BMJ Open (Feb 2021)

Comparison of high-flow nasal oxygen therapy and non-invasive ventilation in ICU patients with acute respiratory failure and a do-not-intubate orders: a multicentre prospective study OXYPAL

  • Denis Frasca,
  • Christophe Guitton,
  • Jean-Pierre Frat,
  • Stephan Ehrmann,
  • Nicolas Terzi,
  • Damien Contou,
  • Jean-Pierre Quenot,
  • Saad Nseir,
  • Didier Thévenin,
  • Arnaud W Thille,
  • Bertrand Guidet,
  • Laura Federici,
  • Jean Reignier,
  • René Robert,
  • Christophe Vinsonneau,
  • Michel Djibré,
  • C Girault,
  • Suela Demiri,
  • Juliette Masse,
  • Olivier Lesieur,
  • Pascal Beuret,
  • Julie Badin,
  • Dalila Benzekri-Llefevre,
  • Hassène Rahmani,
  • Laurent Argaud Argaud,
  • Erwan I'her,
  • Khaldoune Kuteifan,
  • Francois Thouy,
  • Martial Thyrault,
  • Juliette Audibert,
  • Alexandre Boyer,
  • Riad Chelha,
  • G Piton,
  • Nadia Aissaoui

DOI
https://doi.org/10.1136/bmjopen-2020-045659
Journal volume & issue
Vol. 11, no. 2

Abstract

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Introduction A palliative approach to intensive care unit (ICU) patients with acute respiratory failure and a do-not-intubate order corresponds to a poorly evaluated target for non-invasive oxygenation treatments. Survival alone should not be the only target; it also matters to avoid discomfort and to restore the patient’s quality of life. We aim to conduct a prospective multicentre observational study to analyse clinical practices and their impact on outcomes of palliative high-flow nasal oxygen therapy (HFOT) and non-invasive ventilation (NIV) in ICU patients with do-not-intubate orders.Methods and analysis This is an investigator-initiated, multicentre prospective observational cohort study comparing the three following strategies of oxygenation: HFOT alone, NIV alternating with HFOT and NIV alternating with standard oxygen in patients admitted in the ICU for acute respiratory failure with a do-not-intubate order. The primary outcome is the hospital survival within 14 days after ICU admission in patients weaned from NIV and HFOT. The sample size was estimated at a minimum of 330 patients divided into three groups according to the oxygenation strategy applied. The analysis takes into account confounding factors by modelling a propensity score.Ethics and dissemination The study has been approved by the ethics committee and patients will be included after informed consent. The results will be submitted for publication in peer-reviewed journals.Trial registration number NCT03673631