hepa Wash(®) system, was newly introduced. We evaluated the new liver support system as well as the Molecular Adsorbent Recycling System (MARS) in an ischemic porcine model of ALF. METHODS: In the first study animals were randomly allocated to control (n=5) and Hepa Wash (n=6) groups. In a further pilot study, two animals were treated with the MARS-system. All animals received the same medical and surgical procedures. An intraparenchymal intracranial pressure was inserted. Hemodynamic monitoring and goal-directed fluid therapy using the PiCCO system was done. Animals underwent functional end-to-side portacaval shunt and ligation of hepatic arteries. Treatment with albumin dialysis was started after fall of cerebral perfusion pressure to 45 mmHg and continued for 8 h. RESULTS: All animals in the Hepa Wash group survived the 13-hour observation period, except for one that died after stopping treatment. Four of the control animals died within this period (p=0.03). Hepa Wash significantly reduced impairment of cerebral perfusion pressure (23±2 vs. 10±3 mmHg, p=0.006) and mean arterial pressure (37±1 vs. 24±2 mmHg, p=0.006) but had no effect on intracranial pressure (14±1 vs. 15±1 mmHg, p=0.72). Hepa Wash also enhanced cardiac index (4.94±0.32 vs. 3.36±0.25 l/min/m2, p=0.006) and renal function (urine production, 1850 ± 570 vs. 420 ± 180 ml, p=0.045) and eliminated water soluble (creatinine, 1.3±0.2 vs. 3.2±0.3 mg/dl, p=0.01; ammonia 562±124 vs. 1382±92 μg/dl, p=0.006) and protein-bound toxins (nitrate/nitrite 5.54±1.57 vs. 49.82±13.27 μmol/l, p=0.01). No adverse events that could be attributed to the Hepa Wash treatment were observed. CONCLUSIONS: Hepa Wash was a safe procedure and improved multiorgan system failure in pigs with ALF. The survival benefit could be the result of ameliorating different organ functions in association with the detoxification capacity of water soluble and protein-bound toxins.
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spelling pubmed-36590672013-05-21 Evaluation of the Hepa Wash(®) treatment in pigs with acute liver failure Al-Chalabi, Ahmed Matevossian, Edouard v Thaden, Anne-K Luppa, Peter Neiss, Albrecht Schuster, Tibor Yang, Zejian Schreiber, Catherine Schimmel, Patrick Nairz, Ewald Perren, Aurel Radermacher, Peter Huber, Wolfgang Schmid, Roland M Kreymann, Bernhard BMC Gastroenterol Research Article BACKGROUND: Mortality of patients with acute liver failure (ALF) is still unacceptably high. Available liver support systems are still of limited success at improving survival. A new type of albumin dialysis, the Hepa Wash(®) system, was newly introduced. We evaluated the new liver support system as well as the Molecular Adsorbent Recycling System (MARS) in an ischemic porcine model of ALF. METHODS: In the first study animals were randomly allocated to control (n=5) and Hepa Wash (n=6) groups. In a further pilot study, two animals were treated with the MARS-system. All animals received the same medical and surgical procedures. An intraparenchymal intracranial pressure was inserted. Hemodynamic monitoring and goal-directed fluid therapy using the PiCCO system was done. Animals underwent functional end-to-side portacaval shunt and ligation of hepatic arteries. Treatment with albumin dialysis was started after fall of cerebral perfusion pressure to 45 mmHg and continued for 8 h. RESULTS: All animals in the Hepa Wash group survived the 13-hour observation period, except for one that died after stopping treatment. Four of the control animals died within this period (p=0.03). Hepa Wash significantly reduced impairment of cerebral perfusion pressure (23±2 vs. 10±3 mmHg, p=0.006) and mean arterial pressure (37±1 vs. 24±2 mmHg, p=0.006) but had no effect on intracranial pressure (14±1 vs. 15±1 mmHg, p=0.72). Hepa Wash also enhanced cardiac index (4.94±0.32 vs. 3.36±0.25 l/min/m2, p=0.006) and renal function (urine production, 1850 ± 570 vs. 420 ± 180 ml, p=0.045) and eliminated water soluble (creatinine, 1.3±0.2 vs. 3.2±0.3 mg/dl, p=0.01; ammonia 562±124 vs. 1382±92 μg/dl, p=0.006) and protein-bound toxins (nitrate/nitrite 5.54±1.57 vs. 49.82±13.27 μmol/l, p=0.01). No adverse events that could be attributed to the Hepa Wash treatment were observed. CONCLUSIONS: Hepa Wash was a safe procedure and improved multiorgan system failure in pigs with ALF. The survival benefit could be the result of ameliorating different organ functions in association with the detoxification capacity of water soluble and protein-bound toxins. BioMed Central 2013-05-13 /pmc/articles/PMC3659067/ /pubmed/23668774 http://dx.doi.org/10.1186/1471-230X-13-83 Text en Copyright © 2013 Al-Chalabi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Al-Chalabi, Ahmed
Matevossian, Edouard
v Thaden, Anne-K
Luppa, Peter
Neiss, Albrecht
Schuster, Tibor
Yang, Zejian
Schreiber, Catherine
Schimmel, Patrick
Nairz, Ewald
Perren, Aurel
Radermacher, Peter
Huber, Wolfgang
Schmid, Roland M
Kreymann, Bernhard
Evaluation of the Hepa Wash(®) treatment in pigs with acute liver failure
title Evaluation of the Hepa Wash(®) treatment in pigs with acute liver failure
title_full Evaluation of the Hepa Wash(®) treatment in pigs with acute liver failure
title_fullStr Evaluation of the Hepa Wash(®) treatment in pigs with acute liver failure
title_full_unstemmed Evaluation of the Hepa Wash(®) treatment in pigs with acute liver failure
title_short Evaluation of the Hepa Wash(®) treatment in pigs with acute liver failure
title_sort evaluation of the hepa wash(®) treatment in pigs with acute liver failure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659067/
https://www.ncbi.nlm.nih.gov/pubmed/23668774
http://dx.doi.org/10.1186/1471-230X-13-83
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