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Respiratory weakness after mechanical ventilation is associated with one-year mortality - a prospective study
BACKGROUND: Diaphragm dysfunction in mechanically ventilated patients is associated with poor outcome. Maximal inspiratory pressure (MIP) can be used to evaluate inspiratory muscle function. However, it is unclear whether respiratory weakness is independently associated with long-term mortality. The...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967510/ https://www.ncbi.nlm.nih.gov/pubmed/27475524 http://dx.doi.org/10.1186/s13054-016-1418-y |
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author | Medrinal, Clément Prieur, Guillaume Frenoy, Éric Robledo Quesada, Aurora Poncet, Antoine Bonnevie, Tristan Gravier, Francis-Edouard Lamia, Bouchra Contal, Olivier |
author_facet | Medrinal, Clément Prieur, Guillaume Frenoy, Éric Robledo Quesada, Aurora Poncet, Antoine Bonnevie, Tristan Gravier, Francis-Edouard Lamia, Bouchra Contal, Olivier |
author_sort | Medrinal, Clément |
collection | PubMed |
description | BACKGROUND: Diaphragm dysfunction in mechanically ventilated patients is associated with poor outcome. Maximal inspiratory pressure (MIP) can be used to evaluate inspiratory muscle function. However, it is unclear whether respiratory weakness is independently associated with long-term mortality. The aim of this study was to determine if low MIP is independently associated with one-year mortality. METHODS: We conducted a prospective observational cohort study in an 18-bed ICU. Adults requiring at least 24 hours of mechanical ventilation with scheduled extubation and no evidence of pre-existing muscle weakness underwent MIP evaluation just before extubation. Patients were divided into two groups: low MIP (MIP ≤30 cmH(2)O) and high MIP (MIP >30 cmH(2)O). Mortality was recorded for one year after extubation. For the survival analysis, the effect of low MIP was assessed using the log-rank test. The independent effect of low MIP on post mechanical ventilation mortality was analyzed using a multivariable Cox regression model. RESULTS: One hundred and twenty-four patients underwent MIP evaluation (median age 66 years (25(th)–75(th) percentile 56–74), Simplified Acute Physiology Score (SAPS) 2 = 45 (33–57), duration of mechanical ventilation 7 days (4–10)). Fifty-four percent of patients had low MIP. One-year mortality was 31 % (95 % CI 0.21, 0.43) in the low MIP group and 7 % (95 % CI 0.02, 0.16) in the high MIP group. After adjustment for SAPS 2 score, body mass index and duration of mechanical ventilation, low MIP was independently associated with one-year mortality (hazard ratio 4.41, 95 % CI 1.5, 12.9, p = 0.007). Extubation failure was also associated with low MIP (relative risk 3.0, 95 % CI 1, -9.6; p = 0.03) but tracheostomy and ICU length of stay were not. CONCLUSION: Low MIP is frequent in patients on mechanical ventilation and is an independent risk factor for long-term mortality in ICU patients requiring mechanical ventilation. MIP is easily evaluated at the patient’s bedside. TRIAL REGISTRATION: This study was retrospectively registered in www.clinicaltrials.gov (NCT02363231) in February 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-016-1418-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4967510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49675102016-08-01 Respiratory weakness after mechanical ventilation is associated with one-year mortality - a prospective study Medrinal, Clément Prieur, Guillaume Frenoy, Éric Robledo Quesada, Aurora Poncet, Antoine Bonnevie, Tristan Gravier, Francis-Edouard Lamia, Bouchra Contal, Olivier Crit Care Research BACKGROUND: Diaphragm dysfunction in mechanically ventilated patients is associated with poor outcome. Maximal inspiratory pressure (MIP) can be used to evaluate inspiratory muscle function. However, it is unclear whether respiratory weakness is independently associated with long-term mortality. The aim of this study was to determine if low MIP is independently associated with one-year mortality. METHODS: We conducted a prospective observational cohort study in an 18-bed ICU. Adults requiring at least 24 hours of mechanical ventilation with scheduled extubation and no evidence of pre-existing muscle weakness underwent MIP evaluation just before extubation. Patients were divided into two groups: low MIP (MIP ≤30 cmH(2)O) and high MIP (MIP >30 cmH(2)O). Mortality was recorded for one year after extubation. For the survival analysis, the effect of low MIP was assessed using the log-rank test. The independent effect of low MIP on post mechanical ventilation mortality was analyzed using a multivariable Cox regression model. RESULTS: One hundred and twenty-four patients underwent MIP evaluation (median age 66 years (25(th)–75(th) percentile 56–74), Simplified Acute Physiology Score (SAPS) 2 = 45 (33–57), duration of mechanical ventilation 7 days (4–10)). Fifty-four percent of patients had low MIP. One-year mortality was 31 % (95 % CI 0.21, 0.43) in the low MIP group and 7 % (95 % CI 0.02, 0.16) in the high MIP group. After adjustment for SAPS 2 score, body mass index and duration of mechanical ventilation, low MIP was independently associated with one-year mortality (hazard ratio 4.41, 95 % CI 1.5, 12.9, p = 0.007). Extubation failure was also associated with low MIP (relative risk 3.0, 95 % CI 1, -9.6; p = 0.03) but tracheostomy and ICU length of stay were not. CONCLUSION: Low MIP is frequent in patients on mechanical ventilation and is an independent risk factor for long-term mortality in ICU patients requiring mechanical ventilation. MIP is easily evaluated at the patient’s bedside. TRIAL REGISTRATION: This study was retrospectively registered in www.clinicaltrials.gov (NCT02363231) in February 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-016-1418-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-07-31 2016 /pmc/articles/PMC4967510/ /pubmed/27475524 http://dx.doi.org/10.1186/s13054-016-1418-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Medrinal, Clément Prieur, Guillaume Frenoy, Éric Robledo Quesada, Aurora Poncet, Antoine Bonnevie, Tristan Gravier, Francis-Edouard Lamia, Bouchra Contal, Olivier Respiratory weakness after mechanical ventilation is associated with one-year mortality - a prospective study |
title | Respiratory weakness after mechanical ventilation is associated with one-year mortality - a prospective study |
title_full | Respiratory weakness after mechanical ventilation is associated with one-year mortality - a prospective study |
title_fullStr | Respiratory weakness after mechanical ventilation is associated with one-year mortality - a prospective study |
title_full_unstemmed | Respiratory weakness after mechanical ventilation is associated with one-year mortality - a prospective study |
title_short | Respiratory weakness after mechanical ventilation is associated with one-year mortality - a prospective study |
title_sort | respiratory weakness after mechanical ventilation is associated with one-year mortality - a prospective study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967510/ https://www.ncbi.nlm.nih.gov/pubmed/27475524 http://dx.doi.org/10.1186/s13054-016-1418-y |
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