<?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>0034-7531</journal-id>
<journal-title><![CDATA[Revista Cubana de Pediatría]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Cubana Pediatr]]></abbrev-journal-title>
<issn>0034-7531</issn>
<publisher>
<publisher-name><![CDATA[Centro Nacional de Información de Ciencias MédicasEditorial Ciencias Médicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0034-75312019000100008</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Morbilidad y mortalidad neonatal por cardiopatías congénitas]]></article-title>
<article-title xml:lang="en"><![CDATA[Neonatal morbidity and mortality by congenital cardiopathies]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Armas López]]></surname>
<given-names><![CDATA[Marisel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sierra]]></surname>
<given-names><![CDATA[Reinaldo Elias]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rodríguez Collado]]></surname>
<given-names><![CDATA[Yenicel]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Elias Armas]]></surname>
<given-names><![CDATA[Karla Sucet]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Servicio de Neonatologia. Hospital &#8220;Dr. Agostinho Neto&#8221;  ]]></institution>
<addr-line><![CDATA[Guantánamo ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital &#8220;Dr. Agostinho Neto&#8221; Servicio de Cardiologia ]]></institution>
<addr-line><![CDATA[Guantánamo ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Facultad de Medicina de Guantánamo  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2019</year>
</pub-date>
<volume>91</volume>
<numero>1</numero>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S0034-75312019000100008&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S0034-75312019000100008&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S0034-75312019000100008&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN  Introducción:  Las cardiopatías congénitas inciden en 8 x 1 000 recién nacidos vivos en el mundo y en gran medida determinan su mortalidad.  Objetivo:  Precisar la morbilidad y mortalidad neonatal por cardiopatías congénitas.  Métodos:  Estudio descriptivo, longitudinal y prospectivo realizado en 97 recién nacidos con estas cardiopatías, diagnósticados en el Servicio de Neonatología del Hospital &#8220;Dr. Agostinho Neto&#8221; de Guantánamo durante los años 2015- 2017. Se consideró el análisis segmentario, probable mecanismos que la determinan y tipo de cardiopatía.  Resultados:  Se identificaron cardiopatías congénitas en el 12,9 % de los recién nacidos; la letalidad fue de 1,0 %. Lo más común fue que se identificaron modos y tipos de conexión auriculoventricular y ventriculoarterial fisiológicos. Las anomalías en la muerte celular (47,3 %) fue el mecanismo genético y molecular más observado. La cardiopatía más frecuente fue la comunicación interventricular (63,9 %). La mayoría de las cardiopatías se clasificaron como: aisladas (95,9 %), de gravedad moderada (92,8 %), acianóticas (93,8 %), no se asociaran a síndromes o enfermedades genéticas (94,9 %) pero sí a malformaciones extracardiacas (94,9 %). Se manifestaron sobre todo por soplo cardiaco (85,6 %). El diagnóstico de 70,1 % de las cardiopatías se realizó en etapa prenatal.  Conclusiones: Estas afecciones no constituyen un problema de salud en el servicio de este hospital, pero a pesar de que la mayoría de las cardiopatías congénitas se diagnostican en etapa prenatal, se requiere continuar laborando en función de potenciar más su diagnóstico en esta etapa.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Introduction: Neonatal congenital cardiopathies have a global incidence of 8 x 1000 live births and it greatly determines their mortality.  Objective:  To specify the neonatal morbidity and mortality by congenital cardiopathies.  Method:  Descriptive, longitudinal and prospective study of 97 newborns with these cardiopathies diagnosed in the Neonatolgy Service in ´´Dr. Agostinho Neto´´ Hospital, Guantánamo province from 2015 to 2017. It was considered: the segmental analysis, probable mechanisms that determine it and cardiopathy type.  Results: Congenital cardiopathies were identified in 12.9 % of the newborns; the lethality was of 1.0%. The most common aspect was the identification of ways and types of aurículo-ventricular and physiologic ventrículo-arterial connection. Anomalies in the cellular death (47.3 %) were the most frequent genetic and molecular mechanism. The most frequent congenital heart disease was the interventricular communication (63.9 %). Most of the cardiopathies were classified as: isolated (95.9 %); of moderate graveness (92.8 %); acyanotic (93.8 %); not associated to syndromes or genetic diseases (94.9 %) but yes to extracardiac malformations (94.9 %); and they manifested mainly by heart murmur (85.6 ). The diagnosis of 70.1 % of the cardiopathies was carried out in prenatal stage.  Conclusions:  Congenital cardiopathies don't constitute a health problem in the Neonatology service of the Hospital; but instead that these were mainly diagnosed in the prenatal stage, it is required to continue working in function of boosting their prenatal diagnosis.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[recién nacido]]></kwd>
<kwd lng="es"><![CDATA[cardiopatía congénita]]></kwd>
<kwd lng="es"><![CDATA[neonatología]]></kwd>
<kwd lng="en"><![CDATA[newborn]]></kwd>
<kwd lng="en"><![CDATA[congenital cardiopathy]]></kwd>
<kwd lng="en"><![CDATA[neonatology]]></kwd>
</kwd-group>
</article-meta>
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