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  <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">KDY8LzLfmYMfX5LrvvXwmqy</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2012001100005</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(12)09900205</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2012005000065</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigos Originais</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Par&#226;metros ecocardiogr&#225;ficos como preditores de eventos cardiovasculares em pacientes em hemodi&#225;lise</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Siqueira</surname>
            <given-names>Thayse Mayara Arag&#227;o</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ferreira</surname>
            <given-names>Pedro Ant&#244;nio Muniz</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Monteiro J&#250;nior</surname>
            <given-names>Francisco das Chagas</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Salgado Filho</surname>
            <given-names>Natalino</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ferreira</surname>
            <given-names>Adalgisa de Souza Paiva</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Santos Neto</surname>
            <given-names>Eug&#234;nio dos</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Souza</surname>
            <given-names>Francival Leite de</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Cardoso</surname>
            <given-names>Paulo de Tarso</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="city">S&#227;o Lu&#237;s</named-content>
          <named-content content-type="state">Maranh&#227;o</named-content>
        </addr-line>
        <institution content-type="orgname">Universidade Federal do Maranh&#227;o</institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff02">
        <addr-line>
          <named-content content-type="city">S&#227;o Lu&#237;s</named-content>
          <named-content content-type="state"/>
        </addr-line>
        <institution content-type="orgname">Centro de Nefrologia do Maranh&#227;o</institution>
        <country country="BR">Brazil</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>08</month>
        <year>2012</year>
      </pub-date>
      <volume>99</volume>
      <issue>2</issue>
      <fpage>714</fpage>
      <lpage>723</lpage>
      <history>
        <date date-type="received">
          <day>12</day>
          <month>10</month>
          <year>2011</year>
        </date>
        <date date-type="accepted">
          <day>17</day>
          <month>03</month>
          <year>2012</year>
        </date>
        <date date-type="rev-recd">
          <day>12</day>
          <month>10</month>
          <year>2011</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>FUNDAMENTO: Pacientes com doen&#231;a renal cr&#244;nica (DRC) em hemodi&#225;lise possuem altas taxas de morbidade e mortalidade cardiovascular. Apesar de altera&#231;&#245;es ecocardiogr&#225;ficas estruturais e funcionais em pacientes submetidos &#224; hemodi&#225;lise terem sido objeto de diversos estudos de an&#225;lise de sobrevida, o valor progn&#243;stico destas altera&#231;&#245;es ainda n&#227;o est&#225; bem estabelecido na literatura. OBJETIVO: Determinar o valor progn&#243;stico de par&#226;metros ecocardiogr&#225;ficos em pacientes com DRC em hemodi&#225;lise. M&#201;TODOS: Sessenta pacientes consecutivos com DRC em tratamento hemodial&#237;tico foram avaliados clinicamente e submetidos ao ecodopplercardiograma, sendo acompanhados durante 19 &#177; 6 meses. Os desfechos avaliados foram eventos cardiovasculares fatais e n&#227;o fatais e mortalidade geral. O valor preditivo das vari&#225;veis ecocardiogr&#225;ficas foi avaliado pelo modelo de regress&#227;o de Cox, as curvas de sobrevida foram constru&#237;das pelo m&#233;todo de Kaplan-Meier e o teste log rank foi utilizado para compar&#225;-las. RESULTADOS: As taxas de sobrevida livre de eventos cardiovasculares, de mortalidade cardiovascular e de mortalidade global em dois anos foram de 79,4%, 88,5% e 83%, respectivamente. Diabetes, diagn&#243;stico pr&#233;vio de doen&#231;a cardiovascular (DCV), fra&#231;&#227;o de eje&#231;&#227;o, fra&#231;&#227;o de encurtamento, di&#226;metro sist&#243;lico do ventr&#237;culo esquerdo e rela&#231;&#227;o E/e' foram preditores de desfecho cardiovascular na an&#225;lise univariada. Na an&#225;lise multivariada, hist&#243;ria pr&#233;via de DCV (HR = 6,17; IC 95% 1,7 - 22,2; p = 0,005) e disfun&#231;&#227;o diast&#243;lica moderada a grave (HR = 3,76; IC 95% 1,05 - 13,4; p = 0,042) foram fatores de risco independentes para eventos cardiovasculares. CONCLUS&#195;O: Disfun&#231;&#227;o diast&#243;lica de moderada a grave &#233; um preditor independente de eventos cardiovasculares em pacientes em hemodi&#225;lise.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>Ecocardiografia doppler</kwd>
        <kwd>insufici&#234;ncia renal cr&#244;nica</kwd>
        <kwd>an&#225;lise de sobrevida</kwd>
        <kwd>di&#225;lise</kwd>
        <kwd>progn&#243;stico</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>05</day>
        <month>07</month>
        <year>2012</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>
      <bold>Par&#226;metros ecocardiogr&#225;ficos como preditores de eventos cardiovasculares em pacientes em hemodi&#225;lise</bold>
    </p>
    <p>
      <bold>Thayse Mayara Arag&#227;o Siqueira<sup>I</sup>; Pedro Ant&#244;nio Muniz Ferreira<sup>I, II</sup>; Francisco das Chagas Monteiro J&#250;nior<sup>I</sup>; Natalino Salgado Filho<sup>I, II</sup>; Adalgisa de Souza Paiva Ferreira<sup>I</sup>; Eug&#234;nio dos Santos Neto<sup>I</sup>; Francival Leite de Souza<sup>I</sup>; Paulo de Tarso Cardoso<sup>I</sup></bold>
    </p>
    <p><sup>I</sup>Universidade Federal do Maranh&#227;o, S&#227;o Lu&#237;s, MA - Brasil </p>
    <p><sup>II</sup>Centro de Nefrologia do Maranh&#227;o, S&#227;o Lu&#237;s, MA - Brasil</p>
    <p>
      <xref ref-type="corresp" rid="back">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p><bold>FUNDAMENTO:</bold> Pacientes com doen&#231;a renal cr&#244;nica (DRC) em hemodi&#225;lise possuem altas taxas de morbidade e mortalidade cardiovascular. Apesar de altera&#231;&#245;es ecocardiogr&#225;ficas estruturais e funcionais em pacientes submetidos &#224; hemodi&#225;lise terem sido objeto de diversos estudos de an&#225;lise de sobrevida, o valor progn&#243;stico destas altera&#231;&#245;es ainda n&#227;o est&#225; bem estabelecido na literatura. </p>
    <p><bold>OBJETIVO:</bold> Determinar o valor progn&#243;stico de par&#226;metros ecocardiogr&#225;ficos em pacientes com DRC em hemodi&#225;lise. </p>
    <p><bold>M&#201;TODOS:</bold> Sessenta pacientes consecutivos com DRC em tratamento hemodial&#237;tico foram avaliados clinicamente e submetidos ao ecodopplercardiograma, sendo acompanhados durante 19 &#177; 6 meses. Os desfechos avaliados foram eventos cardiovasculares fatais e n&#227;o fatais e mortalidade geral. O valor preditivo das vari&#225;veis ecocardiogr&#225;ficas foi avaliado pelo modelo de regress&#227;o de Cox, as curvas de sobrevida foram constru&#237;das pelo m&#233;todo de Kaplan-Meier e o teste <italic>log rank</italic> foi utilizado para compar&#225;-las. </p>
    <p><bold>RESULTADOS:</bold> As taxas de sobrevida livre de eventos cardiovasculares, de mortalidade cardiovascular e de mortalidade global em dois anos foram de 79,4%, 88,5% e 83%, respectivamente. Diabetes, diagn&#243;stico pr&#233;vio de doen&#231;a cardiovascular (DCV), fra&#231;&#227;o de eje&#231;&#227;o, fra&#231;&#227;o de encurtamento, di&#226;metro sist&#243;lico do ventr&#237;culo esquerdo e rela&#231;&#227;o E/e' foram preditores de desfecho cardiovascular na an&#225;lise univariada. Na an&#225;lise multivariada, hist&#243;ria pr&#233;via de DCV (HR = 6,17; IC 95% 1,7 - 22,2; p = 0,005) e disfun&#231;&#227;o diast&#243;lica moderada a grave (HR = 3,76; IC 95% 1,05 - 13,4; p = 0,042) foram fatores de risco independentes para eventos cardiovasculares. </p>
    <p><bold>CONCLUS&#195;O:</bold> Disfun&#231;&#227;o diast&#243;lica de moderada a grave &#233; um preditor independente de eventos cardiovasculares em pacientes em hemodi&#225;lise.</p>
    <p><bold>Palavras-chave:</bold> Ecocardiografia doppler; insufici&#234;ncia renal cr&#244;nica; an&#225;lise de sobrevida; di&#225;lise; progn&#243;stico.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>As taxas de mortalidade anual em pacientes com doen&#231;a renal cr&#244;nica (DRC) em tratamento dial&#237;tico s&#227;o elevadas. De acordo com o censo de di&#225;lise dos Estados Unidos<sup>1</sup>, a sobrevida de pacientes em hemodi&#225;lise no pa&#237;s foi de 77,4% em um ano e de 34,2% em cinco anos, no per&#237;odo de 1999 a 2003. No Brasil, em 2009, a taxa anual de mortalidade bruta foi de 17,1%<sup>2</sup>.</p>
    <p>As doen&#231;as cardiovasculares (DCV) correspondem a cerca de metade dos &#243;bitos ocorridos em pacientes submetidos &#224; hemodi&#225;lise. Al&#233;m disso, esses pacientes s&#227;o frequentemente submetidos a interna&#231;&#245;es hospitalares e as DCVs s&#227;o respons&#225;veis por aproximadamente um ter&#231;o dessas interna&#231;&#245;es<sup>3</sup>.</p>
    <p>Altera&#231;&#245;es estruturais e funcionais detectadas atrav&#233;s da ecocardiografia, como hipertrofia e disfun&#231;&#227;o sist&#243;lica e diast&#243;lica do ventr&#237;culo esquerdo (VE), s&#227;o bastante prevalentes na popula&#231;&#227;o em hemodi&#225;lise. O diagn&#243;stico ecodopplercardiogr&#225;fico dessas anormalidades tem sido um importante passo para a caracteriza&#231;&#227;o de indiv&#237;duos com maior risco cardiovascular<sup>4,5</sup>.</p>
    <p>Diversos estudos t&#234;m buscado determinar o valor progn&#243;stico de altera&#231;&#245;es, como hipertrofia e disfun&#231;&#227;o sist&#243;lica em pacientes submetidos &#224; hemodi&#225;lise<sup>6-8</sup>. Por&#233;m, estudos avaliando o valor preditivo da disfun&#231;&#227;o diast&#243;lica nessa popula&#231;&#227;o s&#227;o escassos. Desse modo, o objetivo deste estudo foi determinar o valor progn&#243;stico de par&#226;metros ecocardiogr&#225;ficos em pacientes com DRC em tratamento hemodial&#237;tico.</p>
    <p>
      <bold>M&#233;todos</bold>
    </p>
    <p>
      <bold>Desenho do estudo e popula&#231;&#227;o</bold>
    </p>
    <p>Trata-se de um estudo observacional, anal&#237;tico, de coorte e prospectivo, conduzido no Servi&#231;o de Di&#225;lise do Centro de Nefrologia do Maranh&#227;o (CENEFRON). Foram avaliados consecutivamente 60 pacientes portadores de DRC submetidos &#224; hemodi&#225;lise nesse servi&#231;o. As sess&#245;es de hemodi&#225;lise de todos os pacientes eram realizadas tr&#234;s vezes por semana, com dura&#231;&#227;o de quatro horas, em m&#225;quinas volum&#233;tricas (Baxter Tina<italic><sup>&#174;</sup></italic>, EUA; Fresenius 4008S<italic><sup>&#174;</sup></italic> ou Fresenius 4008B<italic><sup>&#174;</sup></italic>, Alemanha). Os filtros de di&#225;lise utilizados eram do tipo polissulfona, de baixo fluxo (Hemoflow, Fresenius<italic><sup>&#174;</sup></italic>, Alemanha), escolhidos de acordo com o c&#225;lculo da superf&#237;cie corporal do paciente.</p>
    <p>Os crit&#233;rios de inclus&#227;o foram idade igual ou superior a 18 anos e tratamento hemodial&#237;tico h&#225; pelo menos tr&#234;s meses. Foram considerados crit&#233;rios de exclus&#227;o: hist&#243;ria recente (inferior a seis meses) de infarto agudo do mioc&#225;rdio (IAM), revasculariza&#231;&#227;o mioc&#225;rdica cir&#250;rgica ou percut&#226;nea, angina inst&#225;vel ou acidente vascular encef&#225;lico (AVE); insufici&#234;ncia card&#237;aca congestiva (ICC) descompensada; doen&#231;a valvular importante; hipertens&#227;o pulmonar; press&#227;o arterial &gt; 160/110 mmHg; fibrila&#231;&#227;o atrial n&#227;o controlada ou arritmia card&#237;aca ventricular complexa (taquicardia ventricular n&#227;o sustentada; extrass&#237;stoles polim&#243;rficas, frequentes, em salvas e aos pares); n&#237;veis glic&#234;micos n&#227;o controlados; neoplasias malignas; infec&#231;&#227;o ativa; regime irregular de di&#225;lise; impossibilidade de se obter o consentimento informado do paciente e janela ecocardiogr&#225;fica inadequada.</p>
    <p>Os pacientes foram avaliados clinicamente e submetidos &#224; realiza&#231;&#227;o de um ecodopplercardiograma durante o per&#237;odo de fevereiro a setembro de 2009, com um intervalo inferior a 30 dias entre os dois procedimentos. Em seguida, foram acompanhados regularmente at&#233; maio de 2011 ou at&#233; a ocorr&#234;ncia de desfecho.</p>
    <p>O projeto foi aprovado pela Comiss&#227;o de Pesquisa do CENEFRON e pelo Comit&#234; de &#201;tica em Pesquisa da Universidade Federal do Maranh&#227;o. Foi obtida a assinatura do Termo de Consentimento Livre e Esclarecido (TCLE) de todos os pacientes inclu&#237;dos no estudo.</p>
    <p>
      <bold>Ecodopplercardiograma</bold>
    </p>
    <p>Os ecocardiogramas transtor&#225;cicos foram realizados em aparelhos ecocardi&#243;grafos do modelo <italic>Vivid 3 Cardiovascular Ultrasound System</italic> (<italic>GE Healthcare, General Electric Company,</italic> EUA), com transdutores de 3 a 7 mHz e com recursos para obten&#231;&#227;o das modalidades de ecocardiograma modo M, bidimensional e Doppler (puls&#225;til, cont&#237;nuo, colorido e tecidual). Os exames foram realizados no per&#237;odo interdial&#237;tico, em at&#233; 24 horas ap&#243;s a sess&#227;o de hemodi&#225;lise, por um &#250;nico profissional m&#233;dico, treinado e capacitado em ecocardiografia, com os pacientes em repouso e na posi&#231;&#227;o de dec&#250;bito lateral esquerdo. As medidas ecocardiogr&#225;ficas seguiram as recomenda&#231;&#245;es da Sociedade Americana de Ecocardiografia<sup>9-12</sup> e, para cada vari&#225;vel, pelo menos tr&#234;s ciclos foram analisados.</p>
    <p>A avalia&#231;&#227;o da geometria do VE foi obtida pela imagem bidimensional, sendo obtidas as seguintes vari&#225;veis: espessura diast&#243;lica final do septo (EDS), espessura diast&#243;lica final da parede posterior (EDP), di&#226;metro diast&#243;lico final do ventr&#237;culo esquerdo (DDVE) e di&#226;metro sist&#243;lico final do ventr&#237;culo esquerdo (DSVE).</p>
    <p>A massa do ventr&#237;culo esquerdo (MVE) foi calculada atrav&#233;s da f&#243;rmula proposta por Devereux e cols.<sup>13</sup> e, ent&#227;o, indexada &#224; &#225;rea da superf&#237;cie corporal (ASC), para obten&#231;&#227;o do &#237;ndice de massa do ventr&#237;culo esquerdo (IMVE = MVE/ASC). A espessura relativa da parede (ERP) foi obtida pela f&#243;rmula EDP + EDS/DDVE. A fra&#231;&#227;o de eje&#231;&#227;o do ventr&#237;culo esquerdo (FE) foi calculada pelo m&#233;todo descrito por Teichholz e cols.<sup>14</sup> e a fra&#231;&#227;o de encurtamento sist&#243;lico do ventr&#237;culo esquerdo, pela f&#243;rmula (DDVE - DSVE) / DDVE. O volume do &#225;trio esquerdo (VAE) foi determinado a partir da planimetria bidimensional, utilizando a t&#233;cnica de Simpson biplanar<sup>15</sup> e, ent&#227;o, indexado &#224; ASC para obten&#231;&#227;o do &#237;ndice de volume do &#225;trio esquerdo (IVAE = VAE/ASC).</p>
    <p>O fluxo mitral foi avaliado em proje&#231;&#227;o apical de quatro c&#226;maras pelo Doppler puls&#225;til. A amostra foi posicionada entre as extremidades distais dos folhetos da v&#225;lvula mitral e, ent&#227;o, foram obtidas as seguintes vari&#225;veis: velocidades diast&#243;licas precoce (E) e tardia (A) transmitral, rela&#231;&#227;o E/A e intervalo de tempo de desacelera&#231;&#227;o da onda E (TDE). O Doppler tecidual foi realizado no corte apical de quatro c&#226;maras para obten&#231;&#227;o das velocidades do anel mitral. A amostra foi colocada na jun&#231;&#227;o da parede lateral do VE com o anel mitral<sup>16</sup>, sendo, ent&#227;o, determinadas as velocidades diast&#243;licas precoce (e') e tardia (a') do anel mitral, al&#233;m das rela&#231;&#245;es e'/a' e E/e'.</p>
    <p>Hipertrofia de ventr&#237;culo esquerdo (HVE) foi diagnosticada quando o IMVE foi &gt; 115 g/m<sup>2</sup> para homens e &gt; 95 g/m<sup>2</sup> para mulheres. A geometria do VE foi classificada de acordo com os valores da ERP e do IMVE como: hipertrofia conc&#234;ntrica (presen&#231;a de HVE e ERP &gt; 0,42), hipertrofia exc&#234;ntrica (presen&#231;a de HVE e ERP <underline>&lt;</underline> 0,42), remodelamento conc&#234;ntrico (aus&#234;ncia de HVE e ERP &gt; 0,42) e geometria normal (aus&#234;ncia de HVE e ERP <underline>&lt;</underline> 0,42). Definiu-se aumento do &#225;trio esquerdo (AE) na presen&#231;a de IVAE &gt; 28 mL/m<sup>2</sup>, enquanto dilata&#231;&#227;o do VE foi definida quando o DDVE foi &gt; 5,9 cm para homens e &gt; 5,3 cm para mulheres<sup>15</sup>.</p>
    <p>Disfun&#231;&#227;o sist&#243;lica foi admitida quando a FE foi menor que 55%<sup>15</sup>. A fun&#231;&#227;o diast&#243;lica do VE foi classificada em quatro padr&#245;es: normal, altera&#231;&#227;o do relaxamento (disfun&#231;&#227;o diast&#243;lica leve), pseudonormal (disfun&#231;&#227;o diast&#243;lica moderada) e restritivo (disfun&#231;&#227;o diast&#243;lica grave). Considerou-se altera&#231;&#227;o do relaxamento quando E/A &lt; 1; padr&#227;o restritivo quando E/A &gt; 2 e padr&#227;o pseudonormal quando E/A foi maior que 1 e menor que 2 em associa&#231;&#227;o a E/e' &gt; 10<sup>17</sup>.</p>
    <p>
      <bold>Dados demogr&#225;ficos, cl&#237;nicos e laboratoriais</bold>
    </p>
    <p>Dados demogr&#225;ficos e cl&#237;nicos, incluindo idade, sexo, hist&#243;ria de tabagismo, comorbidades e tempo de di&#225;lise, foram obtidos a partir de rigorosa an&#225;lise de prontu&#225;rio, al&#233;m de entrevista com o paciente e com o m&#233;dico respons&#225;vel, quando necess&#225;rio. Evento cardiovascular pr&#233;vio foi definido como hist&#243;ria pregressa de angina t&#237;pica ou IAM, AVE isqu&#234;mico ou hemorr&#225;gico e ICC com classe funcional &gt; II.</p>
    <p>Antes da realiza&#231;&#227;o de cada ecodopplercardiograma, efetuaram-se a aferi&#231;&#227;o da press&#227;o arterial e a obten&#231;&#227;o de medidas e raz&#245;es antropom&#233;tricas (peso, altura, ASC, &#237;ndice de massa corp&#243;rea), mensuradas conforme t&#233;cnicas padronizadas e utilizando-se materiais adequados. O &#237;ndice de massa corp&#243;rea (IMC) foi calculado pela divis&#227;o do peso (kg) pelo quadrado da altura (m), considerando-se desnutri&#231;&#227;o quando &lt; 18,5 kg/m<sup>2</sup>. A ASC foi obtida pela f&#243;rmula de Dubois e Dubois<sup>18</sup>.</p>
    <p>Todas as dosagens bioqu&#237;micas foram realizadas em um &#250;nico laborat&#243;rio, localizado no CENEFRON, e esses dados foram coletados a partir da an&#225;lise dos prontu&#225;rios dos pacientes.</p>
    <p>
      <bold>Desfechos</bold>
    </p>
    <p>O desfecho prim&#225;rio, ou desfecho cardiovascular, abrangeu ocorr&#234;ncia de eventos cardiovasculares fatais e n&#227;o fatais. Os eventos cardiovasculares foram definidos por angina com estenose coronariana &gt; 50% &#224; cineangiocoronariografia, IAM n&#227;o fatal, procedimento de revasculariza&#231;&#227;o mioc&#225;rdica, AVE isqu&#234;mico ou hemorr&#225;gico n&#227;o fatal, ICC requerendo interna&#231;&#227;o hospitalar e morte de causa cardiovascular (incluindo morte s&#250;bita, IAM e AVE). O desfecho secund&#225;rio incluiu mortalidade geral.</p>
    <p>Os desfechos foram obtidos a partir de revis&#227;o mensal de documenta&#231;&#227;o m&#233;dica, incluindo registros em prontu&#225;rios e atestados de &#243;bito, al&#233;m de contato com o m&#233;dico e com familiares do paciente. Pacientes que realizaram transplante renal ou que mudaram de modalidade de di&#225;lise foram censurados no estudo.</p>
    <p>
      <bold>An&#225;lise estat&#237;stica</bold>
    </p>
    <p>As an&#225;lises estat&#237;sticas foram realizadas no programa <italic>Statistical Package for Social Sciences - SPSS 17.0<sup>&#174;</sup></italic> (SPSS Inc, EUA). As vari&#225;veis quantitativas foram expressas na forma de m&#233;dia com desvio padr&#227;o ou mediana e as vari&#225;veis categ&#243;ricas, na forma de porcentagem. Para a compara&#231;&#227;o de propor&#231;&#245;es entre os grupos com e sem desfecho, foi utilizado o teste do qui-quadrado e para a compara&#231;&#227;o de vari&#225;veis quantitativas, o teste <italic>t</italic> de Student para amostras independentes. Para estimar as raz&#245;es de risco (<italic>hazard ratios</italic>), realizou-se a an&#225;lise univariada pelo modelo de risco proporcional de Cox e, em seguida, as vari&#225;veis com p &lt; 0,10 foram inclu&#237;das na an&#225;lise multivariada pelo mesmo modelo. As curvas de sobrevida foram constru&#237;das pelo m&#233;todo de Kaplan-Meier e o teste <italic>log rank</italic> foi utilizado para comparar curvas de sobrevida em an&#225;lise univariada. O n&#237;vel de signific&#226;ncia foi definido como p &lt; 0,05.</p>
    <p>
      <bold>Resultados</bold>
    </p>
    <p>A popula&#231;&#227;o estudada foi composta por 31 (51,7%) homens e 29 (49,3%) mulheres, com m&#233;dia de idade de 49,2 &#177; 13,7 anos, variando de 22 a 76 anos. As caracter&#237;sticas demogr&#225;ficas, cl&#237;nicas, bioqu&#237;micas e ecodopplercardiogr&#225;ficas da popula&#231;&#227;o est&#227;o listadas na <xref ref-type="table" rid="t1">Tabela 1</xref>.</p>
    <table-wrap id="t1">
      <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gt01.jpg"/></table-wrap>
    <p>A causa da DRC foi atribu&#237;da &#224; nefroesclerose hipertensiva em 30% dos casos, &#224; glomerulonefrite cr&#244;nica em 30%, &#224; nefropatia diab&#233;tica em 16,7%, &#224; doen&#231;a renal polic&#237;stica em 5%, &#224; pielonefrite cr&#244;nica em 1,7% e a outras afec&#231;&#245;es em 16,7% dos casos.</p>
    <p>Dentre os indiv&#237;duos inclu&#237;dos no estudo, 25% apresentavam diagn&#243;stico pr&#233;vio de DCV: tr&#234;s pacientes com diagn&#243;stico de ICC, seis com hist&#243;ria de angina t&#237;pica ou IAM e seis com hist&#243;ria de AVE.</p>
    <p>As principais altera&#231;&#245;es ecodopplercardiogr&#225;ficas diagnosticadas foram: aumento do AE (49,2%), dilata&#231;&#227;o do VE (20%), HVE (85%), disfun&#231;&#227;o sist&#243;lica (26,7%) e disfun&#231;&#227;o diast&#243;lica (83,6%).</p>
    <p>De acordo com o grau de disfun&#231;&#227;o diast&#243;lica, 16,4% dos pacientes apresentaram fluxo restritivo; 20%, padr&#227;o pseudonormal e 47,3%, altera&#231;&#227;o do relaxamento. Em rela&#231;&#227;o &#224; geometria do VE, 68,3% dos pacientes apresentaram hipertrofia conc&#234;ntrica; 16,7%, hipertrofia exc&#234;ntrica; 8,3%, remodelamento conc&#234;ntrico e 6,7%, geometria normal.</p>
    <p>O seguimento m&#233;dio foi de 19,6 &#177; 6 meses e, durante este per&#237;odo, ocorreram nove &#243;bitos e cinco eventos cardiovasculares n&#227;o fatais. As DCV foram respons&#225;veis por 66,7% dos &#243;bitos ocorridos (tr&#234;s por IAM e tr&#234;s por AVE), enquanto os outros tr&#234;s &#243;bitos foram atribu&#237;dos a outras causas (um por choque hipovol&#234;mico e dois por choque s&#233;ptico). Os eventos cardiovasculares n&#227;o fatais ocorridos foram: um epis&#243;dio de AVE, duas interna&#231;&#245;es hospitalares por ICC descompensada e dois epis&#243;dios de angina com estenose coronariana superior a 50% &#224; cineangiocoronariografia.</p>
    <p>As taxas de sobrevida livre de eventos em um e dois anos, respectivamente, foram de 91,5% e de 79,4% para eventos cardiovasculares, de 96,5% e de 88,5% para mortalidade cardiovascular e de 96,5% e de 83% para mortalidade geral. As <xref ref-type="fig" rid="aop06012f01">Figuras 1</xref> e <xref ref-type="fig" rid="aop06012f02">2</xref> representam as curvas de sobrevida livre de mortalidade cardiovascular e de eventos cardiovasculares fatais e n&#227;o fatais, respectivamente.</p>
    <p content-type="asset">
      <fig id="aop06012f01">
        <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gf01.jpg"/></fig>
    </p>
    <p content-type="asset">
      <fig id="aop06012f02">
        <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gf02.jpg"/></fig>
    </p>
    <p>A <xref ref-type="table" rid="aop06012t02">Tabela 2</xref> demonstra a compara&#231;&#227;o das caracter&#237;sticas demogr&#225;ficas, cl&#237;nicas, bioqu&#237;micas e ecodopplercardiogr&#225;ficas entre os grupos com e sem evento cardiovascular. Os pacientes com desfecho cardiovascular apresentaram maior preval&#234;ncia de diabetes e de evento cardiovascular pr&#233;vio, maior DSVE e menores valores de FE e de fra&#231;&#227;o de encurtamento sist&#243;lico.</p>
    <p content-type="asset">
      <table-wrap id="aop06012t02">
        <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gt02.jpg"/></table-wrap>
    </p>
    <p>O modelo univariado de Cox para eventos cardiovasculares est&#225; apresentado na <xref ref-type="table" rid="t3">Tabela 3</xref>. Na an&#225;lise univariada, diabetes melito, hist&#243;ria pr&#233;via de DCV, DSVE, FE e fra&#231;&#227;o de encurtamento sist&#243;lico mostraram associa&#231;&#227;o significativa com desfecho cardiovascular. A an&#225;lise multivariada incluiu as vari&#225;veis: diabetes melito, evento cardiovascular pr&#233;vio, FE, disfun&#231;&#227;o diast&#243;lica de moderada a grave e rela&#231;&#227;o E/e'. As vari&#225;veis DSVE e fra&#231;&#227;o de encurtamento sist&#243;lico n&#227;o foram inclu&#237;das no modelo de regress&#227;o, pois s&#227;o vari&#225;veis correlacionadas com a FE. No modelo final de regress&#227;o, o diagn&#243;stico pr&#233;vio de DCV e a disfun&#231;&#227;o diast&#243;lica de moderada a grave mostraram-se como fatores de risco independentes para eventos cardiovasculares fatais e n&#227;o fatais (<xref ref-type="table" rid="t4">Tabela 4</xref>).</p>
    <table-wrap id="t3">
      <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gt03.jpg"/></table-wrap>
    <table-wrap id="t4">
      <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gt04.jpg"/></table-wrap>
    <p>A <xref ref-type="table" rid="t5">Tabela 5</xref> apresenta o modelo univariado de Cox para mortalidade cardiovascular. Apenas a hist&#243;ria pr&#233;via de DCV mostrou associa&#231;&#227;o significativa com mortalidade cardiovascular na an&#225;lise univariada. A an&#225;lise multivariada n&#227;o foi realizada, pois, pelo crit&#233;rio de sele&#231;&#227;o de vari&#225;veis para o modelo multivariado (p &lt; 0,1), somente DCV pr&#233;via e desnutri&#231;&#227;o estariam aptas a entrar no modelo final.</p>
    <table-wrap id="t5">
      <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gt05.jpg"/></table-wrap>
    <p>A taxa de sobrevida livre de eventos cardiovasculares no per&#237;odo de seguimento foi de 87,2% e de 55% nos grupos sem e com hist&#243;ria de DCV pr&#233;via, respectivamente (p = 0,007). Enquanto a taxa de sobrevida livre de desfechos cardiovasculares foi de 66,4% no grupo com disfun&#231;&#227;o diast&#243;lica de moderada a grave, no grupo com altera&#231;&#227;o do relaxamento ou fun&#231;&#227;o diast&#243;lica normal foi de 87,3% (p = 0,075). A <xref ref-type="fig" rid="aop06012f03">Figura 3</xref> ilustra as curvas de sobrevida livre de desfecho cardiovascular de acordo com a presen&#231;a ou aus&#234;ncia disfun&#231;&#227;o diast&#243;lica moderada a grave.</p>
    <p content-type="asset">
      <fig id="aop06012f03">
        <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gf03.jpg"/></fig>
    </p>
    <p>
      <bold>Discuss&#227;o</bold>
    </p>
    <p>Este estudo demonstrou taxas de sobrevida livre de mortalidade global de 96,5% em um ano e de 83% em dois anos. Essas taxas s&#227;o compar&#225;veis &#224;s encontradas por Silva e cols.<sup>19</sup>, que verificaram sobrevida de 91% e de 84% em um e dois anos, respectivamente, em estudo realizado no Brasil. Dados obtidos de censos de di&#225;lise mostram taxas de sobrevida de 88,6% em um ano e de 79,1% em dois anos na Europa<sup>20</sup> e de 77,4% em um ano e de 63% em dois anos nos Estados Unidos<sup>1</sup>. As caracter&#237;sticas dos pacientes inclu&#237;dos nesta pesquisa poderiam explicar as diferen&#231;as encontradas. Foram estudados pacientes com m&#233;dias de press&#227;o arterial mais controladas, fato incomum nessa popula&#231;&#227;o. Al&#233;m disso, a m&#233;dia da FE estava preservada nos indiv&#237;duos estudados, caracterizando uma popula&#231;&#227;o de pacientes mais est&#225;veis do ponto de vista da fun&#231;&#227;o sist&#243;lica do VE.</p>
    <p>As DCV foram respons&#225;veis por 66,7% do total de &#243;bitos ocorridos no per&#237;odo de seguimento. A propor&#231;&#227;o encontrada assemelha-se &#224;s relatadas em estudos que avaliaram mortalidade cardiovascular e global em pacientes em tratamento hemodial&#237;tico<sup>6,21</sup>. Por&#233;m estudos multic&#234;ntricos, tais como o HEMO e o AURORA, revelaram taxas inferiores a 50% de mortalidade por doen&#231;as card&#237;acas na popula&#231;&#227;o em di&#225;lise<sup>22,23</sup>. Esses resultados confirmam que as DCV permanecem como a mais importante causa de morbidade e mortalidade nos pacientes em hemodi&#225;lise. Pacientes em hemodi&#225;lise t&#234;m 10 a 20 vezes mais risco de mortalidade cardiovascular quando comparados com a popula&#231;&#227;o geral<sup>24</sup> e isso se deve ao fato de serem indiv&#237;duos expostos tanto a fatores tradicionais quanto a fatores n&#227;o tradicionais para complica&#231;&#245;es cardiovasculares<sup>25</sup>.</p>
    <p>A an&#225;lise univariada sugeriu que fatores de risco tradicionais como diabetes e hist&#243;ria pr&#233;via de DCV est&#227;o relacionados com um risco mais elevado de eventos cardiovasculares. Por outro lado, idade, tabagismo e hipercolesterolemia n&#227;o se mostraram como fatores de risco para a ocorr&#234;ncia de desfecho cardiovascular. Apesar de estudos mostrarem uma maior preval&#234;ncia dos fatores de risco tradicionais na popula&#231;&#227;o com DRC que na popula&#231;&#227;o em geral<sup>26</sup>, as altas taxas de complica&#231;&#245;es cardiovasculares n&#227;o t&#234;m sido totalmente explicadas por tais fatores de risco<sup>24,25</sup>. Adicionalmente, fatores conhecidos por n&#227;o tradicionais, como anemia, m&#225;-nutri&#231;&#227;o, estado inflamat&#243;rio, altera&#231;&#245;es no produto c&#225;lcio-f&#243;sforo, dentre outros, t&#234;m sido implicados como fatores independentes associados com complica&#231;&#245;es cardiovasculares nos pacientes em di&#225;lise<sup>27-30</sup>. Na presente pesquisa, no entanto, esses fatores n&#227;o se relacionaram com um maior risco de morbimortalidade cardiovascular.</p>
    <p>Evid&#234;ncias indicam que os par&#226;metros de disfun&#231;&#227;o sist&#243;lica do VE est&#227;o associados de modo independente com a ocorr&#234;ncia de eventos cardiovasculares fatais e n&#227;o fatais em pacientes em tratamento dial&#237;tico, n&#227;o havendo diferen&#231;a no poder preditivo entre os m&#233;todos utilizados para avali&#225;-la<sup>7</sup>. Neste estudo, verificou-se na an&#225;lise univariada que redu&#231;&#245;es na FE ou na fra&#231;&#227;o de encurtamento sist&#243;lico est&#227;o relacionadas com o aumento do risco de eventos cardiovasculares.</p>
    <p>A HVE &#233; um forte preditor de morbidade e mortalidade cardiovascular nos pacientes em hemodi&#225;lise<sup>31</sup>. A HVE esteve presente em 85% dos pacientes desta pesquisa, taxa semelhante &#224;s reportadas por outros autores<sup>6,32</sup>. Zoccali e cols.<sup>31</sup> revelaram que o aumento do IMVE em pacientes em hemodi&#225;lise foi um preditor independente de eventos cardiovasculares, independentemente dos valores basais da MVE. Neste estudo, o IMVE n&#227;o se associou com morbidade e mortalidade cardiovascular. Esse resultado pode ser atribu&#237;do &#224;s caracter&#237;sticas mais est&#225;veis dos pacientes inclu&#237;dos na amostra e ao per&#237;odo de seguimento deste estudo.</p>
    <p>O VAE &#233; um par&#226;metro potencialmente &#250;til para avaliar disfun&#231;&#227;o diast&#243;lica, estando relacionado &#224; gravidade e &#224; dura&#231;&#227;o da disfun&#231;&#227;o<sup>5</sup>. Em estudo com uma popula&#231;&#227;o em terapia renal substitutiva, Barberato e cols.<sup>33</sup> mostraram que o IVAE foi um preditor de mortalidade. Na presente pesquisa, embora o IVAE estivesse discretamente elevado nos dois grupos, a vari&#225;vel n&#227;o foi preditora independente de eventos cardiovasculares e de mortalidade cardiovascular. Poss&#237;veis explica&#231;&#245;es para a n&#227;o associa&#231;&#227;o poderiam ser: em pacientes an&#234;micos, esse &#237;ndice n&#227;o refletiria disfun&#231;&#227;o diast&#243;lica<sup>34</sup>; os pacientes avaliados n&#227;o faziam parte de uma popula&#231;&#227;o de renais cr&#244;nicos com importante comprometimento da fun&#231;&#227;o sist&#243;lica do VE; e o n&#250;mero de pacientes foi insuficiente para encontrar diferen&#231;as estatisticamente significantes.</p>
    <p>Na an&#225;lise multivariada, o diagn&#243;stico pr&#233;vio de DCV permaneceu como um fator de risco de eventos cardiovasculares fatais e n&#227;o fatais. Zoccali e cols.<sup>7</sup>, em estudo com 254 pacientes em hemodi&#225;lise, Rakhit e cols.<sup>35</sup>, em pesquisa que incluiu 176 pacientes com DRC nos est&#225;gios 4 e 5 em tratamento conservador ou dial&#237;tico, e Cheung e cols.<sup>22</sup>, no estudo multic&#234;ntrico HEMO, descreveram resultado semelhante no modelo final da an&#225;lise multivariada de Cox.</p>
    <p>O presente estudo demonstrou uma elevada preval&#234;ncia de disfun&#231;&#227;o diast&#243;lica entre pacientes portadores de DRC em hemodi&#225;lise, correspondendo a 83,6%, sendo que 36,4% do total de pacientes apresentaram disfun&#231;&#227;o diast&#243;lica de moderada a grave. Estudos realizados com pacientes em hemodi&#225;lise revelaram que a preval&#234;ncia de disfun&#231;&#227;o diast&#243;lica nessa popula&#231;&#227;o pode variar de 63,5% a 87%, dependendo dos crit&#233;rios utilizados para defini&#231;&#227;o e dos pacientes inclu&#237;dos na amostra<sup>36-38</sup>.</p>
    <p>A disfun&#231;&#227;o diast&#243;lica caracteriza-se por altera&#231;&#245;es do relaxamento e da complac&#234;ncia ventricular<sup>5</sup> e a sua alta preval&#234;ncia pode ser explicada pelo fato de a DRC expor o cora&#231;&#227;o &#224; sobrecarga de press&#227;o e volume e a fatores n&#227;o hemodin&#226;micos associados que provocam altera&#231;&#245;es no mioc&#225;rdio<sup>39</sup>. A fibrose mioc&#225;rdica resultante desses processos &#233; um dos principais determinantes da rigidez do VE e da eleva&#231;&#227;o das press&#245;es de enchimento, predispondo ao desenvolvimento de disfun&#231;&#227;o diast&#243;lica<sup>39</sup>.</p>
    <p>A presen&#231;a de disfun&#231;&#227;o diast&#243;lica de moderada a grave foi o &#250;nico crit&#233;rio ecocardiogr&#225;fico preditor independente de eventos cardiovasculares. Um estudo que empregou apenas par&#226;metros derivados do fluxo transvalvar mitral e do fluxo venoso pulmonar para a categoriza&#231;&#227;o da fun&#231;&#227;o diast&#243;lica demonstrou que a disfun&#231;&#227;o diast&#243;lica &#233; um preditor independente de mortalidade em pacientes em terapia renal substitutiva por hemodi&#225;lise<sup>40</sup>.</p>
    <p>Em um estudo publicado recentemente, que avaliou 129 pacientes em hemodi&#225;lise e utilizou crit&#233;rios do Doppler convencional e do Doppler tecidual para classificar disfun&#231;&#227;o diast&#243;lica, Barberato e cols.<sup>37</sup> evidenciaram que a mortalidade geral foi significativamente maior no grupo com disfun&#231;&#227;o diast&#243;lica com padr&#227;o pseudonormal e fluxo restritivo em compara&#231;&#227;o ao grupo com disfun&#231;&#227;o diast&#243;lica do tipo altera&#231;&#227;o do relaxamento ou com fun&#231;&#227;o diast&#243;lica normal. Nesse estudo, a disfun&#231;&#227;o diast&#243;lica avan&#231;ada mostrou-se ainda um preditor independente de eventos cardiovasculares.</p>
    <p>O presente estudo apresenta limita&#231;&#245;es: o n&#250;mero de pacientes estudados poderia influenciar o poder de algumas vari&#225;veis, como o IVAE; o tempo de seguimento, inferior a dois anos, pode ter influenciado na n&#227;o associa&#231;&#227;o dos par&#226;metros da fun&#231;&#227;o do ventr&#237;culo esquerdo com a mortalidade cardiovascular. Os pontos fortes s&#227;o: o estudo &#233; prospectivo e longitudinal; foram utilizadas t&#233;cnicas fact&#237;veis para a an&#225;lise da fun&#231;&#227;o diast&#243;lica de forma n&#227;o invasiva, permitindo an&#225;lises peri&#243;dicas nos pacientes que apresentam altas taxas de eventos cardiovasculares.</p>
    <p>
      <bold>Conclus&#245;es</bold>
    </p>
    <p>Pacientes em hemodi&#225;lise apresentam altas taxas de morbidade e mortalidade cardiovascular. A presen&#231;a de diabetes, o hist&#243;rico pr&#233;vio de DCV e uma FE mais baixa s&#227;o fatores potencialmente relacionados com eventos cardiovasculares. A disfun&#231;&#227;o diast&#243;lica de moderada a grave foi um fator de risco independente de eventos cardiovasculares e, embora novos estudos sejam necess&#225;rios para a valida&#231;&#227;o deste achado, &#233; recomend&#225;vel que a avalia&#231;&#227;o da fun&#231;&#227;o diast&#243;lica, feita atrav&#233;s de par&#226;metros do Doppler pulsado e do Doppler tecidual, seja inclu&#237;da na avalia&#231;&#227;o dos pacientes em tratamento hemodial&#237;tico. Essa medida possibilitar&#225; a detec&#231;&#227;o precoce dos indiv&#237;duos em risco, visando redu&#231;&#227;o de morbidade e mortalidade.</p>
    <p>
      <bold>Potencial Conflito de Interesses</bold>
    </p>
    <p>Declaro n&#227;o haver conflito de interesses pertinentes.</p>
    <p>
      <bold>Fontes de Financiamento</bold>
    </p>
    <p>O presente estudo n&#227;o teve fontes de financiamento externas.</p>
    <p>
      <bold>Vincula&#231;&#227;o Acad&#234;mica</bold>
    </p>
    <p>N&#227;o h&#225; vincula&#231;&#227;o deste estudo a programas de p&#243;s-gradua&#231;&#227;o.</p>
    <p>
      <fn id="back" fn-type="corresp">
        <p>Correspond&#234;ncia:</p>
        <p> Thayse Mayara Arag&#227;o Siqueira </p>
        <p> Rua 39, quadra 40, casa 25, conj. Henrique de La Roque, Ipem S&#227;o Crist&#243;v&#227;o </p>
        <p> CEP 65056-020, S&#227;o Lu&#237;s, MA - Brasil </p>
        <p> E-mail: </p>
        <p><email xlink:href="thayse_siqueira@hotmail.com">thayse_siqueira@hotmail.com</email>, </p>
        <p>
          <email xlink:href="thayse_siqueira@yahoo.com.br">thayse_siqueira@yahoo.com.br</email>
        </p>
      </fn>
    </p>
    <p>Artigo recebido em 12/10/11 </p>
    <p> Revisado em 12/10/11 </p>
    <p> Aceito em 07/03/12</p>
  </body>
  <back>
    <ref-list>
      <ref id="B1">
        <label>1</label>
        <mixed-citation>1. United States Data System. 2010 Annual Data Report. Atlas of Chronic Kidney Disease and End-Stage Renal Disease in the United States. Bethesda, MD: National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases; 2010.</mixed-citation>
        <element-citation publication-type="book">
          <source>2010 Annual Data Report: Atlas of Chronic Kidney Disease and End-Stage Renal Disease in the United States</source>
          <date>
            <year>2010</year>
          </date>
        </element-citation>
      </ref>
      <ref id="B2">
        <mixed-citation>2.  Sesso RCC, Lopes AA, Thom&#233; FS, Lugon JR, Burdmann EA. Censo Brasileiro  de Di&#225;lise, 2009. J Bras Nefrol. 2010;32(4):380-4.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Censo Brasileiro de Di&#225;lise, 2009</article-title>
          <source>J Bras Nefrol</source>
          <date>
            <year>2010</year>
          </date>
          <fpage>380</fpage>
          <lpage>4</lpage>
          <issue>4</issue>
          <volume>32</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Sesso</surname>
              <given-names>RCC</given-names>
            </name>
            <name>
              <surname>Lopes</surname>
              <given-names>AA</given-names>
            </name>
            <name>
              <surname>Thom&#233;</surname>
              <given-names>FS</given-names>
            </name>
            <name>
              <surname>Lugon</surname>
              <given-names>JR</given-names>
            </name>
            <name>
              <surname>Burdmann</surname>
              <given-names>EA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B3">
        <mixed-citation>3.  Parfrey PS, Foley RN. The clinical epidemiology of cardiac disease in chronic  renal failure. J Am Soc Nephrol. 1999;10(7):1606-15.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>The clinical epidemiology of cardiac disease in chronic renal failure</article-title>
          <source>J Am Soc Nephrol</source>
          <date>
            <year>1999</year>
          </date>
          <fpage>1606</fpage>
          <lpage>15</lpage>
          <issue>7</issue>
          <volume>10</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Parfrey</surname>
              <given-names>PS</given-names>
            </name>
            <name>
              <surname>Foley</surname>
              <given-names>RN</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B4">
        <mixed-citation>4.  Bucharles SG, Varela AM, Barberato SH, Pecoits-Filho R. Avalia&#231;&#227;o  e manejo da doen&#231;a cardiovascular em pacientes com doen&#231;a renal  cr&#244;nica. J Bras Nefrol. 2010;32(1):118-25.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Avalia&#231;&#227;o e manejo da doen&#231;a cardiovascular em pacientes com doen&#231;a renal cr&#244;nica</article-title>
          <source>J Bras Nefrol</source>
          <date>
            <year>2010</year>
          </date>
          <fpage>118</fpage>
          <lpage>25</lpage>
          <issue>1</issue>
          <volume>32</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Bucharles</surname>
              <given-names>SG</given-names>
            </name>
            <name>
              <surname>Varela</surname>
              <given-names>AM</given-names>
            </name>
            <name>
              <surname>Barberato</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Pecoits-Filho</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B5">
        <mixed-citation>5.  Barberato SH, Pecoits-Filho R. Altera&#231;&#245;es ecocardiogr&#225;ficas  em pacientes com insufici&#234;ncia renal cr&#244;nica em programa de hemodi&#225;lise.  Arq Bras Cardiol. 2010;94(1):140-6.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Altera&#231;&#245;es ecocardiogr&#225;ficas em pacientes com insufici&#234;ncia renal cr&#244;nica em programa de hemodi&#225;lise</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>2010</year>
          </date>
          <fpage>140</fpage>
          <lpage>6</lpage>
          <issue>1</issue>
          <volume>94</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Barberato</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Pecoits-Filho</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B6">
        <mixed-citation>6.  London GM, Pannier B, Guerin AP, Blacher J, Marchais SJ, Darne B, et al. Alterations  of left ventricular hypertrophy in and survival of patients receiving hemodialysis:  follow-up of an interventional study. J Am Soc Nephrol. 2001;12(12):2759-67.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Alterations of left ventricular hypertrophy in and survival of patients receiving hemodialysis: follow-up of an interventional study</article-title>
          <source>J Am Soc Nephrol</source>
          <date>
            <year>2001</year>
          </date>
          <fpage>2759</fpage>
          <lpage>67</lpage>
          <issue>12</issue>
          <volume>12</volume>
          <person-group person-group-type="author">
            <name>
              <surname>London</surname>
              <given-names>GM</given-names>
            </name>
            <name>
              <surname>Pannier</surname>
              <given-names>B</given-names>
            </name>
            <name>
              <surname>Guerin</surname>
              <given-names>AP</given-names>
            </name>
            <name>
              <surname>Blacher</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Marchais</surname>
              <given-names>SJ</given-names>
            </name>
            <name>
              <surname>Darne</surname>
              <given-names>B</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B7">
        <mixed-citation>7.  Zoccali C, Benedetto FA, Mallamaci F, Tripepi G, Giacone G, Cataliotti A, et al.  Prognostic value of echocardiographic indicators of left ventricular systolic  function in asymptomatic dialysis patients. J Am Soc Nephrol. 2004;15(4):1029-37.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Prognostic value of echocardiographic indicators of left ventricular systolic function in asymptomatic dialysis patients</article-title>
          <source>J Am Soc Nephrol</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>1029</fpage>
          <lpage>37</lpage>
          <issue>4</issue>
          <volume>15</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Zoccali</surname>
              <given-names>C</given-names>
            </name>
            <name>
              <surname>Benedetto</surname>
              <given-names>FA</given-names>
            </name>
            <name>
              <surname>Mallamaci</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Tripepi</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Giacone</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Cataliotti</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B8">
        <mixed-citation>8.  Chen SC, Chang JM, Liu WC, Huang JC, Tsai JC, Lin MY, et al. Echocardiographic  parameters are independently associated with increased cardiovascular events in  patients with chronic kidney disease. Nephrol Dial Transplant. 2012;27(3):1064-70.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Echocardiographic parameters are independently associated with increased cardiovascular events in patients with chronic kidney disease</article-title>
          <source>Nephrol Dial Transplant</source>
          <date>
            <year>2012</year>
          </date>
          <fpage>1064</fpage>
          <lpage>70</lpage>
          <issue>3</issue>
          <volume>27</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Chen</surname>
              <given-names>SC</given-names>
            </name>
            <name>
              <surname>Chang</surname>
              <given-names>JM</given-names>
            </name>
            <name>
              <surname>Liu</surname>
              <given-names>WC</given-names>
            </name>
            <name>
              <surname>Huang</surname>
              <given-names>JC</given-names>
            </name>
            <name>
              <surname>Tsai</surname>
              <given-names>JC</given-names>
            </name>
            <name>
              <surname>Lin</surname>
              <given-names>MY</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B9">
        <mixed-citation>9.  Sahn DJ, DeMaria A, Kisslo J, Weyman A. Recommendations regarding quantitation  in M-mode echocardiography: results of a survey of echocardiographic measurements.  Circulation. 1978;58(6):1072-83.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Recommendations regarding quantitation in M-mode echocardiography: results of a survey of echocardiographic measurements</article-title>
          <source>Circulation</source>
          <date>
            <year>1978</year>
          </date>
          <fpage>1072</fpage>
          <lpage>83</lpage>
          <issue>6</issue>
          <volume>58</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Sahn</surname>
              <given-names>DJ</given-names>
            </name>
            <name>
              <surname>DeMaria</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Kisslo</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Weyman</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B10">
        <mixed-citation>10.  Schiller NB, Shah PM, Crawford M, DeMaria A, Devereux R, Feigenbaum H, et al.  Recommendations for quantitation of the left ventricle by two-dimensional echocardiography.  American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation  of Two-Dimensional Echocardiograms. J Am Soc Echocardiogr. 1989;2(5):358-67.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Recommendations for quantitation of the left ventricle by two-dimensional echocardiography: American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>1989</year>
          </date>
          <fpage>358</fpage>
          <lpage>67</lpage>
          <issue>5</issue>
          <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>
            <name>
              <surname>DeMaria</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Devereux</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Feigenbaum</surname>
              <given-names>H</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B11">
        <mixed-citation>11.  Qui&#241;ones MA, Otto CM, Stoddard M, Waggoner A, Zoghbi WA. Recommendations  for quantification of Doppler echocardiography: a report from the Doppler Quantification  Task Force of the Nomenclature and Standards Committee of the American Society  of Echocardiography. J Am Soc Echocardiogr. 2002;15(2):167-84.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Recommendations for quantification of Doppler echocardiography: a report from the Doppler Quantification Task Force of the Nomenclature and Standards Committee of the American Society of Echocardiography</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>2002</year>
          </date>
          <fpage>167</fpage>
          <lpage>84</lpage>
          <issue>2</issue>
          <volume>15</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Qui&#241;ones</surname>
              <given-names>MA</given-names>
            </name>
            <name>
              <surname>Otto</surname>
              <given-names>CM</given-names>
            </name>
            <name>
              <surname>Stoddard</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Waggoner</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Zoghbi</surname>
              <given-names>WA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B12">
        <mixed-citation>12.  Nagueh SF, Appleton CP, Gillebert TC, Marino PN, Oh JK, Smiseth OA, et al. Recommendations  for the evaluation of left ventricular diastolic function by echocardiography.  J Am Soc Echocardiogr. 2009;22(2):107-33.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Recommendations for the evaluation of left ventricular diastolic function by echocardiography</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>2009</year>
          </date>
          <fpage>107</fpage>
          <lpage>33</lpage>
          <issue>2</issue>
          <volume>22</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Nagueh</surname>
              <given-names>SF</given-names>
            </name>
            <name>
              <surname>Appleton</surname>
              <given-names>CP</given-names>
            </name>
            <name>
              <surname>Gillebert</surname>
              <given-names>TC</given-names>
            </name>
            <name>
              <surname>Marino</surname>
              <given-names>PN</given-names>
            </name>
            <name>
              <surname>Oh</surname>
              <given-names>JK</given-names>
            </name>
            <name>
              <surname>Smiseth</surname>
              <given-names>OA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B13">
        <mixed-citation>13.  Devereux RB, Alonso DR, Lutas EM, Gottlieb GJ, Campo E, Sachs I, et al. Echocardiographic  assessment of left ventricular hypertrophy: comparison to necropsy findings. Am  J Cardiol. 1986;57(6):450-8.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings</article-title>
          <source>Am J Cardiol</source>
          <date>
            <year>1986</year>
          </date>
          <fpage>450</fpage>
          <lpage>8</lpage>
          <issue>6</issue>
          <volume>57</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Devereux</surname>
              <given-names>RB</given-names>
            </name>
            <name>
              <surname>Alonso</surname>
              <given-names>DR</given-names>
            </name>
            <name>
              <surname>Lutas</surname>
              <given-names>EM</given-names>
            </name>
            <name>
              <surname>Gottlieb</surname>
              <given-names>GJ</given-names>
            </name>
            <name>
              <surname>Campo</surname>
              <given-names>E</given-names>
            </name>
            <name>
              <surname>Sachs</surname>
              <given-names>I</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B14">
        <mixed-citation>14.  Teichholz LE, Kreulen T, Herman MV, Gorlin R. Problems in echocardiographic volume  determinations: echocardiographic-angiographic correlations in the presence or  absence of asynergy. Am J Cardiol. 1976;37(1):7-11.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Problems in echocardiographic volume determinations: echocardiographic-angiographic correlations in the presence or absence of asynergy</article-title>
          <source>Am J Cardiol</source>
          <date>
            <year>1976</year>
          </date>
          <fpage>7</fpage>
          <lpage>11</lpage>
          <issue>1</issue>
          <volume>37</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Teichholz</surname>
              <given-names>LE</given-names>
            </name>
            <name>
              <surname>Kreulen</surname>
              <given-names>T</given-names>
            </name>
            <name>
              <surname>Herman</surname>
              <given-names>MV</given-names>
            </name>
            <name>
              <surname>Gorlin</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B15">
        <mixed-citation>15.  Lang RM, Bierig M, Devereux RB, Flachskampf FA, Foster E, Pellikka PA, et al.  Recommendations for chamber quantification: a report from the American Society  of Echocardiography's Guidelines and Standards Committee and the Chamber Quantification  Writing Group, developed in conjunction with the European Association of Echocardiography,  a branch of the European Society of Cardiology. J Am Soc Echocardiogr. 2005;18(12):1440-63.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Recommendations for chamber quantification: a report from the American Society of Echocardiography's Guidelines and Standards Committee and the Chamber Quantification Writing Group, developed in conjunction with the European Association of Echocardiography, a branch of the European Society of Cardiology</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>2005</year>
          </date>
          <fpage>1440</fpage>
          <lpage>63</lpage>
          <issue>12</issue>
          <volume>18</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Lang</surname>
              <given-names>RM</given-names>
            </name>
            <name>
              <surname>Bierig</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Devereux</surname>
              <given-names>RB</given-names>
            </name>
            <name>
              <surname>Flachskampf</surname>
              <given-names>FA</given-names>
            </name>
            <name>
              <surname>Foster</surname>
              <given-names>E</given-names>
            </name>
            <name>
              <surname>Pellikka</surname>
              <given-names>PA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B16">
        <mixed-citation>16.  Kasner M, Westermann D, Steendijk P, Gaub R, Wilkenshoff U, Weitmann K, et al.  Utility of Doppler echocardiography and tissue Doppler imaging in the estimation  of diastolic function in heart failure with normal ejection fraction: a comparative  Doppler-conductance catheterization study. Circulation. 2007;116(6):637-47.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Utility of Doppler echocardiography and tissue Doppler imaging in the estimation of diastolic function in heart failure with normal ejection fraction: a comparative Doppler-conductance catheterization study</article-title>
          <source>Circulation</source>
          <date>
            <year>2007</year>
          </date>
          <fpage>637</fpage>
          <lpage>47</lpage>
          <issue>6</issue>
          <volume>116</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Kasner</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Westermann</surname>
              <given-names>D</given-names>
            </name>
            <name>
              <surname>Steendijk</surname>
              <given-names>P</given-names>
            </name>
            <name>
              <surname>Gaub</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Wilkenshoff</surname>
              <given-names>U</given-names>
            </name>
            <name>
              <surname>Weitmann</surname>
              <given-names>K</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B17">
        <mixed-citation>17.  Khouri SJ, Maly GT, Suh DD, Walsh TE. A practical approach to the echocardiographic  evaluation of diastolic function. J Am Soc Echocardiogr. 2004;17(3):290-7.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>A practical approach to the echocardiographic evaluation of diastolic function</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>290</fpage>
          <lpage>7</lpage>
          <issue>3</issue>
          <volume>17</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Khouri</surname>
              <given-names>SJ</given-names>
            </name>
            <name>
              <surname>Maly</surname>
              <given-names>GT</given-names>
            </name>
            <name>
              <surname>Suh</surname>
              <given-names>DD</given-names>
            </name>
            <name>
              <surname>Walsh</surname>
              <given-names>TE</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B18">
        <mixed-citation>18.  Dubois D, Dubois EF. A formula to estimate the approximate surface area if height  and weight be known. Arch Intern Med. 1916;17:863-71.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>A formula to estimate the approximate surface area if height and weight be known</article-title>
          <source>Arch Intern Med</source>
          <date>
            <year>1916</year>
          </date>
          <fpage>863</fpage>
          <lpage>71</lpage>
          <volume>17</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Dubois</surname>
              <given-names>D</given-names>
            </name>
            <name>
              <surname>Dubois</surname>
              <given-names>EF</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B19">
        <mixed-citation>19.  Silva LA, Mezzomo NF, Pansard HM, Arantes LC, Rempel W, Argenta LC, et al. Sobrevida  em hemodi&#225;lise cr&#244;nica: estudo de uma coorte de 1.009 pacientes em  25 anos. J Bras Nefrol. 2009;31(3):190-7.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Sobrevida em hemodi&#225;lise cr&#244;nica: estudo de uma coorte de 1.009 pacientes em 25 anos</article-title>
          <source>J Bras Nefrol</source>
          <date>
            <year>2009</year>
          </date>
          <fpage>190</fpage>
          <lpage>7</lpage>
          <issue>3</issue>
          <volume>31</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Silva</surname>
              <given-names>LA</given-names>
            </name>
            <name>
              <surname>Mezzomo</surname>
              <given-names>NF</given-names>
            </name>
            <name>
              <surname>Pansard</surname>
              <given-names>HM</given-names>
            </name>
            <name>
              <surname>Arantes</surname>
              <given-names>LC</given-names>
            </name>
            <name>
              <surname>Rempel</surname>
              <given-names>W</given-names>
            </name>
            <name>
              <surname>Argenta</surname>
              <given-names>LC</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B20">
        <mixed-citation>20.  European Renal Association (ERA). European Dialysis and Transplant Association  (EDTA). Registry Annual Report 2009: Academic Medical Center, Department of Medical  Informatics, Amsterdam (The Netherlands); 2011.</mixed-citation>
        <element-citation publication-type="book">
          <source>European Dialysis and Transplant Association (EDTA): Registry Annual Report 2009</source>
          <date>
            <year>2011</year>
          </date>
          <person-group person-group-type="author">
            <name>
              <surname>European Renal Association</surname>
              <given-names>(ERA)</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B21">
        <mixed-citation>21.  Tripepi G, Benedetto FA, Mallamaci F, Tripepi R, Malatino L, Zoccali C. Left atrial  volume in end-stage renal disease: a prospective cohort study. J Hypertens. 2006;24(6):1173-80.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Left atrial volume in end-stage renal disease: a prospective cohort study</article-title>
          <source>J Hypertens</source>
          <date>
            <year>2006</year>
          </date>
          <fpage>1173</fpage>
          <lpage>80</lpage>
          <issue>6</issue>
          <volume>24</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Tripepi</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Benedetto</surname>
              <given-names>FA</given-names>
            </name>
            <name>
              <surname>Mallamaci</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Tripepi</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Malatino</surname>
              <given-names>L</given-names>
            </name>
            <name>
              <surname>Zoccali</surname>
              <given-names>C</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B22">
        <mixed-citation>22.  Cheung AK, Sarnak MJ, Yan G, Berkoben M, Heyka R, Kaufman A, et al. Cardiac diseases  in maintenance hemodialysis patients: results of the HEMO Study. Kidney Int. 2004;65(6):2380-9.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Cardiac diseases in maintenance hemodialysis patients: results of the HEMO Study</article-title>
          <source>Kidney Int</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>2380</fpage>
          <lpage>9</lpage>
          <issue>6</issue>
          <volume>65</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Cheung</surname>
              <given-names>AK</given-names>
            </name>
            <name>
              <surname>Sarnak</surname>
              <given-names>MJ</given-names>
            </name>
            <name>
              <surname>Yan</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Berkoben</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Heyka</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Kaufman</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B23">
        <mixed-citation>23.  Fellstr&#246;m BC, Jardine AG, Schmieder RE, Holdaas H, Bannister K, Beutler J,  et al. Rosuvastatin and cardiovascular events in patients undergoing hemodialysis.  N Engl J Med. 2009;360(14):1395-407.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Rosuvastatin and cardiovascular events in patients undergoing hemodialysis</article-title>
          <source>N Engl J Med</source>
          <date>
            <year>2009</year>
          </date>
          <fpage>1395</fpage>
          <lpage>407</lpage>
          <issue>14</issue>
          <volume>360</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Fellstr&#246;m</surname>
              <given-names>BC</given-names>
            </name>
            <name>
              <surname>Jardine</surname>
              <given-names>AG</given-names>
            </name>
            <name>
              <surname>Schmieder</surname>
              <given-names>RE</given-names>
            </name>
            <name>
              <surname>Holdaas</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Bannister</surname>
              <given-names>K</given-names>
            </name>
            <name>
              <surname>Beutler</surname>
              <given-names>J</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B24">
        <mixed-citation>24.  Foley RN, Parfrey PS, Sarnak MJ. Clinical epidemiology of cardiovascular disease  in chronic renal disease. Am J Kidney Dis. 1998;32(5 Suppl 3):S112-9.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Clinical epidemiology of cardiovascular disease in chronic renal disease</article-title>
          <source>Am J Kidney Dis</source>
          <date>
            <year>1998</year>
          </date>
          <fpage>S112</fpage>
          <lpage>9</lpage>
          <issue>5</issue>
          <volume>32</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Foley</surname>
              <given-names>RN</given-names>
            </name>
            <name>
              <surname>Parfrey</surname>
              <given-names>PS</given-names>
            </name>
            <name>
              <surname>Sarnak</surname>
              <given-names>MJ</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B25">
        <mixed-citation>25.  Zoccali C, Mallamaci F, Tripepi G. Novel cardiovascular risk factors in end-stage  renal disease.J Am Soc Nephrol. 2004;15(Suppl 1):S77-80.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Novel cardiovascular risk factors in end-stage renal disease</article-title>
          <source>J Am Soc Nephrol</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>S77</fpage>
          <lpage>80</lpage>
          <volume>15</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Zoccali</surname>
              <given-names>C</given-names>
            </name>
            <name>
              <surname>Mallamaci</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Tripepi</surname>
              <given-names>G</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B26">
        <mixed-citation>26.  Longenecker JC, Coresh J, Powe NR, Levey AS, Fink NE, Martin A, et al. Traditional  cardiovascular disease risk factors in dialysis patients compared with the general  population: the CHOICE Study. J Am Soc Nephrol. 2002;13(7):1918-27.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Traditional cardiovascular disease risk factors in dialysis patients compared with the general population: the CHOICE Study</article-title>
          <source>J Am Soc Nephrol</source>
          <date>
            <year>2002</year>
          </date>
          <fpage>1918</fpage>
          <lpage>27</lpage>
          <issue>7</issue>
          <volume>13</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Longenecker</surname>
              <given-names>JC</given-names>
            </name>
            <name>
              <surname>Coresh</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Powe</surname>
              <given-names>NR</given-names>
            </name>
            <name>
              <surname>Levey</surname>
              <given-names>AS</given-names>
            </name>
            <name>
              <surname>Fink</surname>
              <given-names>NE</given-names>
            </name>
            <name>
              <surname>Martin</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B27">
        <mixed-citation>27.  Weiner DE, Tighiouart H, Vlagopoulos PT, Griffith JL, Salem DN, Levey AS, et al.  Effects of anemia and left ventricular hypertrophy on cardiovascular disease in  patients with chronic kidney disease. J Am Soc Nephrol. 2005;16(6):1803-10.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Effects of anemia and left ventricular hypertrophy on cardiovascular disease in patients with chronic kidney disease</article-title>
          <source>J Am Soc Nephrol</source>
          <date>
            <year>2005</year>
          </date>
          <fpage>1803</fpage>
          <lpage>10</lpage>
          <issue>6</issue>
          <volume>16</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Weiner</surname>
              <given-names>DE</given-names>
            </name>
            <name>
              <surname>Tighiouart</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Vlagopoulos</surname>
              <given-names>PT</given-names>
            </name>
            <name>
              <surname>Griffith</surname>
              <given-names>JL</given-names>
            </name>
            <name>
              <surname>Salem</surname>
              <given-names>DN</given-names>
            </name>
            <name>
              <surname>Levey</surname>
              <given-names>AS</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B28">
        <mixed-citation>28.  Kakiya R, Shoji T, Tsujimoto Y, Tatsumi N, Hatsuda S, Shinohara K, et al. Body  fat mass and lean mass as predictors of survival in hemodialysis patients. Kidney  Int. 2006;70(3):549-56.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Body fat mass and lean mass as predictors of survival in hemodialysis patients</article-title>
          <source>Kidney Int</source>
          <date>
            <year>2006</year>
          </date>
          <fpage>549</fpage>
          <lpage>56</lpage>
          <issue>3</issue>
          <volume>70</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Kakiya</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Shoji</surname>
              <given-names>T</given-names>
            </name>
            <name>
              <surname>Tsujimoto</surname>
              <given-names>Y</given-names>
            </name>
            <name>
              <surname>Tatsumi</surname>
              <given-names>N</given-names>
            </name>
            <name>
              <surname>Hatsuda</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Shinohara</surname>
              <given-names>K</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B29">
        <mixed-citation>29.  Kalantar-Zadeh K, Kopple JD, Block G, Humphreys MH. A malnutrition-inflammation  score is correlated with morbidity and mortality in maintenance hemodialysis patients.  Am J Kidney Dis. 2001;38(6):1251-63.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>A malnutrition-inflammation score is correlated with morbidity and mortality in maintenance hemodialysis patients</article-title>
          <source>Am J Kidney Dis</source>
          <date>
            <year>2001</year>
          </date>
          <fpage>1251</fpage>
          <lpage>63</lpage>
          <issue>6</issue>
          <volume>38</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Kalantar-Zadeh</surname>
              <given-names>K</given-names>
            </name>
            <name>
              <surname>Kopple</surname>
              <given-names>JD</given-names>
            </name>
            <name>
              <surname>Block</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Humphreys</surname>
              <given-names>MH</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B30">
        <mixed-citation>30.  Block GA, Klassen PS, Lazarus JM, Ofsthun N, Lowrie EG, Chertow GM. Mineral metabolism,  mortality, and morbidity in maintenance hemodialysis. J Am Soc Nephrol. 2004;15(8):2208-18.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Mineral metabolism, mortality, and morbidity in maintenance hemodialysis</article-title>
          <source>J Am Soc Nephrol</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>2208</fpage>
          <lpage>18</lpage>
          <issue>8</issue>
          <volume>15</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Block</surname>
              <given-names>GA</given-names>
            </name>
            <name>
              <surname>Klassen</surname>
              <given-names>PS</given-names>
            </name>
            <name>
              <surname>Lazarus</surname>
              <given-names>JM</given-names>
            </name>
            <name>
              <surname>Ofsthun</surname>
              <given-names>N</given-names>
            </name>
            <name>
              <surname>Lowrie</surname>
              <given-names>EG</given-names>
            </name>
            <name>
              <surname>Chertow</surname>
              <given-names>GM</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B31">
        <mixed-citation>31.  Zoccali C, Benedetto FA, Mallamaci F, Tripepi G, Giacone G, Stancanelli B, et  al. Left ventricular mass monitoring in the follow-up of dialysis patients: prognostic  value of left ventricular hypertrophy progression. Kidney Int. 2004;65(4):1492-8.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Left ventricular mass monitoring in the follow-up of dialysis patients: prognostic value of left ventricular hypertrophy progression</article-title>
          <source>Kidney Int</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>1492</fpage>
          <lpage>8</lpage>
          <issue>4</issue>
          <volume>65</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Zoccali</surname>
              <given-names>C</given-names>
            </name>
            <name>
              <surname>Benedetto</surname>
              <given-names>FA</given-names>
            </name>
            <name>
              <surname>Mallamaci</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Tripepi</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Giacone</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Stancanelli</surname>
              <given-names>B</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B32">
        <mixed-citation>32.  Foley RN, Parfrey PS, Harnett JD, Kent GM, Murray DC, Barr&#233; PE. The prognostic  importance of left ventricular geometry in uremic cardiomyopathy. J Am Soc Nephrol.  1995;5(12):2024-31.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>The prognostic importance of left ventricular geometry in uremic cardiomyopathy</article-title>
          <source>J Am Soc Nephrol</source>
          <date>
            <year>1995</year>
          </date>
          <fpage>2024</fpage>
          <lpage>31</lpage>
          <issue>12</issue>
          <volume>5</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Foley</surname>
              <given-names>RN</given-names>
            </name>
            <name>
              <surname>Parfrey</surname>
              <given-names>PS</given-names>
            </name>
            <name>
              <surname>Harnett</surname>
              <given-names>JD</given-names>
            </name>
            <name>
              <surname>Kent</surname>
              <given-names>GM</given-names>
            </name>
            <name>
              <surname>Murray</surname>
              <given-names>DC</given-names>
            </name>
            <name>
              <surname>Barr&#233;</surname>
              <given-names>PE</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B33">
        <mixed-citation>33.  arberato SH, Pecoits Filho R. Valor progn&#243;stico do &#237;ndice do volume  do &#225;trio esquerdo em pacientes em hemodi&#225;lise. Arq Bras Cardiol.  2007;88(6):643-50.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Valor progn&#243;stico do &#237;ndice do volume do &#225;trio esquerdo em pacientes em hemodi&#225;lise</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>2007</year>
          </date>
          <fpage>643</fpage>
          <lpage>50</lpage>
          <issue>6</issue>
          <volume>88</volume>
          <person-group person-group-type="author">
            <name>
              <surname>arberato</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Pecoits Filho</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B34">
        <mixed-citation>34.  Johnson TV, Symanski JD, Patel SR, Rose GA. Improvement in the assessment of diastolic  function in a clinical echocardiography laboratory following implementation of  a quality improvement initiative. J Am Soc Echocardiogr. 2011;24(11):1169-79.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Improvement in the assessment of diastolic function in a clinical echocardiography laboratory following implementation of a quality improvement initiative</article-title>
          <source>J Am Soc Echocardiogr</source>
          <date>
            <year>2011</year>
          </date>
          <fpage>1169</fpage>
          <lpage>79</lpage>
          <issue>11</issue>
          <volume>24</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Johnson</surname>
              <given-names>TV</given-names>
            </name>
            <name>
              <surname>Symanski</surname>
              <given-names>JD</given-names>
            </name>
            <name>
              <surname>Patel</surname>
              <given-names>SR</given-names>
            </name>
            <name>
              <surname>Rose</surname>
              <given-names>GA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B35">
        <mixed-citation>35.  Rakhit DJ, Zhang XH, Leano R, Armstrong KA, Isbel NM, Marwick TH. Prognostic role  of subclinical left ventricular abnormalities and impact of transplantation in  chronic kidney disease. Am Heart J. 2007;153(4):656-64.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Prognostic role of subclinical left ventricular abnormalities and impact of transplantation in chronic kidney disease</article-title>
          <source>Am Heart J</source>
          <date>
            <year>2007</year>
          </date>
          <fpage>656</fpage>
          <lpage>64</lpage>
          <issue>4</issue>
          <volume>153</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Rakhit</surname>
              <given-names>DJ</given-names>
            </name>
            <name>
              <surname>Zhang</surname>
              <given-names>XH</given-names>
            </name>
            <name>
              <surname>Leano</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Armstrong</surname>
              <given-names>KA</given-names>
            </name>
            <name>
              <surname>Isbel</surname>
              <given-names>NM</given-names>
            </name>
            <name>
              <surname>Marwick</surname>
              <given-names>TH</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B36">
        <mixed-citation>36.  Salgueira M, Milan JA, Moreno Alba R, Amor J, Arest&#233; N, Jim&#233;nez  E, et al. [Cardiac failure and diastolic disfunction in hemodialysis patients:  associated factors]. Nefrologia. 2005;25(6):668-77.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>[Cardiac failure and diastolic disfunction in hemodialysis patients: associated factors]</article-title>
          <source>Nefrologia</source>
          <date>
            <year>2005</year>
          </date>
          <fpage>668</fpage>
          <lpage>77</lpage>
          <issue>6</issue>
          <volume>25</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Salgueira</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Milan</surname>
              <given-names>JA</given-names>
            </name>
            <name>
              <surname>Moreno Alba</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Amor</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Arest&#233;</surname>
              <given-names>N</given-names>
            </name>
            <name>
              <surname>Jim&#233;nez</surname>
              <given-names>E</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B37">
        <mixed-citation>37.  Barberato SH, Bucharles SG, Sousa AM, Costantini CO, Costantini CR, Pecoits-Filho  R. Preval&#234;ncia e impacto progn&#243;stico da disfun&#231;&#227;o diast&#243;lica  na doen&#231;a renal cr&#244;nica em hemodi&#225;lise. Arq Bras Cardiol.  2010;94(4):457-62.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Preval&#234;ncia e impacto progn&#243;stico da disfun&#231;&#227;o diast&#243;lica na doen&#231;a renal cr&#244;nica em hemodi&#225;lise</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>2010</year>
          </date>
          <fpage>457</fpage>
          <lpage>62</lpage>
          <issue>4</issue>
          <volume>94</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Barberato</surname>
              <given-names>SH</given-names>
            </name>
            <name>
              <surname>Bucharles</surname>
              <given-names>SG</given-names>
            </name>
            <name>
              <surname>Sousa</surname>
              <given-names>AM</given-names>
            </name>
            <name>
              <surname>Costantini</surname>
              <given-names>CO</given-names>
            </name>
            <name>
              <surname>Costantini</surname>
              <given-names>CR</given-names>
            </name>
            <name>
              <surname>Pecoits-Filho</surname>
              <given-names>R</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B38">
        <mixed-citation>38.  Manes MT, Gagliardi M, Misuraca G, Rossi S, Chiatto M. [Left ventricular geometric  patterns and cardiac function in patients with chronic renal failure undergoing  hemodialysis]. Monaldi Arch Chest Dis. 2005;64(1):27-32.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>[Left ventricular geometric patterns and cardiac function in patients with chronic renal failure undergoing hemodialysis]</article-title>
          <source>Monaldi Arch Chest Dis</source>
          <date>
            <year>2005</year>
          </date>
          <fpage>27</fpage>
          <lpage>32</lpage>
          <issue>1</issue>
          <volume>64</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Manes</surname>
              <given-names>MT</given-names>
            </name>
            <name>
              <surname>Gagliardi</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Misuraca</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Rossi</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Chiatto</surname>
              <given-names>M</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B39">
        <mixed-citation>39.  Herzog CA, Asinger RW, Berger AK, Charytan DM, D&#237;ez J, Hart RG, et al.  Cardiovascular disease in chronic kidney disease. A clinical update from Kidney  Disease: Improving Global Outcomes (KDIGO). Kidney Int. 2011;80(6):572-86.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Cardiovascular disease in chronic kidney disease: A clinical update from Kidney Disease: Improving Global Outcomes (KDIGO)</article-title>
          <source>Kidney Int</source>
          <date>
            <year>2011</year>
          </date>
          <fpage>572</fpage>
          <lpage>86</lpage>
          <issue>6</issue>
          <volume>80</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Herzog</surname>
              <given-names>CA</given-names>
            </name>
            <name>
              <surname>Asinger</surname>
              <given-names>RW</given-names>
            </name>
            <name>
              <surname>Berger</surname>
              <given-names>AK</given-names>
            </name>
            <name>
              <surname>Charytan</surname>
              <given-names>DM</given-names>
            </name>
            <name>
              <surname>D&#237;ez</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Hart</surname>
              <given-names>RG</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B40">
        <mixed-citation>40.  Zaslavsky LM, Pinotti AF, Gross JL. Diastolic dysfunction and mortality in diabetic  patients on hemodialysis: a 4.25-year controlled prospective study. J Diabetes  Complications. 2005;19(4):194-200.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Diastolic dysfunction and mortality in diabetic patients on hemodialysis: a 4.25-year controlled prospective study</article-title>
          <source>J Diabetes Complications</source>
          <date>
            <year>2005</year>
          </date>
          <fpage>194</fpage>
          <lpage>200</lpage>
          <issue>4</issue>
          <volume>19</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Zaslavsky</surname>
              <given-names>LM</given-names>
            </name>
            <name>
              <surname>Pinotti</surname>
              <given-names>AF</given-names>
            </name>
            <name>
              <surname>Gross</surname>
              <given-names>JL</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">Echocardiographic parameters as cardiovascular event predictors in hemodialysis patients</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>BACKGROUND: Patients with chronic kidney disease (CKD) on hemodialysis have high rates of cardiovascular morbidity and mortality. Although structural and functional echocardiographic alterations in patients undergoing hemodialysis have been the subject of several survival analysis studies, the prognostic value of these alterations is not well established in literature. OBJECTIVE: To determine the prognostic value of echocardiographic parameters in patients with CKD on hemodialysis. METHODS: Sixty consecutive patients with CKD on hemodialysis were clinically evaluated and underwent Doppler echocardiography, being followed for 19 &#177; 6 months. The outcome measures were fatal and nonfatal cardiovascular events and overall mortality. The predictive value of echocardiographic variables was evaluated by Cox regression model and survival curves were constructed using the Kaplan-Meier method and log rank test to compare them. RESULTS: Rates of survival free of cardiovascular events, of cardiovascular and overall mortality in two years were 79.4%, 88.5% and 83% respectively. Diabetes, previous diagnosis of cardiovascular disease (CVD), ejection fraction, fractional shortening, left ventricular systolic diameter and E/e' ratio were predictors of cardiovascular outcome at univariate analysis. In the multivariate analysis, previous history of CVD (HR = 6.17, 95%CI: 1.7 - 22.2, p = 0.005) and moderate to severe diastolic dysfunction (HR = 3.76, 95%CI: 1.05 - 13.4, p = 0.042) were independent risk factors for cardiovascular events. CONCLUSION: Moderate to severe diastolic dysfunction is an independent predictor of cardiovascular events in hemodialysis patients.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Echocardiography, doppler</kwd>
        <kwd>renal insufficiency, chronic</kwd>
        <kwd>survival analysis</kwd>
        <kwd>dialysis</kwd>
        <kwd>prognosis</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <fn id="top-body2">
          <label>
            <bold>Echocardiographic parameters as cardiovascular event predictors in hemodialysis patients</bold>
          </label>
          <p>
            <bold>Thayse Mayara Arag&#227;o Siqueira<sup>I</sup>; Pedro Ant&#244;nio Muniz Ferreira<sup>I, II</sup>; Francisco das Chagas Monteiro J&#250;nior<sup>I</sup>; Natalino Salgado Filho<sup>I, II</sup>; Adalgisa de Souza Paiva Ferreira<sup>I</sup>; Eug&#234;nio dos Santos Neto<sup>I</sup>; Francival Leite de Souza<sup>I</sup>; Paulo de Tarso Cardoso<sup>I</sup></bold>
          </p>
        </fn>
      </p>
      <p><sup>I</sup>Universidade Federal do Maranh&#227;o, S&#227;o Lu&#237;s, MA - Brazil</p>
      <p><sup>II</sup>Centro de Nefrologia do Maranh&#227;o, S&#227;o Lu&#237;s, MA - Brazil</p>
      <p>Mailing Address</p>
      <p>
        <bold>ABSTRACT</bold>
      </p>
      <p><bold>BACKGROUND:</bold> Patients with chronic kidney disease (CKD) on hemodialysis have high rates of cardiovascular morbidity and mortality. Although structural and functional echocardiographic alterations in patients undergoing hemodialysis have been the subject of several survival analysis studies, the prognostic value of these alterations is not well established in literature.</p>
      <p><bold>OBJECTIVE:</bold> To determine the prognostic value of echocardiographic parameters in patients with CKD on hemodialysis.</p>
      <p><bold>METHODS:</bold> Sixty consecutive patients with CKD on hemodialysis were clinically evaluated and underwent Doppler echocardiography, being followed for 19 &#177; 6 months. The outcome measures were fatal and nonfatal cardiovascular events and overall mortality. The predictive value of echocardiographic variables was evaluated by Cox regression model and survival curves were constructed using the Kaplan-Meier method and log rank test to compare them.</p>
      <p><bold>RESULTS:</bold> Rates of survival free of cardiovascular events, of cardiovascular and overall mortality in two years were 79.4%, 88.5% and 83% respectively. Diabetes, previous diagnosis of cardiovascular disease (CVD), ejection fraction, fractional shortening, left ventricular systolic diameter and E/e' ratio were predictors of cardiovascular outcome at univariate analysis. In the multivariate analysis, previous history of CVD (HR = 6.17, 95%CI: 1.7 - 22.2, p = 0.005) and moderate to severe diastolic dysfunction (HR = 3.76, 95%CI: 1.05 - 13.4, p = 0.042) were independent risk factors for cardiovascular events.</p>
      <p><bold>CONCLUSION:</bold> Moderate to severe diastolic dysfunction is an independent predictor of cardiovascular events in hemodialysis patients.</p>
      <p><bold>Keywords:</bold> Echocardiography, doppler; renal insufficiency, chronic; survival analysis; dialysis; prognosis.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>The annual mortality rates in patients with chronic kidney disease (CKD) undergoing dialysis are high. According to the dialysis census of the USA<sup>1</sup>, the survival of hemodialysis patients in the country was 77.4% in one year and 34.2% in five years, from 1999 to 2003. In Brazil, the annual crude mortality was 17.1% in 2009<sup>2</sup>.</p>
      <p>Cardiovascular diseases (CVD) account for approximately 50% of all deaths in patients undergoing hemodialysis. Moreover, these patients are often hospitalized and CVD account for approximately one third of hospital admissions<sup>3</sup>.</p>
      <p>Structural and functional alterations detected by echocardiography, such as left ventricular (LV) hypertrophy and systolic and diastolic dysfunction, are very prevalent in the hemodialysis population. Doppler echocardiographic diagnosis of these abnormalities has been an important step for the characterization of individuals with higher cardiovascular risk<sup>4,5</sup>.</p>
      <p>Several studies have sought to determine the prognostic value of alterations such as LV hypertrophy and systolic dysfunction in patients undergoing hemodialysis<sup>6-8</sup>. However, studies evaluating the predictive value of diastolic dysfunction in this population are scarce. Thus, the objective of this study was to determine the prognostic value of echocardiographic parameters in patients with CKD undergoing hemodialysis.</p>
      <p>
        <bold>Methods</bold>
      </p>
      <p>
        <bold>Study design and population</bold>
      </p>
      <p>This is an observational, analytical, prospective cohort study, carried out in the Dialysis Service of Centro de Nefrologia do Maranh&#227;o (CENEFRON). We evaluated 60 consecutive patients with CKD undergoing hemodialysis in this service. The hemodialysis sessions of all patients were performed three times a week, and lasted four hours, in volumetric machines (Baxter Tina&#174;, USA; Fresenius 4008S&#174; or Fresenius 4008B&#174;, Germany). The dialysis filters used were Polysulfone, low-flow type (Hemoflow, Fresenius&#174;, Germany), chosen according to the calculation of the patient's body surface.</p>
      <p>Inclusion criteria were patients aged 18 years and older, undergoing hemodialysis for at least three months. Exclusion criteria were: recent history (less than six months) of acute myocardial infarction (AMI), percutaneous or surgical revascularization, unstable angina or cerebrovascular accident (CVA), decompensated congestive heart failure (CHF); severe valvular disease; pulmonary hypertension, blood pressure &gt; 160/110 mmHg, uncontrolled atrial fibrillation or complex ventricular arrhythmia (nonsustained ventricular tachycardia, frequent and polymorphic extrasystoles, in pairs and salvoes), uncontrolled blood sugar levels, malignancies, active infection; irregular dialysis regimen; incapacity to obtain informed consent from the patient and inadequate echocardiographic window.</p>
      <p>Patients were clinically evaluated and underwent a Doppler echocardiography during the period of February to September 2009, with an interval &lt; 30 days between the two procedures. Subsequently, they were regularly followed until May 2011 or until the occurrence of outcome.</p>
      <p>The project was approved by the CENEFRON Research and Ethics Committee in Research of Universidade Federal do Maranh&#227;o. We obtained a signed Free and Informed Consent Form (FICF) from all patients included in the study.</p>
      <p>
        <bold>Doppler echocardiogram</bold>
      </p>
      <p>The echocardiograms were performed on echocardiography equipment, model Vivid 3 Cardiovascular Ultrasound System (GE Healthcare, General Electric Company, USA) with a 3-7 mHz transducer and resources to obtain M-mode, two-dimensional and Doppler echocardiography (pulsed continuous, and tissue). The examinations were performed in the interdialytic period, within 24 hours after the dialysis session by a single medical professional, trained and skilled in echocardiography, with patients at rest and in left lateral decubitus position. Echocardiographic measurements followed the recommendations of the American Society of Echocardiography<sup>9-12</sup> and, for each variable, at least three cycles were analyzed.</p>
      <p>The assessment of LV geometry was obtained by two-dimensional image, with the following variables: end-diastolic septal thickness (EDS), end diastolic posterior wall (EDPW), left ventricular end-diastolic diameter of (LVEDD) and left ventricular end-systolic diameter (LVESD).</p>
      <p>The assessment of LV geometry was obtained by the two-dimensional image, with the following variables: end-diastolic septal thickness (EDST), end-diastolic posterior wall thickness (PWT), left ventricular end-diastolic diameter (LVEDD) and left ventricular end-systolic diameter (LVESD).</p>
      <p>The left ventricular mass (LVM) was calculated using the formula proposed by Devereux et al.<sup>13</sup> and then indexed to body surface area (BSA), to obtain the left ventricular mass index (LVMI = LVM / BSA) . The relative wall thickness (RWT) was obtained by the formula EDT + EDS/LVEDD. The left ventricular ejection fraction (LVEF) was calculated by the method described by Teichholz et al.<sup>14</sup> and the left ventricular systolic fractional shortening by the formula (LVEDD - LVESD)/LVEDD. The left atrial volume (LAV) was determined from the two-dimensional planimetry using the biplane method of Simpson<sup>15</sup> and then indexed to the BSA to obtain the left atrial volume index (LAVi = LAV / BSA).</p>
      <p>Mitral flow was measured in apical four-chamber view by pulsed Doppler. The sample was positioned between the distal ends of the mitral valve leaflets, and then the following variables were obtained: early (E) and late (A) transmitral diastolic velocities, E/A ratio and E-wave deceleration time (EDT). Tissue Doppler was performed in the apical four-chamber view to obtain the velocities of the mitral annulus. The sample was placed at the junction of the LV lateral wall with the mitral annulus<sup>16</sup>, and then early (e') and late (a') diastolic velocities of the mitral annulus were identified, as well as the e'/ a' and E/e' ratios.</p>
      <p>Left ventricular hypertrophy (LVH) was diagnosed when LVMI was &gt; 115 g/m<sup>2</sup> for men and &gt; 95 g/m<sup>2</sup> for women.</p>
      <p>LV geometry was classified according to the values of RWT and LVMI as: concentric hypertrophy (presence of LVH and RWT &gt; 0.42), eccentric hypertrophy (presence of LVH and RWT <underline>&lt;</underline> 0.42), concentric remodeling (absence of LVH and RWT &gt; 0.42) and normal geometry (no LVH and RWT <underline>&lt;</underline> 0.42). We defined left atrial (LA) enlargement in the presence of LAVI &gt; 28 mL/m<sup>2</sup>, while LV dilatation was defined when the LVEDD was &gt; 5.9 cm for men and &gt; 5.3 cm for women<sup>15</sup>.</p>
      <p>Systolic dysfunction was considered when the EF was &lt; 55%<sup>15</sup>. LV diastolic function was classified into four patterns: normal, abnormal relaxation (mild diastolic dysfunction), pseudonormal (moderate diastolic dysfunction) and restrictive (severe diastolic dysfunction). It was considered abnormal relaxation when E / A &lt; 1; restrictive pattern when E/A &gt; 2 and pseudonormal pattern when E/A was &gt; 1 and &lt; 2 in association with E/e' &gt; 10<sup>17</sup>.</p>
      <p>
        <bold>Demographic, clinical and laboratory data</bold>
      </p>
      <p>Demographic and clinical data, including age, sex, history of smoking, comorbidities and duration of dialysis were obtained from detailed analysis of medical records and interviews with the patient and the attending physician, when necessary. Previous cardiovascular event was defined as a history of typical angina or myocardial infarction, ischemic or hemorrhagic CVA and congestive heart failure with functional class &gt; II.</p>
      <p>Before performing each Doppler echocardiogram, blood pressure was measured and anthropometric data and ratios were obtained (weight, height, BSA, body mass index), which were measured according to standard procedures and using suitable materials. The body mass index (BMI) was calculated by dividing weight (kg) by squared height (m), considering malnutrition when &lt; 18.5 kg/m<sup>2</sup>. The BSA was obtained using the formula of Dubois and Dubois<sup>18</sup>.</p>
      <p>All biochemical measurements were performed by a single laboratory, located in CENEFRON, and data were collected from patients' charts.</p>
      <p>
        <bold>Outcomes</bold>
      </p>
      <p>The primary endpoint or cardiovascular outcome included fatal and nonfatal cardiovascular events. Cardiovascular events were defined by angina with coronary stenosis &gt; 50% at coronary angiography, nonfatal AMI, myocardial revascularization procedure, nonfatal ischemic or hemorrhagic CVA, CHF requiring hospitalization and death from cardiovascular causes (including sudden death, AMI and CVA). The secondary outcomes included overall mortality.</p>
      <p>Outcomes were obtained from monthly review of medical documentation, including medical records and death certificates, as well as communication with the physician and patient's relatives. Patients who underwent kidney transplant or who switched dialysis modality were censored in the study.</p>
      <p>
        <bold>Statistical analysis</bold>
      </p>
      <p>Statistical analyzes were performed using the Statistical Package for Social Sciences - SPSS &#174; 17.0 (SPSS Inc, USA). Quantitative variables were expressed as mean with standard deviation or median and categorical variables as percentages.</p>
      <p>For comparison of proportions between groups with and without outcome, we used the Chi-square test and for comparison of quantitative variables, Student's <italic>t</italic> test for independent samples. To estimate the hazard ratios (HR), we performed univariate analysis using Cox proportional hazards model by and then, variables with p &lt; 0.10 were included in the multivariate analysis using the same model. Survival curves were constructed using the Kaplan-Meier method and log rank test was used to compare survival curves in univariate analysis. The significance level was defined as p &lt; 0.05.</p>
      <p>
        <bold>Results</bold>
      </p>
      <p>The study population consisted of 31 (51.7%) men and 29 (49.3%) women, with a mean age of 49.2 &#177; 13.7 years, ranging from 22 to 76 years. The demographic, clinical, biochemical and echocardiographic characteristics of the population are listed in <xref ref-type="table" rid="t1-body2">Table 1</xref>.</p>
      <table-wrap id="t1-body2">
        <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gt01-en.jpg"/></table-wrap>
      <p>The cause of CKD was attributed to hypertensive nephrosclerosis in 30% of cases, to chronic glomerulonephritis in 30%, to diabetic nephropathy in 16.7%, to polycystic kidney disease in 5%, to chronic pyelonephritis in 1.7% and to other diseases in 16.7% of cases.</p>
      <p>Among the individuals included in the study, 25% had a previous diagnosis of CVD: three patients diagnosed with CHF, six with a history of typical angina or acute myocardial infarction and six with a history of CVA.</p>
      <p>The main diagnosed echocardiographic alterations were: left atrial enlargement (49.2%), LV dilatation (20%), LVH (85%), systolic dysfunction (26.7%) and diastolic dysfunction (83.6%).</p>
      <p>According to the degree of diastolic dysfunction, 16.4% of patients had restrictive flow; 20% had pseudonormal pattern and 47.3%, abnormal relaxation. Regarding LV geometry, 68.3% of patients had concentric hypertrophy; 16.7%, eccentric hypertrophy, 8.3% had concentric remodeling and 6.7% had normal geometry.</p>
      <p>The mean follow-up was 19.6 &#177; 6 months and during this period, there were nine deaths and five non-fatal cardiovascular events. CVD accounted for 66.7% of all deaths (three AMI and three CVA), while the other three deaths were attributed to other causes (one due to hypovolemic shock and two due to septic shock). The non-fatal cardiovascular events were: a CVA, two hospitalizations for decompensated CHF and two episodes of angina with coronary stenosis &gt; 50% at coronary angiography.</p>
      <p>The event-free survival rates in one and two years were 91.5% and 79.4%, respectively, for cardiovascular events, 96.5% and 88.5% for cardiovascular mortality and 96.5 % and 83% for overall mortality.</p>
      <p><xref ref-type="fig" rid="en_aop06012f01-body2">Figures 1</xref> and <xref ref-type="fig" rid="en_aop06012f02-body2">2</xref> show the survival curves free of cardiovascular mortality and fatal and nonfatal cardiovascular events, respectively.</p>
      <p content-type="asset">
        <fig id="en_aop06012f01-body2">
          <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gf01-en.jpg"/></fig>
      </p>
      <p content-type="asset">
        <fig id="en_aop06012f02-body2">
          <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gf02-en.jpg"/></fig>
      </p>
      <p><xref ref-type="table" rid="en_aop06012t02-body2">Table 2</xref> shows the comparison of demographic, clinical, biochemical and echocardiographic characteristics between groups with and without cardiovascular events. Patients with cardiovascular outcome had a higher prevalence of diabetes and previous cardiovascular event, higher LVSD and lower values of EF and systolic fractional shortening.</p>
      <p content-type="asset">
        <table-wrap id="en_aop06012t02-body2">
          <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gt02-en.jpg"/></table-wrap>
      </p>
      <p>The univariate Cox model for cardiovascular events is shown in <xref ref-type="table" rid="t3-body2">Table 3</xref>. At univariate analysis, diabetes mellitus, prior history of CVD, LVESD, EF and systolic fractional shortening were significantly associated with cardiovascular outcome. Multivariate analysis included variables: diabetes mellitus, previous cardiovascular event, EF, moderate to severe diastolic dysfunction and E/e' ratio. The variables LVESD and systolic fractional shortening were not included in the regression model because they are variables correlated with EF. In the final regression model, prior diagnosis of CVD and moderate to severe diastolic dysfunction showed to be independent risk factors for fatal and nonfatal cardiovascular events (<xref ref-type="table" rid="t4-body2">Table 4</xref>).</p>
      <table-wrap id="t3-body2">
        <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gt03-en.jpg"/></table-wrap>
      <table-wrap id="t4-body2">
        <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gt04-en.jpg"/></table-wrap>
      <p><xref ref-type="table" rid="en_aop06012t05-body2">Table 5</xref> shows the univariate Cox model for cardiovascular mortality. Only a prior history of CVD was significantly associated with cardiovascular mortality in the univariate analysis. Multivariate analysis was not performed, because when using the variable selection criterion for the multivariate model (p &lt;0.1), only prior CVD and malnutrition would be entered in the final model.</p>
      <p content-type="asset">
        <table-wrap id="en_aop06012t05-body2">
          <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gt05-en.jpg"/></table-wrap>
      </p>
      <p>The rate of survival free of cardiovascular events during follow-up was 87.2% and 55% in the groups with and without history of prior CVD, respectively (p = 0.007). While the rate of survival free of cardiovascular events was 66.4% in patients with moderate to severe diastolic dysfunction, in the group with abnormal relaxation or normal diastolic function it was 87.3% (p = 0.075). <xref ref-type="fig" rid="en_aop06012f03-body2">Figure 3</xref> shows the survival curves free of cardiovascular outcome according with the presence or absence of moderate to severe diastolic dysfunction.</p>
      <p content-type="asset">
        <fig id="en_aop06012f03-body2">
          <graphic xlink:href="1678-4170-abc-99-02-0714-00065-gf03-en.jpg"/></fig>
      </p>
      <p>
        <bold>Discussion</bold>
      </p>
      <p>This study showed free survival rates of overall mortality of 96.5% in one year and 83% in two years. These rates are comparable to those found by Silva et al.<sup>19</sup>, who found survival rates of 91% and 84% in one and two years respectively, in a study carried out in Brazil. Data from dialysis censuses show survival rates of 88.6% in one year and 79.1% in two years in Europe<sup>20</sup> and 77.4% in one year and 63% in two years in the USA<sup>1</sup>. The characteristics of patients included in this study could explain the differences found. We studied patients with more controlled mean blood pressure, which is uncommon in this population. Furthermore, the average EF was preserved in the subjects studied, characterizing a population of more stable patients from the point of view of LV systolic function.</p>
      <p>CVD accounted for 66.7% of all deaths during follow-up. The proportion found is similar to those reported in studies on cardiovascular and overall mortality in hemodialysis patients<sup>6,21</sup>. However, multicenter studies, such as the HEMO and AURORA studies, showed rates of less than 50% of mortality due to heart disease in the dialysis population<sup>22,23</sup>. These results confirm that CVD remain the leading cause of morbidity and mortality in hemodialysis patients. Hemodialysis patients have a 10-20-fold higher risk of cardiovascular mortality compared with the general population<sup>24</sup> and this is due to the fact that individuals are exposed to both traditional as well as non-traditional factors for cardiovascular complications<sup>25</sup>.</p>
      <p>Univariate analysis suggested that traditional risk factors such as diabetes and previous history of CVD are related to a higher risk of cardiovascular events. On the other hand, age, smoking, and hypercholesterolemia were not risk factors for the occurrence of cardiovascular outcome. Although some studies showed a higher prevalence of traditional risk factors in the population with CKD than in the general population<sup>26</sup>, high rates of cardiovascular complications have not been fully explained by such risk factors<sup>24,25</sup>. Additionally, factors known to be non-traditional, such as anemia, malnutrition, inflammatory state, alterations in calcium-phosphorus product, among others, have been implicated as independent factors associated with cardiovascular complications in dialysis patients<sup>27-30</sup>. In the present study, however, these factors did not correlate with an increased risk of cardiovascular morbidity and mortality.</p>
      <p>Evidence indicates that the LV systolic dysfunction parameters are independently associated with the occurrence of fatal and nonfatal cardiovascular events in patients on dialysis, with no difference in predictive power between the methods used to evaluate it<sup>7</sup>. In this study, we observed, at univariate analysis, that reductions in EF or systolic fractional shortening are related to increased risk of cardiovascular events.</p>
      <p>LVH is a strong predictor of cardiovascular morbidity and mortality in hemodialysis patients<sup>31</sup>. LVH was present in 85% of patients in this study, a rate similar to the ones reported by other authors<sup>6,32</sup>. Zoccali et al.<sup>31</sup> showed that increased LVMI in hemodialysis patients was an independent predictor of cardiovascular events, regardless of basal LVM values. In this study, LVMI was not associated with cardiovascular morbidity and mortality. This result can be attributed to more stable characteristics of the patients included in the sample and the follow-up period of this study.</p>
      <p>LAV is a potentially useful parameter to assess diastolic dysfunction and is related to the severity and duration of the dysfunction<sup>5</sup>. In a study of a population on renal replacement therapy, Barberato et al.<sup>33</sup> showed that LAVI was a predictor of mortality. In this study, although LAVI was mildly elevated in both groups, the variable was not an independent predictor of cardiovascular events and cardiovascular mortality. Possible explanations for the lack of association might be: in anemic patients, this index does not reflect diastolic dysfunction<sup>34</sup>; the evaluated patients were not part of a population with chronic kidney disease with significant LV systolic function impairment; and the number of patients was insufficient to find statistically significant differences.</p>
      <p>In the multivariate analysis, previous diagnosis of CVD remained a risk factor for fatal and nonfatal cardiovascular events. Zoccali et al.<sup>7</sup> in a study of 254 hemodialysis patients, Rakhit et al.<sup>35</sup> in a study that included 176 patients with CKD stages 4 and 5 on conservative treatment or dialysis, and Cheung et al.<sup>22</sup> in the HEMO multicenter study, described a similar result in the final model of Cox multivariate analysis.</p>
      <p>The present study demonstrated a high prevalence of diastolic dysfunction in patients with CKD on hemodialysis, corresponding to 83.6%, with 36.4% of patients having moderate to severe diastolic dysfunction. Studies carried out in hemodialysis patients showed that the prevalence of diastolic dysfunction in this population can vary from 63.5% to 87%, depending on the criteria used for definition and patients included in the sample<sup>36-38</sup>.</p>
      <p>Diastolic dysfunction is characterized by alterations in ventricular relaxation and compliance<sup>5</sup> and its high prevalence can be explained by the fact that the CKD expose the heart to pressure and volume overload and associated hemodynamic factors that cause myocardial alterations<sup>39</sup>. Myocardial fibrosis resulting from these processes is a major determinant of LV stiffness and elevated filling pressures, predisposing to the development of diastolic dysfunction<sup>39</sup>.</p>
      <p>The presence of moderate to severe diastolic dysfunction was the only independent echocardiographic predictor of cardiovascular events. A study that employed only parameters derived from mitral inflow and pulmonary venous flow for the categorization of diastolic function showed that diastolic dysfunction is an independent predictor of mortality in patients on renal replacement therapy by hemodialysis<sup>40</sup>.</p>
      <p>In a recently published study, which evaluated 129 hemodialysis patients and the used conventional Doppler and tissue Doppler criteria to classify diastolic dysfunction, Barberato et al.<sup>37</sup> showed that overall mortality was significantly higher in patients with diastolic dysfunction with pseudonormal pattern and restrictive flow, when compared to the group with diastolic dysfunction and abnormal relaxation or normal diastolic function. In this study, advanced diastolic dysfunction was showed to be an independent predictor of cardiovascular events.</p>
      <p>The present study has limitations: the number of patients studied could influence the power of some variables, such as LAVI; duration of follow-up &lt; two years, may have influenced the lack of association between left ventricular function parameters and cardiovascular mortality. The strengths are: the study is prospective and longitudinal; feasible techniques were used for the noninvasive analysis of diastolic function, allowing periodic analysis in patients who have high rates of cardiovascular events.</p>
      <p>
        <bold>Conclusions</bold>
      </p>
      <p>Hemodialysis patients have high rates of cardiovascular morbidity and mortality. The presence of diabetes, previous history of CVD and a lower EF are factors potentially related to cardiovascular events. Moderate to severe diastolic dysfunction was an independent risk factor for cardiovascular events, and although further studies are necessary to validate this finding, it is recommended that diastolic function evaluation, made through pulsed Doppler and tissue Doppler parameters, be included in the evaluation of patients undergoing hemodialysis. This measure will enable the early detection of individuals at risk in order to reduce morbidity and mortality.</p>
      <p>
        <bold>Potential Conflict of Interest</bold>
      </p>
      <p>No potential conflict of interest relevant to this article</p>
      <p>was reported.</p>
      <p>
        <bold>Sources of Funding</bold>
      </p>
      <p>There were no external funding sources for this study.</p>
      <p>
        <bold>Study Association</bold>
      </p>
      <p>This study is not associated with any post-graduation program.</p>
      <p>
        <bold>References</bold>
      </p>
    </body>
  </sub-article>
</article>
