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Evaluation of a New Extracorporeal CO(2) Removal Device in an Experimental Setting
Background: Ultra-protective lung ventilation in acute respiratory distress syndrome or early weaning and/or avoidance of mechanical ventilation in decompensated chronic obstructive pulmonary disease may be facilitated by the use of extracorporeal CO(2) removal (ECCO(2)R). We tested the CO(2) remova...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7823796/ https://www.ncbi.nlm.nih.gov/pubmed/33374762 http://dx.doi.org/10.3390/membranes11010008 |
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author | Di Nardo, Matteo Annoni, Filippo Su, Fuhong Belliato, Mirko Lorusso, Roberto Broman, Lars Mikael Malfertheiner, Maximilian Creteur, Jacques Taccone, Fabio Silvio |
author_facet | Di Nardo, Matteo Annoni, Filippo Su, Fuhong Belliato, Mirko Lorusso, Roberto Broman, Lars Mikael Malfertheiner, Maximilian Creteur, Jacques Taccone, Fabio Silvio |
author_sort | Di Nardo, Matteo |
collection | PubMed |
description | Background: Ultra-protective lung ventilation in acute respiratory distress syndrome or early weaning and/or avoidance of mechanical ventilation in decompensated chronic obstructive pulmonary disease may be facilitated by the use of extracorporeal CO(2) removal (ECCO(2)R). We tested the CO(2) removal performance of a new ECCO(2)R (CO(2)RESET) device in an experimental animal model. Methods: Three healthy pigs were mechanically ventilated and connected to the CO(2)RESET device (surface area = 1.8 m(2), EUROSETS S.r.l., Medolla, Italy). Respiratory settings were adjusted to induce respiratory acidosis with the adjunct of an external source of pure CO(2) (target pre membrane lung venous PCO(2) (P(pre)CO(2)): 80–120 mmHg). The amount of CO(2) removed (VCO(2), mL/min) by the membrane lung was assessed directly by the ECCO(2)R device. Results: Before the initiation of ECCO(2)R, the median P(pre)CO(2) was 102.50 (95.30–118.20) mmHg. Using fixed incremental steps of the sweep gas flow and maintaining a fixed blood flow of 600 mL/min, VCO(2) progressively increased from 0 mL/min (gas flow of 0 mL/min) to 170.00 (160.00–200.00) mL/min at a gas flow of 10 L/min. In particular, a high increase of VCO(2) was observed increasing the gas flow from 0 to 2 L/min, then, VCO(2) tended to progressively achieve a steady-state for higher gas flows. No animal or pump complications were observed. Conclusions: Medium-flow ECCO(2)R devices with a blood flow of 600 mL/min and a high surface membrane lung (1.8 m(2)) provided a high VCO(2) using moderate sweep gas flows (i.e., >2 L/min) in an experimental swine models with healthy lungs. |
format | Online Article Text |
id | pubmed-7823796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78237962021-01-24 Evaluation of a New Extracorporeal CO(2) Removal Device in an Experimental Setting Di Nardo, Matteo Annoni, Filippo Su, Fuhong Belliato, Mirko Lorusso, Roberto Broman, Lars Mikael Malfertheiner, Maximilian Creteur, Jacques Taccone, Fabio Silvio Membranes (Basel) Article Background: Ultra-protective lung ventilation in acute respiratory distress syndrome or early weaning and/or avoidance of mechanical ventilation in decompensated chronic obstructive pulmonary disease may be facilitated by the use of extracorporeal CO(2) removal (ECCO(2)R). We tested the CO(2) removal performance of a new ECCO(2)R (CO(2)RESET) device in an experimental animal model. Methods: Three healthy pigs were mechanically ventilated and connected to the CO(2)RESET device (surface area = 1.8 m(2), EUROSETS S.r.l., Medolla, Italy). Respiratory settings were adjusted to induce respiratory acidosis with the adjunct of an external source of pure CO(2) (target pre membrane lung venous PCO(2) (P(pre)CO(2)): 80–120 mmHg). The amount of CO(2) removed (VCO(2), mL/min) by the membrane lung was assessed directly by the ECCO(2)R device. Results: Before the initiation of ECCO(2)R, the median P(pre)CO(2) was 102.50 (95.30–118.20) mmHg. Using fixed incremental steps of the sweep gas flow and maintaining a fixed blood flow of 600 mL/min, VCO(2) progressively increased from 0 mL/min (gas flow of 0 mL/min) to 170.00 (160.00–200.00) mL/min at a gas flow of 10 L/min. In particular, a high increase of VCO(2) was observed increasing the gas flow from 0 to 2 L/min, then, VCO(2) tended to progressively achieve a steady-state for higher gas flows. No animal or pump complications were observed. Conclusions: Medium-flow ECCO(2)R devices with a blood flow of 600 mL/min and a high surface membrane lung (1.8 m(2)) provided a high VCO(2) using moderate sweep gas flows (i.e., >2 L/min) in an experimental swine models with healthy lungs. MDPI 2020-12-23 /pmc/articles/PMC7823796/ /pubmed/33374762 http://dx.doi.org/10.3390/membranes11010008 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Di Nardo, Matteo Annoni, Filippo Su, Fuhong Belliato, Mirko Lorusso, Roberto Broman, Lars Mikael Malfertheiner, Maximilian Creteur, Jacques Taccone, Fabio Silvio Evaluation of a New Extracorporeal CO(2) Removal Device in an Experimental Setting |
title | Evaluation of a New Extracorporeal CO(2) Removal Device in an Experimental Setting |
title_full | Evaluation of a New Extracorporeal CO(2) Removal Device in an Experimental Setting |
title_fullStr | Evaluation of a New Extracorporeal CO(2) Removal Device in an Experimental Setting |
title_full_unstemmed | Evaluation of a New Extracorporeal CO(2) Removal Device in an Experimental Setting |
title_short | Evaluation of a New Extracorporeal CO(2) Removal Device in an Experimental Setting |
title_sort | evaluation of a new extracorporeal co(2) removal device in an experimental setting |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7823796/ https://www.ncbi.nlm.nih.gov/pubmed/33374762 http://dx.doi.org/10.3390/membranes11010008 |
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