<?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>1692-7273</journal-id>
<journal-title><![CDATA[Revista Ciencias de la Salud]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Cienc. Salud]]></abbrev-journal-title>
<issn>1692-7273</issn>
<publisher>
<publisher-name><![CDATA[Editorial Universidad del Rosario]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1692-72732024000300007</article-id>
<article-id pub-id-type="doi">10.12804/revistas.urosario.edu.co/revsalud/a.13287</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Experiencia vivida de las personas con discapacidad auditiva durante la atención sanitaria]]></article-title>
<article-title xml:lang="en"><![CDATA[Lived Experience of People with Hearing Disabilities During Health Care]]></article-title>
<article-title xml:lang="pt"><![CDATA[A experiência vivida por pessoas com deficiência auditiva no setor de saúde]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Fuentes Chiquito]]></surname>
<given-names><![CDATA[Alondra del Rocío]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vázquez Velázquez]]></surname>
<given-names><![CDATA[Natalie]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gutiérrez Velázquez]]></surname>
<given-names><![CDATA[Ana Sofía]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Flores Raygoza]]></surname>
<given-names><![CDATA[Brenda Fernanda]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Tenorio Martínez]]></surname>
<given-names><![CDATA[Hatsumi]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vivero Acosta]]></surname>
<given-names><![CDATA[Estefanía]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Altamira Camacho]]></surname>
<given-names><![CDATA[Ramiro]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
<xref ref-type="aff" rid="A a"/>
<xref ref-type="aff" rid="A3"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Autónoma de Aguascalientes Departamento de Enfermería ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Grupo Nodal Transdisciplinario para la Investigación en Salud  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="Af3">
<institution><![CDATA[,Hospital General de Pabellón Arteaga  ]]></institution>
<addr-line><![CDATA[Aguascalientes ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2024</year>
</pub-date>
<volume>22</volume>
<numero>3</numero>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S1692-72732024000300007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S1692-72732024000300007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S1692-72732024000300007&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Introducción:  La comunicación representa un pilar fundamental al brindar atención sanitaria, lo que permite identificar y tratar las necesidades de las personas que la solicitan. Al presentarse algún grado de discapacidad auditiva, se interponen barreras en la relación de cuidado. El artículo busca explorar la experiencia vivida de las personas con discapacidad auditiva durante la atención sanitaria.  Materiales y métodos:  Estudio cualitativo fenomenológico hermenêutico. Muestreo por método de cadena de referencia hasta alcanzar la saturación de información. Se solicitó autorización a los participantes para relatar, mediante una entrevista fenomenológica, las vivencias respecto a la atención sanitaria que han recibido. Se consideró un rigor ético y metodológico basado en la validez, credibilidad, transferibilidad, consistencia, empleo de consentimiento informado, confidencialidad y manejo de riesgos.  Resultados:  Se contó con la participación de 6 personas con discapacidad auditiva, 3 del sexo femenino y 3 del sexo masculino, cuya edad oscilaba entre los 26 y los 46 años. Se obtuvieron 18 temas que se agruparon en 5 unidades de significado: la interpretación como necesidad básica, el sistema de atención sanitaria como generador de discriminación, reformando la atención sanitaria, estado de ánimo ante la discriminación y Sorge ante la discriminación.  Conclusión:  La experiencia vivida de las personas con discapacidad auditiva indica la privación al derecho de la atención sanitaria de calidad.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Introduction:  Communication represents a fundamental pillar when providing health care, which makes it possible to identify and treat the needs of the people who request it. When presenting some degree of hearing disability, barriers are placed in the care relationship. The objective of this paper is to explore the lived experience of people with hearing disabilities during health care.  Materials and methods:  Hermeneutic phenomenological qualitative study. Sampling by reference chain method until information saturation is reached. Authorization was requested by the participants, to report through a phenomenological interview, the experiences regarding the health care they have received. Ethical and methodological rigor was considered based on validity, credibility, transferability, consistency, use of informed consent, confidentiality, and risk management.  Results:  A total of 6 people with hearing disabilities participated, three female and three males, whose age ranges between 26 and 46 years. Eighteen themes were obtained that were grouped into five meaning units: Interpretation as a basic need; The health care system as a generator of discrimination; Reforming Health Care; State of mind in the face of discrimination and Sorge in the face of discrimination.  Conclusion:  The lived experience of people with hearing disabilities indicates the deprivation of the right to quality health care. The need to remove barriers that contribute to the creation of fair and equitable conditions for all is stressed.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Resumo  Introdução:  A comunicação representa pilar fundamental na prestação de serviços de saúde, permitindo que as necessidades das pessoas que buscam atendimento sejam identificadas e tratadas. Com algum grau de deficiência auditiva, são colocadas barreiras na relação de atendimento. O objetivo deste artigo é explorar a experiência vivida por pessoas com deficiência auditiva durante o atendimento de saúde.  Materiais e métodos:  Estudo qualitativo fenomenológico hermenêutico. Amostragem pelo método da cadeia de referência até atingir a saturação de informações. Aos participantes foi solicitada permissão para relatar, por meio de entrevista fenomenológica, suas experiências com o atendimento de saúde que receberam. O rigor ético e metodológico foi considerado com base na validade, na credibilidade, na transferibilidade, na consistência, no uso do consentimento informado, na confidencialidade e no gerenciamento de riscos.  Resultados:  Seis pessoas com deficiência auditiva, três do sexo feminino e três do sexo masculino, com idades entre 26 e 46 anos, participaram do estudo. Dezoito temas foram obtidos e agrupados em cinco unidades de significado: interpretação como uma necessidade básica; sistema de atenção à saúde como gerador de discriminação; reforma da atenção à saúde; estado de espírito diante da discriminação e Sorge diante da discriminação.  Conclusão:  A experiência vivida pelas pessoas com deficiência auditiva indica a privação do direito à assistência médica de qualidade.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[experiencia vivida]]></kwd>
<kwd lng="es"><![CDATA[discapacidad auditiva]]></kwd>
<kwd lng="es"><![CDATA[atención sanitaria]]></kwd>
<kwd lng="en"><![CDATA[life experiences]]></kwd>
<kwd lng="en"><![CDATA[hearing impairment]]></kwd>
<kwd lng="en"><![CDATA[health care]]></kwd>
<kwd lng="pt"><![CDATA[experiência vivida]]></kwd>
<kwd lng="pt"><![CDATA[deficiência auditiva]]></kwd>
<kwd lng="pt"><![CDATA[assistência médica]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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