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Continuous molecular adsorbent recirculating system treatment in 69 patients listed for liver transplantation

Objective. The molecular adsorbent recirculating system (MARS) is used to purify blood from albumin-bound toxins in patients with liver failure. However, the application of MARS has not demonstrated improved survival in randomized clinical trials and the clinical utility has not been finally establi...

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Autores principales: Olin, Per, Hausken, John, Foss, Aksel, Karlsen, Tom Hemming, Melum, Espen, Haugaa, Håkon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa Healthcare 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673540/
https://www.ncbi.nlm.nih.gov/pubmed/25865318
http://dx.doi.org/10.3109/00365521.2015.1027262
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author Olin, Per
Hausken, John
Foss, Aksel
Karlsen, Tom Hemming
Melum, Espen
Haugaa, Håkon
author_facet Olin, Per
Hausken, John
Foss, Aksel
Karlsen, Tom Hemming
Melum, Espen
Haugaa, Håkon
author_sort Olin, Per
collection PubMed
description Objective. The molecular adsorbent recirculating system (MARS) is used to purify blood from albumin-bound toxins in patients with liver failure. However, the application of MARS has not demonstrated improved survival in randomized clinical trials and the clinical utility has not been finally established. In our department, the use of MARS is now restricted to the most critically ill patients with acute or acute on chronic liver failure. Material and methods. Since 2005, we have treated 69 patients (30 males/39 females with median age of 49 years ranging from 1 months to 70 years) listed for liver transplantation (LT) with MARS. Median model of end-stage liver disease score in patients older than 12 years of age (n = 56) was 33 (interquartile range 26–39). The flow rate was 35–40 mL/kg/h and treatment kits were changed every 8–12 h. The patients were treated for a median of 27 h (range 1–144 h). Results. Fifty-six patients (81%) were transplanted. Nine died before they could be transplanted, and four patients recovered without transplantation. Forty-six (82%) of the transplanted patients were alive 30 days after transplantation. Ammonium decreased modestly from a median of 148 to 124 µM (p = 0.03) during MARS treatment. We detected worsening of coagulopathy with significant decreases in platelet count and fibrinogen concentrations, and increase in International Normalized Ratio. Phosphate and magnesium decreased significantly during MARS treatment. Conclusion. Continuous MARS therapy may bridge liver failure patients to LT under close observation and treatment of coagulopathy and electrolyte disturbances.
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spelling pubmed-46735402015-12-15 Continuous molecular adsorbent recirculating system treatment in 69 patients listed for liver transplantation Olin, Per Hausken, John Foss, Aksel Karlsen, Tom Hemming Melum, Espen Haugaa, Håkon Scand J Gastroenterol Original Article Objective. The molecular adsorbent recirculating system (MARS) is used to purify blood from albumin-bound toxins in patients with liver failure. However, the application of MARS has not demonstrated improved survival in randomized clinical trials and the clinical utility has not been finally established. In our department, the use of MARS is now restricted to the most critically ill patients with acute or acute on chronic liver failure. Material and methods. Since 2005, we have treated 69 patients (30 males/39 females with median age of 49 years ranging from 1 months to 70 years) listed for liver transplantation (LT) with MARS. Median model of end-stage liver disease score in patients older than 12 years of age (n = 56) was 33 (interquartile range 26–39). The flow rate was 35–40 mL/kg/h and treatment kits were changed every 8–12 h. The patients were treated for a median of 27 h (range 1–144 h). Results. Fifty-six patients (81%) were transplanted. Nine died before they could be transplanted, and four patients recovered without transplantation. Forty-six (82%) of the transplanted patients were alive 30 days after transplantation. Ammonium decreased modestly from a median of 148 to 124 µM (p = 0.03) during MARS treatment. We detected worsening of coagulopathy with significant decreases in platelet count and fibrinogen concentrations, and increase in International Normalized Ratio. Phosphate and magnesium decreased significantly during MARS treatment. Conclusion. Continuous MARS therapy may bridge liver failure patients to LT under close observation and treatment of coagulopathy and electrolyte disturbances. Informa Healthcare 2015-09-02 2015-04-11 /pmc/articles/PMC4673540/ /pubmed/25865318 http://dx.doi.org/10.3109/00365521.2015.1027262 Text en © 2015 The Author(s). Published by Taylor & Francis. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Olin, Per
Hausken, John
Foss, Aksel
Karlsen, Tom Hemming
Melum, Espen
Haugaa, Håkon
Continuous molecular adsorbent recirculating system treatment in 69 patients listed for liver transplantation
title Continuous molecular adsorbent recirculating system treatment in 69 patients listed for liver transplantation
title_full Continuous molecular adsorbent recirculating system treatment in 69 patients listed for liver transplantation
title_fullStr Continuous molecular adsorbent recirculating system treatment in 69 patients listed for liver transplantation
title_full_unstemmed Continuous molecular adsorbent recirculating system treatment in 69 patients listed for liver transplantation
title_short Continuous molecular adsorbent recirculating system treatment in 69 patients listed for liver transplantation
title_sort continuous molecular adsorbent recirculating system treatment in 69 patients listed for liver transplantation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673540/
https://www.ncbi.nlm.nih.gov/pubmed/25865318
http://dx.doi.org/10.3109/00365521.2015.1027262
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