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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">f6qfTvNPNTWSXnTYVQszRLs</article-id>
      <article-id pub-id-type="other">00004</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2004001000004</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(04)08200004</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2004001000004</article-id>
      <title-group>
        <article-title>IV Diretrizes Brasileiras de Hipertens&#227;o Arterial</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="COORD">
          <name>
            <surname>Mion Jr.</surname>
            <given-names>D&#233;cio</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Gomes</surname>
            <given-names>Marco Ant&#244;nio Mota</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Nobre</surname>
            <given-names>Fernando</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Amodeo</surname>
            <given-names>Celso</given-names>
          </name>
          <xref ref-type="aff" rid="aff03"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Kohlmann Jr.</surname>
            <given-names>Osvaldo</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Praxedes</surname>
            <given-names>Jos&#233; Nery</given-names>
          </name>
          <xref ref-type="aff" rid="aff03"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Machado</surname>
            <given-names>Carlos Alberto</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Machado</surname>
            <given-names>Carlos Alberto</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Pascoal</surname>
            <given-names>Ist&#234;nio</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Magalh&#227;es</surname>
            <given-names>Luc&#233;lia C.</given-names>
          </name>
        </contrib>
      </contrib-group>
      <aff id="aff03">
        <institution content-type="orgname">Sociedade Brasileira de Nefrologia</institution>
      </aff>
      <aff id="aff01">
        <institution content-type="orgname">Sociedade Brasileira de Hipertens&#227;o</institution>
      </aff>
      <aff id="aff02">
        <institution content-type="orgname">Sociedade Brasileira de Cardiologia</institution>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>03</month>
        <year>2004</year>
      </pub-date>
      <volume>82</volume>
      <issue>suppl 4</issue>
      <fpage>7</fpage>
      <lpage>14</lpage>
      <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>
      <pub-date publication-format="electronic" date-type="pub">
        <day>22</day>
        <month>04</month>
        <year>2004</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>
      <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-e01.jpg"/></p>
    <p>
      <bold>IV Diretrizes Brasileiras de Hipertens&#227;o Arterial</bold>
    </p>
    <p>Realiza&#231;&#227;o </p>
    <p>Sociedade Brasileira de Hipertens&#227;o &#150; SBH </p>
    <p>Sociedade Brasileira de Cardiologia &#150; SBC </p>
    <p>Sociedade Brasileira de Nefrologia &#150; SBN </p>
    <p>Sociedades Patrocinadoras </p>
    <p>Academia Brasileira de Neurologia &#150; ABN </p>
    <p>Associa&#231;&#227;o Brasileira para o Estudo da Obesidade &#150; ABESO </p>
    <p>Federa&#231;&#227;o Brasileira das Sociedades de Ginecologia e Obstetr&#237;cia &#150; FEBRASGO </p>
    <p>Sociedade Brasileira de Cl&#237;nica M&#233;dica &#150; SBCM </p>
    <p>Sociedade Brasileira de Diabetes &#150; SBD </p>
    <p>Sociedade Brasileira de Endocrinologia e Metabologia &#150; SBEM </p>
    <p>Sociedade Brasileira de Geriatria e Gerontologia &#150; SBGG </p>
    <p>Comiss&#227;o Organizadora </p>
    <p>D&#233;cio Mion Jr. (Coordenador) </p>
    <p> Marco Ant&#244;nio Mota Gomes (SBC) </p>
    <p>Fernando Nobre (SBH) </p>
    <p> Celso Amodeo (SBN) </p>
    <p>Osvaldo Kohlmann Jr. (SBH) </p>
    <p> Jos&#233; Nery Praxedes (SBN) </p>
    <p>Carlos Alberto Machado (SBC)</p>
    <p>Comiss&#227;o de Reda&#231;&#227;o </p>
    <p>Carlos Alberto Machado </p>
    <p> Celso Amodeo </p>
    <p>D&#233;cio Mion Jr. </p>
    <p> Fernando Nobre </p>
    <p>Ist&#234;nio Pascoal </p>
    <p> Jos&#233; Nery Praxedes </p>
    <p>Luc&#233;lia C. Magalh&#227;es </p>
    <p> Marco Ant&#244;nio Mota Gomes </p>
    <p>Osvaldo Kohlmann Jr.</p>
    <p>Apoio </p>
    <p>AstraZeneca do Brasil Ltda. </p>
    <p> Aventis Pharma Ltda. </p>
    <p>Bayer S.A. </p>
    <p> Biolab Farmac&#234;utica Ltda. </p>
    <p>Boehringer Ingelheim do Brasil Qu&#237;m. e Farm. Ltda. </p>
    <p> Farmalab Ind. Qu&#237;micas e Farmac&#234;uticas Ltda. </p>
    <p>Laborat&#243;rios Biosint&#233;tica </p>
    <p> Laborat&#243;rios Pfizer Ltda. </p>
    <p>Libbs Farmac&#234;utica Ltda. </p>
    <p> Merck Sharp &amp; Dohme Farmac&#234;utica Ltda. </p>
    <p>Novartis Bioci&#234;ncias S.A. </p>
    <p> Sanofi-Synth&#233;labo Ltda. </p>
    <p>Servier do Brasil Ltda.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>A hipertens&#227;o &#233; um dos principais agravos &#224; sa&#250;de no Brasil. Eleva o custo m&#233;dico-social, principalmente pelas suas complica&#231;&#245;es, como as doen&#231;as c&#233;rebro-vascular, arterial coronariana e vascular de extremidades, al&#233;m da insufici&#234;ncia card&#237;aca e da insufici&#234;ncia renal cr&#244;nica.</p>
    <p>Desde 1963, as doen&#231;as cardiovasculares superaram as outras causas de morte, sendo respons&#225;veis atualmente por 27% dos &#243;bitos. Houve aumento do risco de morte por estas doen&#231;as de 1980 a 1984, seguido de queda at&#233; 1996.</p>
    <p>Diferentemente do quadro norte-americano, que mostrou redu&#231;&#227;o de 60% na mortalidade por doen&#231;a c&#233;rebro-vascular e 53% por doen&#231;a arterial coronariana, no Brasil (<xref ref-type="fig" rid="figura1">Figura 1</xref>) a redu&#231;&#227;o verificada foi de 20% e 13%, respectivamente. As tend&#234;ncias de risco de morte por doen&#231;as cardiovasculares s&#227;o diferentes nas diversas regi&#245;es com queda no Sudeste e Sul, aumento no Centro-Oeste e Nordeste e estabilidade no Norte<sup>1</sup> (<bold>B</bold>).</p>
    <fig id="figura1">
      <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gf01.jpg"/></fig>
    <p>Os estudos de preval&#234;ncia s&#227;o poucos e n&#227;o representativos do pa&#237;s. Os inqu&#233;ritos mostrados na <xref ref-type="fig" rid="f2">Figura 2</xref> apontam alta preval&#234;ncia, da ordem de 22% a 44%<sup>2</sup>(<bold>B</bold>) <sup>3-6</sup> (<bold>A</bold>) <sup>7</sup>(<bold>C</bold>). Em fun&#231;&#227;o desta realidade, deve-se estabelecer programas de controle em todo o pa&#237;s.</p>
    <p content-type="asset">
      <fig id="f2">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gf02.jpg"/></fig>
    </p>
    <p>
      <bold>Diagn&#243;stico e Classifica&#231;&#227;o</bold>
    </p>
    <p>O diagn&#243;stico de hipertens&#227;o &#233; estabelecido com medida de press&#227;o realizada com m&#233;todos e condi&#231;&#245;es descritos na <xref ref-type="table" rid="tabela1">Tabela 1</xref>, de acordo com os n&#237;veis tensionais relacionados na <xref ref-type="table" rid="tabela2">Tabela 2</xref>.</p>
    <table-wrap id="tabela1">
      <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt01.jpg"/></table-wrap>
    <table-wrap id="tabela2">
      <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt02.jpg"/></table-wrap>
    <p>
      <bold>Medida da Press&#227;o Arterial<sup>17,19</sup>(D)</bold>
    </p>
    <p>O aparelho de coluna de merc&#250;rio &#233; o mais adequado. O aner&#243;ide deve ser testado a cada seis meses e os eletr&#244;nicos s&#227;o indicados somente quando validados.</p>
    <p>
      <bold>Rotina Diagn&#243;stica (D)</bold>
    </p>
    <p>Realizar no m&#237;nimo duas medidas da press&#227;o por consulta, na posi&#231;&#227;o sentada, e se as diast&#243;licas apresentarem diferen&#231;as acima de 5 mmHg, fazer novas medidas at&#233; se obter menor diferen&#231;a. Na primeira avalia&#231;&#227;o, as medi&#231;&#245;es devem ser obtidas em ambos os membros superiores. Em caso de diferen&#231;a, utilizar sempre o bra&#231;o de maior press&#227;o. Recomenda-se que as medidas sejam repetidas em pelo menos duas ou mais visitas antes de confirmar o diagn&#243;stico de hipertens&#227;o.</p>
    <p>A medida na posi&#231;&#227;o ortost&#225;tica deve ser feita, pelo menos, na avalia&#231;&#227;o inicial, especialmente em idosos, diab&#233;ticos, portadores de disautonomias, dependentes do &#225;lcool e usu&#225;rios de medica&#231;&#227;o antihipertensiva.</p>
    <p>
      <bold>Crit&#233;rios Diagn&#243;sticos, Classifica&#231;&#227;o e </bold>
      <bold>Recomenda&#231;&#245;es para Seguimento<sup>20</sup>(D)</bold>
    </p>
    <p>Qualquer atribui&#231;&#227;o de valor num&#233;rico &#233; arbitr&#225;ria e qualquer classifica&#231;&#227;o insuficiente. Considerar, al&#233;m dos n&#237;veis de press&#227;o, a presen&#231;a de fatores de risco, comorbidades e les&#227;o de &#243;rg&#227;os alvos relacionados na <xref ref-type="table" rid="tabela3">Tabela 3</xref>.</p>
    <table-wrap id="tabela3">
      <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt03.jpg"/></table-wrap>
    <p>Em crian&#231;as e adolescentes, a press&#227;o arterial &#233; classificada de acordo com os percentis de estatura e sexo. Considera-se hipertens&#227;o arterial valores iguais ou acima do percentil 95.</p>
    <p>
      <bold>Investiga&#231;&#227;o Cl&#237;nica e Decis&#227;o Terap&#234;utica</bold>
    </p>
    <p>S&#227;o objetivos da investiga&#231;&#227;o cl&#237;nica confirmar a eleva&#231;&#227;o persistente da press&#227;o arterial, avaliar les&#245;es de &#243;rg&#227;os-alvo, identificar fatores de risco cardiovascular, diagnosticar doen&#231;as associadas e a etiologia da hipertens&#227;o. Para tanto, realiza-se: a) hist&#243;ria cl&#237;nica - considerando, al&#233;m do habitual, sexo, idade, ra&#231;a, condi&#231;&#227;o socioecon&#244;mica, tabagismo, dura&#231;&#227;o da hipertens&#227;o e n&#237;veis de press&#227;o arterial, sobrepeso e obesidade, sintomas de doen&#231;a arterial coronariana, acidente vascular cerebral ou doen&#231;a arterial coronariana na fam&#237;lia (em mulheres &lt; 65 anos e homens &lt; 55 anos), sintomas e sinais de insufici&#234;ncia card&#237;aca, hist&#243;ria familiar de hipertens&#227;o, doen&#231;a vascular encef&#225;lica, morte prematura/s&#250;bita em familiares pr&#243;ximos, insufici&#234;ncia vascular perif&#233;rica, depress&#227;o, ansiedade, p&#226;nico, doen&#231;a renal, situa&#231;&#227;o familiar, diabete melito, ingest&#227;o de sal e &#225;lcool, consumo de medicamentos ou drogas que possam interferir com a press&#227;o arterial, fatores de risco para aterosclerose, pr&#225;tica de atividade f&#237;sica, dislipidemias, perda de peso e ind&#237;cios de hipertens&#227;o secund&#225;ria, que deve ser sempre pesquisada na presen&#231;a das manifesta&#231;&#245;es caracter&#237;sticas; b) exame f&#237;sico - com &#234;nfase para peso e estatura, sopros mitral e a&#243;rtico, circunfer&#234;ncia abdominal, estertores, roncos, sibilos, sinais de hipertens&#227;o secund&#225;ria, massas abdominais (tumores, aneurismas, hidronefrose, rins polic&#237;sticos) medida da press&#227;o arterial, sopros abdominais (renais, aorta), freq&#252;&#234;ncia de pulso, pulsos braquiais, radiais, fumorais, tibiais pediosos e pediosos, palpa&#231;&#227;o e ausculta de car&#243;tidas, presen&#231;a de edema, estase venosa, exame neurol&#243;gico sum&#225;rio, palpa&#231;&#227;o da tire&#243;ide, fundo de olho, ictus sugestivo de hipertrofia ventricular esquerda/dilata&#231;&#227;o do ventr&#237;culo esquerdo, 3&#170; bulha (disfun&#231;&#227;o sist&#243;lica do ventr&#237;culo esquerdo), hiperfonese de A2; c) avalia&#231;&#227;o laboratorial de rotina - an&#225;lise de urina, dosagens de pot&#225;ssio, creatinina, glicemia de jejum, colesterol total, HDL-colesterol, triglic&#233;rides e eletrocardiograma, pode-se calcular o LDL-colesterol quando a dosagem de triglic&#233;rides for abaixo de 400mg/dl pela f&#243;rmula: LDL-colesterol = colesterol total - HDL-colesterol - triglic&#233;rides/5; d) avalia&#231;&#227;o complementar quando h&#225; ind&#237;cios de hipertens&#227;o secund&#225;ria, les&#227;o em &#243;rg&#227;osalvo ou doen&#231;as associadas<sup>21,22</sup>(<bold>D</bold>).</p>
    <p>Para institui&#231;&#227;o do tratamento, deve-se considerar o n&#237;vel press&#243;rico e o risco do paciente de acordo com as <xref ref-type="table" rid="tabela3">Tabelas 3</xref> e <xref ref-type="table" rid="t4">4</xref>.</p>
    <p content-type="asset">
      <table-wrap id="t4">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt04.jpg"/></table-wrap>
    </p>
    <p>
      <bold>Abordagem Multiprofissional</bold>
    </p>
    <p>Por ser a hipertens&#227;o arterial multifatorial e envolver orienta&#231;&#245;es voltadas para v&#225;rios objetivos, poder&#225; requerer o apoio de outros profissionais de sa&#250;de al&#233;m do m&#233;dico. A forma&#231;&#227;o da equipe multiprofissional ir&#225; proporcionar uma a&#231;&#227;o diferenciada aos hipertensos<sup>24</sup>(<bold>A</bold>).</p>
    <p>
      <bold>A Equipe</bold>
    </p>
    <p>Poder&#225; ser formada por m&#233;dicos, enfermeiros, auxiliares de enfermagem, nutricionistas, psic&#243;logos, assistentes sociais, professores de educa&#231;&#227;o f&#237;sica, farmac&#234;uticos, funcion&#225;rios administrativos e agentes comunit&#225;rios. N&#227;o &#233; necess&#225;rio a exist&#234;ncia de todo esse grupo para a forma&#231;&#227;o da equipe.</p>
    <p>
      <bold>A&#231;&#245;es comuns &#224; Equipe</bold>
    </p>
    <p>Visa a promo&#231;&#227;o &#224; sa&#250;de, a&#231;&#245;es educativas com &#234;nfase nas mudan&#231;as do estilo de vida, corre&#231;&#227;o dos fatores de risco e produ&#231;&#227;o de material educativo; treinamento de profissionais; encaminhamento a outros profissionais, quando indicado; a&#231;&#245;es assistenciais individuais e em grupo; participa&#231;&#227;o em projetos de pesquisa; gerenciamento do programa.</p>
    <p>
      <bold>A&#231;&#245;es Individuais</bold>
    </p>
    <p>A&#231;&#245;es pr&#243;prias de cada profissional, por&#233;m haver&#225; momentos em que as fun&#231;&#245;es ser&#227;o comuns e dever&#227;o ocorrer de modo natural com uniformidade de linguagem e conduta.</p>
    <p>
      <bold>Programas Comunit&#225;rios</bold>
    </p>
    <p>A cria&#231;&#227;o de ligas e associa&#231;&#245;es de hipertensos pode aumentar a ades&#227;o e ser instrumento de press&#227;o junto &#224;s autoridades constitu&#237;das visando melhoria na qualidade da assist&#234;ncia aos portadores de hipertens&#227;o arterial.</p>
    <p>
      <bold>Tratamento n&#227;o Medicamentoso</bold>
    </p>
    <p>
      <bold>Medidas de maior Efic&#225;cia</bold>
    </p>
    <p>Redu&#231;&#227;o do peso corporal e manuten&#231;&#227;o do peso ideal - &#237;ndice de massa corp&#243;rea (peso em quilogramas dividido pelo quadrado da altura em metros) entre 20 e 25 kg/m<sup>2</sup> porque existe rela&#231;&#227;o direta entre peso corp&#243;reo e press&#227;o arterial<sup>25</sup>(<bold>A</bold>).</p>
    <p>Redu&#231;&#227;o da ingest&#227;o de s&#243;dio - &#233; saud&#225;vel ingerir at&#233; 6 g/dia de sal correspondente a 4 colheres de caf&#233; rasas de sal, 4g, e 2g de sal presente nos alimentos naturais, reduzindo o sal adicionado aos alimentos, evitando o saleiro &#224; mesa e alimentos industrializados. A dieta habitual cont&#233;m 10 a 12 g/dia de sal<sup>26</sup>(<bold>A</bold>).</p>
    <p>Maior ingest&#227;o de pot&#225;ssio &#150; dieta rica em vegetais e frutas cont&#233;m 2 a 4g de pot&#225;ssio/dia e pode ser &#250;til na redu&#231;&#227;o da press&#227;o e preven&#231;&#227;o da hipertens&#227;o arterial<sup>27</sup>(<bold>A</bold>). Os substitutos do sal contendo cloreto de pot&#225;ssio e menos cloreto de s&#243;dio (30% a 50%) s&#227;o &#250;teis para reduzir a ingest&#227;o de s&#243;dio e aumentar a de pot&#225;ssio.</p>
    <p>Redu&#231;&#227;o do consumo de bebidas alco&#243;licas<sup>28,29</sup> (<bold>D</bold>) <sup>30,31</sup>(<bold>B</bold>) <sup>32</sup>(<bold>A</bold>) - para os consumidores de &#225;lcool, a ingest&#227;o de bebida alco&#243;lica deve ser limitada a 30g &#225;lcool/dia contidas em 600 ml de cerveja (5% de &#225;lcool) ou 250 ml de vinho (12% de &#225;lcool) ou 60ml de destilados (whisky, vodka, aguardente - 50% de &#225;lcool). Este limite deve ser reduzido &#224; metade para homens de baixo peso, mulheres, indiv&#237;duos com sobrepeso e/ou triglic&#233;rides elevados.</p>
    <p>Exerc&#237;cios f&#237;sicos regulares<sup>33</sup>(<bold>A</bold>) <sup>34</sup>(<bold>D</bold>) &#150; h&#225; rela&#231;&#227;o inversa entre grau de atividade f&#237;sica e incid&#234;ncia de hipertens&#227;o; exerc&#237;cio f&#237;sico regular reduz a press&#227;o (<xref ref-type="table" rid="tabela5">Tabela 5</xref>).</p>
    <table-wrap id="tabela5">
      <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt05.jpg"/></table-wrap>
    <p>
      <bold>Medidas sem Avalia&#231;&#227;o Cient&#237;fica Definitiva</bold>
    </p>
    <p>Suplementa&#231;&#227;o de c&#225;lcio<sup>36,37</sup>(<bold>A</bold>), magn&#233;sio<sup>38</sup>(<bold>D</bold>), dietas vegetarianas e medidas antiestresse.</p>
    <p>
      <bold>Medidas Associadas</bold>
    </p>
    <p>Abandono do tabagismo &#150; deve ser recomendado devido a sua associa&#231;&#227;o com maior incid&#234;ncia e mortalidade cardiovascular e aumento da press&#227;o arterial medida ambulatorialmente<sup>39-41</sup>(<bold>B</bold>). A interrup&#231;&#227;o deve ser acompanhada de restri&#231;&#227;o cal&#243;rica e aumento da atividade f&#237;sica para evitar ganho de peso que pode ocorrer. A exposi&#231;&#227;o ao fumo, tabagismo passivo, tamb&#233;m constitui fator de risco cardiovascular que deve ser evitado<sup>42</sup>(<bold>D</bold>).</p>
    <p>Controle do diabete e das dislipidemias &#150; intoler&#226;ncia &#224; glicose e diabete est&#227;o freq&#252;entemente associadas &#224; hipertens&#227;o arterial, favorecendo a ocorr&#234;ncia de doen&#231;as cardiovasculares e complica&#231;&#245;es do diabete<sup>43</sup>(<bold>A</bold>) <sup>44</sup>(<bold>B</bold>). Sua preven&#231;&#227;o tem como base a dieta hipocal&#243;rica, a pr&#225;tica regular de atividades f&#237;sicas aer&#243;bias e a redu&#231;&#227;o de ingest&#227;o de a&#231;&#250;car simples. Estas medidas visam tamb&#233;m a manuten&#231;&#227;o da press&#227;o arterial abaixo de 130/80 mmHg<sup>45</sup>(<bold>D</bold>). Hipercolesterolemia e hipertrigliceridemia, com HDL-colesterol baixo, s&#227;o importantes fatores de risco cardiovascular<sup>45</sup>(<bold>D</bold>). A base do controle das dislipidemias &#233; representada por mudan&#231;as diet&#233;ticas, com redu&#231;&#227;o do consumo de gordura e substitui&#231;&#227;o parcial das gorduras saturadas por gorduras mono e poliinsaturadas e redu&#231;&#227;o da ingest&#227;o di&#225;ria de colesterol<sup>46</sup>(<bold>D</bold>).</p>
    <p>Evitar medicamentos que elevem a press&#227;o arterial<sup>23</sup>(<bold>D</bold>) relacionados na <xref ref-type="table" rid="tabela6">Tabela 6</xref>, onde se encontram as condutas espec&#237;ficas a cada tipo de medicamento.</p>
    <table-wrap id="tabela6">
      <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt06.jpg"/></table-wrap>
    <p>
      <bold>Tratamento Medicamentoso</bold>
    </p>
    <p>Objetivo - Reduzir a morbidade e mortalidade cardiovasculares do hipertenso. O benef&#237;cio &#233; obtido em pacientes tratados com diur&#233;ticos<sup>47</sup>(<bold>A</bold>), betabloqueadores<sup>47</sup>(<bold>D</bold>), inibidores da enzima conversora da angiotensina - ECA<sup>48</sup>(<bold>A</bold>), antagonistas do receptor AT1 da angiotensina II - AII<sup>49</sup>(<bold>D</bold>) e em pacientes mais idosos com antagonistas de canal de c&#225;lcio<sup>48</sup>(<bold>A</bold>), sendo que a maioria dos estudos terminou por utilizar associa&#231;&#227;o de f&#225;rmacos.</p>
    <p>
      <bold>Meta de Redu&#231;&#227;o da Press&#227;o Arterial</bold>
    </p>
    <p>Deve ser, no m&#237;mimo, para valores inferiores a 140/ 90 mmHg<sup>20</sup>(<bold>D</bold>). Redu&#231;&#245;es para n&#237;veis menores que 130/ 85 mmHg propiciam maior benef&#237;cio<sup>20</sup>(<bold>D</bold>) em pacientes de alto risco cardiovascular<sup>43</sup>(<bold>A</bold>), diab&#233;ticos em especial com microalbumin&#250;ria<sup>50</sup>(<bold>A</bold>), com insufici&#234;ncia card&#237;aca, com nefropatia e na preven&#231;&#227;o prim&#225;ria e secund&#225;ria de acidente vascular cerebral<sup>48</sup>(<bold>A</bold>).</p>
    <p>
      <bold>Princ&#237;pios Gerais do Tratamento Medicamentoso (D):</bold>
    </p>
    <disp-quote>
      <p><bold>&#149;</bold> Medicamento deve ser eficaz por via oral, bem tolerado e permitir o menor n&#250;mero poss&#237;vel de tomadas di&#225;rias;</p>
      <p><bold>&#149;</bold> Em pacientes em est&#225;gio 1, iniciar tratamento com as menores doses efetivas;</p>
      <p><bold>&#149;</bold> Em pacientes nos est&#225;gios 2 e 3, considerar o uso associado de anti-hipertensivos para in&#237;cio de tratamento;</p>
      <p><bold>&#149;</bold> Respeitar m&#237;nimo de quatro semanas para aumentar a dose, substituir a monoterapia ou mudar a associa&#231;&#227;o de f&#225;rmacos;</p>
      <p><bold>&#149;</bold> Instruir o paciente sobre a doen&#231;a, planifica&#231;&#227;o e objetivos terap&#234;uticos, necessidade do tratamento continuado e efeitos adversos dos f&#225;rmacos;</p>
      <p><bold>&#149;</bold> Considerar as condi&#231;&#245;es socioecon&#244;micas.</p>
    </disp-quote>
    <p>
      <bold>Esquemas Terap&#234;uticos</bold>
    </p>
    <p>O tratamento deve ser individualizado e procurar conservar a qualidade de vida do paciente. Qualquer grupo de f&#225;rmacos anti-hipertensivos, com exce&#231;&#227;o dos vasodilatadores de a&#231;&#227;o direta e alfa-bloqueadores, &#233; apropriado para o controle da press&#227;o arterial em monoterapia inicial (<xref ref-type="table" rid="t7">Tabela 7</xref>)<sup>23</sup>(<bold>D</bold>). Os agentes anti-hipertensivos dispon&#237;veis no Brasil est&#227;o nas <xref ref-type="table" rid="tabela8">Tabelas 8</xref> e <xref ref-type="table" rid="tabela9">9</xref>.</p>
    <p content-type="asset">
      <table-wrap id="t7">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt07.jpg"/></table-wrap>
    </p>
    <table-wrap id="tabela8">
      <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt08.jpg"/></table-wrap>
    <table-wrap id="tabela9">
      <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt09.jpg"/></table-wrap>
    <p>A clortalidona se mostrou superior a doxazosina como escolha medicamentosa inicial em pacientes hipertensos mais velhos com outros fatores de risco<sup>50</sup>(<bold>D</bold>) <sup>51</sup>(<bold>A</bold>).</p>
    <p>Para o paciente hipertenso com press&#227;o arterial controlada, a associa&#231;&#227;o de baixas doses de &#225;cido acetil salic&#237;lico pode diminuir a ocorr&#234;ncia de complica&#231;&#245;es cardiovasculares<sup>52</sup>(<bold>A</bold>).</p>
    <p>
      <bold>Preven&#231;&#227;o de Hipertens&#227;o e Fatores de Risco Associados</bold>
    </p>
    <p>Combater a hipertens&#227;o &#233; prevenir o aumento da press&#227;o pela redu&#231;&#227;o dos fatores de risco em toda popula&#231;&#227;o e nos grupos de maior risco de desenvolver a doen&#231;a como o normal lim&#237;trofe (130 - 139/80 &#150; 89 mmHg)<sup>35</sup>(<bold>D</bold>) e aqueles com hist&#243;ria familiar de hipertens&#227;o. O aparecimento da hipertens&#227;o &#233; facilitado pelo excesso de peso<sup>53</sup>(<bold>D</bold>), sedentarismo<sup>34</sup>(<bold>D</bold>), elevada ingest&#227;o de sal<sup>26</sup>(<bold>A</bold>), baixa ingest&#227;o de pot&#225;ssio<sup>46</sup>(<bold>D</bold>) e consumo excessivo de &#225;lcool<sup>31</sup>(<bold>B</bold>). No grupo com press&#227;o normal lim&#237;trofe tamb&#233;m contribuem para o aumento do risco cardiovascular as dislipidemias, intoler&#226;ncia &#224; glicose e diabete, tabagismo, menopausa e estresse emocional<sup>54</sup>(<bold>A</bold>).</p>
    <p>As medidas preventivas incluem: manuten&#231;&#227;o do peso ideal<sup>53</sup>(<bold>D</bold>), pr&#225;tica regular de atividade f&#237;sica<sup>35</sup>(<bold>D</bold>), redu&#231;&#227;o da ingest&#227;o de sal e aumento da de pot&#225;ssio<sup>46</sup>(<bold>D</bold>), evitar a ingest&#227;o de bebidas alco&#243;licas<sup>31</sup>(<bold>B</bold>), seguir dieta saud&#225;vel (<xref ref-type="table" rid="tabela10">Tabela 10</xref>) que deve conter baixo teor de gordura, principalmente saturadas, baixo teor de colesterol, elevado teor de pot&#225;ssio e fibras<sup>46</sup>(<bold>D</bold>) e baixo teor de s&#243;dio<sup>26</sup>(<bold>A</bold>). O valor cal&#243;rico total deve ser ajustado para obten&#231;&#227;o e manuten&#231;&#227;o do peso ideal. A observ&#226;ncia global da dieta &#233; mais importante do que o seguimento de medidas isoladas<sup>55</sup>(<bold>B</bold>).</p>
    <table-wrap id="tabela10">
      <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt10.jpg"/></table-wrap>
    <p>
      <bold>Refer&#234;ncias</bold>
    </p>
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    <p>2. Freitas OC, Carvalho FR, Neves JM, et al. Prevalence of hypertension in the urban population of Catanduva, in the State of Sao Paulo, Brazil. Arq Bras Cardiol 2001; 77: 9-21.</p>
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    <p>12. Foster-Fitzpatrick L, Ortiz A, Sibilano H, Marcantonio R, Braun LT. The effects of crossed leg on blood pressure measurement. Nurs Res 1999; 48: 105-8.</p>
    <p>13. Peters GL, Binder SK, Campbell NR. The effect of crossing legs on blood pressure: a randomized single-blind cross-over study. Blood Press Monit 1999; 4: 97-101.</p>
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    <p>17. Perloff D, Grim C, Flack J, Frohlich ED, Hill M, McDonald M, et al. Human blood pressure determination by sphygmomanometry. Circulation 1993; 88: 2460-70.</p>
    <p>18. The sixth report of the Joint National Committee on prevention, detection, evaluation, and treatment of high blood pressure. Arch Intern Med 1997; 157: 2413-46.</p>
    <p>19. McAlister FA, Straus SE. Measurement of blood pressure: an evidence based review. BMJ 2001; 322: 908-11.</p>
    <p>20. 1999 World Health Organization- International Society of Hypertension Guidelines for the Management of Hypertension. Guidelines Subcommittee. J Hypertens 1999; 17: 151-83.</p>
    <p>21. Zarnke KB, Levine M, McAlister FA, Campbell NR, Myers MG, McKay DW, et al. The 2000 Canadian recommendations for the management of hypertension: part two - diagnosis and assessment of people with high blood pressure. Can J Cardiol 2001; 17: 1249-63.</p>
    <p>22. Vagaonescu T, Phillips RA. Initial Routine Tests for Diagnosis and Risk Stratification of the Patient with Hypertension. In: Weber M (editor). Hypertension Medicine. New Jersey: Humana Press; 2001. p.147-55.</p>
    <p>23. III Consenso Brasileiro de Hipertens&#227;o Arterial. Clin Terap 1998; 24: 233-72.</p>
    <p>24. Boulware E, Daumit GL, Frick KD, Minkovitz CS, Lawrence RS, Powe NR. An evidence-based review of patient-centered behavioral interventions for hypertension. Am J Prev Med 2001; 21: 221-32.</p>
    <p>25. The effects of nonpharmacologic interventions on blood pressure of persons with high normal levels. Results of the Trials of Hypertension Prevention, Phase I. JAMA 1992; 267: 1213-20.</p>
    <p>26. Sacks FM, Svetkey LP, Vollmer WM, Appel LJ, Bray GA, Harsha D, et al. Effects on blood pressure of reduced dietary sodium and the Dietary Approaches to Stop Hypertension (DASH) diet. DASH - Sodium Collaborative Research Group. N Engl J Med 2001; 344: 3-10.</p>
    <p>27. Whelton PK, He J, Cutler JA, Brancati FL, Appel LJ, Follmann D, et al. Effects of oral potassium on blood pressure. Meta-analysis of randomized controlled clinical trials. JAMA 1997; 277: 1624-32.</p>
    <p>28. MacMahon S. Alcohol consumption and hypertension. Hypertension 1987; 9: 111-21.</p>
    <p>29. Krauss RM, Eckel RH, Howard B, Appel LJ, Daniels SR, Deckelbaum RJ, et al. AHA Dietary Guidelines: revision 2000: A statement for healthcare professionals from the Nutrition Committee of the American Heart Association. Stroke 2000; 31: 2751-66.</p>
    <p>30. Puddey IB, Beilin LJ, Vandongen R, Rouse IL, Rogers P. Evidence for a direct effect of alcohol consumption on blood pressure in normotensive men. A randomized controlled trial. Hypertension 1985; 7: 707-13.</p>
    <p>31. Puddey IB, Beilin LJ, Vandongen R. Regular alcohol use raises blood pressure in treated hypertensive subjects: a randomized controlled trial. Lancet 1987; 1: 647-51.</p>
    <p>32. Klatsky AL. Armstrong MA, Friedman GD. Risk of cardiovascular mortality in alcohol drinkers, ex-drinkers and nondrinkers. Am J Cardiol 1990; 66: 1237-42.</p>
    <p>33. Berlin JA, Colditz GA. A meta-analysis of physical activity in the prevention of coronary heart disease. Am J Epidemiol 1990; 132: 612-28.</p>
    <p>34. Paffenbarger RS Jr. Contributions of epidemiology to exercise science and cardiovascular health. Med Sci Sports Exerc 1988; 20: 426-38.</p>
    <p>35. American College of Sports Medicine. ACSM's Guidelines for exercise testing and prescription. Baltimore: Williams &amp; Wilkins, 2000.</p>
    <p>36. Griffith LE, Guyatt GH, Cook RJ, Bucher HC, Cook DJ. The influence of dietary and nondietary calcium supplementation on blood pressure: an updated metaanalysis of randomized trials. Am J Hypertens 1999; 12: 84-92.</p>
    <p>37. Allender PS, Cutler JA, Follmann D, Cappuccio FP, Pryer J, Elliott P. Dietary calcium and blood pressure: a meta-analysis of randomized clinical trials. Ann Intern Med 1996; 124: 825-31.</p>
    <p>38. McAlister FA, Levine M, Zarnke KB, Campbell N, Lewanczuk R, Leenen F, et al. The 2000 Canadian recommendations for the management of hypertension. Part one-therapy. Can J Cardiol 2001; 17: 543-59.</p>
    <p>39. Milkkelsen KL, Winberg N, Hoegholm A, Christensen HR, Bang LE, Nielsen PE, et al. Smoking related to 24-h ambulatory blood pressure and heart rate: a study in 352 normotensive Danish subjects. Am J Hypertens 1997; 10: 483-91.</p>
    <p>40. Mann SJ, James GD, Wang RS, Pickering TG. Elevation of ambulatory systolic blood pressure in hypertensive smokers. A casecontrol study. JAMA 1991; 265: 2226-8.</p>
    <p>41. Verdecchia P, Schillaci G, Borgioni C, Ciucci A, Zampi I, Battistelli M, et al. Cigarette smoking, ambulatory blood pressure and cardiac hypertrophy in essential hypertension. J Hypertens 1995; 13: 1209-15.</p>
    <p>42. Raw M, McNeill A, West R. Smoking cessation: evidence based recommendations for the healthcare system. BMJ 1999; 318: 182-85.</p>
    <p>43. Tight blood pressure control and the risk of macrovascular and microvascular complications in type 2 diabetes: UKPDS 38. UK Prospective Diabetes Study Group. BMJ 1998; 317: 703-13.</p>
    <p>44. Parving HH, Andersen AR, Smidit UM, Svendsen PA. Early agressive antihypertensive treatment reduces rate of decline in kidney function in diabetic nephropathy. Lancet 1983; 1: 1175-8.</p>
    <p>45. American Diabetes Association. Standards of medical care for patients with diabetes mellitus. Diabetes Care 2002; 25: 213-29.</p>
    <p>46. III Diretrizes Brasileiras sobre Dislipidemias de Preven&#231;&#227;o da Aterosclerose do Departamento de Aterosclerose da Sociedade Brasileira de Cardiologia. Arq Bras Cardiol 2001; 77: 1-48.</p>
    <p>47. Psaty BM, Smith NL, Siscovick DS, Koepsell TD, Weiss NS, Heckbert SR, et al. Health outcomes associated with antihypertensive therapies used as first-line agents. A systematic review and metaanalysis. JAMA 1997; 277: 739-45.</p>
    <p>48. Neal B, MacMahon S, Chapman N. Blood Pressure Lowering Treatment Trialists Collaboration. Effects of ACE inhibitors, calcium antagonists and other blood pressure-lowering drugs: results of prospectively designed over views of randomised trials. Blood Pressure Lowering Treatment Trialists' Collaboration. Lancet 2000; 356: 1955-64.</p>
    <p>49. Dahlof B, Devereux RB, Kjeldsen SE, Julius S, Beevers G, Faire U, et al. Cardiovascular morbidity and mortality in the Losartan Intervention For Endpoint reduction in hypertension study (LIFE): a randomised trial against atenolol. Lancet 2002; 359: 995-1003.</p>
    <p>50. Major cardiovascular events in hypertensive patients randomized to doxazosin vs chlorthalidone: the antihypertensive and lipidlowering treatment to prevent heart attack trial (ALLHAT). ALLHAT Collaborative Research Group. JAMA 2000; 283: 1967-75.</p>
    <p>51. Detection, evaluation, and treatment of renovascular hypertension. Final report. Working Group on Renovascular Hypertension. Arch Intern Med 1987; 147: 820-9.</p>
    <p>52. Hansson L, Zanchetti A, Carruthers SG, Dahlof B, Elmfeldt D, Julius S, et al. Effects of intensive blood-pressure lowering and low-dose aspirin in patients with hypertension: principal results of the Hypertension Optimal Treatment (HOT) randomised trial. HOT Study Group. Lancet 1998; 351: 1755-62.</p>
    <p>53. Stamler J. Epidemiologic findings on body mass and blood pressure in adults. Ann Epidemiol 1991; 1: 347-62.</p>
    <p>54. Neaton JD, Wentworth D. Serum cholesterol, blood pressure, cigarette smoking, and death from coronary heart disease. Overall findings and differences by age for 316,099 white men. Multiple Risk Factors Intervention Trial Research Group. Arch Intern Med 1992; 152: 56-64.</p>
    <p>55. Stamler R, Stamler J, Gosh FC, Civinelli J, Fishman J, McKeever P, et al. Primary prevention of hypertension by nutritionalhygienic means. Final report of a randomized, controlled trial. JAMA 1989; 262: 1801-7.</p>
  </body>
  <sub-article article-type="translation" id="TRen" xml:lang="en">
    <front-stub>
      <title-group>
        <article-title xml:lang="en">IV Brazilian Guidelines on Hypertension</article-title>
      </title-group>
    </front-stub>
    <body>
      <p>
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-e01-en.jpg"/></p>
      <p>
        <bold>IV Brazilian Guidelines on Hypertension</bold>
      </p>
      <p>Work performed by</p>
      <p>Brazilian Society of Hypertension &#150; SBH</p>
      <p> Brazilian Society of Cardiology &#150; SBC</p>
      <p> Brazilian Society of Nephrology &#150; SBN</p>
      <p>Sponsors</p>
      <p>Brazilian Academy of Neurology &#150; ABN</p>
      <p> Brazilian Association for the Study of Obesity &#150; ABESO</p>
      <p> Brazilian Federation of Gynecology and Obstetrics Societies &#150; FEBRASGO</p>
      <p> Brazilian Society of Internal Medicine &#150; SBCM</p>
      <p> Brazilian Society of Diabetes &#150; SBD</p>
      <p> Brazilian Society of Endocrinology and Metabolism &#150; SBEM</p>
      <p> Brazilian Society of Geriatrics and Gerontology &#150; SBGG</p>
      <p>Organizing Commission</p>
      <p>D&#233;cio Mion Jr. (Coordenador)</p>
      <p> Marco Ant&#244;nio Mota Gomes (SBC)</p>
      <p>Fernando Nobre (SBH)</p>
      <p> Celso Amodeo (SBN)</p>
      <p>Osvaldo Kohlmann Jr. (SBH)</p>
      <p> Jos&#233; Nery Praxedes (SBN)</p>
      <p>Carlos Alberto Machado (SBC)</p>
      <p>Editing Commission</p>
      <p>Carlos Alberto Machado</p>
      <p> Celso Amodeo</p>
      <p>D&#233;cio Mion Jr.</p>
      <p> Fernando Nobre</p>
      <p>Ist&#234;nio Pascoal</p>
      <p> Jos&#233; Nery Praxedes</p>
      <p>Luc&#233;lia C. Magalh&#227;es</p>
      <p> Marco Ant&#244;nio Mota Gomes</p>
      <p>Osvaldo Kohlmann Jr.</p>
      <p>Support</p>
      <p>AstraZeneca do Brasil Ltda.</p>
      <p> Aventis Pharma Ltda.</p>
      <p>Bayer S.A.</p>
      <p> Biolab Farmac&#234;utica Ltda.</p>
      <p>Boehringer Ingelheim do Brasil Qu&#237;m. e Farm. Ltda.</p>
      <p> Farmalab Ind. Qu&#237;micas e Farmac&#234;uticas Ltda.</p>
      <p>Laborat&#243;rios Biosint&#233;tica</p>
      <p> Laborat&#243;rios Pfizer Ltda.</p>
      <p>Libbs Farmac&#234;utica Ltda.</p>
      <p> Merck Sharp &amp; Dohme Farmac&#234;utica Ltda.</p>
      <p>Novartis Bioci&#234;ncias S.A.</p>
      <p> Sanofi-Synth&#233;labo Ltda.</p>
      <p>Servier do Brasil Ltda.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>Hypertension is one of the most important health problems in Brazil. It raises the social-medical costs, mainly because of its complications such as cerebrovascular diseases, coronary artery diseases and vascular diseases of the extremities, in addition to cardiac heart failure and chronic renal failure.</p>
      <p>Since 1963, cardiovascular diseases have outnumbered other causes of death; they presently account for 27% of all deaths. There was an increase in the mortality risk from these diseases between 1980 and 1984, followed by a decrease until 1996.</p>
      <p>Different from North America, which showed a 60% mortality reduction from cerebrovascular causes and a 53% reduction from coronary artery causes, in Brazil (<xref ref-type="fig" rid="figura1-body2">Figure 1</xref>) the reductions observed were 20% and 13%, respectively. The trends of mortality risk by cardiovascular diseases are different in the various regions of the country; there is a decrease in the Southeast and South, an increase in the Center-West and Northeast, and stable levels in the North<sup>1</sup> (<bold>B</bold>).</p>
      <fig id="figura1-body2">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gf01-en.jpg"/></fig>
      <p>There are few prevalence studies and they do not represent the reality of the country. The investigations shown in <xref ref-type="fig" rid="f2-body2">Figure 2</xref> indicate high prevalence between 22-44%<sup>2</sup> (<bold>B</bold>) <sup>3-6</sup>(<bold>A</bold>) <sup>7</sup>(<bold>C</bold>). Due to this reality, control programs should be established throughout the country.</p>
      <p content-type="asset">
        <fig id="f2-body2">
          <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gf02-en.jpg"/></fig>
      </p>
      <p>
        <bold>Diagnosis and Classification</bold>
      </p>
      <p>Hypertension is diagnosed by measuring blood pressure using the methods and conditions described on <xref ref-type="table" rid="tabela1-body2">Table 1</xref>, according to the blood pressure levels reported on <xref ref-type="table" rid="tabela2-body2">Table 2</xref>.</p>
      <table-wrap id="tabela1-body2">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt01-en.jpg"/></table-wrap>
      <table-wrap id="tabela2-body2">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt02-en.jpg"/></table-wrap>
      <p>
        <bold>Measurement of Arterial Pressure<sup>17,19</sup>(D)</bold>
      </p>
      <p>The mercury column manometer is the most appropriate device. The aneroid variety must be tested every 6 months and the electronic models are indicated only when validated.</p>
      <p>
        <bold>Diagnostic Routine (D)</bold>
      </p>
      <p>A minimum of two blood pressure measurements must be taken at each medical examination, both with the patient seated; if diastolic pressures show differences above 5 mm Hg, new measurements should be taken until a smaller difference is obtained. In a first evaluation, the measurements must be taken in both upper limbs. If a difference is noticed, the arm to be used is the one with the higher blood pressure. Measurements should be repeated in at least 2 or more appointments before the diagnosis of hypertension is confirmed.</p>
      <p>Measurement in orthostatic position must be taken at least during the initial evaluation, especially for the elderly, or for diabetic patients with dysautonomias, alcohol addicts, and users of antihypertensive medication.</p>
      <p>
        <bold>Criteria for Diagnostic Classification and Follow-up Recommendations<sup>20</sup>(D)</bold>
      </p>
      <p>Any numerical value is arbitrarily attributed and any classification is insufficient. One must consider, in addition to the pressure levels, the presence of risk factors, comorbidities and target organs lesions listed on <xref ref-type="table" rid="tabela3-body2">Table 3</xref>.</p>
      <table-wrap id="tabela3-body2">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt03-en.jpg"/></table-wrap>
      <p>Children and adolescents have their arterial pressure classified according to the percentiles of height and gender. Values ? 95 percentile are regarded as arterial hypertension.</p>
      <p>
        <bold>Clinical Investigation and Therapeutic Decision</bold>
      </p>
      <p>The objectives of the clinical investigation include the confirmation of persistent elevation of arterial pressure, evaluation of lesions in target organs, identification of cardiovascular risk factor, diagnosis of associated diseases and etiology of hypertension. To reach this goal, one must consider: a) clinical history &#150; in addition to the usual data of the patient's gender, age, race, socioeconomic status, smoking habits, time since onset of hypertension and blood pressure levels, overweight and obesity, symptoms of coronary artery disease, stroke, or coronary artery disease in family members (in women &lt; 65 years old and men &lt; 55 years old), signs and symptoms of cardiac heart failure, family history of hypertension, cerebral vascular disease, early/sudden death of close family members, peripheral vascular failure, depression, anxiety, panic, renal disease, family situation, diabetes mellitus, salt and alcohol intake, use of medication or drugs that might affect arterial blood pressure, risk factors for atherosclerosis, level of physical activity, dyslipidemia, weight loss and evidence of secondary hypertension, which must always be analyzed when characteristic manifestations are present b) physical examinations &#150; emphasizing weight and height, mitral and aortic murmurs, abdominal circumference, rales, roaring, sibilus, signs of secondary hypertension, abdominal masses (tumors, aneurisms, hydronephrosis, polycystic kidneys), measurements of arterial blood pressure, abdominal murmurs (renal, aortic), pulse rate, brachial, radial, femoral, tibial and pedis pulses, carotid palpation and auscultation, presence of edema, venous stasis, concise neurological exam, thyroid palpation, eye ground exam, ictus suggestive of left ventricular hypertrophy/dilatation, third heart sound (systolic dysfunction of left ventricle), hyperphonesis of A2; c) routine laboratory tests &#150; urinalysis, potassium, creatinine, fasting glucose test, total cholesterol, HDL-cholesterol, triglycerides and electrocardiogram; LDL-cholesterol may be estimated when triglycerides level are below 400mg/dl using the formula: LDL-cholesterol = total cholesterol - HDL-cholesterol - triglycerides/5; d) complementary evaluation if there is evidence of secondary hypertension, target organ injury, or associated diseases<sup>21,22</sup>(<bold>D</bold>).</p>
      <p>To start the treatment, one must consider the blood pressure levels and the patient's risk according to <xref ref-type="table" rid="tabela3-body2">Tables 3</xref> and <xref ref-type="table" rid="t4-body2">4</xref>.</p>
      <p content-type="asset">
        <table-wrap id="t4-body2">
          <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt04-en.jpg"/></table-wrap>
      </p>
      <p>
        <bold>Multiprofessional Approach</bold>
      </p>
      <p>Arterial hypertension is a multifactorial disease and as it involves guidelines directed to various objectives, it may demand help from other healthcare professionals in addition to the physician. The setup of this multiprofessional team will provide a differentiated approach to hypertensive patients<sup>24</sup>(<bold>A</bold>).</p>
      <p>
        <bold>The Team</bold>
      </p>
      <p>It may be composed of physicians, nurses, nurse aides, nutritionists, psychologists, social assistants, physical education teachers, pharmacists, management employees, and community agents. It is not necessary to have this whole group composing the team.</p>
      <p>
        <bold>Team Actions</bold>
      </p>
      <p>They intend to promote health, educational activities emphasizing lifestyle changes, correction of risk factors and production of educational material; training of professionals; referrals to other professionals, when appropriate; individual and group assistance; participation in research projects; program management.</p>
      <p>
        <bold>Individual Actions</bold>
      </p>
      <p>Actions characteristic to each professional; however, there are situations in which the functions are common to more than one professional and they will be performed naturally using uniform language and approach.</p>
      <p>
        <bold>Community Programs</bold>
      </p>
      <p>Forming leagues and associations of hypertensive patients may increase complicance and become an instrument of pressure with authorities in order to improve the quality of assistance offered to hypertensive patients.</p>
      <p>
        <bold>Non-drug Treatment</bold>
      </p>
      <p>
        <bold>Measures of better Effectiveness</bold>
      </p>
      <p>Reduction of body weight and maintenance of ideal body weight &#150; body mass index (weight in kilograms divided by square value of height in meters) between 20 and 25 kg/m<sup>2</sup>, because there is a direct association between body weight and arterial blood pressure<sup>25</sup>(<bold>A</bold>).</p>
      <p>Reduction of sodium intake &#150; it is healthy to ingest up to 6 g/day, which is the equivalent of 4 shallow coffee spoons of salt (4 g) and 2 g of salt present in natural food; it is important to reduce the amount of salt added to food and to avoid having the salt shaker on the table and eating industrialized food. A regular diet contains between 10-12 g/day of sodium<sup>26</sup>(<bold>A</bold>).</p>
      <p>Greater potassium intake &#150; a diet rich in vegetables and fruits contains 2-4 g/day and can be helpful to lower blood pressure, as well as preventing arterial hypertension<sup>27</sup>(<bold>A</bold>). Salt substitutes containing potassium chloride and a lower amount of sodium chloride (30-50%) are helpful to reduce sodium intake and increase potassium intake.</p>
      <p>Reduction of alcoholic beverage consumption<sup>28,29</sup> (<bold>D</bold>) <sup>30,31</sup>(<bold>B</bold>) <sup>32</sup>(<bold>A</bold>) &#150; for alcohol consumers, the ingestion of alcoholic beverages must be limited to 30g of alcohol/day, contained in 600 ml of beer (5% alcohol) or 250 ml of wine (12% alcohol) or 60 ml of distilled drinks (whiskey, vodka, sugar cane liquor - 50% alcohol). This limit must be reduced to half in men with low body weight, women, overweight individuals or those who have high levels of triglycerides.</p>
      <p>Regular physical activities<sup>33</sup>(<bold>A</bold>) <sup>34</sup>(<bold>D</bold>) &#150; there is an inverse relationship between the level of physical activity and the incidence of hypertension; regular physical activity reduces blood pressure (<xref ref-type="table" rid="tabela5-body2">Table 5</xref>).</p>
      <table-wrap id="tabela5-body2">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt05-en.jpg"/></table-wrap>
      <p>
        <bold>Measures without Definitive Scientific Evaluation</bold>
      </p>
      <p>Calcium supplements <sup>36,37</sup>(<bold>A</bold>), magnesium<sup>38</sup>(<bold>D</bold>), vegetarian diets and anti-stress measures.</p>
      <p>
        <bold>Associated Measures</bold>
      </p>
      <p>Quit smoking &#150; this must be recommended because of its association with a higher incidence of cardiovascular mortality, and increased levels of arterial pressure measured on an outpatient basis<sup>39-41</sup>(<bold>B</bold>). Smoke quitting must be accompanied by caloric restriction and increase in physical activity in order to avoid possible weight gain. Exposure to smoke, passive smoking, is also a cardiovascular risk factor which must be avoided<sup>42</sup>(<bold>D</bold>).</p>
      <p>Control of diabetes and dyslipidemias &#150; glucose intolerance and diabetes are frequently associated with arterial hypertension, causing the occurrence of cardiovascular diseases and complications from diabetes<sup>43</sup>(<bold>A</bold>) <sup>44</sup>(<bold>B</bold>). Prevention is based mainly on a hypocaloric diet, regular practice of aerobic physical activities and reduction of simple sugar intake. These measures also intend to keep arterial blood pressure below 130/80 mmHg<sup>45</sup>(<bold>D</bold>). Hypercholesterolemia and e hypertriglyceridemia, with low HDL-cholesterol, are important cardiovascular risk factors<sup>45</sup>(<bold>D</bold>).</p>
      <p>The basis for controlling dyslipidemias is represented by dietary changes with reduction of fat intake and partial replacement of saturated fats by mono- and polyunsaturated fats, as well as reduction of daily cholesterol intake<sup>46</sup>(<bold>D</bold>).</p>
      <p>Avoid medications that increase arterial blood pressure levels<sup>23</sup>(<bold>D</bold>), listed on <xref ref-type="table" rid="tabela6-body2">Table 6</xref> along with specific guidelines for each type of medication.</p>
      <table-wrap id="tabela6-body2">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt06-en.jpg"/></table-wrap>
      <p>
        <bold>Drug Treatment</bold>
      </p>
      <p>Objective &#150; To reduce cardiovascular morbidity and mortality in hypertensive patients. The objective is reached in patients treated with diuretics<sup>47</sup>(<bold>A</bold>), beta blockers<sup>47</sup>(<bold>D</bold>), angiotensine-converting enzyme (ECA) inhibitors<sup>48</sup>(<bold>A</bold>), antagonists of AT1 receptor of angiotensina II &#150; (AII)<sup>49</sup>(<bold>D</bold>) and in older patients who use calcium channel antagonists<sup>48</sup>(<bold>A</bold>); the majority of the studies ended up using an association of drugs.</p>
      <p>
        <bold>Target of Arterial Blood Pressure Reduction</bold>
      </p>
      <p>It should be at least to values below 140/90 mmHg<sup>20</sup>(<bold>D</bold>). Reductions to levels below 130/85 mmHg provide greater benefit<sup>20</sup>(<bold>D</bold>) to patients with high cardiovascular risk<sup>43</sup>(<bold>A</bold>), diabetic patients especially with microalbuminuria<sup>50</sup>(<bold>A</bold>) and heart failure, nephropathy and in primary and secondary prevention of stroke<sup>48</sup>(<bold>A</bold>).</p>
      <p>
        <bold>General Principles of Drug Treatment (D):</bold>
      </p>
      <disp-quote>
        <p><bold>&#149;</bold> The drug must be effective orally, be well tolerated and allow the smallest possible amount of daily doses;</p>
        <p><bold>&#149;</bold> With stage 1 patients, treatment should start with the lowest effective doses possible;</p>
        <p><bold>&#149;</bold> With patients In stages 2 and 3, consider the associated use of an anti-hypertensive drug to start the treatment;</p>
        <p><bold>&#149;</bold> Observe a minimum of four weeks before increasing the dose, replacing monotherapy or changing the drug association;</p>
        <p><bold>&#149;</bold> Explain the patient about the disease, treatment plans and objectives, the importance of complying with the treatment, and adverse effects associated with the drugs;</p>
        <p><bold>&#149;</bold> Consider socioeconomic conditions.</p>
      </disp-quote>
      <p>
        <bold>Therapeutic Planning</bold>
      </p>
      <p>Treatment must be individualized and should maintain the patient's quality of life. Any group of antihypertensive drugs, except direct-acting vasodilators and alpha-blockers, is appropriate to control arterial blood pressure as initial monotherapy (<xref ref-type="table" rid="t7-body2">Table 7</xref>)<sup>23</sup>(<bold>D</bold>). Antihypertensive agents available in Brazil are shown on <xref ref-type="table" rid="tabela8-body2">Tables 8</xref> e <xref ref-type="table" rid="tabela9-body2">9</xref>.</p>
      <p content-type="asset">
        <table-wrap id="t7-body2">
          <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt07-en.jpg"/></table-wrap>
      </p>
      <table-wrap id="tabela8-body2">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt08-en.jpg"/></table-wrap>
      <table-wrap id="tabela9-body2">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt09-en.jpg"/></table-wrap>
      <p>Chlorthalidone has shown to be superior to doxazosin as an initial treatment drug for older hypertensive patients with other risk factors<sup>50</sup>(<bold>D</bold>) <sup>51</sup>(<bold>A</bold>).</p>
      <p>For the hypertensive patient with arterial blood pressure under control, the association of low doses of acetylsalicylic acid may reduce the occurrence of cardiovascular complications<sup>52</sup>(<bold>A</bold>).</p>
      <p>
        <bold>Prevention of Hypertension and Associated Risk Factors</bold>
      </p>
      <p>Fighting hypertension means preventing the increase of blood pressure by reducing the risk factors in the overall population and in groups with higher risk of developing the disease within the normal limit values (130 - 139/ 80 - 89 mmHg)<sup>35</sup>(<bold>D</bold>) and those with a family history of hypertension. Hypertension is also stimulated by excessive body weight<sup>53</sup>(<bold>D</bold>), sedentarism<sup>34</sup>(<bold>D</bold>), high salt intake<sup>26</sup>(<bold>A</bold>), low potassium intake<sup>46</sup>(<bold>D</bold>) and excessive alcohol consumption<sup>31</sup>(<bold>B</bold>). In the group with bordering normal blood pressure levels, factors such as dyslipidemias, glucose intolerance and diabetes, smoking, menopause and emotional stress<sup>54</sup> (<bold>A</bold>) also contribute to the increase of cardiovascular risk.</p>
      <p>Preventive measures include: maintenance of ideal body weight<sup>53</sup>(<bold>D</bold>), regular physical activities<sup>35</sup>(<bold>D</bold>), reduction in salt intake and increase in potassium intake<sup>46</sup>(<bold>D</bold>), avoiding alcoholic beverages<sup>31</sup>(<bold>B</bold>), following a healthy diet (<xref ref-type="table" rid="tabela10-body2">Table 10</xref>) which should have a low fat content, mainly saturated fats, low cholesterol, high potassium content and fibers<sup>46</sup>(<bold>D</bold>), and low sodium content <sup>26</sup>(<bold>A</bold>). The total calorie count must be adjusted for the purpose of achieving and keeping the ideal body weight. Strictly watching the entire diet is more important than following up isolated measures<sup>55</sup> (<bold>B</bold>).</p>
      <table-wrap id="tabela10-body2">
        <graphic xlink:href="1678-4170-abc-82-suppl4-0007-00004-gt10-en.jpg"/></table-wrap>
      <p>
        <bold>References</bold>
      </p>
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      <p>55. Stamler R, Stamler J, Gosh FC, Civinelli J, Fishman J, McKeever P, et al. Primary prevention of hypertension by nutritionalhygienic means. Final report of a randomized, controlled trial. JAMA 1989; 262: 1801-7.</p>
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