Cargando…
A prospective randomized open-label crossover trial of regional citrate anticoagulation vs. anticoagulation free liver dialysis by the Molecular Adsorbents Recirculating System
INTRODUCTION: The Molecular Adsorbent Recycling System (MARS) is used to treat patients with liver failure. Observational data suggest that citrate anticoagulation during MARS is feasible. Comparative studies on the optimal anticoagulation regimen during MARS are lacking. The aim of the current stud...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3396260/ https://www.ncbi.nlm.nih.gov/pubmed/22305273 http://dx.doi.org/10.1186/cc11180 |
_version_ | 1782238090761338880 |
---|---|
author | Meijers, Björn Laleman, Wim Vermeersch, Pieter Nevens, Frederik Wilmer, Alexander Evenepoel, Pieter |
author_facet | Meijers, Björn Laleman, Wim Vermeersch, Pieter Nevens, Frederik Wilmer, Alexander Evenepoel, Pieter |
author_sort | Meijers, Björn |
collection | PubMed |
description | INTRODUCTION: The Molecular Adsorbent Recycling System (MARS) is used to treat patients with liver failure. Observational data suggest that citrate anticoagulation during MARS is feasible. Comparative studies on the optimal anticoagulation regimen during MARS are lacking. The aim of the current study was to evaluate two heparin-free anticoagulation regimens. METHODS: We performed a prospective randomized open-label crossover study of regional citrate anticoagulation against no anticoagulation. Ten patients (age 55 ± 11 years) with liver failure undergoing MARS treatment were included. The primary endpoint was completion of MARS sessions. Secondary endpoints included treatment efficacy and safety. Longevity of MARS treatment was plotted as a Kaplan-Meier estimate. Fisher's exact test was used for contingency table analysis. RESULTS: Of a total of 27 6-hour sessions, four sessions had to be terminated prematurely, three due to occlusive clotting of the extracorporeal circuit and one due to uncontrollable bleeding from the vascular access site. All four events occurred in the group without anticoagulation. Between group comparison demonstrated citrate anticoagulation to significantly increase the likelihood of completed MARS treatment (Fisher's exact test, P 0.04). This translates into higher bilirubin reduction ratios when citrate was applied (reduction ratio 0.25 vs. 0.15, P 0.02). Systemic ionized calcium concentrations were significantly reduced during citrate anticoagulation (P < 0.001) but remained within a safe range. We observed no major adverse events. CONCLUSIONS: Regional citrate anticoagulation in patients with liver failure is feasible. Citrate anticoagulation provides superior patency of the extracorporeal circuit. Avoidance of anticoagulation during MARS results in significant loss of treatment efficacy, due to treatment downtime. Additional studies are required to identify the optimal anticoagulation regimen for extracorporeal circulation in patients with liver failure. |
format | Online Article Text |
id | pubmed-3396260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33962602012-07-13 A prospective randomized open-label crossover trial of regional citrate anticoagulation vs. anticoagulation free liver dialysis by the Molecular Adsorbents Recirculating System Meijers, Björn Laleman, Wim Vermeersch, Pieter Nevens, Frederik Wilmer, Alexander Evenepoel, Pieter Crit Care Research INTRODUCTION: The Molecular Adsorbent Recycling System (MARS) is used to treat patients with liver failure. Observational data suggest that citrate anticoagulation during MARS is feasible. Comparative studies on the optimal anticoagulation regimen during MARS are lacking. The aim of the current study was to evaluate two heparin-free anticoagulation regimens. METHODS: We performed a prospective randomized open-label crossover study of regional citrate anticoagulation against no anticoagulation. Ten patients (age 55 ± 11 years) with liver failure undergoing MARS treatment were included. The primary endpoint was completion of MARS sessions. Secondary endpoints included treatment efficacy and safety. Longevity of MARS treatment was plotted as a Kaplan-Meier estimate. Fisher's exact test was used for contingency table analysis. RESULTS: Of a total of 27 6-hour sessions, four sessions had to be terminated prematurely, three due to occlusive clotting of the extracorporeal circuit and one due to uncontrollable bleeding from the vascular access site. All four events occurred in the group without anticoagulation. Between group comparison demonstrated citrate anticoagulation to significantly increase the likelihood of completed MARS treatment (Fisher's exact test, P 0.04). This translates into higher bilirubin reduction ratios when citrate was applied (reduction ratio 0.25 vs. 0.15, P 0.02). Systemic ionized calcium concentrations were significantly reduced during citrate anticoagulation (P < 0.001) but remained within a safe range. We observed no major adverse events. CONCLUSIONS: Regional citrate anticoagulation in patients with liver failure is feasible. Citrate anticoagulation provides superior patency of the extracorporeal circuit. Avoidance of anticoagulation during MARS results in significant loss of treatment efficacy, due to treatment downtime. Additional studies are required to identify the optimal anticoagulation regimen for extracorporeal circulation in patients with liver failure. BioMed Central 2012 2012-02-03 /pmc/articles/PMC3396260/ /pubmed/22305273 http://dx.doi.org/10.1186/cc11180 Text en Copyright ©2012 Meijers 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 Meijers, Björn Laleman, Wim Vermeersch, Pieter Nevens, Frederik Wilmer, Alexander Evenepoel, Pieter A prospective randomized open-label crossover trial of regional citrate anticoagulation vs. anticoagulation free liver dialysis by the Molecular Adsorbents Recirculating System |
title | A prospective randomized open-label crossover trial of regional citrate anticoagulation vs. anticoagulation free liver dialysis by the Molecular Adsorbents Recirculating System |
title_full | A prospective randomized open-label crossover trial of regional citrate anticoagulation vs. anticoagulation free liver dialysis by the Molecular Adsorbents Recirculating System |
title_fullStr | A prospective randomized open-label crossover trial of regional citrate anticoagulation vs. anticoagulation free liver dialysis by the Molecular Adsorbents Recirculating System |
title_full_unstemmed | A prospective randomized open-label crossover trial of regional citrate anticoagulation vs. anticoagulation free liver dialysis by the Molecular Adsorbents Recirculating System |
title_short | A prospective randomized open-label crossover trial of regional citrate anticoagulation vs. anticoagulation free liver dialysis by the Molecular Adsorbents Recirculating System |
title_sort | prospective randomized open-label crossover trial of regional citrate anticoagulation vs. anticoagulation free liver dialysis by the molecular adsorbents recirculating system |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3396260/ https://www.ncbi.nlm.nih.gov/pubmed/22305273 http://dx.doi.org/10.1186/cc11180 |
work_keys_str_mv | AT meijersbjorn aprospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem AT lalemanwim aprospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem AT vermeerschpieter aprospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem AT nevensfrederik aprospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem AT wilmeralexander aprospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem AT evenepoelpieter aprospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem AT meijersbjorn prospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem AT lalemanwim prospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem AT vermeerschpieter prospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem AT nevensfrederik prospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem AT wilmeralexander prospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem AT evenepoelpieter prospectiverandomizedopenlabelcrossovertrialofregionalcitrateanticoagulationvsanticoagulationfreeliverdialysisbythemolecularadsorbentsrecirculatingsystem |