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Respiratory distress observation scales to predict weaning outcome
BACKGROUND: Whether dyspnea is present before starting a spontaneous breathing trial (SBT) and whether it may affect the outcome of the SBT is unknown. Mechanical Ventilation—Respiratory Distress Observation Scale (MV-RDOS) has been proposed as a reliable surrogate of dyspnea in non-communicative in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169318/ https://www.ncbi.nlm.nih.gov/pubmed/35668459 http://dx.doi.org/10.1186/s13054-022-04028-7 |
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author | Decavèle, Maxens Rozenberg, Emmanuel Niérat, Marie-Cécile Mayaux, Julien Morawiec, Elise Morélot-Panzini, Capucine Similowski, Thomas Demoule, Alexandre Dres, Martin |
author_facet | Decavèle, Maxens Rozenberg, Emmanuel Niérat, Marie-Cécile Mayaux, Julien Morawiec, Elise Morélot-Panzini, Capucine Similowski, Thomas Demoule, Alexandre Dres, Martin |
author_sort | Decavèle, Maxens |
collection | PubMed |
description | BACKGROUND: Whether dyspnea is present before starting a spontaneous breathing trial (SBT) and whether it may affect the outcome of the SBT is unknown. Mechanical Ventilation—Respiratory Distress Observation Scale (MV-RDOS) has been proposed as a reliable surrogate of dyspnea in non-communicative intubated patients. In the present study, we sought (1) to describe the evolution of the MV-RDOS during a SBT and (2) to investigate whether MV-RDOS can predict the outcome of the SBT. METHODS: Prospective, single-center study in a twenty-two bed ICU in a tertiary center. Patients intubated since more 48 h who had failed a first SBT were eligible if they meet classical readiness to wean criteria. The MV-RDOS was assessed before, at 2-min, 15-min and 30-min (end) of the SBT. The presence of clinically important dyspnea was inferred by a MV-RDOS value ≥ 2.6. RESULTS: Fifty-eight patients (age 63 [51–70], SAPS II 66 [51–76]; med [IQR]) were included. Thirty-three (57%) patients failed the SBT, whose 18 (55%) failed before 15-min. Twenty-five (43%) patients successfully passed the SBT. A MV-RDOS ≥ 2.6 was present in ten (17%) patients before to start the SBT. All these ten patients subsequently failed the SBT. A MV-RDOS ≥ 2.6 at 2-min predicted a SBT failure with a 51% sensibility and a 88% specificity (AUC 0.741 95% confidence interval [CI] 0.616–0.866, p = 0.002). Best cut-off value at 2-min was 4.3 and predicted SBT failure with a 27% sensibility and a 96% specificity. CONCLUSION: Despite patients met classical readiness to wean criteria, respiratory distress assessed with the MV-RDOS was frequent at the beginning of SBT. Measuring MV-RDOS before to initiate a SBT could avoid undue procedure and reduce patient’s exposure to unnecessary mechanical ventilation weaning failure and distress. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-022-04028-7. |
format | Online Article Text |
id | pubmed-9169318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91693182022-06-07 Respiratory distress observation scales to predict weaning outcome Decavèle, Maxens Rozenberg, Emmanuel Niérat, Marie-Cécile Mayaux, Julien Morawiec, Elise Morélot-Panzini, Capucine Similowski, Thomas Demoule, Alexandre Dres, Martin Crit Care Research BACKGROUND: Whether dyspnea is present before starting a spontaneous breathing trial (SBT) and whether it may affect the outcome of the SBT is unknown. Mechanical Ventilation—Respiratory Distress Observation Scale (MV-RDOS) has been proposed as a reliable surrogate of dyspnea in non-communicative intubated patients. In the present study, we sought (1) to describe the evolution of the MV-RDOS during a SBT and (2) to investigate whether MV-RDOS can predict the outcome of the SBT. METHODS: Prospective, single-center study in a twenty-two bed ICU in a tertiary center. Patients intubated since more 48 h who had failed a first SBT were eligible if they meet classical readiness to wean criteria. The MV-RDOS was assessed before, at 2-min, 15-min and 30-min (end) of the SBT. The presence of clinically important dyspnea was inferred by a MV-RDOS value ≥ 2.6. RESULTS: Fifty-eight patients (age 63 [51–70], SAPS II 66 [51–76]; med [IQR]) were included. Thirty-three (57%) patients failed the SBT, whose 18 (55%) failed before 15-min. Twenty-five (43%) patients successfully passed the SBT. A MV-RDOS ≥ 2.6 was present in ten (17%) patients before to start the SBT. All these ten patients subsequently failed the SBT. A MV-RDOS ≥ 2.6 at 2-min predicted a SBT failure with a 51% sensibility and a 88% specificity (AUC 0.741 95% confidence interval [CI] 0.616–0.866, p = 0.002). Best cut-off value at 2-min was 4.3 and predicted SBT failure with a 27% sensibility and a 96% specificity. CONCLUSION: Despite patients met classical readiness to wean criteria, respiratory distress assessed with the MV-RDOS was frequent at the beginning of SBT. Measuring MV-RDOS before to initiate a SBT could avoid undue procedure and reduce patient’s exposure to unnecessary mechanical ventilation weaning failure and distress. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-022-04028-7. BioMed Central 2022-06-06 /pmc/articles/PMC9169318/ /pubmed/35668459 http://dx.doi.org/10.1186/s13054-022-04028-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Decavèle, Maxens Rozenberg, Emmanuel Niérat, Marie-Cécile Mayaux, Julien Morawiec, Elise Morélot-Panzini, Capucine Similowski, Thomas Demoule, Alexandre Dres, Martin Respiratory distress observation scales to predict weaning outcome |
title | Respiratory distress observation scales to predict weaning outcome |
title_full | Respiratory distress observation scales to predict weaning outcome |
title_fullStr | Respiratory distress observation scales to predict weaning outcome |
title_full_unstemmed | Respiratory distress observation scales to predict weaning outcome |
title_short | Respiratory distress observation scales to predict weaning outcome |
title_sort | respiratory distress observation scales to predict weaning outcome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169318/ https://www.ncbi.nlm.nih.gov/pubmed/35668459 http://dx.doi.org/10.1186/s13054-022-04028-7 |
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