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High-flow nasal cannula oxygen therapy alone or with non-invasive ventilation during the weaning period after extubation in ICU: the prospective randomised controlled HIGH-WEAN protocol.
Thille, Arnaud W; Muller, Grégoire; Gacouin, Arnaud; Coudroy, Rémi; Demoule, Alexandre; Sonneville, Romain; Beloncle, François; Girault, Christophe; Dangers, Laurence; Lautrette, Alexandre; Cabasson, Séverin; Rouzé, Anahita; Vivier, Emmanuel; Le Meur, Anthony; Ricard, Jean-Damien; Razazi, Keyvan; Barberet, Guillaume; Lebert, Christine; Ehrmann, Stephan; Picard, Walter; Bourenne, Jeremy; Pradel, Gael; Bailly, Pierre; Terzi, Nicolas; Buscot, Matthieu; Lacave, Guillaume; Danin, Pierre-Eric; Nanadoumgar, Hodanou; Gibelin, Aude; Zanre, Lassane; Deye, Nicolas; Ragot, Stéphanie; Frat, Jean-Pierre.
Affiliation
  • Thille AW; Department of Réanimation Médicale, CHU de Poitiers, Poitiers, France.
  • Muller G; Université de Poitiers, INSERM CIC 1402 ALIVE, Poitiers, France.
  • Gacouin A; Médecine Intensive Réanimation, Groupe Hospitalier Régional d'Orléans, Orléans, France.
  • Coudroy R; Service des Maladies Infectieuses et Réanimation Médicale, CHU de Rennes, Hôpital Ponchaillou, Rennes, France.
  • Demoule A; Department of Réanimation Médicale, CHU de Poitiers, Poitiers, France.
  • Sonneville R; Université de Poitiers, INSERM CIC 1402 ALIVE, Poitiers, France.
  • Beloncle F; Service de Pneumologie et Réanimation Médicale du Département R3S, AP-HP, INSERM, UMRS1158 Neurophysiologie Respiratoire Expérimentale et Clinique, Sorbonne Université, Groupe Hospitalier Pitié-Salpêtrière Charles Foix, Paris, France.
  • Girault C; Hôpital Bichat - Claude Bernard, Médecine Intensive Réanimation, AP-HP, Université Paris Diderot, Paris, France.
  • Dangers L; Département de Médecine Intensive - Réanimation, Université d'Angers, CHU d'Angers, Angers, France.
  • Lautrette A; Département de Réanimation Médicale, Normandie Université, UNIROUEN, EA3830-GRHV, Institute for Research and Innovation in Biomedicine (IRIB), CHU de Rouen, Hôpital Charles Nicolle, Rouen, France.
  • Cabasson S; Service de Réanimation Polyvalente, CHU Félix Guyon, Saint Denis de la Réunion, France.
  • Rouzé A; Service de Réanimation Médicale, CHU de Clermont-Ferrand, Hôpital Gabriel Montpied, Clermont-Ferrand, France.
  • Vivier E; Service de Réanimation, Centre hospitalier de la Rochelle, La Rochelle, Nouvelle-Aquitaine, France.
  • Le Meur A; Centre de Réanimation, Université de Lille, CHU de Lille, Lille, France.
  • Ricard JD; Reanimation Polyvalente, Hôpital Saint Joseph Saint Luc, Lyon, France.
  • Razazi K; Médecine Intensive Réanimation, CHU de Nantes, Nantes, France.
  • Barberet G; Réanimation Médico-Chirurgicale, AP-HP, INSERM, Université Paris Diderot, UMR IAME 1137, Sorbonne Paris Cité, Hopital Louis-Mourier, Colombes, France.
  • Lebert C; Service de Réanimation Médicale DHU A-TVB, AP-HP, Hopitaux Universitaires Henri Mondor, Creteil, Île-de-France, France.
  • Ehrmann S; Service de Réanimation Médicale, Groupe Hospitalier Régional Mulhouse Sud Alsace, Site Emile Muller, Mulhouse, France.
  • Picard W; Service de Médecine Intensive et Réanimation, Centre Hospitalier Départemental de Vendée, La Roche-sur-Yon, France.
  • Bourenne J; CHU de Tours, Médecin Intensive Réanimation, CIC 1415, CRICS-TriggerSEP, Centre d'étude des pathologies respiratoires, INSERM U1100, Université de Tours, Tours, France.
  • Pradel G; Service de Réanimation, Centre Hospitalier de Pau, Pau, France.
  • Bailly P; CHU La Timone 2, Médecine Intensive Réanimation, Réanimation des Urgences, Aix-Marseille Université, Marseille, France.
  • Terzi N; Service de Réanimation, Centre Hospitalier Henri Mondor d'Aurillac, Aurillac, France.
  • Buscot M; Médecine Intensive Réanimation, CHU de Brest, Brest, France.
  • Lacave G; Médecine Intensive Réanimation, INSERM, Université Grenoble-Alpes, U1042, HP2, Centre Hospitalier Universitaire Grenoble Alpes, Grenoble, France.
  • Danin PE; Réanimation Médicale Archet 1, Université Cote d'Azur, CHU de Nice, Nice, France.
  • Nanadoumgar H; Service de Réanimation Médico-Chirurgicale, Centre Hospitalier de Versailles, Le Chesnay, France.
  • Gibelin A; Réanimation Médico-Chirurgicale Archet 2, INSERM U 1065, CHU de Nice, Nice, France.
  • Zanre L; Réanimation Chirurgicale, CHU de Poitiers, Poitiers, France.
  • Deye N; Réanimation et USC médico-chirurgicale, CARMAS, AP-HP, Faculté de Médecine Sorbonne Université, Collegium Galilée, Hopital Tenon, Paris, France.
  • Ragot S; Service de Réanimation, Centre Hospitalier Emile Roux, Le Puy-en-Velay, France.
  • Frat JP; Réanimation Médicale et Toxicologique, AP-HP, INSERM UMR-S 942, Hopital Lariboisiere, Paris, France.
BMJ Open ; 8(9): e023772, 2018 09 05.
Article in En | MEDLINE | ID: mdl-30185583
ABSTRACT

INTRODUCTION:

Recent practice guidelines suggest applying non-invasive ventilation (NIV) to prevent postextubation respiratory failure in patients at high risk of extubation failure in intensive care unit (ICU). However, such prophylactic NIV has been only a conditional recommendation given the low certainty of evidence. Likewise, high-flow nasal cannula (HFNC) oxygen therapy has been shown to reduce reintubation rates as compared with standard oxygen and to be as efficient as NIV in patients at high risk. Whereas HFNC may be considered as an optimal therapy during the postextubation period, HFNC associated with NIV could be an additional means of preventing postextubation respiratory failure. We are hypothesising that treatment associating NIV with HFNC between NIV sessions may be more effective than HFNC alone and may reduce the reintubation rate in patients at high risk. METHODS AND

ANALYSIS:

This study is an investigator-initiated, multicentre randomised controlled trial comparing HFNC alone or with NIV sessions during the postextubation period in patients at high risk of extubation failure in the ICU. Six hundred patients will be randomised with a 11 ratio in two groups according to the strategy of oxygenation after extubation. The primary outcome is the reintubation rate within the 7 days following planned extubation. Secondary outcomes include the number of patients who meet the criteria for moderate/severe respiratory failure, ICU length of stay and mortality up to day 90. 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 NCT03121482.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxygen Inhalation Therapy / Ventilator Weaning / Noninvasive Ventilation / Intensive Care Units Type of study: Clinical_trials / Guideline / Risk_factors_studies Limits: Humans Language: En Journal: BMJ Open Year: 2018 Type: Article Affiliation country: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxygen Inhalation Therapy / Ventilator Weaning / Noninvasive Ventilation / Intensive Care Units Type of study: Clinical_trials / Guideline / Risk_factors_studies Limits: Humans Language: En Journal: BMJ Open Year: 2018 Type: Article Affiliation country: France