High-flow nasal oxygen reduces endotracheal intubation: a randomized clinical trial

Background: The benefits of high-flow nasal cannula (HFNC) as primary intervention in patients with acute hypoxemic respiratory failure (AHRF) are still a matter in debate. Our objective was to compare HFNC therapy versus conventional oxygen therapy (COT) in the prevention of endotracheal intubation...

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Main Authors: Ricardo Andino, Gema Vega, Sandra Karina Pacheco, Nuria Arevalillo, Ana Leal, Laura Fernández, María Jesús Rodriguez
Format: Article
Language:English
Published: SAGE Publishing 2020-09-01
Series:Therapeutic Advances in Respiratory Disease
Online Access:https://doi.org/10.1177/1753466620956459
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spelling doaj-cd08fb3e48794a9aaf13f0120ef97c042020-11-25T02:46:18ZengSAGE PublishingTherapeutic Advances in Respiratory Disease1753-46662020-09-011410.1177/1753466620956459High-flow nasal oxygen reduces endotracheal intubation: a randomized clinical trialRicardo AndinoGema VegaSandra Karina PachecoNuria ArevalilloAna LealLaura FernándezMaría Jesús RodriguezBackground: The benefits of high-flow nasal cannula (HFNC) as primary intervention in patients with acute hypoxemic respiratory failure (AHRF) are still a matter in debate. Our objective was to compare HFNC therapy versus conventional oxygen therapy (COT) in the prevention of endotracheal intubation in this group of patients. Methods: An open-label, controlled and single-centre clinical trial was conducted in patients with severe AHRF, defined by a PaO 2 /FIO 2 ratio ⩽200, to compare HFNC with a control group (CG) treated by COT delivered through a face mask, with the need to perform intubation as the primary outcome. The secondary outcomes included tolerance of the HFNC device and to look for the predictive factors for intubation in these patients. Results: A total of 46 patients were included (22 in the COT group and 24 in the HFNC group) 48% of whom needed intubation: 63% in the COT group and 33% in the HFNC group, with significant differences both in intention to treat [χ 2  = 4.2; p  = 0.04, relative risk (RR) = 0.5; confidence interval (CI) 95%: 0.3–1.0] and also in treatment analysis (χ 2  = 4.7; p  = 0.03; RR = 0.5; IC 95%: 0.3–0.9) We obtained a number needed to treat (NNT) = 3 patients treated to avoid an intubation. Intubation occurred significantly later in the HFNC group. Estimated PaO 2 /FIO 2 , respiratory rate and dyspnea were significantly better in the HFNC group. Patients treated with HFNC who required intubation presented significant worsening after the first 8 h, as compared with non-intubated HFNC group patients. Mortality was 22% with no differences. The HFNC group patients were hospitalized for almost half of the time in the intensive care unit (ICU) and in the ward, with significantly less hospital length of stay. A total of 14 patients in the HFNC group (58%) complained of excessive heat and 17% of noise; 3 patients did not tolerate HFNC. Conclusion: Patients with severe acute hypoxemic respiratory failure who tolerate HFNC present a significantly lower need for endotracheal intubation compared with conventional oxygen therapy. Clinical Trial Register EUDRA CT number: 2012-001671-36 The reviews of this paper are available via the supplemental material section.https://doi.org/10.1177/1753466620956459
collection DOAJ
language English
format Article
sources DOAJ
author Ricardo Andino
Gema Vega
Sandra Karina Pacheco
Nuria Arevalillo
Ana Leal
Laura Fernández
María Jesús Rodriguez
spellingShingle Ricardo Andino
Gema Vega
Sandra Karina Pacheco
Nuria Arevalillo
Ana Leal
Laura Fernández
María Jesús Rodriguez
High-flow nasal oxygen reduces endotracheal intubation: a randomized clinical trial
Therapeutic Advances in Respiratory Disease
author_facet Ricardo Andino
Gema Vega
Sandra Karina Pacheco
Nuria Arevalillo
Ana Leal
Laura Fernández
María Jesús Rodriguez
author_sort Ricardo Andino
title High-flow nasal oxygen reduces endotracheal intubation: a randomized clinical trial
title_short High-flow nasal oxygen reduces endotracheal intubation: a randomized clinical trial
title_full High-flow nasal oxygen reduces endotracheal intubation: a randomized clinical trial
title_fullStr High-flow nasal oxygen reduces endotracheal intubation: a randomized clinical trial
title_full_unstemmed High-flow nasal oxygen reduces endotracheal intubation: a randomized clinical trial
title_sort high-flow nasal oxygen reduces endotracheal intubation: a randomized clinical trial
publisher SAGE Publishing
series Therapeutic Advances in Respiratory Disease
issn 1753-4666
publishDate 2020-09-01
description Background: The benefits of high-flow nasal cannula (HFNC) as primary intervention in patients with acute hypoxemic respiratory failure (AHRF) are still a matter in debate. Our objective was to compare HFNC therapy versus conventional oxygen therapy (COT) in the prevention of endotracheal intubation in this group of patients. Methods: An open-label, controlled and single-centre clinical trial was conducted in patients with severe AHRF, defined by a PaO 2 /FIO 2 ratio ⩽200, to compare HFNC with a control group (CG) treated by COT delivered through a face mask, with the need to perform intubation as the primary outcome. The secondary outcomes included tolerance of the HFNC device and to look for the predictive factors for intubation in these patients. Results: A total of 46 patients were included (22 in the COT group and 24 in the HFNC group) 48% of whom needed intubation: 63% in the COT group and 33% in the HFNC group, with significant differences both in intention to treat [χ 2  = 4.2; p  = 0.04, relative risk (RR) = 0.5; confidence interval (CI) 95%: 0.3–1.0] and also in treatment analysis (χ 2  = 4.7; p  = 0.03; RR = 0.5; IC 95%: 0.3–0.9) We obtained a number needed to treat (NNT) = 3 patients treated to avoid an intubation. Intubation occurred significantly later in the HFNC group. Estimated PaO 2 /FIO 2 , respiratory rate and dyspnea were significantly better in the HFNC group. Patients treated with HFNC who required intubation presented significant worsening after the first 8 h, as compared with non-intubated HFNC group patients. Mortality was 22% with no differences. The HFNC group patients were hospitalized for almost half of the time in the intensive care unit (ICU) and in the ward, with significantly less hospital length of stay. A total of 14 patients in the HFNC group (58%) complained of excessive heat and 17% of noise; 3 patients did not tolerate HFNC. Conclusion: Patients with severe acute hypoxemic respiratory failure who tolerate HFNC present a significantly lower need for endotracheal intubation compared with conventional oxygen therapy. Clinical Trial Register EUDRA CT number: 2012-001671-36 The reviews of this paper are available via the supplemental material section.
url https://doi.org/10.1177/1753466620956459
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