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Validation of a new transpulmonary thermodilution system to assess global end-diastolic volume and extravascular lung water

INTRODUCTION: A new system has been developed to assess global end-diastolic volume (GEDV), a volumetric marker of cardiac preload, and extravascular lung water (EVLW) from a transpulmonary thermodilution curve. Our goal was to compare this new system with the system currently in clinical use. METHO...

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Autores principales: Bendjelid, Karim, Giraud, Raphael, Siegenthaler, Nils, Michard, Frederic
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220030/
https://www.ncbi.nlm.nih.gov/pubmed/21092252
http://dx.doi.org/10.1186/cc9332
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author Bendjelid, Karim
Giraud, Raphael
Siegenthaler, Nils
Michard, Frederic
author_facet Bendjelid, Karim
Giraud, Raphael
Siegenthaler, Nils
Michard, Frederic
author_sort Bendjelid, Karim
collection PubMed
description INTRODUCTION: A new system has been developed to assess global end-diastolic volume (GEDV), a volumetric marker of cardiac preload, and extravascular lung water (EVLW) from a transpulmonary thermodilution curve. Our goal was to compare this new system with the system currently in clinical use. METHODS: Eleven anesthetized and mechanically ventilated pigs were instrumented with a central venous catheter and a right (PulsioCath; Pulsion, Munich, Germany) and a left (VolumeView™; Edwards Lifesciences, Irvine, CA, USA) thermistor-tipped femoral arterial catheter. The right femoral catheter was used to measure GEDV and EVLW using the PiCCO(2)™ (Pulsion) method (GEDV(1 )and EVLW(1), respectively). The left femoral catheter was used to measure the same parameters using the new VolumeView™ (Edwards Lifesciences) method (GEDV(2 )and EVLW(2), respectively). Measurements were made during inotropic stimulation (dobutamine), during hypovolemia (bleeding), during hypervolemia (fluid overload), and after inducing acute lung injury (intravenous oleic acid). RESULTS: One hundred and thirty-seven paired measurements were analyzed. GEDV(1 )and GEDV(2 )ranged from 701 to 1,629 ml and from 774 to 1,645 ml, respectively. GEDV(1 )and GEDV(2 )were closely correlated (r(2 )= 0.79), with mean bias of -11 ± 80 ml and percentage error of 14%. EVLW(1 )and EVLW2 ranged from 507 to 2,379 ml and from 495 to 2,222 ml, respectively. EVLW(1 )and EVLW(2 )were closely correlated (r(2 )= 0.97), with mean bias of -5 ± 72 ml and percentage error of 15%. CONCLUSIONS: In animals, and over a very wide range of values, a good agreement was found between the new VolumeView™ system and the PiCCO™ system to assess GEDV and EVLW.
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spelling pubmed-32200302011-11-18 Validation of a new transpulmonary thermodilution system to assess global end-diastolic volume and extravascular lung water Bendjelid, Karim Giraud, Raphael Siegenthaler, Nils Michard, Frederic Crit Care Research INTRODUCTION: A new system has been developed to assess global end-diastolic volume (GEDV), a volumetric marker of cardiac preload, and extravascular lung water (EVLW) from a transpulmonary thermodilution curve. Our goal was to compare this new system with the system currently in clinical use. METHODS: Eleven anesthetized and mechanically ventilated pigs were instrumented with a central venous catheter and a right (PulsioCath; Pulsion, Munich, Germany) and a left (VolumeView™; Edwards Lifesciences, Irvine, CA, USA) thermistor-tipped femoral arterial catheter. The right femoral catheter was used to measure GEDV and EVLW using the PiCCO(2)™ (Pulsion) method (GEDV(1 )and EVLW(1), respectively). The left femoral catheter was used to measure the same parameters using the new VolumeView™ (Edwards Lifesciences) method (GEDV(2 )and EVLW(2), respectively). Measurements were made during inotropic stimulation (dobutamine), during hypovolemia (bleeding), during hypervolemia (fluid overload), and after inducing acute lung injury (intravenous oleic acid). RESULTS: One hundred and thirty-seven paired measurements were analyzed. GEDV(1 )and GEDV(2 )ranged from 701 to 1,629 ml and from 774 to 1,645 ml, respectively. GEDV(1 )and GEDV(2 )were closely correlated (r(2 )= 0.79), with mean bias of -11 ± 80 ml and percentage error of 14%. EVLW(1 )and EVLW2 ranged from 507 to 2,379 ml and from 495 to 2,222 ml, respectively. EVLW(1 )and EVLW(2 )were closely correlated (r(2 )= 0.97), with mean bias of -5 ± 72 ml and percentage error of 15%. CONCLUSIONS: In animals, and over a very wide range of values, a good agreement was found between the new VolumeView™ system and the PiCCO™ system to assess GEDV and EVLW. BioMed Central 2010 2010-11-23 /pmc/articles/PMC3220030/ /pubmed/21092252 http://dx.doi.org/10.1186/cc9332 Text en Copyright ©2010 Engvall et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Bendjelid, Karim
Giraud, Raphael
Siegenthaler, Nils
Michard, Frederic
Validation of a new transpulmonary thermodilution system to assess global end-diastolic volume and extravascular lung water
title Validation of a new transpulmonary thermodilution system to assess global end-diastolic volume and extravascular lung water
title_full Validation of a new transpulmonary thermodilution system to assess global end-diastolic volume and extravascular lung water
title_fullStr Validation of a new transpulmonary thermodilution system to assess global end-diastolic volume and extravascular lung water
title_full_unstemmed Validation of a new transpulmonary thermodilution system to assess global end-diastolic volume and extravascular lung water
title_short Validation of a new transpulmonary thermodilution system to assess global end-diastolic volume and extravascular lung water
title_sort validation of a new transpulmonary thermodilution system to assess global end-diastolic volume and extravascular lung water
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220030/
https://www.ncbi.nlm.nih.gov/pubmed/21092252
http://dx.doi.org/10.1186/cc9332
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