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The course of diaphragm atrophy in ventilated patients assessed with ultrasound: a longitudinal cohort study

INTRODUCTION: Mechanical ventilation and the effect of respiratory muscle unloading on the diaphragm cause ventilator-induced diaphragmatic dysfunction (VIDD). Atrophy of the diaphragmatic muscle is a major part of VIDD, and has a rapid onset in most animal models. We wanted to assess the clinical e...

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Autores principales: Schepens, Tom, Verbrugghe, Walter, Dams, Karolien, Corthouts, Bob, Parizel, Paul M., Jorens, Philippe G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4671211/
https://www.ncbi.nlm.nih.gov/pubmed/26639081
http://dx.doi.org/10.1186/s13054-015-1141-0
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author Schepens, Tom
Verbrugghe, Walter
Dams, Karolien
Corthouts, Bob
Parizel, Paul M.
Jorens, Philippe G.
author_facet Schepens, Tom
Verbrugghe, Walter
Dams, Karolien
Corthouts, Bob
Parizel, Paul M.
Jorens, Philippe G.
author_sort Schepens, Tom
collection PubMed
description INTRODUCTION: Mechanical ventilation and the effect of respiratory muscle unloading on the diaphragm cause ventilator-induced diaphragmatic dysfunction (VIDD). Atrophy of the diaphragmatic muscle is a major part of VIDD, and has a rapid onset in most animal models. We wanted to assess the clinical evolution and risk factors for VIDD in an adult intensive care unit (ICU) by measuring diaphragm thickness using ultrasound. METHOD: We performed a single-centre observational cohort study, including 54 mechanically ventilated patients. The right hemidiaphragm was measured daily at the zone of apposition on the midaxillary line. RESULTS: Mean baseline thickness was 1.9 mm (SD ± 0.4 mm), and mean nadir was 1.3 mm (SD ± 0.4 mm), corresponding with a mean change in thickness of 32 % (95 % CI 27–37 %). Length of mechanical ventilation (MV) was associated with the degree of atrophy, whereas other known risk factors for muscle atrophy in an ICU were not. The largest decrease in thickness occurred during the first 72 hours of MV. CONCLUSIONS: Diaphragm atrophy occurs quickly in mechanically ventilated patients and can accurately be monitored using ultrasound. Length of MV, as opposed to other variables, is associated with the degree of atrophy. CLINICAL TRIAL REGISTRATION: Clinicaltrials.gov NCT02299986. Registered 10/11/2014 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-015-1141-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-46712112015-12-08 The course of diaphragm atrophy in ventilated patients assessed with ultrasound: a longitudinal cohort study Schepens, Tom Verbrugghe, Walter Dams, Karolien Corthouts, Bob Parizel, Paul M. Jorens, Philippe G. Crit Care Research INTRODUCTION: Mechanical ventilation and the effect of respiratory muscle unloading on the diaphragm cause ventilator-induced diaphragmatic dysfunction (VIDD). Atrophy of the diaphragmatic muscle is a major part of VIDD, and has a rapid onset in most animal models. We wanted to assess the clinical evolution and risk factors for VIDD in an adult intensive care unit (ICU) by measuring diaphragm thickness using ultrasound. METHOD: We performed a single-centre observational cohort study, including 54 mechanically ventilated patients. The right hemidiaphragm was measured daily at the zone of apposition on the midaxillary line. RESULTS: Mean baseline thickness was 1.9 mm (SD ± 0.4 mm), and mean nadir was 1.3 mm (SD ± 0.4 mm), corresponding with a mean change in thickness of 32 % (95 % CI 27–37 %). Length of mechanical ventilation (MV) was associated with the degree of atrophy, whereas other known risk factors for muscle atrophy in an ICU were not. The largest decrease in thickness occurred during the first 72 hours of MV. CONCLUSIONS: Diaphragm atrophy occurs quickly in mechanically ventilated patients and can accurately be monitored using ultrasound. Length of MV, as opposed to other variables, is associated with the degree of atrophy. CLINICAL TRIAL REGISTRATION: Clinicaltrials.gov NCT02299986. Registered 10/11/2014 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-015-1141-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-07 2015 /pmc/articles/PMC4671211/ /pubmed/26639081 http://dx.doi.org/10.1186/s13054-015-1141-0 Text en © Schepens et al. 2015 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
Schepens, Tom
Verbrugghe, Walter
Dams, Karolien
Corthouts, Bob
Parizel, Paul M.
Jorens, Philippe G.
The course of diaphragm atrophy in ventilated patients assessed with ultrasound: a longitudinal cohort study
title The course of diaphragm atrophy in ventilated patients assessed with ultrasound: a longitudinal cohort study
title_full The course of diaphragm atrophy in ventilated patients assessed with ultrasound: a longitudinal cohort study
title_fullStr The course of diaphragm atrophy in ventilated patients assessed with ultrasound: a longitudinal cohort study
title_full_unstemmed The course of diaphragm atrophy in ventilated patients assessed with ultrasound: a longitudinal cohort study
title_short The course of diaphragm atrophy in ventilated patients assessed with ultrasound: a longitudinal cohort study
title_sort course of diaphragm atrophy in ventilated patients assessed with ultrasound: a longitudinal cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4671211/
https://www.ncbi.nlm.nih.gov/pubmed/26639081
http://dx.doi.org/10.1186/s13054-015-1141-0
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