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Elevated PaCO(2) levels increase pulmonary artery pressure
Permissive hypercapnia is commonly used in mechanically ventilated patients to avoid lung injury but its effect on pulmonary artery pressure (PAP) is still unclear, particularly in combination with tidal volume (Vt). Therefore, an in vivo study was performed on adult rabbits ventilated with low (9 m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358613/ https://www.ncbi.nlm.nih.gov/pubmed/35440248 http://dx.doi.org/10.1177/00368504221094161 |
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author | Triantaris, Apostolos Aidonidis, Isaak Hatziefthimiou, Apostolia Gourgoulianis, Konstantinos Zakynthinos, Georgios Makris, Demosthenes |
author_facet | Triantaris, Apostolos Aidonidis, Isaak Hatziefthimiou, Apostolia Gourgoulianis, Konstantinos Zakynthinos, Georgios Makris, Demosthenes |
author_sort | Triantaris, Apostolos |
collection | PubMed |
description | Permissive hypercapnia is commonly used in mechanically ventilated patients to avoid lung injury but its effect on pulmonary artery pressure (PAP) is still unclear, particularly in combination with tidal volume (Vt). Therefore, an in vivo study was performed on adult rabbits ventilated with low (9 ml/Kg, LVt group) or high (15 ml/Kg, HVt group) tidal volume (Vt) and alterations in PAP were estimated. Both groups of animals initially were ventilated with FiO(2) 0.3 (Normocapnia-1) followed by inhalation of enriched CO(2) gas mixture (FiCO(2) 0.10) to develop hypercapnia (Hypercapnia-1). After 30 min of hypercapnia, animals were re-ventilated with FiO(2) 0.3 to develop normocapnia (Normocapnia-2) again and then with FiCO(2) 0.10 to develop hypercapnia (Hypercapnia-2). Systolic, diastolic and mean PAP were assessed with a catheter in the pulmonary artery. In HP-1 and HP-2, PaCO(2) increased (p < 0.0001) in both LVt and HVt animals compared to baseline values. pH decreased to ≈7.2 in HP-1 and ≈7.1 in HP −2. In normocapnia, the rise in Vt from 9 to 15 ml/Kg induced an increase in static compliance (Cstat), plateau airway pressure (Pplat) and PAP. Hypercapnia increased PAP in either LVt or HVt animals without significant effect on Cstat or Pplat. A two-way ANOVA revealed that there was not a statistically significant interaction between the effects of hypercapnia and tidal volume on mPAP (p = 0.76). In conclusion, increased Vt per se induced an increase in Cstat, Pplat and PAP in normocapnia. Hypercapnia increased PAP in rabbits ventilated with low or high Vt but this effect was not long-lasting. |
format | Online Article Text |
id | pubmed-10358613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-103586132023-08-09 Elevated PaCO(2) levels increase pulmonary artery pressure Triantaris, Apostolos Aidonidis, Isaak Hatziefthimiou, Apostolia Gourgoulianis, Konstantinos Zakynthinos, Georgios Makris, Demosthenes Sci Prog Original Manuscript Permissive hypercapnia is commonly used in mechanically ventilated patients to avoid lung injury but its effect on pulmonary artery pressure (PAP) is still unclear, particularly in combination with tidal volume (Vt). Therefore, an in vivo study was performed on adult rabbits ventilated with low (9 ml/Kg, LVt group) or high (15 ml/Kg, HVt group) tidal volume (Vt) and alterations in PAP were estimated. Both groups of animals initially were ventilated with FiO(2) 0.3 (Normocapnia-1) followed by inhalation of enriched CO(2) gas mixture (FiCO(2) 0.10) to develop hypercapnia (Hypercapnia-1). After 30 min of hypercapnia, animals were re-ventilated with FiO(2) 0.3 to develop normocapnia (Normocapnia-2) again and then with FiCO(2) 0.10 to develop hypercapnia (Hypercapnia-2). Systolic, diastolic and mean PAP were assessed with a catheter in the pulmonary artery. In HP-1 and HP-2, PaCO(2) increased (p < 0.0001) in both LVt and HVt animals compared to baseline values. pH decreased to ≈7.2 in HP-1 and ≈7.1 in HP −2. In normocapnia, the rise in Vt from 9 to 15 ml/Kg induced an increase in static compliance (Cstat), plateau airway pressure (Pplat) and PAP. Hypercapnia increased PAP in either LVt or HVt animals without significant effect on Cstat or Pplat. A two-way ANOVA revealed that there was not a statistically significant interaction between the effects of hypercapnia and tidal volume on mPAP (p = 0.76). In conclusion, increased Vt per se induced an increase in Cstat, Pplat and PAP in normocapnia. Hypercapnia increased PAP in rabbits ventilated with low or high Vt but this effect was not long-lasting. SAGE Publications 2022-04-19 /pmc/articles/PMC10358613/ /pubmed/35440248 http://dx.doi.org/10.1177/00368504221094161 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Manuscript Triantaris, Apostolos Aidonidis, Isaak Hatziefthimiou, Apostolia Gourgoulianis, Konstantinos Zakynthinos, Georgios Makris, Demosthenes Elevated PaCO(2) levels increase pulmonary artery pressure |
title | Elevated PaCO(2) levels increase pulmonary artery pressure |
title_full | Elevated PaCO(2) levels increase pulmonary artery pressure |
title_fullStr | Elevated PaCO(2) levels increase pulmonary artery pressure |
title_full_unstemmed | Elevated PaCO(2) levels increase pulmonary artery pressure |
title_short | Elevated PaCO(2) levels increase pulmonary artery pressure |
title_sort | elevated paco(2) levels increase pulmonary artery pressure |
topic | Original Manuscript |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358613/ https://www.ncbi.nlm.nih.gov/pubmed/35440248 http://dx.doi.org/10.1177/00368504221094161 |
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