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Inhaled furosemide for relief of air hunger versus sense of breathing effort: a randomized controlled trial

BACKGROUND: Inhaled furosemide offers a potentially novel treatment for dyspnoea, which may reflect modulation of pulmonary stretch receptor feedback to the brain. Specificity of relief is unclear because different neural pathways may account for different components of clinical dyspnoea. Our object...

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Autores principales: Grogono, Joanna C., Butler, Clare, Izadi, Hooshang, Moosavi, Shakeeb H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148783/
https://www.ncbi.nlm.nih.gov/pubmed/30236110
http://dx.doi.org/10.1186/s12931-018-0886-9
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author Grogono, Joanna C.
Butler, Clare
Izadi, Hooshang
Moosavi, Shakeeb H.
author_facet Grogono, Joanna C.
Butler, Clare
Izadi, Hooshang
Moosavi, Shakeeb H.
author_sort Grogono, Joanna C.
collection PubMed
description BACKGROUND: Inhaled furosemide offers a potentially novel treatment for dyspnoea, which may reflect modulation of pulmonary stretch receptor feedback to the brain. Specificity of relief is unclear because different neural pathways may account for different components of clinical dyspnoea. Our objective was to evaluate if inhaled furosemide relieves the air hunger component (uncomfortable urge to breathe) but not the sense of breathing work/effort of dyspnoea. METHODS: A randomised, double blind, placebo-controlled crossover trial in 16 healthy volunteers studied in a university research laboratory. Each participant received 3 mist inhalations (either 40 mg furosemide or 4 ml saline) separated by 30–60 min on 2 test days. Each participant was randomised to mist order ‘furosemide-saline-furosemide’ (n- = 8) or ‘saline-furosemide-saline’ (n = 8) on both days. One day involved hypercapnic air hunger tests (mean ± SD PCO(2) = 50 ± 3.7 mmHg; constrained ventilation = 9 ± 1.5 L/min), the other involved work/effort tests with targeted ventilation (17 ± 3.1 L/min) and external resistive load (20cmH(2)O/L/s). Primary outcome was ratings of air hunger or work/effort every 15 s on a visual analogue scale. During saline inhalations, 1.5 mg furosemide was infused intravenously to match the expected systemic absorption from the lungs when furosemide is inhaled. Corresponding infusions of saline during furosemide inhalations maintained procedural blinding. Average visual analogue scale ratings (%full scale) during the last minute of air hunger or work/effort stimuli were analysed using Linear Mixed Methods. RESULTS: Data from all 16 participants were analysed. Inhaled furosemide relative to inhaled saline significantly improved visual analogues scale ratings of air hunger (Least Squares Mean ± SE − 9.7 ± 2%; p = 0.0015) but not work/effort (+ 1.6 ± 2%; p = 0.903). There were no significant adverse events. CONCLUSIONS: Inhaled furosemide was effective at relieving laboratory induced air hunger but not work/effort in healthy adults; this is consistent with the notion that modulation of pulmonary stretch receptor feedback by inhaled furosemide leads to dyspnoea relief that is specific to air hunger, the most unpleasant quality of dyspnoea. FUNDING: Oxford Brookes University Central Research Fund. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02881866. Retrospectively registered on 29th August 2018.
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spelling pubmed-61487832018-09-24 Inhaled furosemide for relief of air hunger versus sense of breathing effort: a randomized controlled trial Grogono, Joanna C. Butler, Clare Izadi, Hooshang Moosavi, Shakeeb H. Respir Res Research BACKGROUND: Inhaled furosemide offers a potentially novel treatment for dyspnoea, which may reflect modulation of pulmonary stretch receptor feedback to the brain. Specificity of relief is unclear because different neural pathways may account for different components of clinical dyspnoea. Our objective was to evaluate if inhaled furosemide relieves the air hunger component (uncomfortable urge to breathe) but not the sense of breathing work/effort of dyspnoea. METHODS: A randomised, double blind, placebo-controlled crossover trial in 16 healthy volunteers studied in a university research laboratory. Each participant received 3 mist inhalations (either 40 mg furosemide or 4 ml saline) separated by 30–60 min on 2 test days. Each participant was randomised to mist order ‘furosemide-saline-furosemide’ (n- = 8) or ‘saline-furosemide-saline’ (n = 8) on both days. One day involved hypercapnic air hunger tests (mean ± SD PCO(2) = 50 ± 3.7 mmHg; constrained ventilation = 9 ± 1.5 L/min), the other involved work/effort tests with targeted ventilation (17 ± 3.1 L/min) and external resistive load (20cmH(2)O/L/s). Primary outcome was ratings of air hunger or work/effort every 15 s on a visual analogue scale. During saline inhalations, 1.5 mg furosemide was infused intravenously to match the expected systemic absorption from the lungs when furosemide is inhaled. Corresponding infusions of saline during furosemide inhalations maintained procedural blinding. Average visual analogue scale ratings (%full scale) during the last minute of air hunger or work/effort stimuli were analysed using Linear Mixed Methods. RESULTS: Data from all 16 participants were analysed. Inhaled furosemide relative to inhaled saline significantly improved visual analogues scale ratings of air hunger (Least Squares Mean ± SE − 9.7 ± 2%; p = 0.0015) but not work/effort (+ 1.6 ± 2%; p = 0.903). There were no significant adverse events. CONCLUSIONS: Inhaled furosemide was effective at relieving laboratory induced air hunger but not work/effort in healthy adults; this is consistent with the notion that modulation of pulmonary stretch receptor feedback by inhaled furosemide leads to dyspnoea relief that is specific to air hunger, the most unpleasant quality of dyspnoea. FUNDING: Oxford Brookes University Central Research Fund. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02881866. Retrospectively registered on 29th August 2018. BioMed Central 2018-09-20 2018 /pmc/articles/PMC6148783/ /pubmed/30236110 http://dx.doi.org/10.1186/s12931-018-0886-9 Text en © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Grogono, Joanna C.
Butler, Clare
Izadi, Hooshang
Moosavi, Shakeeb H.
Inhaled furosemide for relief of air hunger versus sense of breathing effort: a randomized controlled trial
title Inhaled furosemide for relief of air hunger versus sense of breathing effort: a randomized controlled trial
title_full Inhaled furosemide for relief of air hunger versus sense of breathing effort: a randomized controlled trial
title_fullStr Inhaled furosemide for relief of air hunger versus sense of breathing effort: a randomized controlled trial
title_full_unstemmed Inhaled furosemide for relief of air hunger versus sense of breathing effort: a randomized controlled trial
title_short Inhaled furosemide for relief of air hunger versus sense of breathing effort: a randomized controlled trial
title_sort inhaled furosemide for relief of air hunger versus sense of breathing effort: a randomized controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148783/
https://www.ncbi.nlm.nih.gov/pubmed/30236110
http://dx.doi.org/10.1186/s12931-018-0886-9
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