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Relation between respiratory variations in pulse oximetry plethysmographic waveform amplitude and arterial pulse pressure in ventilated patients
INTRODUCTION: Respiratory variation in arterial pulse pressure is a reliable predictor of fluid responsiveness in mechanically ventilated patients with circulatory failure. The main limitation of this method is that it requires an invasive arterial catheter. Both arterial and pulse oximetry plethysm...
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/PMC1297625/ https://www.ncbi.nlm.nih.gov/pubmed/16277719 http://dx.doi.org/10.1186/cc3799 |
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author | Cannesson, Maxime Besnard, Cyril Durand, Pierre G Bohé, Julien Jacques, Didier |
author_facet | Cannesson, Maxime Besnard, Cyril Durand, Pierre G Bohé, Julien Jacques, Didier |
author_sort | Cannesson, Maxime |
collection | PubMed |
description | INTRODUCTION: Respiratory variation in arterial pulse pressure is a reliable predictor of fluid responsiveness in mechanically ventilated patients with circulatory failure. The main limitation of this method is that it requires an invasive arterial catheter. Both arterial and pulse oximetry plethysmographic waveforms depend on stroke volume. We conducted a prospective study to evaluate the relationship between respiratory variation in arterial pulse pressure and respiratory variation in pulse oximetry plethysmographic (POP) waveform amplitude. METHOD: This prospective clinical investigation was conducted in 22 mechanically ventilated patients. Respiratory variation in arterial pulse pressure and respiratory variation in POP waveform amplitude were recorded simultaneously in a beat-to-beat evaluation, and were compared using a Spearman correlation test and a Bland–Altman analysis. RESULTS: There was a strong correlation (r(2 )= 0.83; P < 0.001) and a good agreement (bias = 0.8 ± 3.5%) between respiratory variation in arterial pulse pressure and respiratory variation in POP waveform amplitude. A respiratory variation in POP waveform amplitude value above 15% allowed discrimination between patients with respiratory variation in arterial pulse pressure above 13% and those with variation of 13% or less (positive predictive value 100%). CONCLUSION: Respiratory variation in arterial pulse pressure above 13% can be accurately predicted by a respiratory variation in POP waveform amplitude above 15%. This index has potential applications in patients who are not instrumented with an intra-arterial catheter. |
format | Text |
id | pubmed-1297625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-12976252005-12-01 Relation between respiratory variations in pulse oximetry plethysmographic waveform amplitude and arterial pulse pressure in ventilated patients Cannesson, Maxime Besnard, Cyril Durand, Pierre G Bohé, Julien Jacques, Didier Crit Care Research INTRODUCTION: Respiratory variation in arterial pulse pressure is a reliable predictor of fluid responsiveness in mechanically ventilated patients with circulatory failure. The main limitation of this method is that it requires an invasive arterial catheter. Both arterial and pulse oximetry plethysmographic waveforms depend on stroke volume. We conducted a prospective study to evaluate the relationship between respiratory variation in arterial pulse pressure and respiratory variation in pulse oximetry plethysmographic (POP) waveform amplitude. METHOD: This prospective clinical investigation was conducted in 22 mechanically ventilated patients. Respiratory variation in arterial pulse pressure and respiratory variation in POP waveform amplitude were recorded simultaneously in a beat-to-beat evaluation, and were compared using a Spearman correlation test and a Bland–Altman analysis. RESULTS: There was a strong correlation (r(2 )= 0.83; P < 0.001) and a good agreement (bias = 0.8 ± 3.5%) between respiratory variation in arterial pulse pressure and respiratory variation in POP waveform amplitude. A respiratory variation in POP waveform amplitude value above 15% allowed discrimination between patients with respiratory variation in arterial pulse pressure above 13% and those with variation of 13% or less (positive predictive value 100%). CONCLUSION: Respiratory variation in arterial pulse pressure above 13% can be accurately predicted by a respiratory variation in POP waveform amplitude above 15%. This index has potential applications in patients who are not instrumented with an intra-arterial catheter. BioMed Central 2005 2005-08-23 /pmc/articles/PMC1297625/ /pubmed/16277719 http://dx.doi.org/10.1186/cc3799 Text en Copyright © 2005 Cannesson et al.; licensee BioMed Central Ltd. |
spellingShingle | Research Cannesson, Maxime Besnard, Cyril Durand, Pierre G Bohé, Julien Jacques, Didier Relation between respiratory variations in pulse oximetry plethysmographic waveform amplitude and arterial pulse pressure in ventilated patients |
title | Relation between respiratory variations in pulse oximetry plethysmographic waveform amplitude and arterial pulse pressure in ventilated patients |
title_full | Relation between respiratory variations in pulse oximetry plethysmographic waveform amplitude and arterial pulse pressure in ventilated patients |
title_fullStr | Relation between respiratory variations in pulse oximetry plethysmographic waveform amplitude and arterial pulse pressure in ventilated patients |
title_full_unstemmed | Relation between respiratory variations in pulse oximetry plethysmographic waveform amplitude and arterial pulse pressure in ventilated patients |
title_short | Relation between respiratory variations in pulse oximetry plethysmographic waveform amplitude and arterial pulse pressure in ventilated patients |
title_sort | relation between respiratory variations in pulse oximetry plethysmographic waveform amplitude and arterial pulse pressure in ventilated patients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1297625/ https://www.ncbi.nlm.nih.gov/pubmed/16277719 http://dx.doi.org/10.1186/cc3799 |
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