<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0186-4866</journal-id>
<journal-title><![CDATA[Medicina interna de México]]></journal-title>
<abbrev-journal-title><![CDATA[Med. interna Méx.]]></abbrev-journal-title>
<issn>0186-4866</issn>
<publisher>
<publisher-name><![CDATA[Edición y Farmacia S.A. de C.V.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0186-48662019000100005</article-id>
<article-id pub-id-type="doi">10.24245/mim.v35i1.2120</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Estratificación de la gravedad del síndrome de insuficiencia respiratoria aguda a las 24 horas de su diagnóstico]]></article-title>
<article-title xml:lang="en"><![CDATA[Stratification of the severity of the acute respiratory distress syndrome at 24 hours after diagnosis]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sánchez-Zúñiga]]></surname>
<given-names><![CDATA[Martín de Jesús]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Carrillo-Esper]]></surname>
<given-names><![CDATA[Raúl]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Garnica-Escamilla]]></surname>
<given-names><![CDATA[Marco Antonio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Medveczky-Ordoñes]]></surname>
<given-names><![CDATA[Nikolette Iren]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Carrillo-Córdova]]></surname>
<given-names><![CDATA[Dulce María]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Instituto Nacional de Rehabilitación Dr. Luis Guillermo Ibarra Ibarra  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Instituto Nacional de Rehabilitación Dr. Luis Guillermo Ibarra Ibarra  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Instituto Nacional de Rehabilitación Dr. Luis Guillermo Ibarra Ibarra  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Hospital General de México Dr. Eduardo Liceaga  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af5">
<institution><![CDATA[,Instituto Nacional de Ciencias Médicas y Nutrición Dr. Salvador Zubirán  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>02</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>02</month>
<year>2019</year>
</pub-date>
<volume>35</volume>
<numero>1</numero>
<fpage>5</fpage>
<lpage>15</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0186-48662019000100005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0186-48662019000100005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0186-48662019000100005&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  OBJETIVO: Identificar si hay cambios en la estratificación de la gravedad del síndrome de insuficiencia respiratoria aguda al ingreso y 24 horas después.  MATERIAL Y MÉTODO: Estudio retrospectivo observacional de pacientes que cumplieron criterios de Berlín para síndrome de insuficiencia respiratoria aguda (SIRA) de cualquier origen y que se reestratificaron a las 24 horas con la misma escala analizados durante un periodo de 4 meses durante 2017. Se recabaron los datos de biomarcadores inflamatorios y de la mecánica ventilatoria.  RESULTADOS: Se incluyeron 17 pacientes, de los que 11 fallecieron (65%) y 6 (35%) egresaron a domicilio. La estratificación inicial de los pacientes de acuerdo con la gravedad de la hipoxemia (PaO2/FiO2) mostró 2 (11%) sin SIRA, 3 (17%) con SIRA leve, en 10 (58%) fue moderado y en 2 (11%) grave. A las 24 horas de iniciado el tratamiento convencional, la estratificación de gravedad (PaO2/FiO2) mostró: 9 (52%) sin SIRA, 6 (35.2%) con hipoxemia leve, en uno (5.8%) moderada y en uno (5.8%) grave.  CONCLUSIONES: Es necesario estratificar al ingreso y a las 24 horas la gravedad del SIRA, a pesar de que no se mostró ninguna diferencia en el patrón de respuesta inflamatoria a través de la medición de marcadores séricos de uso clínico habitual.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  OBJECTIVE: To identify if there are changes in the stratification of acute respiratory distress syndrome severity at hospitalization and 24 hours later.  MATERIAL AND METHOD: A retrospective observational study was done describing patients studied over a 4-month period during 2017, who met Berlin criteria for acute respiratory distress syndrome (ARDS) of any origin and who re-stratified at 24 hours, with the same scale. The data of inflammatory biomarkers and ventilatory mechanics were collected.  RESULTS: There were included 17 patients, from which 11 patients (64%) died and 6 (35%) were discharged to home. The initial stratification of patients according to the severity of the hypoxemia (PaO2/FiO2) showed 2 (11%) without ARDS, 3 (17%) mild, 10 (58%) moderate, and 2 (11%) severe. At 24 hours after conventional treatment, gravity stratification (PaO2/FiO2) showed: 9 (52%) without ARDS, 6 (35.2%) with mild hypoxemia, in one (5.8%) moderate and in one (5.8%) severe.  CONCLUSIONS: It is necessary to stratify at the time of admission and at 24 hours the severity of the ARDS, although no difference was shown in the pattern of inflammatory response through the measurement of serum markers of usual clinical use.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Síndrome de insuficiencia respiratoria aguda]]></kwd>
<kwd lng="es"><![CDATA[SIRA]]></kwd>
<kwd lng="es"><![CDATA[hipoxemia]]></kwd>
<kwd lng="es"><![CDATA[biomarcadores]]></kwd>
<kwd lng="en"><![CDATA[Acute respiratory distress syndrome]]></kwd>
<kwd lng="en"><![CDATA[ARDS]]></kwd>
<kwd lng="en"><![CDATA[Hypoxemia]]></kwd>
<kwd lng="en"><![CDATA[Biomarkers]]></kwd>
</kwd-group>
</article-meta>
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