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Low-flow CO(2) removal integrated into a renal-replacement circuit can reduce acidosis and decrease vasopressor requirements

INTRODUCTION: Lung-protective ventilation in patients with ARDS and multiorgan failure, including renal failure, is often paralleled with a combined respiratory and metabolic acidosis. We assessed the effectiveness of a hollow-fiber gas exchanger integrated into a conventional renal-replacement circ...

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Autores principales: Forster, Christian, Schriewer, Jens, John, Stefan, Eckardt, Kai-Uwe, Willam, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056563/
https://www.ncbi.nlm.nih.gov/pubmed/23883472
http://dx.doi.org/10.1186/cc12833
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author Forster, Christian
Schriewer, Jens
John, Stefan
Eckardt, Kai-Uwe
Willam, Carsten
author_facet Forster, Christian
Schriewer, Jens
John, Stefan
Eckardt, Kai-Uwe
Willam, Carsten
author_sort Forster, Christian
collection PubMed
description INTRODUCTION: Lung-protective ventilation in patients with ARDS and multiorgan failure, including renal failure, is often paralleled with a combined respiratory and metabolic acidosis. We assessed the effectiveness of a hollow-fiber gas exchanger integrated into a conventional renal-replacement circuit on CO(2) removal, acidosis, and hemodynamics. METHODS: In ten ventilated critically ill patients with ARDS and AKI undergoing renal- and respiratory-replacement therapy, effects of low-flow CO(2) removal on respiratory acidosis compensation were tested by using a hollow-fiber gas exchanger added to the renal-replacement circuit. This was an observational study on safety, CO(2)-removal capacity, effects on pH, ventilator settings, and hemodynamics. RESULTS: CO(2) elimination in the low-flow circuit was safe and was well tolerated by all patients. After 4 hours of treatment, a mean reduction of 17.3 mm Hg (−28.1%) pCO(2) was observed, in line with an increase in pH. In hemodynamically instable patients, low-flow CO(2) elimination was paralleled by hemodynamic improvement, with an average reduction of vasopressors of 65% in five of six catecholamine-dependent patients during the first 24 hours. CONCLUSIONS: Because no further catheters are needed, besides those for renal replacement, the implementation of a hollow-fiber gas exchanger in a renal circuit could be an attractive therapeutic tool with only a little additional trauma for patients with mild to moderate ARDS undergoing invasive ventilation with concomitant respiratory acidosis, as long as no severe oxygenation defects indicate ECMO therapy.
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spelling pubmed-40565632014-06-16 Low-flow CO(2) removal integrated into a renal-replacement circuit can reduce acidosis and decrease vasopressor requirements Forster, Christian Schriewer, Jens John, Stefan Eckardt, Kai-Uwe Willam, Carsten Crit Care Research INTRODUCTION: Lung-protective ventilation in patients with ARDS and multiorgan failure, including renal failure, is often paralleled with a combined respiratory and metabolic acidosis. We assessed the effectiveness of a hollow-fiber gas exchanger integrated into a conventional renal-replacement circuit on CO(2) removal, acidosis, and hemodynamics. METHODS: In ten ventilated critically ill patients with ARDS and AKI undergoing renal- and respiratory-replacement therapy, effects of low-flow CO(2) removal on respiratory acidosis compensation were tested by using a hollow-fiber gas exchanger added to the renal-replacement circuit. This was an observational study on safety, CO(2)-removal capacity, effects on pH, ventilator settings, and hemodynamics. RESULTS: CO(2) elimination in the low-flow circuit was safe and was well tolerated by all patients. After 4 hours of treatment, a mean reduction of 17.3 mm Hg (−28.1%) pCO(2) was observed, in line with an increase in pH. In hemodynamically instable patients, low-flow CO(2) elimination was paralleled by hemodynamic improvement, with an average reduction of vasopressors of 65% in five of six catecholamine-dependent patients during the first 24 hours. CONCLUSIONS: Because no further catheters are needed, besides those for renal replacement, the implementation of a hollow-fiber gas exchanger in a renal circuit could be an attractive therapeutic tool with only a little additional trauma for patients with mild to moderate ARDS undergoing invasive ventilation with concomitant respiratory acidosis, as long as no severe oxygenation defects indicate ECMO therapy. BioMed Central 2013 2013-07-24 /pmc/articles/PMC4056563/ /pubmed/23883472 http://dx.doi.org/10.1186/cc12833 Text en Copyright © 2013 Forster 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
Forster, Christian
Schriewer, Jens
John, Stefan
Eckardt, Kai-Uwe
Willam, Carsten
Low-flow CO(2) removal integrated into a renal-replacement circuit can reduce acidosis and decrease vasopressor requirements
title Low-flow CO(2) removal integrated into a renal-replacement circuit can reduce acidosis and decrease vasopressor requirements
title_full Low-flow CO(2) removal integrated into a renal-replacement circuit can reduce acidosis and decrease vasopressor requirements
title_fullStr Low-flow CO(2) removal integrated into a renal-replacement circuit can reduce acidosis and decrease vasopressor requirements
title_full_unstemmed Low-flow CO(2) removal integrated into a renal-replacement circuit can reduce acidosis and decrease vasopressor requirements
title_short Low-flow CO(2) removal integrated into a renal-replacement circuit can reduce acidosis and decrease vasopressor requirements
title_sort low-flow co(2) removal integrated into a renal-replacement circuit can reduce acidosis and decrease vasopressor requirements
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056563/
https://www.ncbi.nlm.nih.gov/pubmed/23883472
http://dx.doi.org/10.1186/cc12833
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