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Limited value of pulse wave analysis in assessing arterial wave reflection and stiffness in the pulmonary artery

We explored the use of the augmentation index (AI) based on pulse wave analysis (PWA) in the pulmonary circulation as a measure of wave reflection and arterial stiffness in individuals with and without pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH). R...

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Autores principales: Su, Junjing, Simonsen, Ulf, Mellemkjaer, Soren, Howard, Luke S., Manisty, Charlotte, Hughes, Alun D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461033/
https://www.ncbi.nlm.nih.gov/pubmed/34558215
http://dx.doi.org/10.14814/phy2.15024
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author Su, Junjing
Simonsen, Ulf
Mellemkjaer, Soren
Howard, Luke S.
Manisty, Charlotte
Hughes, Alun D.
author_facet Su, Junjing
Simonsen, Ulf
Mellemkjaer, Soren
Howard, Luke S.
Manisty, Charlotte
Hughes, Alun D.
author_sort Su, Junjing
collection PubMed
description We explored the use of the augmentation index (AI) based on pulse wave analysis (PWA) in the pulmonary circulation as a measure of wave reflection and arterial stiffness in individuals with and without pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH). Right heart catheterization was performed using a pressure and Doppler flow sensor–tipped catheter to obtain simultaneous pressure and flow velocity measurements in the pulmonary artery in 10 controls, 11 PAH patients, and 11 CTEPH patients. PWA was applied to the measured pressure, while wave intensity analysis (WIA) and wave separation analysis (WSA) were performed using both the pressure and velocity to determine the magnitudes and timings of reflected waves. Type C (AI < 0) pressure waveform dominated in controls and type A (AI > 12%) waveform dominated in PAH patients, while there was a mixture of types A, B, and C among CTEPH patients. AI was greater and the inflection time shorter in CTEPH compared to PAH patients. There was a poor correlation between AI and arterial wave speed as well as measures of wave reflection derived from WIA and WSA. The infection point did not match the timing of the backward compression wave in ~50% of the cases. In patients with type C waveforms, the inflection time correlated well to the timing of the late systolic forward decompression wave caused by ventricular relaxation. In conclusion quantifying pulmonary arterial wave reflection and stiffness using AI based on PWA may be inaccurate and should therefore be discouraged.
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spelling pubmed-84610332021-09-28 Limited value of pulse wave analysis in assessing arterial wave reflection and stiffness in the pulmonary artery Su, Junjing Simonsen, Ulf Mellemkjaer, Soren Howard, Luke S. Manisty, Charlotte Hughes, Alun D. Physiol Rep Original Articles We explored the use of the augmentation index (AI) based on pulse wave analysis (PWA) in the pulmonary circulation as a measure of wave reflection and arterial stiffness in individuals with and without pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH). Right heart catheterization was performed using a pressure and Doppler flow sensor–tipped catheter to obtain simultaneous pressure and flow velocity measurements in the pulmonary artery in 10 controls, 11 PAH patients, and 11 CTEPH patients. PWA was applied to the measured pressure, while wave intensity analysis (WIA) and wave separation analysis (WSA) were performed using both the pressure and velocity to determine the magnitudes and timings of reflected waves. Type C (AI < 0) pressure waveform dominated in controls and type A (AI > 12%) waveform dominated in PAH patients, while there was a mixture of types A, B, and C among CTEPH patients. AI was greater and the inflection time shorter in CTEPH compared to PAH patients. There was a poor correlation between AI and arterial wave speed as well as measures of wave reflection derived from WIA and WSA. The infection point did not match the timing of the backward compression wave in ~50% of the cases. In patients with type C waveforms, the inflection time correlated well to the timing of the late systolic forward decompression wave caused by ventricular relaxation. In conclusion quantifying pulmonary arterial wave reflection and stiffness using AI based on PWA may be inaccurate and should therefore be discouraged. John Wiley and Sons Inc. 2021-09-23 /pmc/articles/PMC8461033/ /pubmed/34558215 http://dx.doi.org/10.14814/phy2.15024 Text en © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Su, Junjing
Simonsen, Ulf
Mellemkjaer, Soren
Howard, Luke S.
Manisty, Charlotte
Hughes, Alun D.
Limited value of pulse wave analysis in assessing arterial wave reflection and stiffness in the pulmonary artery
title Limited value of pulse wave analysis in assessing arterial wave reflection and stiffness in the pulmonary artery
title_full Limited value of pulse wave analysis in assessing arterial wave reflection and stiffness in the pulmonary artery
title_fullStr Limited value of pulse wave analysis in assessing arterial wave reflection and stiffness in the pulmonary artery
title_full_unstemmed Limited value of pulse wave analysis in assessing arterial wave reflection and stiffness in the pulmonary artery
title_short Limited value of pulse wave analysis in assessing arterial wave reflection and stiffness in the pulmonary artery
title_sort limited value of pulse wave analysis in assessing arterial wave reflection and stiffness in the pulmonary artery
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461033/
https://www.ncbi.nlm.nih.gov/pubmed/34558215
http://dx.doi.org/10.14814/phy2.15024
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