<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.1 20151215//EN" "https://jats.nlm.nih.gov/publishing/1.1/JATS-journalpublishing1.dtd">
<article xmlns:xlink="http://www.w3.org/1999/xlink" specific-use="sps-1.9" dtd-version="1.1" xml:lang="pt" article-type="research-article">
  <front>
    <journal-meta>
      <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-loc>S&#227;o Paulo, SP, Brazil</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v3">TFM4qRjP3jjkppYGXnVrWHH</article-id>
      <article-id pub-id-type="other">00017</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2006001600017</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(06)08700317</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2006001600017</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigos Originais</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Avalia&#231;&#227;o de pacientes assintom&#225;ticos com forma cr&#244;nica da doen&#231;a de Chagas atrav&#233;s da an&#225;lise do eletrocardiograma din&#226;mico, ecocardiograma e do pept&#237;deo natriur&#233;tico tipo B</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Marques</surname>
            <given-names>Divina Seila de Oliveira</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Canesin</surname>
            <given-names>Manoel Fernandes</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Barutta J&#250;nior</surname>
            <given-names>Flavio</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Fuganti</surname>
            <given-names>Claudio Jos&#233;</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Barretto</surname>
            <given-names>Antonio Carlos Pereira</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="city">Londrina</named-content>
          <named-content content-type="state"/>
        </addr-line>
        <institution content-type="orgname">Universidade Estadual de Londrina</institution>
        <institution content-type="orgdiv1">Faculdade de Medicina </institution>
        <institution content-type="orgdiv2">Hospital de Cl&#237;nicas</institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff02">
        <addr-line>
          <named-content content-type="city">S&#227;o Paulo</named-content>
          <named-content content-type="state"/>
        </addr-line>
        <institution content-type="orgname">Universidade de S&#227;o Paulo</institution>
        <institution content-type="orgdiv1">FM </institution>
        <institution content-type="orgdiv2">Hospital das Cl&#237;nicas</institution>
        <country country="BR">Brazil</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>09</month>
        <year>2006</year>
      </pub-date>
      <volume>87</volume>
      <issue>3</issue>
      <fpage>336</fpage>
      <lpage>343</lpage>
      <history>
        <date date-type="received">
          <day>20</day>
          <month>07</month>
          <year>2004</year>
        </date>
        <date date-type="accepted">
          <day>12</day>
          <month>09</month>
          <year>2005</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/4.0/" xml:lang="en">
          <license-p>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</license-p>
        </license>
      </permissions>
      <abstract>
        <p>OBJETIVO: Avaliar pacientes assintom&#225;ticos com forma cr&#244;nica da doen&#231;a de Chagas em rela&#231;&#227;o a preval&#234;ncia de arritmias ventriculares, disfun&#231;&#227;o ventricular esquerda e n&#237;veis plasm&#225;ticos do pept&#237;deo natriur&#233;tico tipo B (BNP). M&#201;TODOS: Avalia&#231;&#227;o cl&#237;nica, eletrocardiograma (ECG), &#237;ndice cardiotor&#225;cico (ICT), eletrocardiograma din&#226;mico, ecocardiograma e dosagem BNP foram realizados em 106 pacientes do Ambulat&#243;rio de Doen&#231;a de Chagas, distribu&#237;dos em tr&#234;s grupos: GI (50-ECG normal), GIIA (31-ECG com altera&#231;&#245;es caracter&#237;sticas de doen&#231;a de Chagas) e GIIB (25-ECG com outras altera&#231;&#245;es). RESULTADOS: Altera&#231;&#245;es eletrocardiogr&#225;ficas mais prevalentes no GIIA: bloqueio completo do ramo direito, bloqueio divisional &#226;ntero-superior esquerdo (35% cada) e &#225;reas inativas (32%), GIIB: altera&#231;&#227;o da repolariza&#231;&#227;o inferolateral (28%) e sobrecarga ventricular esquerda (24%). Os valores m&#233;dios do ICT foram semelhantes (p = 0,383). A preval&#234;ncia de arritmia ventricular foi maior nos grupos GIIA (77%) e GIIB (75%) do que no GI (46%) (p = 0,002). A disfun&#231;&#227;o ventricular foi mais prevalente no GIIA (52%) e GIIB (32%) do que no GI (14%) (p = 0,001). A disfun&#231;&#227;o sist&#243;lica foi mais prevalente no GIIA (29%) do que no GIIB (20%) e GI (2%) (p &lt; 0,001). A disfun&#231;&#227;o diast&#243;lica foi mais prevalente no GIIA (42%) e no GIIB (28%) do que no GI (12%) (p = 0,005). Os valores m&#233;dios do pept&#237;deo natriur&#233;tico tipo B foram, respectivamente, 30 &#177; 88 pg/ml no GI, 66 &#177; 194 no GIIA e 24 &#177; 82 no GIIB (p = 0,121). CONCLUS&#195;O: Pacientes assintom&#225;ticos com forma cr&#244;nica da doen&#231;a de Chagas e ECG alterado t&#234;m maior preval&#234;ncia de arritmias e disfun&#231;&#227;o ventricular esquerda do que pacientes com ECG normal. Os n&#237;veis plasm&#225;ticos do BNP foram semelhantes entre os grupos.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>Doen&#231;a de Chagas</kwd>
        <kwd>eletrocardiografia ambulatorial</kwd>
        <kwd>ecocardiografia Doppler</kwd>
        <kwd>pept&#237;deo natriur&#233;tico cerebral</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>16</day>
        <month>10</month>
        <year>2006</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>
      <bold>ARTIGOS ORIGINAIS</bold>
    </p>
    <p>Avalia&#231;&#227;o de pacientes assintom&#225;ticos com forma cr&#244;nica da doen&#231;a de Chagas atrav&#233;s da an&#225;lise do eletrocardiograma din&#226;mico, ecocardiograma e do pept&#237;deo natriur&#233;tico tipo B </p>
    <p>
      <bold>Divina Seila de Oliveira Marques; Manoel Fernandes Canesin; Flavio Barutta J&#250;nior; Claudio Jos&#233; Fuganti; Antonio Carlos Pereira Barretto</bold>
    </p>
    <p>Hospital de Cl&#237;nicas da Faculdade de Medicina da Universidade Estadual de Londrina e Instituto do Cora&#231;&#227;o do Hospital das Cl&#237;nicas da FMUSP - Londrina, PR &#150; S&#227;o Paulo, SP</p>
    <p>
      <xref ref-type="corresp" rid="end">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p><bold>OBJETIVO: </bold>Avaliar pacientes assintom&#225;ticos com forma cr&#244;nica da doen&#231;a de Chagas em rela&#231;&#227;o a preval&#234;ncia de arritmias ventriculares, disfun&#231;&#227;o ventricular esquerda e n&#237;veis plasm&#225;ticos do pept&#237;deo natriur&#233;tico tipo B (BNP). </p>
    <p><bold>M&#201;TODOS: </bold>Avalia&#231;&#227;o cl&#237;nica, eletrocardiograma (ECG), &#237;ndice cardiotor&#225;cico (ICT), eletrocardiograma din&#226;mico, ecocardiograma e dosagem BNP foram realizados em 106 pacientes do Ambulat&#243;rio de Doen&#231;a de Chagas, distribu&#237;dos em tr&#234;s grupos: GI (50-ECG normal), GIIA (31-ECG com altera&#231;&#245;es caracter&#237;sticas de doen&#231;a de Chagas) e GIIB (25-ECG com outras altera&#231;&#245;es). </p>
    <p><bold>RESULTADOS: </bold>Altera&#231;&#245;es eletrocardiogr&#225;ficas mais prevalentes no GIIA: bloqueio completo do ramo direito, bloqueio divisional &#226;ntero-superior esquerdo (35% cada) e &#225;reas inativas (32%), GIIB: altera&#231;&#227;o da repolariza&#231;&#227;o inferolateral (28%) e sobrecarga ventricular esquerda (24%). Os valores m&#233;dios do ICT foram semelhantes (p = 0,383). A preval&#234;ncia de arritmia ventricular foi maior nos grupos GIIA (77%) e GIIB (75%) do que no GI (46%) (p = 0,002). A disfun&#231;&#227;o ventricular foi mais prevalente no GIIA (52%) e GIIB (32%) do que no GI (14%) (p = 0,001). A disfun&#231;&#227;o sist&#243;lica foi mais prevalente no GIIA (29%) do que no GIIB (20%) e GI (2%) (p &lt; 0,001). A disfun&#231;&#227;o diast&#243;lica foi mais prevalente no GIIA (42%) e no GIIB (28%) do que no GI (12%) (p = 0,005). Os valores m&#233;dios do pept&#237;deo natriur&#233;tico tipo B foram, respectivamente, 30 &#177; 88 pg/ml no GI, 66 &#177; 194 no GIIA e 24 &#177; 82 no GIIB (p = 0,121). </p>
    <p><bold>CONCLUS&#195;O: </bold>Pacientes assintom&#225;ticos com forma cr&#244;nica da doen&#231;a de Chagas e ECG alterado t&#234;m maior preval&#234;ncia de arritmias e disfun&#231;&#227;o ventricular esquerda do que pacientes com ECG normal. Os n&#237;veis plasm&#225;ticos do BNP foram semelhantes entre os grupos.</p>
    <p><bold>Palavras-chave: </bold>Doen&#231;a de Chagas, eletrocardiografia ambulatorial, ecocardiografia Doppler, pept&#237;deo natriur&#233;tico cerebral.</p>
    <p>A doen&#231;a de Chagas caracteriza-se pela grande diversidade cl&#237;nica. O n&#250;mero estimado de indiv&#237;duos infectados corresponde a cerca de tr&#234;s milh&#245;es, constituindo-se em um dos maiores problemas de sa&#250;de p&#250;blica do pa&#237;s<sup>1-3</sup>.</p>
    <p>Aproximadamente 60% dos indiv&#237;duos infectados permanecer&#227;o na forma indeterminada (FI); 25% a 35% desenvolver&#227;o cardiopatia, dentre eles 10% poder&#227;o desenvolver cardiopatia grave. Manifesta-se sob a forma de arritmias e/ou dist&#250;rbios de condu&#231;&#227;o, insufici&#234;ncia card&#237;aca, acidentes tromboemb&#243;licos e morte s&#250;bita<sup>4,5</sup>.</p>
    <p>No conhecimento da hist&#243;ria natural da doen&#231;a de Chagas altera&#231;&#245;es no eletrocardiograma (ECG) precedem o aparecimento de sintomas, anormalidades ao exame f&#237;sico e na radiografia de t&#243;rax<sup>6</sup>. Como o significado cl&#237;nico de altera&#231;&#245;es do ECG em indiv&#237;duos assintom&#225;ticos ainda n&#227;o est&#225; bem estabelecido, &#233; poss&#237;vel encontr&#225;-los entre aqueles que rec&#233;m adentraram na cl&#225;ssica fase cr&#244;nica e apresentam discretas altera&#231;&#245;es at&#233; em indiv&#237;duos com altera&#231;&#245;es eletrocardiogr&#225;ficas mais avan&#231;adas<sup>7</sup>. </p>
    <p>Al&#233;m do ECG e da radiografia de t&#243;rax, a utiliza&#231;&#227;o da eletrocardiografia din&#226;mica permitiu melhor conhecimento das arritmias ventriculares, reconhecidas desde os relatos iniciais da forma card&#237;aca da doen&#231;a de Chagas. Apesar de sua presen&#231;a estar associada com maior incid&#234;ncia de morte s&#250;bita<sup>8</sup>, algumas caracter&#237;sticas, como a sua preval&#234;ncia nas diferentes formas cl&#237;nicas, a rela&#231;&#227;o com sintomas e disfun&#231;&#227;o ventricular, ainda n&#227;o est&#227;o bem definidas e diferem de um estudo para outro, na depend&#234;ncia da amostra populacional e da metodologia empregada<sup>9</sup>. </p>
    <p>O ecocardiograma &#233; &#250;til ao trazer a possibilidade de diagnosticar e acompanhar o acometimento card&#237;aco, principalmente a disfun&#231;&#227;o ventricular, em especial a disfun&#231;&#227;o ventricular sist&#243;lica, reconhecida como o principal fator progn&#243;stico da miocardiopatia chag&#225;sica<sup>10,11</sup>. A disfun&#231;&#227;o ventricular diast&#243;lica que geralmente precede a disfun&#231;&#227;o sist&#243;lica n&#227;o tem seu valor progn&#243;stico ainda definido. M&#233;todos recentes, como a utiliza&#231;&#227;o da imagem do Doppler tissular quantificando a velocidade de fluxo no mioc&#225;rdio, t&#234;m demonstrado grande valor com maior sensibilidade na detec&#231;&#227;o de padr&#245;es pseudonormais de disfun&#231;&#227;o diast&#243;lica do que a velocidade de fluxo mitral detectada pelo Doppler pulsado<sup>12,13</sup>. </p>
    <p>A dosagem do pept&#237;deo natriur&#233;tico cerebral ou tipo B (BNP) tem demonstrado utilidade no diagn&#243;stico de disfun&#231;&#245;es sist&#243;licas e diast&#243;licas do ventr&#237;culo esquerdo<sup>14,15</sup>. O BNP &#233; um pept&#237;deo hormonalmente ativo, secretado pelos ventr&#237;culos, e suas concentra&#231;&#245;es plasm&#225;ticas aumentam de acordo com a severidade da insufici&#234;ncia card&#237;aca (IC) baseada na classifica&#231;&#227;o da New York Heart Association<sup>16</sup>. Em pacientes com doen&#231;a de Chagas, poucos estudos foram realizados avaliando o valor plasm&#225;tico desse pept&#237;deo<sup>17,18</sup>. </p>
    <p>Nosso objetivo foi avaliar prospectivamente a preval&#234;ncia de arritmias ventriculares, preval&#234;ncia de disfun&#231;&#227;o ventricular esquerda e n&#237;veis plasm&#225;ticos do BNP em pacientes assintom&#225;ticos, com forma cr&#244;nica da doen&#231;a de Chagas e ECG alterado, divididos em dois grupos: GIIA (ECG com altera&#231;&#245;es caracter&#237;sticas) e GIIB (ECG com altera&#231;&#245;es n&#227;o caracter&#237;sticas de doen&#231;a de Chagas) comparados a um grupo de pacientes com doen&#231;a de Chagas e ECG normal (GI).</p>
    <p>
      <bold>M&#201;TODOS</bold>
    </p>
    <p>Estudo transversal, prospectivo, aprovado pelo Comit&#234; de &#201;tica em Pesquisa da institui&#231;&#227;o, no qual foram avaliados 329 pacientes com infec&#231;&#227;o pelo Trypanosoma cruzi, confirmada pela positividade sorol&#243;gica em pelo menos duas entre tr&#234;s t&#233;cnicas diferentes (hemaglutina&#231;&#227;o indireta, imunofluoresc&#234;ncia indireta e ELISA) atendidos no ambulat&#243;rio de doen&#231;a de Chagas no per&#237;odo de abril a novembro de 2002. Todos os pacientes foram submetidos a anamnese e exame f&#237;sico e selecionados ap&#243;s an&#225;lise dos crit&#233;rios de exclus&#227;o: 1) idade menor que dezoito e maior que cinq&#252;enta anos; 2) presen&#231;a de sintomas sugestivos de insufici&#234;ncia card&#237;aca<sup>19</sup> e/ou arritmia<sup>20</sup>; 3) hipertens&#227;o arterial &#150; definida como hist&#243;ria pr&#233;via, uso de medica&#231;&#227;o anti-hipertensiva ou, no momento da inclus&#227;o, press&#227;o arterial diast&#243;lica (PAD) &gt; 89 e/ou press&#227;o arterial sist&#243;lica (PAS) &gt;139<sup>21</sup>; 4) diabetes mellitus &#150; definida como glicose de jejum <underline>&gt;</underline>126 mg/dl ou refer&#234;ncia de uso regular de medica&#231;&#227;o hipoglicemiante<sup>22</sup>; 5) hist&#243;ria de: doen&#231;a pulmonar obstrutiva cr&#244;nica; 6) disfun&#231;&#245;es end&#243;crinas; 7) cardiopatia de outras etiologias; 8) gravidez no momento da inclus&#227;o. Foram selecionados 106 pacientes que, ap&#243;s esclarecimento sobre os objetivos da pesquisa, assinaram termo de consentimento escrito. </p>
    <p>Ap&#243;s an&#225;lise do eletrocardiograma (ECG) os pacientes foram distribu&#237;dos em tr&#234;s grupos: 1) GI &#150; pacientes com ECG normal; 2) GIIA &#150; pacientes com ECG com altera&#231;&#245;es caracter&#237;sticas (bloqueios atrioventriculares, bloqueio completo do ramo direito e/ou bloqueio divisional &#226;ntero-superior esquerdo do feixe de Hiss; &#225;reas inativas; bradicardia sinusal quando acompanhada por extra-s&#237;stoles ventriculares ou altera&#231;&#245;es prim&#225;rias da repolariza&#231;&#227;o ventricular<sup>23</sup>); e 3) GIIB &#150; pacientes com altera&#231;&#245;es n&#227;o-caracter&#237;sticas de doen&#231;a de Chagas. </p>
    <p>A seguir, foram realizados os seguintes exames; a) radiografia de t&#243;rax e c&#225;lculo do &#237;ndice cardiotor&#225;cico (ICT) conforme t&#233;cnica j&#225; descrita<sup>24</sup>; b) eletrocardiograma din&#226;mico de 24 horas utilizando-se um gravador port&#225;til de dois canais Dynamis 4000 (Cardios Sistemas, S&#227;o Paulo, Brasil) e an&#225;lise com programa Premier 4 (Diagnostic Monitoring Software, Nevada, EUA). Foram avaliados a presen&#231;a e o n&#250;mero de EVS em 24 horas, taquicardia ventricular sustentada (TVS): tr&#234;s ou mais ectopias ventriculares sucessivas com dura&#231;&#227;o igual ou superior a 30 s e n&#227;o sustentada (TVNS): tr&#234;s ou mais ectopias ventriculares sucessivas com dura&#231;&#227;o menor que 30 s.<sup>25</sup>; c) ecocardiograma utilizando-se um ecocardi&#243;grafo modelo "Vivid 3" (GE Medical Systems, Milwaukee, EUA), seguindo crit&#233;rios da Sociedade Americana de Ecocardiografia. </p>
    <p>Os par&#226;metros analisados foram: fra&#231;&#227;o de eje&#231;&#227;o do ventr&#237;culo esquerdo (FEVE) avaliada pelo m&#233;todo biplano de discos de Simpson, com valor normal igual ou maior que 50%<sup>26</sup>; contra&#231;&#227;o regional do ventr&#237;culo esquerdo, utilizando-se o modelo de dezesseis segmentos preconizado pela Sociedade Americana de Ecocardiografia e classificados como normais ou anormais (hipocin&#233;ticos, acin&#233;ticos ou discin&#233;ticos)<sup>27</sup>, rela&#231;&#227;o da amplitude da onda E&#146; (velocidade m&#225;xima da movimenta&#231;&#227;o do anel mitral no in&#237;cio da di&#225;stole) e amplitude da onda A&#146; (velocidade m&#225;xima da movimenta&#231;&#227;o do anel mitral no final da di&#225;stole) (E&#146;/A&#146;) utilizando-se o Doppler tecidual da movimenta&#231;&#227;o do anel mitral medido na parede septal no corte apical quatro c&#226;maras, com valor normal quando maior ou igual a 1<sup>28</sup>. Disfun&#231;&#227;o ventricular foi considerada na presen&#231;a de disfun&#231;&#227;o sist&#243;lica e/ou diast&#243;lica do ventr&#237;culo esquerdo.</p>
    <p>Disfun&#231;&#227;o ventricular sist&#243;lica foi definida na presen&#231;a de disfun&#231;&#227;o ventricular global e/ou regional. Disfun&#231;&#227;o ventricular sist&#243;lica global foi definida na presen&#231;a de FEVE menor do que 50%. Disfun&#231;&#227;o ventricular diast&#243;lica foi definida na presen&#231;a de E&#146;/A&#146;&lt;1, d) BNP: foram colhidas amostras de 5 ml de sangue total e colocado em um tubo contendo &#225;cido etilenodiaminotetraac&#233;tico (EDTA) como anticoagulante, ap&#243;s centrifuga&#231;&#227;o, o plasma foi obtido e armazenado a temperatura de -20 &#186;C. A an&#225;lise quantitativa foi realizada pelo m&#233;todo de imunoensaio de fluoresc&#234;ncia-Triage BNP (Biosite, San Diego, EUA) ap&#243;s a amostra de plasma estar em temperatura ambiente e homogeneizada. </p>
    <p>As an&#225;lises estat&#237;sticas foram realizadas utilizando-se os programas Epi Info 6 &#150; vers&#227;o 6.04 e SAS &#150; Statistical Analysis System vers&#227;o 6.11. As vari&#225;veis cont&#237;nuas foram expressas pela m&#233;dia e desvio-padr&#227;o (DP). As vari&#225;veis categ&#243;ricas atrav&#233;s de freq&#252;&#234;ncias absolutas e relativas. Para se testar a homogeneidade dos grupos em rela&#231;&#227;o &#224;s propor&#231;&#245;es foi utilizado o teste qui-quadrado ou o teste exato de Fisher. Para a an&#225;lise da hip&#243;tese de igualdade entre tr&#234;s grupos utilizou-se a An&#225;lise de vari&#226;ncia a um fator, com as compara&#231;&#245;es m&#250;ltiplas atrav&#233;s de Bonferroni. Quando a suposi&#231;&#227;o de normalidade dos dados foi rejeitada foi utilizado o teste n&#227;o-param&#233;trico de Kruskal-Wallis, com as compara&#231;&#245;es m&#250;ltiplas atrav&#233;s de Dunn. O n&#237;vel de signific&#226;ncia utilizado para os testes foi de 5%.</p>
    <p>
      <bold>RESULTADOS</bold>
    </p>
    <p>Na <xref ref-type="table" rid="tab01">Tabela 1</xref> podemos observar as vari&#225;veis demogr&#225;ficas e cl&#237;nicas observadas nos grupos estudados.</p>
    <table-wrap id="tab01">
      <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gt01.jpg"/></table-wrap>
    <p>As altera&#231;&#245;es no ECG mais freq&#252;entes encontradas no grupo GIIA foram o bloqueio de ramo direito e o bloqueio divisional &#226;ntero-superior esquerdo, com freq&#252;&#234;ncia de 35% cada, seguida por &#225;reas inativas em 32%. No grupo GIIB foram a altera&#231;&#227;o da repolariza&#231;&#227;o &#237;nfero-lateral e a sobrecarga ventricular esquerda, com freq&#252;&#234;ncia de 28% e 24%, respectivamente.</p>
    <p>Os valores m&#233;dios do ICT foram semelhantes entre os grupos: GI - 0,41 &#177; 0,05; GIIA - 0,43 &#177; 0,05 e GIIB - 0,43 &#177; 0,05 (p = 0,383). </p>
    <p>Dentre os 106 pacientes 102 apresentaram eletrocardiograma din&#226;mico com condi&#231;&#245;es de serem analisados: 48 (96%) do GI, 30 do GIIA (97%) e 24 (96%) do GIIB. A preval&#234;ncia de arritmia ventricular foi semelhante entre os grupos com altera&#231;&#245;es no ECG (GIIA e GIIB) e significativamente maior do que o grupo com ECG normal (GI) (<xref ref-type="fig" rid="fig01">fig.1</xref>).</p>
    <fig id="fig01">
      <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gf01.jpg"/></fig>
    <p>A m&#233;dia de extra-s&#237;stoles ventriculares nas 24 horas (EVS/24H) foi significativamente maior no grupo GIIA (1138,00 &#177; 2779) do que no grupo GI (51,68 &#177; 161) e GIIB (115,40 &#177; 297) (p &lt; 0,05). Apresentaram TVNS seis participantes do estudo, um (2%) do grupo GI e cinco (16,6%) do grupo GIIA.</p>
    <p>A disfun&#231;&#227;o ventricular foi mais prevalente nos grupos GIIA e GIIB e significativamente maior que no grupo GI (<xref ref-type="fig" rid="fig02">fig. 2</xref>). Na an&#225;lise univariada de risco relativo (RR) observou-se uma associa&#231;&#227;o positiva de disfun&#231;&#227;o ventricular e os grupos GIIA e GIIB em rela&#231;&#227;o ao grupo GI. Os pacientes do grupo GIIA tem RR de 3,69 (IC 95%= 1,71-7,94; p &lt; 0,001). Os pacientes do grupo GIIB tem RR de 2,72 (IC 95%= 1,13-6,54; p = 0,024). </p>
    <fig id="fig02">
      <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gf02.jpg"/></fig>
    <p>Disfun&#231;&#227;o ventricular sist&#243;lica (DS) foi observada em um (2%) paciente do grupo GI, 9 (29%) pacientes do grupo GIIA e cinco (20%) pacientes do grupo GIIB (p &lt; 0,001) (<xref ref-type="fig" rid="fig03">fig. 3</xref>).</p>
    <fig id="fig03">
      <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gf03.jpg"/></fig>
    <p>Os pacientes do grupo GI n&#227;o apresentaram disfun&#231;&#227;o ventricular sist&#243;lica global, observada em quatro (13%) pacientes do grupo GIIA e dois (8%) pacientes do grupo GIIB (p = 0,020).</p>
    <p>Apresentaram disfun&#231;&#227;o sist&#243;lica regional doze (11,3%) pacientes: um (2%) paciente do GI, sete (23%) pacientes do grupo GIIA e quatro (16%) pacientes do grupo GIIB (p = 0,005). A localiza&#231;&#227;o da disfun&#231;&#227;o sist&#243;lica regional no grupo GI foi na regi&#227;o apical. Na <xref ref-type="fig" rid="fig04">figura 4</xref>, observa-se a freq&#252;&#234;ncia absoluta e localiza&#231;&#227;o da disfun&#231;&#227;o sist&#243;lica regional nos grupos GIIA e GIIB. A regi&#227;o apical foi a mais acometida. </p>
    <fig id="fig04">
      <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gf04.jpg"/></fig>
    <p>A preval&#234;ncia de disfun&#231;&#227;o diast&#243;lica foi semelhante nos grupos GIIA e GIIB e significativamente maior do que no grupo GI (p = 0,009) (<xref ref-type="fig" rid="fig05">fig. 5</xref>). </p>
    <fig id="fig05">
      <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gf05.jpg"/></fig>
    <p>N&#227;o houve diferen&#231;a estat&#237;stica na compara&#231;&#227;o das m&#233;dias dos valores plasm&#225;ticos do BNP entre os grupos (p = 0,121). </p>
    <p>A an&#225;lise descritiva dos valores do BNP nos grupos estudados &#233; apresentada na <xref ref-type="table" rid="tab02">tabela 2</xref></p>
    <table-wrap id="tab02">
      <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gt02.jpg"/></table-wrap>
    <p>
      <bold>DISCUSS&#195;O</bold>
    </p>
    <p>O desafio atual no manejo do paciente infectado &#233; o diagn&#243;stico precoce e a preven&#231;&#227;o da evolu&#231;&#227;o das formas cl&#237;nicas da fase cr&#244;nica, com a indica&#231;&#227;o de terap&#234;utica adequada e preven&#231;&#227;o das complica&#231;&#245;es<sup>29</sup>. </p>
    <p>Neste estudo, no qual foram estudados pacientes assintom&#225;ticos, sem diagn&#243;stico pr&#233;vio de cardiopatia, procurou-se avaliar a rela&#231;&#227;o entre a presen&#231;a de altera&#231;&#245;es no ECG e a preval&#234;ncia de arritmias, disfun&#231;&#227;o ventricular e valor plasm&#225;tico do BNP. Nessa avalia&#231;&#227;o, o ponto de partida foi a an&#225;lise da presen&#231;a de altera&#231;&#245;es eletrocardiogr&#225;ficas, pois, apesar de todo o avan&#231;o tecnol&#243;gico, o ECG ainda &#233; o exame b&#225;sico solicitado na avalia&#231;&#227;o inicial do paciente com doen&#231;a de Chagas, e pode ser a &#250;nica proped&#234;utica complementar presente na maioria dos servi&#231;os de sa&#250;de, principalmente nos lugares mais carentes onde geralmente se concentra a maioria dos pacientes infectados.</p>
    <p>O valor do ECG em identificar disfun&#231;&#227;o ventricular sist&#243;lica levando a insufici&#234;ncia card&#237;aca foi avaliado por Davie e cols.<sup>30</sup>, que observaram um valor preditivo positivo de 35% e valor preditivo negativo de 98% para diagn&#243;stico de disfun&#231;&#227;o ventricular sist&#243;lica em pacientes com ECG anormal. Estudando anormalidades no ECG e sua rela&#231;&#227;o com fun&#231;&#227;o ventricular sist&#243;lica (volumes ventriculares e FE pela angiografia) na doen&#231;a de Chagas, Casado e cols..<sup>31</sup> observaram uma rela&#231;&#227;o entre a diminui&#231;&#227;o da fun&#231;&#227;o sist&#243;lica ventricular esquerda com a progress&#227;o e associa&#231;&#227;o de anormalidades no ECG. </p>
    <p>Neste estudo observou-se que tanto em rela&#231;&#227;o &#224; presen&#231;a de arritmias ventriculares como de disfun&#231;&#227;o ventricular os grupos com altera&#231;&#227;o no ECG tiveram preval&#234;ncias semelhantes e significativamente maiores que o grupo com ECG normal. Carrasco e cols.<sup>32</sup>, analisando quatro grupos de pacientes: ECG normal, ECG normal e disfun&#231;&#227;o segmentar regional, ECG anormal e disfun&#231;&#227;o ventricular global, ECG anormal e insufici&#234;ncia card&#237;aca, observaram preval&#234;ncias de arritmia ventricular em 30%, 53%, 86% e 99% dos pacientes, respectivamente. Rassi Junior e cols.<sup>9</sup> encontraram preval&#234;ncias de 85% na popula&#231;&#227;o normal, 74% na FI e 88% nas formas card&#237;acas, n&#227;o discriminando se esses eram sintom&#225;ticos ou assintom&#225;ticos. </p>
    <p>Quando analisada a freq&#252;&#234;ncia de EVS nos grupos, a m&#233;dia de EVS/24 horas foi significativamente maior no grupo GIIA do que nos grupos GIIB e GI. Na literatura, semelhan&#231;a em rela&#231;&#227;o a incid&#234;ncia, n&#250;mero e complexidade das EVS foi encontrada entre a FI e indiv&#237;duos sem cardiopatia. Como a ocorr&#234;ncia de arritmias aumenta proporcionalmente com o grau de comprometimento verificado no ECG de repouso, as EVS s&#227;o menos freq&#252;entes nos pacientes com forma cr&#244;nica com altera&#231;&#245;es m&#237;nimas do ECG e mais freq&#252;entes e complexas quando o paciente apresenta altera&#231;&#245;es caracter&#237;sticas, principalmente quando associadas &#224; disfun&#231;&#227;o do ventr&#237;culo esquerdo<sup>33</sup>. </p>
    <p>Observou-se preval&#234;ncia de TVNS em 16,6% do grupo GIIA e 2% do grupo GI, menos freq&#252;ente do que as observadas por Rassi Jr e cols.<sup>9</sup>: 42% em grupo de chag&#225;sicos com ECG caracter&#237;stico, 16% em pacientes com ECG n&#227;o-caracter&#237;stico e 1% de pacientes na FI. </p>
    <p>Em nosso estudo, a an&#225;lise univariada de risco relativo (RR) demonstrou que pacientes com altera&#231;&#245;es eletrocardiogr&#225;ficas caracter&#237;sticas de doen&#231;a de Chagas (GIIA) t&#234;m risco de 3,69, e os pacientes com altera&#231;&#245;es eletrocardiogr&#225;ficas n&#227;o-caracter&#237;sticas de doen&#231;a de Chagas (GIIB) t&#234;m risco de 2,72 vezes de ter disfun&#231;&#227;o ventricular do que os pacientes com ECG normal (GI). Disfun&#231;&#227;o ventricular sist&#243;lica global caracterizada por FEVE abaixo de 50% foi observada em seis pacientes, quatro do grupo GIIA e dois do grupo GIIB. FEVE abaixo de 40% foi observada em dois (6,5%) pacientes do grupo GIIA.</p>
    <p>A disfun&#231;&#227;o ventricular sist&#243;lica, cuja preval&#234;ncia na popula&#231;&#227;o geral &#233; de 2% a 4%, &#233; o substrato anat&#244;mico de cerca de dois ter&#231;os dos pacientes com insufici&#234;ncia card&#237;aca (IC)<sup>34</sup>. </p>
    <p>Mady e cols.<sup>11</sup>, avaliando pacientes com IC por doen&#231;a de Chagas em classes funcionais da NYHA de II a IV, observaram que a FEVE &#233; um importante &#237;ndice para an&#225;lise de sobrevida nesses grupos. Segundo a literatura, a disfun&#231;&#227;o sist&#243;lica na doen&#231;a de Chagas, analisada pelo ECO, varia conforme a forma cl&#237;nica da doen&#231;a e a metodologia aplicada nos diversos trabalhos. Quando analisada a FI, encontram-se desde relatos de registro normal da fun&#231;&#227;o ventricular sist&#243;lica<sup>35</sup> at&#233; aumentos significativos das dimens&#245;es e volumes do VE e diminui&#231;&#227;o da FE em rela&#231;&#227;o a um grupo controle<sup>36</sup>. Quando comparados a FI e pacientes com altera&#231;&#245;es m&#237;nimas no ECG, Ianni e cols.<sup>37</sup> n&#227;o observaram diferen&#231;a significativa entre os grupos em rela&#231;&#227;o &#224; fra&#231;&#227;o de encurtamento do ventr&#237;culo esquerdo. Por&#233;m, Pereira-Barretto e cols.<sup>38</sup> observaram uma preval&#234;ncia de 4,5% de fun&#231;&#227;o ventricular deprimida em pacientes com ECG normal e 45,7% a 66% de presen&#231;a de disfun&#231;&#227;o ventricular em pacientes com ECG alterado, dependendo da altera&#231;&#227;o eletrocardiogr&#225;fica presente. Perez e cols.<sup>39</sup> obtiveram preval&#234;ncia de 29% de disfun&#231;&#227;o ventricular global em grupo de chag&#225;sicos n&#227;o selecionados.</p>
    <p>Disfun&#231;&#227;o sist&#243;lica regional foi mais freq&#252;ente no grupo GIIA do que nos grupos GIIB e GI (respectivamente 23%, 16% e 2%). A regi&#227;o apical foi a mais acometida em todos os pacientes. Altera&#231;&#245;es segmentares da contratilidade s&#227;o encontradas em at&#233; 74% dos pacientes chag&#225;sicos, sendo caracter&#237;stica da doen&#231;a de Chagas principalmente quando localizada na regi&#227;o apical, na aus&#234;ncia de cardiopatia isqu&#234;mica<sup>40</sup>. Apar&#237;cio e cols.<sup>41</sup> observaram 12% de hipocinesia do septo interventricular em pacientes assintom&#225;ticos com ECG normal, quando avaliado pelo ECO modo M. Na FI, Ortiz e cols.<sup>42</sup> observaram freq&#252;&#234;ncia de 26% de altera&#231;&#245;es segmentares, restritas &#224; regi&#227;o p&#243;stero-apical. C&#226;mara<sup>43</sup>, avaliando pacientes com ECG alterado, observou freq&#252;&#234;ncia de 68% de altera&#231;&#245;es segmentares, 64% delas localizadas na regi&#227;o apical e a presen&#231;a de aneurisma apical em 42% dos pacientes.</p>
    <p>A disfun&#231;&#227;o diast&#243;lica foi mais freq&#252;ente que a disfun&#231;&#227;o sist&#243;lica, e foi significativamente mais freq&#252;ente no grupo GIIA (41,9%) do que nos demais grupos. </p>
    <p>O Doppler tecidual foi utilizado, pois sua sensibilidade na detec&#231;&#227;o de disfun&#231;&#227;o diast&#243;lica &#233; maior do que o m&#233;todo cl&#225;ssico que analisa o fluxo transmitral pelo Doppler pulsado, diferenciando inclusive o padr&#227;o pseudonormal<sup>12,28</sup>. &#201; reconhecido que o fluxo transmitral &#233; influenciado por in&#250;meros fatores, dentre eles a press&#227;o atrial esquerda. Aumentos na press&#227;o atrial esquerda acima do aumento da press&#227;o resultantes da diminui&#231;&#227;o do relaxamento ventricular resulta, freq&#252;entemente, em uma pseudonormaliza&#231;&#227;o do fluxo transmitral. </p>
    <p>A disfun&#231;&#227;o diast&#243;lica em popula&#231;&#227;o geral n&#227;o-selecionada apresenta uma preval&#234;ncia maior que a disfun&#231;&#227;o sist&#243;lica, cerca de 11%<sup>44</sup>. J&#225; em pacientes chag&#225;sicos a disfun&#231;&#227;o diast&#243;lica varia de 27,6% a 83%, de acordo com o m&#233;todo de avalia&#231;&#227;o utilizado e a forma cl&#237;nica da doen&#231;a<sup>45</sup>. Os primeiros estudos de disfun&#231;&#227;o diast&#243;lica na doen&#231;a de Chagas com m&#233;todos n&#227;o-invasivos utilizaram o ECO modo M, associado ao fonocardiograma e ao apexcardiograma, seguidos por estudos acoplando o modo bidimensional com Doppler e, finalmente, o Doppler tissular. Independentemente do m&#233;todo utilizado, h&#225; ind&#237;cios de que a disfun&#231;&#227;o diast&#243;lica &#233; freq&#252;ente e pode estar presente em pacientes assintom&#225;ticos, precedendo a disfun&#231;&#227;o sist&#243;lica e sua preval&#234;ncia aumenta de acordo com a progress&#227;o da cardiopatia chag&#225;sica cr&#244;nica<sup>12,43,45,46</sup>.</p>
    <p>Os pept&#237;deos natriur&#233;ticos s&#227;o produzidos pelas c&#233;lulas card&#237;acas e s&#227;o neuro-horm&#244;nios com propriedades diur&#233;ticas, natriur&#233;ticas e vasodilatadoras<sup>16</sup>. </p>
    <p>Estudos sugerem que a an&#225;lise dos n&#237;veis s&#233;ricos ou plasm&#225;ticos do BNP podem ser utilizados para confirmar o diagn&#243;stico de IC, para medir o grau de comprometimento do ventr&#237;culo esquerdo, para quantificar a classe funcional, para estimar o progn&#243;stico e prever futuros eventos card&#237;acos e para avaliar a efici&#234;ncia da terapia na IC<sup>15,47-49</sup>.</p>
    <p>Neste estudo, no momento de inclus&#227;o os pacientes eram assintom&#225;ticos e foram divididos conforme as altera&#231;&#245;es encontradas no ECG. Valor plasm&#225;tico m&#233;dio mais elevado de BNP foi observado no grupo GIIA em rela&#231;&#227;o aos grupos GI e GIIB, por&#233;m sem signific&#226;ncia estat&#237;stica.</p>
    <p>Em estudos publicados avaliando pacientes com doen&#231;a de Chagas, os pacientes foram classificados conforme o grau de comprometimento da fun&#231;&#227;o sist&#243;lica do VE e comparados a um grupo controle, independentemente da presen&#231;a de altera&#231;&#227;o no ECG<sup>17,18</sup>. </p>
    <p>Ribeiro e cols.<sup>17</sup> obtiveram valores m&#233;dios de BNP semelhantes entre o grupo controle e os pacientes com FEVE &gt; 40%, e significativamente menores em rela&#231;&#227;o aos pacientes com FEVE &lt; 40%. Com o ponto de corte de 60,7 pmol/l a sensibilidade foi de 80% e a especificidade de 93% para FEVE &lt; 40% em pacientes com anormalidades no ECG ou no ICT. Walther e cols.<sup>18</sup>, em estudo semelhante, obtiveram valores significativamente menores no grupo controle do que nos pacientes chag&#225;sicos, mesmo com FEVE &gt; 40%. Com ponto de corte de 18,1 pmol/l a sensibilidade foi de 86% e a especificidade de 91% para diagn&#243;stico de pacientes com FEVE &lt; 40%. </p>
    <p> No presente estudo, os resultados apresentados podem ter sido influenciados pelo tamanho da amostra e pelos crit&#233;rios que permitiram a inclus&#227;o somente de pacientes assintom&#225;ticos que apresentaram baixa freq&#252;&#234;ncia de disfun&#231;&#227;o ventricular sist&#243;lica mais acentuada. Os dois pacientes com FEVE &lt; 40% apresentaram os maiores valores plasm&#225;ticos de BNP: 589 pg/ml e 946 pg/ml.</p>
    <p>Outra particularidade observada foi que, em quatro pacientes, todas do sexo feminino, os valores do BNP foram maiores que 100 pg/ml, sem estas apresentarem disfun&#231;&#227;o ventricular e quatro pacientes que apresentaram disfun&#231;&#227;o ventricular discreta os valores do BNP foram inferiores a 100 pg/ml. Desses, tr&#234;s eram do sexo masculino e um do sexo feminino. Estudos pr&#233;vios demonstram que os valores do BNP s&#227;o influenciados pelo sexo tanto em popula&#231;&#245;es normais quanto em popula&#231;&#245;es com IC. O sexo feminino tem valores mais elevados de BNP do que o sexo masculino<sup>50</sup>. </p>
    <p>Todos os pacientes que apresentaram disfun&#231;&#227;o sist&#243;lica global receberam tratamento medicamentoso padr&#227;o com captopril na dose m&#225;xima tolerada, e em dois pacientes foi associado tamb&#233;m o carvedilol. Tr&#234;s pacientes que apresentaram disfun&#231;&#227;o ventricular e TVNS foram tratados tamb&#233;m com amiodarona.</p>
    <p>Nossos resultados demonstram que em pacientes com doen&#231;a de Chagas e altera&#231;&#245;es eletrocardiogr&#225;ficas, mesmo assintom&#225;ticos, outros m&#233;todos diagn&#243;sticos como o ecocardiograma e o eletrocardiograma din&#226;mico de 24 horas, al&#233;m do eletrocardiograma e da radiografia de t&#243;rax, t&#234;m importante valor na avalia&#231;&#227;o inicial. As limita&#231;&#245;es do estudo se concentram na casu&#237;stica limitada pelos r&#237;gidos crit&#233;rios de inclus&#227;o e exclus&#227;o, aus&#234;ncia de um grupo controle de indiv&#237;duos n&#227;o-infectados e na aus&#234;ncia de seguimento. </p>
    <p>Como a doen&#231;a de Chagas &#233; uma doen&#231;a de evolu&#231;&#227;o lenta e os pacientes desse estudo continuar&#227;o seu acompanhamento, estima-se poder esclarecer, ap&#243;s um per&#237;odo adequado de acompanhamento, quest&#245;es ainda n&#227;o definidas. Dentre elas, os aspectos evolutivos em longo prazo dos pacientes com doen&#231;a de Chagas e altera&#231;&#245;es n&#227;o-caracter&#237;sticas no eletrocardiograma, al&#233;m do valor progn&#243;stico da disfun&#231;&#227;o ventricular diast&#243;lica e do BNP nos grupos estudados.</p>
    <p>
      <bold>Potencial Conflito de Interesses</bold>
    </p>
    <p>Declaro n&#227;o haver conflitos de interesses pertinentes.</p>
    <p>
      <fn id="end" fn-type="corresp">
        <label>
          <bold>Correspond&#234;ncia:</bold>
        </label>
        <p> Divina Seila de Oliveira Marques </p>
        <p> Rua Robert Koch, 60 </p>
        <p> 86038-440 &#150; Londrina, PR </p>
        <p> E-mail: </p>
        <p>
          <email xlink:href="d.seila@cardiol.br">d.seila@cardiol.br</email>
        </p>
      </fn>
    </p>
    <p>Recebido em 20/07/04 </p>
    <p> Aceito em 12/09/05</p>
  </body>
  <back>
    <ref-list>
      <ref id="B1">
        <mixed-citation>1. Dias JCP. A doen&#231;a de Chagas e seu    controle na Am&#233;rica Latina. Uma an&#225;lise de possibilidades. Cad    Sa&#250;de Publ. 1993;9:201-9. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>A doen&#231;a de Chagas e seu controle na Am&#233;rica Latina: Uma an&#225;lise de possibilidades</article-title>
          <source>Cad Sa&#250;de Publ.</source>
          <date>
            <year>1993</year>
          </date>
          <fpage>201</fpage>
          <lpage>9</lpage>
          <volume>9</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Dias</surname>
              <given-names>JCP.</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B2">
        <mixed-citation>2. Schmunis GA. Tripanossom&#237;ase americana:    seu impacto nas Am&#233;ricas e perspectivas de elimina&#231;&#227;o.    In: Dias JCP, Coura JR. Cl&#237;nica e Terap&#234;utica da Doen&#231;a    de Chagas. Rio de Janeiro: Fiocruz; 1997: 11-23.</mixed-citation>
        <element-citation publication-type="book">
          <source>Cl&#237;nica e Terap&#234;utica da Doen&#231;a de Chagas</source>
          <date>
            <year>1997</year>
          </date>
          <fpage>11</fpage>
          <lpage>23</lpage>
          <person-group person-group-type="author">
            <name>
              <surname>Schmunis</surname>
              <given-names>GA</given-names>
            </name>
            <name>
              <surname>Dias</surname>
              <given-names>JCP</given-names>
            </name>
            <name>
              <surname>Coura</surname>
              <given-names>JR</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B3">
        <mixed-citation>3. Akhavan D. An&#225;lise de custo-efetividade    do programa de controle da doen&#231;a de chagas no Brasil: relat&#243;rio    final. Bras&#237;lia: OPAS; 2000. </mixed-citation>
        <element-citation publication-type="book">
          <source>An&#225;lise de custo-efetividade do programa de controle da doen&#231;a de chagas no Brasil: relat&#243;rio final</source>
          <date>
            <year>2000</year>
          </date>
          <person-group person-group-type="author">
            <name>
              <surname>Akhavan</surname>
              <given-names>D</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B4">
        <mixed-citation>4. Mac&#234;do VO. Influ&#234;ncia da exposi&#231;&#227;o    &#224; reinfec&#231;&#227;o na evolu&#231;&#227;o da doen&#231;a    de Chagas (estudo longitudinal de cinco anos). Tese (Livre-doc&#234;ncia) -    Rio de Janeiro, 1973 - Universidade Federal do Rio de Janeiro.</mixed-citation>
        <element-citation publication-type="thesis">
          <source>Influ&#234;ncia da exposi&#231;&#227;o &#224; reinfec&#231;&#227;o na evolu&#231;&#227;o da doen&#231;a de Chagas (estudo longitudinal de cinco anos)</source>
          <date>
            <year>1973</year>
          </date>
          <person-group person-group-type="author">
            <name>
              <surname>Mac&#234;do</surname>
              <given-names>VO</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B5">
        <mixed-citation>5. Dias JCP. Hist&#243;ria natural da doen&#231;a    de Chagas. In: Rassi Junior A, ed. Simp&#243;sio "ABC" Doen&#231;a de Chagas.    Arq Bras Cardiol 1995;65(4):359-66. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Hist&#243;ria natural da doen&#231;a de Chagas</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>1995</year>
          </date>
          <fpage>359</fpage>
          <lpage>66</lpage>
          <issue>4</issue>
          <volume>65</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Dias</surname>
              <given-names>JCP</given-names>
            </name>
            <name>
              <surname>Rassi Junior</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B6">
        <mixed-citation>6. Garzon SAC, Lorga AM, Nicolau JC. Eletrocardiografia    na cardiopatia chag&#225;sica. Rev Soc Cardiol Est S&#227;o Paulo 1994;4(2):    33-43. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Eletrocardiografia na cardiopatia chag&#225;sica</article-title>
          <source>Rev Soc Cardiol Est S&#227;o Paulo</source>
          <date>
            <year>1994</year>
          </date>
          <fpage>33</fpage>
          <lpage>43</lpage>
          <issue>2</issue>
          <volume>4</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Garzon</surname>
              <given-names>SAC</given-names>
            </name>
            <name>
              <surname>Lorga</surname>
              <given-names>AM</given-names>
            </name>
            <name>
              <surname>Nicolau</surname>
              <given-names>JC</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B7">
        <mixed-citation>7. Marin-Neto JA, Sim&#245;es MV, Sarabanda    AVL. Doen&#231;a card&#237;aca no indiv&#237;duo assintom&#225;tico    com mol&#233;stia de Chagas. Rev Soc Cardiol Est S&#227;o Paulo 1997;7(6):726-34.    </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Doen&#231;a card&#237;aca no indiv&#237;duo assintom&#225;tico com mol&#233;stia de Chagas</article-title>
          <source>Rev Soc Cardiol Est S&#227;o Paulo</source>
          <date>
            <year>1997</year>
          </date>
          <fpage>726</fpage>
          <lpage>34</lpage>
          <issue>6</issue>
          <volume>7</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Marin-Neto</surname>
              <given-names>JA</given-names>
            </name>
            <name>
              <surname>Sim&#245;es</surname>
              <given-names>MV</given-names>
            </name>
            <name>
              <surname>Sarabanda</surname>
              <given-names>AVL</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B8">
        <mixed-citation>8. Rassi J&#250;nior A, Rassi SG, Rassi A.    Sudden death in Chagas disease. Arq Bras Cardiol 2001;76(1):86-96.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Sudden death in Chagas&#8217; disease</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>2001</year>
          </date>
          <fpage>86</fpage>
          <lpage>96</lpage>
          <issue>1</issue>
          <volume>76</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Rassi J&#250;nior</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Rassi</surname>
              <given-names>SG</given-names>
            </name>
            <name>
              <surname>Rassi</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B9">
        <mixed-citation>9. Rassi Junior A, Rassi AG, Rassi SG, Rassi    Junior L, Rassi A. Arritmias ventriculares na doen&#231;a de Chagas. Particularidades    diagn&#243;sticas, progn&#243;sticas e terap&#234;uticas. Arq Bras Cardiol    1995;65(4):377-87. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Arritmias ventriculares na doen&#231;a de Chagas: Particularidades diagn&#243;sticas, progn&#243;sticas e terap&#234;uticas</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>1995</year>
          </date>
          <fpage>377</fpage>
          <lpage>87</lpage>
          <issue>4</issue>
          <volume>65</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Rassi Junior</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Rassi</surname>
              <given-names>AG</given-names>
            </name>
            <name>
              <surname>Rassi</surname>
              <given-names>SG</given-names>
            </name>
            <name>
              <surname>Rassi Junior</surname>
              <given-names>L</given-names>
            </name>
            <name>
              <surname>Rassi</surname>
              <given-names>A.</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B10">
        <mixed-citation>10. Costa Rocha MO, Ribeiro ALP, Torres RM, Tostes    VTV. M&#233;todos n&#227;o-invasivos de an&#225;lise funcional card&#237;aca.    In: Dias JCP, Coura JR. Cl&#237;nica e Terap&#234;utica da doen&#231;a    de Chagas. Rio de Janeiro: Fiocruz; 1997: 237-53.</mixed-citation>
        <element-citation publication-type="book">
          <source>Cl&#237;nica e Terap&#234;utica da doen&#231;a de Chagas</source>
          <date>
            <year>1997</year>
          </date>
          <fpage>237</fpage>
          <lpage>53</lpage>
          <person-group person-group-type="author">
            <name>
              <surname>Costa Rocha</surname>
              <given-names>MO</given-names>
            </name>
            <name>
              <surname>Ribeiro</surname>
              <given-names>ALP</given-names>
            </name>
            <name>
              <surname>Torres</surname>
              <given-names>RM</given-names>
            </name>
            <name>
              <surname>Tostes</surname>
              <given-names>VTV</given-names>
            </name>
            <name>
              <surname>Dias</surname>
              <given-names>JCP</given-names>
            </name>
            <name>
              <surname>Coura</surname>
              <given-names>JR</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B11">
        <mixed-citation>11. Mady C, Cardoso RHA, Barretto AC, Da Luz    PL, Bellotti G, Pillegi F. Survival and predictor of survival in patients with    congestive heart failure due to Chagas disease. Circulation 1994;(90):3098-102.    </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Survival and predictor of survival in patients with congestive heart failure due to Chagas&#8217; disease</article-title>
          <source>Circulation</source>
          <date>
            <year>1994</year>
          </date>
          <fpage>3098</fpage>
          <lpage>102</lpage>
          <volume>90</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Mady</surname>
              <given-names>C</given-names>
            </name>
            <name>
              <surname>Cardoso</surname>
              <given-names>RHA</given-names>
            </name>
            <name>
              <surname>Barretto</surname>
              <given-names>AC</given-names>
            </name>
            <name>
              <surname>Da Luz</surname>
              <given-names>PL</given-names>
            </name>
            <name>
              <surname>Bellotti</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Pillegi</surname>
              <given-names>F</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B12">
        <mixed-citation>12. Barros MVL, Rocha MOC, Ribeiro ALP, Machado    FS. Tissue Doppler Imaging Enables the Identification of Diastolic Dysfunction    of Pseudonormal Pattern in ChagasDisease. J Am Soc Echocardiogr 2001;14(5):353-59.    </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Tissue Doppler Imaging Enables the Identification of Diastolic Dysfunction of Pseudonormal Pattern in Chagas&#8217;Disease</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>2001</year>
          </date>
          <fpage>353</fpage>
          <lpage>59</lpage>
          <issue>5</issue>
          <volume>14</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Barros</surname>
              <given-names>MVL</given-names>
            </name>
            <name>
              <surname>Rocha</surname>
              <given-names>MOC</given-names>
            </name>
            <name>
              <surname>Ribeiro</surname>
              <given-names>ALP</given-names>
            </name>
            <name>
              <surname>Machado</surname>
              <given-names>FS</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B13">
        <mixed-citation>13. Farias CA, Rodriguez L, Garcia MJ, Sun JP,    Klein AL, Thomas JD. Assessment of diastolic function by tissue Doppler echocardiography,    comparision with standard transmitral and pulmonary venous flow. J Am Soc Echocardiogr    1999;(12):609-17.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Assessment of diastolic function by tissue Doppler echocardiography, comparision with standard transmitral and pulmonary venous flow</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>1999</year>
          </date>
          <fpage>609</fpage>
          <lpage>17</lpage>
          <volume>12</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Farias</surname>
              <given-names>CA</given-names>
            </name>
            <name>
              <surname>Rodriguez</surname>
              <given-names>L</given-names>
            </name>
            <name>
              <surname>Garcia</surname>
              <given-names>MJ</given-names>
            </name>
            <name>
              <surname>Sun</surname>
              <given-names>JP</given-names>
            </name>
            <name>
              <surname>Klein</surname>
              <given-names>AL</given-names>
            </name>
            <name>
              <surname>Thomas</surname>
              <given-names>JD</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B14">
        <mixed-citation>14. Maisel AK, Jen B, Krishnaswamy P, et al.    Utility of B-natriuretic peptide as a rapid, point-of-care test for screening    patients undergoing echocardiography to determine left ventricular dysfunction.    Am Heart J 2001;3(141):367-74. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Utility of B-natriuretic peptide as a rapid, point-of-care test for screening patients undergoing echocardiography to determine left ventricular dysfunction</article-title>
          <source>Am Heart J</source>
          <date>
            <year>2001</year>
          </date>
          <fpage>367</fpage>
          <lpage>74</lpage>
          <issue>141</issue>
          <volume>3</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Maisel</surname>
              <given-names>AK</given-names>
            </name>
            <name>
              <surname>Jen</surname>
              <given-names>B</given-names>
            </name>
            <name>
              <surname>Krishnaswamy</surname>
              <given-names>P</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B15">
        <mixed-citation>15. Lubien E, Demaria A, Krisnaswamy P. Utility    of B-natriuretic peptide in detecting diastolic dysfunction. Comparision with    Doppler velocity recordings. Circulation 2002;(105):595-601. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Utility of B-natriuretic peptide in detecting diastolic dysfunction: Comparision with Doppler velocity recordings</article-title>
          <source>Circulation</source>
          <date>
            <year>2002</year>
          </date>
          <fpage>595</fpage>
          <lpage>601</lpage>
          <volume>105</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Lubien</surname>
              <given-names>E</given-names>
            </name>
            <name>
              <surname>Demaria</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Krisnaswamy</surname>
              <given-names>P.</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B16">
        <mixed-citation>16. Levin ER, Gardner DG, Samson WW. Mechanisms    of Disease: Natriuretic Peptides. N Engl J Med 1998;(339):321-28.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Mechanisms of Disease: Natriuretic Peptides</article-title>
          <source>N Engl J Med</source>
          <date>
            <year>1998</year>
          </date>
          <fpage>321</fpage>
          <lpage>28</lpage>
          <volume>339</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Levin</surname>
              <given-names>ER</given-names>
            </name>
            <name>
              <surname>Gardner</surname>
              <given-names>DG</given-names>
            </name>
            <name>
              <surname>Samson</surname>
              <given-names>WW</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B17">
        <mixed-citation>17. Ribeiro ALP, Reis AM, Barros MVL, et al.    Brain Natriuretic Peptide and Left Ventricular Dysfunction in Chagas' Disease.    Lancet 2002;360:461-2. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Brain Natriuretic Peptide and Left Ventricular Dysfunction in Chagas' Disease</article-title>
          <source>Lancet</source>
          <date>
            <year>2002</year>
          </date>
          <fpage>461</fpage>
          <lpage>2</lpage>
          <volume>360</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Ribeiro</surname>
              <given-names>ALP</given-names>
            </name>
            <name>
              <surname>Reis</surname>
              <given-names>AM</given-names>
            </name>
            <name>
              <surname>Barros</surname>
              <given-names>MVL</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B18">
        <mixed-citation>18. Walther T, Heringer-Walther S, Wessel N,    Heinz-Peter S, Moreira MCV. Brain natriuretic peptide as a predictor of cardiomyopathy    in Chagas Disease. Lancet 2003;61(9368):1567.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Brain natriuretic peptide as a predictor of cardiomyopathy in Chagas&#8217; Disease</article-title>
          <source>Lancet</source>
          <date>
            <year>2003</year>
          </date>
          <fpage>1567</fpage>
          <issue>9368</issue>
          <volume>61</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Walther</surname>
              <given-names>T</given-names>
            </name>
            <name>
              <surname>Heringer-Walther</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Wessel</surname>
              <given-names>N</given-names>
            </name>
            <name>
              <surname>Heinz-Peter</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Moreira</surname>
              <given-names>MCV</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B19">
        <mixed-citation>19. Sociedade Brasileira de Cardiologia. II Diretrizes    da Sociedade Brasileira da Cardiologia para o Diagn&#243;stico e Tratamento    da Insufici&#234;ncia Card&#237;aca. Arq Bras Cardiol 1999; 72 Suppl.1.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>II Diretrizes da Sociedade Brasileira da Cardiologia para o Diagn&#243;stico e Tratamento da Insufici&#234;ncia Card&#237;aca</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>1999</year>
          </date>
          <volume>72</volume>
        </element-citation>
      </ref>
      <ref id="B20">
        <mixed-citation>20. Sociedade Brasileira de Cardiologia. Diretriz    para Avalia&#231;&#227;o e Tratamento de Pacientes com Arritmia Card&#237;aca.    Arq Bras Cardiol 2002; 79 Suppl 5. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Diretriz para Avalia&#231;&#227;o e Tratamento de Pacientes com Arritmia Card&#237;aca</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>2002</year>
          </date>
          <volume>79</volume>
        </element-citation>
      </ref>
      <ref id="B21">
        <mixed-citation>21. Sociedade Brasileira de Cardiologia. IV Diretrizes    Brasileiras de Hipertens&#227;o Arterial. Arq Bras Cardiol 2004; 82 Suppl.4.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>IV Diretrizes Brasileiras de Hipertens&#227;o Arterial</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>2004</year>
          </date>
          <volume>82</volume>
        </element-citation>
      </ref>
      <ref id="B22">
        <mixed-citation>22. The Expert Committee on the Diagnosis and    Classification of Diabetes Mellitus. Report of the Expert Committee on the Diagnosis    and Classification of Diabetes Mellitus. Diabetes Care 1997;20(7):1186-97.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>The Expert Committee on the Diagnosis and Classification of Diabetes Mellitus: Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus</article-title>
          <source>Diabetes Care</source>
          <date>
            <year>1997</year>
          </date>
          <fpage>1186</fpage>
          <lpage>97</lpage>
          <issue>7</issue>
          <volume>20</volume>
        </element-citation>
      </ref>
      <ref id="B23">
        <mixed-citation>23. Mac&#234;do V. Inqu&#233;rito eletrocardiogr&#225;fico    Nacional para doen&#231;a de Chagas. Rev Soc Bras Med Trop 1993;(26)Suppl.    2:12-3. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Inqu&#233;rito eletrocardiogr&#225;fico Nacional para doen&#231;a de Chagas</article-title>
          <source>Rev Soc Bras Med Trop</source>
          <date>
            <year>1993</year>
          </date>
          <fpage>12</fpage>
          <lpage>3</lpage>
          <volume>26</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Mac&#234;do</surname>
              <given-names>V</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B24">
        <mixed-citation>24. Medeiros Sobrinho JO. Radiologia do Cora&#231;&#227;o.    S&#227;o Paulo: Sarvier; 1980. </mixed-citation>
        <element-citation publication-type="book">
          <source>Radiologia do Cora&#231;&#227;o</source>
          <date>
            <year>1980</year>
          </date>
          <person-group person-group-type="author">
            <name>
              <surname>Medeiros Sobrinho</surname>
              <given-names>JO</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B25">
        <mixed-citation>25. Fagundes MLA, Boghossian SH. Taquicardias    ventriculares. O uso do Holter na identifica&#231;&#227;o dos poss&#237;veis    mecanismos eletrofisiol&#243;gicos. In: Souza OF, Pereira LS, Maia IG. O sistema    Holter e outros m&#233;todos nas arritmias card&#237;acas. Rio de Janeiro:    Revinter, 2001:125-33.</mixed-citation>
        <element-citation publication-type="book">
          <source>O sistema Holter e outros m&#233;todos nas arritmias card&#237;acas</source>
          <date>
            <year>2001</year>
          </date>
          <fpage>125</fpage>
          <lpage>33</lpage>
          <person-group person-group-type="author">
            <name>
              <surname>Fagundes</surname>
              <given-names>MLA</given-names>
            </name>
            <name>
              <surname>Boghossian</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Souza</surname>
              <given-names>OF</given-names>
            </name>
            <name>
              <surname>Pereira</surname>
              <given-names>LS</given-names>
            </name>
            <name>
              <surname>Maia</surname>
              <given-names>IG</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B26">
        <mixed-citation>26. Folland ED, Parisi AF, Moynihan PF, Jones    DR, Feldman CL, Tow DE. Assessment of left ventricular ejection fraction and    volumes by real-time, two-dimensional echocardiography. A comparison of cineangiographic    and radionuclide techniques. Circulation 1979;60(4):760-6. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Assessment of left ventricular ejection fraction and volumes by real-time, two-dimensional echocardiography: A comparison of cineangiographic and radionuclide techniques</article-title>
          <source>Circulation</source>
          <date>
            <year>1979</year>
          </date>
          <fpage>760</fpage>
          <lpage>6</lpage>
          <issue>4</issue>
          <volume>60</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Folland</surname>
              <given-names>ED</given-names>
            </name>
            <name>
              <surname>Parisi</surname>
              <given-names>AF</given-names>
            </name>
            <name>
              <surname>Moynihan</surname>
              <given-names>PF</given-names>
            </name>
            <name>
              <surname>Jones</surname>
              <given-names>DR</given-names>
            </name>
            <name>
              <surname>Feldman</surname>
              <given-names>CL</given-names>
            </name>
            <name>
              <surname>Tow</surname>
              <given-names>DE</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B27">
        <mixed-citation>27. Schiller NB, Shah PM, Crawford M, et al.    Recommendations for quantitation of the left ventricle by two-dimensional echocardiography.    J Am Soc Echocardiogr 1989;2:358-65.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Recommendations for quantitation of the left ventricle by two-dimensional echocardiography</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>1989</year>
          </date>
          <fpage>358</fpage>
          <lpage>65</lpage>
          <volume>2</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Schiller</surname>
              <given-names>NB</given-names>
            </name>
            <name>
              <surname>Shah</surname>
              <given-names>PM</given-names>
            </name>
            <name>
              <surname>Crawford</surname>
              <given-names>M</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B28">
        <mixed-citation>28. Sohn DW, Chai IH, Lee DJ, et al. Assessment    of mitral annulus velocity by Doppler tissue imaging in the evaluation of left    ventricular diastolic function. J Am Coll Cardiol 1997;30(2):474-80.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Assessment of mitral annulus velocity by Doppler tissue imaging in the evaluation of left ventricular diastolic function</article-title>
          <source>J Am Coll Cardiol</source>
          <date>
            <year>1997</year>
          </date>
          <fpage>474</fpage>
          <lpage>80</lpage>
          <issue>2</issue>
          <volume>30</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Sohn</surname>
              <given-names>DW</given-names>
            </name>
            <name>
              <surname>Chai</surname>
              <given-names>IH</given-names>
            </name>
            <name>
              <surname>Lee</surname>
              <given-names>DJ</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B29">
        <mixed-citation>29. Dias JCP. O controle da Doen&#231;a de    Chagas no Brasil. In: Silveira AC, Arias AR, Segura E, Guill&#233;n G, Russomando    G, Schenone H, Dias JCP, Padilha JV, Lorca M, Salvatella R. El control de la    enfermedad de Chagas en los pa&#237;ses del Cono Sur de Am&#233;rica: Hist&#243;ria    de uma iniciativa internacional. 1991/2001. Uberaba: Faculdade de Medicina do    Tri&#226;ngulo Mineiro; 2002:146-250.</mixed-citation>
        <element-citation publication-type="book">
          <source>El control de la enfermedad de Chagas en los pa&#237;ses del Cono Sur de Am&#233;rica: Hist&#243;ria de uma iniciativa internacional. 1991/2001</source>
          <date>
            <year>2002</year>
          </date>
          <fpage>146</fpage>
          <lpage>250</lpage>
          <person-group person-group-type="author">
            <name>
              <surname>Dias</surname>
              <given-names>JCP</given-names>
            </name>
            <name>
              <surname>Silveira</surname>
              <given-names>AC</given-names>
            </name>
            <name>
              <surname>Arias</surname>
              <given-names>AR</given-names>
            </name>
            <name>
              <surname>Segura</surname>
              <given-names>E</given-names>
            </name>
            <name>
              <surname>Guill&#233;n</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Russomando</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Schenone</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Dias</surname>
              <given-names>JCP</given-names>
            </name>
            <name>
              <surname>Padilha</surname>
              <given-names>JV</given-names>
            </name>
            <name>
              <surname>Lorca</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Salvatella</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B30">
        <mixed-citation>30. Davie AP, Francis CM, Love MP, et al. Value    of the electrocardiogram in identifying heart failure due to left ventricular    systolic dysfunction. BMJ 1996;312(7025):222.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Value of the electrocardiogram in identifying heart failure due to left ventricular systolic dysfunction</article-title>
          <source>BMJ</source>
          <date>
            <year>1996</year>
          </date>
          <fpage>222</fpage>
          <issue>7025</issue>
          <volume>312</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Davie</surname>
              <given-names>AP</given-names>
            </name>
            <name>
              <surname>Francis</surname>
              <given-names>CM</given-names>
            </name>
            <name>
              <surname>Love</surname>
              <given-names>MP</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B31">
        <mixed-citation>31. Casado J, Davila DF, Donis JH, et al. Electrocardiographic    abnormalities and left ventricular systolic function in Chagas heart disease.    Int J Cardiol 1990;27(1):55-62.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Electrocardiographic abnormalities and left ventricular systolic function in Chagas&#8217; heart disease</article-title>
          <source>Int J Cardiol</source>
          <date>
            <year>1990</year>
          </date>
          <fpage>55</fpage>
          <lpage>62</lpage>
          <issue>1</issue>
          <volume>27</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Casado</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Davila</surname>
              <given-names>DF</given-names>
            </name>
            <name>
              <surname>Donis</surname>
              <given-names>JH</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B32">
        <mixed-citation>32. Carrasco HA, Guerrero L, Parada H, Molina    C, Vegas E, Chuecos R. Ventricular Arrhythmias and Left Ventricular Myocardial    function in chronic chagasic patients. Int J Cardiol 1990;28(1):35-41. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Ventricular Arrhythmias and Left Ventricular Myocardial function in chronic chagasic patients</article-title>
          <source>Int J Cardiol</source>
          <date>
            <year>1990</year>
          </date>
          <fpage>35</fpage>
          <lpage>41</lpage>
          <issue>1</issue>
          <volume>28</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Carrasco</surname>
              <given-names>HA</given-names>
            </name>
            <name>
              <surname>Guerrero</surname>
              <given-names>L</given-names>
            </name>
            <name>
              <surname>Parada</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Molina</surname>
              <given-names>C</given-names>
            </name>
            <name>
              <surname>Vegas</surname>
              <given-names>E</given-names>
            </name>
            <name>
              <surname>Chuecos</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B33">
        <mixed-citation>33. Grupi CJ, Moffa PJ, Barbosa AS, et al. Holter    monitoring in Chagas heart disease. SPaulo Med Journ 1995;113(2):835-40. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Holter monitoring in Chagas&#8217; heart disease</article-title>
          <source>SPaulo Med Journ</source>
          <date>
            <year>1995</year>
          </date>
          <fpage>835</fpage>
          <lpage>40</lpage>
          <issue>2</issue>
          <volume>113</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Grupi</surname>
              <given-names>CJ</given-names>
            </name>
            <name>
              <surname>Moffa</surname>
              <given-names>PJ</given-names>
            </name>
            <name>
              <surname>Barbosa</surname>
              <given-names>AS</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B34">
        <mixed-citation>34. McDonagh TA, Morrison CCE, Lawrence A, et    al. Symptomatic and asymptomatic left-ventricular systolic dysfunction in an    urban population. Lancet 1997;350:829-33. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Symptomatic and asymptomatic left-ventricular systolic dysfunction in an urban population</article-title>
          <source>Lancet</source>
          <date>
            <year>1997</year>
          </date>
          <fpage>829</fpage>
          <lpage>33</lpage>
          <volume>350</volume>
          <person-group person-group-type="author">
            <name>
              <surname>McDonagh</surname>
              <given-names>TA</given-names>
            </name>
            <name>
              <surname>Morrison</surname>
              <given-names>CCE</given-names>
            </name>
            <name>
              <surname>Lawrence</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B35">
        <mixed-citation>35. Acquatella H, Schiller NB, Puigb&#243;    JJ, et al. Mode M and two-dimensional echocardiography in chronic Chagasheart    disease. A clinical and pathologic study. Circulation 1980;62:787-99.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Mode M and two-dimensional echocardiography in chronic Chagas&#8217;heart disease: A clinical and pathologic study</article-title>
          <source>Circulation</source>
          <date>
            <year>1980</year>
          </date>
          <fpage>787</fpage>
          <lpage>99</lpage>
          <volume>62</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Acquatella</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Schiller</surname>
              <given-names>NB</given-names>
            </name>
            <name>
              <surname>Puigb&#243;</surname>
              <given-names>JJ</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B36">
        <mixed-citation>36. Friedmann AA, Armelin E, Nelken JR, Zerbini    CAF, Coimbra MA, Serro-Azul LG. Estudo ecocardiogr&#225;fico do desempenho    ventricular em fase pr&#233;-cl&#237;nica da doen&#231;a de Chagas. Rev    Hosp Clin Fac Med S&#227;o Paulo 1980;35(4):165-70. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Estudo ecocardiogr&#225;fico do desempenho ventricular em fase pr&#233;-cl&#237;nica da doen&#231;a de Chagas</article-title>
          <source>Rev Hosp Clin Fac Med S&#227;o Paulo</source>
          <date>
            <year>1980</year>
          </date>
          <fpage>165</fpage>
          <lpage>70</lpage>
          <issue>4</issue>
          <volume>35</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Friedmann</surname>
              <given-names>AA</given-names>
            </name>
            <name>
              <surname>Armelin</surname>
              <given-names>E</given-names>
            </name>
            <name>
              <surname>Nelken</surname>
              <given-names>JR</given-names>
            </name>
            <name>
              <surname>Zerbini</surname>
              <given-names>CAF</given-names>
            </name>
            <name>
              <surname>Coimbra</surname>
              <given-names>MA</given-names>
            </name>
            <name>
              <surname>Serro-Azul</surname>
              <given-names>LG</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B37">
        <mixed-citation>37. Ianni BM, Alfieri RG, Chalela WA, et al.    Avalia&#231;&#227;o do comprometimento card&#237;aco em pacientes na forma    indeterminada e com altera&#231;&#245;es discretas ao eletrocardiograma:    atrav&#233;s do teste de esfor&#231;o e da ecocardiografia unidimensional.    Ars cvrandi cardiol 1985;7(56):8-14. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Avalia&#231;&#227;o do comprometimento card&#237;aco em pacientes na forma indeterminada e com altera&#231;&#245;es discretas ao eletrocardiograma: atrav&#233;s do teste de esfor&#231;o e da ecocardiografia unidimensional</article-title>
          <source>Ars cvrandi cardiol</source>
          <date>
            <year>1985</year>
          </date>
          <fpage>8</fpage>
          <lpage>14</lpage>
          <issue>56</issue>
          <volume>7</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Ianni</surname>
              <given-names>BM</given-names>
            </name>
            <name>
              <surname>Alfieri</surname>
              <given-names>RG</given-names>
            </name>
            <name>
              <surname>Chalela</surname>
              <given-names>WA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B38">
        <mixed-citation>38. Pereira-Barretto AC, Bellotti G, Deperon    SP, et al. O valor do eletrocardiograma na avalia&#231;&#227;o da fun&#231;&#227;o    mioc&#225;rdica nos portadores de doen&#231;a de Chagas. Arq Bras Cardiol    1989;52(2):69-73.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>O valor do eletrocardiograma na avalia&#231;&#227;o da fun&#231;&#227;o mioc&#225;rdica nos portadores de doen&#231;a de Chagas</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>1989</year>
          </date>
          <fpage>69</fpage>
          <lpage>73</lpage>
          <issue>2</issue>
          <volume>52</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Pereira-Barretto</surname>
              <given-names>AC</given-names>
            </name>
            <name>
              <surname>Bellotti</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Deperon</surname>
              <given-names>SP</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B39">
        <mixed-citation>39. Perez AA, Ribeiro ALP, Barros MVL, et al.    Valor do estudo radiol&#243;gico do t&#243;rax no diagn&#243;stico de    disfun&#231;&#227;o ventricular esquerda na doen&#231;a de Chagas. Arq    Bras Cardiol 2003;80(2):202-13. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Valor do estudo radiol&#243;gico do t&#243;rax no diagn&#243;stico de disfun&#231;&#227;o ventricular esquerda na doen&#231;a de Chagas</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>2003</year>
          </date>
          <fpage>202</fpage>
          <lpage>13</lpage>
          <issue>2</issue>
          <volume>80</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Perez</surname>
              <given-names>AA</given-names>
            </name>
            <name>
              <surname>Ribeiro</surname>
              <given-names>ALP</given-names>
            </name>
            <name>
              <surname>Barros</surname>
              <given-names>MVL</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B40">
        <mixed-citation>40. Pereira R. Recursos Diagn&#243;sticos na    Cardiopatia Chag&#225;sica: Ecocardiografia. In: Malta J. Doen&#231;a de    Chagas. S&#227;o Paulo: Sarvier; 1996: 110-12.</mixed-citation>
        <element-citation publication-type="book">
          <source>Doen&#231;a de Chagas</source>
          <date>
            <year>1996</year>
          </date>
          <fpage>110</fpage>
          <lpage>12</lpage>
          <person-group person-group-type="author">
            <name>
              <surname>Pereira</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Malta</surname>
              <given-names>J</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B41">
        <mixed-citation>41. Apar&#237;cio O, Artezana GA, Carlier Y,    Desjeux P. Ecocardiografia modo "M" en la enfermedad de Chagas. Ann Soc Belge    M&#233;d Trop 1985;65(Suppl 1):41-50.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Ecocardiografia modo "M" en la enfermedad de Chagas</article-title>
          <source>Ann Soc Belge M&#233;d Trop</source>
          <date>
            <year>1985</year>
          </date>
          <fpage>41</fpage>
          <lpage>50</lpage>
          <issue>1</issue>
          <volume>65</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Apar&#237;cio</surname>
              <given-names>O</given-names>
            </name>
            <name>
              <surname>Artezana</surname>
              <given-names>GA</given-names>
            </name>
            <name>
              <surname>Carlier</surname>
              <given-names>Y</given-names>
            </name>
            <name>
              <surname>Desjeux</surname>
              <given-names>P</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B42">
        <mixed-citation>42. Ortiz J, Pereira-Barretto AC, Matsumoto AY,    et al. Altera&#231;&#227;o contr&#225;til segmentar na forma indeterminada    da doen&#231;a de Chagas: estudo ecocardiogr&#225;fico. Arq Bras Cardiol    1987;49(4):217-20.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Altera&#231;&#227;o contr&#225;til segmentar na forma indeterminada da doen&#231;a de Chagas: estudo ecocardiogr&#225;fico</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>1987</year>
          </date>
          <fpage>217</fpage>
          <lpage>20</lpage>
          <issue>4</issue>
          <volume>49</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Ortiz</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Pereira-Barretto</surname>
              <given-names>AC</given-names>
            </name>
            <name>
              <surname>Matsumoto</surname>
              <given-names>AY</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B43">
        <mixed-citation>43. C&#226;mara EJ. Segmental changes in contractility    of the left heart ventricle in Chagas cardiopathy with and without ventricular    dilatation. Arq Bras Cardiol 1993;60(3):151-5.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Segmental changes in contractility of the left heart ventricle in Chagas cardiopathy with and without ventricular dilatation</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>1993</year>
          </date>
          <fpage>151</fpage>
          <lpage>5</lpage>
          <issue>3</issue>
          <volume>60</volume>
          <person-group person-group-type="author">
            <name>
              <surname>C&#226;mara</surname>
              <given-names>EJ</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B44">
        <mixed-citation>44. Fischer M, Baessler A, Hense HW, et al. Prevalence    of left ventricular diastolic dysfunction in the community: Results from a Doppler    echocardiographic-based survey of a population sample. Eur Heart J 2003;24(4):320-8.    </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Prevalence of left ventricular diastolic dysfunction in the community: Results from a Doppler echocardiographic-based survey of a population sample</article-title>
          <source>Eur Heart J</source>
          <date>
            <year>2003</year>
          </date>
          <fpage>320</fpage>
          <lpage>8</lpage>
          <issue>4</issue>
          <volume>24</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Fischer</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Baessler</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Hense</surname>
              <given-names>HW</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B45">
        <mixed-citation>45. Combellas I, Puigb&#243; JJ, Acquatella    H, Toledo F, Gomez JR. Echocardiographic Features of Impaired Left Ventricular    diastolic function in Chagas heart disease. Br Heart J 1985;53:298-309.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Echocardiographic Features of Impaired Left Ventricular diastolic function in Chagas heart disease</article-title>
          <source>Br Heart J</source>
          <date>
            <year>1985</year>
          </date>
          <fpage>298</fpage>
          <lpage>309</lpage>
          <volume>53</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Combellas</surname>
              <given-names>I</given-names>
            </name>
            <name>
              <surname>Puigb&#243;</surname>
              <given-names>JJ</given-names>
            </name>
            <name>
              <surname>Acquatella</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Toledo</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Gomez</surname>
              <given-names>JR</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B46">
        <mixed-citation>46. Migliore RA, Adaniya ME, Tamagusuku H, Lapuente    A. Evaluacion de la funcion diastolica en la enfermedad de Chagas mediante Doppler    tisular pulsado. Medicina 2003;63(6):692-6. </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Evaluacion de la funcion diastolica en la enfermedad de Chagas mediante Doppler tisular pulsado</article-title>
          <source>Medicina</source>
          <date>
            <year>2003</year>
          </date>
          <fpage>692</fpage>
          <lpage>6</lpage>
          <issue>6</issue>
          <volume>63</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Migliore</surname>
              <given-names>RA</given-names>
            </name>
            <name>
              <surname>Adaniya</surname>
              <given-names>ME</given-names>
            </name>
            <name>
              <surname>Tamagusuku</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Lapuente</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B47">
        <mixed-citation>47. Cowie MR, Struthers AD, Wood DA, et al. Value    of natriuretic peptides in assessment of patients with possible new heart failure    in primary care. Lancet 1997;350:1347-51.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Value of natriuretic peptides in assessment of patients with possible new heart failure in primary care</article-title>
          <source>Lancet</source>
          <date>
            <year>1997</year>
          </date>
          <fpage>1347</fpage>
          <lpage>51</lpage>
          <volume>350</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Cowie</surname>
              <given-names>MR</given-names>
            </name>
            <name>
              <surname>Struthers</surname>
              <given-names>AD</given-names>
            </name>
            <name>
              <surname>Wood</surname>
              <given-names>DA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B48">
        <mixed-citation>48. Cheng V, Kazanagra R, Garcia A, et al. A    rapid bedside test for B-type peptide predicts treatment outcomes in patients    admitted for decompensate heart failure: a pilot study. J Am Coll Cardiol 2001;37(2):386-91.    </mixed-citation>
        <element-citation publication-type="journal">
          <article-title>A rapid bedside test for B-type peptide predicts treatment outcomes in patients admitted for decompensate heart failure: a pilot study</article-title>
          <source>J Am Coll Cardiol</source>
          <date>
            <year>2001</year>
          </date>
          <fpage>386</fpage>
          <lpage>91</lpage>
          <issue>2</issue>
          <volume>37</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Cheng</surname>
              <given-names>V</given-names>
            </name>
            <name>
              <surname>Kazanagra</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Garcia</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B49">
        <mixed-citation>49. Wang TJ, Larson MG, Levy D, et al. Plasma    natriuretic peptide levels and the risk of cardiovascular events and death.    N Engl J Med 2004;350(7):655-63.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Plasma natriuretic peptide levels and the risk of cardiovascular events and death</article-title>
          <source>N Engl J Med</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>655</fpage>
          <lpage>63</lpage>
          <issue>7</issue>
          <volume>350</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Wang</surname>
              <given-names>TJ</given-names>
            </name>
            <name>
              <surname>Larson</surname>
              <given-names>MG</given-names>
            </name>
            <name>
              <surname>Levy</surname>
              <given-names>D</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B50">
        <mixed-citation>50. Redfield MM, Rodeheffer RJ, Jacobsen SJ,    Mahoney DW, Bailey KR, Burnet JC. Plasma Brain natriuretic peptide concentration:    impact of age and gender. J Am Coll Cardiol 2002;40(5):976-82.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Plasma Brain natriuretic peptide concentration: impact of age and gender</article-title>
          <source>J Am Coll Cardiol</source>
          <date>
            <year>2002</year>
          </date>
          <fpage>976</fpage>
          <lpage>82</lpage>
          <issue>5</issue>
          <volume>40</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Redfield</surname>
              <given-names>MM</given-names>
            </name>
            <name>
              <surname>Rodeheffer</surname>
              <given-names>RJ</given-names>
            </name>
            <name>
              <surname>Jacobsen</surname>
              <given-names>SJ</given-names>
            </name>
            <name>
              <surname>Mahoney</surname>
              <given-names>DW</given-names>
            </name>
            <name>
              <surname>Bailey</surname>
              <given-names>KR</given-names>
            </name>
            <name>
              <surname>Burnet</surname>
              <given-names>JC</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
    </ref-list>
  </back>
  <sub-article article-type="translation" id="TRen" xml:lang="en">
    <front-stub>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Original Articles</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title xml:lang="en">Evaluation of asymptomatic patients with chronic Chagas&#8217; disease through ambulatory electrocardiogram, echocardiogram and B-Type natriuretic peptide analyses</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>OBJECTIVE: To evaluate asymptomatic patients with chronic Chagas&#8217; disease to determine prevalence of ventricular arrhythmias, left ventricular dysfunction, and B-type natriuretic peptide (BNP) plasma levels. METHODS: One hundred and six patients from the Chagas&#8217; disease outpatient clinic underwent clinical evaluation, electrocardiogram (ECG), cardiothoracic index (CTI), ambulatory electrocardiogram (Holter monitoring), echocardiogram, and BNP measurement and then were distributed into three groups: GI, with normal ECG (n = 50); GIIA, with ECG changes characteristic of Chagas&#8217; disease (n = 31); and GIIB, with other ECG changes (n = 25). RESULTS: The most common electrocardiographic changes were the following. GIIA: complete right bundle branch block (35%), left anterior hemiblock (35%), and electrically inactive areas (32%); GIIB: inferolateral repolarization change (28%), and left ventricular overload (24%). Mean CTI index values were similar (p = 0.383). Ventricular arrhythmia prevalence was higher in the GIIA (77%) and GIIB (75%) groups than in the GI group (46%) (p = 0.002). Ventricular dysfunction was more prevalent in the GIIA (52%) and GIIB (32%) groups than in the GI group (14%) (p = 0.001). Systolic dysfunction was more prevalent in the GIIA group (29%) than in the GIIB (20%) and GI groups (2%) (p &lt; 0.001). Diastolic dysfunction was more prevalent in the GIIA (42%) and GIIB (28%) groups than in the GI group (12%) (p = 0.005). Mean B-type natriuretic peptide levels were 30 &#177; 88 pg/mL in the GI group, 66 &#177; 194 in the GIIA group and 24 &#177; 82 for the GIIB group (p = 0.121), respectively. CONCLUSION: Arrhythmias and left ventricular dysfunction are more prevalent in asymptomatic patients with chronic Chagas&#8217; disease and abnormal ECG than in patients with normal ECG. Plasma BNP levels were similar among the groups.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Chagas&#8217; disease</kwd>
        <kwd>ambulatory electrocardiography</kwd>
        <kwd>Doppler echocardiography</kwd>
        <kwd>brain natriuretic peptide</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>ORIGINAL ARTICLE</bold>
      </p>
      <p>Evaluation of asymptomatic patients with chronic chagas&#146; disease through ambulatory electrocardiogram, echocardiogram and B-type natriuretic peptide analyses </p>
      <p>
        <bold>Divina Seila de Oliveira Marques; Manoel Fernandes Canesin; Flavio Barutta J&#250;nior; Claudio Jos&#233; Fuganti; Antonio Carlos Pereira Barretto</bold>
      </p>
      <p>Hospital de Cl&#237;nicas da Faculdade de Medicina da Universidade Estadual de Londrina e Instituto do Cora&#231;&#227;o do Hospital das Cl&#237;nicas da FMUSP - Londrina, PR &#150; S&#227;o Paulo, SP - Brazil</p>
      <p>
        <xref ref-type="corresp" rid="end-body2">Mailing address</xref>
      </p>
      <p>
        <bold>ABSTRACT</bold>
      </p>
      <p><bold>OBJECTIVE: </bold>To evaluate asymptomatic patients with chronic Chagas&#146; disease to determine prevalence of ventricular arrhythmias, left ventricular dysfunction, and B-type natriuretic peptide (BNP) plasma levels.</p>
      <p><bold>METHODS:</bold> One hundred and six patients from the Chagas&#146; disease outpatient clinic underwent clinical evaluation, electrocardiogram (ECG), cardiothoracic index (CTI), ambulatory electrocardiogram (Holter monitoring), echocardiogram, and BNP measurement and then were distributed into three groups: GI, with normal ECG (n = 50); GIIA, with ECG changes characteristic of Chagas&#146; disease (n = 31); and GIIB, with other ECG changes (n = 25).</p>
      <p><bold>RESULTS:</bold> The most common electrocardiographic changes were the following. GIIA: complete right bundle branch block (35%), left anterior hemiblock (35%), and electrically inactive areas (32%); GIIB: inferolateral repolarization change (28%), and left ventricular overload (24%). Mean CTI index values were similar (p = 0.383). Ventricular arrhythmia prevalence was higher in the GIIA (77%) and GIIB (75%) groups than in the GI group (46%) (p = 0.002). Ventricular dysfunction was more prevalent in the GIIA (52%) and GIIB (32%) groups than in the GI group (14%) (p = 0.001). Systolic dysfunction was more prevalent in the GIIA group (29%) than in the GIIB (20%) and GI groups (2%) (p &lt; 0.001). Diastolic dysfunction was more prevalent in the GIIA (42%) and GIIB (28%) groups than in the GI group (12%) (p = 0.005). Mean B-type natriuretic peptide levels were 30 &#177; 88 pg/mL in the GI group, 66 &#177; 194 in the GIIA group and 24 &#177; 82 for the GIIB group (p = 0.121), respectively.</p>
      <p><bold>CONCLUSION:</bold> Arrhythmias and left ventricular dysfunction are more prevalent in asymptomatic patients with chronic Chagas&#146; disease and abnormal ECG than in patients with normal ECG. Plasma BNP levels were similar among the groups. </p>
      <p><bold>Key words: </bold>Chagas&#146; disease, ambulatory electrocardiography, Doppler echocardiography, brain natriuretic peptide.</p>
      <p>Chagas&#146; disease is characterized by a large clinical diversity. It is one of the major public health problems in Brazil, with an estimated 3 million people infected<sup>1-3</sup>. </p>
      <p>Approximately 60% of the infected individuals will remain in the indeterminate form (IF); 25% to 35% will develop heart disease, 10% of them severely. Chagas&#146; disease manifests itself as arrhythmias and/or conduction disturbances, heart failure, thromboembolic accidents and sudden death<sup>4,5</sup>.</p>
      <p>It is known that, in the natural history of Chagas&#146; disease, electrocardiographic changes precede symptoms&#146; onset, as well as physical examination and chest radiography abnormalities<sup>6</sup>. Since the clinical significance of ECG changes in asymptomatic individuals has not yet been well established, they may be found in patients who have recently entered the classic chronic phase and show either slight or more advanced electrocardiographic changes<sup>7</sup>.</p>
      <p>In addition to ECG and chest radiography, the use of ambulatory electrocardiogram allows a better understanding of ventricular arrhythmias, detected since the first reports on the cardiac form of Chagas&#146; disease. Although ventricular arrhythmias are associated with higher incidence of sudden death<sup>8</sup>, some characteristics, such as their presence in the different clinical forms of Chagas&#146; disease and their relationship with symptoms and ventricular dysfunction, are not yet well defined and differ from one study to another, depending on the sample population and methodology employed<sup>9</sup>.</p>
      <p>Echocardiograms are helpful in that they make it possible to diagnose and follow heart involvement, particularly ventricular dysfunction and, especially, systolic ventricular dysfunction, known to be the main prognostic factor of chagasic cardiomyopathy<sup>10,11</sup>. The prognostic value of the diastolic ventricular dysfunction that usually precedes systolic dysfunction is yet to be defined. Novel methods, such as tissue Doppler imaging to quantify myocardial flow velocity, have shown to be invaluable tools, because they are more sensitive in detecting pseudonormal patterns of diastolic dysfunction than pulsed Doppler mitral flow<sup>12,13</sup>.</p>
      <p>Measurement of brain natriuretic peptide (BNP), also referred to as B-type natriuretic peptide, is useful in the diagnosis of left ventricular systolic and diastolic dysfunctions<sup>14,15</sup>. The BNP is a hormonally active peptide secreted by the heart ventricles, and its plasma concentrations increase according to the severity of the heart failure (HF) based on the New York Heart Association classification<sup>16</sup>. Few studies have been conducted to evaluate this peptide plasma levels in Chagas&#146; disease patients<sup>17,18</sup>. </p>
      <p>We aimed at prospectively evaluating ventricular arrhythmia and left ventricular dysfunction prevalence, as well as BNP plasma levels, in asymptomatic patients with chronic Chagas&#146; disease and abnormal ECG, divided into two groups: GIIA (ECG with changes characteristic of Chagas&#146; disease) and GIIB (ECG with changes non-characteristic of Chagas&#146;s disease), compared with a group of chagasic patients with normal ECG (GI). </p>
      <p>
        <bold>METHODS</bold>
      </p>
      <p>In this prospective, cross-sectional study approved by the institution&#146;s Research Ethics Committee, 329 patients seen at the Chagas&#146; disease outpatient clinic from April to November 2002 and confirmed seropositive for Trypanosoma cruzi infection by at least two of three different techniques (indirect hemagglutination, indirect immunofluorescence, and ELISA) were evaluated. All patients underwent history taking and physical examination after the following exclusion criteria were applied: 1) younger than 18 or older than 50; 2) symptoms suggestive of heart failure<sup>19</sup> and/or arrhythmia;<sup>20</sup> 3) arterial hypertension &#150; defined as previous history, use of antihypertensive drugs or, at the time of inclusion, diastolic blood pressure (DBP) &gt; 89 and/or systolic blood pressure (SBP) &gt; 139;<sup>21</sup> 4) diabetes mellitus &#150; defined as fasting glucose <underline>&gt;</underline>126 mg/dL or regular use of hypoglycemic agents;<sup>22</sup> 5) history of chronic obstructive pulmonary disease; (6) endocrine dysfunctions; 7) heart disease of other etiologies; 8) pregnancy at the time of inclusion. One hundred and six patients were selected and, after being fully informed about the purpose of the study, they signed an informed consent. </p>
      <p>After electrocardiogram (ECG) analysis, patients were distributed into three different groups: 1) GI &#150; patients with normal ECG; 2) GIIA &#150; patients with characteristic ECG changes (atrioventricular blocks, complete right bundle branch block, and/or left anterior hemiblock in the His bundle; electrically inactive areas; sinus bradicardia accompanied by ventricular extrasystoles or primary changes in ventricular repolarization);<sup>23</sup> and 3) GIIB &#150; patients with ECG changes non-characteristic of Chagas&#146; disease. </p>
      <p>Next, the following examinations were performed: a) Chest radiography and cardiothoracic index measurement (CTI) according to the technique already described<sup>24</sup>; b) A 24-hour ambulatory electrocardiogram using a two-channel portable tape recorder Dynamis 4000 (Cardios Sistemas, S&#227;o Paulo, Brazil) and analysis using Premier 4 holter software (Diagnostic Monitoring Software, Nevada, USA). Evaluation included the presence and number of ventricular extrasystoles (VES) in 24 hours: sustained ventricular tachycardia (SVT), defined as three or more consecutive ventricular ectopies lasting 30 seconds or longer, and nonsustained ventricular tachycardia (NSVT), defined as three or more consecutive ventricular ectopies lasting less than 30 seconds<sup>25</sup>; c) Echocardiogram using a "Vivid 3" echocardiograph (GE Medical Systems, Milwaukee, EUA), following the American Society of Echocardiography criteria. </p>
      <p>The following parameters were analyzed: left ventricular ejection fraction (LVEF) assessed by Simpson&#146;s biplane method, with a normal value of 50% or more<sup>26</sup>; regional left ventricular contraction, using the 16-segment model recommended by the American Society of Echocardiography and classified as normal and abnormal (hypokinetic, akinetic or dyskinetic)<sup>27</sup>; E&#146; wave (peak velocity of the mitral annulus motion during early diastole) to A&#146; wave (peak velocity of the mitral annulus motion during end-diastole) ratio (E&#146;/A&#146;) using tissue Doppler imaging of mitral annulus motion on the septal wall in the apical four-chamber view, with normal value <underline>&gt;</underline> 1<sup>28</sup>. Ventricular dysfunction was considered in the presence of left ventricular systolic and/or diastolic dysfunction. Ventricular systolic dysfunction was defined in the presence of global and/or regional ventricular dysfunction. Global ventricular systolic dysfunction was defined in the presence of LVEF &lt; 50%. Diastolic ventricular dysfunction was defined in the presence of E'/A&#146;&lt;1. </p>
      <p> d) BNP: five-mL blood samples were collected and drawn into tubes containing ethylenediaminetetraacetic acid (EDTA) as anticoagulant. After centrifugation, plasma was separated and stored at -20&#176;C. The Triage&#174; BNP fluorescence immunoassay test was used for quantitative measurement (Biosite, San Diego, USA) after the plasma sample was equilibrated to room temperature and mixed thoroughly. </p>
      <p>Statistical analyses were performed using Epi Info 6 version 6.04 and SAS &#150; Statistical Analysis System version 6.11. Continuous variables were expressed as mean and standard deviation (SD), and categorical variables were expressed as absolute and relative frequencies. The chi-square test or Fisher&#146;s exact test was performed to test the groups&#146; homogeneity relative to proportions. One-factor analysis of variance was used for the hypothesis of equality among the three groups, with the multiple comparison procedure employing the Bonferroni method. When the assumption of data normality was rejected, the Kruskal-Wallis non-parametric test was applied, using Dunn&#146;s method of multiple comparisons. The significance level was set at 5%. </p>
      <p>
        <bold>RESULTS</bold>
      </p>
      <p>The most frequent ECG changes found in the GIIA group were right bundle branch block and left anterior hemiblock, with 35% each, followed by electrically inactive areas in 32%. In the GIIB group they were inferolateral repolarization changes and left ventricular overload, with 28% and 24%, respectively.</p>
      <p>Mean CTI values were similar among the groups. GI, 0.41 &#177; 0.05; GIIA, 0.43 &#177; 0.05; and GIIB, 0.43 &#177; 0.05 (p = 0.383). </p>
      <p>Among the 106 patients, 102 had ambulatory electrocardiograms that could be analyzed: 48 (96%) in the GI group, 30 in the GIIA group (97%), and 24 (96%) in the GIIB group. Ventricular arrhythmia prevalence was similar between groups with ECG changes (GIIA e GIIB) and significantly higher than in the group with normal ECG (GI) (<xref ref-type="fig" rid="fig01-body2">Fig. 1</xref>).</p>
      <fig id="fig01-body2">
        <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gf01-en.jpg"/></fig>
      <p>Mean ventricular extrasystole in the 24 hours (24H/VES) was significantly higher in the GIIA group (1138.00 &#177; 2779) than in the GI (51.68 &#177; 161) and GIIB groups (115.40 &#177; 297) (p &lt; 0.05). Six study participants experienced NSVT, one (2%) from the GI group and five (16.6%) from the GIIA group.</p>
      <p>Ventricular dysfunction was more prevalent in the GIIA and GIIB groups and significantly higher than in the GI group (<xref ref-type="fig" rid="fig02-body2">Figure 2</xref>). In the univariate analysis of relative risk (RR) a positive association between ventricular dysfunction and the GIIA and GIIB groups was found compared to the GI group. Patients in the GIIA group showed a positive RR of 3.69 (95% CI = 1.71-7.94; p &lt; 0.001), and patients in the GIIB group showed a positive RR of 2.72 (95% CI = 1.13-6.54; p = 0.024). </p>
      <fig id="fig02-body2">
        <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gf02-en.jpg"/></fig>
      <p>Ventricular systolic dysfunction (SD) was found in one patient (2%) of the GI group, 9 patients (29%) of the GIIA group, and 5 patients (20%) of the GIIB group (p &lt; 0.001) (<xref ref-type="fig" rid="fig03-body2">Fig. 3</xref>).</p>
      <fig id="fig03-body2">
        <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gf03-en.jpg"/></fig>
      <p>No patient in the GI group showed global systolic dysfunction, found in four patients (13%) of the GIIA group and two patients (8%) of the GIIB group (p = 0.020).</p>
      <p>Twelve patients (11.3%) showed regional systolic dysfunction: one patient (2%) of the GI group, seven patients (23%) of the GIIA group and four patients (16%) of the GIIB group (p = 0.005). In the GI group, regional systolic dysfunction was located in the apical region. <xref ref-type="fig" rid="fig04-body2">Figure 4</xref> shows the absolute frequency and site of regional systolic dysfunction in the GIIA and GIIB groups. The apical region was the most affected. </p>
      <fig id="fig04-body2">
        <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gf04-en.jpg"/></fig>
      <p>Diastolic dysfunction prevalence was similar in the GIIA and GIIB groups and significantly higher than in the GI group (p = 0.009) (<xref ref-type="fig" rid="fig05-body2">Fig. 5</xref>). </p>
      <fig id="fig05-body2">
        <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gf05-en.jpg"/></fig>
      <p>No statistically significant difference was found when mean BNP plasma level was compared among the groups (p = 0.121). </p>
      <p>Descriptive analysis of BNP values in the groups studied is shown in <xref ref-type="table" rid="tab02-body2">Table 2</xref>.</p>
      <p>
        <graphic xlink:href="1678-4170-abc-87-03-0336-00017-e01-en.jpg"/></p>
      <table-wrap id="tab02-body2">
        <graphic xlink:href="1678-4170-abc-87-03-0336-00017-gt01-en.jpg"/></table-wrap>
      <p>
        <bold>DISCUSSION</bold>
      </p>
      <p>Current challenges in the management of infected patients are early diagnosis and halting the progression of Chagas&#146;s disease clinical forms in the chronic phase, indicating the appropriate treatment and preventing complications<sup>29</sup>.</p>
      <p>This study, in which asymptomatic patients with no previous diagnosis of heart disease were assessed, sought to evaluate the relationship between ECG changes and prevalence of arrhythmias, ventricular dysfunction and BNP plasma concentrations. The starting point in this evaluation was electrocardiographic changes analysis, because, despite all technological advances, ECG remains the basic examination required in the baseline evaluation of Chagas&#146; disease patients, and may be the only complementary propaedeutic in most healthcare services, especially in poverty-stricken regions where there is usually a greater predominance of infected patients.</p>
      <p>The usefulness of ECG in identifying systolic ventricular dysfunction leading to heart failure was evaluated by Davie et al<sup>30</sup>, who observed a 35% positive predictive value and a 98% negative predictive value for the diagnosis of systolic ventricular dysfunction in patients with abnormal ECG. Studying ECG abnormalities and their relationship with ventricular systolic function (ventricular volumes and EF by angiography) in Chagas&#146; disease, Casado et al<sup>31</sup> found a relationship between decreased left ventricular systolic function and the progression and association of ECG abnormalities. </p>
      <p>In this study, prevalence of ventricular arrhythmias and ventricular dysfunction was found to be similar in the abnormal-ECG groups and significantly higher than in the normal-ECG group. Carrasco et al<sup>32</sup> analyzed four groups of patients - with normal ECG, with normal ECG and regional segmental dysfunction, with abnormal ECG and global ventricular dysfunction, and with abnormal ECG and heart failure - and found prevalence of ventricular arrhythmia in 30%, 53%, 86%, and 99% of these patients, respectively. Rassi Junior et al<sup>9</sup> found prevalence of 85% in the normal population, 74% in the indeterminate form (IF) and 88% in the cardiac forms, but did not specify whether they were symptomatic or asymptomatic. </p>
      <p> When VES was analyzed in the three groups, mean VES in 24 hours was significantly higher in the GIIA group than in the GIIB and GI groups. Similar VES incidence, number and complexity were found in literature among individuals in the indeterminate form and individuals with no heart disease. As arrhythmia occurrence increases proportionally to the degree of involvement on resting ECG, the VESs are less frequent in patients with chronic Chagas&#146; disease and minimal ECG changes and more frequent and complex when the patient shows characteristic changes, especially when associated with left ventricular dysfunction<sup>33</sup>.</p>
      <p> NSVT prevalence was 16.6% in the GIIA group and 2% in the GI group, lower than those observed by Rassi Junior et al<sup>9</sup>, who found 42% in the chagasic group with characteristic ECG, 16% in patients with non-characteristic ECG, and 1% among the IF patients. </p>
      <p>In our study, univariate analysis showed that the relative risk (RR) of experiencing ventricular dysfunction is 3.69-fold in patients with electrocardiographic changes characteristic of Chagas&#146;s disease (GIIA) and 2.72-fold in patients with electrocardiographic changes non-characteristic of Chagas&#146;s disease (GIIB) than in patients with normal ECG (GI). Six patients showed global ventricular systolic dysfunction, characterized by LVEF &gt; 50%, four in the GIIA group and two in the GIIB group. The LVEF was lower than 40% in two patients (6.5%) of the GIIA group.</p>
      <p>Ventricular systolic dysfunction, present in 2% to 4% of the general population, is the anatomical substrate for around two-thirds of patients with heart failure (HF)<sup>34</sup>.</p>
      <p>Mady et al<sup>11</sup> evaluated patients with HF in NYHA functional class II or III secondary to Chagas&#146; disease and found that LVEF is an important index for survival analysis in these groups. According to literature, systolic dysfunction in Chagas&#146; disease, measured by echo, varies depending on the clinical form of the disease and the methodology followed in the many studies. In regard to the indeterminate form, reports range from normal ventricular systolic function<sup>35</sup> to significant increases in LV dimension and volume and decrease in EF compared to a control group<sup>36</sup>. Ianni et al<sup>37 </sup>compared the IF in patients with minimal ECG changes and found no significant difference between groups regarding LV fractional shortening. However, Pereira-Barretto et al.<sup>38</sup> found a 4.5% incidence of depressed ventricular function in patients with normal ECG and 45.7% and 66% of ventricular dysfunction in patients with abnormal ECG, depending on the electrocardiographic change. Perez et al<sup>39</sup> reported a 29% incidence of global ventricular dysfunction in a non-selected group of chagasic patients.</p>
      <p>Regional systolic dysfunction was more frequent in the GIIA group than in the GIIB and GI groups (23%, 16% and 2%, respectively). The apical region was the most affected in all patients. Segmental changes in contractility are found in up to 74% of chagasic patients and are typical of Chagas&#146; disease, especially when located in the apical region, in the absence of ischemic heart disease<sup>40</sup>. Apar&#237;cio et al<sup>41</sup> found 12% of interventricular septum hypokinesia in asymptomatic patients with normal ECG measured by M-mode ECHO. In the IF, Ortiz et al<sup>42</sup> found a 26% segmental change incidence, restricted to the posterior apical region. C&#226;mara<sup>43</sup> evaluated patients with abnormal ECG and found a 68% segmental change frequency, 64% of them in the apical region, and also the presence of apical aneurysm in 42% of the patients.</p>
      <p>Diastolic dysfunction was more common than systolic dysfunction, and was significantly more frequent in the GIIA group (41,9%) than in the other groups. </p>
      <p>Tissue Doppler was used, because in addition to being more sensitive in detecting diastolic dysfunction than the classic method of transmittal flow analysis by pulsed Doppler, it differentiates the pseudonormal pattern<sup>12,28</sup>. It is known that transmitral flow is affected by a host of factors, among them left atrial pressure. Increases in the left atrial pressure above blood pressure increase as the result of ventricular relaxation often lead to a pseudonormalization of the transmittal flow. </p>
      <p>Diastolic dysfunction in the non-selected general population is more prevalent than systolic dysfunction, about 11%<sup>44</sup>. In chagasic patients, however, it ranges from 27.6% to 83%, according to the evaluation method employed and the clinical form of the disease<sup>45</sup>. Early studies on diastolic dysfunction in Chagas&#146; disease through non-invasive methods used M-mode ECHO associated with phonocardiogram and apexcardiogram followed by two-dimensional echocardiogram coupled with Doppler flow studies and, finally, tissue Doppler. Regardless of the method used, evidence exists that diastolic dysfunction is common and may be present in asymptomatic patients, preceding systolic dysfunction; and its prevalence increases according to the progression of chronic Chagas cardiomyopathy<sup>12,43,45,46</sup>.</p>
      <p>Natriuretic peptides are neurohormones produced by the heart cells with natriuretic, diuretic and vasodilatory properties<sup>16</sup>.</p>
      <p>Studies suggest that serum or plasma BNP measurements may be useful to confirm HF diagnosis, assess the degree of left ventricle involvement, quantify the functional class, estimate the prognosis and anticipate cardiac events, and evaluate the therapeutic efficacy in HF<sup>15,47-49</sup>.</p>
      <p>In this study, patients were asymptomatic at the time of inclusion and were divided according to the ECG changes found. The highest mean BNP plasma level was found in the GIIA group, compared with the GI and GIIB groups, although the difference did not achieve statistical significance.</p>
      <p>In published studies evaluating Chagas&#146; disease patients, studied population was classified according to the degree of LV systolic function involvement and compared with a control group, regardless of the presence of ECG changes<sup>17,18</sup>.</p>
      <p>Ribeiro et al<sup>17</sup> found similar mean BNP values between the control group and patients with LVEF &gt; 40%, and significantly lower than those of patients with LVEF &lt; 40%. Setting the cut-off point at 60.7 pmol/L, a sensitivity of 80% and specificity of 93% were found for LVEF &lt; 40% in patients with abnormal ECG ou CTI. Walther et al<sup>18</sup>, in a similar study, found significant lower values in the control group than in the group of chagasic patients even with LVEF &gt; 40%. Using a cut-off point of 18.1 pmol/L, the sensibility was 86% and the specificity was 91% for the diagnosis of patients with LVEF &lt; 40%.</p>
      <p> In the present study, results might have been affected by the sample size and criteria that allowed the inclusion only of asymptomatic patients with low frequency of more marked ventricular systolic dysfunction. The two patients with LVEF &lt; 40% showed the highest BNP plasma levels: 589 pg/mL and 946 pg/mL.</p>
      <p>Another peculiarity was that, in four patients (all female), BNP levels were higher than 100 pg/mL, and these women showed no ventricular dysfunction; and in four patients with slight ventricular dysfunction, BNP levels were lower than 100 pg/mL. Of these, three were male and one was female. Previous studies showed that BNP levels are affected by gender both in normal population and HF population. The female gender is associated with higher BNP levels than the male gender<sup>50</sup>.</p>
      <p>All patients with global systolic dysfunction received standard drug treatment with captopril at the maximum tolerated dose, and for two patients carvedilol was also associated. Three patients who experienced ventricular dysfunction and NSVT were treated also with amiodarone.</p>
      <p>Our results demonstrate that in patients with Chagas&#146; disease and electrocardiographic changes, even those who are asymptomatic, other diagnostic methods such as echocardiogram and 24-hour ambulatory electrocardiogram, in addition to standard electrocardiogram and chest radiography, play key roles in the initial evaluation. Study limitations include the small number of patients due to the strict inclusion and exclusion criteria, absence of a control group of non-infected individuals, and lack of follow-up. </p>
      <p>As Chagas&#146; disease is a slow-progressing disease and patients enrolled in this study will remain under follow-up, it is believed that, after an adequate period, some pending issues may be clarified. Among them, the long-term evolutive aspects of Chagas&#146; disease patients and non-characteristic changes in ECG, and the prognostic value of diastolic ventricular dysfunction and BNP levels in the groups studied.</p>
      <p>
        <bold>Potencial Conflict of Interest</bold>
      </p>
      <p>No potential conflict of interest relevant to this article was reported.</p>
      <p>
        <bold>REFERENCES</bold>
      </p>
      <p>
        <fn id="end-body2" fn-type="corresp">
          <p>Mailing address:</p>
          <p> Divina Seila de Oliveira Marques</p>
          <p> Rua Robert Koch, 60</p>
          <p> 86038-440 &#150; Londrina, PR - Brazil</p>
          <p> E-mail: </p>
          <p>
            <email xlink:href="d.seila@cardiol.br">d.seila@cardiol.br</email>
          </p>
        </fn>
      </p>
      <p>Received on 07/20/04</p>
      <p> Accepted on 09/12/05</p>
    </body>
  </sub-article>
</article>
