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  <front>
    <journal-meta>
      <journal-id journal-id-type="nlm-ta">Arq Bras Cardiol</journal-id>
      <journal-id journal-id-type="publisher-id">abc</journal-id>
      <journal-title-group>
        <journal-title>Arquivos Brasileiros de Cardiologia</journal-title>
        <abbrev-journal-title abbrev-type="publisher">Arq. Bras. Cardiol.</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">0066-782X</issn>
      <issn pub-type="epub">1678-4170</issn>
      <publisher>
        <publisher-name>Sociedade Brasileira de Cardiologia - SBC</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id specific-use="scielo-v3" pub-id-type="publisher-id">FHSjsTTWMfQnvsQ3TKPfx8D</article-id>
      <article-id specific-use="scielo-v2" pub-id-type="publisher-id">S0066-782X2024000900310</article-id>
      <article-id pub-id-type="other">00310</article-id>
      <article-id pub-id-type="doi">10.36660/abc.20230875</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigo Original</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Progn&#243;stico de Pacientes Chag&#225;sicos e n&#227;o Chag&#225;sicos Submetidos a Implante de Marca-passo e Ressincronizador Card&#237;aco em Centro Terci&#225;rio</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0002-4892-6297</contrib-id>
          <name>
            <surname>Vasconcelos</surname>
            <given-names>La&#237;s Toledo de</given-names>
          </name>
          <role>Concep&#231;&#227;o e desenho da pesquisa</role>
          <role>An&#225;lise e interpreta&#231;&#227;o dos dados e Revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do</role>
          <role>Obten&#231;&#227;o de dados</role>
          <role>Reda&#231;&#227;o do manuscrito</role>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Martins</surname>
            <given-names>Larissa Natany Almeida</given-names>
          </name>
          <role>An&#225;lise estat&#237;stica</role>
          <xref ref-type="aff" rid="aff2">
            <sup>2</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Fran&#231;a</surname>
            <given-names>Anna Terra</given-names>
          </name>
          <role>Obten&#231;&#227;o de dados</role>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Castilho</surname>
            <given-names>F&#225;bio Morato de</given-names>
          </name>
          <role>Concep&#231;&#227;o e desenho da pesquisa</role>
          <role>An&#225;lise e interpreta&#231;&#227;o dos dados e Revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do</role>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ribeiro</surname>
            <given-names>Ant&#244;nio Luiz Pinho</given-names>
          </name>
          <role>Concep&#231;&#227;o e desenho da pesquisa</role>
          <role>An&#225;lise e interpreta&#231;&#227;o dos dados e Revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do</role>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
          <xref ref-type="corresp" rid="c1"/>
        </contrib>
        <aff id="aff1">
          <label>1</label>
          <institution content-type="orgname">Hospital das Cl&#237;nicas da Universidade Federal de Minas Gerais</institution>
          <institution content-type="orgdiv1">Faculdade de Medicina</institution>
          <institution content-type="orgdiv2">Departamento de Cl&#237;nica M&#233;dica</institution>
          <addr-line>
            <named-content content-type="city">Belo Horizonte</named-content>
            <named-content content-type="state">MG</named-content>
          </addr-line>
          <country country="BR">Brasil</country>
          <institution content-type="original">Programa de P&#243;s-gradua&#231;&#227;o em Ci&#234;ncias Aplicadas &#224; Sa&#250;de do Adulto &#8211; Departamento de Cl&#237;nica M&#233;dica - Faculdade de Medicina e Servi&#231;o de Cardiologia e Cirurgia Cardiovascular do Hospital das Cl&#237;nicas da Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG &#8211; Brasil</institution>
        </aff>
        <aff id="aff2">
          <label>2</label>
          <institution content-type="orgname">Universidade Federal de Minas Gerais</institution>
          <institution content-type="orgdiv1">Departamento de Estat&#237;stica</institution>
          <addr-line>
            <named-content content-type="city">Belo Horizonte</named-content>
            <named-content content-type="state">MG</named-content>
          </addr-line>
          <country country="BR">Brasil</country>
          <institution content-type="original">Departamento de Estat&#237;stica da Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG &#8211; Brasil</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="c1"><label>Correspond&#234;ncia:</label><bold>Ant&#244;nio Luiz Pinho Ribeiro</bold> &#8226; Centro de Telessa&#250;de &#8211; Hospital das Cl&#237;nicas UFMG &#8211; Av. Professor Alfredo Balena, 110, 1&#176; Andar, Ala Sul, Sala 107. CEP <postal-code>30130-100</postal-code>, Belo Horizonte, MG &#8211; Brasil E-mail: <email>tom1963br@yahoo.com.br</email> </corresp>
        <fn fn-type="edited-by">
          <label>Editor respons&#225;vel pela revis&#227;o:</label>
          <p>Mauricio Scanavacca</p>
        </fn>
        <fn fn-type="conflict">
          <label>Potencial conflito de interesse</label>
          <p>N&#227;o h&#225; conflito com o presente artigo.</p>
        </fn>
      </author-notes>
      <pub-date date-type="pub" publication-format="electronic">
        <day>18</day>
        <month>10</month>
        <year>2024</year>
      </pub-date>
      <pub-date date-type="collection" publication-format="electronic">
        <year>2024</year>
      </pub-date>
      <volume>121</volume>
      <issue>9</issue>
      <elocation-id>e20230875</elocation-id>
      <history>
        <date date-type="received">
          <day>16</day>
          <month>01</month>
          <year>2024</year>
        </date>
        <date date-type="rev-recd">
          <day>21</day>
          <month>05</month>
          <year>2024</year>
        </date>
        <date date-type="accepted">
          <day>24</day>
          <month>07</month>
          <year>2024</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/" xml:lang="en">
          <license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License</license-p>
        </license>
      </permissions>
      <abstract>
        <title>Resumo</title>
        <sec>
          <title>Fundamento:</title>
          <p>A cardiomiopatia chag&#225;sica (CCh) &#233; respons&#225;vel pelo implante de marca-passo (MP) em muitos pacientes, tendo sido associada a progn&#243;stico adverso.</p>
        </sec>
        <sec>
          <title>Objetivos:</title>
          <p>Comparar o progn&#243;stico da popula&#231;&#227;o chag&#225;sica e n&#227;o chag&#225;sica submetida ao implante de MP e ressincronizador card&#237;aco.</p>
        </sec>
        <sec>
          <title>M&#233;todos:</title>
          <p>Estudo observacional, retrospectivo, que analisou coorte de pacientes submetidos a implante desses dispositivos, em centro terci&#225;rio, de outubro 2007 a dezembro de 2017, comparando o grupo de pacientes chag&#225;sicos com os n&#227;o-chag&#225;sicos. O m&#233;todo n&#227;o param&#233;trico de Kaplan-Meier foi utilizado para calcular a sobrevida dos pacientes. O n&#237;vel de signific&#226;ncia adotado na an&#225;lise estat&#237;stica foi de 5%. O desfecho prim&#225;rio foi a mortalidade por qualquer causa, enquanto os desfechos secund&#225;rios foram a ocorr&#234;ncia de interna&#231;&#227;o e o desfecho combinado interna&#231;&#227;o e morte.</p>
        </sec>
        <sec>
          <title>Resultados:</title>
          <p>Um total de 911 pacientes foram inclu&#237;dos, sendo que 23,4% apresentavam CCh. Em an&#225;lise de Cox ajustada por sexo e idade, a doen&#231;a de Chagas (dCh) n&#227;o esteve associada ao risco aumentado de morte (HR: 1,14, IC:95%, 0,86-1,51, p=0,365), interna&#231;&#227;o (HR: 0,79, IC:95%, 0,61-1,04, p=0,09) ou desfecho combinado morte e interna&#231;&#227;o (HR: 0,90, IC:95%, 0,72-1,12, p=0,49).</p>
        </sec>
        <sec>
          <title>Conclus&#245;es:</title>
          <p>A dCh n&#227;o se associou ao aumento do risco de morte, interna&#231;&#227;o, ou desfecho combinado morte e interna&#231;&#227;o, mesmo ap&#243;s ajuste para sexo e idade. Tais resultados se contrap&#245;em aos de estudos pr&#233;vios e sugerem modifica&#231;&#227;o da qualidade do cuidado ao paciente cardiopata.</p>
        </sec>
      </abstract>
      <kwd-group xml:lang="pt">
        <title>Palavras-chave:</title>
        <kwd>Marca-passo Artificial</kwd>
        <kwd>Estimula&#231;&#227;o Card&#237;aca Artificial</kwd>
        <kwd>Cardiomiopatia Chag&#225;sica</kwd>
      </kwd-group>
      <counts>
        <fig-count count="8"/>
        <table-count count="6"/>
        <equation-count count="0"/>
        <ref-count count="27"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <fig id="f4">
      <caption>
        <title>Avalia&#231;&#227;o progn&#243;stica de pacientes chag&#225;sicos e n&#227;o chag&#225;sicos submetidos &#224; implante de marca-passo. HR: Hazard Ratio; IC: Intervalo de Confian&#231;a.</title>
      </caption>
      <graphic xlink:href="1678-4170-abc-121-09-e20230875-30875-gf01.tif"/></fig>
    <sec sec-type="intro">
      <title>Introdu&#231;&#227;o</title>
      <p>A estimula&#231;&#227;o el&#233;trica card&#237;aca se destaca como uma das maiores conquistas na &#225;rea da cardiologia no s&#233;culo XX.<sup><xref ref-type="bibr" rid="B1">1</xref></sup> Nas &#250;ltimas d&#233;cadas, observa-se aumento do n&#250;mero de implantes, que pode ser atribu&#237;do ao envelhecimento populacional, aos avan&#231;os tecnol&#243;gicos desses aparelhos, e ao aumento do n&#250;mero de indica&#231;&#245;es cl&#237;nicas.<sup><xref ref-type="bibr" rid="B2">2</xref>,<xref ref-type="bibr" rid="B3">3</xref></sup></p>
      <p>Desses implantes, a CCh ainda &#233; respons&#225;vel por parte significativa das indica&#231;&#245;es de estimula&#231;&#227;o card&#237;aca artificial permanente em nosso pa&#237;s,<sup><xref ref-type="bibr" rid="B4">4</xref></sup> embora observe-se queda gradual e progressiva de implantes de MP por essa etiologia, refletindo um melhor controle epidemiol&#243;gico da dCh em territ&#243;rio nacional.<sup><xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B6">6</xref></sup></p>
      <p>Apesar da redu&#231;&#227;o de sua preval&#234;ncia, em especial na Am&#233;rica Latina, a dCh evoluindo com CCh ainda apresenta elevada morbimortalidade no Brasil, com pior progn&#243;stico do que o das cardiomiopatias n&#227;o inflamat&#243;rias.<sup><xref ref-type="bibr" rid="B7">7</xref></sup> Entretanto, h&#225; poucos estudos que avaliaram caracter&#237;sticas epidemiol&#243;gicas associadas aos preditores de mortalidade de pacientes com MP e CCh.<sup><xref ref-type="bibr" rid="B4">4</xref>,<xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B8">8</xref>,<xref ref-type="bibr" rid="B9">9</xref></sup></p>
      <p>O presente estudo objetivou comparar a evolu&#231;&#227;o de pacientes chag&#225;sicos e n&#227;o chag&#225;sicos submetidos a implante de MP e ressincronizador em um centro terci&#225;rio brasileiro.</p>
    </sec>
    <sec sec-type="methods">
      <title>M&#233;todos</title>
      <p>Trata-se de estudo observacional, retrospectivo e longitudinal. Foram inclu&#237;dos todos os pacientes submetidos a implante de MP e ressincronizador no centro terci&#225;rio em quest&#227;o de outubro de 2007 a dezembro de 2017. O projeto de pesquisa foi aprovado pelo Comit&#234; de &#201;tica em Pesquisa da institui&#231;&#227;o, em conson&#226;ncia com os termos da Resolu&#231;&#227;o n&#176; 466/12 do Conselho Nacional de Sa&#250;de com parecer sob o n&#250;mero CAAE: 56119122.0.0000.5149.</p>
      <p>As informa&#231;&#245;es dos pacientes foram obtidas a partir de um banco de dados constitu&#237;do por informa&#231;&#245;es do prontu&#225;rio eletr&#244;nico do Laborat&#243;rio de dispositivos card&#237;acos implant&#225;veis (LDCI) de um hospital terci&#225;rio refer&#234;ncia SUS de Minas Gerais com seguimento at&#233; dezembro de 2018. O banco de dados foi elaborado por meio do m&#233;todo de Processamento de Linguagem Natural (PLN), uma ferramenta de intelig&#234;ncia artificial que permitiu extrair as informa&#231;&#245;es de interesse contidas em texto livre do prontu&#225;rio eletr&#244;nico.<sup><xref ref-type="bibr" rid="B10">10</xref></sup> Posteriormente obteve-se o registro de todas as autoriza&#231;&#245;es de interna&#231;&#227;o hospitalar (AIHs) do Sistema de Informa&#231;&#245;es Hospitalares do SUS (SIH-SUS) para procedimentos cardiovasculares da cidade de Belo Horizonte, bem como do registro de &#243;bito no Sistema de Informa&#231;&#227;o sobre Mortalidade (SIM) do Departamento de Inform&#225;tica do Sistema &#218;nico de Sa&#250;de (DATASUS) de Minas Gerais. O pareamento final dos pacientes comuns dessas fontes de informa&#231;&#245;es gerou o banco de dados final do estudo.</p>
      <p>Foram exclu&#237;dos os pacientes que eram acompanhados, mas n&#227;o tiveram o dispositivo implantado no hospital no per&#237;odo do estudo, pacientes que tiveram o dispositivo explantado definitivamente por qualquer motivo, pacientes que n&#227;o tinham registro de acompanhamento no LDCI do hospital, menores de 18 anos e pacientes portadores de cardiodesfibrilador implant&#225;vel (CDI) isoladamente.</p>
      <p>Foram analisadas as vari&#225;veis presen&#231;a ou aus&#234;ncia de dCh (exposi&#231;&#227;o), sexo e idade. Os dispositivos implantados foram divididos em: Marca-passo (unicameral ou bicameral) ou ressincronizador (multiss&#237;tio) isolado ou com CDI. A vari&#225;vel interna&#231;&#227;o foi obtida a partir dos dados de AIH, sendo considerada positiva quando o paciente tinha pelo menos uma interna&#231;&#227;o por motivo cardiovascular ap&#243;s a data do implante do dispositivo.</p>
      <p>O desfecho prim&#225;rio analisado foi a mortalidade por qualquer causa, sendo feita compara&#231;&#227;o entre os grupos de pacientes chag&#225;sicos e n&#227;o chag&#225;sicos. Os desfechos secund&#225;rios analisados foram a ocorr&#234;ncia de interna&#231;&#227;o, desfecho combinado interna&#231;&#227;o e mortalidade por qualquer causa, compara&#231;&#227;o da mortalidade entre chag&#225;sicos e n&#227;o chag&#225;sicos em cada uma das tr&#234;s eras e compara&#231;&#227;o de mortalidade por qualquer causa de acordo com o tipo de dispositivo.</p>
      <p>Os pacientes foram ainda divididos em tr&#234;s eras, de acordo com a data de implante do dispositivo. O tempo total de inclus&#227;o do estudo foi dividido em 3 per&#237;odos de 41 meses cada: outubro de 2007 a fevereiro de 2011 (era 1), mar&#231;o de 2011 a julho de 2014 (era 2), agosto de 2014 a dezembro de 2017 (era 3), com o intuito de se avaliar se houve diferen&#231;a de mortalidade entre chag&#225;sicos e n&#227;o chag&#225;sico em cada uma das diferentes eras.</p>
      <sec>
        <title>An&#225;lise estat&#237;stica</title>
        <p>Para a an&#225;lise dos dados, foi utilizado o programa R (vers&#227;o 4.3 Viena, &#193;ustria). Os dados obtidos de vari&#225;veis cont&#237;nuas foram apresentados como m&#233;dia e desvio-padr&#227;o, se eles apresentavam distribui&#231;&#227;o normal ou mediana e percentis 25 e 75, se eles n&#227;o apresentavam distribui&#231;&#227;o normal. Para avalia&#231;&#227;o da vari&#225;vel idade realizou-se o teste T de Student de compara&#231;&#227;o de m&#233;dias. Para as compara&#231;&#245;es das vari&#225;veis entre os grupos de chag&#225;sicos e n&#227;o chag&#225;sicos foi utilizado o teste T de Student. Os testes de independ&#234;ncia X&#178; e de Kruskal-Wallis foram utilizados para avalia&#231;&#227;o de vari&#225;veis cont&#237;nuas com as demais caracter&#237;sticas de base dos pacientes e dispositivos estudados ao longo dos per&#237;odos. O m&#233;todo n&#227;o param&#233;trico de Kaplan-Meier foi utilizado para calcular a sobrevida dos pacientes. O n&#237;vel de signific&#226;ncia estat&#237;stica foi definido para valores de p inferiores a 0,05, calculados pelo teste <italic>Logrank</italic>. O modelo multivariado de regress&#227;o proporcional de Cox, com estimativas de <italic>Hazard ratio</italic> (HR) e intervalos de confian&#231;a de 95%, foi usado para analisar o efeito nas covari&#225;veis nos desfechos estudados. A suposi&#231;&#227;o de Cox proporcional foi verificada usando-se as curvas de sobreviv&#234;ncia de log-log.</p>
        <p>Foi realizada uma an&#225;lise de sensibilidade avaliando-se o desfecho mortalidade por qualquer causa de acordo com o tipo de dispositivo na popula&#231;&#227;o chag&#225;sica e n&#227;o chag&#225;sica ap&#243;s a exclus&#227;o do ressincronizador e do ressincronizador com CDI, por se tratarem de dispositivos mais complexos e com distribui&#231;&#227;o desigual nas duas popula&#231;&#245;es, para se avaliar se os resultados se mantinham consistentes.</p>
      </sec>
    </sec>
    <sec sec-type="results">
      <title>Resultados</title>
      <p>Dos 2819 pacientes cadastrados no LDCI do hospital em que a pesquisa foi realizada, foram inclu&#237;dos 911 pacientes submetidos a implante de MP e ressincronizador durante o per&#237;odo estudado (<xref ref-type="fig" rid="f1">Figura 1</xref>). A m&#233;dia de idade dos pacientes inclu&#237;dos foi de 68 anos (variando de 20 a 97 anos), sendo 48,5% do sexo masculino. Do total de pacientes, 23,4% apresentavam CCh. A idade m&#233;dia de implante de MP na popula&#231;&#227;o portadora de CCh foi de 65 anos e dos n&#227;o portadores foi de 69 anos. Em rela&#231;&#227;o aos dispositivos card&#237;acos implant&#225;veis, na popula&#231;&#227;o chag&#225;sica, 77,5% implantaram MP Bicameral, 16,4% MP unicameral, 3,3% ressincronizador e 2,8% ressincronizador com CDI (<xref ref-type="table" rid="t1">Tabela 1</xref>).</p>
      <fig id="f1">
        <label>Figura 1</label>
        <caption>
          <title>Fluxograma de sele&#231;&#227;o dos pacientes. *Pacientes que fazem acompanhamento no LDCI do HC-UFMG, mas o implante inicial do dispositivo foi realizado em outro hospital ou em per&#237;odo diferente do per&#237;odo do presente estudo.</title>
        </caption>
        <graphic xlink:href="1678-4170-abc-121-09-e20230875-30875-gf02.tif"/></fig>
      <table-wrap id="t1">
        <label>Tabela 1</label>
        <caption>
          <title>Caracter&#237;sticas de base da popula&#231;&#227;o</title>
        </caption>
        <table frame="hsides" rules="groups">
          <colgroup width="19%">
            <col width="1%"/>
            <col/>
            <col/>
            <col/>
            <col/>
            <col/>
          </colgroup>
          <thead style="border-top: thin solid; border-bottom: thin solid; border-color: #000000">
            <tr style="background-color:#76B4CF">
              <th align="left" colspan="2" valign="middle">Caracter&#237;sticas</th>
              <th align="center" valign="middle">Chag&#225;sicos (N=213)</th>
              <th align="center" valign="middle">N&#227;o Chag&#225;sicos (N=698)</th>
              <th align="center" valign="middle">Total (N=911)</th>
              <th align="center" valign="middle">Valor p</th>
            </tr>
          </thead>
          <tbody style="border-bottom: thin solid; border-color: #000000">
            <tr>
              <td align="left" colspan="2" valign="middle">
                <bold>Idade &#8211; anos</bold>
              </td>
              <td align="center" valign="middle">65 (23-93)</td>
              <td align="center" valign="middle">69 (20-97)</td>
              <td align="center" valign="middle">68 (20-97)</td>
              <td align="center" valign="middle">&lt;0,001</td>
            </tr>
            <tr style="background-color:#C7DFEC">
              <td align="left" colspan="2" valign="middle">
                <bold>Sexo Masculino &#8211; n (%)</bold>
              </td>
              <td align="center" valign="middle">96 (21,7%)</td>
              <td align="center" valign="middle">346(78,3%)</td>
              <td align="center" valign="middle">442 (48,5%)</td>
              <td align="center" valign="middle">0,284</td>
            </tr>
            <tr>
              <td align="left" colspan="2" valign="middle">
                <bold>Dispositivos- n (%)</bold>
              </td>
              <td align="center" valign="middle"/>
              <td align="center" valign="middle"/>
              <td align="center" valign="middle"/>
              <td align="center" valign="middle">&lt;0,001</td>
            </tr>
            <tr>
              <td align="left" valign="middle"/>
              <td align="left" valign="middle">MP unicameral</td>
              <td align="center" valign="middle">35 (16,4%)</td>
              <td align="center" valign="middle">114 (16,3%)</td>
              <td align="center" valign="middle">149 (16,4%)</td>
              <td align="center" valign="middle"/>
            </tr>
            <tr>
              <td align="left" valign="middle"/>
              <td align="left" valign="middle">MP bicameral</td>
              <td align="center" valign="middle">165 (77,5%)</td>
              <td align="center" valign="middle">409 (58,6%)</td>
              <td align="center" valign="middle">574 (63%)</td>
              <td align="center" valign="middle"/>
            </tr>
            <tr>
              <td align="left" valign="middle"/>
              <td align="left" valign="middle">Ressincronizador</td>
              <td align="center" valign="middle">7 (3,3%)</td>
              <td align="center" valign="middle">126 (18,1%)</td>
              <td align="center" valign="middle">133 (14,6%)</td>
              <td align="center" valign="middle"/>
            </tr>
            <tr>
              <td align="left" valign="middle"/>
              <td align="left" valign="middle">Ressincronizador e CDI</td>
              <td align="center" valign="middle">6 (2,8%)</td>
              <td align="center" valign="middle">49 (7,0%)</td>
              <td align="center" valign="middle">55 (6,04%)</td>
              <td align="left" valign="middle"/>
            </tr>
          </tbody>
        </table>
        <table-wrap-foot>
          <fn id="TFN1">
            <p>MP: marca-passo; CDI: cardiodesfibrilador implant&#225;vel.</p>
          </fn>
        </table-wrap-foot>
      </table-wrap>
      <p>O tempo m&#233;dio de seguimento foi de 64,2 meses para o desfecho mortalidade, 60,6 meses para o desfecho interna&#231;&#227;o e 57,4 meses para o desfecho mortalidade e interna&#231;&#227;o.</p>
      <p>Ocorreram 306 (33,6%) mortes, sendo 80 (37,6%) na popula&#231;&#227;o chag&#225;sica e 226 (32,4%) na popula&#231;&#227;o n&#227;o chag&#225;sica (p=0,187). As interna&#231;&#245;es por causas cardiovasculares ocorreram em 275 (30,2%) pacientes, sendo que 76 (35,7%) tinham diagn&#243;stico de dCh e 199 (38,5%) n&#227;o tinham esse diagn&#243;stico (p=0,056). O desfecho combinado de mortalidade e interna&#231;&#227;o ocorreu em 419 (46%) pacientes, sendo que 109 (51,2%) eram chag&#225;sicos e 310 (44,4%) n&#227;o chag&#225;sicos (p=0,098).</p>
      <p>As curvas de Kaplan-Meier, usando teste de logrank com p=0,99, n&#227;o demonstraram diferen&#231;a de mortalidade entre os grupos chag&#225;sicos e n&#227;o chag&#225;sicos (<xref ref-type="fig" rid="f2">Figura 2</xref>), assim como n&#227;o demostraram diferen&#231;a entres os dois grupos em nenhuma das diferentes eras (<inline-supplementary-material mime-subtype="pdf" mimetype="application" xlink:href="1678-4170-abc-121-09-e20230875-30875-suppl01.pdf">Figura 4 &#8211; anexo</inline-supplementary-material>).</p>
      <fig id="f2">
        <label>Figura 2</label>
        <caption>
          <title>Curva de Kaplan Meier com sobrevida livre de morte segundo etiologia. Chagas=0: Aus&#234;ncia de Doen&#231;a de Chagas; Chagas=1: Presen&#231;a de Doen&#231;a de Chagas. As curvas de sobrevida foram comparadas usando o teste de long rank, p=0,99.</title>
        </caption>
        <graphic xlink:href="1678-4170-abc-121-09-e20230875-30875-gf03.tif"/></fig>
      <p>Aus&#234;ncia de diferen&#231;a tamb&#233;m foi observada na an&#225;lise das curvas do desfecho combinado mortalidade e interna&#231;&#227;o entre os dois grupos (<xref ref-type="fig" rid="f3">Figura 3</xref>).</p>
      <fig id="f3">
        <label>Figura 3</label>
        <caption>
          <title>Curva de Kaplan Meier com sobrevida livre do desfecho combinado mortalidade e interna&#231;&#227;o segundo etiologia. Chagas=0: Aus&#234;ncia de Doen&#231;a de Chagas; Chagas=1: Presen&#231;a de Doen&#231;a de Chagas. As curvas de sobrevida foram comparadas usando o teste de long rank, p=0,25.</title>
        </caption>
        <graphic xlink:href="1678-4170-abc-121-09-e20230875-30875-gf04.tif"/></fig>
      <p>As curvas de Kaplan-Meier para avalia&#231;&#227;o de mortalidade em pacientes com MP bicameral n&#227;o mostraram diferen&#231;a entre chag&#225;sicos e n&#227;o chag&#225;sicos, assim como as curvas para pacientes com MP unicameral (<inline-supplementary-material mime-subtype="pdf" mimetype="application" xlink:href="1678-4170-abc-121-09-e20230875-30875-suppl02.pdf">Figura 5 &#8211; anexo</inline-supplementary-material>). N&#227;o foi poss&#237;vel fazer essa an&#225;lise para os pacientes com os dispositivos ressincronizador isolado e ressincronizador com CDI, pois o n&#250;mero de pacientes chag&#225;sicos com esses dispositivos foi muito pequeno. Procedeu-se uma an&#225;lise de sensibilidade, ap&#243;s exclus&#227;o dos pacientes com ressincronizador (isolado ou associado ao CDI), analisando em conjunto somente os pacientes com MP unicameral e bicameral. As curvas de Kaplan-Meier dessa an&#225;lise tamb&#233;m n&#227;o mostraram diferen&#231;a de mortalidade entre chag&#225;sicos e n&#227;o chag&#225;sicos (<inline-supplementary-material mime-subtype="pdf" mimetype="application" xlink:href="1678-4170-abc-121-09-e20230875-30875-suppl03.pdf">Figura 6 &#8211; anexo</inline-supplementary-material>).</p>
      <p>No modelo de Cox, em an&#225;lise univariada, a presen&#231;a de dCh tamb&#233;m n&#227;o esteve associada a mortalidade por qualquer causa, tanto na an&#225;lise por todos os dispositivos quanto na an&#225;lise por cada tipo de dispositivo. O sexo masculino e a idade, por sua vez, relacionaram-se com o aumento do risco de morte (<inline-supplementary-material mime-subtype="pdf" mimetype="application" xlink:href="1678-4170-abc-121-09-e20230875-30875-suppl04.pdf">Tabela 3 &#8211; anexo</inline-supplementary-material>).</p>
      <p>Na an&#225;lise multivariada no modelo de Cox, ajustada por sexo e idade, os resultados se mantiveram e a dCh n&#227;o esteve associada ao risco aumentado de morte, interna&#231;&#227;o, ou desfecho combinado morte e interna&#231;&#227;o (<xref ref-type="fig" rid="f4">Figura Central</xref>), mesmo quando analisado nas diferentes eras (<xref ref-type="table" rid="t2">Tabela 2</xref>).</p>
      <table-wrap id="t2">
        <label>Tabela 2</label>
        <caption>
          <title>Modelo de Regress&#227;o Cox para avalia&#231;&#227;o da popula&#231;&#227;o Chag&#225;sica &#8211; An&#225;lise Multivariada (ajustada para sexo e idade)</title>
        </caption>
        <table frame="hsides" rules="groups">
          <colgroup width="33%">
            <col width="1%"/>
            <col/>
            <col/>
            <col/>
          </colgroup>
          <thead style="border-top: thin solid; border-bottom: thin solid; border-color: #000000">
            <tr style="background-color:#76B4CF">
              <th align="left" colspan="2" valign="middle">Doen&#231;a de Chagas</th>
              <th align="center" valign="middle">HR (IC- 95%)</th>
              <th align="center" valign="middle">Valor p</th>
            </tr>
          </thead>
          <tbody style="border-bottom: thin solid; border-color: #000000">
            <tr>
              <td align="left" colspan="2" valign="middle">
                <bold>Mortalidade Total</bold>
              </td>
              <td align="center" valign="middle">1,14 (0,86-1,51)</td>
              <td align="center" valign="middle">0,365</td>
            </tr>
            <tr style="background-color:#C7DFEC">
              <td align="left" colspan="2" valign="middle">
                <bold>Mortalidade por Eras</bold>
              </td>
              <td align="left" valign="middle"/>
              <td align="left" valign="middle"/>
            </tr>
            <tr style="background-color:#C7DFEC">
              <td align="left" valign="middle"/>
              <td align="left" valign="middle">Era 1</td>
              <td align="center" valign="middle">1,17 (0,83-1,66)</td>
              <td align="center" valign="middle">0,38</td>
            </tr>
            <tr style="background-color:#C7DFEC">
              <td align="left" valign="middle"/>
              <td align="left" valign="middle">Era 2</td>
              <td align="center" valign="middle">0,87 (0,53-1,41)</td>
              <td align="center" valign="middle">0,56</td>
            </tr>
            <tr style="background-color:#C7DFEC">
              <td align="left" valign="middle"/>
              <td align="left" valign="middle">Era 3</td>
              <td align="center" valign="middle">1,29 (0,57-2,90)</td>
              <td align="center" valign="middle">0,55</td>
            </tr>
            <tr>
              <td align="left" colspan="2" valign="middle">
                <bold>Interna&#231;&#227;o</bold>
              </td>
              <td align="center" valign="middle">0,79 (0,61-1,04)</td>
              <td align="center" valign="middle">0,09</td>
            </tr>
            <tr style="background-color:#C7DFEC">
              <td align="left" colspan="2" valign="middle">
                <bold>Mortalidade e interna&#231;&#227;o</bold>
              </td>
              <td align="center" valign="middle">0,90 (0,72-1,12)</td>
              <td align="center" valign="middle">0,49</td>
            </tr>
          </tbody>
        </table>
        <table-wrap-foot>
          <fn id="TFN3">
            <p>HR: hazard ratio; IC: intervalo de confian&#231;a.</p>
          </fn>
        </table-wrap-foot>
      </table-wrap>
      <table-wrap id="t3">
        <label>Tabela 3</label>
        <caption>
          <title>Modelo de Regress&#227;o Cox para avalia&#231;&#227;o do desfecho mortalidade &#8211; An&#225;lise Univariada</title>
        </caption>
        <table frame="hsides" rules="groups">
          <colgroup width="33%">
            <col width="1%"/>
            <col/>
            <col/>
            <col/>
          </colgroup>
          <thead style="border-top: thin solid; border-bottom: thin solid; border-color: #000000">
            <tr style="background-color:#76B4CF">
              <th align="left" colspan="2" valign="middle">Vari&#225;veis</th>
              <th align="center" valign="middle">HR (IC - 95%)</th>
              <th align="center" valign="middle">Valor p</th>
            </tr>
          </thead>
          <tbody style="border-bottom: thin solid; border-color: #000000">
            <tr>
              <td align="left" colspan="2" valign="middle">Idade</td>
              <td align="center" valign="middle">1,02 (1,01-1,03)</td>
              <td align="center" valign="middle">p&lt;0,001</td>
            </tr>
            <tr style="background-color:#C7DFEC">
              <td align="left" colspan="2" valign="middle">
                <bold>Sexo Masculino</bold>
              </td>
              <td align="center" valign="middle">1,49 (1,16-1,92)</td>
              <td align="center" valign="middle">p=0,002</td>
            </tr>
            <tr>
              <td align="left" colspan="2" valign="middle">
                <bold>Chagas</bold>
              </td>
              <td align="center" valign="middle"/>
              <td align="center" valign="middle"/>
            </tr>
            <tr>
              <td align="left" valign="middle"/>
              <td align="left" valign="middle">Mortalidade Total</td>
              <td align="center" valign="middle">0,99 (0,75-1,30)</td>
              <td align="center" valign="middle">p=0,91</td>
            </tr>
            <tr style="background-color:#C7DFEC">
              <td align="left" colspan="2" valign="middle">
                <bold>Mortalidade por dispositivo</bold>
              </td>
              <td align="left" valign="middle"/>
              <td align="left" valign="middle"/>
            </tr>
            <tr style="background-color:#C7DFEC">
              <td align="left" valign="middle"/>
              <td align="left" valign="middle">MP bicameral</td>
              <td align="center" valign="middle">1,1 (0,79-1,53)</td>
              <td align="center" valign="middle">p=0,59</td>
            </tr>
            <tr style="background-color:#C7DFEC">
              <td align="left" valign="middle"/>
              <td align="left" valign="middle">MP unicameral</td>
              <td align="center" valign="middle">0,84 (0,51-1,37)</td>
              <td align="center" valign="middle">p= 0,49</td>
            </tr>
          </tbody>
        </table>
        <table-wrap-foot>
          <fn id="TFN2">
            <p>HR: hazard ratio; IC: intervalo de confian&#231;a.</p>
          </fn>
        </table-wrap-foot>
      </table-wrap>
    </sec>
    <sec sec-type="discussion">
      <title>Discuss&#227;o</title>
      <p>Como principal achado desta pesquisa destaca-se a aus&#234;ncia de diferen&#231;a de mortalidade entre os pacientes com MP e ressincronizador chag&#225;sicos quando comparados aos n&#227;o chag&#225;sicos. Esse resultado contrasta com estudos pr&#233;vios sobre o tema, que demonstram que, na compara&#231;&#227;o com outras cardiopatias dilatadas, os pacientes chag&#225;sicos apresentam pior progn&#243;stico,<sup><xref ref-type="bibr" rid="B8">8</xref>,<xref ref-type="bibr" rid="B11">11</xref>,<xref ref-type="bibr" rid="B12">12</xref></sup> normalmente relacionado &#224; alta incid&#234;ncia de morte s&#250;bita (respons&#225;vel por 55 a 65% das mortes nesses pacientes), al&#233;m de morte n&#227;o card&#237;aca e das diversas arritmias.<sup><xref ref-type="bibr" rid="B4">4</xref>,<xref ref-type="bibr" rid="B11">11</xref>,<xref ref-type="bibr" rid="B13">13</xref>,<xref ref-type="bibr" rid="B14">14</xref></sup> Quando comparados pacientes chag&#225;sicos e n&#227;o chag&#225;sicos com MP, Rincon et al. tamb&#233;m encontraram pior evolu&#231;&#227;o cl&#237;nica no chag&#225;sico, com maior incid&#234;ncia de arritmias ventriculares.<sup><xref ref-type="bibr" rid="B8">8</xref></sup></p>
      <p>Outra manifesta&#231;&#227;o grave que pode resultar em desfecho fatal, consequente ao acometimento card&#237;aco pela dCh &#233; a insufici&#234;ncia card&#237;aca (IC) avan&#231;ada, que responde por 25 a 30% dos &#243;bitos dessa popula&#231;&#227;o.<sup><xref ref-type="bibr" rid="B7">7</xref>,<xref ref-type="bibr" rid="B11">11</xref>,<xref ref-type="bibr" rid="B15">15</xref></sup> Esses pacientes, ao evolu&#237;rem com disfun&#231;&#227;o ventricular e piora de classe funcional, apresentam maior gravidade resultando em pior qualidade de vida, maiores taxas de mortalidade e interna&#231;&#227;o.<sup><xref ref-type="bibr" rid="B7">7</xref></sup> Por isso requerem tratamento cl&#237;nico e farmacol&#243;gico especializado com acompanhamento multidisciplinar regular,<sup><xref ref-type="bibr" rid="B7">7</xref>,<xref ref-type="bibr" rid="B16">16</xref></sup> fazendo com que se tornem mais sens&#237;veis &#224;s circunst&#226;ncias econ&#244;micas e sociais que impactam de forma desigual no bin&#244;mio sa&#250;de-doen&#231;a.<sup><xref ref-type="bibr" rid="B4">4</xref>,<xref ref-type="bibr" rid="B17">17</xref>,<xref ref-type="bibr" rid="B18">18</xref></sup></p>
      <p>Por outro lado, a estrutura&#231;&#227;o de servi&#231;os de refer&#234;ncia para o manejo e seguimento de pessoas com doen&#231;as cr&#244;nicas promovem uma melhor ader&#234;ncia aos tratamentos farmacol&#243;gicos e n&#227;o farmacol&#243;gicos, melhoram a qualidade de vida e reduzem taxas de mortalidade e interna&#231;&#245;es hospitalares.<sup><xref ref-type="bibr" rid="B4">4</xref></sup> O centro em que se realizou esse estudo passou por melhorias constantes de estrutura&#231;&#227;o para atendimento a esse tipo de pacientes nas &#250;ltimas duas d&#233;cadas. Por conseguinte, os resultados encontrados tamb&#233;m poderiam ser atribu&#237;dos &#224; organiza&#231;&#227;o, bom acompanhamento e tratamento das cardiopatias em geral, com a incorpora&#231;&#227;o de equipe especializada na condu&#231;&#227;o de arritmias e de IC ocorridas.<sup><xref ref-type="bibr" rid="B16">16</xref>,<xref ref-type="bibr" rid="B19">19</xref></sup> A avalia&#231;&#227;o de mortalidade em 3 eras diferentes, refor&#231;a a qualidade do cuidado ao longo do seguimento ao demonstrar a aus&#234;ncia de diferen&#231;a de mortalidade entre as popula&#231;&#245;es chag&#225;sicas e n&#227;o chag&#225;sica, independente do per&#237;odo analisado.</p>
      <p>No que diz respeito &#224;s caracter&#237;sticas gerais da popula&#231;&#227;o deste estudo, observou-se que a idade avan&#231;ada e o sexo masculino foram preditores de maior mortalidade em an&#225;lise univariada de Cox. Esses resultados se assemelham aos de outros estudos que avaliaram o perfil cl&#237;nico de portadores de MP, que demonstraram que a idade dos pacientes com dCh foi inferior &#224; da popula&#231;&#227;o n&#227;o chag&#225;sica na ocasi&#227;o do implante<sup><xref ref-type="bibr" rid="B8">8</xref>,<xref ref-type="bibr" rid="B9">9</xref></sup> e que o sexo feminino apresenta melhor sobrevida ap&#243;s o implante de MP.<sup><xref ref-type="bibr" rid="B20">20</xref></sup> Diante disso, todos os resultados foram ajustados por essas vari&#225;veis, mantendo sem diferen&#231;a nos desfechos morte, interna&#231;&#227;o e desfecho combinado morte e interna&#231;&#227;o entre a popula&#231;&#227;o chag&#225;sica e n&#227;o chag&#225;sica.</p>
      <p>Em s&#237;ntese, esse estudo demonstrou resultados relevantes com rela&#231;&#227;o ao progn&#243;stico dos pacientes com dispositivos card&#237;acos eletr&#244;nicos implant&#225;veis (DCEI) chag&#225;sicos e n&#227;o chag&#225;sicos. A confec&#231;&#227;o de um grande banco de dados, por meio do uso de uma ferramenta lingu&#237;stica de intelig&#234;ncia artificial (PLN) permitiu avaliar uma significativa coorte de indiv&#237;duos com MP e ressincronizador, com grande representa&#231;&#227;o de pacientes com dCh.</p>
      <p>Como limita&#231;&#245;es deve-se considerar que o uso do PLN n&#227;o possui sensibilidade de 100%,<sup><xref ref-type="bibr" rid="B10">10</xref></sup> podendo levar a perdas de desfechos, por&#233;m a sele&#231;&#227;o de uma amostragem aleat&#243;ria do resultado do PLN com confer&#234;ncia manual e ajuste, demonstrou boa precis&#227;o e sensibilidade do m&#233;todo. Outra limita&#231;&#227;o a ser apontada foi a exclus&#227;o dos portadores de CDI isolado que s&#227;o possivelmente mais graves e mais propensos a apresentar arritmias graves.<sup><xref ref-type="bibr" rid="B13">13</xref>,<xref ref-type="bibr" rid="B21">21</xref></sup> No entanto, isso se aplicaria igualmente aos pacientes chag&#225;sicos e n&#227;o chag&#225;sicos com o dispositivo em quest&#227;o. Al&#233;m disso, um estudo complementar que utilizou o mesmo banco de dados e avaliou apenas a popula&#231;&#227;o com o dispositivo CDI chag&#225;sica e n&#227;o chag&#225;sica ao longo do mesmo per&#237;odo, n&#227;o encontrou diferen&#231;a de mortalidade por qualquer causa entre os dois grupos.<sup><xref ref-type="bibr" rid="B14">14</xref></sup> A distribui&#231;&#227;o desigual de dispositivos mais complexos, como o ressincronizador isolado e associado ao CDI, implantados em n&#250;mero proporcionalmente maior na popula&#231;&#227;o n&#227;o chag&#225;sica, tamb&#233;m seria outra limita&#231;&#227;o. &#201; bem estabelecido que na CCh, existem restri&#231;&#245;es, que s&#227;o preditoras de pior resposta na terapia de ressincroniza&#231;&#227;o card&#237;aca (TRC).<sup><xref ref-type="bibr" rid="B4">4</xref>,<xref ref-type="bibr" rid="B22">22</xref>&#8211;<xref ref-type="bibr" rid="B27">27</xref></sup> No entanto, essa poss&#237;vel influ&#234;ncia dos dispositivos na mortalidade dos pacientes deste estudo foi avaliada por meio de uma an&#225;lise de sensibilidade com a exclus&#227;o dos pacientes portadores de ressincronizador e ressincronizador com CDI, e o resultado se manteve sem diferen&#231;a de mortalidade entre a popula&#231;&#227;o chag&#225;sica e n&#227;o chag&#225;sica.</p>
      <p>Por fim, &#233; importante salientar que, por ter car&#225;ter retrospectivo e observacional, esta an&#225;lise est&#225; sujeita &#224; qualidade das informa&#231;&#245;es contidas nos prontu&#225;rios, os quais n&#227;o apresentavam detalhamento das condi&#231;&#245;es cl&#237;nicas e laboratoriais dos pacientes e n&#227;o contemplavam dados sobre a terapia medicamentosa aplicada em cada popula&#231;&#227;o, sendo necess&#225;rios outros estudos, preferencialmente prospectivos, para confirmar os resultados encontrados.</p>
    </sec>
    <sec sec-type="conclusions">
      <title>Conclus&#245;es</title>
      <p>A presen&#231;a de dCh n&#227;o esteve associada ao risco aumentado de morte, interna&#231;&#227;o ou desfecho combinado morte e interna&#231;&#227;o nessa coorte de pacientes portadores de MP e ressincronizador card&#237;aco. Esses resultados se mantiveram consistentes mesmo quando analisados em diferentes eras de seguimento e ajustados por sexo e idade.</p>
    </sec>
  </body>
  <back>
    <fn-group>
      <fn fn-type="financial-disclosure" id="fn1">
        <label>Fontes de financiamento</label>
        <p>O presente estudo n&#227;o teve fontes de financiamento externas.</p>
      </fn>
      <fn fn-type="other" id="fn2">
        <label>Vincula&#231;&#227;o acad&#234;mica</label>
        <p>Este artigo &#233; parte de disserta&#231;&#227;o de Mestrado de La&#237;s Toledo de Vasconcelos pelo Programa de P&#243;s-gradua&#231;&#227;o em Ci&#234;ncias Aplicadas &#224; Sa&#250;de do Adulto, Faculdade de Medicina da Universidade Federal de Minas Gerais.</p>
      </fn>
      <fn fn-type="other" id="fn3">
        <label>Aprova&#231;&#227;o &#233;tica e consentimento informado</label>
        <p>Este estudo foi aprovado pelo Comit&#234; de &#201;tica da Universidade Federal de Minas Gerais sob o n&#250;mero de protocolo CAAE 56119122.0.0000.5149. Todos os procedimentos envolvidos nesse estudo est&#227;o de acordo com a Declara&#231;&#227;o de Helsinki de 1975, atualizada em 2013.</p>
      </fn>
    </fn-group>
    <ack>
      <title>Agradecimentos</title>
      <p>&#192; Faculdade de Medicina do Hospital das Cl&#237;nicas da Universidade Federal de Minas Gerais (UFMG) e ao Programa de P&#243;s-gradua&#231;&#227;o em Ci&#234;ncias Aplicadas &#224; Sa&#250;de do Adulto por estimularem o estudo cient&#237;fico e a pesquisa.</p>
      <p>Aos professores F&#225;bio Morato de Castilho e Ant&#244;nio Luiz Pinho Ribeiro por orientarem e contribu&#237;rem com a elabora&#231;&#227;o desse artigo e &#224; colega cardiologista e arritmologista Anna Terra Fran&#231;a pela elabora&#231;&#227;o do grande banco de dados que originou este estudo.</p>
    </ack>
    <ref-list>
      <title>Refer&#234;ncias</title>
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  <sub-article article-type="translation" id="S1" xml:lang="en">
    <front-stub>
      <article-id pub-id-type="doi">10.36660/abc.20230875i</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Original Article</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Prognostic Evaluation of Chagasic and Non-Chagasic Patients Undergoing Pacemaker Implantation and Cardiac Resynchronization in a Tertiary Center</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0002-4892-6297</contrib-id>
          <name>
            <surname>Vasconcelos</surname>
            <given-names>La&#237;s Toledo de</given-names>
          </name>
          <role>Conception and design of the research</role>
          <role>Analysis and interpretation of the data and Critical revision of the manuscript for content</role>
          <role>Acquisition of data</role>
          <role>Writing of the manuscript</role>
          <xref ref-type="aff" rid="aff3">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Martins</surname>
            <given-names>Larissa Natany Almeida</given-names>
          </name>
          <role>Statistical analysis</role>
          <xref ref-type="aff" rid="aff4">
            <sup>2</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Fran&#231;a</surname>
            <given-names>Anna Terra</given-names>
          </name>
          <role>Acquisition of data</role>
          <xref ref-type="aff" rid="aff3">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Castilho</surname>
            <given-names>F&#225;bio Morato de</given-names>
          </name>
          <role>Conception and design of the research</role>
          <role>Analysis and interpretation of the data and Critical revision of the manuscript for content</role>
          <xref ref-type="aff" rid="aff3">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ribeiro</surname>
            <given-names>Ant&#244;nio Luiz Pinho</given-names>
          </name>
          <role>Conception and design of the research</role>
          <role>Analysis and interpretation of the data and Critical revision of the manuscript for content</role>
          <xref ref-type="aff" rid="aff3">
            <sup>1</sup>
          </xref>
          <xref ref-type="corresp" rid="c2"/>
        </contrib>
        <aff id="aff3">
          <label>1</label>
          <addr-line>
            <named-content content-type="city">Belo Horizonte</named-content>
            <named-content content-type="state">MG</named-content>
          </addr-line>
          <country country="BR">Brazil</country>
          <institution content-type="original">Programa de P&#243;s-gradua&#231;&#227;o em Ci&#234;ncias Aplicadas &#224; Sa&#250;de do Adulto &#8211; Departamento de Cl&#237;nica M&#233;dica - Faculdade de Medicina e Servi&#231;o de Cardiologia e Cirurgia Cardiovascular do Hospital das Cl&#237;nicas da Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG &#8211; Brazil</institution>
        </aff>
        <aff id="aff4">
          <label>2</label>
          <addr-line>
            <named-content content-type="city">Belo Horizonte</named-content>
            <named-content content-type="state">MG</named-content>
          </addr-line>
          <country country="BR">Brazil</country>
          <institution content-type="original">Departamento de Estat&#237;stica da Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG &#8211; Brazil</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="c2"><label>Mailing Address:</label><bold>Ant&#244;nio Luiz Pinho Ribeiro</bold> &#8226; Centro de Telessa&#250;de &#8211; Hospital das Cl&#237;nicas UFMG &#8211; Av. Professor Alfredo Balena, 110, 1&#176; Andar, Ala Sul, Sala 107. Postal Code <postal-code>30130-100</postal-code>, Belo Horizonte, MG &#8211; Brazil E-mail: <email>tom1963br@yahoo.com.b</email> </corresp>
        <fn fn-type="edited-by">
          <label>Editor responsible for the review:</label>
          <p>Mauricio Scanavacca</p>
        </fn>
        <fn fn-type="conflict">
          <label>Potential conflict of interest</label>
          <p>No potential conflict of interest relevant to this article was reported.</p>
        </fn>
      </author-notes>
      <abstract>
        <title>Abstract</title>
        <sec>
          <title>Background:</title>
          <p>Chagas cardiomyopathy (ChCC) is one of the causes of the implantation of pacemakers (PM) in many patients and has been associated with an adverse prognosis.</p>
        </sec>
        <sec>
          <title>Objectives:</title>
          <p>To compare the prognosis of the chagasic and non-chagasic populations undergoing PM and cardiac resynchronizer implantation.</p>
        </sec>
        <sec>
          <title>Methods:</title>
          <p>Observational, retrospective study, which analyzed a cohort of patients who underwent implantation of these devices, in a tertiary center, from October 2007 to December 2017, comparing the chagasic group with non-chagasic patients. The non-parametric Kaplan-Meier method was used to calculate patient survival. The significance level adopted in the statistical analysis was 5%. The primary outcome was mortality from any cause, while the secondary outcomes were the occurrence of hospitalization and the combination of hospitalization and death.</p>
        </sec>
        <sec>
          <title>Results:</title>
          <p>A total of 911 patients were included, of which 23.4% had ChCC. In a Cox analysis adjusted for sex and age, Chagas disease (ChD) was not associated with an increased risk of death (HR: 1.14, CI:95%, 0.86-1.51, p=0.365), hospitalization (HR: 0.79, CI:95%, 0.61-1.04, p=0.09) or combined outcome of death and hospitalization (HR: 0.90, CI:95%, 0.72-1 .12, p=0.49).</p>
        </sec>
        <sec>
          <title>Conclusions:</title>
          <p>ChD was not associated with an increased risk of death, hospitalization, or combined outcome of death and hospitalization, even after adjustment for sex and age. These results contrast with those of previous studies and suggest changes in the quality of care of patients with cardiomyopathy.</p>
        </sec>
      </abstract>
      <kwd-group xml:lang="en">
        <title>Keywords:</title>
        <kwd>Artificial Pacemaker</kwd>
        <kwd>Artificial Cardiac Pacing</kwd>
        <kwd>Chagas Cardiomyopathy</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <sec sec-type="intro">
        <title>Introduction</title>
        <p>Cardiac electrical stimulation stands out as one of the greatest achievements in the field of cardiology in the 20th century.<sup><xref ref-type="bibr" rid="B1">1</xref></sup> Over the past decades, there has been an increase in the number of implants, which can be attributed to population aging, technological advancements in these devices, and an increase in clinical indications.<sup><xref ref-type="bibr" rid="B2">2</xref>,<xref ref-type="bibr" rid="B3">3</xref></sup></p>
        <p>Among these implants, ChCC still accounts for a significant portion of permanent artificial cardiac stimulation indications in our country.<sup><xref ref-type="bibr" rid="B4">4</xref></sup> However, there has been a gradual decline in PM implants due to this etiology, reflecting improved epidemiological control of ChD in the national territory.<sup><xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B6">6</xref></sup></p>
        <p>Despite the reduction in its prevalence, especially in Latin America, ChD evolving with ChCC still presents high morbidity and mortality rates in Brazil, with a worse prognosis than non-inflammatory cardiomyopathies.<sup><xref ref-type="bibr" rid="B7">7</xref></sup> However, few studies have evaluated epidemiological characteristics associated with mortality predictors in patients with PM and ChCC.<sup><xref ref-type="bibr" rid="B4">4</xref>,<xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B8">8</xref>,<xref ref-type="bibr" rid="B9">9</xref></sup></p>
        <p>The present study aimed to compare the outcomes of Chagas and non-Chagas patients undergoing PM and cardiac resynchronization therapy (CRT) implantation at a Brazilian tertiary center.</p>
      </sec>
      <sec sec-type="methods">
        <title>Methods</title>
        <p>This is an observational, retrospective, and longitudinal study. All patients who underwent PM and CRT implantation at the specified tertiary center from October 2007 to December 2017 were included. The research project was approved by the Research Ethics Committee of the institution, following the terms of Resolution No. 466/12 of the National Health Council, under the protocol number CAAE: 56119122.0.0000.5149.</p>
        <fig id="f8">
          <caption>
            <title>Prognostic evaluation of Chagas and non-Chagas patients undergoing pacemaker implantation. HR: Hazard Ratio; CI: Confidence Interval.</title>
          </caption>
          <graphic xlink:href="1678-4170-abc-121-09-e20230875-30875-gf01-en.tif"/></fig>
        <p>Patient information was obtained from a database of electronic health record data from the Laboratory of Implantable Cardiac Devices (LICD) at a Unified Health System reference tertiary hospital in Minas Gerais, with follow-up until December 2018. The database was created using Natural Language Processing (NLP), an artificial intelligence tool that extracted relevant information from free-text electronic health records.<sup><xref ref-type="bibr" rid="B10">10</xref></sup> Subsequently, records of all hospital admission authorizations from the Unified Health System Hospital Information System for cardiovascular procedures in the city of Belo Horizonte were obtained, along with death records from the Mortality Information System of the Department of Informatics of the Unified Health System (DATASUS) in Minas Gerais. The final patient dataset was generated by matching common patients from these information sources.</p>
        <p>Patients who were followed but did not have the device implanted during the study period, those who had the device definitively explanted for any reason, patients without follow-up records in the LICD of the hospital, minors under 18 years of age, and patients with isolated implantable cardioverter-defibrillators (ICDs) were excluded.</p>
        <p>The analyzed variables included the presence or absence of Chd (exposure), sex, and age. The implanted devices were categorized as pacemakers (single-chamber or dual-chamber) or resynchronization devices (multisite) alone or combined with ICDs. The hospitalization variable was obtained from hospital admission authorization data and was considered positive when the patient had at least one cardiovascular-related hospitalization after the device implantation date.</p>
        <p>The primary outcome analyzed was all-cause mortality, comparing Chagas and non-Chagas patients. Secondary outcomes included hospitalization occurrence, combined hospitalization and all-cause mortality, mortality comparison between Chagas and non-Chagas patients in each of the three eras, and mortality comparison by device type.</p>
        <p>Patients were further divided into three eras based on the device implantation date. The total study inclusion time was divided into three 41-month periods: October 2007 to February 2011 (era 1), March 2011 to July 2014 (era 2), and August 2014 to December 2017 (era 3), aiming to assess differences in mortality between Chagas and non-Chagas patients in each of these different eras.</p>
        <sec>
          <title>Statistical analysis</title>
          <p>For data analysis, we used the R program (version 4.3, Vienna, Austria). Continuous variables were presented as mean and standard deviation if they followed a normal distribution, or as median and interquartile range (percentiles 25 and 75) if they did not. The Shapiro-Wilk test was used to assess data normality. Categorical variables were expressed as absolute numbers and proportions. To evaluate the age variable, the Student's T-test was performed to compare means. To compare variables between groups of chagas and non-chagas patients, the Student's T test was also used. The chi-square test (X&#178;) and Kruskal-Wallis test were used to evaluate continuous variables to assess other baseline characteristics of patients and studied devices over the study periods. The non-parametric Kaplan-Meier method was used to calculate patient survival. The statistical significance level was set at p-values less than 0.05. A multivariate Cox proportional hazards regression model, with a hazard ratio (HR), estimates, and 95% confidence intervals, was used to analyze the effect of covariates on the studied outcomes. The proportional hazards assumption was verified using log-log survival curves.</p>
          <p>We also conducted a sensitivity analysis by evaluating all-cause mortality according to device type in the Chagas and non-Chagas populations after excluding resynchronization devices and resynchronization devices combined with ICDs. These exclusions were made due to the complexity and unequal distribution of these devices in the two populations, aiming to assess whether the results remained consistent.</p>
        </sec>
      </sec>
      <sec sec-type="results">
        <title>Results</title>
        <p>Out of the 2819 patients registered in the LICD at the hospital where the research was conducted, 911 patients who underwent PM and CRT implantation during the study period were included (<xref ref-type="fig" rid="f5">Figure 1</xref>). The mean age of the included patients was 68 years (ranging from 20 to 97 years), with 48.5% being male. Among all patients, 23.4% had ChCC. The mean age at PM implantation in the Chagas population was 65 years, while in the non-Chagas population, it was 69 years. Regarding implantable cardiac devices, in the Chagas population, 77.5% received dual-chamber PMs, 16.4% received single-chamber PMs, 3.3% received CRT devices, and 2.8% received CRT devices combined with ICDs (<xref ref-type="table" rid="t4">Table 1</xref>).</p>
        <fig id="f5">
          <label>Figure 1</label>
          <caption>
            <title>Patient Selection Flowchart. *Patients undergoing follow-up at the tertiaty center's cardiac device laboratory, but the initial implantation of the device was performed in another hospital or at a different time period to the present study.</title>
          </caption>
          <graphic xlink:href="1678-4170-abc-121-09-e20230875-30875-gf02-en.tif"/></fig>
        <table-wrap id="t4">
          <label>Table 1</label>
          <caption>
            <title>Baseline characteristics of the population</title>
          </caption>
          <table frame="hsides" rules="groups">
            <colgroup width="19%">
              <col width="1%"/>
              <col/>
              <col/>
              <col/>
              <col/>
              <col/>
            </colgroup>
            <thead style="border-top: thin solid; border-bottom: thin solid; border-color: #000000">
              <tr style="background-color:#76B4CF">
                <th align="left" colspan="2" valign="middle">Characteristics</th>
                <th align="center" valign="middle">Chagas (N=213)</th>
                <th align="center" valign="middle">Non-Chagas (N=698)</th>
                <th align="center" valign="middle">Total (N=911)</th>
                <th align="center" valign="middle">p-Value</th>
              </tr>
            </thead>
            <tbody style="border-bottom: thin solid; border-color: #000000">
              <tr>
                <td align="left" colspan="2" valign="middle">
                  <bold>Age &#8211; years</bold>
                </td>
                <td align="center" valign="middle">65 (23-93)</td>
                <td align="center" valign="middle">69 (20-97)</td>
                <td align="center" valign="middle">68 (20-97)</td>
                <td align="center" valign="middle">&lt;0.001</td>
              </tr>
              <tr style="background-color:#C7DFEC">
                <td align="left" colspan="2" valign="middle">
                  <bold>Male sex- n (%)</bold>
                </td>
                <td align="center" valign="middle">96 (21.7%)</td>
                <td align="center" valign="middle">346(78.3%)</td>
                <td align="center" valign="middle">442 (48.5%)</td>
                <td align="center" valign="middle">0.284</td>
              </tr>
              <tr>
                <td align="left" colspan="2" valign="middle">
                  <bold>Devices- n (%)</bold>
                </td>
                <td align="center" valign="middle"/>
                <td align="center" valign="middle"/>
                <td align="center" valign="middle"/>
                <td align="center" valign="middle">&lt;0.001</td>
              </tr>
              <tr>
                <td align="left" valign="middle"/>
                <td align="left" valign="middle">Single-chamber PM</td>
                <td align="center" valign="middle">35 (16.4%)</td>
                <td align="center" valign="middle">114 (16.3%)</td>
                <td align="center" valign="middle">149 (16.4%)</td>
                <td align="center" valign="middle"/>
              </tr>
              <tr>
                <td align="left" valign="middle"/>
                <td align="left" valign="middle">Dual chamber PM</td>
                <td align="center" valign="middle">165 (77.5%)</td>
                <td align="center" valign="middle">409 (58.6%)</td>
                <td align="center" valign="middle">574 (63%)</td>
                <td align="center" valign="middle"/>
              </tr>
              <tr>
                <td align="left" valign="middle"/>
                <td align="left" valign="middle">CRT</td>
                <td align="center" valign="middle">7 (3.3%)</td>
                <td align="center" valign="middle">126 (18.1%)</td>
                <td align="center" valign="middle">133 (14.6%)</td>
                <td align="center" valign="middle"/>
              </tr>
              <tr>
                <td align="left" valign="middle"/>
                <td align="left" valign="middle">CRT with ICD</td>
                <td align="center" valign="middle">6 (2.8%)</td>
                <td align="center" valign="middle">49 (7.0%)</td>
                <td align="center" valign="middle">55 (6.04%)</td>
                <td align="left" valign="middle"/>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="TFN4">
              <p>PM: pacemaker; ICD: implantable cardioverter-defibrillators; CRT: cardiac resynchronization therapy.</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
        <p>The mean follow-up duration was 64.2 months for mortality, 60.6 months for hospitalization, and 57.4 months for the combined outcome of mortality and hospitalization.</p>
        <p>A total of 306 deaths (33,6%) occurred, with 80 (37.6%) in the Chagas population and 226 (32.4%) in the non-Chagas population (p=0.187). Cardiovascular-related hospitalizations occurred in 275 (30.2%) patients, with 76 (35.7%) having a diagnosis of Chd and 199 (38.5%) without this diagnosis (p=0.056). The combined outcome of mortality and hospitalization occurred in 419 (46%) patients, with 109 (51.2%) being Chagas patients and 310 (44.4%) non-Chagas patients (p=0.098).</p>
        <p>Kaplan-Meier survival curves, using the log-rank test with p=0.99, did not demonstrate a difference in mortality between the Chagas and non-Chagas groups (<xref ref-type="fig" rid="f6">Figure 2</xref>), nor did they show differences between the two groups in any of the different eras (<inline-supplementary-material mime-subtype="pdf" mimetype="application" xlink:href="1678-4170-abc-121-09-e20230875-30875-suppl01-en.pdf">Figure 4 &#8211; see appendix</inline-supplementary-material>).</p>
        <fig id="f6">
          <label>Figure 2</label>
          <caption>
            <title>Kaplan-Meier Survival Curve for All-Cause Mortality by Etiology. Chagas=0: Absence of Chagas Disease; Chagas=1: Presence of Chagas Disease. Survival curves were compared using the long rank test, p=0.99.</title>
          </caption>
          <graphic xlink:href="1678-4170-abc-121-09-e20230875-30875-gf03-en.tif"/></fig>
        <p>Moreover, no difference was observed in the analysis of combined mortality and hospitalization curves between the two groups (<xref ref-type="fig" rid="f7">Figure 3</xref>).</p>
        <fig id="f7">
          <label>Figure 3</label>
          <caption>
            <title>Kaplan-Meier Survival Curve for Combined Mortality and Hospitalization by Etiology. Absence of Chagas Disease; Chagas=1: Presence of Chagas Disease. Survival curves were compared using the long rank test, p=0.25.</title>
          </caption>
          <graphic xlink:href="1678-4170-abc-121-09-e20230875-30875-gf04-en.tif"/></fig>
        <p>The Kaplan-Meier curves for mortality evaluation in patients with dual-chamber PMs showed no difference between Chagas and non-Chagas patients, as well as for patients with single-chamber PMs (<inline-supplementary-material mime-subtype="pdf" mimetype="application" xlink:href="1678-4170-abc-121-09-e20230875-30875-suppl02-en.pdf">Figure 5 &#8211; see appendix</inline-supplementary-material>). Unfortunately, we could not perform this analysis for patients with isolated CRT devices and CRT devices combined with ICDs due to the small number of Chagas patients with these devices. We conducted a sensitivity analysis by excluding patients with CRT devices (isolated or combined with ICDs) and analyzing only patients with single-chamber and dual-chamber PMs together. The Kaplan-Meier curves from this analysis also did not show a difference in mortality between Chagas and non-Chagas patients (<inline-supplementary-material mime-subtype="pdf" mimetype="application" xlink:href="1678-4170-abc-121-09-e20230875-30875-suppl03-en.pdf">Figure 6 &#8211; see appendix</inline-supplementary-material>).</p>
        <p>In the Cox univariate analysis, the presence of Chd was not associated with all-cause mortality, even when considering all devices and analyzing each device type separately. However, male sex and age were related to an increased risk of death (<inline-supplementary-material mime-subtype="pdf" mimetype="application" xlink:href="1678-4170-abc-121-09-e20230875-30875-suppl04-en.pdf">Table 3 -see appendix</inline-supplementary-material>).</p>
        <p>In the multivariate Cox model, adjusted for sex and age, the results remained consistent and Chd was not associated with an increased risk of death, hospitalization, or the combined outcome of mortality and hospitalization (<xref ref-type="fig" rid="f8">Central Figure</xref>), even when analyzed across different eras (<xref ref-type="table" rid="t5">Table 2</xref>).</p>
        <table-wrap id="t5">
          <label>Table 2</label>
          <caption>
            <title>Cox Regression Model for the Chagas Population &#8211; Multivariate Analysis (adjusted for sex and age)</title>
          </caption>
          <table frame="hsides" rules="groups">
            <colgroup width="33%">
              <col width="1%"/>
              <col/>
              <col/>
              <col/>
            </colgroup>
            <thead style="border-top: thin solid; border-bottom: thin solid; border-color: #000000">
              <tr style="background-color:#76B4CF">
                <th align="left" colspan="2" valign="middle">Chagas Disease</th>
                <th align="center" valign="middle">HR (CI- 95%)</th>
                <th align="center" valign="middle">p- Value</th>
              </tr>
            </thead>
            <tbody style="border-bottom: thin solid; border-color: #000000">
              <tr>
                <td align="left" colspan="2" valign="middle">
                  <bold>Total Mortality</bold>
                </td>
                <td align="center" valign="middle">1.14 (0.86-1.51)</td>
                <td align="center" valign="middle">0.365</td>
              </tr>
              <tr style="background-color:#C7DFEC">
                <td align="left" colspan="2" valign="middle">
                  <bold>Mortality by Eras</bold>
                </td>
                <td align="left" valign="middle"/>
                <td align="left" valign="middle"/>
              </tr>
              <tr style="background-color:#C7DFEC">
                <td align="left" valign="middle"/>
                <td align="left" valign="middle">Era 1</td>
                <td align="center" valign="middle">1.17 (0.83-1.66)</td>
                <td align="center" valign="middle">0.38</td>
              </tr>
              <tr style="background-color:#C7DFEC">
                <td align="left" valign="middle"/>
                <td align="left" valign="middle">Era 2</td>
                <td align="center" valign="middle">0.87 (0.53-1.41)</td>
                <td align="center" valign="middle">0.56</td>
              </tr>
              <tr style="background-color:#C7DFEC">
                <td align="left" valign="middle"/>
                <td align="left" valign="middle">Era 3</td>
                <td align="center" valign="middle">1.29 (0.57-2.90)</td>
                <td align="center" valign="middle">0.55</td>
              </tr>
              <tr>
                <td align="left" colspan="2" valign="middle">
                  <bold>Hospitalization</bold>
                </td>
                <td align="center" valign="middle">0.79 (0.61-1.04)</td>
                <td align="center" valign="middle">0.09</td>
              </tr>
              <tr style="background-color:#C7DFEC">
                <td align="left" colspan="2" valign="middle">
                  <bold>Mortality and Hospitalization</bold>
                </td>
                <td align="center" valign="middle">0.90 (0.72-1.12)</td>
                <td align="center" valign="middle">0.49</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="TFN6">
              <p>HR: hazard ratio; CI: confidence interval.</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
        <table-wrap id="t6">
          <label>Table 3</label>
          <caption>
            <title>Cox Proportional Hazards Model for Mortality Outcome Assessment &#8211; Univariate Analysis</title>
          </caption>
          <table frame="hsides" rules="groups">
            <colgroup width="33%">
              <col width="1%"/>
              <col/>
              <col/>
              <col/>
            </colgroup>
            <thead style="border-top: thin solid; border-bottom: thin solid; border-color: #000000">
              <tr style="background-color:#76B4CF">
                <th align="left" colspan="2" valign="middle">Variables</th>
                <th align="center" valign="middle">HR (CI- 95%)</th>
                <th align="center" valign="middle">p- Value</th>
              </tr>
            </thead>
            <tbody style="border-bottom: thin solid; border-color: #000000">
              <tr>
                <td align="left" colspan="2" valign="middle">
                  <bold>Age</bold>
                </td>
                <td align="center" valign="middle">1.02 (1.01-1.03)</td>
                <td align="center" valign="middle">p&lt;0.001</td>
              </tr>
              <tr style="background-color:#C7DFEC">
                <td align="left" colspan="2" valign="middle">
                  <bold>Male Sex</bold>
                </td>
                <td align="center" valign="middle">1.49 (1.16-1.92)</td>
                <td align="center" valign="middle">p=0.002</td>
              </tr>
              <tr>
                <td align="left" colspan="2" valign="middle">
                  <bold>Chagas</bold>
                </td>
                <td align="center" valign="middle"/>
                <td align="center" valign="middle"/>
              </tr>
              <tr>
                <td align="left" valign="middle"/>
                <td align="left" valign="middle">Overall Mortality</td>
                <td align="center" valign="middle">0.99 (0.75-1.30)</td>
                <td align="center" valign="middle">p=0.91</td>
              </tr>
              <tr style="background-color:#C7DFEC">
                <td align="left" colspan="2" valign="middle">
                  <bold>Device-related Mortality</bold>
                </td>
                <td align="left" valign="middle"/>
                <td align="left" valign="middle"/>
              </tr>
              <tr style="background-color:#C7DFEC">
                <td align="left" valign="middle"/>
                <td align="left" valign="middle">Biventricular Pacemaker</td>
                <td align="center" valign="middle">1.1 (0.79-1.53)</td>
                <td align="center" valign="middle">p=0.59</td>
              </tr>
              <tr style="background-color:#C7DFEC">
                <td align="left" valign="middle"/>
                <td align="left" valign="middle">Univentricular Pacemaker</td>
                <td align="center" valign="middle">0.84 (0.51-1.37)</td>
                <td align="center" valign="middle">p= 0.49</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="TFN5">
              <p>HR: hazard ratio; CI: confidence interval.</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
      </sec>
      <sec sec-type="discussion">
        <title>Discussion</title>
        <p>The primary finding of this study highlights the absence of a difference in mortality between Chagas patients with PM and CRT devices compared to non-Chagas patients. This result contrasts with previous studies that have shown worse prognoses for Chagas patients when compared to other dilated cardiopathies.<sup><xref ref-type="bibr" rid="B8">8</xref>,<xref ref-type="bibr" rid="B11">11</xref>,<xref ref-type="bibr" rid="B12">12</xref></sup> Typically, this worse prognosis is associated with a high incidence of sudden cardiac death (responsible for 55% to 65% of deaths in these patients), as well as non-cardiac deaths and various arrhythmias.<sup><xref ref-type="bibr" rid="B4">4</xref>,<xref ref-type="bibr" rid="B11">11</xref>,<xref ref-type="bibr" rid="B13">13</xref>,<xref ref-type="bibr" rid="B14">14</xref></sup> In a comparison between Chagas and non-Chagas patients with PM, Rincon et al. also found worse clinical outcomes in Chagas patients, with a higher incidence of ventricular arrhythmias.<sup><xref ref-type="bibr" rid="B8">8</xref></sup></p>
        <p>Another serious manifestation resulting in fatal outcomes due to cardiac involvement in Chagas disease is advanced heart failure (HF), accounting for 25% to 30% of deaths in this population.<sup><xref ref-type="bibr" rid="B7">7</xref>,<xref ref-type="bibr" rid="B11">11</xref>,<xref ref-type="bibr" rid="B15">15</xref></sup> As Chagas patients progress with ventricular dysfunction and worsening functional class, their severity increases, leading to a poorer quality of life, higher mortality rates, and hospitalizations.<sup><xref ref-type="bibr" rid="B7">7</xref></sup> Consequently, they require specialized clinical and pharmacological treatment with regular multidisciplinary follow-up,<sup><xref ref-type="bibr" rid="B7">7</xref>,<xref ref-type="bibr" rid="B16">16</xref></sup> becoming more sensitive to economic and social circumstances that disproportionately impact the health-disease continuum.<sup><xref ref-type="bibr" rid="B4">4</xref>,<xref ref-type="bibr" rid="B17">17</xref>,<xref ref-type="bibr" rid="B18">18</xref></sup></p>
        <p>On the other hand, establishing reference services for managing and monitoring individuals with chronic diseases promotes better adherence to pharmacological and non-pharmacological treatments, improves quality of life, and reduces mortality and hospitalization rates.<sup><xref ref-type="bibr" rid="B4">4</xref></sup> The center where this study was conducted underwent continuous structural improvements to provide care for such patients over the past two decades. Therefore, the present results could also be attributed to the organization, effective follow-up, and treatment of cardiopathies in general, including specialized teams managing arrhythmias and heart failure.<sup><xref ref-type="bibr" rid="B16">16</xref>,<xref ref-type="bibr" rid="B19">19</xref></sup> The evaluation of mortality across three different eras reinforces the quality of care over time, demonstrating no difference in mortality between Chagas and non-Chagas populations, regardless of the analyzed period.</p>
        <p>Regarding the general characteristics of the study population, advanced age and male sex were predictors of higher mortality in the univariate Cox analysis. These results align with other studies that evaluated the clinical profile of pacemaker recipients, showing that Chagas patients were younger than the non-Chagas population at the time of implantation.<sup><xref ref-type="bibr" rid="B8">8</xref>,<xref ref-type="bibr" rid="B9">9</xref></sup> Additionally, female patients tend to have better survival after pacemaker implantation.<sup><xref ref-type="bibr" rid="B20">20</xref></sup> Considering these factors, all results were adjusted for age and sex, maintaining no difference in mortality, hospitalization, or the combined outcome of mortality and hospitalization between the Chagas and non-Chagas populations.</p>
        <p>In summary, this study demonstrated relevant findings regarding the prognosis of patients with implantable electronic cardiac devices, both for those with Chagas disease and those without. The creation of a large database using natural language processing allowed for the evaluation of a significant cohort of individuals with PM and CRT, with a substantial representation of Chagas patients.</p>
        <p>However, there are some limitations to consider. First, the use of NLP does not achieve 100% sensitivity,<sup><xref ref-type="bibr" rid="B10">10</xref></sup> which may result in some loss of outcomes. Nevertheless, the random sampling of NLP results with manual review and adjustments demonstrated good accuracy and sensitivity. Second, the exclusion of patients with isolated ICDs, who are supposed to have more severe cardiomyopathy and prone to present with serious arrhythmias,<sup><xref ref-type="bibr" rid="B13">13</xref>,<xref ref-type="bibr" rid="B21">21</xref></sup> could have selected a less severe group. Still, this would apply equally to chagasic and non-chagasic patients with the device in question. Additionally, a complementary study using the same database, focusing solely on the ICD population (Chagas and non-Chagas), found no difference in all-cause mortality between the two groups.<sup><xref ref-type="bibr" rid="B14">14</xref></sup></p>
        <p>Unequal distribution of more complex devices, such as isolated CRT and CRT combined with ICDs, could also be considered a limitation. It is well-established that Chagas disease imposes restrictions that predict a poorer response to cardiac resynchronization therapy.<sup><xref ref-type="bibr" rid="B4">4</xref>,<xref ref-type="bibr" rid="B22">22</xref>&#8211;<xref ref-type="bibr" rid="B27">27</xref></sup> However, the potential influence of these devices on patient mortality was evaluated through sensitivity analysis, excluding patients with CRT devices, and the results remained consistent, showing no difference in mortality between the Chagas and non-Chagas populations.</p>
        <p>Finally, it is essential to note that this retrospective and observational analysis relies on the quality of information in medical records, which lacked detailed clinical and laboratory conditions of patients and did not include data on medication therapy. Therefore, further studies, preferably prospective ones, are necessary to confirm these findings.</p>
      </sec>
      <sec sec-type="conclusions">
        <title>Conclusion</title>
        <p>The presence of Chagas disease was not associated with an increased risk of death, hospitalization, or the combined outcome of mortality and hospitalization in this cohort of patients with pacemakers and cardiac resynchronization devices. These results remained consistent even when analyzed across different follow-up periods and adjusted for sex and age.</p>
      </sec>
    </body>
    <back>
      <fn-group>
        <fn fn-type="financial-disclosure" id="fn4">
          <label>Sources of funding</label>
          <p>There were no external funding sources for this study.</p>
        </fn>
        <fn fn-type="other" id="fn6">
          <label>Study association</label>
          <p>This study is part of a master's thesis of La&#237;s Toledo de Vasconcelos, for the Programa de P&#243;s-Gradua&#231;&#227;o de Ci&#234;ncias Aplicadas &#224; Sa&#250;de do Adulto da Faculdade de medicina da Universidade Federal de Minas Gerais (UFMG).</p>
        </fn>
        <fn fn-type="other" id="fn7">
          <label>Ethics approval and consent to participate</label>
          <p>This study was approved by the Ethics Committee of the Universidade Federal de Minas Gerais under the protocol number CAAE 56119122.0.0000.5149. All the procedures in this study were in accordance with the 1975 Helsinki Declaration, updated in 2013.</p>
        </fn>
      </fn-group>
      <app-group>
        <app id="app2">
          <title>*Supplemental Materials</title>
          <p>For additional information, please <ext-link ext-link-type="uri" xlink:href="http://abccardiol.org/supplementary-material/2024/12109/2023-0875_AO_Appendix.pdf">click here</ext-link>.</p>
        </app>
      </app-group>
    </back>
  </sub-article>
</article>
