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          "titulo" => "References"
        ]
      ]
    ]
    "pdfFichero" => "main.pdf"
    "tienePdf" => true
    "fechaRecibido" => "2020-07-08"
    "fechaAceptado" => "2020-08-07"
    "PalabrasClave" => array:2 [
      "en" => array:1 [
        0 => array:4 [
          "clase" => "keyword"
          "titulo" => "Keywords"
          "identificador" => "xpalclavsec1350707"
          "palabras" => array:4 [
            0 => "Sudden death"
            1 => "Hypertrophic cardiomyopathy"
            2 => "Heart failure"
            3 => "Cardiomyopathies"
          ]
        ]
      ]
      "pt" => array:1 [
        0 => array:4 [
          "clase" => "keyword"
          "titulo" => "Palavras-chave"
          "identificador" => "xpalclavsec1350708"
          "palabras" => array:4 [
            0 => "Morte s&#250;bita"
            1 => "Miocardiopatia hipertr&#243;fica"
            2 => "Insufici&#234;ncia card&#237;aca"
            3 => "Miocardiopatias"
          ]
        ]
      ]
    ]
    "tieneResumen" => true
    "resumen" => array:2 [
      "en" => array:3 [
        "titulo" => "Abstract"
        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Introduction and objectives</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">According to current international guidelines&#44; hypertrophic cardiomyopathy &#40;HCM&#41; patients should be managed in specialized units&#46; However&#44; there is lack of data on the impact of the creation of these units in the management of HCM patients&#46; Our goal was to assess the impact of the creation of an Inherited Inherited Diseases Cardiac Unit &#40;ICDU&#41; in the current management of patients with HCM&#46;</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Methods</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">We analyzed 114 consecutive patients &#40;62&#46;6&#177;8 years old&#44; 70&#46;2&#37; males&#41; with HCM&#46; Variables related to optimal management of HCM patients and their family study were recorded&#44; as well as guidance on the risk of sudden death&#46; We analyzed whether patients were assessed by the ICDU or at a general cardiology consultation &#40;GCC&#41;&#46;</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Results</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">50 patients were assessed in the IDCU and 64 in the GCC&#46; Familial screening was more frequent in patients assessed by the IDCU &#40;45&#46;3&#37; vs&#46; 4&#37;&#59; p&#60;0&#46;01&#41;&#44; requesting more genetic studies of the index case &#40;70&#46;3&#37; vs&#46; 14&#37;&#59; p&#60;0&#46;01&#41; and cardiac magnetic resonance &#40;53&#46;1&#37; vs&#46; 18&#37;&#59; p&#60;0&#46;01&#41;&#46; Sudden death risk score was performed more frequently in patients after the creation of an IDCU &#40;67&#46;2&#37; vs&#46; 28&#37;&#59; p&#60;0&#46;01&#41;&#46; Treatment with beta-blockers was similar in both groups &#40;72&#37; vs&#46; 78&#46;1&#37;&#59; p&#61;0&#46;24&#41;&#46; An implantable cardiac defibrillator was indicated similarly in both groups &#40;12&#46;5&#37; in ICDU and 6&#37; in GC&#59; p&#61;0&#46;24&#41;&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Conclusions</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">The implementation of an IDCU improved the quality of the medical care for HCM patients by performing a better study of the patients and their families&#46;</p></span>"
        "secciones" => array:4 [
          0 => array:2 [
            "identificador" => "abst0005"
            "titulo" => "Introduction and objectives"
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          1 => array:2 [
            "identificador" => "abst0010"
            "titulo" => "Methods"
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          2 => array:2 [
            "identificador" => "abst0015"
            "titulo" => "Results"
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          3 => array:2 [
            "identificador" => "abst0020"
            "titulo" => "Conclusions"
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      ]
      "pt" => array:3 [
        "titulo" => "Resumo"
        "resumen" => "<span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Introdu&#231;&#227;o e objetivos</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">De acordo com as recomenda&#231;&#245;es internacionais atuais&#44; o tratamento de doentes com miocardiopatia hipertr&#243;fica &#40;MCH&#41; deve ser efetuado em unidades especializadas&#46; No entanto&#44; h&#225; escassez de dados sobre o impacto da cria&#231;&#227;o de uma unidade de doen&#231;as card&#237;acas heredit&#225;rias &#40;UDCH&#41; no tratamento dos doentes com MCH&#46;</p></span> <span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">M&#233;todos</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Analis&#225;mos 114 doentes consecutivos &#40;62&#44;6&#177;8 anos&#44; 70&#44;2&#37; homens&#41; com MCH&#46; Foram registadas as vari&#225;veis relacionadas com o tratamento aprimorado destes doentes e o respetivo estudo familiar&#44; assim como o aconselhamento sobre o risco de morte s&#250;bita&#46; Verific&#225;mos se os doentes foram avaliados em UDCH em consulta geral de cardiologia &#40;GC&#41;&#46;</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Resultados</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Foram avaliados respetivamente 50 e 64 doentes na UDCH e na CG&#46; O rastreio familiar foi mais frequente em doentes avaliados na UDCH &#40;45&#44;3&#37; <span class="elsevierStyleItalic">versus</span> 4&#37;&#44; p&#60;0&#44;01&#41; requerendo a UDCH mais estudos gen&#233;ticos no caso &#237;ndice &#40;70&#44;3&#37; <span class="elsevierStyleItalic">versus</span> 14&#37;&#44; p&#60;0&#44;01&#41; e mais resson&#226;ncia magn&#233;tica card&#237;aca &#40;53&#44;1&#37; <span class="elsevierStyleItalic">versus</span> 18&#37;&#44; p&#60;0&#44;01&#41;&#46; O <span class="elsevierStyleItalic">score</span> de risco de morte s&#250;bita foi realizado com mais frequ&#234;ncia em doentes ap&#243;s a cria&#231;&#227;o da UDCH &#40;67&#44;2&#37; <span class="elsevierStyleItalic">versus</span> 28&#37;&#44; p&#60;0&#44;001&#41;&#46; O tratamento com betabloqueantes foi semelhante em ambos os grupos &#40;72&#37; <span class="elsevierStyleItalic">versus</span> 78&#44;1&#37;&#44; p&#61;0&#44;24&#41;&#46; Foi indicado desfibrilhador card&#237;aco implant&#225;vel de forma semelhante em ambos os grupos &#40;12&#44;5&#37; na UDCH e 6&#37; na CG&#44; p&#61;0&#44;24&#41;&#46;</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conclus&#245;es</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">A implanta&#231;&#227;o de uma UDCH melhorou a qualidade do atendimento m&#233;dico aos doentes com MCH atrav&#233;s de um estudo mais completo dos doentes e das suas fam&#237;lias&#46;</p></span>"
        "secciones" => array:4 [
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            "identificador" => "abst0025"
            "titulo" => "Introdu&#231;&#227;o e objetivos"
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          1 => array:2 [
            "identificador" => "abst0030"
            "titulo" => "M&#233;todos"
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          2 => array:2 [
            "identificador" => "abst0035"
            "titulo" => "Resultados"
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          3 => array:2 [
            "identificador" => "abst0040"
            "titulo" => "Conclus&#245;es"
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    ]
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        "etiqueta" => "Table 1"
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          "leyenda" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">HCM&#58; hypertrophic cardiomyopathy&#59; SCD&#58; sudden cardiac death&#46;</p>"
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">General Consultation &#40;n&#61;50&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">Assessment of relatives&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">29 &#40;45&#46;3&#37;&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t">&#60;0&#46;01&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">Genetic test performance&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">7 &#40;14&#37;&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">45 &#40;70&#46;3&#37;&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t">HCM Risk-SCD Score&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">14 &#40;28&#37;&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">Exercise test&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">Cardiac magnetic resonance&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">Defibrillator indication&nbsp;\t\t\t\t\t\t\n
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          "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Main actions related to the assessment of patients with hypertrophic cardiomyopathy in clinical practice&#46;</p>"
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    "bibliografia" => array:2 [
      "titulo" => "References"
      "seccion" => array:1 [
        0 => array:2 [
          "identificador" => "bibs0015"
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                0 => array:2 [
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                    0 => array:2 [
                      "titulo" => "The Portuguese Registry of hypertrophic cardiomyopathy&#58; overall results"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:3 [
                            0 => "N&#46; Cardim"
                            1 => "D&#46; Brito"
                            2 => "L&#46; Rocha Lopes"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:5 [
                        "tituloSerie" => "Rev Port Cardiol &#40;English Ed&#41;"
                        "fecha" => "2018"
                        "volumen" => "37"
                        "paginaInicial" => "1"
                        "paginaFinal" => "10"
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                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Plan of action for inherited cardiovascular diseases&#58; synthesis of recommendations and action algorithms"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:3 [
                            0 => "R&#46; Barriales-Villa"
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                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:5 [
                        "tituloSerie" => "Rev Espa&#241;ola Cardiol &#40;English Ed&#41;"
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Short Communication
Impact of the creation of specialized units for patients with hypertrophic cardiomyopathy
Impacto da criação de uma unidade especializada no atendimento de doentes com miocardiopatia hipertrófica
Martín Negreira-Caamañoa,
Autor para correspondência
martin.negcam@gmail.com

Corresponding author.
, Jesús Piqueras-Floresb, Inmaculada Vivo-Ortegab, María Arántzazu-González-Marínc, Manuel Muñoz-Garcíaa, Alberto Jiménez-Lozanod
a Cardiology Department, University General Hospital of Ciudad Real, Spain
b Inherited Cardiac Diseases Unit, Cardiology Department, University General Hospital of Ciudad Real, Spain
c Department of Pediatrics, University General Hospital of Ciudad Real, Spain
d Castilla La-Mancha University, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Hypertrophic cardiomyopathy &#40;HCM&#41; is the most frequent cardiomyopathy and represents a major health burden&#44; causing heart failure and sudden death &#40;SD&#41; among young patients&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">1</span></a> In its management&#44; a variety of areas of cardiology work in partnership as the assessment of these patients is a complex process that should be developed into specialized units&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">2</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">The impact of these units is also complex and hard to measure&#46; Before our study&#44; there was no data that we are aware of on the impact of a specialized unit in the clinical assessment of patients with HCM&#46; We present our initial experience in the assessment of these patients in an Inherited Cardiac Diseases Unit &#40;ICDU&#41;&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">We analyzed 114 consecutive HCM patients diagnosed by imaging testing according to current guidelines&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">3</span></a> Fifty patients were assessed in a general cardiology consultation &#40;GCC&#41; and sixty-four in an ICDCU&#46; The main clinical courses of action related to HCM clinical assessment were analyzed&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">70&#46;2&#37; of patients were male and the mean age was 62&#46;6&#177;8 years&#46; Prevalence of cardiovascular risk factors was higher in the GCC group&#44; where more patients had hypertension &#40;85&#37; vs&#46; 39&#46;1&#37;&#59; p&#60;0&#46;01&#41; and dyslipidemia &#40;23&#46;9&#37; vs&#46; 19&#46;5&#37;&#59; p&#61;0&#46;03&#41;&#46; Atrial fibrillation was also more prevalent in the GCC group &#40;42&#46;9&#37; vs&#46; 21&#46;9&#37;&#59; p&#61;0&#46;017&#41;&#46; Family history of sudden cardiac death &#40;SCD&#41; was found in 28&#46;1&#37; of patients assessed in the ICDU and in 4&#37; of those assessed assessed in the GCCs &#40;p&#60;0&#46;01&#41;&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">The most frequent phenotype was septal hypertrophy &#40;70&#46;2&#37;&#41;&#44; followed by apical &#40;14&#46;9&#37;&#41;&#46; 38&#46;6&#37; of patients had left ventricle outflow tract obstruction&#44; which was similar in both groups &#40;p&#61;0&#46;51&#41;&#44; with a mean peak gradient of 52&#46;3&#177;28 mmHg in GCC and 67&#46;9&#177;42 mmHg in ICDU &#40;p&#61;0&#46;19&#41;&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall"><a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a> shows the main characteristic related to the clinical management of the patients&#46; In patients assessed in the IDCU&#44; family screening occurred more frequently&#44; as well as recording the family history and family tree&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0035" class="elsevierStylePara elsevierViewall">The main tests required for a complete assessment of HCM<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">2&#44;4</span></a> &#40;including cardiac magnetic resonance&#44; exercise test and genetic test&#41; were performed more frequently in patients assessed in the IDCU&#46; SCD risk assessment&#44; using the HCM risk-SCD Score was also performed more often in the IDCU&#46; Beta-blockers were administered in high numbers in both groups&#46; Implantable cardioverter defibrillators were indicated much more frequently by the IDCU&#44; although statistical significance was not reached&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">In spite of the limited conclusions that can be drawn from a single experience&#44; our results endorse the benefits of specialized units for the clinical assessment of HCM patients&#46; They fulfil all the care needs of patients and their families&#44; providing a comprehensive approach that is usually impossible at general consultations&#46; The differences observed could be derived from the higher grade of staff training and implementation of specific protocols for each specific disease&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Financial disclosures</span><p id="par0045" class="elsevierStylePara elsevierViewall">The authors have no financial disclosures&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Conflicts of interest</span><p id="par0050" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
    "textoCompletoSecciones" => array:1 [
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          "identificador" => "xres1483540"
          "titulo" => "Abstract"
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              "identificador" => "abst0005"
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    "pdfFichero" => "main.pdf"
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    "fechaRecibido" => "2020-07-08"
    "fechaAceptado" => "2020-08-07"
    "PalabrasClave" => array:2 [
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        0 => array:4 [
          "clase" => "keyword"
          "titulo" => "Keywords"
          "identificador" => "xpalclavsec1350707"
          "palabras" => array:4 [
            0 => "Sudden death"
            1 => "Hypertrophic cardiomyopathy"
            2 => "Heart failure"
            3 => "Cardiomyopathies"
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        0 => array:4 [
          "clase" => "keyword"
          "titulo" => "Palavras-chave"
          "identificador" => "xpalclavsec1350708"
          "palabras" => array:4 [
            0 => "Morte s&#250;bita"
            1 => "Miocardiopatia hipertr&#243;fica"
            2 => "Insufici&#234;ncia card&#237;aca"
            3 => "Miocardiopatias"
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    "resumen" => array:2 [
      "en" => array:3 [
        "titulo" => "Abstract"
        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Introduction and objectives</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">According to current international guidelines&#44; hypertrophic cardiomyopathy &#40;HCM&#41; patients should be managed in specialized units&#46; However&#44; there is lack of data on the impact of the creation of these units in the management of HCM patients&#46; Our goal was to assess the impact of the creation of an Inherited Inherited Diseases Cardiac Unit &#40;ICDU&#41; in the current management of patients with HCM&#46;</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Methods</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">We analyzed 114 consecutive patients &#40;62&#46;6&#177;8 years old&#44; 70&#46;2&#37; males&#41; with HCM&#46; Variables related to optimal management of HCM patients and their family study were recorded&#44; as well as guidance on the risk of sudden death&#46; We analyzed whether patients were assessed by the ICDU or at a general cardiology consultation &#40;GCC&#41;&#46;</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Results</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">50 patients were assessed in the IDCU and 64 in the GCC&#46; Familial screening was more frequent in patients assessed by the IDCU &#40;45&#46;3&#37; vs&#46; 4&#37;&#59; p&#60;0&#46;01&#41;&#44; requesting more genetic studies of the index case &#40;70&#46;3&#37; vs&#46; 14&#37;&#59; p&#60;0&#46;01&#41; and cardiac magnetic resonance &#40;53&#46;1&#37; vs&#46; 18&#37;&#59; p&#60;0&#46;01&#41;&#46; Sudden death risk score was performed more frequently in patients after the creation of an IDCU &#40;67&#46;2&#37; vs&#46; 28&#37;&#59; p&#60;0&#46;01&#41;&#46; Treatment with beta-blockers was similar in both groups &#40;72&#37; vs&#46; 78&#46;1&#37;&#59; p&#61;0&#46;24&#41;&#46; An implantable cardiac defibrillator was indicated similarly in both groups &#40;12&#46;5&#37; in ICDU and 6&#37; in GC&#59; p&#61;0&#46;24&#41;&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Conclusions</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">The implementation of an IDCU improved the quality of the medical care for HCM patients by performing a better study of the patients and their families&#46;</p></span>"
        "secciones" => array:4 [
          0 => array:2 [
            "identificador" => "abst0005"
            "titulo" => "Introduction and objectives"
          ]
          1 => array:2 [
            "identificador" => "abst0010"
            "titulo" => "Methods"
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          2 => array:2 [
            "identificador" => "abst0015"
            "titulo" => "Results"
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            "titulo" => "Conclusions"
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      "pt" => array:3 [
        "titulo" => "Resumo"
        "resumen" => "<span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Introdu&#231;&#227;o e objetivos</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">De acordo com as recomenda&#231;&#245;es internacionais atuais&#44; o tratamento de doentes com miocardiopatia hipertr&#243;fica &#40;MCH&#41; deve ser efetuado em unidades especializadas&#46; No entanto&#44; h&#225; escassez de dados sobre o impacto da cria&#231;&#227;o de uma unidade de doen&#231;as card&#237;acas heredit&#225;rias &#40;UDCH&#41; no tratamento dos doentes com MCH&#46;</p></span> <span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">M&#233;todos</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Analis&#225;mos 114 doentes consecutivos &#40;62&#44;6&#177;8 anos&#44; 70&#44;2&#37; homens&#41; com MCH&#46; Foram registadas as vari&#225;veis relacionadas com o tratamento aprimorado destes doentes e o respetivo estudo familiar&#44; assim como o aconselhamento sobre o risco de morte s&#250;bita&#46; Verific&#225;mos se os doentes foram avaliados em UDCH em consulta geral de cardiologia &#40;GC&#41;&#46;</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Resultados</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Foram avaliados respetivamente 50 e 64 doentes na UDCH e na CG&#46; O rastreio familiar foi mais frequente em doentes avaliados na UDCH &#40;45&#44;3&#37; <span class="elsevierStyleItalic">versus</span> 4&#37;&#44; p&#60;0&#44;01&#41; requerendo a UDCH mais estudos gen&#233;ticos no caso &#237;ndice &#40;70&#44;3&#37; <span class="elsevierStyleItalic">versus</span> 14&#37;&#44; p&#60;0&#44;01&#41; e mais resson&#226;ncia magn&#233;tica card&#237;aca &#40;53&#44;1&#37; <span class="elsevierStyleItalic">versus</span> 18&#37;&#44; p&#60;0&#44;01&#41;&#46; O <span class="elsevierStyleItalic">score</span> de risco de morte s&#250;bita foi realizado com mais frequ&#234;ncia em doentes ap&#243;s a cria&#231;&#227;o da UDCH &#40;67&#44;2&#37; <span class="elsevierStyleItalic">versus</span> 28&#37;&#44; p&#60;0&#44;001&#41;&#46; O tratamento com betabloqueantes foi semelhante em ambos os grupos &#40;72&#37; <span class="elsevierStyleItalic">versus</span> 78&#44;1&#37;&#44; p&#61;0&#44;24&#41;&#46; Foi indicado desfibrilhador card&#237;aco implant&#225;vel de forma semelhante em ambos os grupos &#40;12&#44;5&#37; na UDCH e 6&#37; na CG&#44; p&#61;0&#44;24&#41;&#46;</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conclus&#245;es</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">A implanta&#231;&#227;o de uma UDCH melhorou a qualidade do atendimento m&#233;dico aos doentes com MCH atrav&#233;s de um estudo mais completo dos doentes e das suas fam&#237;lias&#46;</p></span>"
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          "leyenda" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">HCM&#58; hypertrophic cardiomyopathy&#59; SCD&#58; sudden cardiac death&#46;</p>"
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">Genetic test performance&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">7 &#40;14&#37;&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">45 &#40;70&#46;3&#37;&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">Cardiac magnetic resonance&nbsp;\t\t\t\t\t\t\n
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Informação do artigo
ISSN: 08702551
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