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Bench-to-bedside review: Permissive hypercapnia
Current protective lung ventilation strategies commonly involve hypercapnia. This approach has resulted in an increase in the clinical acceptability of elevated carbon dioxide tension, with hypoventilation and hypercapnia 'permitted' in order to avoid the deleterious effects of high lung s...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1065087/ https://www.ncbi.nlm.nih.gov/pubmed/15693984 http://dx.doi.org/10.1186/cc2918 |
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author | O' Croinin, Donall Ni Chonghaile, Martina Higgins, Brendan Laffey, John G |
author_facet | O' Croinin, Donall Ni Chonghaile, Martina Higgins, Brendan Laffey, John G |
author_sort | O' Croinin, Donall |
collection | PubMed |
description | Current protective lung ventilation strategies commonly involve hypercapnia. This approach has resulted in an increase in the clinical acceptability of elevated carbon dioxide tension, with hypoventilation and hypercapnia 'permitted' in order to avoid the deleterious effects of high lung stretch. Advances in our understanding of the biology of hypercapnia have prompted consideration of the potential for hypercapnia to play an active role in the pathogenesis of inflammation and tissue injury. In fact, hypercapnia may protect against lung and systemic organ injury independently of ventilator strategy. However, there are no clinical data evaluating the direct effects of hypercapnia per se in acute lung injury. This article reviews the current clinical status of permissive hypercapnia, discusses insights gained to date from basic scientific studies of hypercapnia and acidosis, identifies key unresolved concerns regarding hypercapnia, and considers the potential clinical implications for the management of patients with acute lung injury. |
format | Text |
id | pubmed-1065087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-10650872005-03-16 Bench-to-bedside review: Permissive hypercapnia O' Croinin, Donall Ni Chonghaile, Martina Higgins, Brendan Laffey, John G Crit Care Review Current protective lung ventilation strategies commonly involve hypercapnia. This approach has resulted in an increase in the clinical acceptability of elevated carbon dioxide tension, with hypoventilation and hypercapnia 'permitted' in order to avoid the deleterious effects of high lung stretch. Advances in our understanding of the biology of hypercapnia have prompted consideration of the potential for hypercapnia to play an active role in the pathogenesis of inflammation and tissue injury. In fact, hypercapnia may protect against lung and systemic organ injury independently of ventilator strategy. However, there are no clinical data evaluating the direct effects of hypercapnia per se in acute lung injury. This article reviews the current clinical status of permissive hypercapnia, discusses insights gained to date from basic scientific studies of hypercapnia and acidosis, identifies key unresolved concerns regarding hypercapnia, and considers the potential clinical implications for the management of patients with acute lung injury. BioMed Central 2005 2004-08-05 /pmc/articles/PMC1065087/ /pubmed/15693984 http://dx.doi.org/10.1186/cc2918 Text en Copyright © 2004 BioMed Central Ltd |
spellingShingle | Review O' Croinin, Donall Ni Chonghaile, Martina Higgins, Brendan Laffey, John G Bench-to-bedside review: Permissive hypercapnia |
title | Bench-to-bedside review: Permissive hypercapnia |
title_full | Bench-to-bedside review: Permissive hypercapnia |
title_fullStr | Bench-to-bedside review: Permissive hypercapnia |
title_full_unstemmed | Bench-to-bedside review: Permissive hypercapnia |
title_short | Bench-to-bedside review: Permissive hypercapnia |
title_sort | bench-to-bedside review: permissive hypercapnia |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1065087/ https://www.ncbi.nlm.nih.gov/pubmed/15693984 http://dx.doi.org/10.1186/cc2918 |
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