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A Non Invasive Estimate of Dead Space Ventilation from Exercise Measurements
RATIONALE: During exercise, heart failure patients (HF) show an out-of-proportion ventilation increase, which in patients with COPD is blunted. When HF and COPD coexist, the ventilatory response to exercise is unpredictable. OBJECTIVES: We evaluated a human model of respiratory impairment in 10 COPD...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907547/ https://www.ncbi.nlm.nih.gov/pubmed/24498096 http://dx.doi.org/10.1371/journal.pone.0087395 |
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author | Gargiulo, Paola Apostolo, Anna Perrone-Filardi, Pasquale Sciomer, Susanna Palange, Paolo Agostoni, Piergiuseppe |
author_facet | Gargiulo, Paola Apostolo, Anna Perrone-Filardi, Pasquale Sciomer, Susanna Palange, Paolo Agostoni, Piergiuseppe |
author_sort | Gargiulo, Paola |
collection | PubMed |
description | RATIONALE: During exercise, heart failure patients (HF) show an out-of-proportion ventilation increase, which in patients with COPD is blunted. When HF and COPD coexist, the ventilatory response to exercise is unpredictable. OBJECTIVES: We evaluated a human model of respiratory impairment in 10 COPD-free HF patients and in 10 healthy subjects, tested with a progressive workload exercise with different added dead space. We hypothesized that increased serial dead space upshifts the VE vs. VCO(2) relationship and that the VE-axis intercept might be an index of dead space ventilation. MEASUREMENTS: All participants performed a cardiopulmonary exercise test with 0, 250 and 500 mL of additional dead space. Since DS does not contribute to gas exchange, ventilation relative to dead space is ventilation at VCO(2) = 0, i.e. VE-axis intercept. We compared dead space volume, estimated dividing VE-axis intercept by the intercept on respiratory rate axis of the respiratory rate vs. VCO(2) relationship with standard method measured DS. MAIN RESULTS: In HF, adding dead space increased VE-axis intercept (+0 mL = 4.98±1.63 L; +250 mL = 9.69±2.91 L; +500 mL = 13.26±3.18 L; p<0.001) and upshifted the VE vs.VCO(2) relationship, with a minor slope rise (+0 mL = 27±4 L; +250 = 28±5; +500 = 29±4; p<0.05). In healthy, adding dead space increased VE-axis intercept (+0 mL = 4.9±1.4 L; +250 = 9.3±2.4; +500 = 13.1±3.04; p<0.001) without slope changes. Measured and estimated dead space volumes were similar both in HF and healthy subjects. CONCLUSIONS: VE-axis intercept is related to dead space ventilation and dead space volume can be non-invasively estimated. |
format | Online Article Text |
id | pubmed-3907547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39075472014-02-04 A Non Invasive Estimate of Dead Space Ventilation from Exercise Measurements Gargiulo, Paola Apostolo, Anna Perrone-Filardi, Pasquale Sciomer, Susanna Palange, Paolo Agostoni, Piergiuseppe PLoS One Research Article RATIONALE: During exercise, heart failure patients (HF) show an out-of-proportion ventilation increase, which in patients with COPD is blunted. When HF and COPD coexist, the ventilatory response to exercise is unpredictable. OBJECTIVES: We evaluated a human model of respiratory impairment in 10 COPD-free HF patients and in 10 healthy subjects, tested with a progressive workload exercise with different added dead space. We hypothesized that increased serial dead space upshifts the VE vs. VCO(2) relationship and that the VE-axis intercept might be an index of dead space ventilation. MEASUREMENTS: All participants performed a cardiopulmonary exercise test with 0, 250 and 500 mL of additional dead space. Since DS does not contribute to gas exchange, ventilation relative to dead space is ventilation at VCO(2) = 0, i.e. VE-axis intercept. We compared dead space volume, estimated dividing VE-axis intercept by the intercept on respiratory rate axis of the respiratory rate vs. VCO(2) relationship with standard method measured DS. MAIN RESULTS: In HF, adding dead space increased VE-axis intercept (+0 mL = 4.98±1.63 L; +250 mL = 9.69±2.91 L; +500 mL = 13.26±3.18 L; p<0.001) and upshifted the VE vs.VCO(2) relationship, with a minor slope rise (+0 mL = 27±4 L; +250 = 28±5; +500 = 29±4; p<0.05). In healthy, adding dead space increased VE-axis intercept (+0 mL = 4.9±1.4 L; +250 = 9.3±2.4; +500 = 13.1±3.04; p<0.001) without slope changes. Measured and estimated dead space volumes were similar both in HF and healthy subjects. CONCLUSIONS: VE-axis intercept is related to dead space ventilation and dead space volume can be non-invasively estimated. Public Library of Science 2014-01-30 /pmc/articles/PMC3907547/ /pubmed/24498096 http://dx.doi.org/10.1371/journal.pone.0087395 Text en © 2014 Gargiulo et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Gargiulo, Paola Apostolo, Anna Perrone-Filardi, Pasquale Sciomer, Susanna Palange, Paolo Agostoni, Piergiuseppe A Non Invasive Estimate of Dead Space Ventilation from Exercise Measurements |
title | A Non Invasive Estimate of Dead Space Ventilation from Exercise Measurements |
title_full | A Non Invasive Estimate of Dead Space Ventilation from Exercise Measurements |
title_fullStr | A Non Invasive Estimate of Dead Space Ventilation from Exercise Measurements |
title_full_unstemmed | A Non Invasive Estimate of Dead Space Ventilation from Exercise Measurements |
title_short | A Non Invasive Estimate of Dead Space Ventilation from Exercise Measurements |
title_sort | non invasive estimate of dead space ventilation from exercise measurements |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907547/ https://www.ncbi.nlm.nih.gov/pubmed/24498096 http://dx.doi.org/10.1371/journal.pone.0087395 |
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