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  <titleInfo>
    <title>High-flow or standard oxygen in acute hypoxemic respiratory failure</title>
  </titleInfo>
  <name type="personal">
    <namePart>Frat, Jean-Pierre</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
    <role>
      <roleTerm type="text">Autor</roleTerm>
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  </name>
  <name type="personal">
    <namePart>Quenot, Jean-Pierre</namePart>
  </name>
  <name type="personal">
    <namePart>Guitton, Christophe</namePart>
  </name>
  <name type="personal">
    <namePart>Coudroy, Rémi</namePart>
  </name>
  <name type="personal">
    <namePart>Gacouin, Arnaud</namePart>
  </name>
  <name type="personal">
    <namePart>Badie, Julio</namePart>
  </name>
  <name type="personal">
    <namePart>Demoule, Alexandre</namePart>
  </name>
  <name type="personal">
    <namePart>Contou, Damien</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">pe</placeTerm>
    </place>
    <issuance>monographic</issuance>
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  <language>
    <languageTerm authority="iso639-2b" type="code">spa</languageTerm>
  </language>
  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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  <physicalDescription>
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    <extent>páginas: 2095-2106</extent>
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  <abstract>Background: Data are needed on the effect of oxygen delivered through a high-flow nasal cannula, as compared with standard oxygen therapy, on intubation and mortality in patients with acute hypoxemic respiratory failure. Methods: In this multicenter, open-label trial, we randomly assigned patients who had acute hypoxemic respiratory failure to receive high-flow-oxygen or standard-oxygen therapy. All the patients had a ratio of the partial pressure of arterial oxygen to the fraction of inspired oxygen of 200 or less, a respiratory rate of more than 25 breaths per minute, and pulmonary infiltrate on chest imaging. The primary outcome was death by day 28. Results: A total of 1116 patients underwent randomization. Of these patients, 1110 (556 in the high-flow-oxygen group and 554 in the standard-oxygen group) were included in the analysis. Mortality at day 28 was 14.6% (in 81 of 556 patients) in the high-flow-oxygen group and 14.6% (in 81 of 554 patients) in the standard-oxygen group (difference, −0.05 percentage points; 95% confidence interval [CI], −4.21 to 4.10; P=0.98). The incidence of intubation by day 28 was 42.4% (in 236 of 556 patients) in the high-flow-oxygen group and 48.4% (in 268 of 554 patients) in the standard-oxygen group (difference, −5.93 percentage points; 95% CI, −11.78 to −0.08). Serious adverse events (cardiac arrest or pneumothorax) occurred during spontaneous breathing in 13 patients (2.3%) in the high-flow-oxygen group and in 6 patients (1.1%) in the standard-oxygen group. Conclusions: Among patients with acute hypoxemic respiratory failure, the use of oxygen delivered through a high-flow nasal cannula did not significantly reduce mortality at day 28. </abstract>
  <subject>
    <topic>CUIDADOS INTENSIVOS</topic>
  </subject>
  <subject>
    <topic>MEDICINA DE URGENCIAS</topic>
  </subject>
  <subject>
    <topic>MEDICINA CLINICA HOSPITALARIA</topic>
  </subject>
  <subject>
    <topic>VENTILACION MECANICA</topic>
  </subject>
  <subject>
    <topic>NEUMOLOGÍA</topic>
  </subject>
  <relatedItem type="host">
    <titleInfo>
      <title>The New England Journal of Medicine</title>
    </titleInfo>
    <originInfo>
      <publisher>Massachusetts NEJM Group</publisher>
    </originInfo>
    <identifier>NEJM011</identifier>
    <identifier type="issn">0028-4793</identifier>
    <identifier type="local">ESSALUD</identifier>
  </relatedItem>
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    <recordCreationDate encoding="marc">      </recordCreationDate>
    <recordChangeDate encoding="iso8601">20260819164758.0</recordChangeDate>
    <recordIdentifier>ESSALUD</recordIdentifier>
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