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Computer simulation allows goal-oriented mechanical ventilation in acute respiratory distress syndrome
INTRODUCTION: To prevent further lung damage in patients with acute respiratory distress syndrome (ARDS), it is important to avoid overdistension and cyclic opening and closing of atelectatic alveoli. Previous studies have demonstrated protective effects of using low tidal volume (V(T)), moderate po...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206452/ https://www.ncbi.nlm.nih.gov/pubmed/17352801 http://dx.doi.org/10.1186/cc5719 |
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author | Uttman, Leif Ögren, Helena Niklason, Lisbet Drefeldt, Björn Jonson, Björn |
author_facet | Uttman, Leif Ögren, Helena Niklason, Lisbet Drefeldt, Björn Jonson, Björn |
author_sort | Uttman, Leif |
collection | PubMed |
description | INTRODUCTION: To prevent further lung damage in patients with acute respiratory distress syndrome (ARDS), it is important to avoid overdistension and cyclic opening and closing of atelectatic alveoli. Previous studies have demonstrated protective effects of using low tidal volume (V(T)), moderate positive end-expiratory pressure and low airway pressure. Aspiration of dead space (ASPIDS) allows a reduction in V(T )by eliminating dead space in the tracheal tube and tubing. We hypothesized that, by applying goal-orientated ventilation based on iterative computer simulation, V(T )can be reduced at high respiratory rate and much further reduced during ASPIDS without compromising gas exchange or causing high airway pressure. METHODS: ARDS was induced in eight pigs by surfactant perturbation and ventilator-induced lung injury. Ventilator resetting guided by computer simulation was then performed, aiming at minimal V(T), plateau pressure 30 cmH(2)O and isocapnia, first by only increasing respiratory rate and then by using ASPIDS as well. RESULTS: V(T )decreased from 7.2 ± 0.5 ml/kg to 6.6 ± 0.5 ml/kg as respiratory rate increased from 40 to 64 ± 6 breaths/min, and to 4.0 ± 0.4 ml/kg when ASPIDS was used at 80 ± 6 breaths/min. Measured values of arterial carbon dioxide tension were close to predicted values. Without ASPIDS, total positive end-expiratory pressure and plateau pressure were slightly higher than predicted, and with ASPIDS they were lower than predicted. CONCLUSION: In principle, computer simulation may be used in goal-oriented ventilation in ARDS. Further studies are needed to investigate potential benefits and limitations over extended study periods. |
format | Text |
id | pubmed-2206452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22064522008-01-23 Computer simulation allows goal-oriented mechanical ventilation in acute respiratory distress syndrome Uttman, Leif Ögren, Helena Niklason, Lisbet Drefeldt, Björn Jonson, Björn Crit Care Research INTRODUCTION: To prevent further lung damage in patients with acute respiratory distress syndrome (ARDS), it is important to avoid overdistension and cyclic opening and closing of atelectatic alveoli. Previous studies have demonstrated protective effects of using low tidal volume (V(T)), moderate positive end-expiratory pressure and low airway pressure. Aspiration of dead space (ASPIDS) allows a reduction in V(T )by eliminating dead space in the tracheal tube and tubing. We hypothesized that, by applying goal-orientated ventilation based on iterative computer simulation, V(T )can be reduced at high respiratory rate and much further reduced during ASPIDS without compromising gas exchange or causing high airway pressure. METHODS: ARDS was induced in eight pigs by surfactant perturbation and ventilator-induced lung injury. Ventilator resetting guided by computer simulation was then performed, aiming at minimal V(T), plateau pressure 30 cmH(2)O and isocapnia, first by only increasing respiratory rate and then by using ASPIDS as well. RESULTS: V(T )decreased from 7.2 ± 0.5 ml/kg to 6.6 ± 0.5 ml/kg as respiratory rate increased from 40 to 64 ± 6 breaths/min, and to 4.0 ± 0.4 ml/kg when ASPIDS was used at 80 ± 6 breaths/min. Measured values of arterial carbon dioxide tension were close to predicted values. Without ASPIDS, total positive end-expiratory pressure and plateau pressure were slightly higher than predicted, and with ASPIDS they were lower than predicted. CONCLUSION: In principle, computer simulation may be used in goal-oriented ventilation in ARDS. Further studies are needed to investigate potential benefits and limitations over extended study periods. BioMed Central 2007 2007-03-12 /pmc/articles/PMC2206452/ /pubmed/17352801 http://dx.doi.org/10.1186/cc5719 Text en Copyright © 2007 Uttman 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 Uttman, Leif Ögren, Helena Niklason, Lisbet Drefeldt, Björn Jonson, Björn Computer simulation allows goal-oriented mechanical ventilation in acute respiratory distress syndrome |
title | Computer simulation allows goal-oriented mechanical ventilation in acute respiratory distress syndrome |
title_full | Computer simulation allows goal-oriented mechanical ventilation in acute respiratory distress syndrome |
title_fullStr | Computer simulation allows goal-oriented mechanical ventilation in acute respiratory distress syndrome |
title_full_unstemmed | Computer simulation allows goal-oriented mechanical ventilation in acute respiratory distress syndrome |
title_short | Computer simulation allows goal-oriented mechanical ventilation in acute respiratory distress syndrome |
title_sort | computer simulation allows goal-oriented mechanical ventilation in acute respiratory distress syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206452/ https://www.ncbi.nlm.nih.gov/pubmed/17352801 http://dx.doi.org/10.1186/cc5719 |
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