Evidence map›Paper›PMID 30357270›Full record

Trial reportJAMA2018

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.

Elie Azoulay, Virginie Lemiale, Djamel Mokart, Saad Nseir, Laurent Argaud, Frédéric Pène, Loay Kontar, Fabrice Bruneel, Kada Klouche, François Barbier and 24 more

Registry-linked trialOpen access · bronzeAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02739451 (A Randomised Controlled Trial of High-Flow Nasal Oxygen Versus Standard Oxygen Therapy in Critically Ill Immunocompromised Patients), which is not on this map. Cited by 149 papers, 15 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
149citing papers in PubMed, 15 pooled it
26.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02739451 nacompletednot on this map

A Randomised Controlled Trial of High-Flow Nasal Oxygen Versus Standard Oxygen Therapy in Critically Ill Immunocompromised Patients

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2016 to 2017Enrolled776ConditionsAcute Respiratory FailureArmsstandard oxygen, HFNO
3 · Its place in the literature

Who cites it

149 citing papers in PubMed, 15 syntheses or guidelines pooled it, 309 citations in OpenAlex.

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89 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

34 authors at 20 institutions in 1 country.

Elie AzoulayMedical Intensive Care Unit and Department of Biostatistics, APHP, Hôpital St-Louis, Paris, France.
Virginie LemialeMedical Intensive Care Unit and Department of Biostatistics, APHP, Hôpital St-Louis, Paris, France.
Djamel MokartIntensive Care Unit, Paoli Calmettes Institut, Marseille, France.
Saad NseirCritical Care Center, CHU de Lille, Lille, France.
Laurent ArgaudMedical Intensive Care Unit, Hospices Civils de Lyon, Hôpital Edouard Herriot, Lyon, France.
Frédéric PèneMedical Intensive Care Unit, Hôpital Cochin, APHP, Université Paris Descartes, Paris, France.
Loay KontarMedical Intensive Care Unit, INSERM U1088, Amiens University Hospital, Amiens, France.
Fabrice BruneelMedical Intensive Care Unit, André Mignot Hospital, Versailles, France.
Kada KloucheMedical Intensive Care Unit, CHU de Montpellier, Montpellier, France.
François BarbierMedical Intensive Care Unit, La Source Hospital, CHR Orléans, Orléans, France.
Jean ReignierMedical Intensive Care Unit, Hotel Dieu, CHU de Nantes, Nantes, France.
Lilia Berrahil-MeksenIntensive Care Unit, Institut Gustave Roussy, Villejuif, France.
Guillaume LouisIntensive Care Unit, CHR de Metz-Thionville, Metz, France.
Jean-Michel ConstantinDepartment of Perioperative Medicine, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Julien MayauxMedical Intensive Care Unit and Respiratory Division, APHP, Hôpital Pitié-Salpêtrière, Sorbonne University, Paris, France.
Florent WalletIntensive Care Unit, Lyon Sud Medical Center, Lyon, France.
Achille KouatchetMedical Intensive Care Unit, CHRU, Angers, France.
Vincent PeigneIntensive Care Unit, Centre Hospitalier Métropole-Savoie, Chambery, France.
Igor ThéodoseMedical Intensive Care Unit and Department of Biostatistics, APHP, Hôpital St-Louis, Paris, France.
Pierre PerezMedical Intensive Care Unit, Hôpital Brabois, Vandoeuvre Les Nancy, France.
Christophe GiraultMedical Intensive Care Unit, Hôpital Charles Nicolle, Rouen, France.
Samir JaberMontpellier University Hospital, PhyMedExp, INSERM U-1046, CNRS 34295 Montpellier, France.
Johanna OzielMedical Intensive Care Unit, Avicenne University Hospital, Bobigny, France.
Martine NyungaIntensive Care Unit, Roubaix hospital, Roubaix, France.
Nicolas TerziMedical Intensive Care Unit, CHU de Grenoble Alpes, Grenoble, France.
Lila BouadmaMedical Intensive Care Unit, CHU Bichat, Paris, France.
Christine LebertIntensive Care Unit, Centre Hospitalier Départemental Les Oudairies, La Roche Sur Yon, France.
Alexandre LautretteMedical Intensive Care Unit, Gabriel-Montpied University Hospital, Clermont-Ferrand, France.
Naike BigéMedical Intensive Care Unit, CHU St-Antoine, Paris, France.
Jean-Herlé RaphalenDepartment of Anesthesia and Critical Care, Necker Hospital, Paris, France.
Laurent PapazianRéanimation des Détresses Respiratoires et Infections Sévères, Assistance Publique-Hôpitaux de Marseille, Hôpital Nord, Aix-Marseille Université, Faculté de Médecine, Marseille, France.
Michael DarmonRespiratory Intensive Care Unit, Hôpital Cochin, Paris, France.
Sylvie ChevretMedical Intensive Care Unit and Department of Biostatistics, APHP, Hôpital St-Louis, Paris, France.
Alexandre DemouleMedical Intensive Care Unit and Respiratory Division, APHP, Hôpital Pitié-Salpêtrière, Sorbonne University, Paris, France.
Assistance Publique – Hôpitaux de Paris · FRSorbonne Université · FRAix-Marseille Université · FRCentre Hospitalier Départemental Vendée · FRCentre Hospitalier de Roubaix · FRCentre Hospitalier Métropole Savoie · FRCentre Hospitalier Régional de Metz-Thionville · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire de Nantes · FRCentre hospitalier universitaire d'Orléans · FRCentre National de la Recherche Scientifique · FRHôpital André Mignot · FRHôpital Bichat-Claude-Bernard · FRHôpital Charles-Nicolle · FRHôpital Cochin · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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 1:1 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, Pao2:Fio2 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 Pao2:Fio2 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 Pao2:Fio2 (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.

Indexed as

High-Frequency VentilationImmunocompromised HostAdultAgedCritical IllnessFemaleHumansMaleMiddle AgedNoninvasive VentilationOxygen Inhalation TherapyRespiratory InsufficiencySurvival Analysis

Identifiers

PMID30357270
PMCPMC6583581
OpenAlexW2898161514

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.