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Mouthpiece ventilation in the management of dyspnea: A single-arm pilot study

BACKGROUND: Noninvasive ventilation may relieve dyspnea in advanced diseases, but noninvasive ventilation through mouthpiece has not been tested in palliative care. AIM: To assess the feasibility of mouthpiece ventilation in relieving dyspnea among patients with advanced disease. DESIGN: In this pro...

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Autores principales: Lehto, Juho T, Leivo-Korpela, Sirpa, Korhonen, Tarja, Rantala, Heidi A, Raunio, Hanna, Lyly-Yrjänäinen, Tiina, Lehtimäki, Lauri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495670/
https://www.ncbi.nlm.nih.gov/pubmed/32579086
http://dx.doi.org/10.1177/0269216320935003
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author Lehto, Juho T
Leivo-Korpela, Sirpa
Korhonen, Tarja
Rantala, Heidi A
Raunio, Hanna
Lyly-Yrjänäinen, Tiina
Lehtimäki, Lauri
author_facet Lehto, Juho T
Leivo-Korpela, Sirpa
Korhonen, Tarja
Rantala, Heidi A
Raunio, Hanna
Lyly-Yrjänäinen, Tiina
Lehtimäki, Lauri
author_sort Lehto, Juho T
collection PubMed
description BACKGROUND: Noninvasive ventilation may relieve dyspnea in advanced diseases, but noninvasive ventilation through mouthpiece has not been tested in palliative care. AIM: To assess the feasibility of mouthpiece ventilation in relieving dyspnea among patients with advanced disease. DESIGN: In this prospective single-arm pilot study, the change in dyspnea by mouthpiece ventilation was measured with numeric rating scale (0–10) and 100-mm visual analogue scale. Overall, benefit and adverse events of the therapy were also assessed. SETTING/PARTICIPANTS: Twenty-two patients with an advanced disease and dyspnea from the Tampere University Hospital or Pirkanmaa Hospice were treated with mouthpiece ventilation. The patients used mouthpiece ventilation as long as they preferred, but for a minimum of 5 min. RESULTS: After the treatment period lasting a median of 13.5 min, mean decrease in dyspnea was −1.1 (95 % confidence interval = −2.2 to −0.1, p = 0.034) on numeric rating scale and −11.8 mm (95 % confidence interval = −19.9 to −3.7, p = 0.006) on visual analogue scale. Nonetheless, there was a high variability in this effect between individual patients. About half of the patients found mouthpiece ventilation beneficial. No serious adverse events occurred, but dry mouth was the most common adverse event. Anxiety did not increase with mouthpiece ventilation. CONCLUSION: Mouthpiece ventilation is feasible and may relieve dyspnea in some patients with an advanced disease. Further studies are needed, and these might concentrate on stable patients in early palliative care. Before initiation, this study was registered at clinicaltrials.gov (study no. NCT03012737).
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spelling pubmed-74956702020-09-24 Mouthpiece ventilation in the management of dyspnea: A single-arm pilot study Lehto, Juho T Leivo-Korpela, Sirpa Korhonen, Tarja Rantala, Heidi A Raunio, Hanna Lyly-Yrjänäinen, Tiina Lehtimäki, Lauri Palliat Med Short Reports BACKGROUND: Noninvasive ventilation may relieve dyspnea in advanced diseases, but noninvasive ventilation through mouthpiece has not been tested in palliative care. AIM: To assess the feasibility of mouthpiece ventilation in relieving dyspnea among patients with advanced disease. DESIGN: In this prospective single-arm pilot study, the change in dyspnea by mouthpiece ventilation was measured with numeric rating scale (0–10) and 100-mm visual analogue scale. Overall, benefit and adverse events of the therapy were also assessed. SETTING/PARTICIPANTS: Twenty-two patients with an advanced disease and dyspnea from the Tampere University Hospital or Pirkanmaa Hospice were treated with mouthpiece ventilation. The patients used mouthpiece ventilation as long as they preferred, but for a minimum of 5 min. RESULTS: After the treatment period lasting a median of 13.5 min, mean decrease in dyspnea was −1.1 (95 % confidence interval = −2.2 to −0.1, p = 0.034) on numeric rating scale and −11.8 mm (95 % confidence interval = −19.9 to −3.7, p = 0.006) on visual analogue scale. Nonetheless, there was a high variability in this effect between individual patients. About half of the patients found mouthpiece ventilation beneficial. No serious adverse events occurred, but dry mouth was the most common adverse event. Anxiety did not increase with mouthpiece ventilation. CONCLUSION: Mouthpiece ventilation is feasible and may relieve dyspnea in some patients with an advanced disease. Further studies are needed, and these might concentrate on stable patients in early palliative care. Before initiation, this study was registered at clinicaltrials.gov (study no. NCT03012737). SAGE Publications 2020-06-24 2020-10 /pmc/articles/PMC7495670/ /pubmed/32579086 http://dx.doi.org/10.1177/0269216320935003 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Short Reports
Lehto, Juho T
Leivo-Korpela, Sirpa
Korhonen, Tarja
Rantala, Heidi A
Raunio, Hanna
Lyly-Yrjänäinen, Tiina
Lehtimäki, Lauri
Mouthpiece ventilation in the management of dyspnea: A single-arm pilot study
title Mouthpiece ventilation in the management of dyspnea: A single-arm pilot study
title_full Mouthpiece ventilation in the management of dyspnea: A single-arm pilot study
title_fullStr Mouthpiece ventilation in the management of dyspnea: A single-arm pilot study
title_full_unstemmed Mouthpiece ventilation in the management of dyspnea: A single-arm pilot study
title_short Mouthpiece ventilation in the management of dyspnea: A single-arm pilot study
title_sort mouthpiece ventilation in the management of dyspnea: a single-arm pilot study
topic Short Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495670/
https://www.ncbi.nlm.nih.gov/pubmed/32579086
http://dx.doi.org/10.1177/0269216320935003
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