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  <controlfield tag="001">ESSALUD</controlfield>
  <controlfield tag="005">20260819164758.0</controlfield>
  <controlfield tag="007">ta</controlfield>
  <controlfield tag="008">      t        pe ||||| |||| 00| 0 spa d</controlfield>
  <datafield tag="040" ind1=" " ind2=" ">
    <subfield code="a">BMG</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Frat, Jean-Pierre </subfield>
    <subfield code="e">Autor</subfield>
    <subfield code="9">54172</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">High-flow or standard oxygen in acute hypoxemic respiratory failure</subfield>
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  <datafield tag="300" ind1=" " ind2=" ">
    <subfield code="a">p&#xE1;ginas: 2095-2106</subfield>
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    <subfield code="a">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, &#x2212;0.05 percentage points; 95% confidence interval [CI], &#x2212;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, &#x2212;5.93 percentage points; 95% CI, &#x2212;11.78 to &#x2212;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. </subfield>
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    <subfield code="a">CUIDADOS INTENSIVOS</subfield>
    <subfield code="9">5208</subfield>
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    <subfield code="a">MEDICINA DE URGENCIAS</subfield>
    <subfield code="9">53820</subfield>
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    <subfield code="a">MEDICINA CLINICA HOSPITALARIA</subfield>
    <subfield code="9">53754</subfield>
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    <subfield code="a">VENTILACION MECANICA</subfield>
    <subfield code="9">37360</subfield>
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    <subfield code="a">NEUMOLOG&#xCD;A</subfield>
    <subfield code="9">25628</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Quenot, Jean-Pierre</subfield>
    <subfield code="9">54173</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Guitton, Christophe </subfield>
    <subfield code="9">54174</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Coudroy, R&#xE9;mi  </subfield>
    <subfield code="9">54175</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Gacouin, Arnaud </subfield>
    <subfield code="9">54176</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Badie, Julio </subfield>
    <subfield code="9">54177</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Demoule, Alexandre  </subfield>
    <subfield code="9">54178</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Contou, Damien </subfield>
    <subfield code="9">54179</subfield>
  </datafield>
  <datafield tag="773" ind1="0" ind2=" ">
    <subfield code="0">22717</subfield>
    <subfield code="9">22648</subfield>
    <subfield code="d">Massachusetts NEJM Group</subfield>
    <subfield code="o">NEJM011</subfield>
    <subfield code="t">The New England Journal of Medicine </subfield>
    <subfield code="w">ESSALUD</subfield>
    <subfield code="x">0028-4793</subfield>
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  <datafield tag="942" ind1=" " ind2=" ">
    <subfield code="c">ARTICULOS</subfield>
    <subfield code="e">2026-08-19</subfield>
    <subfield code="z">sqb</subfield>
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  <datafield tag="999" ind1=" " ind2=" ">
    <subfield code="c">22834</subfield>
    <subfield code="d">22834</subfield>
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