<?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>1657-4702</journal-id>
<journal-title><![CDATA[Revista Latinoamericana de Bioética]]></journal-title>
<abbrev-journal-title><![CDATA[rev.latinoam.bioet.]]></abbrev-journal-title>
<issn>1657-4702</issn>
<publisher>
<publisher-name><![CDATA[Universidad Militar Nueva Granada]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1657-47022020000200041</article-id>
<article-id pub-id-type="doi">10.18359/rlbi.4703</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[A bioética da intervenção como possibilidade de inclusão social de pacientes com doença falciforme em tempos de COVID-19]]></article-title>
<article-title xml:lang="es"><![CDATA[La bioética de la intervención como posibilidad de inclusión social de pacientes con enfermedad de células falciformes en tiempos de COVID-19]]></article-title>
<article-title xml:lang="en"><![CDATA[Intervention bioethics as a social inclusion possibility for sickle cell anemia patients in times of COVID-19]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gustin]]></surname>
<given-names><![CDATA[Clara]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pimentel]]></surname>
<given-names><![CDATA[Willian]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sarsur]]></surname>
<given-names><![CDATA[Marcelo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Dadalto]]></surname>
<given-names><![CDATA[Luciana]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Pontifícia Universidade Católica de Minas Gerais  ]]></institution>
<addr-line><![CDATA[Belo Horizonte ]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidade Estadual do Rio de Janeiro  ]]></institution>
<addr-line><![CDATA[Belo Horizonte ]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Universidade Federal de Minas Gerais  ]]></institution>
<addr-line><![CDATA[Belo Horizonte ]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Universidade Federal de Minas Gerais  ]]></institution>
<addr-line><![CDATA[Belo Horizonte ]]></addr-line>
<country>Brazil</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2020</year>
</pub-date>
<volume>20</volume>
<numero>2</numero>
<fpage>41</fpage>
<lpage>53</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S1657-47022020000200041&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S1657-47022020000200041&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S1657-47022020000200041&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Resumo: este artigo discute a exclusão social vivida pelos indivíduos brasileiros com a doença falciforme, sob a perspectiva da bioética de intervenção. Trata-se de uma enfermidade na qual o afetado herda de seus progenitores o gene responsável pelo formato diferenciado da hemoglobina; ademais, apresenta maior incidência na população negra, uma vez que a alteração do formato da hemoglobina foi resultado da evolução do próprio corpo para evitar a contração da malária no continente africano. Além da exclusão social que a população negra sofre, há, ainda, um maior grau de preconceito advindo dos efeitos da doença. Revela-se que as dificuldades enfrentadas pelos acometidos são agravadas em decorrência da COVID-19. Portanto, a criação de políticas públicas que se alicercem nos parâmetros da bioética da intervenção, cujo foco principal é a vulnerabilidade e os desafios persistentes da sociedade, é proposta como possível ação para minorar as consequências da doença falciforme na população por ela afetada.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen: el artículo discute la exclusión social vivida por individuos brasileños con la enfermedad de células falciformes, desde la perspectiva de la bioética de intervención. Se trata de uma enfermedad en que el afectado hereda de sus progenitores el gen responsable del formato diferenciado da hemoglobina; asimismo, presenta más incidencia en población negra, una vez que la alteración del formato da hemoglobina resultó de la evolución del propio cuerpo para evitar la malaria en el continente africano. Además de la exclusión social que la población negra sufre, hay aun un mayor grado de discriminación que proviene de los efectos de la enfermedad. Se revela que las dificultades afrontadas por los enfermos se ven agravadas debido a la COVID-19. Por lo tanto, la creación de políticas públicas que se fundamenten en los parámetros de la bioética de la intervención, cuyo enfoque principal es la vulnerabilidad y los retos persistentes de la sociedad, se propone como posible acción de reducir las consecuencias de la enfermedad falciforme en la población afectada.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract: This paper discusses from the perspective of intervention bioethics the social exclusion experienced by Brazilian individuals suffering from sickle cell anemia. It is an inherited disease where the gene responsible for the hemoglobin differential format is generationally passed on. It has more incidence in the afro-descendant population than any other, given that this hemoglobin format alteration was an evolutionary response to prevent malaria in the African continent. Besides the social exclusion that this population suffers, there is an even greater degree of discrimination resulting from the disease's effects. It has been recently discovered that COVID-19 has worsened the difficulties faced by patients with this disease. Therefore, drafting intervention-bioethics-based public policies whose main focus relies on vulnerability and the persistent challenges of society is proposed as a possible action to reduce the consequences of patients suffering from sickle-cell anemia.]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[doença falciforme]]></kwd>
<kwd lng="pt"><![CDATA[exclusão social]]></kwd>
<kwd lng="pt"><![CDATA[bioética da intervenção]]></kwd>
<kwd lng="pt"><![CDATA[COVID-19]]></kwd>
<kwd lng="es"><![CDATA[enfermedad falciforme]]></kwd>
<kwd lng="es"><![CDATA[exclusión social]]></kwd>
<kwd lng="es"><![CDATA[bioética de la intervención]]></kwd>
<kwd lng="es"><![CDATA[COVID-19]]></kwd>
<kwd lng="en"><![CDATA[Sickle-cell anemia]]></kwd>
<kwd lng="en"><![CDATA[Social exclusion]]></kwd>
<kwd lng="en"><![CDATA[Intervention Bioethics]]></kwd>
<kwd lng="en"><![CDATA[COVID-19]]></kwd>
</kwd-group>
</article-meta>
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