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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">mt5FfpDfRVSsWkPwk4RQKgz</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2013000600002</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(13)10000600002</article-id>
      <article-id pub-id-type="doi">10.5935/abc.20130101</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigos Originais</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Comportamento da s&#237;ndrome coronariana aguda: resultados de um registro brasileiro</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Piegas</surname>
            <given-names>Leopoldo Soares</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Avezum</surname>
            <given-names>&#193;lvaro</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Guimar&#227;es</surname>
            <given-names>H&#233;lio Penna</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Muniz</surname>
            <given-names>Antonio Jos&#233;</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Reis</surname>
            <given-names>Helder J. L.</given-names>
          </name>
          <xref ref-type="aff" rid="aff03"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Santos</surname>
            <given-names>Elizabete Silva dos</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Knobel</surname>
            <given-names>Marcos</given-names>
          </name>
          <xref ref-type="aff" rid="aff04"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Souza</surname>
            <given-names>Roberta de</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="city">S&#227;o Paulo</named-content>
          <named-content content-type="state">S&#227;o Paulo</named-content>
        </addr-line>
        <institution content-type="orgname">Instituto Dante Pazzanese de Cardiologia</institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff04">
        <addr-line>
          <named-content content-type="city">S&#227;o Paulo</named-content>
          <named-content content-type="state">S&#227;o Paulo</named-content>
        </addr-line>
        <institution content-type="orgname">Hospital Israelita Albert Einstein</institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff03">
        <addr-line>
          <named-content content-type="city">Bel&#233;m</named-content>
          <named-content content-type="state"/>
        </addr-line>
        <institution content-type="orgname">Hospital das Cl&#237;nicas Gaspar Vianna</institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff02">
        <addr-line>
          <named-content content-type="city">Juiz de Fora</named-content>
          <named-content content-type="state">Minas Gerais</named-content>
        </addr-line>
        <institution content-type="orgname">Santa Casa de Miseric&#243;rdia de Juiz de Fora</institution>
        <country country="BR">Brazil</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>06</month>
        <year>2013</year>
      </pub-date>
      <volume>100</volume>
      <issue>6</issue>
      <fpage>502</fpage>
      <lpage>510</lpage>
      <history>
        <date date-type="received">
          <day>09</day>
          <month>04</month>
          <year>2012</year>
        </date>
        <date date-type="accepted">
          <day>19</day>
          <month>11</month>
          <year>2012</year>
        </date>
        <date date-type="rev-recd">
          <day>24</day>
          <month>09</month>
          <year>2012</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: O Brasil carece de registros multic&#234;ntricos publicados de s&#237;ndrome coronariana aguda. OBJETIVO: O Registro Brasileiro de S&#237;ndrome Coronariana Aguda &#233; um estudo multic&#234;ntrico nacional com objetivo de apresentar dados representativos das caracter&#237;sticas cl&#237;nicas, e manejo e evolu&#231;&#227;o hospitalares dessa s&#237;ndrome. M&#201;TODOS: Participaram 23 hospitais de 14 cidades. Foram eleg&#237;veis pacientes que se apresentaram com suspeita de s&#237;ndrome coronariana aguda nas primeiras 24 horas, com quadro cl&#237;nico sugestivo, associado a altera&#231;&#245;es eletrocardiogr&#225;ficas compat&#237;veis e/ou marcadores de necrose. O seguimento foi realizado at&#233; o &#243;bito ou a alta hospitalar. RESULTADOS: Entre os anos de 2003 e 2008, foram inclu&#237;dos 2.693 pacientes com diagn&#243;stico de s&#237;ndrome coronariana aguda, sendo 864 (32,1%) mulheres. O diagn&#243;stico final foi de angina inst&#225;vel para 1.141 (42,4%) pacientes, com mortalidade de 3,06% deles; de infarto agudo do mioc&#225;rdio sem supradesn&#237;vel de ST para 529 (19,6%) pacientes, com mortalidade de 6,8% deles; e de infarto agudo do mioc&#225;rdio com supradesn&#237;vel de ST para 950 (35,3%) pacientes, com mortalidade de 8,1% deles; tiveram diagn&#243;stico n&#227;o confirmado 73 (2,7%) pacientes, com mortalidade de 1,36% deles. A mortalidade global foi de 5,53%. O modelo de regress&#227;o log&#237;stica m&#250;ltipla identificou o g&#234;nero feminino (OR=1,45), o diabetes melito (OR=1,59), o &#237;ndice de massa corporal (OR=1,27) e a interven&#231;&#227;o coronariana percut&#226;nea (OR=0,70) como fatores de risco de &#243;bito, para demografia e interven&#231;&#245;es. Um modelo para &#243;bito por complica&#231;&#245;es maiores identificou choque cardiog&#234;nico/Edema Agudo de Pulm&#227;o (OR=4,57), reinfarto (OR=3,48), acidente vascular cerebral (OR=21,56), sangramento grave (OR=3,33), parada cardiorrespirat&#243;ria (OR=40,27) e classe funcional de Killip (OR=3,37). CONCLUS&#195;O: Os dados do Registro Brasileiro de S&#237;ndrome Coronariana Aguda n&#227;o diferem de outros coletados fora do pa&#237;s. Seus achados poder&#227;o ajudar a promover um melhor planejamento e manejo do atendimento da s&#237;ndrome coronariana aguda a n&#237;vel p&#250;blico e privado.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>S&#237;ndrome Coronariana Aguda</kwd>
        <kwd>Estudos Multic&#234;ntricos como Assunto</kwd>
        <kwd>Registros de Doen&#231;as</kwd>
        <kwd>Infarto do Mioc&#225;rdio</kwd>
        <kwd>Evolu&#231;&#227;o Cl&#237;nica</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>14</day>
        <month>05</month>
        <year>2013</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>
      <bold>Comportamento da s&#237;ndrome coronariana aguda. Resultados de um registro brasileiro</bold>
    </p>
    <p>
      <bold>Leopoldo Soares Piegas<sup>I</sup>; &#193;lvaro Avezum<sup>I</sup>; H&#233;lio Penna Guimar&#227;es<sup>I</sup>; Antonio Jos&#233; Muniz<sup>II</sup>; Helder J. L. Reis<sup>III</sup>; Elizabete Silva dos Santos<sup>I</sup>; Marcos Knobel<sup>IV</sup>; Roberta de Souza<sup>I</sup></bold>
    </p>
    <p><sup>I</sup>Instituto Dante Pazzanese de Cardiologia, S&#227;o Paulo, SP </p>
    <p><sup>II</sup>Santa Casa de Miseric&#243;rdia de Juiz de Fora, Juiz de Fora, MG </p>
    <p><sup>III</sup>Hospital das Cl&#237;nicas Gaspar Vianna, Bel&#233;m, PA </p>
    <p><sup>IV</sup>Hospital Israelita Albert Einstein, S&#227;o Paulo, SP - Brasil</p>
    <p>
      <xref ref-type="corresp" rid="end">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p><bold>FUNDAMENTO:</bold> O Brasil carece de registros multic&#234;ntricos publicados de s&#237;ndrome coronariana aguda. </p>
    <p><bold>OBJETIVO:</bold> O Registro Brasileiro de S&#237;ndrome Coronariana Aguda &#233; um estudo multic&#234;ntrico nacional com objetivo de apresentar dados representativos das caracter&#237;sticas cl&#237;nicas, e manejo e evolu&#231;&#227;o hospitalares dessa s&#237;ndrome. </p>
    <p><bold>M&#201;TODOS:</bold> Participaram 23 hospitais de 14 cidades. Foram eleg&#237;veis pacientes que se apresentaram com suspeita de s&#237;ndrome coronariana aguda nas primeiras 24 horas, com quadro cl&#237;nico sugestivo, associado a altera&#231;&#245;es eletrocardiogr&#225;ficas compat&#237;veis e/ou marcadores de necrose. O seguimento foi realizado at&#233; o &#243;bito ou a alta hospitalar. </p>
    <p><bold>RESULTADOS:</bold> Entre os anos de 2003 e 2008, foram inclu&#237;dos 2.693 pacientes com diagn&#243;stico de s&#237;ndrome coronariana aguda, sendo 864 (32,1%) mulheres. O diagn&#243;stico final foi de angina inst&#225;vel para 1.141 (42,4%) pacientes, com mortalidade de 3,06% deles; de infarto agudo do mioc&#225;rdio sem supradesn&#237;vel de ST para 529 (19,6%) pacientes, com mortalidade de 6,8% deles; e de infarto agudo do mioc&#225;rdio com supradesn&#237;vel de ST para 950 (35,3%) pacientes, com mortalidade de 8,1% deles; tiveram diagn&#243;stico n&#227;o confirmado 73 (2,7%) pacientes, com mortalidade de 1,36% deles. A mortalidade global foi de 5,53%. O modelo de regress&#227;o log&#237;stica m&#250;ltipla identificou o g&#234;nero feminino (OR=1,45), o diabetes melito (OR=1,59), o &#237;ndice de massa corporal (OR=1,27) e a interven&#231;&#227;o coronariana percut&#226;nea (OR=0,70) como fatores de risco de &#243;bito, para demografia e interven&#231;&#245;es. Um modelo para &#243;bito por complica&#231;&#245;es maiores identificou choque cardiog&#234;nico/Edema Agudo de Pulm&#227;o (OR=4,57), reinfarto (OR=3,48), acidente vascular cerebral (OR=21,56), sangramento grave (OR=3,33), parada cardiorrespirat&#243;ria (OR=40,27) e classe funcional de Killip (OR=3,37). </p>
    <p><bold>CONCLUS&#195;O:</bold> Os dados do Registro Brasileiro de S&#237;ndrome Coronariana Aguda n&#227;o diferem de outros coletados fora do pa&#237;s. Seus achados poder&#227;o ajudar a promover um melhor planejamento e manejo do atendimento da s&#237;ndrome coronariana aguda a n&#237;vel p&#250;blico e privado.</p>
    <p><bold>Palavras-Chave:</bold> S&#237;ndrome Coronariana Aguda, Estudos Multic&#234;ntricos como Assunto, Registros de Doen&#231;as, Infarto do Mioc&#225;rdio, Evolu&#231;&#227;o Cl&#237;nica.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>No ano de 2010, as doen&#231;as do aparelho circulat&#243;rio, terceira causa de interna&#231;&#227;o hospitalar, com 210.046 interna&#231;&#245;es por doen&#231;a isqu&#234;mica do cora&#231;&#227;o, foram respons&#225;veis, no Brasil, por 29% das mortes, de um total de 1.133.761. O n&#250;mero absoluto de &#243;bitos por doen&#231;as isqu&#234;micas do cora&#231;&#227;o naquele ano foi de 99.408 &#243;bitos ou 52,11 &#243;bitos/100 mil habitantes, e os &#243;bitos por doen&#231;as cerebrovasculares foi de 99.159 ou 51,98 &#243;bitos/100.000 habitantes<sup>1</sup>. A preval&#234;ncia da Doen&#231;a Arterial Coronariana (DAC) na popula&#231;&#227;o adulta est&#225; estimada em 5 a 8%<sup>2</sup>.</p>
    <p>Em 2010, foram registrados 79.954 &#243;bitos associados &#224; S&#237;ndrome Coronariana Aguda (SCA). Esses n&#250;meros totalizam os &#243;bitos por angina e Infarto Agudo do Mioc&#225;rdio (IAM), correspondendo a 7,05% do total de &#243;bitos no ano, ou 24,67% dos &#243;bitos por doen&#231;as do aparelho circulat&#243;rio<sup>1</sup>.</p>
    <p>As SCA representam importante causa de interna&#231;&#227;o, sendo o IAM, em 2009, a terceira causa de hospitaliza&#231;&#227;o no Sistema &#218;nico de Sa&#250;de (SUS). Representou 10,2% das interna&#231;&#245;es, n&#250;mero que ultrapassa 25% na popula&#231;&#227;o com mais de 50 anos de idade.</p>
    <p>A principal fonte de cobertura de sa&#250;de no pa&#237;s &#233; dada pelo SUS, sendo os planos de sa&#250;de respons&#225;veis por 25,9% (Intervalo de Confian&#231;a de 95% - IC95% = 25,4-26,4) da popula&#231;&#227;o no ano de 2008. As SCA foram respons&#225;veis pelo maior gasto com interna&#231;&#245;es, correspondendo a um total de R$1,9 bilh&#227;o ou 19% do custo total com hospitaliza&#231;&#245;es<sup>3</sup>.</p>
    <p>Pelo SUS, em 2011, a estimativa de custo direto da SCA era de R$ 522.286.726,00, correspondendo a 0,77% do or&#231;amento total e, pelo Sistema Suplementar, de R$ 515.138.617,00, sendo os custos indiretos de R$ 2,8 bilh&#245;es, estimando-se em R$ 3,8 bilh&#245;es o custo total<sup>4</sup>.</p>
    <p>O conhecimento do comportamento hospitalar dos pacientes com SCA &#233; fundamental para a estratifica&#231;&#227;o do risco hospitalar imediato e, a longo prazo, para os sobreviventes do epis&#243;dio agudo, al&#233;m de mostrar como estes pacientes s&#227;o tratados em nosso meio.</p>
    <p>In&#250;meros registros internacionais de SCA t&#234;m sido publicados, alguns inclusive com participa&#231;&#227;o de centros brasileiros<sup>5-8</sup>. Registros nacionais s&#227;o escassos e inclu&#237;ram pacientes de um &#250;nico centro, n&#227;o representativo da cultura nacional<sup>9</sup>. O Registro Brasileiro de S&#237;ndromes Coronariana Agudas (RBSCA), parcialmente apresentado em congressos nacionais<sup>10 </sup>e internacionais<sup>11</sup>, pretende preencher essa lacuna, municiando os interessados com tais informa&#231;&#245;es em falta. Tem por objetivo apresentar os resultados de um volumoso registro nacional, multic&#234;ntrico, representativo das caracter&#237;sticas, manejo e evolu&#231;&#227;o hospitalar da SCA no pa&#237;s.</p>
    <p>
      <bold>M&#233;todos</bold>
    </p>
    <p>
      <bold>Delineamento do estudo</bold>
    </p>
    <p>O RBSCA &#233; um estudo prospectivo, nacional, multic&#234;ntrico, n&#227;o financiado, delineado para captar as informa&#231;&#245;es hospitalares de pacientes com suspeita de SCA, internados em servi&#231;o de emerg&#234;ncia de hospitais convidados a participar do estudo, em distintas partes do territ&#243;rio brasileiro, de modo a refletir o comportamento da SCA em hospitais com as caracter&#237;sticas descritas adiante. Os hospitais convidados deveriam ter pr&#233;via experi&#234;ncia em estudos cl&#237;nicos, assim como os investigadores principais, tradi&#231;&#227;o na &#225;rea de pesquisa.</p>
    <p>
      <bold>Hospitais, investigadores e popula&#231;&#227;o</bold>
    </p>
    <p>Participaram do RBSCA 23 hospitais, localizados em 14 cidades, sendo quatro privados, 15 filantr&#243;picos e quatro p&#250;blicos. Destes, seis n&#227;o atendiam o SUS. Todos dispunham de unidade coronariana ou sala de emerg&#234;ncia com monitoriza&#231;&#227;o eletrocardiogr&#225;fica, laborat&#243;rio de hemodin&#226;mica e estavam capacitados a realizar procedimentos de interven&#231;&#227;o coronariana percut&#226;nea e cirurgia card&#237;aca (<xref ref-type="app" rid="anex">Anexo 1</xref>).</p>
    <p>Os investigadores principais tinham titulo de especialista<sup>20</sup> pela Sociedade Brasileira de Cardiologia (SBC) e/ou titula&#231;&#227;o acad&#234;mica<sup>14</sup>.</p>
    <p>A popula&#231;&#227;o alvo era composta pelos pacientes internados em servi&#231;o de emerg&#234;ncia ou unidade coronariana com diagn&#243;stico de SCA.</p>
    <p>
      <bold>Elegibilidade</bold>
    </p>
    <p>Foram eleg&#237;veis aqueles pacientes que se apresentassem para atendimento de emerg&#234;ncia com suspeita de SCA, com quadro cl&#237;nico sugestivo, associado a altera&#231;&#245;es eletrocardiogr&#225;ficas compat&#237;veis e/ou marcadores de necrose alterados. Foram inclu&#237;dos apenas pacientes com at&#233; 24 horas do in&#237;cio dos sintomas. O seguimento foi realizado at&#233; a alta hospitalar ou &#243;bito, o que ocorresse primeiro.</p>
    <p>
      <bold>Crit&#233;rios de inclus&#227;o</bold>
    </p>
    <p>
      <bold>Para IAM com Supradesn&#237;vel de ST (IAMST):</bold>
    </p>
    <p>&#149; altera&#231;&#245;es definitivas de Eletrocardiograma (ECG) indicando IAMST: eleva&#231;&#227;o persistente de ST (<underline>&gt;</underline> 0,2 mV em duas deriva&#231;&#245;es precordiais cont&#237;guas, ou <underline>&gt;</underline> 0,1 mV em pelo menos duas deriva&#231;&#245;es de membro), ou novo bloqueio de ramo esquerdo, ou altera&#231;&#245;es de ECG indicando Infarto do Mioc&#225;rdio posterior verdadeiro;</p>
    <p>&#149; eleva&#231;&#227;o dos marcadores bioqu&#237;micos de necrose;</p>
    <p>
      <bold>Para IAM sem Supradesn&#237;vel de ST (IAMST):</bold>
    </p>
    <p>&#149; altera&#231;&#245;es caracter&#237;sticas no ECG compat&#237;veis com isquemia (por exemplo: depress&#227;o ST <underline>&gt;</underline> 1 mm em pelo menos duas deriva&#231;&#245;es adjacentes, ou invers&#227;o de onda T &gt; 3 mm, ou qualquer altera&#231;&#227;o din&#226;mica no segmento ST, ou eleva&#231;&#227;o transit&#243;ria de ST);</p>
    <p>&#149; eleva&#231;&#227;o dos marcadores bioqu&#237;micos de necrose.</p>
    <p>
      <bold>Angina Inst&#225;vel (AI):</bold>
    </p>
    <p>&#149; altera&#231;&#245;es caracter&#237;sticas no ECG compat&#237;veis com isquemia (por exemplo: depress&#227;o ST <underline>&gt;</underline> 1 mm em pelo menos duas deriva&#231;&#245;es adjacentes, ou invers&#227;o de onda T &gt; 3 mm, ou qualquer altera&#231;&#227;o din&#226;mica no segmento ST, ou eleva&#231;&#227;o transit&#243;ria de ST).;</p>
    <p>&#149; aus&#234;ncia de eleva&#231;&#227;o dos marcadores bioqu&#237;micos de necrose.</p>
    <p>
      <bold>Todos</bold>
    </p>
    <p>consentimento informado assinado;</p>
    <p>in&#237;cio dos sintomas sugestivos de SCA <underline>&lt;</underline> 24 horas.</p>
    <p>
      <bold>Crit&#233;rios de exclus&#227;o</bold>
    </p>
    <p>Foram crit&#233;rios para exclus&#227;o de pacientes deste estudo:</p>
    <p>&#149; idade inferior a 18 anos;</p>
    <p>&#149; admiss&#227;o no hospital com sintomas suspeitos de apresentar uma SCA, por&#233;m n&#227;o confirmada pela hist&#243;ria cl&#237;nica, exame f&#237;sico e exames complementares (marcadores bioqu&#237;micos de necrose).</p>
    <p>
      <bold>Coleta de dados</bold>
    </p>
    <p>As informa&#231;&#245;es foram recolhidas em formul&#225;rio eletr&#244;nico e enviadas via <italic>internet</italic> ao Centro Coordenador, localizado no Instituto Dante Pazzanese de Cardiologia. Esse formul&#225;rio, com 182 quesitos, abrangeu identifica&#231;&#227;o, antecedentes pessoais, demografia, diagn&#243;stico, evolu&#231;&#227;o hospitalar, complica&#231;&#245;es, tratamento farmacol&#243;gico, interven&#231;&#245;es hospitalares e condi&#231;&#245;es de alta. Quando detectadas discrep&#226;ncias em rela&#231;&#227;o aos dados recebidos, era feito contato com Centro Investigador.</p>
    <p>O Protocolo do Estudo foi aprovado pelos Comit&#234;s de &#201;tica dos hospitais participantes, e os pacientes inclu&#237;dos assinaram um Termo de Consentimento Livre e Esclarecido, conforme resolu&#231;&#227;o no. 196 do Conselho Nacional de Sa&#250;de, de 10 de outubro de 1996.</p>
    <p>
      <bold>An&#225;lise estat&#237;stica</bold>
    </p>
    <p>Fatores (medidas qualitativas) e covari&#225;veis (medidas quantitativas) foram comparados na presen&#231;a ou na aus&#234;ncia de &#243;bito. As medidas qualitativas foram resumidas em estat&#237;sticas descritivas de frequ&#234;ncias absoluta (n) e relativa (n), nas categorias nos grupos com aus&#234;ncia e presen&#231;a de &#243;bito. A associa&#231;&#227;o isolada (univariada) entre essas medidas e o &#243;bito foi avaliada por teste do qui-quadrado de Pearson ou exato de Fisher<sup>12</sup>. As medidas quantitativas (vari&#225;veis cont&#237;nuas) foram expressas por mediana e intervalo interquart&#237;lico (IIQ) = (percentil 25 - percentil 75). Para a compara&#231;&#227;o isolada (univariada) dessas medidas entre os grupos, foram aplicados testes n&#227;o param&#233;tricos de Mann-Whitney<sup>13</sup>. Para melhor entender os preditores de risco de &#243;bito, foram realizadas duas an&#225;lises de modelos de regress&#227;o log&#237;stica m&#250;ltipla<sup>14</sup>: uma para identificar fatores da demografia e das interven&#231;&#245;es hospitalares associadas, e outra para identificar a influ&#234;ncia das complica&#231;&#245;es maiores no &#243;bito. Efeitos ou diferen&#231;as foram considerados estatisticamente significativos quando encontrados valores de p &lt; 0,05. Todas as an&#225;lises estat&#237;sticas foram realizadas com aux&#237;lio do programa <italic>Statistical Package for Social Sciences</italic> (SPSS), vers&#227;o 19.</p>
    <p>
      <bold>Resultados</bold>
    </p>
    <p>Entre os anos de 2003 e 2008, foram inclu&#237;dos 2.693 pacientes com diagn&#243;stico de SCA, sendo 864 (32,1%) mulheres. A mediana da idade foi de 63 anos. O diagn&#243;stico final foi de AI para 1.141 (42,4%) pacientes, IAMNST para 529 (19,6%), IAMST para 950 (35,3%) e diagn&#243;stico n&#227;o confirmado para 73 (2.7%).</p>
    <p>A compara&#231;&#227;o das caracter&#237;sticas basais entre sobreviventes e &#243;bitos durante a interna&#231;&#227;o hospitalar &#233; apresentada na <xref ref-type="table" rid="aop_4817tab01">Tabela 1</xref>. As diferen&#231;as significativas das vari&#225;veis dos sobreviventes em rela&#231;&#227;o ao que foram a &#243;bito foram mediana da idade (62 <italic>versus</italic> 71 anos), g&#234;nero feminino (31,6 <italic>versus</italic> 41,6%), hist&#243;ria familiar de DAC (29,5% <italic>versus</italic> 44,5%), acidente vascular cerebral (4,9 <italic>versus </italic>10,1%), ICC (7,2 <italic>versus</italic> 18,8%), diabetes melito (27,2 <italic>versus</italic> 38,3%), interven&#231;&#227;o coron&#225;ria percut&#226;nea (ICP) pr&#233;via (18,2 <italic>versus</italic> 11,4%), frequ&#234;ncia card&#237;aca (75 <italic>versus</italic> 82 bpm), press&#227;o arterial sist&#243;lica (130 <italic>versus</italic> 120 mmHg), press&#227;o arterial diast&#243;lica (80 <italic>versus</italic> 70 mmHg), &#237;ndice de massa corp&#243;rea (26,1 <italic>versus</italic> 25,4), fra&#231;&#227;o MB creatinoquinase do m&#250;sculo card&#237;aco - CKMB (70.4 <italic>versus</italic> 12) e fra&#231;&#227;o de eje&#231;&#227;o (50 <italic>versus</italic> 55%).</p>
    <p content-type="asset">
      <table-wrap id="aop_4817tab01">
        <graphic xlink:href="1678-4170-abc-100-06-0502-30101-gt01.jpg"/></table-wrap>
    </p>
    <p>Na <xref ref-type="table" rid="aop_4817tab02">Tabela 2</xref>, que analisa o uso de f&#225;rmacos, observa-se que maior mortalidade esteve relacionada &#224; utiliza&#231;&#227;o de betabloqueadores por via intravenosa (8,2 <italic>versus</italic> 16,8%), nitratos (66,4 <italic>versus</italic> 80,5 %), Heparina de Baixo Peso Molecular (HBPM) (55,0 <italic>versus</italic> 69,8%), tirofiban (10,4 <italic>versus </italic>36,9%), amiodarona (6,8 <italic>versus</italic> 28,9%), lidoca&#237;na (2,3 <italic>versus</italic> 6,7%) e diur&#233;ticos (27,2 <italic>versus</italic> 52,3%). Houve redu&#231;&#227;o na mortalidade relacionada ao uso de betabloqueadores orais (79,1 <italic>versus </italic>38,9%); bloqueadores dos canais de c&#225;lcio (10,1 <italic>versus</italic> 4,7%); Heparina N&#227;o Fracionada (HNF) (31,3 <italic>versus</italic> 23,5%); clopidogrel (63,7 <italic>versus</italic> 49,7%); Inibidores da Enzima de Convers&#227;o da Angiotensina (IECA) (67,3 <italic>versus</italic> 56,4%); IECA e/ou Bloqueadores dos Receptores de Angiotensina (BRA) (70,5 <italic>versus</italic> 57,7%) e estatinas (78,8 <italic>versus</italic> 48,3%); al&#233;m das associa&#231;&#245;es aspirina, betabloqueadores orais e estatina (63,2 <italic>versus</italic> 22,1%) e aspirina, betabloqueadores orais, estatina e IECA (45,4 <italic>versus</italic> 16,1%).</p>
    <p content-type="asset">
      <table-wrap id="aop_4817tab02">
        <graphic xlink:href="1678-4170-abc-100-06-0502-30101-gt02.jpg"/></table-wrap>
    </p>
    <p>A <xref ref-type="table" rid="aop_4817tab03">Tabela 3</xref> analisa complica&#231;&#245;es/procedimentos associadas ao &#243;bito: choque cardiog&#234;nico/edema pulmonar (3,5 <italic>versus</italic> 75,8%), insufici&#234;ncia card&#237;aca (7,75 <italic>versus</italic> 59,1%), Killip classe II (10,8 <italic>versus</italic> 14,0%); Killip classe III (2,8 <italic>versus</italic> 15,1%), Killip classe IV (1,7 <italic>versus</italic> 65,5%), disfun&#231;&#227;o ventricular esquerda moderada (22,0 <italic>versus</italic> 31,7%) e grave (8,9 <italic>versus</italic> 26,8%), IAM/novo IAM (1,4 <italic>versus</italic> 11,4%), angina recorrente (6,1 <italic>versus</italic> 14,1%), arritmias necessitando de tratamento (6,0 <italic>versus</italic> 53,7%), acidente vascular cerebral (0,5 <italic>versus</italic> 4,0%), sangramento maior (4,0 <italic>versus</italic> 22,8%), parada card&#237;aca (1,0 <italic>versus</italic> 62,4%), complica&#231;&#245;es mec&#226;nicas (0,4 <italic>versus</italic> 3,4%), cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica (10,9 <italic>versus</italic> 22,1%), marca-passo (1,4 <italic>versus</italic> 14,1%) e bal&#227;o intra-a&#243;rtico (0,6 <italic>versus</italic> 7,4%). Estiveram associadas &#224; sobrevida angiografia coronariana (85,1 <italic>versus</italic> 75,0%), fun&#231;&#227;o ventricular esquerda normal (38,9 <italic>versus</italic> 12,2%) e discreta (30,2 <italic>versus</italic> 29,3%) e interven&#231;&#227;o coronariana percut&#226;nea (53,6 <italic>versus</italic> 36,8%).</p>
    <p content-type="asset">
      <table-wrap id="aop_4817tab03">
        <graphic xlink:href="1678-4170-abc-100-06-0502-30101-gt03.jpg"/></table-wrap>
    </p>
    <p>O diagn&#243;stico final mais frequente foi AI, seguido por IAMST e IAMNST, conforme observado na <xref ref-type="table" rid="aop_4817tab04">Tabela 4</xref>.</p>
    <p content-type="asset">
      <table-wrap id="aop_4817tab04">
        <graphic xlink:href="1678-4170-abc-100-06-0502-30101-gt04.jpg"/></table-wrap>
    </p>
    <p>O modelo de regress&#227;o log&#237;stica m&#250;ltipla dos fatores da demografia e das interven&#231;&#245;es hospitalares associadas ao &#243;bito, apresentados na <xref ref-type="table" rid="aop_4817tab05">Tabela 5</xref>, mostrou aumento de risco do g&#234;nero feminino (OR = 1,45; IC95% = 1,16-1,81), diabetes melito (OR = 1,59; IC95% 1,27-1,98) e IMC (OR = 1,27; IC95% = 1,23-1,30) e fator protetor da interven&#231;&#227;o coronariana (OR = 0,70; IC95% = 0,57-0,86). A <xref ref-type="table" rid="aop_4817tab06">Tabela 6</xref> mostra as estimativas do risco de &#243;bito das complica&#231;&#245;es maiores intra-hospitalares: choque cardiog&#234;nico/EAP, reinfarto do mioc&#225;rdio, acidente vascular cerebral, sangramento grave, parada cardiorrespirat&#243;ria e classe funcional de Killip.</p>
    <p content-type="asset">
      <table-wrap id="aop_4817tab05">
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    </p>
    <p content-type="asset">
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    </p>
    <p>
      <bold>Discuss&#227;o</bold>
    </p>
    <p>Os registros cl&#237;nicos constituem excelente oportunidade para avaliar a apresenta&#231;&#227;o cl&#237;nica, o comportamento, o tratamento e a evolu&#231;&#227;o de uma doen&#231;a e dos pacientes por ela afetados. Estudos cl&#237;nicos randomizados, embora tamb&#233;m forne&#231;am informa&#231;&#245;es cl&#237;nicas, seguem crit&#233;rios de inclus&#227;o espec&#237;ficos, limitando a amostra. J&#225; nos registros, os pacientes n&#227;o s&#227;o selecionados e seus achados refletem com mais propriedade o chamado "mundo real", no qual os cardiologistas trabalham e vivenciam sua rotina di&#225;ria.</p>
    <p>Nesta abordagem do banco de dados do RBSCA, procurou-se analisar, em conjunto, todo o espectro da SCA, sem individualizar os tr&#234;s quadros cl&#237;nicos (AI, IAMNST e IAMST). Foram inclu&#237;dos 2.693 pacientes e procurou-se estabelecer a import&#226;ncia das principais vari&#225;veis analisadas e relacion&#225;-las com as complica&#231;&#245;es e &#243;bitos observados durante a interna&#231;&#227;o.</p>
    <p>Semelhante a outros registros contempor&#226;neos de SCA, neste, a AI foi tamb&#233;m o diagn&#243;stico mais frequente (42%), com mortalidade de 3,06%, seguido pelo IAMST (35%), com mortalidade de 8,10%, IAMNST (20%), com mortalidade de 6,80%, e diagn&#243;stico n&#227;o comprovado 2,7%, com mortalidade 1,36%. A mortalidade global da SCA foi de 5,53%. </p>
    <p>Registro recente de um hospital nacional especializado identificou mortalidade hospitalar em AI/IAMNST de 4,8% e mortalidade no IAMST de 6,4%, sem diferen&#231;a significativa entre esses diagn&#243;sticos<sup>9</sup>. Em outro registro nacional unic&#234;ntrico, que incluiu 411 pacientes, a mortalidade intra-hospitalar para angina inst&#225;vel foi de 4,1%, IAM de 12,5% e total de 9,0%<sup>15</sup>.</p>
    <p>No <italic>Brazilian Registry on Acute Coronary Syndromes</italic> (BRACE), foram analisadas as diferen&#231;as regionais sobre utiliza&#231;&#227;o de f&#225;rmacos e terap&#234;uticas de reperfus&#227;o (fibrinol&#237;ticos e angioplastia prim&#225;ria) em 1.150 pacientes<sup>16</sup>. </p>
    <p>O Registro Brasileiro da Pr&#225;tica Cl&#237;nica em S&#237;ndromes Coronariana Agudas da Sociedade Brasileira de Cardiologia (ACCEPT-SBC) &#233; um registro observacional, prospectivo, que visa documentar a pr&#225;tica cl&#237;nica hospitalar da SCA efetivada em hospitais p&#250;blicos e privados brasileiros. Incluiu 24 hospitais e 2.475 pacientes com diagn&#243;stico confirmado de SCA<sup>17,18</sup>. A <xref ref-type="table" rid="aop_4817tab07">Tabela 7</xref> compara as principais diferen&#231;as dispon&#237;veis em rela&#231;&#227;o ao Registro Brasileiro da Pr&#225;tica Cl&#237;nica em S&#237;ndromes Coronariana Agudas da Sociedade Brasileira de Cardiologia (ACCEPT-SBC) e o RBSCA.</p>
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      <table-wrap id="aop_4817tab07">
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    </p>
    <p>Embora uma compara&#231;&#227;o estat&#237;stica n&#227;o seja poss&#237;vel, devido aos dados do BRACE e ACCEPT-SBC n&#227;o estarem dispon&#237;veis de maneira individualizada, as compara&#231;&#245;es num&#233;ricas dispon&#237;veis n&#227;o apresentam grandes discord&#226;ncias (<xref ref-type="table" rid="aop_4817tab07">Tabela 7</xref>). Apenas as mortalidades no ACCEPT-SBC e RBSCA s&#227;o diferentes (2,75 e 5,53%), respectivamente, provavelmente devido &#224;s caracter&#237;sticas dos hospitais e pacientes, visto que apenas 50% dos hospitais do ACCEPT-SBC atendiam o SUS, enquanto no RBSCA esse n&#250;mero atingiu 74%. No ACCEPT-SBC, a cinecoronariografia foi realizada em 80,6%, ICP em 50,8% e cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica (CRM) em 6,1%; no RBSCA, esses n&#250;meros foram de 84,5%, 52,7%, 11,6%, respectivamente.</p>
    <p>No registro espanhol Mascara<sup>19</sup>, que incluiu 7.923 pacientes, a mortalidade total hospitalar foi de 5,7%, sendo na AI/IAMNST de 3,9%, no IAMST de 7,6% e na SCA n&#227;o classificada de 8,8%. Dados do registro GRACE, de 2002, mostraram uma mortalidade hospitalar na AI de 3%, IAMNST de 5% e no IAMST de 7%. No registro norte-americano Action<sup>20</sup>, que incluiu 22.025 com IAMST, a mortalidade hospitalar foi de 6,0% e, no IAMNST, que incluiu 32.741 pacientes, a mortalidade foi de 4,0%. Esses dados mostraram um alinhamento dos achados do RBSCA com outros registros.</p>
    <p>No RBSCA, os riscos mais frequentemente associados ao aparecimento da SCA e que tiveram preval&#234;ncia &gt; 40% foram hipertens&#227;o arterial, angina pr&#233;via, dislipidemia, hist&#243;ria familiar de DAC e tratamento farmacol&#243;gico para DAC. Outras condi&#231;&#245;es basais associadas &#224; mortalidade, embora menos frequentes (&lt; 40%), foram: g&#234;nero feminino, tabagismo (negativa), acidente vascular cerebral, insufici&#234;ncia card&#237;aca, insufici&#234;ncia renal cr&#244;nica, diabetes melito, interven&#231;&#227;o coronariana percut&#226;nea. Frequ&#234;ncia card&#237;aca, press&#227;o arterial sist&#243;lica e diast&#243;lica, IMC e diagn&#243;stico de alta estiveram associados a uma maior mortalidade hospitalar.</p>
    <p>As complica&#231;&#245;es relacionadas ao &#243;bito foram: choque cardiog&#234;nico/edema agudo de pulm&#227;o, insufici&#234;ncia card&#237;aca, novo infarto, angina recorrente, arritmias necessitando tratamento, acidente vascular cerebral, sangramento maior, parada card&#237;aca e complica&#231;&#245;es mec&#226;nicas. Aqueles que necessitaram de cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica, marca-passos e bal&#227;o intra-a&#243;rtico (possivelmente casos de maior gravidade), tamb&#233;m foram &#224; &#243;bito com maior frequ&#234;ncia. A interven&#231;&#227;o coronariana percut&#226;nea comportou-se como procedimento protetor.</p>
    <p>Dos f&#225;rmacos de uso intra-hospitalar, destacaram-se como mais frequentemente utilizados a aspirina, os betabloqueadores, os nitratos, o clopidogrel, as heparinas, as estatinas e os IECA. Fizeram uso da associa&#231;&#227;o aspirina, betabloqueadores orais e estatina 60,9%, enquanto 43,8% associaram IECA a esses medicamentos. Redu&#231;&#227;o na mortalidade esteve associada ao uso de betabloqueadores orais, bloqueadores dos canais de c&#225;lcio, HNF, clopidogrel, IECA, estatinas, associa&#231;&#227;o aspirina, betabloqueadores orais e estatina e associa&#231;&#227;o aspirina, betabloqueadores orais, estatina e IECA. Essas duas associa&#231;&#245;es s&#227;o padr&#245;es no tratamento da SCA, sendo a associa&#231;&#227;o com IECA mais utilizada na presen&#231;a de disfun&#231;&#227;o ventricular esquerda. A mortalidade foi significativamente maior nos que receberam betabloqueadores por via intravenosa, nitratos, tirofiban, amiodarona e lidoca&#237;na, diur&#233;ticos. Neste tipo de estudo, &#233; dif&#237;cil caracterizar-se medica&#231;&#245;es como protetoras ou n&#227;o. A indica&#231;&#227;o de determinados f&#225;rmacos, como diur&#233;ticos e antiarr&#237;tmicos, est&#225;, muitas vezes, associada a gravidade do quadro cl&#237;nico. Observa-se que a orienta&#231;&#227;o terap&#234;utica tem seguido as orienta&#231;&#245;es preconizadas pelas diretrizes nacionais<sup>21,22</sup>.</p>
    <p>
      <bold>Limita&#231;&#245;es do registro</bold>
    </p>
    <p>Embora os investigadores convidados fossem todos experientes em pesquisa clinica (<xref ref-type="app" rid="anex">Anexo 1</xref>) n&#227;o houve monitoriza&#231;&#227;o nem auditoria local para verifica&#231;&#227;o das informa&#231;&#245;es, pela falta de recursos financeiros. Todas as informa&#231;&#245;es coletadas foram relatadas pelos servi&#231;os participantes. Apenas dados discrepantes ou faltantes foram averiguados.</p>
    <p>Os hospitais participantes, concentrados , nas Regi&#245;es Sul e Sudeste, s&#227;o hospitais terci&#225;rios, equipados para procedimentos de interven&#231;&#227;o, percut&#226;nea ou cir&#250;rgica, representando um perfil diferenciado para o atendimento da SCA. </p>
    <p>Embora solicitado que a inclus&#227;o fosse cont&#237;nua, &#233; poss&#237;vel que isso n&#227;o se tenha ocorrido, assim como podem n&#227;o ter sido inclu&#237;dos aqueles que faleceram no atendimento inicial.</p>
    <p>
      <bold>Implica&#231;&#245;es cl&#237;nicas</bold>
    </p>
    <p>O RBSCA &#233; um registro robusto, com uma amostra significativa de pacientes com SCA internados em 23 hospitais brasileiros. Esse registro se preocupou em identificar a totalidade de pacientes internados, fugindo da individualiza&#231;&#227;o unit&#225;ria dessa s&#237;ndrome, o que poderia comprometer resultados, pela dificuldade muitas vezes encontrada na caracteriza&#231;&#227;o diagn&#243;stica. Os dados foram coletados por via da <italic>internet</italic>, uniformizando as informa&#231;&#245;es e evitando erros frequentemente cometidos pela coleta escrita. Por serem terci&#225;rios os hospitais participantes, tais dados devem refletir o que de melhor se faz para o tratamento desses pacientes em nosso meio.</p>
    <p>
      <bold>Conclus&#227;o</bold>
    </p>
    <p>Esse registro de SCA anteriormente teve seus achados parciais divulgados tanto a n&#237;vel nacional<sup>10,20</sup> como internacional<sup>11,21</sup>. Seus resultados, embora com as habituais limita&#231;&#245;es de compara&#231;&#245;es, n&#227;o diferem de dados coletados em outros registros, dentro e fora do pa&#237;s, sendo consistentes com estes.</p>
    <p>O entendimento de seus achados pode ajudar no mapeamento de nossas inconsist&#234;ncias e na melhoria do planejamento do atendimento p&#250;blico e privado da SCA.</p>
    <p>
      <bold>Contribui&#231;&#227;o dos autores</bold>
    </p>
    <p>Concep&#231;&#227;o e desenho da pesquisa: Piegas LS, Avezum A, Guimar&#227;es HP; Obten&#231;&#227;o de dados: Piegas LS, Avezum A, Guimar&#227;es HP, Muniz AJ, Reis HJL, Santos ES, Knobel M, Souza R; An&#225;lise e interpreta&#231;&#227;o dos dados: Piegas LS, Avezum A, Guimar&#227;es HP, Souza R; An&#225;lise estat&#237;stica: Piegas LS, Souza R; Obten&#231;&#227;o de financiamento e Revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do intelectual: Piegas LS; Reda&#231;&#227;o do manuscrito: Piegas LS, Avezum A, Souza R.</p>
    <p>
      <bold>Potencial Conflito de Interesses</bold>
    </p>
    <p>Declaro n&#227;o haver conflito de interesses pertinentes.</p>
    <p>
      <bold>Fontes de Financiamento</bold>
    </p>
    <p>O presente estudo n&#227;o teve fontes de financiamento externas.</p>
    <p>
      <bold>Vincula&#231;&#227;o Acad&#234;mica</bold>
    </p>
    <p>N&#227;o h&#225; vincula&#231;&#227;o deste estudo a programas de p&#243;s-gradua&#231;&#227;o.</p>
    <p>
      <fn id="end" fn-type="corresp">
        <label>
          <bold>Correspond&#234;ncia:</bold>
        </label>
        <p> Leopoldo Soares Piegas </p>
        <p> Rua Abilio Soares, 227. Cj. 32 </p>
        <p> CEP 04005-000. S&#227;o Paulo. SP - Brasil </p>
        <p> E-mail: </p>
        <p>
          <email xlink:href="lpiegas@uol.com.br">lpiegas@uol.com.br</email>
        </p>
      </fn>
    </p>
    <p>Artigo recebido em 09/04/12, revisado em 24/09/12, aceito em 19/11/12.</p>
    <p/>
    <p>Bahia: <italic>Salvador</italic> - Funda&#231;&#227;o Bahiana de Cardiologia (24) (A Rabelo Jr, E C Porto); Hospital Portugu&#234;s (19) (M S Teixeira, J P Esteves). Minas Gerais: <italic>Belo Horizonte - </italic>Hospital Socor (2) (L R A Castro, J C F Garcia); Hospital Madre Tereza (173) (R L Marino, B C A Marino); <italic>Juiz de Fora</italic> - Santa Casa de Miseric&#243;rdia de Juiz de Fora (567) (A J Muniz). Par&#225;: <italic>Bel&#233;m</italic> - Funda&#231;&#227;o P&#250;blica Estadual Hospital de Cl&#237;nicas Gaspar Vianna (450) (H J L Reis, M S Carneiro). Paran&#225;: <italic>Maring&#225; - </italic>Hospital Santa Rita - Associa&#231;&#227;o Beneficente Bom Samaritano (73) (R D Mora Jr, E K Hayashi);<italic> Curitiba</italic> - Hospital Universit&#225;rio Evang&#233;lico de Curitiba (192) (P R F Rossi, C M C Branco). Pernambuco: <italic>Recife - </italic>Hospital Agamenon Magalh&#227;es (11) (J B M X Moraes Jr); Real Hospital Portugu&#234;s (S T Montenegro) (9) . Rio de Janeiro: <italic>Rio de Janeiro - </italic>Hospital Barra D`Or (48) (A C B S Figueiredo, M A N Rati). Rio Grande do Sul: <italic>Passo Fundo - </italic>Hospital S&#227;o Vicente de Paulo (19) (R T Tumelero, N T Duda); <italic>Porto Alegre - </italic>Hospital M&#227;e de Deus (30) (CP Jaeger, E R Manenti); Hospital S&#227;o Francisco - ISCMPA (6) (P E Le&#227;es, C Blacher); Hospital S&#227;o Lucas de PUCRS (104) (L C Bodanese, A V Azevedo). S&#227;o Paulo: <italic>S&#227;o Paulo - </italic>Hospital Israelita Albert Einstein (255) (M Knobel, M Makdisse); Instituto do Cora&#231;&#227;o - HCFMUSP (12) (J C Nicolau, L M Baracioli); Instituto Dante Pazzanese de Cardiologia (439) (E S Santos, M P Pereira); Hospital do Cora&#231;&#227;o - HCOR (17) (I M R Fernandes, E R Romano); <italic>S&#227;o Jos&#233; do Rio Preto - </italic>Hospital de Base/Faculdade de Medicina de S&#227;o Jos&#233; do Rio Preto (96) (L N Maia, M A B T Lemos); Instituto de Mol&#233;stias Cardiovasculares - IMC (60) (G V Greque, J C A Ayoub); <italic>Campinas - </italic>Hospital e Maternidade Celso Pierro - PUC Campinas (63) (J F K Saraiva, M L Paiva); <italic>Mar&#237;lia - </italic>Instituto do Cora&#231;&#227;o e Santa Casa de Miseric&#243;rdia de Mar&#237;lia (24) (A Rodrigues, J C F Braga).</p>
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        </element-citation>
      </ref>
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        <mixed-citation>20. ACTION Registry-GWTG DATA: July 1.2008 - June 30, 2009. [Acessed on 2010 July 10]. Available from: <ext-link ext-link-type="uri" xlink:href="http://www.outcome.com">http://www.outcome.com</ext-link></mixed-citation>
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      <ref id="B21">
        <mixed-citation>21. Nicolau JC, Timerman A, Piegas LS, Marin-Neto JA, Rassi A Jr. Guidelines for unstable angina and non-ST-segment elevation myocardial infarction of the Brazilian Society of Cardiology (II Edition, 2007). Arq Bras Cardiol. 2007;89(4):e89-e131.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Guidelines for unstable angina and non-ST-segment elevation myocardial infarction of the Brazilian Society of Cardiology (II Edition, 2007)</article-title>
          <source>Arq Bras Cardiol</source>
          <date>
            <year>2007</year>
          </date>
          <fpage>e89</fpage>
          <lpage>e131</lpage>
          <issue>4</issue>
          <volume>89</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Nicolau</surname>
              <given-names>JC</given-names>
            </name>
            <name>
              <surname>Timerman</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Piegas</surname>
              <given-names>LS</given-names>
            </name>
            <name>
              <surname>Marin-Neto</surname>
              <given-names>JA</given-names>
            </name>
            <name>
              <surname>Rassi Jr</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B22">
        <mixed-citation>22. Piegas LS, Feitosa G, Mattos LA, Nicolau JC, Rossi Neto JM, Timerman A, et al; Sociedade Brasileira de Cardiologia. IV Diretriz da Sociedade Brasileira de Cardiologia sobre tratamento do infarto agudo do mioc&#225;rdio com supradesn&#237;vel do segmento ST. Arq Bras Cardiol. 2009;93(6 supl. 2):e179-e264.</mixed-citation>
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          <source>Arq Bras Cardiol</source>
          <date>
            <year>2009</year>
          </date>
          <fpage>e179</fpage>
          <lpage>e264</lpage>
          <issue>6</issue>
          <volume>93</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Piegas</surname>
              <given-names>LS</given-names>
            </name>
            <name>
              <surname>Feitosa</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Mattos</surname>
              <given-names>LA</given-names>
            </name>
            <name>
              <surname>Nicolau</surname>
              <given-names>JC</given-names>
            </name>
            <name>
              <surname>Rossi Neto</surname>
              <given-names>JM</given-names>
            </name>
            <name>
              <surname>Timerman</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
    </ref-list>
    <app-group>
      <app id="anex">
        <label>Anexo 1</label>
        <title> - Hospitais, inclus&#245;es e investigadores </title>
      </app>
    </app-group>
  </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">Acute coronary syndrome behavior: results of a Brazilian registry</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>BACKGROUND: Brazil lacks published multicenter registries of acute coronary syndrome. OBJECTIVE: The Brazilian Registry of Acute Coronary Syndrome is a multicenter national study aiming at providing data on clinical aspects, management and hospital outcomes of acute coronary syndrome in our country. METHODS: A total of 23 hospitals from 14 cities, participated in this study. Eligible patients were those who came to the emergency wards with suspected acute coronary syndrome within the first 24 hours of symptom onset, associated with compatible electrocardiographic alterations and/or altered necrosis biomarkers. Follow-up lasted until hospital discharge or death, whichever occurred first. RESULTS: Between 2003 and 2008, 2,693 ACS patients were enrolled, of which 864 (32.1%) were females. T he final diagnosis was unstable angina in 1,141 patients, (42.4%), with a mortality rate of 3.06%, non-ST elevation acute myocardial infarction (AMI) in 529 (19.6%), with mortality of 6.8%, ST-elevation AMI 950 (35.3%), with mortality of 8.1% and non-confirmed diagnosis 73 (2.7%), with mortality of 1.36%. The overall mortality was 5.53%. The multiple logistic regression model identified the following as risk factors for death regarding demographic factors and interventions: female gender (OR=1.45), diabetes mellitus (OR=1.59), body mass index (OR=1.27) and percutaneous coronary intervention (OR=0.70). A second model for death due to major complications identified: cardiogenic shock/acute pulmonary edema (OR=4.57), reinfarction (OR=3.48), stroke (OR=21.56), major bleeding (OR=3.33), cardiopulmonary arrest (OR=40.27) and Killip functional class (OR=3.37). CONCLUSION: The Brazilian Registry of Acute Coronary Syndrome data do not differ from other data collected abroad. The understanding of their findings may help promote better planning and management of acute coronary syndrome care in public and private health services.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Acute Coronary Syndrome</kwd>
        <kwd>Multicenter Studies as Topic</kwd>
        <kwd>Diseases Registries</kwd>
        <kwd>Clinical Evolution</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <fn id="enda-body2">
          <label>
            <bold>Acute coronary syndrome behavior: results of a Brazilian registry</bold>
          </label>
          <p>
            <bold>Leopoldo Soares Piegas<sup>I</sup>; &#193;lvaro Avezum<sup>I</sup>; H&#233;lio Penna Guimar&#227;es<sup>I</sup>; Antonio Jos&#233; Muniz<sup>II</sup>; Helder J. L. Reis<sup>III</sup>; Elizabete Silva dos Santos<sup>I</sup>; Marcos Knobel<sup>IV</sup>; Roberta de Souza<sup>I</sup></bold>
          </p>
        </fn>
      </p>
      <p><sup>I</sup>Instituto Dante Pazzanese de Cardiologia, S&#227;o Paulo, SP</p>
      <p><sup>II</sup>Santa Casa de Miseric&#243;rdia de Juiz de Fora, Juiz de Fora, MG</p>
      <p><sup>III</sup>Hospital das Cl&#237;nicas Gaspar Vianna, Bel&#233;m, PA</p>
      <p><sup>IV</sup>Hospital Israelita Albert Einstein, S&#227;o Paulo, SP - Brazil</p>
      <p>Mailing Address</p>
      <p>
        <bold>ABSTRACT</bold>
      </p>
      <p><bold>BACKGROUND:</bold> Brazil lacks published multicenter registries of acute coronary syndrome.</p>
      <p><bold>OBJECTIVE:</bold> The Brazilian Registry of Acute Coronary Syndrome is a multicenter national study aiming at providing data on clinical aspects, management and hospital outcomes of acute coronary syndrome in our country.</p>
      <p><bold>METHODS:</bold> A total of 23 hospitals from 14 cities, participated in this study. Eligible patients were those who came to the emergency wards with suspected acute coronary syndrome within the first 24 hours of symptom onset, associated with compatible electrocardiographic alterations and/or altered necrosis biomarkers. Follow-up lasted until hospital discharge or death, whichever occurred first.</p>
      <p><bold>RESULTS:</bold> Between 2003 and 2008, 2,693 ACS patients were enrolled, of which 864 (32.1%) were females. T he final diagnosis was unstable angina in 1,141 patients, (42.4%), with a mortality rate of 3.06%, non-ST elevation acute myocardial infarction (AMI) in 529 (19.6%), with mortality of 6.8%, ST-elevation AMI 950 (35.3%), with mortality of 8.1% and non-confirmed diagnosis 73 (2.7%), with mortality of 1.36%. The overall mortality was 5.53%. The multiple logistic regression model identified the following as risk factors for death regarding demographic factors and interventions: female gender (OR=1.45), diabetes mellitus (OR=1.59), body mass index (OR=1.27) and percutaneous coronary intervention (OR=0.70). A second model for death due to major complications identified: cardiogenic shock/acute pulmonary edema (OR=4.57), reinfarction (OR=3.48), stroke (OR=21.56), major bleeding (OR=3.33), cardiopulmonary arrest (OR=40.27) and Killip functional class (OR=3.37).</p>
      <p><bold>CONCLUSION:</bold> The Brazilian Registry of Acute Coronary Syndrome data do not differ from other data collected abroad. The understanding of their findings may help promote better planning and management of acute coronary syndrome care in public and private health services.</p>
      <p><bold>Keywords:</bold> Acute Coronary Syndrome; Multicenter Studies as Topic; Diseases Registries; Clinical Evolution.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>In the year 2010, circulatory system diseases, the third leading cause of hospitalization, with 210,046 hospitalizations due to ischemic heart disease were responsible, in Brazil, for 29% of deaths, of a total of 1,133,761. The absolute number of deaths from ischemic heart disease in that year was 99,408 deaths or 52.11 deaths/100,000 inhabitants, whereas deaths from cerebrovascular diseases was 99,159 or 51.98 deaths/100,000 inhabitants<sup>1</sup>. The prevalence of Coronary Artery Disease (CAD) in the adult population is estimated at 5-8%<sup>2</sup>.</p>
      <p>In 2010, there were 79,954 deaths associated with acute coronary syndrome (ACS). These figures account for the total number of deaths from angina and acute myocardial infarction (AMI), corresponding to 7.05% of total deaths in the year, or 24.67% of deaths from circulatory system diseases<sup>1</sup>.</p>
      <p>The ACS is also an important cause of hospitalization, with AMI being the third leading cause of hospitalization under the Brazilian Unified Health System (SUS) in 2009. It represented 10.2% of hospital admissions, a number that exceeds 25% of the population older than 50 years.</p>
      <p>The main source of health coverage in the country is provided by SUS, whereas private health insurance accounted for 25.9% (95% confidence interval - 95% CI = 25.4 to 26.4) of the population in 2008. ACS was responsible for the highest costs with hospital admissions, corresponding to a total of R$ 1.9 billion or 19% of total cost with hospitalizations<sup>3</sup>.</p>
      <p>Regarding the health coverage provided by SUS, in 2011, the estimated direct cost of the ACS was R $ 522,286,726.00, corresponding to 0.77% of the total budget, whereas the Private Health System cost was R$ 515,138,617.00, with indirect costs of $ 2.8 billion and the total cost estimated at R$ 3.8 billion<sup>4</sup>.</p>
      <p>The knowledge of hospital behavior of patients with ACS is essential for immediate in-hospital risk stratification and in the long term, for the acute episode survivors, as well as to show how these patients are managed in our country.</p>
      <p>Several international ACS registries have been published, including some with the participation of Brazilians centers<sup>5-8</sup>. National registries are scarce and included patients from a single center, not representative of the national reality<sup>9</sup>. The Brazilian Registry of Acute Coronary Syndromes (RBSCA), partially presented in national<sup>10</sup> and international<sup>11 </sup>congresses, aims to fill this gap, providing this information to interested professionals. It aims to disclose the results of a large national multicenter registry, representative of the characteristics, management and hospital evolution of ACS in the country.</p>
      <p>
        <bold>Methods</bold>
      </p>
      <p>
        <bold>Study design</bold>
      </p>
      <p>RBSCA is a prospective, national, multicenter, non-funded study, designed to assess in-hospital data from patients with suspected ACS, admitted to the emergency department of hospitals invited to participate in the study, in different parts of Brazil, aiming to reflect the behavior of ACS in hospitals with the characteristics described below. The invited hospitals should have prior experience in clinical trials, as well as the main investigators, who should be experienced in research activities.</p>
      <p>
        <bold>Hospitals, investigators and population</bold>
      </p>
      <p>A total of 23 hospitals located in 14 cities participated in the RBSCA, of which four were private, 15 were philanthropic and four were public. Of these, six did not provide health care services through SUS. All had coronary care units or emergency rooms with electrocardiographic monitoring, hemodynamic laboratory and were able to carry out percutaneous coronary intervention and cardiac surgery procedures (<a href="#appe" link-type="internal">Appendix 1</a>).</p>
      <p>The principal investigators were Board Certified<sup>20</sup> by the Brazilian Cardiology Society (SBC) and / or had an academic degree<sup>14</sup>.</p>
      <p>The target population consisted of patients admitted to the emergency department or coronary care unit with a diagnosis of ACS.</p>
      <p>
        <bold>Eligibility</bold>
      </p>
      <p>Eligible patients were those who presented to the emergency room with suspected ACS, with a suggestive clinical picture, associated with compatible ECG alterations and/or altered necrosis markers. We included only patients with up to 24 hours of symptom onset. Follow-up was performed until hospital discharge or death, whichever occurred first. </p>
      <p>
        <bold>For AMI with ST-segment elevation (STEMI):</bold>
      </p>
      <p>&#149; conclusive electrocardiogram (ECG) alterations indicating STEMI: Persistent elevation of ST (<underline>&gt;</underline> 0.2 mV in two contiguous precordial leads, or <underline>&gt;</underline> 0.1 mV in at least two limb leads) or new left bundle branch block, or ECG alterations indicating true posterior AMI;</p>
      <p>&#149; increase in biochemical markers of necrosis;</p>
      <p>
        <bold>For AMI with no ST elevation (NSTEMI):</bold>
      </p>
      <p>&#149; alterations in ECG features compatible with ischemia (e.g., ST depression <underline>&gt;</underline> 1 mm in at least two adjacent leads or T-wave inversion &gt; 3 mm or any dynamic alteration in ST segment or transient ST elevation);</p>
      <p>&#149; increase in biochemical markers of necrosis.</p>
      <p>
        <bold>Unstable angina (UA):</bold>
      </p>
      <p>&#149; characteristic ECG alterations compatible with ischemia (e.g., ST depression 1 mm in at least two adjacent leads or T-wave inversion &gt; 3 mm or any dynamic alteration in ST segment or transient ST elevation).; </p>
      <p>&#149; no increase in biochemical markers of necrosis</p>
      <p>
        <bold>All</bold>
      </p>
      <p>&#149; signed informed consent form;</p>
      <p>&#149; onset of symptoms suggestive of ACS <underline>&lt;</underline> 24 hours.</p>
      <p>
        <bold>Exclusion criteria</bold>
      </p>
      <p>&#149; The exclusion criteria included:</p>
      <p>&#149; age &lt; 18 years;</p>
      <p>hospital admission with symptoms suggesting ACS, but not confirmed by clinical history, physical examination and laboratory tests (biochemical markers of necrosis).</p>
      <p>
        <bold>Data collection</bold>
      </p>
      <p>Data were collected and sent in electronic form through the internet to the Coordinating Center, located at Instituto Dante Pazzanese de Cardiologia. This form, containing 182 questions, included identification, personal history, demographics, diagnosis, hospital evolution, complications, drug treatment, interventions and hospital discharge status. When there were discrepancies in relation to the received data, the Research Center was contacted.</p>
      <p>The study protocol was approved by the Ethics Committees of the participating hospitals, and enrolled patients signed the free and informed consent form, according to Resolution #196 of the National Health Council, of October 10, 1996.</p>
      <p>
        <bold>Statistical Analysis</bold>
      </p>
      <p>Factors (qualitative measures) and covariates (quantitative measures) were compared in the presence or absence of death. Qualitative measures were summarized in descriptive statistics of absolute (n) and relative (n) frequencies, in the categories of the groups with the absence and presence of death. The association alone (univariate) between these measures and death was evaluated by Pearson's Chi-square test or Fisher's exact test<sup>12</sup>. Quantitative measures (continuous variables) were expressed as median and interquartile range (IQR) = (25<sup>th</sup> percentile-75<sup>th</sup> percentile).</p>
      <p>The nonparametric Mann-Whitney test was used for the comparison alone (univariate) of these measures between groups<sup>13</sup>. To better understand the predictors of risk of death, two analyses of multiple logistic regression models were performed<sup>14</sup>: one to identify demographic factors and associated in-hospital interventions, and another to identify the influence of major complications on death. Effects or differences were considered statistically significant when p values &lt; 0.05 were found. All statistical analyses were performed using the Statistical Package for Social Sciences (SPSS), release 19.</p>
      <p>
        <bold>Results</bold>
      </p>
      <p>Between 2003 and 2008, 2693 patients diagnosed with ACS were included in the study, of which 864 (32.1%) were women. The median age was 63 years. The final diagnosis was UA in 1141 (42.4%) patients, NSTEMI in 529 (19.6%), STEMI in 950 (35.3%) and unconfirmed diagnosis in 73 (2.7%).</p>
      <p>Comparison of baseline characteristics between survivors and deaths during hospitalization is shown in <xref ref-type="table" rid="en_aop_4817tab01-body2">Table 1</xref>. The significant differences of the variables in survivors, when compared to the ones who died were median age (62 <italic>versus </italic>71 years), female gender (31.6 <italic>versus</italic> 41.6%), family history of CAD (29.5% <italic>versus</italic> 44.5% versus 29.5%), cerebrovascular accident (4.9 <italic>versus</italic> 10.1%), CHF (7.2 <italic>versus</italic> 18.8%), diabetes mellitus (27.2 <italic>versus</italic> 38.3%), prior percutaneous coronary intervention (PCI) (18.2 <italic>versus</italic> 11.4%), heart rate (75 <italic>versus</italic> 82 bpm), systolic blood pressure (130 <italic>versus</italic> 120 mmHg), diastolic blood pressure (80 <italic>versus</italic> 70 mmHg), body mass index (26.1 <italic>versus </italic>25.4), creatine kinase MB fraction of cardiac muscle - CKMB (70.4 <italic>versus</italic> 12) and ejection fraction (50 <italic>versus</italic> 55).</p>
      <p content-type="asset">
        <table-wrap id="en_aop_4817tab01-body2">
          <graphic xlink:href="1678-4170-abc-100-06-0502-30101-gt01-en.jpg"/></table-wrap>
      </p>
      <p>In <xref ref-type="table" rid="en_aop_4817tab02-body2">Table 2</xref>, which assesses drug use, it can be observed that higher mortality was related to the intravenous use of beta-blockers (8.2 <italic>versus</italic> 16.8%), nitrates (66.4 <italic>versus </italic>80.5%), Low Molecular Weight Heparin (LMWH) (55.0 versus 69.8%), tirofiban (10.4 <italic>versus</italic> 36.9%), amiodarone (6.8 <italic>versus</italic> 28.9%), lidocaine (2.3 <italic>versus</italic> 6.7%) and diuretics (27.2 <italic>versus</italic> 52.3%). There was a decrease in mortality associated with the use of oral beta-blockers (79.1 <italic>versus</italic> 38.9%), calcium channel blockers (10.1 <italic>versus</italic> 4.7%), unfractionated heparin (UFH) (31.3 <italic>versus</italic> 23.5%), clopidogrel (63.7 <italic>versus</italic> 49.7%); Angiotensin-Converting Enzyme Inhibitors (ACEI) (67.3 <italic>versus</italic> 56.4%), ACEI and/or Angiotensin-receptor blockers (ARBs) (70.5 <italic>versus</italic> 57.7%) and statins (78.8 <italic>versus</italic> 48.3%); in addition to the aspirin, oral beta-blockers and statin (63.2 <italic>versus</italic> 22.1%) and aspirin, oral beta-blockers, statins and ACEI associations (45.4 <italic>versus</italic> 16.1%).</p>
      <p content-type="asset">
        <table-wrap id="en_aop_4817tab02-body2">
          <graphic xlink:href="1678-4170-abc-100-06-0502-30101-gt02-en.jpg"/></table-wrap>
      </p>
      <p><xref ref-type="table" rid="en_aop_4817tab03-body2">Table 3</xref> analyzes complications/procedures associated with death: cardiogenic shock/pulmonary edema (3.5 <italic>versus</italic> 75.8%), heart failure (7.75 <italic>versus </italic>59.1%), Killip class II (10.8 <italic>versus</italic> 14.0%) , Killip class III (2.8 <italic>versus </italic>15.1%), Killip class IV (1.7 <italic>versus</italic> 65.5%), moderate (22.0 <italic>versus </italic>31.7%) and severe (8.9 <italic>versus</italic> 26.8%) left ventricular function, AMI/new AMI (1.4 <italic>versus</italic> 11.4%), recurrent angina (6.1 <italic>versus </italic>14.1%), arrhythmia requiring treatment (6.0 <italic>versus</italic> 53.7%), cerebrovascular accident (CVA) (0.5 <italic>versus</italic> 4.0%), major bleeding (4.0 <italic>versus</italic> 22.8%), cardiac arrest (1.0 <italic>versus </italic>62.4%), mechanical complications (0.4 <italic>versus</italic> 3.4%), CABG (10.9 <italic>versus</italic> 22.1%), pacemaker (1.4 <italic>versus</italic> 14.1%) and intra-aortic balloon (0.6 <italic>versus</italic> 7.4%). Coronary angiography (85.1 <italic>versus</italic> 75.0%), normal (38.9 <italic>versus</italic> 12.2%) and mild (30.2 <italic>versus</italic> 29.3%) left ventricular function and percutaneous coronary intervention (53.6 <italic>versus</italic> 36.8%) were associated with survival.</p>
      <p content-type="asset">
        <table-wrap id="en_aop_4817tab03-body2">
          <graphic xlink:href="1678-4170-abc-100-06-0502-30101-gt03-en.jpg"/></table-wrap>
      </p>
      <p>The most frequent final diagnosis was UA, followed by STEMI and NSTEMI, as shown in <xref ref-type="table" rid="en_aop_4817tab04-body2">Table 4</xref>.</p>
      <p content-type="asset">
        <table-wrap id="en_aop_4817tab04-body2">
          <graphic xlink:href="1678-4170-abc-100-06-0502-30101-gt04-en.jpg"/></table-wrap>
      </p>
      <p>The multiple logistic regression model of demographic factors and in-hospital interventions associated with death, shown in <xref ref-type="table" rid="en_aop_4817tab05-body2">Table 5</xref>, disclosed an increased risk of female gender (OR = 1.45, 95% CI: 1.16 to 1.81), diabetes mellitus (OR = 1.59, 95% CI: 1.27 to 1.98) and BMI (OR = 1.27, 95% CI: 1.23 to 1.30) and protective factor of the coronary intervention (OR = 0.70 95%CI: 0.57 to 0.86). <xref ref-type="table" rid="en_aop_4817tab06-body2">Table 6</xref> shows the estimates of the mortality risk of major in-hospital complications: cardiogenic shock/APE, myocardial reinfarction, CVA, severe bleeding, cardiorespiratory arrest and Killip functional class.</p>
      <p content-type="asset">
        <table-wrap id="en_aop_4817tab05-body2">
          <graphic xlink:href="1678-4170-abc-100-06-0502-30101-gt05-en.jpg"/></table-wrap>
      </p>
      <p content-type="asset">
        <table-wrap id="en_aop_4817tab06-body2">
          <graphic xlink:href="1678-4170-abc-100-06-0502-30101-gt06-en.jpg"/></table-wrap>
      </p>
      <p>
        <bold>Discussion</bold>
      </p>
      <p>Clinical records are an excellent opportunity to evaluate the clinical presentation, behavior, treatment and outcome of a disease and the patients affected by it. Randomized clinical trials, while also providing clinical information, follow specific inclusion criteria, thus limiting the sample. In registries, patients are not selected and their findings more properly reflect the so-called "real world", in which cardiologists work and live their daily routine.</p>
      <p>Regarding this approach of the RBSCA database, we sought to analyze the entire spectrum of ACS, without differentiating the three clinical pictures (UA, NSTEMI and STEMI). A total of 2693 patients were included and we sought to establish the importance of the main variables analyzed and correlate them with the complications and deaths observed during hospitalization.</p>
      <p>Similar to other contemporary ACS registries, the present one also showed that UA was the most frequent diagnosis (42%), with a mortality of 3.06%, followed by STEMI (35%), with a mortality of 8.10%, NSTEMI (20%), with a mortality of 6.80%, and undefined diagnosis, 2.7%, with 1.36% mortality. The overall mortality in ACS was 5.53%.</p>
      <p>A recent registry of a national specialized hospital identified in-hospital mortality for UA/NSTEMI of 4.8% and mortality for STEMI of 6.4%, with no significant difference between these diagnoses<sup>9</sup>. In another single-center national registry, which included 411 patients, in-hospital mortality was 4.1% for unstable angina, 12.5% for AMI and total mortality of 9.0%<sup>15</sup>.</p>
      <p>The Brazilian Registry on Acute Coronary Syndromes (BRACE) analyzed regional differences on the use of drugs and reperfusion therapies (fibrinolytics and primary angioplasty) in 1,150 patients<sup>16</sup>.</p>
      <p>The Brazilian Registry of Clinical Practice in Acute Coronary Syndrome of the Brazilian Society of Cardiology (ACCEPT-SBC) is a prospective, observational registry that aims to document the in-hospital clinical practice of ACS carried in public and private hospitals in Brazil. It included 24 hospitals and 2,475 patients with a confirmed diagnosis of ACS<sup>17,18</sup>. <xref ref-type="table" rid="en_aop_4817tab07-body2">Table 7</xref> compares the main differences found in relation to the Brazilian Registry of Clinical Practice in Acute Coronary Syndromes of the Brazilian Society of Cardiology (ACCEPT-SBC) and RBSCA.</p>
      <p content-type="asset">
        <table-wrap id="en_aop_4817tab07-body2">
          <graphic xlink:href="1678-4170-abc-100-06-0502-30101-gt07-en.jpg"/></table-wrap>
      </p>
      <p>Although a statistical comparison is not possible because data from the BRACE and ACCEPT-SBC are not available on an individual basis, the available numerical comparisons show no large discrepancies (<xref ref-type="table" rid="en_aop_4817tab07-body2">Table 7</xref>). Only mortalities in ACCEPT-SBC and RBSCA are different (2.75 and 5.53%), respectively, probably due to the characteristics of hospitals and patients, since only 50% of hospitals met the ACCEPT-SBC treated SUS patients, while in RBSCA this figure reached 74%. In ACCEPT-SBC, coronary angiography was performed in 80.6%, PCI in 50.8% and coronary artery bypass graft surgery (CABG) in 6.1% of patients; in RBSCA, these figures were 84.5%, 52.7 % and 11.6%, respectively. </p>
      <p>In the Spanish registry Mascara<sup>19</sup>, which included 7,923 patients, the in-hospital overall mortality was 5.7%, with 3.9% for UA/NSTEMI, 7.6% for STEMI and 8.8% for unclassified ACS. Data from the GRACE registry, of 2002, showed an in-hospital mortality of 3% for UA, 5% for NSTEMI and 7% for STEMI. In the U.S. registry Action<sup>20</sup>, which included 22,025 patients with STEMI, the in-hospital mortality rate was 6.0% and in NSTEMI, which included 32,741 patients, mortality was 4.0%. These data showed the findings of RBSCA to be in agreement with those from other registries.</p>
      <p>In RBSCA, the risks most often associated with ACS onset and that had prevalence &gt; 40% were arterial hypertension, prior angina, dyslipidemia, family history of CAD and drug treatment for CAD. Other baseline conditions associated with mortality, although less frequent (&lt; 40%) were female gender, smoking (negative), CVA, heart failure, chronic renal failure, diabetes mellitus and percutaneous coronary intervention. Heart rate, systolic and diastolic blood pressure, BMI and diagnosis at discharge were associated with a higher in-hospital mortality.</p>
      <p>Complications associated with death were cardiogenic shock/acute pulmonary edema, heart failure, reinfarction, recurrent angina, arrhythmias requiring treatment, CVA, major bleeding, cardiac arrest and mechanical complications. Those who required coronary artery bypass surgery, pacemakers and intra-aortic balloon (possibly more severe cases), also showed higher incidence of death. Percutaneous coronary intervention was shown to be a protective factor.</p>
      <p>Of the drugs used in-hospital, the most frequently used were aspirin, beta-blockers, nitrates, clopidogrel, heparins, statins and ACE inhibitors. A total of 60.9% of patients used the aspirin, beta blockers and oral statin association, while 43.8% associated ACE inhibitors to these drugs. Decrease in mortality was associated with the use of oral beta-blockers, calcium channel blockers, UFH, clopidogrel, ACE inhibitors, statins, the association of aspirin, beta-blockers and statins and the association of aspirin, oral beta-blockers, statins and ACE inhibitors. These two associations are standard in the treatment of ACS, and the association with ACE inhibitors is more often used in the presence of left ventricular dysfunction.</p>
      <p>The mortality was significantly higher among those who received intravenous beta-blockers, nitrates, tirofiban, amiodarone, lidocaine, diuretics. In this type of study, it is difficult to characterize medications as being protective or not. The prescription of certain drugs, such as diuretics and antiarrhythmics, is often associated with clinical severity. It has been observed that the therapy prescribed follows the recommendations established by national guidelines<sup>21,22</sup>.</p>
      <p>
        <bold>Registry Limitations</bold>
      </p>
      <p>Although the invited investigators were all experienced in clinical research (<a href="#appe" link-type="internal">Appendix 1</a>) there was no local monitoring or auditing for information verification, due to lack of financial resources. All information collected was reported by participating services. Only missing or discrepant data were verified.</p>
      <p>The participating hospitals, concentrated in the South and Southeast regions, are tertiary hospitals equipped for interventional procedures, either percutaneous or surgical, representing a differentiated profile for ACS care.</p>
      <p>Although continuous inclusion was requested, it is possible that it has not occurred and those who died during the initial care may not have been included.</p>
      <p>
        <bold>Clinical Implications</bold>
      </p>
      <p>RBSCA is a robust registry, with a significant sample of ACS patients admitted to 23 hospitals in Brazil. This registry aimed to identify all inpatients, avoiding the unit individualization of this syndrome, which could compromise results, due to the difficulty found in diagnostic characterization. Data were collected through the internet, providing consistent information and preventing mistakes often committed when collecting written data. As the participating hospitals are tertiary institutions, these data must reflect the best treatment these patients receive in our country.</p>
      <p>
        <bold>Conclusion</bold>
      </p>
      <p>This ACS registry has had its partial findings previously disclosed both at national<sup>10,20 </sup>and international level<sup>11,21</sup>. Its results, although with the usual limitations of comparisons, do not differ from data collected by other registries, inside and outside the country, being consistent with them.</p>
      <p>Understanding these findings may help in mapping our inconsistencies and improving the planning of public and private care of ACS.</p>
      <p>
        <bold>Author contributions</bold>
      </p>
      <p>Conception and design of the research: Piegas LS, Avezum A, Guimar&#227;es HP; Acquisition of data: Piegas LS, Avezum A, Guimar&#227;es HP, Muniz AJ, Reis HJL, Santos ES, Knobel M, Souza R; Analysis and interpretation of the data: Piegas LS, Avezum A, Guimar&#227;es HP, Souza R; Statistical analysis: Piegas LS, Souza R; Obtaining funding and Critical revision of the manuscript for intellectual content: Piegas LS; Writing of the manuscript: Piegas LS, Avezum A, Souza R.</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>There were no external funding sources for this study.</p>
      <p>
        <bold>Study Association</bold>
      </p>
      <p>This study is not associated with any post-graduation program.</p>
      <p>
        <bold>References</bold>
      </p>
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  </sub-article>
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