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Negative results for ketamine use in severe acute bronchospasm: a randomised controlled trial

Background: Ketamine has bronchodilation properties. The aim of the single-centre, evaluator-blinded, randomised clinical trial study was to evaluate whether continuous infusion of ketamine is associated with improvement in respiratory mechanics correlated with bronchospasm relief, as compared with...

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Autores principales: Nedel, Wagner L., Costa, Rafael L., Mendez, Gabriela, Marin, Luiz G., Vargas, Taiani, Marques, Leonardo da S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172964/
https://www.ncbi.nlm.nih.gov/pubmed/32876408
http://dx.doi.org/10.5114/ait.2020.97765
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author Nedel, Wagner L.
Costa, Rafael L.
Mendez, Gabriela
Marin, Luiz G.
Vargas, Taiani
Marques, Leonardo da S.
author_facet Nedel, Wagner L.
Costa, Rafael L.
Mendez, Gabriela
Marin, Luiz G.
Vargas, Taiani
Marques, Leonardo da S.
author_sort Nedel, Wagner L.
collection PubMed
description Background: Ketamine has bronchodilation properties. The aim of the single-centre, evaluator-blinded, randomised clinical trial study was to evaluate whether continuous infusion of ketamine is associated with improvement in respiratory mechanics correlated with bronchospasm relief, as compared with continuous infusion of fentanyl. Methods: Adult patients submitted to invasive mechanical ventilation were included if they had an acute severe bronchospasm, due to status asthmaticus or COPD exacerbation. They were randomised to ketamine or a standard IV analgesia with fentanyl, both in bolus and continuous infusion. Measurements of respiratory mechanics (airway resistance – R(smax), dynamic compliance – C(dyn) and intrinsic PEEP – PEEPi) both at baseline and 3 and 24 h after randomisation were performed. The main outcome of this study was to evaluate the improvement of R(smax) in 3 h of continuous infusion of the study drugs. Results: Ketamine use was not associated with greater reduction in R(smax) when compared with fentanyl, either after 3 h (0 cm H(2)O L(−1) s(−1) ± 6 vs. −3 cm H(2)O L(−1) s(−1) ± 7.7, respectively; P = 0.16) or after 24 h (−3 cm H(2)O L(−1) s(−1) ± 17 vs. −3.5 cm H(2)O L(−1) s(−1) ± 13.7, respectively; P = 0.73). Patients randomized to the ketamine group did not have better improvements in delta PEEPi as compared with fentanyl in 3 h (P = 0.77) or in 24 h (P = 0.72). Conclusions: In this study, ketamine use was not associated with improvement in ventilatory variables associated with bronchospasm.
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spelling pubmed-101729642023-05-17 Negative results for ketamine use in severe acute bronchospasm: a randomised controlled trial Nedel, Wagner L. Costa, Rafael L. Mendez, Gabriela Marin, Luiz G. Vargas, Taiani Marques, Leonardo da S. Anaesthesiol Intensive Ther Original and Clinical Articles Background: Ketamine has bronchodilation properties. The aim of the single-centre, evaluator-blinded, randomised clinical trial study was to evaluate whether continuous infusion of ketamine is associated with improvement in respiratory mechanics correlated with bronchospasm relief, as compared with continuous infusion of fentanyl. Methods: Adult patients submitted to invasive mechanical ventilation were included if they had an acute severe bronchospasm, due to status asthmaticus or COPD exacerbation. They were randomised to ketamine or a standard IV analgesia with fentanyl, both in bolus and continuous infusion. Measurements of respiratory mechanics (airway resistance – R(smax), dynamic compliance – C(dyn) and intrinsic PEEP – PEEPi) both at baseline and 3 and 24 h after randomisation were performed. The main outcome of this study was to evaluate the improvement of R(smax) in 3 h of continuous infusion of the study drugs. Results: Ketamine use was not associated with greater reduction in R(smax) when compared with fentanyl, either after 3 h (0 cm H(2)O L(−1) s(−1) ± 6 vs. −3 cm H(2)O L(−1) s(−1) ± 7.7, respectively; P = 0.16) or after 24 h (−3 cm H(2)O L(−1) s(−1) ± 17 vs. −3.5 cm H(2)O L(−1) s(−1) ± 13.7, respectively; P = 0.73). Patients randomized to the ketamine group did not have better improvements in delta PEEPi as compared with fentanyl in 3 h (P = 0.77) or in 24 h (P = 0.72). Conclusions: In this study, ketamine use was not associated with improvement in ventilatory variables associated with bronchospasm. Termedia Publishing House 2020-08-06 2020-08 /pmc/articles/PMC10172964/ /pubmed/32876408 http://dx.doi.org/10.5114/ait.2020.97765 Text en Copyright © Polish Society of Anaesthesiology and Intensive Therapy https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access journal, all articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/) ), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original and Clinical Articles
Nedel, Wagner L.
Costa, Rafael L.
Mendez, Gabriela
Marin, Luiz G.
Vargas, Taiani
Marques, Leonardo da S.
Negative results for ketamine use in severe acute bronchospasm: a randomised controlled trial
title Negative results for ketamine use in severe acute bronchospasm: a randomised controlled trial
title_full Negative results for ketamine use in severe acute bronchospasm: a randomised controlled trial
title_fullStr Negative results for ketamine use in severe acute bronchospasm: a randomised controlled trial
title_full_unstemmed Negative results for ketamine use in severe acute bronchospasm: a randomised controlled trial
title_short Negative results for ketamine use in severe acute bronchospasm: a randomised controlled trial
title_sort negative results for ketamine use in severe acute bronchospasm: a randomised controlled trial
topic Original and Clinical Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172964/
https://www.ncbi.nlm.nih.gov/pubmed/32876408
http://dx.doi.org/10.5114/ait.2020.97765
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