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  <front>
    <journal-meta>
      <journal-id journal-id-type="nlm-ta">Arq Bras Cardiol</journal-id>
      <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>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v3">dqRp7Pj4s9BwDkxYn4dCkjB</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2016004200207</article-id>
      <article-id pub-id-type="publisher-id" specific-use="previous-pid">S0066-782X2016005021101</article-id>
      <article-id pub-id-type="doi">10.5935/abc.20160111</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Original Articles</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Syntax Score and Major Adverse Cardiac Events in Patients with Suspected Coronary Artery Disease: Results from a Cohort Study in a University-Affiliated Hospital in Southern Brazil</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Fuchs</surname>
            <given-names>Felipe C.</given-names>
          </name>
          <xref ref-type="corresp" rid="c1"/>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ribeiro</surname>
            <given-names>Jorge P.</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
          <xref ref-type="fn" rid="fn1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Fuchs</surname>
            <given-names>Fl&#225;vio D.</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Wainstein</surname>
            <given-names>Marco V.</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Bergoli</surname>
            <given-names>Luis C.</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Wainstein</surname>
            <given-names>Rodrigo V.</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Zen</surname>
            <given-names>Vanessa</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Kerkhoff</surname>
            <given-names>Alessandra C.</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Moreira</surname>
            <given-names>Leila B.</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Fuchs</surname>
            <given-names>Sandra C.</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <aff id="aff1">
          <institution content-type="orgname">Universidade Federal do Rio Grande do Sul</institution>
          <institution content-type="orgdiv1">Hospital de Cl&#237;nicas de Porto Alegre</institution>
          <addr-line>
            <named-content content-type="city">Porto Alegre</named-content>
            <named-content content-type="state">RS</named-content>
          </addr-line>
          <country country="BR">Brazil</country>
          <institution content-type="original">Hospital de Cl&#237;nicas de Porto Alegre - Universidade Federal do Rio Grande do Sul, Porto Alegre, RS - Brazil</institution>
          <institution content-type="normalized">Universidade Federal do Rio Grande do Sul</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="c1"><bold>Mailing Address: Felipe Costa Fuchs</bold>. Servi&#231;o de Cardiologia, Hospital de Cl&#237;nicas de Porto Alegre. Rua Ramiro, Barcelos, 2350, Santa Cec&#237;lia. Postal Code 90035-903, Porto Alegre, RS - Brazil. E-mail: <email>fcfuchs@terra.com.br</email>
				</corresp>
        <fn fn-type="con">
          <p>
            <bold>Author contributions</bold>
          </p>
          <p>Conception and design of the research: Fuchs FC, Ribeiro JP, Fuchs FD, Moreira LB, Fuchs SC; Acquisition of data: Fuchs FC, Wainstein MV, Bergoli LC, Wainstein RV, Zen V, Kerkhoff AC; Analysis and interpretation of the data and Critical revision of the manuscript for intellectual content: Fuchs FC, Ribeiro JP, Fuchs FD, Bergoli LC, Wainstein RV, Zen V, Kerkhoff AC, Moreira LB, Fuchs SC;Statistical analysis and Writing of the manuscript: Fuchs FC, Ribeiro JP, Fuchs FD, Fuchs SC; Obtaining financing: Ribeiro JP, Moreira LB, Fuchs SC.</p>
        </fn>
        <fn fn-type="conflict">
          <p>
            <bold>Potential Conflict of Interest</bold>
          </p>
          <p>No potential conflict of interest relevant to this article was reported.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub">
        <day>08</day>
        <month>08</month>
        <year>2016</year>
      </pub-date>
      <pub-date pub-type="collection">
        <month>9</month>
        <year>2016</year>
      </pub-date>
      <volume>107</volume>
      <issue>3</issue>
      <fpage>207</fpage>
      <lpage>215</lpage>
      <history>
        <date date-type="received">
          <day>05</day>
          <month>07</month>
          <year>2015</year>
        </date>
        <date date-type="rev-recd">
          <day>21</day>
          <month>03</month>
          <year>2016</year>
        </date>
        <date date-type="accepted">
          <day>01</day>
          <month>04</month>
          <year>2016</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/" xml:lang="en">
          <license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
        </license>
      </permissions>
      <abstract>
        <title>Abstract</title>
        <sec>
          <title>Background:</title>
          <p>The importance of coronary anatomy in predicting cardiovascular events is well known. The use of traditional anatomical scores in routine angiography, however, has not been incorporated to clinical practice. SYNTAX score (SXscore) is a scoring system that estimates the anatomical extent of coronary artery disease (CAD). Its ability to predict outcomes based on a baseline diagnostic angiography has not been tested to date.</p>
        </sec>
        <sec>
          <title>Objective:</title>
          <p>To evaluate the performance of the SXscore in predicting major adverse cardiac events (MACE) in patients referred for diagnostic angiography.</p>
        </sec>
        <sec>
          <title>Methods:</title>
          <p>Prospective cohort of 895 patients with suspected CAD referred for elective diagnostic coronary angiography from 2008 to 2011, at a university-affiliated hospital in Brazil. They had their SXscores calculated and were stratified in three categories: no significant CAD (n = 495), SXscore<sub>LOW-INTERMEDIATE</sub>: &lt; 23 (n = 346), and SXscore<sub>HIGH</sub>: &#8805; 23 (n = 54). Primary outcome was a composite of cardiac death, myocardial infarction, and late revascularization. Secondary endpoints were the components of MACE and death from any cause.</p>
        </sec>
        <sec>
          <title>Results:</title>
          <p>On average, patients were followed up for 1.8 &#177; 1.4 years. The primary outcome occurred in 2.2%, 15.3%, and 20.4% in groups with no significant CAD, SXscore<sub>LOW-INTERMEDIATE</sub>, and SXscore<sub>HIGH</sub>, respectively (p &lt; 0.001). All-cause death was significantly higher in the SXscore<sub>HIGH</sub> compared with the 'no significant CAD' group, 16.7% and 3.8% (p &lt; 0.001), respectively. After adjustment for confounding factors, all outcomes remained associated with the SXscore.</p>
        </sec>
        <sec>
          <title>Conclusions:</title>
          <p>SXscore independently predicts MACE in patients submitted to diagnostic coronary angiography. Its routine use in this setting could identify patients with worse prognosis.</p>
        </sec>
      </abstract>
      <kwd-group xml:lang="en">
        <title>Keywords:</title>
        <kwd>Coronary Artery Disease / epidemiology</kwd>
        <kwd>Probability</kwd>
        <kwd>Cineangiography</kwd>
        <kwd>Syntax Score</kwd>
        <kwd>Cohort Studies</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec sec-type="intro">
      <title>Introduction</title>
      <p>The importance of coronary anatomy in predicting cardiovascular events has been known for decades, when studies like CASS (Coronary Artery Study) registry were published.<xref ref-type="bibr" rid="B1">1</xref> This large cohort study showed the ability of anatomical scores of coronary artery disease (CAD) to predict events, but their routine use was not incorporated to clinical practice.<xref ref-type="bibr" rid="B2">2</xref> Nowadays, standard of care indicates functional, noninvasive, assessment of ischemia, such as stress-echocardiogram, nuclear imaging and magnetic resonance imaging, to evaluate patients with known or suspected CAD.<xref ref-type="bibr" rid="B3">3</xref> Nonetheless, a significant number of patients are eventually submitted to coronary angiography for diagnostic confirmation.<xref ref-type="bibr" rid="B3">3</xref> Therefore, re-assessing the performance of anatomical scores to predict outcomes, in a context of newer clinical and interventional therapies, is potentially worthwhile. Currently, the SYNTAX (Synergy between percutaneous coronary intervention with Taxus and Cardiac Surgery) Score (SXscore), a more elaborate method to quantify anatomic lesions, is an available online tool that estimates the anatomical extent of CAD.<xref ref-type="bibr" rid="B4">4</xref>
			</p>
      <p>The SXscore is a comprehensive angiographic scoring system based on coronary anatomy and lesion characteristics.<xref ref-type="bibr" rid="B4">4</xref> It was initially developed to determine the extent of CAD and lesion complexity, which reflect the difficulties in performing myocardial revascularization, particularly percutaneous coronary interventions (PCI). In the SYNTAX trial, high SXscore values (above 33) identified patients in whom coronary artery bypass grafting (CABG) resulted in better outcomes than in patients submitted to percutaneous revascularization.<xref ref-type="bibr" rid="B5">5</xref> Five-year follow-up of this trial identified patients with scores above 22 as more suitable for CABG.<xref ref-type="bibr" rid="B6">6</xref>
			</p>
      <p>The SXscore was developed as a tool in the decision-making process and, later on, its usefulness was expanded as a predicting score of major adverse cardiac events (MACE) in patients submitted to PCI.<xref ref-type="bibr" rid="B7">7</xref><sup>-</sup><xref ref-type="bibr" rid="B14">14</xref> Those studies included elective and urgent revascularization procedures. However, the majority of coronary angiographies are done for diagnostic purposes.<xref ref-type="bibr" rid="B15">15</xref> The prognostic performance of the SXscore in that setting has not been reported to date, and is the aim of this investigation.</p>
    </sec>
    <sec>
      <title>Objective</title>
      <p>To evaluate the performance of the SXscore in predicting MACE in patients referred for diagnostic angiography.</p>
    </sec>
    <sec sec-type="methods">
      <title>Methods</title>
      <sec>
        <title>Study design and population</title>
        <p>This cohort study enrolled patients with suspected CAD referred for elective, diagnostic coronary angiography, from 2008 to 2011, at a reference tertiary university-affiliated hospital (Hospital de Cl&#237;nicas de Porto Alegre), in Southern Brazil. The patients were referred by cardiologists from the public health system and private practices, and underwent cardiac catheterization due to suspected CAD with or without previous noninvasive testing for ischemia. Patients referred for angiography due to suspected CAD and associated valvular heart disease were also included. Men and women aged 40 years or over were eligible for the study, excluding those with previous coronary revascularization (surgical or percutaneous), class III or IV heart failure, chronic renal disease (previous medical diagnosis or serum creatinine greater than 1.5 mg/dL), history of cancer, or severe psychiatric illness. Patients admitted to the hospital for acute coronary syndromes were not included.</p>
      </sec>
      <sec>
        <title>Enrollment and study procedures</title>
        <p>The study protocol was approved by the hospital's Ethics Committee, which is accredited by the Office for Human Research Protections as an Institutional Review Board, and informed, written consent was obtained. Interviews pertaining demographic information, lifestyle characteristics, and past medical history were done using a standardized questionnaire. After the angiographies, the patients' attending physicians were responsible for assessing the need for revascularization and all medical treatment. The follow-up was conducted from 2008 to 2012.</p>
      </sec>
      <sec>
        <title>SYNTAX score and angiographic analysis</title>
        <p>SXscores were calculated prospectively by scoring all coronary lesions producing a &#8805; 50% diameter stenosis in vessels &#8805; 1.5 mm, using the algorithm that is available at the SYNTAX score website.<xref ref-type="bibr" rid="B16">16</xref> Subsequently, they were categorized as: SXscore<sub>HIGH</sub> (&#8805; 23); SXscore<sub>LOW-INTERMEDIATE</sub> (&lt; 23); and no significant CAD (reference category). Two interventional cardiologists (FCF, LCCB) independently performed the angiographic visual analysis for the assessment of the score. They were trained in calculating the SXscore using the website tutorial. Afterwards, they scored another 80 cases, which were extensively discussed with senior interventional cardiologists. Inter- and intra-observer agreement for determination of the SXscore was evaluated in another group of 90 angiographies.</p>
      </sec>
      <sec>
        <title>Study endpoints</title>
        <p>The primary endpoint was MACE, defined as a time to first event among cardiac death, myocardial infarction (MI) or late revascularization. Myocardial infarction and revascularization followed by death in the same hospitalization were adjudicated as cardiac deaths. Cardiac death was defined, additionally, as sudden death. Myocardial infarction was diagnosed by an increase or decrease of biomarkers, in the presence of symptoms, ECG abnormalities suggestive of ischemia.<xref ref-type="bibr" rid="B17">17</xref> Some patients were treated for acute MI in other hospitals and the diagnosis was defined on the basis of the discharge diagnosis. Late revascularization was either PCI or CABG.</p>
        <p>Percutaneous and surgical revascularizations based on diagnostic angiography findings, performed until three months after the angiography, were defined as index procedures and not considered outcomes. Interventions performed during follow-up, non-directly related to the diagnostic angiography, were defined as late revascularizations and included in the primary outcome. Secondary endpoints were cardiac death, cardiovascular death (fatal MI or stroke), MI, coronary revascularization, and overall mortality.</p>
        <p>All deaths were confirmed through verbal autopsy,<xref ref-type="bibr" rid="B18">18</xref> death certificate (obtained at the Government's Health Department, which has all state death records), or hospital records. Myocardial infarction was established by hospitalization, with diagnosis informed by a physician. An independent Clinical Events Committee adjudicated all endpoints. Data collection regarding the outcomes underwent control of quality to verify reliability, and another investigator checked 5% of the verbal autopsies.</p>
      </sec>
      <sec>
        <title>Sample size calculation and statistical analysis</title>
        <p>The questionnaires were coded and entered into a database using Epinfo 2004 software (version 3.3.2, Centers for Disease Control and Prevention, Atlanta, USA), with data entry quality control to verify amplitude and consistency. A sample size of 588 participants would be necessary to identify a hazard ratio (HR) of at least 2.4, with 80% power and 5% significance level (two-tailed), considering that 5% of unexposed and 12% of exposed to the highest score, a 1:1.5 ratio, respectively, would present a primary endpoint. Considering the lack of previous reports about the performance of SXscore to predict events in this context, sample size was increased to 906 participants to include enough patients with high scores (&gt;23) to provide adequate statistical power. Epi Info 2004, Statcalc module, was used for sample size calculation.</p>
        <p>Inter and intra-observer reliability was assessed by crosschecking 90 angiograms evaluated by two interventional cardiologists and reviewed by a third one. Agreement using Kappa coefficient was done, and interpreted according to Feiss et al.<xref ref-type="bibr" rid="B19">19</xref> Substantial agreement was defined by a Kappa coefficient of 0.7, considering the proportion of patients with SXscore &gt; 23, being 30% according to observer 1 and 20% by observer 2, with accuracy of 0.2. Intraclass correlation coefficients were also calculated.</p>
        <p>Recommendations of the STARD<xref ref-type="bibr" rid="B20">20</xref> were used to plan and report this study. Data are presented by mean &#177;SD, percentages and HR with 95% confidence intervals (CI). Receiver operating characteristic (ROC) curve was used to calculate C-statistic and the area under the curve. Kaplan-Meier survival curve for MACE was calculated for patients according to SXscores. Multivariate analysis of the predictive power of the SXscore was performed using Cox regression, which allowed the estimation of HR and 95% CI. Variables associated to the outcome in the bivariate analysis (P &#8804; 0.2) were eligible as confounding factors. Considering that many variables are intermediates in the causation of MACE, they were individually evaluated to be included or not in the analysis. The same model was run having the number of diseased vessels (none, one and multivessel) as exposure variable. The analyses were carried out using the Statistical Package for Social Sciences (SPSS(r), version 17, Chicago, IL, USA) software, and a p value &lt;0.05 was regarded as statistically significant.</p>
      </sec>
    </sec>
    <sec sec-type="results">
      <title>Results</title>
      <p>Study flowchart is presented in <xref ref-type="fig" rid="f1">Figure 1</xref>. Among 928 eligible patients, 895 patients with SXscore were included in the cohort and were followed up on average for 1.8 &#177; 1.4 years. After angiography, 314 (35.1%) patients were submitted to PCI or CABG, and 82 (9.2%) to valve replacement (index procedure). New interventions were done during the follow-up (late revascularizations) in 54 patients (35 percutaneous and 19 surgical). Myocardial infarction occurred in 16 patients, cardiac death in 13, cardiovascular death in 22, and all-cause death in 40 patients. MACE was established in 73 patients.</p>
      <p>
        <fig id="f1">
          <label>Figure 1</label>
          <caption>
            <title>Flowchart of patients. PCI: percutaneous coronary intervention; CABG: coronary artery bypass grafting; MI: myocardial infarction; CAD: coronary artery disease; CV: cardiovascular; MACE: major adverse cardiac events. * Valve replacement patients were excluded from the outcome analysis. <sup>&#358;</sup> MACE as defined in methods section.</title>
          </caption>
          <graphic xlink:href="1678-4170-abc-107-03-0207-60111-gf01.jpg"/></fig>
      </p>
      <p>Spearman coefficient between the SXscores calculated by the two interventional cardiologists was 0.902 (p &lt; 0.001), and the interobserver agreement between them was 0.94 (95% CI: 0.91-0.96). Kappa coefficient was 0.83 for the two interventional cardiologists. There were 495 patients with a score of 0 (55.4%) and 400 (44.6%) with positive scores, ranging from 1 to 43, with a mean of 12.6 (95% CI: 11.7-13.4). Patients with coronary lesions &#8805; 50% diameter stenosis in vessels &#8805;1.5 mm were classified as SXscore<sub>LOW-INTERMEDIATE</sub> (n = 345) or SXscore<sub>HIGH</sub> (n = 54).</p>
      <p>Baseline clinical and angiographic characteristics according to patient categories are presented in <xref ref-type="table" rid="t1">Table 1</xref>. The mean age of patients with SXscore<sub>HIGH</sub> was higher than that of patients with SXscore<sub>LOW-INTERMEDIATE</sub>. The proportion of men, patients with diabetes mellitus and hypertension was higher among patients with SXscore<sub>HIGH</sub> as well. Clinical indications for diagnostic coronary angiography were not remarkably different by the SXscore, but more patients in the SXscore<sub>LOW-INTERMEDIATE</sub> had typical CAD symptoms and more patients without significant CAD had other symptoms. As expected, prevalence of multivessel disease and all markers of increased lesion complexity, such as the presence of total occlusions, bifurcations and small vessel disease, were significantly more frequent in the SXscore<sub>HIGH</sub> category.</p>
      <table-wrap id="t1">
        <label>Table 1</label>
        <caption>
          <title>Baseline clinical characteristics</title>
        </caption>
        <table frame="hsides" rules="groups">
          <colgroup width="20%">
            <col/>
            <col/>
            <col/>
            <col/>
            <col/>
          </colgroup>
          <thead>
            <tr>
              <th align="left">Baseline characteristics</th>
              <th align="center">No significant CAD n = 495</th>
              <th align="center">SXscore<sub>LOW-INTERMEDIATE</sub> n = 346</th>
              <th align="center">SXscore<sub>HIGH</sub> n = 54</th>
              <th align="center">p value</th>
            </tr>
          </thead>
          <tbody>
            <tr>
              <td align="left">Age</td>
              <td align="center">59.1 &#177; 10.4</td>
              <td align="center">60.8 &#177; 9.6</td>
              <td align="center">63.6 &#177; 8.6</td>
              <td align="center">0.002</td>
            </tr>
            <tr>
              <td align="left">Male</td>
              <td align="center">234 (47.3)</td>
              <td align="center">226 (65.3)</td>
              <td align="center">39 (72.2)</td>
              <td align="center">&lt; 0.001</td>
            </tr>
            <tr>
              <td align="left">Diabetes mellitus</td>
              <td align="center">92 (18.6)</td>
              <td align="center">85 (24.6)</td>
              <td align="center">18 (33.3)</td>
              <td align="center">0.01</td>
            </tr>
            <tr>
              <td align="left">Current smoking</td>
              <td align="center">65 (13.2)</td>
              <td align="center">51 (15.0)</td>
              <td align="center">3 (5.6)</td>
              <td align="center">0.08</td>
            </tr>
            <tr>
              <td align="left">Hypertension</td>
              <td align="center">344 (69.8)</td>
              <td align="center">260 (76.5)</td>
              <td align="center">45 (83.3)</td>
              <td align="center">0.02</td>
            </tr>
            <tr>
              <td align="left">Symptoms of CAD only</td>
              <td align="center">128 (25.9)</td>
              <td align="center">115 (33.4)</td>
              <td align="center">14 (25.9)</td>
              <td align="center">0.05</td>
            </tr>
            <tr>
              <td align="left">With a positive noninvasive test</td>
              <td align="center">209 (42.2)</td>
              <td align="center">139 (40.2)</td>
              <td align="center">28 (51.9)</td>
              <td align="center">0.3</td>
            </tr>
            <tr>
              <td align="left">Valve disease with suspected CAD</td>
              <td align="center">14 (2.8)</td>
              <td align="center">3 (0.9)</td>
              <td align="center">1 (1.9)</td>
              <td align="center">0.14</td>
            </tr>
            <tr>
              <td align="left">Other complaints</td>
              <td align="center">46 (9.3)</td>
              <td align="center">13 (3.8)</td>
              <td align="center">1 (1.9)</td>
              <td align="center">0.002</td>
            </tr>
            <tr>
              <td align="left">Angiographic analysis<xref ref-type="table-fn" rid="TFN02">*</xref>
							</td>
              <td align="center">
							</td>
              <td align="center">
							</td>
              <td align="center">
							</td>
              <td align="center">
							</td>
            </tr>
            <tr>
              <td align="left">Right dominance</td>
              <td align="center">-</td>
              <td align="center">309 (89.3)</td>
              <td align="center">51 (94.4)</td>
              <td align="center">0.3</td>
            </tr>
            <tr>
              <td align="left">N&#186;. lesions per patient</td>
              <td align="center">-</td>
              <td align="center">1.8 &#177; 1.0</td>
              <td align="center">3.9 &#177; 1.5</td>
              <td align="center">&lt; 0.001</td>
            </tr>
            <tr>
              <td align="left">Total occlusions</td>
              <td align="center">-</td>
              <td align="center">88 (25.4)</td>
              <td align="center">41 (75.9)</td>
              <td align="center">&lt; 0.001</td>
            </tr>
            <tr>
              <td align="left">Bifurcations</td>
              <td align="center">-</td>
              <td align="center">125 (36.1)</td>
              <td align="center">44 (81.5)</td>
              <td align="center">&lt; 0.001</td>
            </tr>
            <tr>
              <td align="left">Small vessels /diffuse disease</td>
              <td align="center">-</td>
              <td align="center">68 (19.7)</td>
              <td align="center">26 (48.1)</td>
              <td align="center">&lt; 0.001</td>
            </tr>
            <tr>
              <td align="left">Left main</td>
              <td align="center">-</td>
              <td align="center">13 (13.8)</td>
              <td align="center">13 (24.1)</td>
              <td align="center">&lt; 0.001</td>
            </tr>
            <tr>
              <td align="left">Left anterior descending</td>
              <td align="center">-</td>
              <td align="center">218 (63.0)</td>
              <td align="center">47 (87.0)</td>
              <td align="center">&lt; 0.001</td>
            </tr>
            <tr>
              <td align="left">Left circumflex</td>
              <td align="center">-</td>
              <td align="center">109 (31.5)</td>
              <td align="center">36 (66.7)</td>
              <td align="center">&lt; 0.001</td>
            </tr>
            <tr>
              <td align="left">Right coronary artery</td>
              <td align="center">-</td>
              <td align="center">169 (48.8)</td>
              <td align="center">43 (79.6)</td>
              <td align="center">&lt; 0.001</td>
            </tr>
            <tr>
              <td align="left">One vessel disease</td>
              <td align="center">-</td>
              <td align="center">196 (56.7)</td>
              <td align="center">4 (7.4)</td>
              <td align="center">&lt; 0.001</td>
            </tr>
            <tr>
              <td align="left">Multivessel disease or LM</td>
              <td align="center">-</td>
              <td align="center">150 (43.3)</td>
              <td align="center">50 (92.6)</td>
              <td align="center">&lt; 0.001</td>
            </tr>
          </tbody>
        </table>
        <table-wrap-foot>
          <fn id="TFN01">
            <p>Values are given as n (%) or mean &#177;SD. LM: left main; CAD: coronary artery disease.</p>
          </fn>
          <fn id="TFN02">
            <label>*</label>
            <p>Assessment using the SYNTAX score definitions.</p>
          </fn>
        </table-wrap-foot>
      </table-wrap>
      <sec>
        <title>Procedures after index angiography</title>
        <p>The proportion of patients submitted to PCI, CABG and valve replacement based on the index diagnostic angiography according to patient category is presented in <xref ref-type="table" rid="t2">Table 2</xref>. As expected, more patients with higher scores were submitted to CABG. Despite having no significant CAD based on angiographic assessment done for this study, 3.4% of patients were submitted to PCI.</p>
        <table-wrap id="t2">
          <label>Table 2</label>
          <caption>
            <title>Treatment after the index angiography and cumulative clinical outcomes across patient categories</title>
          </caption>
          <table frame="hsides" rules="groups">
            <colgroup width="20%">
              <col/>
              <col/>
              <col/>
              <col/>
              <col/>
            </colgroup>
            <thead>
              <tr>
                <th align="left">Type of procedure</th>
                <th align="center">No significant CAD n = 495</th>
                <th align="center">SXscore<sub>LOW-INTERMEDIATE</sub> n = 346</th>
                <th align="center">SXscore<sub>HIGH</sub> n = 54</th>
                <th align="center">p value</th>
              </tr>
            </thead>
            <tbody>
              <tr>
                <td align="left">
                  <bold>Interventions:</bold>
                </td>
                <td align="center">
								</td>
                <td align="center">
								</td>
                <td align="center">
								</td>
                <td align="center">&lt; 0.001</td>
              </tr>
              <tr>
                <td align="left">Percutaneous Coronary Intervention</td>
                <td align="center">17 (3.4)</td>
                <td align="center">208 (60.3)</td>
                <td align="center">14 (25.9)</td>
                <td align="center">
								</td>
              </tr>
              <tr>
                <td align="left">Coronary Artery Bypass Surgery</td>
                <td align="center">0</td>
                <td align="center">46 (13.3)</td>
                <td align="center">29 (53.7)</td>
                <td align="center">
								</td>
              </tr>
              <tr>
                <td align="left">Isolated valve replacement<xref ref-type="table-fn" rid="TFN04">*</xref>
								</td>
                <td align="center">78 (15.8)</td>
                <td align="center">4 (1.2)</td>
                <td align="center">0</td>
                <td align="center">
								</td>
              </tr>
              <tr>
                <td align="left">No invasive intervention</td>
                <td align="center">400 (80.8)</td>
                <td align="center">88 (25.4)</td>
                <td align="center">11 (20.4)</td>
                <td align="center">
								</td>
              </tr>
              <tr>
                <td align="left">All-cause death</td>
                <td align="center">16 (3.9)</td>
                <td align="center">11 (3.3)</td>
                <td align="center">9 (16.7)</td>
                <td align="center">&lt; 0.001</td>
              </tr>
              <tr>
                <td align="left">Cardiac death and MI</td>
                <td align="center">4 (1.0)</td>
                <td align="center">13 (3.9)</td>
                <td align="center">9 (16.7)</td>
                <td align="center">&lt; 0.001</td>
              </tr>
              <tr>
                <td align="left">Cardiovascular death</td>
                <td align="center">9 (2.2)</td>
                <td align="center">6 (1.8)</td>
                <td align="center">7 (13)</td>
                <td align="center">&lt; 0.001</td>
              </tr>
              <tr>
                <td align="left">MACE</td>
                <td align="center">9 (2.2)</td>
                <td align="center">53 (15.7)</td>
                <td align="center">11 (20.4)</td>
                <td align="center">&lt; 0.001</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="TFN03">
              <p>Values are given as n (%).</p>
            </fn>
            <fn id="TFN04">
              <label>*</label>
              <p>patients excluded from outcome analysis. MI: myocardial infarction; MACE: MI, cardiac death, and late revascularization.</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
      </sec>
      <sec>
        <title>Clinical outcomes</title>
        <p>The cumulative incidence of clinical outcomes across patient groups is shown in <xref ref-type="table" rid="t2">Table 2</xref>. All-cause death was significantly higher in SXscore<sub>HIGH</sub> patients as compared with patients without significant CAD, 16.7% and 3.9% (p &lt; 0.001), respectively. Cardiovascular death, non-fatal MI, and late revascularization were more frequent in the SXscore<sub>HIGH</sub> as well. After adjustment for confounding factors, all outcomes remained associated with the SXscore (<xref ref-type="table" rid="t3">Table 3</xref>). Risk ratios for MACE, cardiac death or non-fatal MI and non-fatal MI alone were significantly associated with SXscore<sub>LOW-INTERMEDIATE</sub> as well. Patients in the SXscore<sub>HIGH</sub> category had a 12.5 (95% CI: 5.1-30.6) higher chance of presenting the primary outcome than those without significant CAD. This finding was similar among men (10.1; 95% CI: 3.9-25.9) and women (11.5; 95% CI: 1.1-117.3). Further adjustment for index revascularization did not change the estimates significantly. After adjustment for confounding factors, the primary outcome was also associated with the SXscore as a continuous variable (HR 1.06; 95% CI: 1.04-1.08). The area under the ROC curve was 0.73 (95% CI: 0.68-0.79) (<xref ref-type="fig" rid="f2">Figure 2</xref>).</p>
        <table-wrap id="t3">
          <label>Table 3</label>
          <caption>
            <title>Hazard ratios<xref ref-type="table-fn" rid="TFN06">*</xref> for major clinical outcomes according to patient categories</title>
          </caption>
          <table frame="hsides" rules="groups">
            <colgroup width="20%">
              <col/>
              <col/>
              <col/>
              <col/>
              <col/>
            </colgroup>
            <thead>
              <tr>
                <th align="left">Type of Event</th>
                <th align="center">No significant CAD<xref ref-type="table-fn" rid="TFN07">&#8224;</xref> n = 495</th>
                <th align="center">SXscore<sub>LOW-INTERMEDIATE</sub> n = 346</th>
                <th align="center">SXscore<sub>HIGH</sub> n = 54</th>
                <th align="center">p value</th>
              </tr>
            </thead>
            <tbody>
              <tr>
                <td align="left">All-cause death</td>
                <td align="center">1.0</td>
                <td align="center">0.8 (0.4-1.7)</td>
                <td align="center">4.3 (1.8-10.1)</td>
                <td align="center">&lt; 0.001</td>
              </tr>
              <tr>
                <td align="left">Cardiovascular death</td>
                <td align="center">1.0</td>
                <td align="center">0.7 (0.3-2.1)</td>
                <td align="center">5.7 (2.0-15.9)</td>
                <td align="center">&lt; 0.001</td>
              </tr>
              <tr>
                <td align="left">Cardiac death</td>
                <td align="center">1.0</td>
                <td align="center">1.3 (0.3-5.9)</td>
                <td align="center">11.8 (2.9-48.5)</td>
                <td align="center">&lt; 0.001</td>
              </tr>
              <tr>
                <td align="left">MACE<xref ref-type="table-fn" rid="TFN08">&#8225;</xref>
								</td>
                <td align="center">1.0</td>
                <td align="center">7.2 (3.5-14.7)</td>
                <td align="center">12.5 (5.1-30.6)</td>
                <td align="center">&lt; 0.001</td>
              </tr>
              <tr>
                <td align="left">Cardiac death or MI</td>
                <td align="center">1.0</td>
                <td align="center">3.5 (1.1-10.8)</td>
                <td align="center">16.0 (4.9-52.9)</td>
                <td align="center">&lt; 0.001</td>
              </tr>
              <tr>
                <td align="left">MI</td>
                <td align="center">1.0</td>
                <td align="center">12.6 (1.6-98.3)</td>
                <td align="center">33.9 (3.7-308.0)</td>
                <td align="center">0.007</td>
              </tr>
              <tr>
                <td align="left">Late Revascularization</td>
                <td align="center">1.0</td>
                <td align="center">9.9 (4.2-23.4)</td>
                <td align="center">4.0 (0.8-20.0)</td>
                <td align="center">&lt; 0.001</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="TFN05">
              <p>MI: myocardial infarction.</p>
            </fn>
            <fn id="TFN06">
              <label>*</label>
              <p>Adjusted for age, sex and diabetes.</p>
            </fn>
            <fn id="TFN07">
              <label>&#8224;</label>
              <p>Reference category,</p>
            </fn>
            <fn id="TFN08">
              <label>&#8225;</label>
              <p>MACE: MI, cardiac death, and late revascularization.</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
        <p>
          <fig id="f2">
            <label>Figure 2</label>
            <caption>
              <title>ROC curve for the SYNTAX score.</title>
            </caption>
            <graphic xlink:href="1678-4170-abc-107-03-0207-60111-gf02.jpg"/></fig>
        </p>
        <p>MACE-free survival curves for patients according to SXscores are presented in <xref ref-type="fig" rid="f3">Figure 3</xref>, showing that curves diverged immediately after angiography and further during follow-up. Risk ratios for MACE according to the number of diseased vessels, compared to none, were 6.9 (95% CI: 3.4-13.9) for one-vessel disease and 10.2 (5.2-20.1) for multivessel disease. Despite the intrinsic relationship of this classification and the SXscore, 42.0% of the patients with multivessel disease were classified in the SXscore<sub>LOW-INTERMEDIATE</sub> category.</p>
        <p>
          <fig id="f3">
            <label>Figure 3</label>
            <caption>
              <title>Kaplan-Meier Curve for MACE according to patient category. CAD: coronary artery disease.</title>
            </caption>
            <graphic xlink:href="1678-4170-abc-107-03-0207-60111-gf03.jpg"/></fig>
        </p>
      </sec>
    </sec>
    <sec sec-type="discussion">
      <title>Discussion</title>
      <p>This study demonstrated that, in patients submitted to diagnostic angiography for suspected CAD, the SXscore was able to predict the primary endpoint of cardiac death, non-fatal MI and late revascularization, independently of age, sex, presence of diabetes and index revascularization. There was a 6% increased risk in having a MACE for each additional point in the score. Patients with SXscore<sub>HIGH</sub> had a significantly increased risk for all-cause, cardiovascular and cardiac death.</p>
      <p>Previous studies have shown the ability of the SXscore to predict MACE in different scenarios. LEADERS,<xref ref-type="bibr" rid="B9">9</xref><sup>,</sup><xref ref-type="bibr" rid="B10">10</xref> SIRTAX<xref ref-type="bibr" rid="B11">11</xref> and RESOLUTE<xref ref-type="bibr" rid="B8">8</xref> studies included patients with acute coronary syndromes as well as patients submitted to elective PCI. MI-SYNTAXscore Study,<xref ref-type="bibr" rid="B12">12</xref> STRATEGY and MULTISTRATEGY<xref ref-type="bibr" rid="B13">13</xref> studies were done in patients with acute MI. The ACUITY<xref ref-type="bibr" rid="B7">7</xref> trial included patients with acute coronary syndromes. Finally, Serruys et al. summarized the results of five studies, analyzing data from 6.508 patients, with the same results.<xref ref-type="bibr" rid="B14">14</xref> Differently from our research, all of those studies included only patients submitted to percutaneous revascularization procedures, and none of them focused on patients with suspected or stable CAD. The group of patients without significant CAD, although many had CAD with diameter stenosis lesser than 50%, served as the reference category to compare outcomes with those of patients in the SXscore<sub>LOW-INTERMEDIATE</sub> and SXscore<sub>HIGH</sub> categories. We understand that our proposal is different from the application originally proposed for the score, in which patients without lesions treatable with surgery or percutaneously are excluded, but it is in line with the objectives of the study.</p>
      <p>The comparison of the SXscore performance with the traditional CAD anatomical scores was not explored in our investigation. The presence of positive SXscores (44.6%) was similar to the frequency of patients with significant CAD (47%) detected by quantitative angiographic analysis done in a proportion of the patients of our cohort.<xref ref-type="bibr" rid="B21">21</xref> Traditional angiographic scores have also predicted the incidence of MACE in previous studies,<xref ref-type="bibr" rid="B2">2</xref> but those scores do not take into account difficulties in performing myocardial revascularization. Despite their prognostic ability, they have not been incorporated to clinical practice, where the number of diseased vessels has been used to estimate the anatomical severity of disease. In this cohort, patients with one-vessel and multivessel disease had a risk for MACE approximately similar to the SXscore low-intermediate and high, respectively. Nonetheless, almost half of the patients with multivessel disease were classified in the SXscore<sub>LOW-INTERMEDIATE</sub> category.</p>
      <p>Based on the results of the SYNTAX trial,<xref ref-type="bibr" rid="B5">5</xref> in which patients with low SYNTAX scores had similar outcomes regardless of the type of revascularization, our findings have a clinical implication - patients who would otherwise be referred to CABG could also be revascularized percutaneously. Considering that visual characterization of multivessel disease leads to referring patients to surgical revascularization, calculation of the SXscore could better stratify patients who would indeed benefit from this procedure (SXscore<sub>HIGH</sub> category).</p>
      <p>In this study, patients underwent an elective procedure and, as a result, there was a large proportion of patients with no significant CAD, who might also have lesions below 50%. Those patients did not fulfill the criteria for a positive score and served as a comparison group. Therefore, patients were classified into two categories: 1 to 22, and equal to 23 or greater, which correspond to the later defined categories of low-intermediate (0-22) and high (23 or higher).<xref ref-type="bibr" rid="B6">6</xref> The proportion of patients classified as SXscore<sub>LOW-INTERMEDIATE</sub> and submitted to percutaneous revascularization was higher than patients submitted to surgical revascularization, which reflects the current clinical practice and complies with the findings of the 5-year follow-up of the randomized clinical SYNTAX trial.<xref ref-type="bibr" rid="B6">6</xref> At the time the study was conducted, drug-eluting stents were not available for use in the Brazilian public health system. In addition, current evidence indicates surgical revascularization for patients with high SXscores.<xref ref-type="bibr" rid="B6">6</xref> Patients with high surgical risk who were not deemed eligible for surgical revascularization by surgeons received percutaneous treatment. There was an unexpected finding of 3.4% of patients without significant CAD who were submitted to PCI. Patients with non-obstructive CAD represent a large proportion of patients undergoing coronary angiography. Subjective evaluation of coronary anatomy associated with the clinical and noninvasive information might have influenced the decision-making process and could explain this finding.</p>
      <p>Our study has some limitations and strengths that should be addressed. We restricted our analysis to anatomical criteria, considering neither left ventricular function nor myocardial ischemia and viability. Nonetheless, our patients did not have clinically unstable disease or classes III or IV heart failure, and the anatomical criteria frequently prevail to reach a therapeutic decision. In addition, a recent post-hoc analysis of the COURAGE trial has demonstrated that anatomical criteria and not ischemia burden were able to predict cardiovascular events.<xref ref-type="bibr" rid="B22">22</xref> Although most follow-up procedures have been conducted in our hospital, different types of stents were implanted, which could affect the likelihood of stent thrombosis or reinterventions.<xref ref-type="bibr" rid="B23">23</xref> However, analysis including only MI and cardiac death did not change the estimates. Exclusion of patients submitted to valve replacement did not change the results either. Another limitation is the number of events, which accounted for the large confidence intervals. Despite having investigated almost 1,000 patients, more than 50% did not have significant CAD, which reflects real life practice of a tertiary center performing diagnostic angiographies. Studies with larger sample size and conducted at other centers are necessary to confirm our findings and their external validity. The high inter-observer reproducibility of the examiners is among the strengths of our investigation, similar to some<xref ref-type="bibr" rid="B24">24</xref> but different from other studies.<xref ref-type="bibr" rid="B25">25</xref><sup>,</sup><xref ref-type="bibr" rid="B26">26</xref> This performance could be explained by the extensive training in assessing SXscore done by the interventional cardiologists and the fact that both underwent training at the same hospital.</p>
      <sec>
        <title>Clinical Implications</title>
        <p>In clinical practice, the number of epicardial vessels with more than 50% stenosis is used to assess prognostic information, and angiographic scores are rarely used. Recently, the use of scores has been shown to improve the standardization of clinical decision-making. For instance, the EUROSCORE<xref ref-type="bibr" rid="B27">27</xref> or the STS score<xref ref-type="bibr" rid="B28">28</xref> are routinely used in the decision making process for the indication of CABG.<xref ref-type="bibr" rid="B29">29</xref> For the management of multivessel CAD, current guidelines formally recommend the use of the SXscore as well as the EUROSCORE.<xref ref-type="bibr" rid="B30">30</xref> Our data expand the indications of the SXscore for the prognostic evaluation of patients referred for diagnostic angiography.</p>
      </sec>
    </sec>
    <sec sec-type="conclusions">
      <title>Conclusion</title>
      <p>In conclusion, in patients with suspected CAD submitted to elective coronary angiography, SXscore independently predicts MACE. Its routine use in this setting could identify patients with worse prognosis.</p>
    </sec>
  </body>
  <back>
    <fn-group>
      <fn fn-type="other" id="fn1">
        <p>(in memorian)</p>
      </fn>
      <fn fn-type="supported-by">
        <p>
          <bold>Sources of Funding</bold>
        </p>
        <p>This study was partially funded by CNPq and Funda&#231;&#227;o para o incentivo em Pesquisa do Hospital de Cl&#237;nicas de Porto Alegre.</p>
      </fn>
      <fn fn-type="other">
        <p>
          <bold>Study Association</bold>
        </p>
        <p>This article is part of the thesis of master submitted by Felipe C. Fuchs, from Faculdade de Medicina da Universidade Federal do Rio Grande do Sul.</p>
      </fn>
    </fn-group>
    <ack>
      <title>Acknowledgements</title>
      <p>This study was partially supported by the National Council for Scientific and Technological Development (CNPq), Brazil; Research Funding of Hospital de Cl&#237;nicas de Porto Alegre (FIPE-HCPA), Porto Alegre, Brazil.</p>
    </ack>
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  <sub-article article-type="translation" id="s1" xml:lang="pt">
    <front-stub>
      <title-group>
        <article-title>Syntax Escore e Eventos Card&#237;acos Adversos Maiores em Pacientes com Suspeita de Doen&#231;a Arterial Coronariana: Resultados de um Estudo de Coorte em Hospital Universit&#225;rio no Sul do Brasil</article-title>
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          <name>
            <surname>Fuchs</surname>
            <given-names>Felipe C.</given-names>
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          <xref ref-type="corresp" rid="c2"/>
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          <name>
            <surname>Ribeiro</surname>
            <given-names>Jorge P.</given-names>
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          <xref ref-type="aff" rid="aff2"/>
          <xref ref-type="fn" rid="fn2"/>
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        <contrib contrib-type="author">
          <name>
            <surname>Fuchs</surname>
            <given-names>Fl&#225;vio D.</given-names>
          </name>
          <xref ref-type="aff" rid="aff2"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
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            <given-names>Marco V.</given-names>
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          <xref ref-type="aff" rid="aff2"/>
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            <given-names>Luis C.</given-names>
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            <given-names>Rodrigo V.</given-names>
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            <given-names>Vanessa</given-names>
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        <contrib contrib-type="author">
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            <given-names>Alessandra C.</given-names>
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        <contrib contrib-type="author">
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            <given-names>Leila B.</given-names>
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        <contrib contrib-type="author">
          <name>
            <surname>Fuchs</surname>
            <given-names>Sandra C.</given-names>
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        </contrib>
        <aff id="aff2">
          <institution content-type="original">Hospital de Cl&#237;nicas de Porto Alegre - Universidade Federal do Rio Grande do Sul, Porto Alegre, RS - Brasil</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="c2"><bold>Correspond&#234;ncia: Felipe Costa Fuchs</bold>, Servi&#231;o de Cardiologia, Hospital de Cl&#237;nicas de Porto Alegre. Rua Ramiro Barcelos, 2350, Santa Cec&#237;lia. CEP 90035-903, Porto Alegre, RS - Brasil. E-mail: <email>fcfuchs@terra.com.br</email>
				</corresp>
        <fn fn-type="con">
          <p>Contribui&#231;&#227;o dos autores</p>
          <p>Concep&#231;&#227;o e desenho da pesquisa: Fuchs FC, Ribeiro JP, Fuchs FD, Wainstein MV, Moreira LB, Fuchs SC; Obten&#231;&#227;o de dados: Fuchs FC, Wainstein MV, Bergoli LC, Wainstein RV, Zen V, Kerkhoff AC; An&#225;lise e interpreta&#231;&#227;o dos dados e Revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do intelectual importante: Fuchs FC, Ribeiro JP, Fuchs FD, Bergoli LC, Wainstein RV, Zen V, Kerkhoff AC, Moreira LB, Fuchs SC; An&#225;lise estat&#237;stica e Reda&#231;&#227;o do manuscrito: Fuchs FC, Ribeiro JP, Fuchs FD, Fuchs SC; Obten&#231;&#227;o de financiamento: Ribeiro JP, Moreira LB, Fuchs SC.</p>
        </fn>
        <fn fn-type="conflict">
          <p>
            <bold>Potencial conflito de interesse</bold>
          </p>
          <p>Declaro n&#227;o haver conflito de interesses pertinentes.</p>
        </fn>
      </author-notes>
      <abstract>
        <title>Resumo</title>
        <sec>
          <title>Fundamento:</title>
          <p>A import&#226;ncia da anatomia coronariana na predi&#231;&#227;o de eventos cardiovasculares &#233; bem conhecida. O uso de escores anat&#244;micos tradicionais na cineangiocoronariografia de rotina, entretanto, n&#227;o foi incorporado &#224; pr&#225;tica cl&#237;nica. O SYNTAX escore (SXescore) &#233; um sistema de escore que estima a extens&#227;o anat&#244;mica da doen&#231;a arterial coronariana (DAC). Sua capacidade para predizer desfechos com base na cineangiocoronariografia diagn&#243;stica de base ainda n&#227;o foi testada.</p>
        </sec>
        <sec>
          <title>Objetivo:</title>
          <p>Avaliar o desempenho do SXescore para predizer eventos card&#237;acos adversos maiores (MACE) em pacientes encaminhados para cineangiocoronariografia diagn&#243;stica.</p>
        </sec>
        <sec>
          <title>M&#233;todos:</title>
          <p>Coorte prospectiva de 895 pacientes com suspeita de DAC encaminhados para cineangiocoronariografia diagn&#243;stica eletiva de 2008 a 2011, em hospital universit&#225;rio no Brasil. Os pacientes tiveram seus SXescores calculados e foram estratificados em tr&#234;s categorias: 'sem DAC significativa' (n = 495); SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub>: &lt; 23 (n = 346); e SXescore<sub>ALTO</sub>: &#8805; 23 (n = 54). O desfecho prim&#225;rio foi composto de morte card&#237;aca, infarto do mioc&#225;rdio e revasculariza&#231;&#227;o tardia. Os desfechos secund&#225;rios foram MACE e morte por todas as causas.</p>
        </sec>
        <sec>
          <title>Resultados:</title>
          <p>Em m&#233;dia, os pacientes foram acompanhados por 1,8 &#177; 1,4 anos. Desfecho prim&#225;rio ocorreu em 2,2%, 15,3% e 20,4% nos grupos 'sem DAC significativa', SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub> e SXescore<sub>ALTO</sub>, respectivamente (p &lt; 0,001). Morte por todas as causas foi significativamente mais frequente no grupo de SXescore<sub>ALTO</sub> comparado ao grupo 'sem DAC significativa', 16,7% e 3,8% (p &lt; 0,001), respectivamente. Ap&#243;s ajuste para fatores de confus&#227;o, todos os desfechos permaneceram associados com o SXescore.</p>
        </sec>
        <sec>
          <title>Conclus&#227;o:</title>
          <p>O SXescore prediz independentemente MACE em pacientes submetidos a cineangiocoronariografia diagn&#243;stica. Seu uso rotineiro nesse contexto poderia identificar pacientes de pior progn&#243;stico.</p>
        </sec>
      </abstract>
      <kwd-group xml:lang="pt">
        <title>Palavras-chave:</title>
        <kwd>Doen&#231;a da Art&#233;ria Coronariana / epidemiologia</kwd>
        <kwd>Probabilidade</kwd>
        <kwd>Cineangiografia</kwd>
        <kwd>Syntax Escore</kwd>
        <kwd>Estudos de Coortes</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <sec sec-type="intro">
        <title>Introdu&#231;&#227;o</title>
        <p>A import&#226;ncia da anatomia coronariana na predi&#231;&#227;o de eventos cardiovasculares &#233; conhecida h&#225; d&#233;cadas, quando da publica&#231;&#227;o de estudos como o Registro CASS (<italic>Coronary Artery Study</italic>).<xref ref-type="bibr" rid="B1">1</xref> Esse grande estudo de coorte mostrou a capacidade de escores anat&#244;micos para doen&#231;a arterial coronariana (DAC) para predizer eventos, mas seu uso rotineiro n&#227;o foi incorporado &#224; pr&#225;tica cl&#237;nica.<xref ref-type="bibr" rid="B2">2</xref> Atualmente, indica-se avalia&#231;&#227;o funcional e n&#227;o invasiva de isquemia, como ecocardiografia de estresse, cintilografia mioc&#225;rdica e resson&#226;ncia magn&#233;tica, para avaliar pacientes com DAC conhecida ou com suspeita dessa doen&#231;a.<xref ref-type="bibr" rid="B3">3</xref> No entanto, um significativo n&#250;mero de pacientes acaba sendo submetido a cineangiocoronariografia para confirma&#231;&#227;o diagn&#243;stica.<xref ref-type="bibr" rid="B3">3</xref> Consequentemente, a reavalia&#231;&#227;o do desempenho de escores anat&#244;micos para predi&#231;&#227;o de desfechos, em um contexto de novas terapias cl&#237;nicas e intervencionistas, pode ter seu valor. Atualmente, o SYNTAX (<italic>Synergy between percutaneous coronary intervention with Taxus and Cardiac Surgery</italic>) Escore (SXescore), um m&#233;todo mais elaborado para quantificar les&#245;es anat&#244;micas, &#233; uma ferramenta dispon&#237;vel <italic>online</italic> que estima a extens&#227;o anat&#244;mica da DAC.<xref ref-type="bibr" rid="B4">4</xref>
				</p>
        <p>O SXescore &#233; um abrangente sistema de escore angiogr&#225;fico baseado na anatomia coronariana e nas caracter&#237;sticas da les&#227;o.<xref ref-type="bibr" rid="B4">4</xref> Foi inicialmente desenvolvido para determinar a extens&#227;o da DAC e a complexidade da les&#227;o, que refletem as dificuldades na realiza&#231;&#227;o da revasculariza&#231;&#227;o mioc&#225;rdica, em particular da interven&#231;&#227;o coronariana percut&#226;nea (ICP). No ensaio SYNTAX, valores altos de SXescore (acima de 33) identificaram pacientes nos quais a cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica resultou em melhores desfechos do que o de pacientes submetidos a revasculariza&#231;&#227;o percut&#226;nea.<xref ref-type="bibr" rid="B5">5</xref> O seguimento de cinco anos desse ensaio identificou a cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica como sendo mais adequada para pacientes com escores acima de 22.<xref ref-type="bibr" rid="B6">6</xref>
				</p>
        <p>O SXescore foi desenvolvido como uma ferramenta do processo de tomada de decis&#227;o, tendo sua utiliza&#231;&#227;o sido estendida mais tarde como escore de predi&#231;&#227;o de eventos card&#237;acos adversos maiores (MACE) em pacientes submetidos a ICP.<xref ref-type="bibr" rid="B7">7</xref><sup>-</sup><xref ref-type="bibr" rid="B14">14</xref> Tais estudos inclu&#237;ram procedimentos de revasculariza&#231;&#227;o eletivos e de urg&#234;ncia. Entretanto, a maioria das cineangiocoronariografias &#233; realizada com prop&#243;sito diagn&#243;stico.<xref ref-type="bibr" rid="B15">15</xref> O desempenho progn&#243;stico do SXescore nesse contexto ainda n&#227;o foi relatado, constituindo o objetivo desta investiga&#231;&#227;o.</p>
      </sec>
      <sec>
        <title>Objetivo</title>
        <p>Avaliar o desempenho do SXescore para predi&#231;&#227;o de MACE em pacientes encaminhados para cineangiocoronariografia diagn&#243;stica.</p>
      </sec>
      <sec sec-type="methods">
        <title>M&#233;todos</title>
        <sec>
          <title>Desenho e popula&#231;&#227;o do estudo</title>
          <p>Este estudo de coorte arrolou pacientes com suspeita de DAC encaminhados para cineangiocoronariografia diagn&#243;stica eletiva de 2008 a 2011, em um hospital universit&#225;rio terci&#225;rio de refer&#234;ncia (Hospital de Cl&#237;nicas de Porto Alegre), no sul do Brasil. Os pacientes foram encaminhados por cardiologistas do sistema p&#250;blico de sa&#250;de e da pr&#225;tica privada, tendo sido submetidos a cateteriza&#231;&#227;o card&#237;aca devido a suspeita de DAC com ou sem exame n&#227;o invasivo pr&#233;vio para isquemia. Pacientes encaminhados para cineangiocoronariografia devido a suspeita de DAC e doen&#231;a card&#237;aca valvular associada tamb&#233;m foram inclu&#237;dos. Homens e mulheres com idade m&#237;nima de 40 anos eram eleg&#237;veis para este estudo, excluindo aqueles com revasculariza&#231;&#227;o coronariana pr&#233;via (cir&#250;rgica ou percut&#226;nea), insufici&#234;ncia card&#237;aca classes III ou IV, doen&#231;a renal cr&#244;nica (diagn&#243;stico m&#233;dico pr&#233;vio ou creatinina s&#233;rica superior a 1,5 mg/dl), hist&#243;ria de c&#226;ncer, ou enfermidade psiqui&#225;trica grave. Os pacientes hospitalizados por s&#237;ndrome coronariana aguda n&#227;o foram inclu&#237;dos.</p>
        </sec>
        <sec>
          <title>Arrolamento e procedimentos do estudo</title>
          <p>O protocolo do estudo foi aprovado pelo Comit&#234; de &#201;tica em Pesquisa com Seres Humanos do hospital, tendo-se obtido termo de consentimento livre e informado. Entrevistas com informa&#231;&#227;o demogr&#225;fica, caracter&#237;sticas de estilo de vida e hist&#243;ria m&#233;dica foram realizadas usando-se um question&#225;rio padronizado. Ap&#243;s as cineangiocoronariografias, coube aos m&#233;dicos assistentes avaliar a necessidade de revasculariza&#231;&#227;o e todo o tratamento m&#233;dico. O seguimento foi realizado de 2008 a 2012.</p>
        </sec>
        <sec>
          <title>SYNTAX escore e an&#225;lise angiogr&#225;fica</title>
          <p>Os SXescores foram calculados prospectivamente com todas as les&#245;es coronarianas que produzissem uma estenose de di&#226;metro &#8805; 50% nos vasos &#8805; 1,5 mm, usando o algoritmo dispon&#237;vel no <italic>website</italic> do SYNTAX escore.<xref ref-type="bibr" rid="B16">16</xref> Subsequentemente, foram categorizados como se segue: SXescore<sub>ALTO</sub> (&#8805; 23); SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub> (&lt; 23); e 'sem DAC significativa' (categoria de refer&#234;ncia). Dois cardiologistas intervencionistas (FCF, LCCB) realizaram independentemente a an&#225;lise angiogr&#225;fica visual para avalia&#231;&#227;o do escore. Foram treinados para calcular o SXescore usando o tutorial do <italic>website</italic>. Em seguida, eles atribu&#237;ram escore a outros 80 casos, que foram exaustivamente discutidos com cardiologistas intervencionistas seniores. Avaliou-se a concord&#226;ncia inter- e intraobservador para determina&#231;&#227;o do SXescore em outro grupo de 90 cineangiocoronariografias.</p>
        </sec>
        <sec>
          <title>Desfechos do estudo</title>
          <p>O desfecho prim&#225;rio foi MACE, definido como o tempo at&#233; o primeiro evento (morte card&#237;aca, infarto do mioc&#225;rdio (IM) ou revasculariza&#231;&#227;o tardia). Infarto do mioc&#225;rdio e revasculariza&#231;&#227;o seguidos de morte na mesma hospitaliza&#231;&#227;o foram adjudicados como morte card&#237;aca, assim como morte s&#250;bita. O IM foi diagnosticado por aumento de biomarcadores, na presen&#231;a de sintomas e anormalidades eletrocardiogr&#225;ficas sugestivas de isquemia.<xref ref-type="bibr" rid="B17">17</xref> Alguns pacientes foram tratados para IM agudo em outros hospitais, sendo o diagn&#243;stico definido com base no diagn&#243;stico de alta. A revasculariza&#231;&#227;o tardia foi ICP ou cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica.</p>
          <p>Revasculariza&#231;&#245;es percut&#226;neas e cir&#250;rgicas, tendo por base achados de cineangiocoronariografia diagn&#243;stica, realizadas at&#233; tr&#234;s meses ap&#243;s a cineangiocoronariografia, foram definidas como procedimentos-&#237;ndice e n&#227;o considerados desfechos. As interven&#231;&#245;es realizadas durante o seguimento, n&#227;o diretamente relacionadas &#224; cineangiocoronariografia diagn&#243;stica, foram definidas como revasculariza&#231;&#245;es tardias e inclu&#237;das no desfecho prim&#225;rio. Os desfechos secund&#225;rios foram morte card&#237;aca, morte cardiovascular (IM fatal ou acidente vascular encef&#225;lico), IM, revasculariza&#231;&#227;o coronariana e mortalidade global.</p>
          <p>Todas as mortes foram confirmadas por necropsia verbal,<xref ref-type="bibr" rid="B18">18</xref> declara&#231;&#227;o de &#243;bito (fornecida pelo Minist&#233;rio da Sa&#250;de, que det&#233;m todos os registros de &#243;bito dos estados) ou registro hospitalar. O IM foi estabelecido por hospitaliza&#231;&#227;o, com diagn&#243;stico informado por m&#233;dico. Um Comit&#234; de Eventos Cl&#237;nicos independente adjudicou todos os desfechos. A coleta de dados referentes aos desfechos foi submetida a controle de qualidade para verificar confiabilidade, tendo outro investigador checado 5% das necropsias verbais.</p>
        </sec>
        <sec>
          <title>C&#225;lculo do tamanho amostral e an&#225;lise estat&#237;stica</title>
          <p>Os question&#225;rios foram codificados e passados para um banco de dados usando o programa Epinfo 2004 (vers&#227;o 3.3.2, Centro para Controle e Preven&#231;&#227;o de Doen&#231;a, Atlanta, EUA), com controle de qualidade da entrada de dados para verificar amplitude e consist&#234;ncia. Um tamanho amostral de 588 participantes seria necess&#225;rio para identificar uma raz&#227;o de risco (<italic>hazard ratio</italic> - HR) de pelo menos 2,4, com poder de 80% e n&#237;vel de signific&#226;ncia de 5% (bicaudal), considerando que 5% de n&#227;o expostos e 12% de expostos ao mais alto escore, uma taxa de 1:1,5, respectivamente, apresentariam um desfecho prim&#225;rio. Considerando a aus&#234;ncia de relato pr&#233;vio sobre o desempenho do SXescore para predizer eventos nesse contexto, aumentou-se o tamanho amostral para 906 participantes para incluir um n&#250;mero suficiente de pacientes com escores altos (&gt; 23) para fornecer poder estat&#237;stico adequado. Epi Info 2004, Statcalc module, foi usado para calcular o tamanho amostral.</p>
          <p>A confiabilidade inter- e intraobservador foi avaliada atrav&#233;s de checagem cruzada de 90 angiogramas analisados por dois cardiologistas intervencionistas e revisados por um terceiro. O coeficiente kappa foi usado para avaliar concord&#226;ncia, com interpreta&#231;&#227;o segundo Fleiss et al.<xref ref-type="bibr" rid="B19">19</xref> Concord&#226;ncia substancial foi definida como coeficiente kappa de 0,7, considerando-se a propor&#231;&#227;o de pacientes com SXescore &gt; 23, sendo 30% segundo o observador 1 e 20% segundo o observador 2, com acur&#225;cia de 0,2. Os coeficientes de correla&#231;&#227;o intraclasse tamb&#233;m foram calculados.</p>
          <p>As recomenda&#231;&#245;es STARD<xref ref-type="bibr" rid="B20">20</xref> foram usadas para planejar e relatar este estudo. Os dados foram apresentados como m&#233;dia &#177; desvio padr&#227;o (DP), porcentagens e HR com intervalo de confian&#231;a (IC) de 95%. Usou-se curva ROC (<italic>Receiver Operating Characteristic</italic>) para calcular a estat&#237;stica C e a &#225;rea sub a curva. A curva de sobrevida de Kaplan-Meier para MACE foi calculada para pacientes de acordo com os SXescores. Realizou-se an&#225;lise multivariada do poder de predi&#231;&#227;o do SXescore usando regress&#227;o de Cox, que permitiu a estimativa de HR e IC 95%. As vari&#225;veis associadas com o desfecho na an&#225;lise bivariada (p &#8804; 0,2) foram eleg&#237;veis como fatores de confus&#227;o. Considerando que muitas vari&#225;veis s&#227;o intermedi&#225;rias na causa de MACE, elas foram avaliadas individualmente quanto &#224; sua inclus&#227;o na an&#225;lise. Usou-se o mesmo modelo para o n&#250;mero de vasos comprometidos (nenhum, um e m&#250;ltiplos) como vari&#225;vel de exposi&#231;&#227;o. As an&#225;lises foram realizadas com o programa <italic>Statistical Package for Social Sciences</italic> (SPSS(r), vers&#227;o 17, Chicago, IL, EUA), adotando-se o valor de p &lt; 0,05 como estatisticamente significativo.</p>
        </sec>
      </sec>
      <sec sec-type="results">
        <title>Resultados</title>
        <p>O fluxograma do estudo &#233; apresentado na <xref ref-type="fig" rid="f4">Figura 1</xref>. Dos 928 pacientes eleg&#237;veis, 895 com SXescore foram inclu&#237;dos na coorte e acompanhados em m&#233;dia por 1,8 &#177; 1,4 anos. Ap&#243;s a cineangiocoronariografia, 314 (35,1%) pacientes foram submetidos a ICP ou cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica, e 82 (9,2%), a substitui&#231;&#227;o de v&#225;lvula (procedimento-&#237;ndice). Novas interven&#231;&#245;es foram realizadas durante o seguimento (revasculariza&#231;&#245;es tardias) em 54 pacientes (35 percut&#226;neas e 19 cir&#250;rgicas). Infarto do mioc&#225;rdio ocorreu em 16 pacientes, morte card&#237;aca em 13, morte cardiovascular em 22, e morte por todas as causas em 40 pacientes. Estabeleceu-se a presen&#231;a de MACE em 73 pacientes.</p>
        <p>
          <fig id="f4">
            <label>Figura 1</label>
            <caption>
              <title>Fluxograma dos pacientes do estudo. ICP: interven&#231;&#227;o coronariana percut&#226;nea; CRM: cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica; IM: infarto do mioc&#225;rdio; DAC: doen&#231;a arterial coronariana; CV: cardiovascular; MACE: eventos card&#237;acos adversos maiores.* Pacientes de substitui&#231;&#227;o valvar foram exclu&#237;dos da an&#225;lise de desfecho. <sup>&#358;</sup> MACE como definido na se&#231;&#227;o M&#233;todos.</title>
            </caption>
            <graphic xlink:href="1678-4170-abc-107-03-0207-60111-gf01-pt.jpg"/></fig>
        </p>
        <p>O coeficiente de correla&#231;&#227;o de Spearman entre os SXescores calculados pelos dois cardiologistas intervencionistas foi 0,902 (p &lt; 0,001), sendo a concord&#226;ncia interobservador entre eles de 0,94 (IC 95%: 0,91-0,96). O coeficiente Kappa foi 0,83 para os dois cardiologistas intervencionistas. Houve 495 pacientes com escore de 0 (55,4%) e 400 (44,6%) com escores positivos, variando de 1 a 43, com m&#233;dia de 12,6 (IC 95%: 11,7-13,4). Os pacientes com les&#245;es coronarianas com estenose de di&#226;metro &#8805; 50% em vasos &#8805;1,5 mm foram classificados como SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub> (n = 345) ou SXescore<sub>ALTO</sub> (n = 54).</p>
        <p>As caracter&#237;sticas cl&#237;nicas e angiogr&#225;ficas basais conforme as categorias dos pacientes s&#227;o apresentadas na <xref ref-type="table" rid="t4">Tabela 1</xref>. A idade m&#233;dia dos pacientes com SXescore<sub>ALTO</sub> foi mais elevada do que aquela dos pacientes com SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub>. Al&#233;m disso, a propor&#231;&#227;o de pacientes do sexo masculino, com diabetes mellitus e hipertens&#227;o foi maior entre aqueles com SXescore<sub>ALTO</sub>. As indica&#231;&#245;es cl&#237;nicas para cineangiocoronariografia diagn&#243;stica n&#227;o diferiram significativamente conforme o SXescore, ainda que maior n&#250;mero de pacientes com SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub> tivesse sintomas t&#237;picos de DAC, e maior n&#250;mero de pacientes 'sem DAC significativa' apresentasse outros sintomas. Como esperado, a preval&#234;ncia de doen&#231;a multiarterial e de todos os marcadores para les&#227;o de alta complexidade, como oclus&#227;o total, bifurca&#231;&#245;es e doen&#231;a de pequenos vasos, foi significativamente maior na categoria de SXescore<sub>ALTO</sub>.</p>
        <table-wrap id="t4">
          <label>Tabela 1</label>
          <caption>
            <title>Caracter&#237;sticas cl&#237;nicas basais segundo as categorias de SXescore dos pacientes</title>
          </caption>
          <table frame="hsides" rules="groups">
            <colgroup width="20%">
              <col/>
              <col/>
              <col/>
              <col/>
              <col/>
            </colgroup>
            <thead>
              <tr>
                <th align="left">Caracter&#237;sticas basais</th>
                <th align="center">Sem DAC significativa n = 495</th>
                <th align="center">SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub> n = 346</th>
                <th align="center">SXescore<sub>ALTO</sub> n = 54</th>
                <th align="center">Valor de p</th>
              </tr>
            </thead>
            <tbody>
              <tr>
                <td align="left">Idade</td>
                <td align="center">59,1 &#177; 10,4</td>
                <td align="center">60,8 &#177; 9,6</td>
                <td align="center">63,6 &#177; 8,6</td>
                <td align="center">0,002</td>
              </tr>
              <tr>
                <td align="left">Masculino</td>
                <td align="center">234 (47,3)</td>
                <td align="center">226 (65,3)</td>
                <td align="center">39 (72,2)</td>
                <td align="center">&lt; 0,001</td>
              </tr>
              <tr>
                <td align="left">Diabetes mellitus</td>
                <td align="center">92 (18,6)</td>
                <td align="center">85 (24,6)</td>
                <td align="center">18 (33,3)</td>
                <td align="center">0,01</td>
              </tr>
              <tr>
                <td align="left">Tabagismo atual</td>
                <td align="center">65 (13,2)</td>
                <td align="center">51 (15,0)</td>
                <td align="center">3 (5,6)</td>
                <td align="center">0,08</td>
              </tr>
              <tr>
                <td align="left">Hipertens&#227;o</td>
                <td align="center">344 (69,8)</td>
                <td align="center">260 (76,5)</td>
                <td align="center">45 (83,3)</td>
                <td align="center">0,02</td>
              </tr>
              <tr>
                <td align="left">Apenas sintomas sugestivos de DAC</td>
                <td align="center">128 (25,9)</td>
                <td align="center">115 (33,4)</td>
                <td align="center">14 (25,9)</td>
                <td align="center">0,05</td>
              </tr>
              <tr>
                <td align="left">Com teste n&#227;o invasivo positivo</td>
                <td align="center">209 (42,2)</td>
                <td align="center">139 (40,2)</td>
                <td align="center">28 (51,9)</td>
                <td align="center">0,3</td>
              </tr>
              <tr>
                <td align="left">Valvopatia com suspeita de DAC</td>
                <td align="center">14 (2,8)</td>
                <td align="center">3 (0,9)</td>
                <td align="center">1 (1,9)</td>
                <td align="center">0,14</td>
              </tr>
              <tr>
                <td align="left">Outras queixas</td>
                <td align="center">46 (9,3)</td>
                <td align="center">13 (3,8)</td>
                <td align="center">1 (1,9)</td>
                <td align="center">0,002</td>
              </tr>
              <tr>
                <td align="left">
                  <bold>An&#225;lise angiogr&#225;fica<xref ref-type="table-fn" rid="TFN10">*</xref></bold>
                </td>
                <td align="center">
								</td>
                <td align="center">
								</td>
                <td align="center">
								</td>
                <td align="center">
								</td>
              </tr>
              <tr>
                <td align="left">Domin&#226;ncia direita</td>
                <td align="center">-</td>
                <td align="center">309 (89,3)</td>
                <td align="center">51 (94,4)</td>
                <td align="center">0,3</td>
              </tr>
              <tr>
                <td align="left">No. les&#245;es por paciente</td>
                <td align="center">-</td>
                <td align="center">1,8 &#177; 1,0</td>
                <td align="center">3,9 &#177; 1,5</td>
                <td align="center">&lt; 0,001</td>
              </tr>
              <tr>
                <td align="left">Oclus&#227;o total</td>
                <td align="center">-</td>
                <td align="center">88 (25,4)</td>
                <td align="center">41 (75,9)</td>
                <td align="center">&lt; 0,001</td>
              </tr>
              <tr>
                <td align="left">Bifurca&#231;&#245;es</td>
                <td align="center">-</td>
                <td align="center">125 (36,1)</td>
                <td align="center">44 (81,5)</td>
                <td align="center">&lt; 0,001</td>
              </tr>
              <tr>
                <td align="left">Pequenos vasos/doen&#231;a difusa</td>
                <td align="center">-</td>
                <td align="center">68 (19,7)</td>
                <td align="center">26 (48,1)</td>
                <td align="center">&lt; 0,001</td>
              </tr>
              <tr>
                <td align="left">Tronco de coron&#225;ria esquerda</td>
                <td align="center">-</td>
                <td align="center">13 (13,8)</td>
                <td align="center">13 (24,1)</td>
                <td align="center">&lt; 0,001</td>
              </tr>
              <tr>
                <td align="left">Descendente anterior esquerda</td>
                <td align="center">-</td>
                <td align="center">218 (63,0)</td>
                <td align="center">47 (87,0)</td>
                <td align="center">&lt; 0,001</td>
              </tr>
              <tr>
                <td align="left">Circunflexa</td>
                <td align="center">-</td>
                <td align="center">109 (31,5)</td>
                <td align="center">36 (66,7)</td>
                <td align="center">&lt; 0,001</td>
              </tr>
              <tr>
                <td align="left">Coron&#225;ria direita</td>
                <td align="center">-</td>
                <td align="center">169 (48,8)</td>
                <td align="center">43 (79,6)</td>
                <td align="center">&lt; 0,001</td>
              </tr>
              <tr>
                <td align="left">Doen&#231;a uniarterial</td>
                <td align="center">-</td>
                <td align="center">196 (56,7)</td>
                <td align="center">4 (7,4)</td>
                <td align="center">&lt; 0,001</td>
              </tr>
              <tr>
                <td align="left">Doen&#231;a multiarterial ou tronco</td>
                <td align="center">-</td>
                <td align="center">150 (43,3)</td>
                <td align="center">50 (92,6)</td>
                <td align="center">&lt; 0,001</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="TFN09">
              <p>Valores apresentados como n (%) ou m&#233;dia &#177; DP. DAC: doen&#231;a arterial coronariana; SXescore: Syntax Escore.</p>
            </fn>
            <fn id="TFN10">
              <label>*</label>
              <p>Avalia&#231;&#227;o usando as defini&#231;&#245;es do SYNTAX Escore</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
        <sec>
          <title>Procedimentos ap&#243;s a cineangiocoronariografia-&#237;ndice</title>
          <p>A propor&#231;&#227;o de pacientes submetidos a ICP, cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica e substitui&#231;&#227;o valvar com base na cineangiocoronariografia-&#237;ndice diagn&#243;stica, de acordo com a categoria do paciente, &#233; apresentada na <xref ref-type="table" rid="t5">Tabela 2</xref>. Como esperado, maior n&#250;mero de pacientes com escores altos foi submetido a cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica. Ainda que, na avalia&#231;&#227;o angiogr&#225;fica de base realizada neste estudo, tenham sido classificados como 'sem DAC significativa', 3,4% desses pacientes foram submetidos a ICP.</p>
          <table-wrap id="t5">
            <label>Tabela 2</label>
            <caption>
              <title>Tratamento ap&#243;s cineangiocoronariografia-&#237;ndice e desfechos cl&#237;nicos cumulativos segundo as categorias de SXescore dos pacientes</title>
            </caption>
            <table frame="hsides" rules="groups">
              <colgroup width="20%">
                <col/>
                <col/>
                <col/>
                <col/>
                <col/>
              </colgroup>
              <thead>
                <tr>
                  <th align="left">Tipo de procedimento</th>
                  <th align="center">Sem DAC significativa n = 495</th>
                  <th align="center">SXescoren<sub>BAIXO-INTERMEDI&#193;RIO</sub> n = 346</th>
                  <th align="center">SXescore<sub>ALTO</sub> n = 54</th>
                  <th align="center">Valor de p</th>
                </tr>
              </thead>
              <tbody>
                <tr>
                  <td align="left">
                    <bold>Interven&#231;&#245;es</bold>
                  </td>
                  <td align="center">
									</td>
                  <td align="center">
									</td>
                  <td align="center">
									</td>
                  <td align="center">&lt; 0,001</td>
                </tr>
                <tr>
                  <td align="left">Interven&#231;&#227;o coronariana percut&#226;nea</td>
                  <td align="center">17 (3,4)</td>
                  <td align="center">208 (60,3)</td>
                  <td align="center">14 (25,9)</td>
                  <td align="center">
									</td>
                </tr>
                <tr>
                  <td align="left">Cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica</td>
                  <td align="center">0</td>
                  <td align="center">46 (13,3)</td>
                  <td align="center">29 (53,7)</td>
                  <td align="center">
									</td>
                </tr>
                <tr>
                  <td align="left">Substitui&#231;&#227;o valvar isolada<xref ref-type="table-fn" rid="TFN12">*</xref>
									</td>
                  <td align="center">78 (15,8)</td>
                  <td align="center">4 (1,2)</td>
                  <td align="center">0</td>
                  <td align="center">
									</td>
                </tr>
                <tr>
                  <td align="left">Sem interven&#231;&#227;o invasiva</td>
                  <td align="center">400 (80,8)</td>
                  <td align="center">88 (25,4)</td>
                  <td align="center">11 (20,4)</td>
                  <td align="center">
									</td>
                </tr>
                <tr>
                  <td align="left">Morte por todas as causas</td>
                  <td align="center">16 (3,9)</td>
                  <td align="center">11 (3,3)</td>
                  <td align="center">9 (16,7)</td>
                  <td align="center">&lt; 0,001</td>
                </tr>
                <tr>
                  <td align="left">Morte card&#237;aca e IM</td>
                  <td align="center">4 (1,0)</td>
                  <td align="center">13 (3,9)</td>
                  <td align="center">9 (16,7)</td>
                  <td align="center">&lt; 0,001</td>
                </tr>
                <tr>
                  <td align="left">Morte cardiovascular</td>
                  <td align="center">9 (2,2)</td>
                  <td align="center">6 (1,8)</td>
                  <td align="center">7 (13)</td>
                  <td align="center">&lt; 0,001</td>
                </tr>
                <tr>
                  <td align="left">MACE</td>
                  <td align="center">9 (2,2)</td>
                  <td align="center">53 (15,7)</td>
                  <td align="center">11 (20,4)</td>
                  <td align="center">&lt; 0,001</td>
                </tr>
              </tbody>
            </table>
            <table-wrap-foot>
              <fn id="TFN11">
                <p>Valores apresentados como n (%).</p>
              </fn>
              <fn id="TFN12">
                <label>*</label>
                <p>pacientes exclu&#237;dos da an&#225;lise de desfecho. DAC: doen&#231;a arterial coronariana; IM: infarto do mioc&#225;rdio; MACE: eventos card&#237;acos adversos maiores; IM: morte card&#237;aca e revasculariza&#231;&#227;o tardia.</p>
              </fn>
            </table-wrap-foot>
          </table-wrap>
        </sec>
        <sec>
          <title>Desfechos cl&#237;nicos</title>
          <p>A incid&#234;ncia cumulativa de desfechos cl&#237;nicos nos grupos &#233; apresentada na <xref ref-type="table" rid="t5">Tabela 2</xref>. Morte por todas as causas foi significativamente mais alta em pacientes com SXescore<sub>ALTO</sub> quando comparados &#224;queles do grupo 'sem DAC significativa', 16,7% e 3,9% (p &lt; 0,001), respectivamente. Morte cardiovascular, IM n&#227;o fatal e revasculariza&#231;&#227;o tardia foram mais frequentes no grupo com SXescore<sub>ALTO</sub>. Ap&#243;s ajuste para fatores de confus&#227;o, todos os desfechos permaneceram associados com o SXescore (<xref ref-type="table" rid="t6">Tabela 3</xref>). As HR para MACE, morte card&#237;aca ou IM n&#227;o fatal e IM n&#227;o fatal apenas mostraram-se significativamente associadas a SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub>. Os pacientes da categoria SXescore<sub>ALTO</sub> apresentaram uma chance 12,5 vezes maior (IC 95%: 5,1-30,6) de desfecho prim&#225;rio do que aqueles 'sem DAC significativa'. Tal achado foi semelhante em homens (10,1; IC 95%: 3,9-25,9) e mulheres (11,5; IC 95%: 1,1-117,3). Ajuste posterior para revasculariza&#231;&#227;o-&#237;ndice n&#227;o alterou as estimativas de maneira significativa. Ap&#243;s ajuste para os fatores de confus&#227;o, o desfecho prim&#225;rio tamb&#233;m se associou ao SXescore como uma vari&#225;vel cont&#237;nua (HR 1,06; IC 95%: 1,04-1,08). A &#225;rea sob a curva ROC foi de 0,73 (IC 95%: 0,68-0,79) (<xref ref-type="fig" rid="f5">Figura 2</xref>).</p>
          <table-wrap id="t6">
            <label>Tabela 3</label>
            <caption>
              <title>Raz&#227;o de risco (HR)<xref ref-type="table-fn" rid="TFN14">*</xref> para desfechos cl&#237;nicos maiores segundo as categorias de SXescore dos pacientes</title>
            </caption>
            <table frame="hsides" rules="groups">
              <colgroup width="20%">
                <col/>
                <col/>
                <col/>
                <col/>
                <col/>
              </colgroup>
              <thead>
                <tr>
                  <th align="left">Tipo de evento</th>
                  <th align="center">Sem DAC significativa <xref ref-type="table-fn" rid="TFN15">&#8224;</xref> n = 495</th>
                  <th align="center">SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub> n = 346</th>
                  <th align="center">SXescore<sub>ALTO</sub> n = 54</th>
                  <th align="center">Valor de p</th>
                </tr>
              </thead>
              <tbody>
                <tr>
                  <td align="left">Morte por todas as causas</td>
                  <td align="center">1,0</td>
                  <td align="center">0,8 (0,4-1,7)</td>
                  <td align="center">4,3 (1,8-10,1)</td>
                  <td align="center">&lt; 0,001</td>
                </tr>
                <tr>
                  <td align="left">Morte cardiovascular</td>
                  <td align="center">1,0</td>
                  <td align="center">0,7 (0,3-2,1)</td>
                  <td align="center">5,7 (2,0-15,9)</td>
                  <td align="center">&lt; 0,001</td>
                </tr>
                <tr>
                  <td align="left">Morte card&#237;aca</td>
                  <td align="center">1,0</td>
                  <td align="center">1,3 (0,3-5,9)</td>
                  <td align="center">11,8 (2,9-48,5)</td>
                  <td align="center">&lt; 0,001</td>
                </tr>
                <tr>
                  <td align="left">MACE<xref ref-type="table-fn" rid="TFN16">&#8225;</xref>
									</td>
                  <td align="center">1,0</td>
                  <td align="center">7,2 (3,5-14,7)</td>
                  <td align="center">12,5 (5,1-30,6)</td>
                  <td align="center">&lt; 0,001</td>
                </tr>
                <tr>
                  <td align="left">Morte card&#237;aca ou IM</td>
                  <td align="center">1,0</td>
                  <td align="center">3,5 (1,1-10,8)</td>
                  <td align="center">16,0 (4,9-52,9)</td>
                  <td align="center">&lt; 0,001</td>
                </tr>
                <tr>
                  <td align="left">IM</td>
                  <td align="center">1,0</td>
                  <td align="center">12,6 (1,6-98,3)</td>
                  <td align="center">33,9 (3,7-308,0)</td>
                  <td align="center">0,007</td>
                </tr>
                <tr>
                  <td align="left">Revasculariza&#231;&#227;o tardia</td>
                  <td align="center">1,0</td>
                  <td align="center">9,9 (4,2-23,4)</td>
                  <td align="center">4,0 (0,8-20,0)</td>
                  <td align="center">&lt; 0,001</td>
                </tr>
              </tbody>
            </table>
            <table-wrap-foot>
              <fn id="TFN13">
                <p>DAC: doen&#231;a arterial coronariana; IM: infarto do mioc&#225;rdio; MACE: eventos card&#237;acos adversos maiores.</p>
              </fn>
              <fn id="TFN14">
                <label>*</label>
                <p>Ajustada para idade, sexo e diabetes.</p>
              </fn>
              <fn id="TFN15">
                <label>&#8224;</label>
                <p>Categoria de refer&#234;ncia.</p>
              </fn>
              <fn id="TFN16">
                <label>&#8225;</label>
                <p>MACE: IM, morte card&#237;aca e revasculariza&#231;&#227;o tardia.</p>
              </fn>
            </table-wrap-foot>
          </table-wrap>
          <p>
            <fig id="f5">
              <label>Figura 2</label>
              <caption>
                <title>Curva ROC para o SYNTAX Escore. AUC: &#225;rea sob a curva.</title>
              </caption>
              <graphic xlink:href="1678-4170-abc-107-03-0207-60111-gf02-pt.jpg"/></fig>
          </p>
          <p>As curvas de sobrevida sem MACE para os pacientes de acordo com os SXescores s&#227;o apresentadas na <xref ref-type="fig" rid="f6">Figura 3</xref>. Pode-se ver que as curvas divergiram imediatamente ap&#243;s a cineangiocoronariografia e mais ainda durante o seguimento. As HR para MACE de acordo com o n&#250;mero de vasos comprometidos, em compara&#231;&#227;o a nenhum vaso, foram 6,9 (IC 95%: 3,4-13,9) para doen&#231;a uniarterial e 10,2 (5,2-20,1) para doen&#231;a multiarterial. A despeito da rela&#231;&#227;o intr&#237;nseca dessa classifica&#231;&#227;o com o SXescore, 42,0% dos pacientes com doen&#231;a multiarterial foram classificados na categoria de SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub>.</p>
          <p>
            <fig id="f6">
              <label>Figura 3</label>
              <caption>
                <title>Curva de Kaplan-Meier para eventos card&#237;acos adversos maiores (MACE) de acordo com a categoria do SYNTAX Escore (SXescore) do paciente. DAC: doen&#231;a arterial coronariana.</title>
              </caption>
              <graphic xlink:href="1678-4170-abc-107-03-0207-60111-gf03-pt.jpg"/></fig>
          </p>
        </sec>
      </sec>
      <sec sec-type="discussion">
        <title>Discuss&#227;o</title>
        <p>Este estudo demonstrou que, em pacientes submetidos a cineangiocoronariografia diagn&#243;stica devido a suspeita de DAC, o SXescore p&#244;de predizer o desfecho prim&#225;rio de morte card&#237;aca, IM n&#227;o fatal e revasculariza&#231;&#227;o tardia, independentemente de idade, sexo, presen&#231;a de diabetes e revasculariza&#231;&#227;o-&#237;ndice. Houve aumento de 6% no risco de MACE para cada ponto adicional no escore. Os pacientes com SXescore<sub>ALTO</sub> apresentaram um risco significativamente elevado de morte por todas as causas, cardiovascular e card&#237;aca.</p>
        <p>Estudos pr&#233;vios relataram a capacidade do SXescore para predizer MACE em diferentes cen&#225;rios. Os estudos LEADERS,<xref ref-type="bibr" rid="B9">9</xref><sup>,</sup><xref ref-type="bibr" rid="B10">10</xref> SIRTAX<xref ref-type="bibr" rid="B11">11</xref> e RESOLUTE<xref ref-type="bibr" rid="B8">8</xref> inclu&#237;ram pacientes com s&#237;ndromes coronarianas agudas e ainda aqueles submetidos a ICP eletiva. Os estudos MI-SYNTAXscore,<xref ref-type="bibr" rid="B12">12</xref> STRATEGY e MULTISTRATEGY<xref ref-type="bibr" rid="B13">13</xref> foram realizados em pacientes com IM agudo. O ensaio ACUITY<xref ref-type="bibr" rid="B7">7</xref> incluiu pacientes com s&#237;ndromes coronarianas agudas. Por fim, Garg et al.<xref ref-type="bibr" rid="B14">14</xref> resumiram os resultados de cinco estudos, analisando dados de 6.508 pacientes, com os mesmos resultados. Diferentemente da nossa pesquisa, todos aqueles estudos inclu&#237;ram apenas pacientes submetidos a procedimentos de revasculariza&#231;&#227;o percut&#226;nea, nenhum deles tendo focado em pacientes com suspeita de DAC ou com DAC est&#225;vel. O grupo de pacientes 'sem DAC significativa', ainda que muitos tivessem DAC com estenose de di&#226;metro inferior a 50%, serviu como categoria de refer&#234;ncia para comparar os desfechos com os de pacientes nas categorias SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub> e SXescore<sub>ALTO</sub>. Sabemos ser nossa proposta diferente da aplica&#231;&#227;o original do escore, na qual pacientes sem les&#245;es trat&#225;veis por cirurgia ou por via percut&#226;nea foram exclu&#237;dos, mas alinha-se com os objetivos deste estudo.</p>
        <p>A compara&#231;&#227;o do desempenho do SXescore com escores anat&#244;micos tradicionais para DAC n&#227;o foi explorada na nossa investiga&#231;&#227;o. A presen&#231;a de SXescores positivos (44,6%) foi similar &#224; frequ&#234;ncia de pacientes com DAC significativa (47%) detectada por an&#225;lise angiogr&#225;fica quantitativa realizada em uma propor&#231;&#227;o de pacientes da nossa coorte.<xref ref-type="bibr" rid="B21">21</xref> Escores angiogr&#225;ficos tradicionais tamb&#233;m predisseram a incid&#234;ncia de MACE em estudos pr&#233;vios,<xref ref-type="bibr" rid="B2">2</xref> mas tais escores n&#227;o consideram as dificuldades da realiza&#231;&#227;o de revasculariza&#231;&#227;o mioc&#225;rdica. A despeito de sua capacidade progn&#243;stica, eles n&#227;o foram incorporados &#224; pr&#225;tica cl&#237;nica, na qual o n&#250;mero de vasos comprometidos foi usado para estimar a gravidade anat&#244;mica da doen&#231;a. Nesta coorte, os pacientes com doen&#231;a uniarterial e multiarterial apresentaram risco de MACE aproximadamente similar ao dos pacientes com SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub> e SXescore<sub>ALTO</sub>, respectivamente. No entanto, quase metade dos pacientes com doen&#231;a multiarterial foi classificada na categoria SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub>.</p>
        <p>Com base nos resultados do estudo SYNTAX,<xref ref-type="bibr" rid="B5">5</xref> no qual pacientes com baixos escores SYNTAX apresentaram desfechos similares a despeito do tipo de revasculariza&#231;&#227;o, nossos achados t&#234;m uma implica&#231;&#227;o cl&#237;nica - pacientes que, de outra maneira, seriam encaminhados para cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica tamb&#233;m poderiam ser revascularizados por via percut&#226;nea. Considerando que a caracteriza&#231;&#227;o visual de doen&#231;a multiarterial leva ao encaminhamento de pacientes para revasculariza&#231;&#227;o cir&#250;rgica, o c&#225;lculo do SXescore poderia melhor estratificar pacientes que de fato se beneficiariam daquele procedimento (categoria SXescore<sub>ALTO</sub>).</p>
        <p>Neste estudo, os pacientes foram submetidos a procedimento eletivo e, como resultado, houve uma grande propor&#231;&#227;o de pacientes 'sem DAC significativa', que tamb&#233;m poderiam ter les&#245;es menores do que 50%. Tais pacientes n&#227;o preenchiam os crit&#233;rios para um escore positivo e serviram como grupo de compara&#231;&#227;o. Assim, os pacientes foram classificados em duas categorias: 1 a 22, e igual ou maior do que 23, correspondendo &#224;s posteriormente definidas categorias 'baixo-intermedi&#225;rio' (0-22) e 'alto' (igual ou maior do que 23).<xref ref-type="bibr" rid="B6">6</xref> O n&#250;mero de pacientes classificados como SXescore<sub>BAIXO-INTERMEDI&#193;RIO</sub> e submetidos a revasculariza&#231;&#227;o percut&#226;nea foi maior do que o de pacientes submetidos a revasculariza&#231;&#227;o cir&#250;rgica, refletindo a pr&#225;tica cl&#237;nica corrente e em conformidade com os achados de acompanhamento de cinco anos do ensaio cl&#237;nico randomizado SYNTAX.<xref ref-type="bibr" rid="B6">6</xref> Na &#233;poca em que o estudo foi conduzido, os <italic>stents</italic> farmacol&#243;gicos n&#227;o eram dispon&#237;veis para uso no sistema de sa&#250;de p&#250;blica brasileiro. Al&#233;m disso, atualmente indica-se revasculariza&#231;&#227;o cir&#250;rgica para pacientes com SXescore alto.<xref ref-type="bibr" rid="B6">6</xref> Pacientes com alto risco cir&#250;rgico, considerados ineleg&#237;veis para revasculariza&#231;&#227;o cir&#250;rgica pelos cirurgi&#245;es receberam tratamento percut&#226;neo. Houve um achado inesperado de 3,4% de pacientes 'sem DAC significativa' submetidos a ICP. Pacientes com DAC n&#227;o obstrutiva representam uma grande propor&#231;&#227;o daqueles submetidos a cineangiocoronariografia. A avalia&#231;&#227;o subjetiva da anatomia coronariana associada a informa&#231;&#227;o cl&#237;nica e n&#227;o invasiva pode ter influenciado o processo de tomada de decis&#227;o e poderia explicar tal achado.</p>
        <p>Nosso estudo tem algumas limita&#231;&#245;es e pontos fortes que devem ser abordados. Restringimos nossa an&#225;lise ao crit&#233;rio anat&#244;mico, sem considerar fun&#231;&#227;o ventricular esquerda, isquemia ou viabilidade mioc&#225;rdica. No entanto, nossos pacientes n&#227;o tinham doen&#231;a inst&#225;vel do ponto de vista cl&#237;nico e nem insufici&#234;ncia card&#237;aca classe III ou IV, tendo os crit&#233;rios anat&#244;micos frequentemente prevalecido para a tomada de decis&#227;o terap&#234;utica. Al&#233;m disso, uma recente an&#225;lise <italic>post-hoc</italic> do ensaio COURAGE demonstrou que os crit&#233;rios anat&#244;micos e n&#227;o a carga isqu&#234;mica foram capazes de predizer eventos cardiovasculares.<xref ref-type="bibr" rid="B22">22</xref> Embora a maioria dos procedimentos de seguimento tenha sido realizada em nosso hospital, diferentes tipos de <italic>stent</italic> foram implantados, o que pode ter afetado a probabilidade de trombose no <italic>stent</italic> ou de reinterven&#231;&#245;es.<xref ref-type="bibr" rid="B23">23</xref> Entretanto, an&#225;lise incluindo apenas IM e morte card&#237;aca n&#227;o alterou as estimativas, e a exclus&#227;o de pacientes submetidos a substitui&#231;&#227;o valvar n&#227;o alterou os resultados. Outra limita&#231;&#227;o &#233; o n&#250;mero de eventos, respons&#225;vel pelos amplos intervalos de confian&#231;a. Ainda que tiv&#233;ssemos investigado quase 1.000 pacientes, mais de 50% n&#227;o tinham DAC significativa, refletindo a pr&#225;tica da vida real de um centro terci&#225;rio que realiza cineangiocoronariografias diagn&#243;sticas. Estudos com maiores tamanhos amostrais e conduzidos em outros centros s&#227;o necess&#225;rios para confirmar nossos achados e sua validade externa. A alta reprodutibilidade interobservador dos examinadores &#233; um dos pontos fortes da nossa investiga&#231;&#227;o, semelhante &#224; de alguns estudos,<xref ref-type="bibr" rid="B24">24</xref> mas diferente da de outros.<xref ref-type="bibr" rid="B25">25</xref><sup>,</sup><xref ref-type="bibr" rid="B26">26</xref> Tal desempenho poderia ser explicado pelo extenso treinamento na avalia&#231;&#227;o do SXescore realizado pelos cardiologistas intervencionistas e o fato de que ambos foram treinados no mesmo hospital.</p>
        <sec>
          <title>Implica&#231;&#245;es cl&#237;nicas</title>
          <p>Na pr&#225;tica cl&#237;nica, o n&#250;mero de vasos epic&#225;rdicos com estenose superior a 50% &#233; usado para fornecer informa&#231;&#227;o progn&#243;stica, sendo os escores angiogr&#225;ficos raramente usados. Recentemente, o uso de escores mostrou melhorar a padroniza&#231;&#227;o da tomada de decis&#227;o cl&#237;nica. Por exemplo, o EUROESCORE<xref ref-type="bibr" rid="B27">27</xref> e o escore STS<xref ref-type="bibr" rid="B28">28</xref> s&#227;o usados de rotina no processo de tomada de decis&#227;o para a indica&#231;&#227;o de cirurgia de revasculariza&#231;&#227;o mioc&#225;rdica.<xref ref-type="bibr" rid="B29">29</xref> Para a conduta em DAC multiarterial, as atuais diretrizes formalmente recomendam o uso do SXescore, assim como do EUROESCORE.<xref ref-type="bibr" rid="B30">30</xref> Nossos dados expandem as indica&#231;&#245;es do SXescore para avalia&#231;&#227;o progn&#243;stica de pacientes encaminhados para cineangiocoronariografia diagn&#243;stica.</p>
        </sec>
      </sec>
      <sec sec-type="conclusions">
        <title>Conclus&#227;o</title>
        <p>Em pacientes com suspeita de DAC submetidos a cineangiocoronariografia eletiva, o SXescore prediz independentemente MACE. Seu uso rotineiro nesse contexto poderia identificar pacientes com pior progn&#243;stico.</p>
      </sec>
    </body>
    <back>
      <fn-group>
        <fn fn-type="other" id="fn2">
          <p>(in memorian)</p>
        </fn>
        <fn fn-type="supported-by">
          <p>
            <bold>Fontes de financiamento</bold>
          </p>
          <p>O presente estudo foi parcialmente financiado pelo CNPq e Funda&#231;&#227;o para o incentivo em Pesquisa do Hospital de Cl&#237;nicas de Porto Alegre.</p>
        </fn>
        <fn fn-type="other">
          <p>
            <bold>Vincula&#231;&#227;o acad&#234;mica</bold>
          </p>
          <p>Este artigo &#233; parte de Disserta&#231;&#227;o de Mestrado de Felipe C. Fuchs pela Faculdade de Medicina da Universidade Federal do Rio Grande do Sul.</p>
        </fn>
      </fn-group>
      <ack>
        <title>Agradecimentos</title>
        <p>Este estudo foi parcialmente financiado pelo Conselho Nacional de Desenvolvimento Cient&#237;fico e Tecnol&#243;gico (CNPq), Brasil; Fundo de Pesquisa do Hospital de Cl&#237;nicas de Porto Alegre (FIPE-HCPA), Porto Alegre, Brasil.</p>
      </ack>
    </back>
  </sub-article>
</article>
