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Respiratory Impedance is Associated with Ventilation and Diffusing Capacity in Patients with Idiopathic Pulmonary Fibrosis Combined with Emphysema

PURPOSE: Pulmonary fibrosis and emphysema result in relatively maintained ventilation and reduced diffusing capacity. This pulmonary functional impairment complicates the evaluation of pulmonary function in patients with combined pulmonary fibrosis and emphysema (CPFE). Therefore, a single and easy-...

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Autores principales: Yamamoto, Yuji, Hirata, Haruhiko, Shiroyama, Takayuki, Kuge, Tomoki, Matsumoto, Kinnosuke, Yoneda, Midori, Yamamoto, Makoto, Naito, Yujiro, Suga, Yasuhiko, Fukushima, Kiyoharu, Miyake, Kotaro, Koyama, Shohei, Iwahori, Kota, Nagatomo, Izumi, Takeda, Yoshito, Kumanogoh, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9255903/
https://www.ncbi.nlm.nih.gov/pubmed/35801120
http://dx.doi.org/10.2147/COPD.S368162
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author Yamamoto, Yuji
Hirata, Haruhiko
Shiroyama, Takayuki
Kuge, Tomoki
Matsumoto, Kinnosuke
Yoneda, Midori
Yamamoto, Makoto
Naito, Yujiro
Suga, Yasuhiko
Fukushima, Kiyoharu
Miyake, Kotaro
Koyama, Shohei
Iwahori, Kota
Nagatomo, Izumi
Takeda, Yoshito
Kumanogoh, Atsushi
author_facet Yamamoto, Yuji
Hirata, Haruhiko
Shiroyama, Takayuki
Kuge, Tomoki
Matsumoto, Kinnosuke
Yoneda, Midori
Yamamoto, Makoto
Naito, Yujiro
Suga, Yasuhiko
Fukushima, Kiyoharu
Miyake, Kotaro
Koyama, Shohei
Iwahori, Kota
Nagatomo, Izumi
Takeda, Yoshito
Kumanogoh, Atsushi
author_sort Yamamoto, Yuji
collection PubMed
description PURPOSE: Pulmonary fibrosis and emphysema result in relatively maintained ventilation and reduced diffusing capacity. This pulmonary functional impairment complicates the evaluation of pulmonary function in patients with combined pulmonary fibrosis and emphysema (CPFE). Therefore, a single and easy-to-use pulmonary function index to evaluate patients with CPFE warrants further studies. Respiratory impedance can easily be provided by oscillometry and might be a candidate index to evaluate pulmonary function in patients with CPFE. As a preliminary study to assess the utility of respiratory impedance, we investigated the associations of physiological indices, including respiratory impedance, in patients with idiopathic pulmonary fibrosis (IPF) with and without emphysema. PATIENTS AND METHODS: This retrospective study evaluated patients with IPF who did and did not satisfy the diagnostic criteria of CPFE. All patients underwent oscillometry, spirometry, and diffusing capacity for carbon monoxide (D(LCO)). Correlations of the obtained physiological indices were analyzed. RESULTS: In total, 47 patients were included (18 and 29 patients with CPFE and IPF, respectively). Respiratory reactance (Xrs) at 5 Hz (X5) in the inspiratory phase was associated with forced vital capacity (FVC) % predicted in patients with CPFE (r(S)=0.576, P=0.012) and IPF (r(S)=0.539, P=0.003). Inspiratory X5 positively correlated with D(LCO) % predicted only in patients CPFE (r(S)=0.637, P=0.004). CONCLUSION: Emphysema might associate Xrs with ventilation and diffusing capacity in patients with IPF and emphysema. Given the multiple correlations of Xrs with FVC and D(LCO), this study warrants further studies to verify the utility of oscillometry in a large-scale study for patients with CPFE.
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spelling pubmed-92559032022-07-06 Respiratory Impedance is Associated with Ventilation and Diffusing Capacity in Patients with Idiopathic Pulmonary Fibrosis Combined with Emphysema Yamamoto, Yuji Hirata, Haruhiko Shiroyama, Takayuki Kuge, Tomoki Matsumoto, Kinnosuke Yoneda, Midori Yamamoto, Makoto Naito, Yujiro Suga, Yasuhiko Fukushima, Kiyoharu Miyake, Kotaro Koyama, Shohei Iwahori, Kota Nagatomo, Izumi Takeda, Yoshito Kumanogoh, Atsushi Int J Chron Obstruct Pulmon Dis Original Research PURPOSE: Pulmonary fibrosis and emphysema result in relatively maintained ventilation and reduced diffusing capacity. This pulmonary functional impairment complicates the evaluation of pulmonary function in patients with combined pulmonary fibrosis and emphysema (CPFE). Therefore, a single and easy-to-use pulmonary function index to evaluate patients with CPFE warrants further studies. Respiratory impedance can easily be provided by oscillometry and might be a candidate index to evaluate pulmonary function in patients with CPFE. As a preliminary study to assess the utility of respiratory impedance, we investigated the associations of physiological indices, including respiratory impedance, in patients with idiopathic pulmonary fibrosis (IPF) with and without emphysema. PATIENTS AND METHODS: This retrospective study evaluated patients with IPF who did and did not satisfy the diagnostic criteria of CPFE. All patients underwent oscillometry, spirometry, and diffusing capacity for carbon monoxide (D(LCO)). Correlations of the obtained physiological indices were analyzed. RESULTS: In total, 47 patients were included (18 and 29 patients with CPFE and IPF, respectively). Respiratory reactance (Xrs) at 5 Hz (X5) in the inspiratory phase was associated with forced vital capacity (FVC) % predicted in patients with CPFE (r(S)=0.576, P=0.012) and IPF (r(S)=0.539, P=0.003). Inspiratory X5 positively correlated with D(LCO) % predicted only in patients CPFE (r(S)=0.637, P=0.004). CONCLUSION: Emphysema might associate Xrs with ventilation and diffusing capacity in patients with IPF and emphysema. Given the multiple correlations of Xrs with FVC and D(LCO), this study warrants further studies to verify the utility of oscillometry in a large-scale study for patients with CPFE. Dove 2022-07-01 /pmc/articles/PMC9255903/ /pubmed/35801120 http://dx.doi.org/10.2147/COPD.S368162 Text en © 2022 Yamamoto et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Yamamoto, Yuji
Hirata, Haruhiko
Shiroyama, Takayuki
Kuge, Tomoki
Matsumoto, Kinnosuke
Yoneda, Midori
Yamamoto, Makoto
Naito, Yujiro
Suga, Yasuhiko
Fukushima, Kiyoharu
Miyake, Kotaro
Koyama, Shohei
Iwahori, Kota
Nagatomo, Izumi
Takeda, Yoshito
Kumanogoh, Atsushi
Respiratory Impedance is Associated with Ventilation and Diffusing Capacity in Patients with Idiopathic Pulmonary Fibrosis Combined with Emphysema
title Respiratory Impedance is Associated with Ventilation and Diffusing Capacity in Patients with Idiopathic Pulmonary Fibrosis Combined with Emphysema
title_full Respiratory Impedance is Associated with Ventilation and Diffusing Capacity in Patients with Idiopathic Pulmonary Fibrosis Combined with Emphysema
title_fullStr Respiratory Impedance is Associated with Ventilation and Diffusing Capacity in Patients with Idiopathic Pulmonary Fibrosis Combined with Emphysema
title_full_unstemmed Respiratory Impedance is Associated with Ventilation and Diffusing Capacity in Patients with Idiopathic Pulmonary Fibrosis Combined with Emphysema
title_short Respiratory Impedance is Associated with Ventilation and Diffusing Capacity in Patients with Idiopathic Pulmonary Fibrosis Combined with Emphysema
title_sort respiratory impedance is associated with ventilation and diffusing capacity in patients with idiopathic pulmonary fibrosis combined with emphysema
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9255903/
https://www.ncbi.nlm.nih.gov/pubmed/35801120
http://dx.doi.org/10.2147/COPD.S368162
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