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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">KwwSQDn6szLgDfRrYJ7888d</article-id>
      <article-id pub-id-type="other">00010</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2010000200010</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(10)09400210</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2010005000003</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigos Originais</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Mortalidade global e cardiovascular e fatores de risco de pacientes em hemodi&#225;lise</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Almeida</surname>
            <given-names>F&#225;tima Aparecida A.</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Machado</surname>
            <given-names>Felipe Carrh&#225;</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Moura Junior</surname>
            <given-names>Jos&#233; Andrade</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Guimar&#227;es</surname>
            <given-names>Arm&#234;nio Costa</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="state">Bahia</named-content>
        </addr-line>
        <institution content-type="orgname">Escola Bahiana de Medicina e Sa&#250;de P&#250;blica</institution>
        <country country="BR">Brazil</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>02</month>
        <year>2010</year>
      </pub-date>
      <volume>94</volume>
      <issue>2</issue>
      <fpage>201</fpage>
      <lpage>206</lpage>
      <history>
        <date date-type="accepted">
          <day>15</day>
          <month>05</month>
          <year>2009</year>
        </date>
        <date date-type="rev-recd">
          <day>14</day>
          <month>12</month>
          <year>2008</year>
        </date>
        <date date-type="received">
          <day>20</day>
          <month>08</month>
          <year>2008</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: Mortalidade global e cardiovascular (CV) elevada de pacientes em hemodi&#225;lise. OBJETIVO: Avalia&#231;&#227;o da mortalidade global e CV e identifica&#231;&#227;o do risco de pacientes em hemodi&#225;lise. M&#201;TODOS: Estudo observacional, prospectivo. Estudados 334 pacientes em tr&#234;s anos. Desfechos prim&#225;rios: mortalidade global e CV. Sobrevida avaliada pelo m&#233;todo de Kaplan-Meier. Identifica&#231;&#227;o de vari&#225;veis de risco pela Regress&#227;o de Cox, bi e multivariada. RESULTADOS: Foram estudados 189 (56,6%) homens, idade 48,8 &#177; 14,2 anos, maioria de n&#227;o brancos (295[88,3%]) e com escolaridade de 0 a menor que 8 anos (211[63,2%]). Mortalidade total de 21,6% (72/334), 50% sobrevivendo 146 meses, e mortalidade CV de 41,7%(30/72), 75% sobrevivendo 141 meses. Na an&#225;lise bivariada, o RR de &#243;bito n&#227;o cardiovascular (ONCV) e CV aumentou com Idade &gt;60 anos, Hb &lt; 9,0 g/dl e glicemia de jejum &gt;126 mg/dl; de ONCV apenas, com baixa escolaridade, viuvez, Hb&lt;11,0 g/dl, Ht&lt;33,0%, glicemia de jejum &gt;100 mg/dl, produto Ca x P &lt;42 e creatinina &gt;9,2 mg/dl; diminuiu com PA&gt;140/90 mmHg (antes da sess&#227;o de HD) e Ht&gt;36%; de &#243;bito CV apenas, aumentou com creatinina &gt;9,4 mg/dl. Na an&#225;lise multivariada, o RR de ONCV e CV aumentou com idade &gt;60 anos e Hb&lt;9 g/dl; o RR de &#243;bito CV aumentou com glicemia&gt;126 mg/dl e o de ONCV com taxa de remo&#231;&#227;o de ureia na hemodi&#225;lise (Kt/V) &lt;1,2. CONCLUS&#195;O: A mortalidade global e CV de pacientes em hemodi&#225;lise &#233; elevada. Os fatores de risco independentes para ONCV e CV foram idade &gt;60 anos e Hb&lt;9 g/dl, para &#243;bito CV apenas glicemia &gt;126 mg/dl e ONCV Kt/V&lt;1,2. Vale assinalar a import&#226;ncia do monitoramento na corre&#231;&#227;o e preven&#231;&#227;o desses tr&#234;s &#250;ltimos fatores.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>Mortalidade</kwd>
        <kwd>letalidade</kwd>
        <kwd>di&#225;lise renal</kwd>
        <kwd>fal&#234;ncia renal cr&#244;nica</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>15</day>
        <month>01</month>
        <year>2010</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>ARTIGO ORIGINAL </p>
    <p> EPIDEMOLOGIA</p>
    <p>
      <bold>Mortalidade global e cardiovascular e fatores de risco de pacientes em hemodi&#225;lise</bold>
    </p>
    <p>
      <bold>F&#225;tima Aparecida A. Almeida; Felipe Carrh&#225; Machado; Jos&#233; Andrade Moura Junior; Arm&#234;nio Costa Guimar&#227;es</bold>
    </p>
    <p>Escola Bahiana de Medicina e Sa&#250;de P&#250;blica, BA - Brasil</p>
    <p>
      <xref ref-type="corresp" rid="back">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p><bold>FUNDAMENTO: </bold> Mortalidade global e cardiovascular (CV) elevada de pacientes em hemodi&#225;lise. </p>
    <p><bold>OBJETIVO:</bold> Avalia&#231;&#227;o da mortalidade global e CV e identifica&#231;&#227;o do risco de pacientes em hemodi&#225;lise. </p>
    <p><bold>M&#201;TODOS:</bold> Estudo observacional, prospectivo. Estudados 334 pacientes em tr&#234;s anos. Desfechos prim&#225;rios: mortalidade global e CV. Sobrevida avaliada pelo m&#233;todo de Kaplan-Meier. Identifica&#231;&#227;o de vari&#225;veis de risco pela Regress&#227;o de Cox, bi e multivariada. </p>
    <p><bold>RESULTADOS:</bold> Foram estudados 189 (56,6%) homens, idade 48,8 &#177; 14,2 anos, maioria de n&#227;o brancos (295[88,3%]) e com escolaridade de 0 a menor que 8 anos (211[63,2%]). Mortalidade total de 21,6% (72/334), 50% sobrevivendo 146 meses, e mortalidade CV de 41,7%(30/72), 75% sobrevivendo 141 meses. Na an&#225;lise bivariada, o RR de &#243;bito n&#227;o cardiovascular (ONCV) e CV aumentou com Idade <underline>&gt;</underline>60 anos, Hb <underline>&lt;</underline> 9,0 g/dl e glicemia de jejum <underline>&gt;</underline>126 mg/dl; de ONCV apenas, com baixa escolaridade, viuvez, Hb&lt;11,0 g/dl, Ht&lt;33,0%, glicemia de jejum <underline>&gt;</underline>100 mg/dl, produto Ca x P &lt;42 e creatinina <underline>&gt;</underline>9,2 mg/dl; diminuiu com PA<underline>&gt;</underline>140/90 mmHg (antes da sess&#227;o de HD) e Ht&gt;36%; de &#243;bito CV apenas, aumentou com creatinina <underline>&gt;</underline>9,4 mg/dl. Na an&#225;lise multivariada, o RR de ONCV e CV aumentou com idade <underline>&gt;</underline>60 anos e Hb&lt;9 g/dl; o RR de &#243;bito CV aumentou com glicemia<underline>&gt;</underline>126 mg/dl e o de ONCV com taxa de remo&#231;&#227;o de ureia na hemodi&#225;lise (Kt/V) &lt;1,2. </p>
    <p><bold>CONCLUS&#195;O:</bold> A mortalidade global e CV de pacientes em hemodi&#225;lise &#233; elevada. Os fatores de risco independentes para ONCV e CV foram idade <underline>&gt;</underline>60 anos e Hb&lt;9 g/dl, para &#243;bito CV apenas glicemia <underline>&gt;</underline>126 mg/dl e ONCV Kt/V&lt;1,2. Vale assinalar a import&#226;ncia do monitoramento na corre&#231;&#227;o e preven&#231;&#227;o desses tr&#234;s &#250;ltimos fatores.</p>
    <p><bold>Palavras-chave: </bold> Mortalidade, letalidade/doen&#231;as cardiovasculares, di&#225;lise renal, fal&#234;ncia renal cr&#244;nica.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>A doen&#231;a renal cr&#244;nica &#233; considerada um problema de sa&#250;de p&#250;blica e sua incid&#234;ncia vem aumentando em raz&#227;o do crescimento no n&#250;mero de diab&#233;ticos, hipertensos e do envelhecimento da popula&#231;&#227;o. No Brasil, segundo o Censo de 2006 da Sociedade Brasileira de Nefrologia, havia 70.872 pacientes em tratamento dial&#237;tico, com 64.306 em uso de hemodi&#225;lise<sup>1</sup>. A mortalidade cardiovascular (CV) de pacientes em hemodi&#225;lise costuma ser elevada (40%-50% da popula&#231;&#227;o de renais cr&#244;nicos), sendo 10 a 20 vezes superior &#224; da popula&#231;&#227;o geral<sup>2</sup>. Concorrem para isso os fatores de risco tradicionais e aqueles relacionados &#224; insufici&#234;ncia renal e ao processo de hemodi&#225;lise, como anemia, inflama&#231;&#227;o cr&#244;nica, desnutri&#231;&#227;o, hipertrofia ventricular esquerda, eleva&#231;&#227;o do produto c&#225;lcio e f&#243;sforo e Kt/v baixo<sup>3</sup>.</p>
    <p>Objetivando identificar a incid&#234;ncia com que ocorrem esses eventos em nosso meio e quais os fatores de risco a eles associados, realizou-se um estudo de coorte prospectivo, por tr&#234;s anos, em um Centro de Hemodi&#225;lise, em Salvador, BA.</p>
    <p>
      <bold>M&#233;todos</bold>
    </p>
    <p>Estudo longitudinal, incluindo 334 pacientes, avaliados cl&#237;nica e laboratorialmente, de 4/2/2004 a 31/1/2007. Foram estudados pacientes com idade igual ou superior a 18 anos e que assinaram o TCLE. O estudo incluiu pacientes que j&#225; vinham em hemodi&#225;lise e aqueles que entraram em hemodi&#225;lise ap&#243;s o seu in&#237;cio, tendo, por&#233;m, as curvas de sobrevida, relativas &#224; mortalidade global e CV, sido aferidas a partir da data de in&#237;cio da hemodi&#225;lise, em todos. Os indiv&#237;duos foram submetidos a exame cl&#237;nico, com a press&#227;o arterial aferida antes e durante a sess&#227;o de hemodi&#225;lise, segundo os crit&#233;rios da Sociedade Brasileira de Hipertens&#227;o, utilizando-se esfigmoman&#244;metro aneroide, marca Tycos. A avalia&#231;&#227;o laboratorial de rotina incluiu hemoglobina, hemat&#243;crito, leucograma, ferro s&#233;rico, glicemia, albumina, creatinina, ureia, pot&#225;ssio, produto CaxP e Kt/v (avalia a efici&#234;ncia da hemodi&#225;lise, com base na taxa de remo&#231;&#227;o de ureia, regulando, assim, o volume a ser depurado na sess&#227;o). Al&#233;m disso, 284 pacientes realizaram dosagens de colesterol total (CT), HDL-C e triglicer&#237;deos (TG). O LDL-C foi calculado pela f&#243;rmula de Friedewald [LDL-C = (TC-HDL-C) - (TG/5)] para n&#237;veis de TG menores que 400 mg/dL. Cento e cinquenta e oito pacientes realizaram radiografia do t&#243;rax, em p&#243;stero-anterior e o &#237;ndice cardiotor&#225;cico (ICT) foi considerado alterado se superior a 50%. Em 179 pacientes, foi realizado eletrocardiograma nas 12 deriva&#231;&#245;es, sendo o diagn&#243;stico de hipertrofia ventricular esquerda (HVE) feito segundo os crit&#233;rios de <italic>Sokolow-Lyon</italic> e da Universidade de <italic>Cornell</italic><sup>4</sup>. As vari&#225;veis cont&#237;nuas foram expressas em m&#233;dia &#177; DP ou mediana e intervalo interquart&#237;lico, segundo a normalidade ou assimetria da sua distribui&#231;&#227;o, respectivamente, e as categ&#243;ricas em percentuais. Foram avaliadas a mortalidade global, a mortalidade CV e a mortalidade n&#227;o cardiovascular (NCV). As curvas de sobrevida foram constru&#237;das pelo m&#233;todo de <italic>Kaplan-Meier</italic>. Para a avalia&#231;&#227;o dos fatores de risco relacionados &#224; mortalidade, foram comparados as mortalidades NCV e CV. A an&#225;lise bivariada foi realizada pelo modelo de regress&#227;o de Cox com intervalo de confian&#231;a de 95%. Para o ajuste dos modelos multivariados de COX foi usado o algoritmo <italic>backword,</italic> com inclus&#227;o de vari&#225;veis que na an&#225;lise bivariada apresentaram p&lt;0.15. O banco de dados utilizado foi o EPINFO, vers&#227;o 6, e a an&#225;lise de regress&#227;o de Cox foi feita pelo STATA, vers&#227;o 10. O estudo foi aprovado pelo Comit&#234; de &#201;tica da Funda&#231;&#227;o Bahiana para o Desenvolvimento das Ci&#234;ncias.</p>
    <p>
      <bold>Resultados</bold>
    </p>
    <p>Foram estudados 334 pacientes, com m&#233;dia de idade de 48,8 &#177; 14,2 anos, 189(56,6%) homens, 295(88,8%) pardos e negros e 211(63,2%) com baixa escolaridade, variando de 0 (33) a menos de 8 (178). A <xref ref-type="table" rid="t01">Tabela 1</xref> ilustra dados demogr&#225;ficos, cl&#237;nicos e laboratoriais desses pacientes, segundo a sua condi&#231;&#227;o de vivos ou mortos, ap&#243;s tr&#234;s anos de observa&#231;&#227;o. A m&#233;dia de idade nos &#243;bitos foi significativamente mais elevada (56,9&#177;14,6[23-87] <italic>versus</italic> 46,6 &#177; 14,9[18-88] anos, P&lt;0,001) e houve uma preval&#234;ncia maior de antecedente de infarto agudo do mioc&#225;rdio (7[19,7%] <italic>versus</italic> 3[3,4%], P=0,027). Vivos e mortos n&#227;o diferiram em rela&#231;&#227;o &#224; cor da pele, estado civil, escolaridade e outros antecedentes de risco cardiovascular. O mesmo ocorreu com a press&#227;o arterial e o peso. A avalia&#231;&#227;o laboratorial mostrou, nos &#243;bitos, um maior grau de anemia (9,8 &#177; 2,5 g/dl <italic>versus</italic> 10,7 &#177; 2,1 g/dl, P=0,001 e Ht 30,6 &#177; 6,6% <italic>versus</italic> 32,9 &#177; 7,0%, P=0,001), hiperglicemia (121,5[88,0]mg/dl <italic>versus</italic> 94,0[40,0]mg/dl, P&lt;0,001), menor concentra&#231;&#227;o plasm&#225;tica de creatinina (7,6&#177;4,1 mg/dl <italic>versus</italic> 9,5&#177;3,8 mg/dl, P&lt;0,001) e tend&#234;ncia a uma maior cardiomegalia, nos 158 pacientes em que o RX do t&#243;rax foi realizado (ICT, 57,2[5,9] versus 53,1[9,8], P&lt;0,055).</p>
    <p content-type="asset">
      <table-wrap id="t01">
        <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gt01.jpg"/></table-wrap>
    </p>
    <p>Observa-se, tamb&#233;m, na <xref ref-type="table" rid="t01">Tabela 1</xref>, que a maior parte dos 72 &#243;bitos, 30 (41,7%), ocorreu por causa CV, distribu&#237;da entre causa card&#237;aca, 26/30 (86,7%), a principal, e vascular cerebral, 4/30 (13,3%); seguida de causa infecciosa,16/72 (22,2%). Cerca de um quarto, 20 (27,8%), desses pacientes faleceu por causas classificadas como CID-10, R 68.8 (sintomas relacionados com outras causas).</p>
    <p>A curva de sobrevida em rela&#231;&#227;o ao &#243;bito por todas as causas mostra que 50% dos pacientes sobreviveram 146 meses (12,2 anos) ap&#243;s o in&#237;cio da hemodi&#225;lise (<xref ref-type="fig" rid="f1">Figura 1</xref>), ao passo que, em rela&#231;&#227;o ao &#243;bito CV, 75% sobreviveram cerca de 141 meses (11,7 anos) (<xref ref-type="fig" rid="f2">Figura 2</xref>).</p>
    <fig id="f1">
      <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gf01.jpg"/></fig>
    <fig id="f2">
      <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gf02.jpg"/></fig>
    <p>A compara&#231;&#227;o, por an&#225;lise bivariada, de fatores de risco associados &#224; mortalidade NCV e CV, respectivamente, mostrou que Idade <underline>&gt;</underline> 60 anos, Hb<underline>&lt;</underline>9,0 g/dl e glicemia de jejum <underline>&gt;</underline>126 mg/dl aumentaram significativamente os dois tipos de &#243;bito (<xref ref-type="table" rid="t02">Tabela 2</xref>). O risco de &#243;bito NCV tamb&#233;m aumentou significativamente com escolaridade at&#233; o primeiro grau incompleto, viuvez, Hb&lt;11,0 g/dl, Ht&lt;33%, glicemia de jejum <underline>&gt;</underline>100 mg/dl, produto Ca x P &lt;42, e Kt/V <underline>&lt;</underline>1,2, e diminuiu com PA<underline>&gt;</underline>140/90 mmHg, antes da sess&#227;o de HD, e Ht&gt;36%. Por sua vez, creatinina de <underline>&gt;</underline>9,2 mg/dl aumentou significativamente o risco de &#243;bito NCV e de <underline>&gt;</underline>9,4 mg/dl o de &#243;bito CV, respectivamente. Por&#233;m, no modelo multivariado, composto por estas vari&#225;veis de risco (<xref ref-type="table" rid="t03">Tabela 3</xref>), somente idade <underline>&gt;</underline>60 anos e Hb<underline>&lt;</underline> 9,0 g/dl permaneceram como vari&#225;veis de risco independentes para &#243;bito NCV e CV; glicemia <underline>&gt;</underline>126 mg/dl manteve-se como risco independente para &#243;bito CV e Kt/V <underline>&lt;</underline>1,2 para &#243;bito NCV.</p>
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    <p content-type="asset">
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    <p>
      <bold>Discuss&#227;o</bold>
    </p>
    <p>O elevado obitu&#225;rio por todas as causas e, especificamente, por causa CV est&#225; de acordo com dados da literatura, indicando que a doen&#231;a renal terminal, mesmo na &#233;poca atual do tratamento avan&#231;ado por hemodi&#225;lise cr&#244;nica, constitui condi&#231;&#227;o de alto risco, global e cardiovascular<sup>3</sup>. No particular, a an&#225;lise das curvas de sobrevida indica que a doen&#231;a cardiovascular, al&#233;m da sua mais elevada frequ&#234;ncia, associou-se com um per&#237;odo mais curto de hemodi&#225;lise. Os fatores de risco, os antecedentes cardiovasculares mais frequentes dentre os &#243;bitos e a presen&#231;a de cardiomegalia, como indicado pelo aumento do ICT, s&#227;o sugestivos da gravidade da doen&#231;a vascular nesses pacientes e, certamente, contribu&#237;ram para esse desfecho. Dentre os fatores de risco, destacaram-se, como atuando de modo independente, idade igual ou superior a 60 anos e Hb<underline>&lt;</underline> 9,0 g/dl, tanto para ONCV como CV, hiperglicemia igual ou superior a 126 mg/dl para &#243;bito CV e a taxa de remo&#231;&#227;o da ureia (Kt/V) inferior a 1,2 para ONCV. Ao lado dessas vari&#225;veis, uma s&#233;rie de covari&#225;veis mostrou influ&#234;ncia em rela&#231;&#227;o &#224; mortalidade, embora n&#227;o de modo isolado, mas por uma atua&#231;&#227;o conjunta que, contudo, deve ser valorizada do ponto de vista cl&#237;nico. Nesse contexto est&#227;o viuvez, valores normais da PA, antes da sess&#227;o de hemodi&#225;lise, graus menores de anemia (Hb &gt;9,0 g/dl e &lt;11,0 g/dl), hiperglicemia de jejum entre 100 e 126 mg/dl e valores diminu&#237;dos da fosfatemia. Apesar da sua import&#226;ncia etiopatog&#234;nica, dislipidemia, n&#237;veis mais baixos de albumina s&#233;rica, hiperfosfatemia, hipercalemia e hipertrofia exc&#234;ntrica do VE n&#227;o apareceram como diferencial de risco nessa amostra, o que, evidentemente, n&#227;o minimiza os cuidados preventivos e terap&#234;uticos relativos a esse. Vale salientar a pouca diminui&#231;&#227;o da concentra&#231;&#227;o de albumina s&#233;rica, sem diferen&#231;a significativa entre vivos e &#243;bitos, embora maior nestes &#250;ltimos. Esses n&#237;veis m&#233;dios de albumina iguais ou acima de 3,4 g/dl, nessa popula&#231;&#227;o de pacientes em hemodi&#225;lise, s&#227;o sugestivos do estado nutricional pouco comprometido desses pacientes, contribuindo para uma menor mortalidade.</p>
    <p>Dentre os tr&#234;s fatores de risco independentes, o mais importante, pela sua amplitude de atua&#231;&#227;o patog&#234;nica e possibilidade de controle, &#233; a anemia. Ela constitui, em pacientes com DRT (Doen&#231;a Renal Terminal), o mais frequente e negligenciado fator de risco para &#243;bito por causa NCV e CV, talvez n&#227;o devidamente valorizado por ser comum e n&#227;o estar classificado dentre os tradicionais<sup>3</sup>. Neste estudo, para cada grama de diminui&#231;&#227;o da Hb abaixo de 9,0 g/dl, o RR de morte NCV aumentaria cerca de 2,37 vezes e de morte CV de 3,4 vezes. Mesmo assim, essa condi&#231;&#227;o permanece inadequadamente tratada na fase pr&#233;-dial&#237;tica da doen&#231;a renal<sup>5,6</sup>, agravando-se na fase dial&#237;tica<sup>6</sup>, apesar da dispensa&#231;&#227;o atual pelo SUS de eritropoietina. Vale salientar que, al&#233;m dos efeitos sist&#234;micos da anemia cr&#244;nica, ela &#233; causa importante de hipertrofia exc&#234;ntrica do cora&#231;&#227;o e de fibrose mioc&#225;rdica, fatores condicionantes para o advento de ICC<sup>6,7</sup>, aos quais se associam elevada preval&#234;ncia de hipertens&#227;o (70% dos pacientes neste estudo), inflama&#231;&#227;o cr&#244;nica, resist&#234;ncia a insulina (glicemia de jejum alterada) e diabetes tipo 2<sup>8</sup>, todos fatores concorrentes no processo de aterosclerose<sup>9</sup>. A baixa escolaridade, embora uma quest&#227;o de maior amplitude social e complexa na sua solu&#231;&#227;o em curto e m&#233;dio prazos, deve ser valorizada, pois afeta de modo significativo esse estrato social ao qual pertence a maioria dos pacientes em HD. Um suporte educacional cont&#237;nuo por parte da equipe interdisciplinar, necess&#225;ria ao apoio a esse tipo de programa, pode constituir uma solu&#231;&#227;o vi&#225;vel. A idade, como fator de risco progressivo, na sua caracter&#237;stica biol&#243;gica, est&#225; a indicar a necessidade de um controle mais rigoroso dos m&#250;ltiplos fatores de risco no idoso, presentes nesses pacientes e j&#225; relatados na literatura<sup>3</sup>.</p>
    <p>Quanto &#224;s outras covari&#225;veis de risco identificadas pela an&#225;lise bivariada, merece coment&#225;rio espec&#237;fico a quest&#227;o da PA, com RR diminu&#237;do em 45% se igual ou maior que 140/90 mmHg, antes da sess&#227;o de HD, o aumento do RR com um produto Ca x P &lt;42 e a neutralidade do perfil lip&#237;dico. A presen&#231;a de uma correla&#231;&#227;o do tipo em U entre PA sist&#243;lica (PAS) e mortalidade de pacientes em HD foi relatada por Zager e cols.<sup>10</sup>, indo ao encontro dos dados atuais e mostrando que o n&#237;vel &#243;timo de PAS ainda n&#227;o est&#225; determinado e que merece ser motivo de estudos longitudinais. O risco aumentado de mortalidade global pela diminui&#231;&#227;o do produto Ca x P n&#227;o est&#225; relatado na literatura, mesmo em pacientes que fizeram uso do cloridrato de sevelamer<sup>11-14</sup>, medicamento recente, espec&#237;fico para o controle da hiperfosfatemia. Diante disso, vale registrar o achado, com vistas a uma avalia&#231;&#227;o futura. Uma das limita&#231;&#245;es do estudo foi o fato de iniciarmos os exames complementares (perfil lip&#237;dico, dosagem de magn&#233;sio, ECG e Rx do t&#243;rax) ap&#243;s algum tempo do in&#237;cio da pesquisa, o que fez que alguns pacientes n&#227;o pudessem participar da avalia&#231;&#227;o, por terem falecido ou por se recusarem a fazer os exames. Outra, naturalmente, decorre do car&#225;ter observacional da pesquisa, em que os dados foram obtidos em raz&#227;o do protocolo de rotina do Servi&#231;o e n&#227;o da aplica&#231;&#227;o de um protocolo de pesquisa. Por fim, limita&#231;&#227;o de ordem financeira, que impediu que a avalia&#231;&#227;o das altera&#231;&#245;es card&#237;acas fosse feita, tamb&#233;m, pela ecocardiografia e que n&#227;o tivesse sido determinada a prote&#237;na C reativa de alta sensibilidade, a fim de ser avaliada o grau do processo inflamat&#243;rio que ocorre nesses pacientes.</p>
    <p>
      <bold>Conclus&#245;es</bold>
    </p>
    <p>A mortalidade de pacientes em uso de hemodi&#225;lise, como terapia substitutiva renal, ainda &#233; elevada e a doen&#231;a cardiovascular contribui sobremaneira para essas taxas. Riscos independentes de mortalidade n&#227;o cardiovascular e cardiovascular foram idade <underline>&gt;</underline>60 anos e concentra&#231;&#227;o de Hb <underline>&lt;</underline>9,0 g/dl; glicemia de jejum <underline>&gt;</underline>126 mg/dl foi risco independente de mortalidade cardiovascular e a taxa de remo&#231;&#227;o de ureia durante a hemodi&#225;lise (Kt/V) menor que 1,2 de mortalidade n&#227;o cardiovascular. Vale chamar a aten&#231;&#227;o para a possibilidade de monitoramento, corre&#231;&#227;o e preven&#231;&#227;o desses fatores independentes, modific&#225;veis, de mortalidade.</p>
    <p>
      <bold>Agradecimentos</bold>
    </p>
    <p>A Carlos Teles, pela an&#225;lise estat&#237;stica; e a Gabrielita C. Machado, pela ajuda na revis&#227;o bibliogr&#225;fica.</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 foi financiado por FAPESB.</p>
    <p>
      <bold>Vincula&#231;&#227;o Acad&#234;mica</bold>
    </p>
    <p>Este artigo &#233; parte de tese de Doutorado de F&#225;tima Aparecida Afonso Almeida pela Escola Bahiana de Medicina e Sa&#250;de P&#250;blica.</p>
    <p>
      <fn id="back" fn-type="corresp">
        <p>Correspond&#234;ncia:</p>
        <p> Arm&#234;nio Costa Guimar&#227;es </p>
        <p> Rua Guadalajara, 841/101 - Morro do Gato - Ondina </p>
        <p> 40140-460 - Salvador, BA - Brasil </p>
        <p> E-mail: </p>
        <p><email xlink:href="acosta@cardiol.br">acosta@cardiol.br</email>, </p>
        <p>
          <email xlink:href="armenioguimaraes@terra.com.br">armenioguimaraes@terra.com.br</email>
        </p>
      </fn>
    </p>
    <p>Artigo recebido em 20/08/08; revisado recebido em 14/12/08; aceito em 15/05/09.</p>
  </body>
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            </name>
            <name>
              <surname>Flores</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Kalantar-Zadeh</surname>
              <given-names>K</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">Global and cardiovascular mortality and risk factors in patients under hemodialysis treatment</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>BACKGROUND: There is a high global and cardiovascular mortality rate among patients who need hemodialysis. OBJECTIVE: To assess global and cardiovascular mortality and to identify the risk factors in patients who undergo hemodialysis. METHODS: Observational, prospective study. A total of 334 patients were studied within three years. Primary outcomes: global and cardiovascular mortality. Survival was assessed through Kaplan-Meier method, and the risk variables were identified by means of bivariate and multivariate Cox regression. RESULTS: A total of 189 men (56.6%), aging 48.8 &#177; 14.2, majority non-white (295, 88.3%) and who did finished the elementary school (211, 63.2%). Global mortality rate was 21.6%, with a 50% rate of 146-month survival; cardiovascular mortality rate was 41.7% (30/72), with a 75% rate of 141-month survival. In the bivariate analysis, the relative risk (RR) for non-cardiovascular and cardiovascular death increased when age &gt;60 years old was Hb&lt;9.0 g/dl and fast glycemia &gt;126 mg/dl. Only non-cardiovascular death with low school grade and widow, Hb&lt;11.0 g/dl, Ht&lt;33.0%, fast glycemia&gt;100 mg/dl, Ca product x P&lt;42 and creatinine &gt;9.2 mg/dl decreased with blood pressure (BP) &gt;140/90 mmHg (before hemodialysis session) and Ht&gt;36%; Obit due only to cardiovascular factors increased with creatinine &gt;9.4 mg/dl. In the multivariate analysis, non-cardiovascular and cardiovascular RR increased with age &gt;60 years old and Hb&lt;9 g/dl; cardiovascular death RR increased with glycemia &gt;126 mg/dl, and non-cardiovascular death RR increased with urea removal rate in hemodialysis (Kt/V) &lt;1,2. CONCLUSION: Global and cardiovascular mortality of patients who need hemodialysis is high. Independent risk factors for non cardiovascular and cardiovascular causes of death were age &gt;60 years old and Hb&lt;9 g/dl, for cardiovascular cause of death only, was fasting blood glucose &gt;126 mg/dL, and for non-cardiovascular cause of death, Kt/V&lt;1,2.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Mortality</kwd>
        <kwd>letality</kwd>
        <kwd>renal dialysis</kwd>
        <kwd>kidney failure chronic</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>ORIGINAL ARTICLE</bold>
      </p>
      <p>
        <fn id="top-body2">
          <label>
            <bold>Global and cardiovascular mortality and risk factors in patients under hemodialysis treatment</bold>
          </label>
          <p>
            <bold>F&#225;tima Aparecida A. Almeida; Felipe Carrh&#225; Machado; Jos&#233; Andrade Moura Junior; Arm&#234;nio Costa Guimar&#227;es</bold>
          </p>
        </fn>
      </p>
      <p>Escola Bahiana de Medicina e Sa&#250;de P&#250;blica, BA - Brazil</p>
      <p>Mailing address</p>
      <p>
        <bold>ABSTRACT</bold>
      </p>
      <p><bold>BACKGROUND: </bold> There is a high global and cardiovascular mortality rate among patients who need hemodialysis.</p>
      <p><bold>OBJECTIVE: </bold> To assess global and cardiovascular mortality and to identify the risk factors in patients who undergo hemodialysis.</p>
      <p><bold>METHODS: </bold> Observational. prospective study. A total of 334 patients were studied within three years. Primary outcomes: global and cardiovascular mortality. Survival was assessed through Kaplan-Meier method. and the risk variables were identified by means of bivariate and multivariate Cox regression.</p>
      <p><bold>RESULTS:</bold> A total of 189 men (56.6%). aging 48.8 &#177; 14.2. majority non-white (295. 88.3%) and who did finished the elementary school (211. 63.2%). Global mortality rate was 21.6%. with a 50% rate of 146-month survival; cardiovascular mortality rate was 41.7% (30/72). with a 75% rate of 141-month survival. In the bivariate analysis. the relative risk (RR) for non-cardiovascular and cardiovascular death increased when age <underline>&gt;</underline>60 years old was Hb <underline>&lt;</underline>9.0 g/dL and fast glycemia <underline>&gt;</underline>126 mg/dL. Only non-cardiovascular death with low school grade and widow. Hb&lt;11.0 g/dL. Ht&lt;33.0%. fast glycemia<underline>&gt;</underline>100 mg/dL. Ca product x P&lt;42 and creatinine <underline>&gt;</underline>9.2 mg/dL decreased with blood pressure (BP) <underline>&gt;</underline>140/90 mmHg (before hemodialysis session) and Ht&gt;36%; Obit due only to cardiovascular factors increased with creatinine <underline>&gt;</underline>9.4 mg/dL. In the multivariate analysis. non-cardiovascular and cardiovascular RR increased with age <underline>&gt;</underline>60 years old and Hb&lt;9 g/dL; cardiovascular death RR increased with glycemia <underline>&gt;</underline>126 mg/dL. and non-cardiovascular death RR increased with urea removal rate in hemodialysis (Kt/V) &lt;1.2.</p>
      <p><bold>CONCLUSION:</bold> Global and cardiovascular mortality of patients who need hemodialysis is high. Independent risk factors for non cardiovascular and cardiovascular causes of death were age <underline>&gt;</underline>60 years old and Hb&lt;9 g/dL. for cardiovascular cause of death only. was fasting blood glucose <underline>&gt;</underline>126 mg/dL. and for non-cardiovascular cause of death. Kt/V&lt;1.2.</p>
      <p><bold>Key words:</bold> Mortality; letality/cardiovascular diseases; renal dialysis; kidney failure chronic.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>Chronic kidney disease is considered to be a public health problem, and its incidence has been consequently increasing due to diabetes and hypertension cases and to the ageing of population. In Brazil, according to the 2006 Census of <italic>Sociedade Brasileira de Nefrologia</italic>, there were 70,872 patients under dialysis treatment, with 64,306 under hemodialysis treatment<sup>1</sup>. Cardiovascular mortality among hemodialysis patients is usually elevated (40 to 50% of the population with chronic kidney failure), a rate that is 10 to 20 times higher than in general population<sup>2</sup>. Traditional risk factors, as well as those related to renal insufficiency and to hemodialysis process, such as anemia, chronic inflammation, malnutrition, left ventricle hypertrophy, increase in calcium-phosphorus product and low Kt/v, participate in this rate<sup>3</sup>.</p>
      <p>In order to identify the frequency of such events and the associated risk factors, a cohort prospective study was carried out during three years in a hemodialysis center of Salvador, Bahia, Brazil.</p>
      <p>
        <bold>Methods</bold>
      </p>
      <p>Longitudinal study which included 334 patients submitted to clinical and laboratorial assessment from February 2nd 2004 to January 1st 2007. Patients with 18 years old or more and who signed the informed consent were studied. The study included patients who were already under treatment with hemodialysis and those who started the treatment after that date. However, the survival curves for global and cardiovascular mortality were gauged from the day of the first hemodyalisis session, for all. All patients were submitted to clinical examination, as the blood pressure was checked before and during the hemodialysis session, according the Brazilian Society of Hemodyalisis criteria, by means of an aneroid sphygmomanometer (Tycos<sup>&#174;</sup>). Routine laboratorial assessment included hemoglobin, hematocrit, leucogram, serum iron, glycemia, albumin, creatinine, urea, potassium, Ca x P product and Kt/v (which assesses the efficacy of hemodialysis based on urea emotion rate, as regulating the volume to be cleaned in the session). Moreover, 284 patients took total cholesterol (TC) dosage, HDL cholesterol and triglycerides (TG). LDL cholesterol was calculated through Friedewald formula [LDL-C = (TC-HDL-C) - (TG/5)] for levels of TG lower than 400 mg/dL. A total of 158 patients went through posterior-anterior thoracic radiography, and the cardiothoracic index (CTI) was considered altered when superior to 50%. In 179 patients, electrocardiogram was carried out in the 12 derivations, and left ventricle hypertrophy (LVH) was diagnosed based on Sokolow-Lyon criteria and on Cornell University<sup>4</sup>. Continuum variables were expressed in mean &#177; standard deviation (SD) or median and interquartile interval, according to normality or asymmetry of its distribution, respectively, and the categorical variables were expressed in percentiles. Global, cardiovascular and non-cardiovascular mortality were assessed. Survival curves were built through Kaplan-Meier method. For the evaluation of mortality-related risk factors, non-cardiovascular and cardiovascular mortalities were compared. Bivariate analysis was carried out through Cox regression model, with 95% confidence interval. For the adjustment of Cox multivariate models, the backward algorithm was used, as variables of bivariate analysis which presented p&lt;0.15 were included. Epi-Info version 6 was the utilized database, and Cox regression analysis was made through STATA software, version 10. The study was approved by the Ethics Committee of <italic>Funda&#231;&#227;o Bahiana para o Desenvolvimento das Ci&#234;ncias.</italic></p>
      <p>
        <bold>Results</bold>
      </p>
      <p>A total of 334 patients were assessed, with mean age of 48.8 &#177; 14.2 years old, 189 (56.6%) males, 295 (88.8%) mulattos and black individuals, and 211 (63.2%) with a low education level, including illiterates (33), and those with incomplete first grade (178). <xref ref-type="table" rid="en_10t01-body2">Table 1</xref> shows the patients' demographic, clinical and laboratorial data according to their conditions of alive or dead, after a three-year observation. Death cases were significantly older (56.9&#177;14.6 [23-87] <italic>versus</italic> 46.6&#177;14.9 [18-88] years old, p&lt;0.001), and presented with a higher prevalence of antecedents of acute myocardial infarction (7 [19.7%] <italic>versus</italic> 3 [3.4%], p=0,027).88] years old, p&lt;0.001). The alive and dead people did not differ with regard to skin color, marital status, educational level and other cardiovascular risk antecedents. The same occurred in relation to blood pressure and weight. The laboratorial assessment showed, in obits, a higher anemia grade (9.8 &#177; 2.5 g/dL <italic>versus</italic> 10.7 &#177; 2.1 g/dL, p=0.001 e Ht 30.6 &#177; 6.6% <italic>versus</italic> 32.9 &#177; 7.0%, p=0.001), hyperglycemia (121.5 [88.0] mg/dL <italic>versus</italic> 94.0 [40.0] mg/dL, p&lt;0,001), lower plasmatic creatinine concentration (7.6&#177;4.1 mg/dL <italic>versus</italic> 9.5&#177;3.8 mg/dL, p&lt;0.001) and tendency to higher cardiomegaly in the 158 patients that went through thoracic X-ray (CTI), 57.2 [5.9] <italic>versus</italic> 53.1 [9.8], p&lt;0.055).</p>
      <p content-type="asset">
        <table-wrap id="en_10t01-body2">
          <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gt01-en.jpg"/></table-wrap>
      </p>
      <p>In <xref ref-type="table" rid="en_10t01-body2">Table 1</xref>, it is possible to observe that the majority of the 72 obits (30, 41.7%) occurred due to cardiovascular cause, which is divided into cardiac, 26/30 (86.7%), which is the main one, and cerebral vascular causes, 4/30 (13.3%), followed by infectious cause, 16/72 (22.2%). Approximately a quarter of these patients, 20 (27.8%), died by causes qualified as CID-10, R 68.8 (other causes-related symptoms).</p>
      <p>Survival curve regarding obit by all causes shows that 50% of the patients survive 146 months (12.2 years) after the beginning of hemodialysis treatment (<xref ref-type="fig" rid="f1-body2">Figure 1</xref>), while 75% of the patients survived for approximately 141 months with regard to cardiovascular obits (11.7 years) (<xref ref-type="fig" rid="f2-body2">Figure 2</xref>).</p>
      <fig id="f1-body2">
        <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gf01-en.jpg"/></fig>
      <fig id="f2-body2">
        <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gf02-en.jpg"/></fig>
      <p>The comparison through bivariate analysis of risk factor associated with non-cardiovascular and cardiovascular mortality, respectively, showed that age <underline>&gt;</underline>60 years old, Hb<underline>&lt;</underline>9.0 g/dL and fast glycemia <underline>&gt;</underline>126 mg/dL significantly increased both kind of obits (<xref ref-type="table" rid="en_10t02-body2">Table 2</xref>). Non-cardiovascular obit risk also increased significantly with incomplete first grade school, widowers, Hb&lt;11.0 g/dL, Ht&lt;33%, fast glycemia <underline>&gt;</underline>100 mg/dL, Ca x P product &lt;42 and Kt/V <underline>&lt;</underline>1.2, and decreases with BP<underline>&gt;</underline>140/90 mmHg before hemodialysis session, and Ht&gt;36%. Creatinine <underline>&gt;</underline>9.2 mg/dL, on the other hand, significantly increased non-cardiovascular obit risk, while <underline>&gt;</underline>9.4 mg/dL increased cardiovascular obit risk, respectively. Therefore, in multivariate model, in which these risk variables are comprised (<xref ref-type="table" rid="en_10t03-body2">Table 3</xref>), only age <underline>&gt;</underline>60 years and Hb<underline>&lt;</underline>9.0 g/dL remained as independent risk variables for non-cardiovascular and cardiovascular obit; glycemia <underline>&gt;</underline>126 mg/dL remained as independent risk for cardiovascular obit and Kt/V<underline>&lt;</underline>1,2 as independent risk for non-cardiovascular obit.</p>
      <p content-type="asset">
        <table-wrap id="en_10t02-body2">
          <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gt02-en.jpg"/></table-wrap>
      </p>
      <p content-type="asset">
        <table-wrap id="en_10t03-body2">
          <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gt03-en.jpg"/></table-wrap>
      </p>
      <p>
        <bold>Discussion</bold>
      </p>
      <p>The numerous obit occurrences by all causes, specifically by cardiovascular cause, is in compliance with literature data, indicating that chronic kidney failure, even at the period of advanced chronic hemodialysis treatment, is a high risk condition for global and cardiovascular obit<sup>3</sup>. In private, the analysis of the survival curves indicates that the cardiovascular disease, besides its elevated frequency, was associated with a shorter period of hemodialysis treatment. The risk factors, the frequent cardiovascular antecedents among obit cases and the presence of cardiomegaly, as indicated by increase in CTI, are suggestive of severity of vascular disease in these patients and, certainly, contributed to this outcome. Among risk factors, the emphasis in given the following variables as independent factors: age equal or superior to 60 years old and Hb<underline>&lt;</underline> 9,0 g/dL for non-cardiovascular as much as cardiovascular risk, hyperglycemia equal or superior to 126 mg/dL for cardiovascular obit and urea removal rate (Kt/V) inferior to 1.2 for non-cardiovascular obit. Along with these variables, a series of co-variables showed to be influent with regard to mortality, although not in an isolate way, but by a conjunct action that, however, must be considered from the clinical point of view. This context comprises widowers, normal blood pressure values before hemodialysis session, lower grades of anemia (Hb &gt;9.0 g/dL and &lt;11.0 g/dL), fast hyperglycemia between 100 and 126 mg/dL and reduced phosphatemia values. Despite their ethiopathogenic importance, dislipidemia, lower serum albumin levels, hyperphosphatemia, hyperkalemia and eccentric left ventricle hypertrophy are nor presented as a differential risk in this sample, which evidently does not reduce the related preventive and therapeutic care. It is worth to emphasize the small reduction of serum albumin concentration that did not present a significant difference between life and death cases, though it was higher in the latter. These median albumin levels equal or superior to 3.4 g/dL, in these hemodialysis patients, are suggestive of a jeopardized nutritional status, which may contribute to a low mortality rate.</p>
      <p>Among the three mentioned independent risk factors, the most important one, due to its pathogenic actuation amplitude and control possibility, is anemia. In patients with end stage renal disease, it represents the most frequent and neglected risk factor for non-cardiovascular and cardiovascular obit, which may not be adequately valorized because it is common and is not placed among traditional ones<sup>3</sup>. In the present paper, for each diminution Hb gram inferior to 9.0 g/dL, the relative risk for non-cardiovascular obit would increase in approximately 2.37 times, and for cardiovascular obit, in 3.4 times. Still, this condition remains inadequately treated during predialysis phase of renal disease<sup>5,6</sup>, with aggravation in dialysis phase<sup>6</sup>, despite the current availability of erythropoietin by SUS. It is important to point out that, beside the systemic effects of chronic anemia, it is an important cause of eccentric hypertrophy of the heart and of myocardial fibrosis, factors that may lead to congestive heart failure<sup>6,7</sup>, to which an elevate prevalence for hypertension is related (70% of the patients in this study), chronic inflammation, insulin resistance (altered fast glycemia) and type 2 diabetes<sup>8</sup>, all factors that contribute to the atherosclerosis process<sup>9</sup>. Though low educational level is a matter of social amplitude and complex in its short and medium-term solution, it must be taken into account, for it affects significantly the portion of the society that comprises the majority of the patients in hemodialysis treatment. A continuum educational support offered by the interdisciplinary team, which is necessary for supporting this type of program, may constitute a feasible solution. Age, as a progressive risk factor and in its biological characteristics, indicates the necessity of a more rigorous control of the multiple risk factors present in the elderly and already mentioned in the literature<sup>3</sup>.</p>
      <p>With regard to the other risk co-variables identified by the bivariate analysis, the matters of blood pressure with reduced relative risk in 45% when equal to or higher than 140/90 mmHg before hemodialysis session, as well as the increase of relative risk with Ca x P product &lt;42 and lipidic profile neutrality deserve a specific comment. The presence of a U correlation between systolic blood pressure (SBP) and mortality of patients under hemodialysis treatment was reported by Zager et al<sup>10</sup>, which is in compliance with current data and shows that the optimum level for SBP is not yet determined, and should be motif for longitudinal studies. The increased risk of global mortality by the reduced Ca x P product is not reported in the literature, even in patients that were given sevelamer chloride<sup>11-14</sup>, a current medication that is specific for hyperphophatemia control. Face to that, the findings should be registered for the purpose of future assessment. One of the limitations of this study was the fact that the complementary examinatios (lipidic profile, magnesium dosage, echocardiogram and thoracic X-ray) were initiated a period after the beginning of the research, which kept some patients from participating in the evaluation due to obit or refusal to go through the examinations. Another limitation, naturally, comes from the observational characteristics of the research, as data were obtained by means of the routine protocol of the institution, and not of the applicability of a research protocol. At last, a financial limitation did not allow cardiac alterations to be also assessed by echocardiography, and the high sensibility C-reactive protein to be determined in order to assess the grade of the inflammatory process that happens in these patients.</p>
      <p>
        <bold>Conclusions</bold>
      </p>
      <p>The mortality of patients under hemodialysis treatment as substitutive renal therapy is still elevated, and cardiovascular disease strongly contributes for such rates. Independent non-cardiovascular and cardiovascular mortality risks were: age <underline>&gt;</underline>60 years old and Hb <underline>&lt;</underline>9.0 g/dL; fast glycemia <underline>&gt;</underline>126 mg/dL was an independent cardiovascular mortality risk and urea removal rate during hemodialysis (Kt/V) lower than 1.2 of non-cardiovascular mortality. It is important to emphasize the possibility of monitoring, correction and prevention of such independent, modifiable mortality factors.</p>
      <p>
        <bold>Acknowledgments</bold>
      </p>
      <p>The authors would like to thank Carlos Teles for the statistical analysis and Gabrielita C. Machado for the help in the bibliographical review.</p>
      <p>
        <bold>Potential Conflict of Interest</bold>
      </p>
      <p>No potential conflict of interest relevant to this article was reported.</p>
      <p>
        <bold>Sources of Funding</bold>
      </p>
      <p>This study was funded by FAPESB.</p>
      <p>
        <bold>Study Association</bold>
      </p>
      <p>This article is part of the thesis of doctoral submitted by F&#225;tima Aparecida Afonso Almeida, from Escola Bahiana de Medicina e Sa&#250;de P&#250;blica.</p>
      <p>
        <bold>References</bold>
      </p>
    </body>
  </sub-article>
  <sub-article article-type="translation" id="TRes" xml:lang="es">
    <front-stub>
      <article-categories/>
      <title-group>
        <article-title xml:lang="es">Mortalidad global y cardiovascular y factores de riesgo de pacientes en hemodi&#225;lisis</article-title>
      </title-group>
      <abstract xml:lang="es">
        <p>FUNDAMENTO: Mortalidad global y cardiovascular (CV) elevada de pacientes en hemodi&#225;lisis OBJETIVO: Evaluaci&#243;n de la mortalidad global y CV e identificaci&#243;n del riesgo de paciente en hemodi&#225;lisis. M&#201;TODOS: Estudio observacional, prospectivo. Estudiados 334 pacientes en tres a&#241;os. Desenlaces primarios: mortalidad global y CV. Sobrevida evaluada por el m&#233;todo de Kaplan-Meier. Identificaci&#243;n de variables de riesgo por la Regresi&#243;n de Cox, bi y multivariada. RESULTADOS: Se estudiaron 189 (56,6%) hombres, edad 48,8 &#177; 14,2 a&#241;os, mayor&#237;a no blancos (295[88,3%]) y con escolaridad de 0 a menor que 8 a&#241;os (211[63,2%]). Mortalidad total de 21,6% (72/334), 50% sobreviviendo 146 meses, y mortalidad CV de 41,7% (30/72), 75% sobreviviendo 141 meses. En el an&#225;lisis bivariado, el RR de &#243;bito no cardiovascular (ONCV) y CV aument&#243; con edad &gt; 60 a&#241;os, Hb &lt; 9,0 g/dl y glucemia en ayunas &gt; 126 mg/dl; s&#243;lo de ONCV, con baja escolaridad, viudez, Hb &lt; 11,0 g/dl, Ht &lt; 33,0%, glucemia en ayunas &gt; 100 mg/dl, producto Ca x P &lt; 42 y creatinina &gt; 9,2 mg/dl; disminuy&#243; con PA &gt; 140/90 mmHg (antes de la sesi&#243;n de HD) y Ht &gt; 36%; de &#243;bito CV solamente, aument&#243; con creatinina &gt; 9,4 mg/dl. En el an&#225;lisis multivariado, el RR de ONCV y CV aumento con edad &gt; 60 a&#241;os y Hb &lt; 9 g/dl; el RR de &#243;bito CV aument&#243; con glucemia &gt; 126 mg/dl y el de ONCV con tasa de remoci&#243;n de urea en la hemodi&#225;lisis (Kt/V) &lt; 1,2. CONCLUSI&#211;N: La mortalidad global y CV de pacientes en hemodi&#225;lisis es elevada. Los factores de riesgo independientes para ONCV y CV fueron edad &gt; 60 a&#241;os y Hb &lt; 9 g/dl, para &#243;bito CV s&#243;lo glicemia &gt; 126 mg/dl y ONCV Kt/V &lt; 1,2. Cabe se&#241;alar la importancia del monitoreo en la correcci&#243;n y prevenci&#243;n de estos tres &#250;ltimos factores.</p>
      </abstract>
      <kwd-group xml:lang="es">
        <kwd>Mortalidad</kwd>
        <kwd>letalidad</kwd>
        <kwd>di&#225;lisis renal</kwd>
        <kwd>falla renal cr&#243;nica</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>ART&#205;CULO ORIGINAL</bold>
      </p>
      <p>
        <fn id="top-body3">
          <label>
            <bold>Mortalidad global y cardiovascular y factores de riesgo de pacientes en hemodi&#225;lisis</bold>
          </label>
          <p>
            <bold>F&#225;tima Aparecida A. Almeida; Felipe Carrh&#225; Machado; Jos&#233; Andrade Moura Junior; Arm&#234;nio Costa Guimar&#227;es</bold>
          </p>
        </fn>
      </p>
      <p>Escola Bahiana de Medicina e Sa&#250;de P&#250;blica, BA - Brasil</p>
      <p>Correspondencia</p>
      <p>
        <bold>RESUMEN</bold>
      </p>
      <p><bold>FUNDAMENTO: </bold> Mortalidad global y cardiovascular (CV) elevada de pacientes en hemodi&#225;lisis</p>
      <p><bold>OBJETIVO: </bold> Evaluaci&#243;n de la mortalidad global y CV e identificaci&#243;n del riesgo de paciente en hemodi&#225;lisis.</p>
      <p><bold>M&#201;TODOS: </bold> Estudio observacional, prospectivo. Estudiados 334 pacientes en tres a&#241;os. Desenlaces primarios: mortalidad global y CV. Sobrevida evaluada por el m&#233;todo de Kaplan-Meier. Identificaci&#243;n de variables de riesgo por la Regresi&#243;n de Cox, bi y multivariada.</p>
      <p><bold>RESULTADOS: </bold> Se estudiaron 189 (56,6%) hombres, edad 48,8 &#177; 14,2 a&#241;os, mayor&#237;a no blancos (295[88,3%]) y con escolaridad de 0 a menor que 8 a&#241;os (211[63,2%]). Mortalidad total de 21,6% (72/334), 50% sobreviviendo 146 meses, y mortalidad CV de 41,7% (30/72), 75% sobreviviendo 141 meses. En el an&#225;lisis bivariado, el RR de &#243;bito no cardiovascular (ONCV) y CV aument&#243; con edad <underline>&gt;</underline> 60 a&#241;os, Hb <underline>&lt;</underline> 9,0 g/dl y glucemia en ayunas <underline>&gt;</underline> 126 mg/dl; s&#243;lo de ONCV, con baja escolaridad, viudez, Hb &lt; 11,0 g/dl, Ht &lt; 33,0%, glucemia en ayunas <underline>&gt;</underline> 100 mg/dl, producto Ca x P &lt; 42 y creatinina <underline>&gt;</underline> 9,2 mg/dl; disminuy&#243; con PA <underline>&gt;</underline> 140/90 mmHg (antes de la sesi&#243;n de HD) y Ht &gt; 36%; de &#243;bito CV solamente, aument&#243; con creatinina <underline>&gt;</underline> 9,4 mg/dl. En el an&#225;lisis multivariado, el RR de ONCV y CV aumento con edad <underline>&gt;</underline> 60 a&#241;os y Hb &lt; 9 g/dl; el RR de &#243;bito CV aument&#243; con glucemia <underline>&gt;</underline> 126 mg/dl y el de ONCV con tasa de remoci&#243;n de urea en la hemodi&#225;lisis (Kt/V) &lt; 1,2.</p>
      <p><bold>CONCLUSI&#211;N: </bold> La mortalidad global y CV de pacientes en hemodi&#225;lisis es elevada. Los factores de riesgo independientes para ONCV y CV fueron edad <underline>&gt;</underline> 60 a&#241;os y Hb &lt; 9 g/dl, para &#243;bito CV s&#243;lo glicemia <underline>&gt;</underline> 126 mg/dl y ONCV Kt/V &lt; 1,2. Cabe se&#241;alar la importancia del monitoreo en la correcci&#243;n y prevenci&#243;n de estos tres &#250;ltimos factores.</p>
      <p><bold>Palabras clave: </bold> Mortalidad, letalidad/enfermedades cardiovasculares, di&#225;lisis renal, falla renal cr&#243;nica.</p>
      <p>
        <bold>Introducci&#243;n</bold>
      </p>
      <p>La enfermedad renal cr&#243;nica est&#225; considerada un problema de salud p&#250;blica y su incidencia viene aumentando en raz&#243;n el crecimiento en el n&#250;mero de diab&#233;ticos, hipertensos y del envejecimiento de la poblaci&#243;n. En Brasil, de acuerdo con el Censo de 2006 de la Sociedad Brasile&#241;a de Nefrolog&#237;a, hab&#237;a 70.872 pacientes en tratamiento dial&#237;tico, con 64.306 en uso de hemodi&#225;lisis<sup>1</sup>. La mortalidad cardiovascular (CV) de pacientes en hemodi&#225;lisis suele ser elevada (40%-50% de la poblaci&#243;n de renales cr&#243;nicos), siendo de 10 a 20 veces superior al de la poblaci&#243;n en general<sup>2</sup>. Contribuyen para ello los factores de riesgo tradicionales y aquellos relacionados a la insuficiencia renal y al proceso de hemodi&#225;lisis, como anemia, inflamaci&#243;n cr&#243;nica, desnutrici&#243;n, hipertrofia ventricular izquierda, elevaci&#243;n del producto calcio y f&#243;sforo y Kt/v bajo.</p>
      <p>Buscando identificar la incidencia con que ocurren estos eventos en nuestro medio y cu&#225;les son los factores de riesgo asociados a &#233;stos, se realiz&#243; un estudio de cohorte prospectivo, por tres a&#241;os, en un Centro de Hemodi&#225;lisis, en Salvador, BA.</p>
      <p>
        <bold>M&#233;todos</bold>
      </p>
      <p>Estudio longitudinal, incluyendo 334 pacientes, evaluados cl&#237;nica y laboratorialmente, del 4/2/2004 al 31/1/2007. Se estudiaron pacientes con edad igual o superior a 18 a&#241;os y que firmaron el TCLI. El estudio incluy&#243; pacientes que ya ven&#237;an en hemodi&#225;lisis y aquellos que entraron en hemodi&#225;lisis despu&#233;s de su inicio, siendo, sin embargo, las curvas de sobrevida, relativas a la mortalidad global y CV, calculadas a partir de la fecha de inicio de la hemodi&#225;lisis, en todos. Los individuos fueron sometidos a examen cl&#237;nico, midiendo la presi&#243;n arterial antes y durante la sesi&#243;n de hemodi&#225;lisis, seg&#250;n los criterios de la Sociedad Brasile&#241;a de Hipertensi&#243;n, utilizando esfigmoman&#243;metro aneroide, marca Tycos. La evaluaci&#243;n de laboratorio de rutina incluy&#243; hemoglobina, hematocrito, leucograma, hierro s&#233;rico, glucemia, alb&#250;mina, creatinina, urea, potasio, producto CaxP y Kt/v (eval&#250;a la eficiencia de la hemodi&#225;lisis, con base en la tasa de remoci&#243;n de urea, regulando as&#237; el volumen a ser depurado en la sesi&#243;n). Adem&#225;s de ello, 284 pacientes realizaron an&#225;lisis de colesterol total (CT), HDL-C y triglic&#233;ridos (TG). El LDL-C se calcul&#243; por la f&#243;rmula de Friedewald [LDL-C = (TC-HDL-C) - (TG/5)] para niveles de TG menores que 400 mg/dl. Se realiz&#243; radiograf&#237;a de t&#243;rax en postero-anterior, en 158 pacientes, y el &#237;ndice cardiotor&#225;cico (ICT) se consider&#243; alterado cuando era superior al 50%. En 179 pacientes se realiz&#243; electrocardiograma en las 12 derivaciones, realiz&#225;ndose el diagn&#243;stico de hipertrofia ventricular izquierda (HVI) seg&#250;n los criterios de <italic>Sokolow--Lyon</italic> y de la Universidad de <italic>Cornell</italic><sup>4</sup>. Las variables continuas se expresaron en promedio &#177; SD o mediana e intervalo intercuart&#237;lico, seg&#250;n la normalidad o asimetr&#237;a de su distribuci&#243;n, respectivamente, y las categ&#243;ricas en porcentajes. Se evaluaron la mortalidad global, la mortalidad CV y la mortalidad no cardiovascular (NCV). Las curvas de sobrevida se construyeron por el m&#233;todo de <italic>Kaplan-Meier.</italic> Para la evaluaci&#243;n de los factores de riesgo relacionados con la mortalidad, se compararon las mortalidades NCV y CV. El an&#225;lisis bivariado se realiz&#243; por el modelo de regresi&#243;n de Cox con intervalo de confianza del 95%. Para el ajuste de los modelos multivariados de COX se us&#243; el algoritmo <italic>backword,</italic> con inclusi&#243;n de variables que en el an&#225;lisis bivariado presentaron p &lt; 0,15. El banco de datos utilizado fue el EPINFO, versi&#243;n 6, y el an&#225;lisis de regresi&#243;n de Cox se realiz&#243; por el STATA, versi&#243;n 10. El estudio fue aprobado por el Comit&#233; de &#201;tica de la Fundaci&#243;n Bahiana para el Desarrollo de las Ciencias.</p>
      <p>
        <bold>Resultados</bold>
      </p>
      <p>Se estudiaron 334 pacientes, con promedio de edades de 48,8 &#177; 14,2 a&#241;os, 189 (56,6%) hombres, 295 (88,8%) pardos y negros y 211 (63,2%) con baja escolaridad, variando de 0 (33) a menos de 8 (178). La <xref ref-type="table" rid="es_10t01-body3">Tabla 1</xref> ilustra datos demogr&#225;ficos, cl&#237;nicos y anal&#237;ticos de estos pacientes, seg&#250;n su condici&#243;n de vivos o muertos, despu&#233;s de tres a&#241;os de observaci&#243;n. El promedio de edad en los &#243;bitos fue significativamente m&#225;s elevada (56,9 &#177; 14,6[23-87] <italic>versus</italic> 46,6 &#177; 14,9[18-88] a&#241;os, P &lt; 0,001) y hubo una prevalencia mayor de antecedente de infarto agudo de miocardio (7[19,7%] <italic>versus</italic> 3[3,4%], P = 0,027). Vivos o muertos no difirieron con relaci&#243;n al color de la piel, estado civil, escolaridad y otros antecedentes de riesgo cardiovascular. Lo mismo sucedi&#243; con la presi&#243;n arterial y el peso. La evaluaci&#243;n de laboratorio mostr&#243;, en los &#243;bitos, un mayor grado de anemia (9,8 &#177; 2,5 g/dl <italic>versus</italic> 10,7 &#177; 2,1 g/dl, P = 0,001 y Ht 30,6 &#177; 6,6% <italic>versus</italic> 32,9 &#177; 7,0%, P = 0,001), hiperglucemia (121,5[88,0]mg/dl <italic>versus</italic> 94,0[40,0]mg/dl, P &lt; 0,001), menor concentraci&#243;n plasm&#225;tica de creatinina (7,6 &#177; 4,1 mg/dl <italic>versus</italic> 9,5 &#177; 3,8 mg/dl, P &lt; 0,001) y tendencia a una mayor cardiomegalia, en los 158 pacientes en que se realiz&#243; el RX de t&#243;rax (ICT, 57,2[5,9] <italic>versus</italic> 53,1[9,8], P &lt; 0,055).</p>
      <p content-type="asset">
        <table-wrap id="es_10t01-body3">
          <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gt01-es.jpg"/></table-wrap>
      </p>
      <p>Se observa tambi&#233;n en la <xref ref-type="table" rid="es_10t01-body3">Tabla 1</xref>, que la mayor parte de los 72 &#243;bitos, 30 (41,7%), ocurri&#243; por causa CV, distribuida entre causa card&#237;aca, 26/30 (86,7%), la principal, y vascular cerebral, 4/30 (13,3%); seguida de causa infecciosa,16/72 (22,2%). Cerca de un cuarto, 20 (27,8%), de esos pacientes falleci&#243; por causas clasificadas como CIE-10, R 68.8 (s&#237;ntomas relacionados con otras causas).</p>
      <p>La curva de sobrevida con relaci&#243;n al &#243;bito por todas las causas muestra que el 50% de los pacientes sobrevivieron 146 (12,2 a&#241;os) despu&#233;s del inicio de la hemodi&#225;lisis (<xref ref-type="fig" rid="f1-body3">Figura 1</xref>), al paso que, con relaci&#243;n al &#243;bito CV, el 75% sobrevivi&#243; cerca de 141 meses (11,7 a&#241;os) (<xref ref-type="fig" rid="f2-body3">Figura 2</xref>).</p>
      <fig id="f1-body3">
        <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gf01-es.jpg"/></fig>
      <fig id="f2-body3">
        <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gf02-es.jpg"/></fig>
      <p>La comparaci&#243;n, por an&#225;lisis bivariado, de factores de riesgo asociados a la mortalidad NCV y CV, respectivamente, mostr&#243; que edad <underline>&gt;</underline> 60 a&#241;os, Hb <underline>&lt;</underline> 9,0 g/dl y glucemia en ayunas <underline>&gt;</underline> 126 mg/dl aumentaron significativamente los dos tipos de &#243;bito (<xref ref-type="table" rid="t2-body3">Tabla 2</xref>). El riesgo de &#243;bito NCV tambi&#233;n aument&#243; significativamente con escolaridad hasta el primer grado incompleto, viudez, Hb &lt; 11,0 g/dl, Ht &lt; 33%, glucemia en ayunas <underline>&gt;</underline> 100 mg/dl, producto Ca x P &lt; 42, y Kt/V <underline>&lt;</underline> 1,2, y disminuy&#243; con PA <underline>&gt;</underline> 140/90 mmHg, antes de la sesi&#243;n de HD, y Ht &gt; 36%. A su vez, creatinina <underline>&gt;</underline> 9,2 mg/dl aument&#243; significativamente el riesgo de &#243;bito NCV y <underline>&gt;</underline> 9,4 mg/dl el de &#243;bito CV, respectivamente Sin embargo, en el modelo multivariado, compuesto por estas variables de riesgo (<xref ref-type="table" rid="t3-body3">Tabla 3</xref>), s&#243;lo edad <underline>&gt;</underline> 60 a&#241;os y Hb <underline>&lt;</underline> 9,0 g/dl permanecieron como variables de riesgo independientes para &#243;bito NCV y CV; glucemia <underline>&gt;</underline> 126 mg/dl se mantuvo como riesgo independiente para &#243;bito CV y Kt/V <underline>&lt;</underline> 1,2 para &#243;bito NCV</p>
      <table-wrap id="t2-body3">
        <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gt02-es.jpg"/></table-wrap>
      <table-wrap id="t3-body3">
        <graphic xlink:href="1678-4170-abc-94-02-0201-00003-gt03-es.jpg"/></table-wrap>
      <p>
        <bold>Discusi&#243;n</bold>
      </p>
      <p>El elevado obituario por todas las causas y, espec&#237;ficamente, por causa CV est&#225; de acuerdo con los datos de la bibliograf&#237;a, indicando que la enfermedad renal terminal, aun en la &#233;poca actual del tratamiento avanzado por hemodi&#225;lisis cr&#243;nica, constituye condici&#243;n de alto riesgo, global y cardiovascular<sup>3</sup>. En particular, el an&#225;lisis de las curvas de sobrevida indica que la enfermedad cardiovascular, adem&#225;s de su m&#225;s elevada frecuencia, se asoci&#243; con un per&#237;odo m&#225;s corto de hemodi&#225;lisis. Los factores de riesgo, los antecedentes cardiovasculares m&#225;s frecuentes entre los &#243;bitos y la presencia de cardiomegalia, como lo indica el aumento del ICT, sugieren la gravedad de la enfermedad vascular en estos pacientes y, ciertamente, contribuyeron para este desenlace. Entre los factores de riesgo, se destacaron, como actuando de modo independiente, edad igual o superior a 60 a&#241;os y Hb <underline>&lt;</underline> 9,0 g/dl, tanto para ONCV como CV, hiperglicemia igual o superior a 126 mg/dl para &#243;bito CV y la tasa de remoci&#243;n de urea (Kt/V) inferior a 1,2 para ONCV. Al lado de esas variables, una serie de covariables mostr&#243; influencia en relaci&#243;n a la mortalidad, aunque no de modo aislado, pero por una actuaci&#243;n conjunta que, con todo, debe ser valorizada desde el punto de vista cl&#237;nico. En este contexto est&#225;n: viudez, valores normales de la PA, antes de la sesi&#243;n de hemodi&#225;lisis, grados menores de anemia (Hb &gt; 9,0 g/dl y &lt; 11,0 g/dl), hiperglucemia en ayunas entre 100 y 126 mg/dl y valores disminuidos de la fosfatemia. A pesar de su importancia etiopatog&#233;nica, dislipidemia, niveles m&#225;s bajos de alb&#250;mina s&#233;rica, hiperfosfatemia, hipercalemia e hipertrofia exc&#233;ntrica del VI no aparecen como diferencial de riesgo en esta muestra, lo que evidentemente no minimiza los cuidados preventivos y terap&#233;uticos relativos a &#233;ste. Vale destacar la poca disminuci&#243;n de la concentraci&#243;n de alb&#250;mina s&#233;rica, sin diferencia significativa entre vivos y &#243;bitos, aunque es mayor en estos &#250;ltimos. Esos niveles medios de alb&#250;mina iguales o por encima de 3,4 g/dl, en esa poblaci&#243;n de pacientes en hemodi&#225;lisis, sugieren un estado nutricional poco comprometido de estos pacientes, contribuyendo para una menor mortalidad.</p>
      <p>Entre los tres factores de riesgo independientes, el m&#225;s importante, por su amplitud de actuaci&#243;n patog&#233;nica y posibilidad de control, es la anemia. &#201;sta constituye, pacientes con ERT (Enfermedad Renal Terminal), el m&#225;s frecuente y descuidado factor de riesgo para &#243;bito por causa NCV y CV, tal vez no debidamente valorizado por ser com&#250;n y no estar clasificado entre los tradicionales<sup>3</sup>. En este estudio, para cada gramo de disminuci&#243;n de la Hb por debajo de 9,0 g/dl, el RR de muerte NCV aumentar&#237;a cerca de 2,37 veces y de muerte CV de 3,4 veces. Aun as&#237;, esta condici&#243;n permanece inadecuadamente tratada en la fase predial&#237;tica de la enfermedad renal<sup>5,6</sup>, agrav&#225;ndose en la fase dial&#237;tica<sup>6</sup>, a pesar de la entrega actual por el Sistema &#218;nico de Salud de eritropoietina. Cabe destacar que, adem&#225;s de los efectos sist&#233;micos de la anemia cr&#243;nica, &#233;sta es causa importante de hipertrofia exc&#233;ntrica del coraz&#243;n y de fibrosis mioc&#225;rdica, factores condicionantes para el advenimiento de ICC<sup>6,7</sup>, a los cuales se asocian elevada prevalencia de hipertensi&#243;n (70% de los pacientes en este estudio), inflamaci&#243;n cr&#243;nica, resistencia a insulina (glucemia en ayunas alterada) y diabetes tipo 2<sup>8</sup>, todos factores contribuyentes al proceso de aterosclerosis<sup>9</sup>. La baja escolaridad, aunque es una cuesti&#243;n de mayor amplitud social y compleja en su soluci&#243;n en el corto y medio plazo, debe ser valorizada, pues afecta de modo significativo este estrato social al cual pertenece la mayor&#237;a de los pacientes en HD. Un soporte educacional continuo por parte del equipo interdisciplinario, necesario al apoyo a este tipo de programa, puede constituir una soluci&#243;n viable. La edad, como factor de riesgo progresivo, en su caracter&#237;stica biol&#243;gica, indicar&#225; la necesidad de un control m&#225;s riguroso de los m&#250;ltiples factores de riesgo en el adulto mayor, presentes en estos pacientes y ya relatados en la bibliograf&#237;a<sup>3</sup>.</p>
      <p>En cuanto a las otras covariables de riesgo identificadas por el an&#225;lisis bivariado, merece comentario espec&#237;fico la cuesti&#243;n de la PA, como RR disminuido en el 45% si era igual o mayor que 140/90 mmHg, antes de la sesi&#243;n de HD, el aumento del RR con un producto Ca x P &lt; 42 y la neutralidad del perfil lip&#237;dico. La presencia de una correlaci&#243;n del tipo U entre PA sist&#243;lica (PAS) y mortalidad de pacientes en HD fue relatada por Zager et al<sup>10</sup>, concordando con los datos actuales y mostrando que el nivel &#243;ptimo de PAS todav&#237;a no est&#225; determinado y que merece ser motivo de estudios longitudinales. El riesgo aumentado de mortalidad global por la disminuci&#243;n del producto Ca x P no est&#225; relatado en la bibliograf&#237;a, aun en pacientes que hicieron uso del clorhidrato de sevelamer<sup>11-14</sup>, medicamento reciente, espec&#237;fico para el control de la hiperfosfatemia. Frente a esto, vale registrar el hallazgo, con miras a una evaluaci&#243;n futura. Una de las limitaciones del estudio fue el hecho de iniciar los ex&#225;menes complementarios (perfil lip&#237;dico, determinaci&#243;n de magnesio, ECG y Rx de t&#243;rax) despu&#233;s de alg&#250;n tiempo de inicio de la investigaci&#243;n, lo que hizo que algunos pacientes no pudieran participar en la evaluaci&#243;n, por haber fallecido o por negarse a hacer los ex&#225;menes. Otra, naturalmente, deriva del car&#225;cter observacional de la investigaci&#243;n, en que los datos se obtuvieron en raz&#243;n del protocolo de rutina del Servicio y no de la aplicaci&#243;n de un protocolo de investigaci&#243;n. Por fin, limitaci&#243;n de orden financiero, que impidi&#243; que se realizara la evaluaci&#243;n de las alteraciones card&#237;acas, tambi&#233;n por ecocardiograma y que no se haya determinado la prote&#237;na C reactiva de alta sensibilidad, a fin de evaluar el grado del proceso inflamatorio que ocurre en estos pacientes.</p>
      <p>
        <bold>Conclusiones</bold>
      </p>
      <p>La mortalidad de pacientes en uso de hemodi&#225;lisis, como terapia sustitutiva renal, todav&#237;a es elevada y la enfermedad cardiovascular contribuye de sobremanera para esas tasas. Riesgos independientes de mortalidad no cardiovascular y cardiovascular fueron edad <underline>&gt;</underline> 60 a&#241;os y concentraci&#243;n de Hb <underline>&lt;</underline> 9,0 g/dl; glucemia en ayunas <underline>&gt;</underline> 126 mg/dl fue riesgo independiente de mortalidad cardiovascular y la tasa de remoci&#243;n de urea durante la hemodi&#225;lisis (Kt/V) menor que 1,2 de mortalidad no cardiovascular. Vale llamar la atenci&#243;n para la posibilidad de monitoreo, correcci&#243;n y prevenci&#243;n de estos factores independientes, modificables, de mortalidad.</p>
      <p>
        <bold>Agradecimientos</bold>
      </p>
      <p>A Carlos Teles, por el an&#225;lisis estad&#237;stico, y a Gabrielita C. Machado, por la ayuda en la revisi&#243;n bibliogr&#225;fica.</p>
      <p>
        <bold>Potencial Conflicto de Intereses</bold>
      </p>
      <p>Declaro no haber conflicto de intereses pertinentes.</p>
      <p>
        <bold>Fuentes de Financiaci&#243;n</bold>
      </p>
      <p>El presente estudio fue financiado por FAPESB.</p>
      <p>
        <bold>Vinculaci&#243;n Acad&#233;mica</bold>
      </p>
      <p>Este art&#237;culo forma parte de la tesis de doctorado de F&#225;tima Aparecida Afonso Almeida de la Escuela Bahiana de Medicina y Salud P&#250;blica.</p>
      <p>
        <bold>Referencias</bold>
      </p>
    </body>
  </sub-article>
</article>
