Your browser doesn't support javascript.
loading
Effect of High-Flow Nasal Oxygen vs Standard Oxygen on 28-Day Mortality in Immunocompromised Patients With Acute Respiratory Failure: The HIGH Randomized Clinical Trial.
Azoulay, Elie; Lemiale, Virginie; Mokart, Djamel; Nseir, Saad; Argaud, Laurent; Pène, Frédéric; Kontar, Loay; Bruneel, Fabrice; Klouche, Kada; Barbier, François; Reignier, Jean; Berrahil-Meksen, Lilia; Louis, Guillaume; Constantin, Jean-Michel; Mayaux, Julien; Wallet, Florent; Kouatchet, Achille; Peigne, Vincent; Théodose, Igor; Perez, Pierre; Girault, Christophe; Jaber, Samir; Oziel, Johanna; Nyunga, Martine; Terzi, Nicolas; Bouadma, Lila; Lebert, Christine; Lautrette, Alexandre; Bigé, Naike; Raphalen, Jean-Herlé; Papazian, Laurent; Darmon, Michael; Chevret, Sylvie; Demoule, Alexandre.
Afiliação
  • Azoulay E; Medical Intensive Care Unit and Department of Biostatistics, APHP, Hôpital St-Louis, Paris, France.
  • Lemiale V; Medical Intensive Care Unit and Department of Biostatistics, APHP, Hôpital St-Louis, Paris, France.
  • Mokart D; Intensive Care Unit, Paoli Calmettes Institut, Marseille, France.
  • Nseir S; Critical Care Center, CHU de Lille, Lille, France.
  • Argaud L; Medical Intensive Care Unit, Hospices Civils de Lyon, Hôpital Edouard Herriot, Lyon, France.
  • Pène F; Medical Intensive Care Unit, Hôpital Cochin, APHP, Université Paris Descartes, Paris, France.
  • Kontar L; Medical Intensive Care Unit, INSERM U1088, Amiens University Hospital, Amiens, France.
  • Bruneel F; Medical Intensive Care Unit, André Mignot Hospital, Versailles, France.
  • Klouche K; Medical Intensive Care Unit, CHU de Montpellier, Montpellier, France.
  • Barbier F; Medical Intensive Care Unit, La Source Hospital, CHR Orléans, Orléans, France.
  • Reignier J; Medical Intensive Care Unit, Hotel Dieu, CHU de Nantes, Nantes, France.
  • Berrahil-Meksen L; Intensive Care Unit, Institut Gustave Roussy, Villejuif, France.
  • Louis G; Intensive Care Unit, CHR de Metz-Thionville, Metz, France.
  • Constantin JM; Department of Perioperative Medicine, CHU Clermont-Ferrand, Clermont-Ferrand, France.
  • Mayaux J; Medical Intensive Care Unit and Respiratory Division, APHP, Hôpital Pitié-Salpêtrière, Sorbonne University, Paris, France.
  • Wallet F; Intensive Care Unit, Lyon Sud Medical Center, Lyon, France.
  • Kouatchet A; Medical Intensive Care Unit, CHRU, Angers, France.
  • Peigne V; Intensive Care Unit, Centre Hospitalier Métropole-Savoie, Chambery, France.
  • Théodose I; Medical Intensive Care Unit and Department of Biostatistics, APHP, Hôpital St-Louis, Paris, France.
  • Perez P; Medical Intensive Care Unit, Hôpital Brabois, Vandoeuvre Les Nancy, France.
  • Girault C; Medical Intensive Care Unit, Hôpital Charles Nicolle, Rouen, France.
  • Jaber S; Montpellier University Hospital, PhyMedExp, INSERM U-1046, CNRS 34295 Montpellier, France.
  • Oziel J; Medical Intensive Care Unit, Avicenne University Hospital, Bobigny, France.
  • Nyunga M; Intensive Care Unit, Roubaix hospital, Roubaix, France.
  • Terzi N; Medical Intensive Care Unit, CHU de Grenoble Alpes, Grenoble, France.
  • Bouadma L; Medical Intensive Care Unit, CHU Bichat, Paris, France.
  • Lebert C; Intensive Care Unit, Centre Hospitalier Départemental Les Oudairies, La Roche Sur Yon, France.
  • Lautrette A; Medical Intensive Care Unit, Gabriel-Montpied University Hospital, Clermont-Ferrand, France.
  • Bigé N; Medical Intensive Care Unit, CHU St-Antoine, Paris, France.
  • Raphalen JH; Department of Anesthesia and Critical Care, Necker Hospital, Paris, France.
  • Papazian L; Réanimation des Détresses Respiratoires et Infections Sévères, Assistance Publique-Hôpitaux de Marseille, Hôpital Nord, Aix-Marseille Université, Faculté de Médecine, Marseille, France.
  • Darmon M; Respiratory Intensive Care Unit, Hôpital Cochin, Paris, France.
  • Chevret S; Medical Intensive Care Unit and Department of Biostatistics, APHP, Hôpital St-Louis, Paris, France.
  • Demoule A; Medical Intensive Care Unit and Respiratory Division, APHP, Hôpital Pitié-Salpêtrière, Sorbonne University, Paris, France.
JAMA ; 320(20): 2099-2107, 2018 11 27.
Article em En | MEDLINE | ID: mdl-30357270
ABSTRACT
Importance High-flow nasal oxygen therapy is increasingly used for acute hypoxemic respiratory failure (AHRF).

Objective:

To determine whether high-flow oxygen therapy decreases mortality among immunocompromised patients with AHRF compared with standard oxygen therapy. Design, Setting, and

Participants:

The HIGH randomized clinical trial enrolled 776 adult immunocompromised patients with AHRF (Pao2 <60 mm Hg or Spo2 <90% on room air, or tachypnea >30/min or labored breathing or respiratory distress, and need for oxygen ≥6 L/min) at 32 intensive care units (ICUs) in France between May 19, 2016, and December 31, 2017.

Interventions:

Patients were randomized 11 to continuous high-flow oxygen therapy (n = 388) or to standard oxygen therapy (n = 388). Main Outcomes and

Measures:

The primary outcome was day-28 mortality. Secondary outcomes included intubation and mechanical ventilation by day 28, Pao2Fio2 ratio over the 3 days after intubation, respiratory rate, ICU and hospital lengths of stay, ICU-acquired infections, and patient comfort and dyspnea.

Results:

Of 778 randomized patients (median age, 64 [IQR, 54-71] years; 259 [33.3%] women), 776 (99.7%) completed the trial. At randomization, median respiratory rate was 33/min (IQR, 28-39) vs 32 (IQR, 27-38) and Pao2Fio2 was 136 (IQR, 96-187) vs 128 (IQR, 92-164) in the intervention and control groups, respectively. Median SOFA score was 6 (IQR, 4-8) in both groups. Mortality on day 28 was not significantly different between groups (35.6% vs 36.1%; difference, -0.5% [95% CI, -7.3% to +6.3%]; hazard ratio, 0.98 [95% CI, 0.77 to 1.24]; P = .94). Intubation rate was not significantly different between groups (38.7% vs 43.8%; difference, -5.1% [95% CI, -12.3% to +2.0%]). Compared with controls, patients randomized to high-flow oxygen therapy had a higher Pao2Fio2 (150 vs 119; difference, 19.5 [95% CI, 4.4 to 34.6]) and lower respiratory rate after 6 hours (25/min vs 26/min; difference, -1.8/min [95% CI, -3.2 to -0.2]). No significant difference was observed in ICU length of stay (8 vs 6 days; difference, 0.6 [95% CI, -1.0 to +2.2]), ICU-acquired infections (10.0% vs 10.6%; difference, -0.6% [95% CI, -4.6 to +4.1]), hospital length of stay (24 vs 27 days; difference, -2 days [95% CI, -7.3 to +3.3]), or patient comfort and dyspnea scores. Conclusions and Relevance Among critically ill immunocompromised patients with acute respiratory failure, high-flow oxygen therapy did not significantly decrease day-28 mortality compared with standard oxygen therapy. Trial Registration clinicaltrials.gov Identifier NCT02739451.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxigenoterapia / Insuficiência Respiratória / Ventilação de Alta Frequência / Hospedeiro Imunocomprometido Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxigenoterapia / Insuficiência Respiratória / Ventilação de Alta Frequência / Hospedeiro Imunocomprometido Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França