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array:24 [ "pii" => "S1579212913001900" "issn" => "15792129" "doi" => "10.1016/j.arbr.2013.10.008" "estado" => "S300" "fechaPublicacion" => "2013-12-01" "aid" => "808" "copyright" => "SEPAR" "copyrightAnyo" => "2013" "documento" => "article" "crossmark" => 0 "subdocumento" => "fla" "cita" => "Arch Bronconeumol. 2013;49:534-47" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 9780 "formatos" => array:3 [ "EPUB" => 153 "HTML" => 7630 "PDF" => 1997 ] ] "Traduccion" => array:1 [ "es" => array:19 [ "pii" => "S0300289613002263" "issn" => "03002896" "doi" => "10.1016/j.arbres.2013.07.008" "estado" => "S300" "fechaPublicacion" => "2013-12-01" "aid" => "808" "copyright" => "SEPAR" "documento" => "article" "crossmark" => 0 "subdocumento" => "fla" "cita" => "Arch Bronconeumol. 2013;49:534-47" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 138621 "formatos" => array:3 [ "EPUB" => 171 "HTML" => 123289 "PDF" => 15161 ] ] "es" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Normativa SEPAR</span>" "titulo" => "Consenso nacional sobre el diagnóstico, estratificación de riesgo y tratamiento de los pacientes con tromboembolia pulmonar" "tienePdf" => "es" "tieneTextoCompleto" => "es" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "534" "paginaFinal" => "547" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "National Consensus on the Diagnosis, Risk Stratification and Treatment of Patients with Pulmonary Embolism" ] ] "contieneTextoCompleto" => array:1 [ "es" => true ] "contienePdf" => array:1 [ "es" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figura 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 2263 "Ancho" => 3137 "Tamanyo" => 361981 ] ] "descripcion" => array:1 [ "es" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Estratificación pronóstica y tratamiento de la tromboembolia pulmonar en fase aguda. BNP: péptido natriurético cerebral; DVD: disfunción ventricular derecha; Fx: fondaparinux; HBPM: heparina de bajo peso molecular; HFABP: proteína ligadora de ácidos grasos cardiacos; HNF: heparina no fraccionada; hsTnT: troponina T de alta sensibilidad; PESI: Pulmonary Embolism Severity Index; PESIs: PESI simplificada; TVP: trombosis venosa profunda; UCI: unidad de cuidados intensivos.*Shock cardiogénico o presión arterial sistólica<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>90<span class="elsevierStyleHsp" style=""></span>mm Hg mantenida, no debida a hipovolemia, sepsis o arritmias cardiacas.</p> <p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">La línea discontinua indica ausencia de evidencia definitiva (fibrinólisis) o de experiencia clínica amplia (rivaroxaban).</p> <p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Para aquellas situaciones no contempladas en el algoritmo, se recomienda hospitalización y tratamiento anticoagulante convencional.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Fernando Uresandi, Manuel Monreal, Ferrán García-Bragado, Pere Domenech, Ramón Lecumberri, Pilar Escribano, José Luis Zamorano, Sonia Jiménez, Pedro Ruiz-Artacho, Francisco Lozano, Antonio Romera, David Jiménez" "autores" => array:13 [ 0 => array:2 [ "nombre" => "Fernando" "apellidos" => "Uresandi" ] 1 => array:2 [ "nombre" => "Manuel" "apellidos" => "Monreal" ] 2 => array:2 [ "nombre" => "Ferrán" "apellidos" => "García-Bragado" ] 3 => array:2 [ "nombre" => "Pere" "apellidos" => "Domenech" ] 4 => array:2 [ "nombre" => "Ramón" "apellidos" => "Lecumberri" ] 5 => array:2 [ "nombre" => "Pilar" "apellidos" => "Escribano" ] 6 => array:2 [ "nombre" => "José Luis" "apellidos" => "Zamorano" ] 7 => array:2 [ "nombre" => "Sonia" "apellidos" => "Jiménez" ] 8 => array:2 [ "nombre" => "Pedro" "apellidos" => "Ruiz-Artacho" ] 9 => array:2 [ "nombre" => "Francisco" "apellidos" => "Lozano" ] 10 => array:2 [ "nombre" => "Antonio" "apellidos" => "Romera" ] 11 => array:2 [ "nombre" => "David" "apellidos" => "Jiménez" ] 12 => array:1 [ "colaborador" => "en representación del Consenso nacional sobre el diagnóstico, estratificación de riesgo y tratamiento de los pacientes con tromboembolia pulmonar" ] ] ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S1579212913001900" "doi" => "10.1016/j.arbr.2013.10.008" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1579212913001900?idApp=UINPBA00003Z" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0300289613002263?idApp=UINPBA00003Z" "url" => "/03002896/0000004900000012/v1_201312040037/S0300289613002263/v1_201312040037/es/main.assets" ] ] "itemSiguiente" => array:19 [ "pii" => "S1579212913001924" "issn" => "15792129" "doi" => "10.1016/j.arbr.2013.10.010" "estado" => "S300" "fechaPublicacion" => "2013-12-01" "aid" => "784" "copyright" => "SEPAR" "documento" => "simple-article" "crossmark" => 0 "subdocumento" => "crp" "cita" => "Arch Bronconeumol. 2013;49:548-50" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 4405 "formatos" => array:3 [ "EPUB" => 120 "HTML" => 3201 "PDF" => 1084 ] ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Case report</span>" "titulo" => "Alpha-1-Antitrypsin Deficiency Associated With the Mattawa Variant" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "548" "paginaFinal" => "550" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Déficit de alfa-1-antitripsina asociado a la variante Matawa" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1104 "Ancho" => 2599 "Tamanyo" => 274980 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Sequence corresponding to exon 5 SERPINA1. (A) Normal sequence. (B) Sequence corresponding to the patient, which shows insertion of a thymine (T) instead of an adenine (A) at codon 376 in exon 5 of heterozygosity for the PI-Mattawa allele. The SERPINA1 gene coding sequence (exons 2–5) was analyzed using previously described primers for exons 3–5 and 5′ACGTGGTGTCAATCCCTGATCACTG3′ Ex2F primers and ex2R 5′TATGGGAACAGCTGG3′ for exon 2, with reference to the comparative SERPINA1_Transcript_ENST00000440909.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Beatriz Lara, Beatriz Martínez-Delgado, Maria Luisa Torres, Sandra Marín-Arguedas, Ana Bustamante, Marc Miravitlles" "autores" => array:6 [ 0 => array:2 [ "nombre" => "Beatriz" "apellidos" => "Lara" ] 1 => array:2 [ "nombre" => "Beatriz" "apellidos" => "Martínez-Delgado" ] 2 => array:2 [ "nombre" => "Maria Luisa" "apellidos" => "Torres" ] 3 => array:2 [ "nombre" => "Sandra" "apellidos" => "Marín-Arguedas" ] 4 => array:2 [ "nombre" => "Ana" "apellidos" => "Bustamante" ] 5 => array:2 [ "nombre" => "Marc" "apellidos" => "Miravitlles" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "es" => array:9 [ "pii" => "S030028961300152X" "doi" => "10.1016/j.arbres.2013.05.004" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S030028961300152X?idApp=UINPBA00003Z" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1579212913001924?idApp=UINPBA00003Z" "url" => "/15792129/0000004900000012/v1_201312010030/S1579212913001924/v1_201312010030/en/main.assets" ] "itemAnterior" => array:19 [ "pii" => "S1579212913001742" "issn" => "15792129" "doi" => "10.1016/j.arbr.2013.09.011" "estado" => "S300" "fechaPublicacion" => "2013-12-01" "aid" => "751" "copyright" => "SEPAR" "documento" => "article" "crossmark" => 0 "subdocumento" => "fla" "cita" => "Arch Bronconeumol. 2013;49:529-33" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ 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"djc_69_98@yahoo.com" ] "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">l</span>" "identificador" => "aff0060" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">¿</span>" "identificador" => "cor0005" ] ] ] 12 => array:2 [ "colaborador" => "on behalf of the National Consensus on Diagnosis, Risk Stratification and Treatment of Patients With Pulmonary Thromboembolism" "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">1</span>" "identificador" => "fn1" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">2</span>" "identificador" => "fn2" ] ] ] ] "afiliaciones" => array:12 [ 0 => array:3 [ "entidad" => "Servicio de Neumología, Hospital de Cruces, Bilbao, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Servicio de Medicina Interna, Hospital Germans Trias I Pujol, Badalona, Spain" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Servicio de Medicina Interna, Hospital Universitario de Gerona Dr. Josep Trueta, Gerona, Spain" "etiqueta" => "c" "identificador" => "aff0015" ] 3 => array:3 [ "entidad" => "Servicio de Hematología, Hospital Universitario de Bellvitge, Barcelona, Spain" "etiqueta" => "d" "identificador" => "aff0020" ] 4 => array:3 [ "entidad" => "Servicio de Hematología, Clínica Universitaria de Navarra, Pamplona, Spain" "etiqueta" => "e" "identificador" => "aff0025" ] 5 => array:3 [ "entidad" => "Servicio de Cardiología, Hospital Doce de Octubre, Madrid, Spain" "etiqueta" => "f" "identificador" => "aff0030" ] 6 => array:3 [ "entidad" => "Servicio de Cardiología, Hospital Ramón y Cajal, IRYCIS, Madrid, Spain" "etiqueta" => "g" "identificador" => "aff0035" ] 7 => array:3 [ "entidad" => "Servicio de Urgencias, Hospital Clinic, Barcelona, Spain" "etiqueta" => "h" "identificador" => "aff0040" ] 8 => array:3 [ "entidad" => "Servicio de Urgencias, Hospital Clínico San Carlos, Madrid, Spain" "etiqueta" => "i" "identificador" => "aff0045" ] 9 => array:3 [ "entidad" => "Servicio de Angiología y Cirugía Vascular, Hospital Universitario de Bellvitge, Barcelona, Spain" "etiqueta" => "j" "identificador" => "aff0050" ] 10 => array:3 [ "entidad" => "Servicio de Angiología y Cirugía Vascular, Hospital Clínico Universitario, Salamanca, Spain" "etiqueta" => "k" "identificador" => "aff0055" ] 11 => array:3 [ "entidad" => "Servicio de Neumología, Hospital Ramón y Cajal, IRYCIS, Madrid, Spain" "etiqueta" => "l" "identificador" => "aff0060" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Consenso nacional sobre el diagnóstico, estratificación de riesgo y tratamiento de los pacientes con tromboembolia pulmonar" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 4041 "Ancho" => 2253 "Tamanyo" => 312359 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Diagnostic algorithm for the hemodynamically stable outpatient. (A) Angio-CT, computed tomography angiography. <span class="elsevierStyleSup">1</span>Refers to high sensitivity D-dimer. In the case of less sensitive D-dimer, PE can only be ruled out in patients with low clinical probability or PE unlikely. <span class="elsevierStyleSup">2</span>In case of high clinical probability and negative multidetector angio-CT, additional diagnostic tests are suggested (V/Q scan and/or Doppler ultrasound of lower extremities). (B) DVT, deep vein thrombosis. <span class="elsevierStyleSup">1</span>Refers to low or intermediate probability V/Q scans. <span class="elsevierStyleSup">2</span>In case of high clinical probability, inconclusive perfusion scan, and negative ultrasound of lower extremities, the need for multidetector angio-CT should be assessed with the appropriate specialist.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Pulmonary embolism (PE) is a public health problem of the first order. Although less common than other vascular diseases, such as myocardial infarction or cerebrovascular disease, PE is equally as serious. The Spanish Medical Societies involved in the care of these patients have drawn up a consensus document that aims to update the recommendations for the diagnosis, prognosis and treatment of this disease using the best available evidence. This consensus document makes <span class="elsevierStyleItalic">recommendations</span> or <span class="elsevierStyleItalic">suggestions</span> based on the interpretation of the available evidence and its quality, risk-benefit balance of the interventions, and the cost. This was based on two documents: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed.: American College of Chest Physicians (ACCP). Evidence-Based Clinical Practice Guidelines<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> and the National Institute for Health and Clinical Excellence (NICE) clinical guidelines on venous thromboembolic (VTE) diseases.<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Both documents use the GRADE system<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> to establish recommendations. A systematic review of the literature published between January 2012 and March 2013 was also performed. Based on these documents and the systematic literature review, two authors (FU and DJ) prepared a manuscript that formed the basis for the final discussion (in a face-to-face meeting) by a panel composed of the coordinators of each of the participating Scientific Societies. All the recommendations or suggestions were agreed between the attendees at this session. Consensus was reached by discussion between the panel members, considering the potential risks and benefits of the interventions, routine clinical practice, recommendations of other guidelines, patient preference, and equity criteria. The authors of the document also took into account clinical situations in which a lack of evidence justifies waiting until research results become available in the future.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Concept, Pathogenesis, Risk Factors and Epidemiology</span><p id="par0010" class="elsevierStylePara elsevierViewall">PE occurs when a detached thrombus (embolism) from any part of the venous territory becomes lodged in the pulmonary arteries. Although the origin of the embolism may be venous thrombosis in any location (upper extremities, prostatic, uterine and renal veins and right heart chambers), in most cases (90%–95%) it is a lower extremity (LE) deep vein thrombosis (DVT), often asymptomatic.</p><p id="par0015" class="elsevierStylePara elsevierViewall">The risk factors (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>) for developing PE are related with one or several of the etiopathogenic mechanisms of the disease: stasis, endothelial lesion and hypercoagulability. These guidelines classify them as major or minor, depending on whether their prothrombotic risk is high or moderate-low, respectively. When the VTE is associated with precipitating risk factors, it is classified as <span class="elsevierStyleItalic">provoked</span> or <span class="elsevierStyleItalic">secondary</span>. When there are no precipitating factors, it is known as <span class="elsevierStyleItalic">unprovoked</span>, <span class="elsevierStyleItalic">spontaneous</span> or <span class="elsevierStyleItalic">idiopathic</span>.</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">There is an estimated incidence of PE of 1 case per 1000 population per year, although the real incidence is likely to be higher. According to data from the Spanish Ministry for Health, 22 250 cases of PE were diagnosed in 2010, with an in-hospital mortality of 8.9%.</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Diagnosis</span><p id="par0025" class="elsevierStylePara elsevierViewall">No single test is sensitive and specific enough to confirm or rule out acute symptomatic PE. The diagnosis of the disease must therefore be combined with clinical suspicion, D-dimer results and imaging tests. Following widely accepted diagnostic algorithms improves the prognosis in patients assessed for suspected PE.<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> A diagnostic algorithm has been proposed for hemodynamically stable patients with suspected PE (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>A and B) and another for unstable patients (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>).</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">The diagnostic process does not justify delays in initiating anticoagulant treatment, which should be administered early in patients with intermediate or high clinical suspicion.<ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">•</span><p id="par0035" class="elsevierStylePara elsevierViewall">It is recommended to start anticoagulant treatment early (before the results of diagnostic tests become available) in patients with an intermediate or high probability of PE.</p></li></ul></p><span id="sec0225" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Clinical Suspicion</span><p id="par0040" class="elsevierStylePara elsevierViewall">The diagnosis of acute symptomatic PE should be considered in all patients who report new onset dyspnea, worsening of their usual dyspnea, chest pain, syncope or hypotension with no alternative explanation, particularly when the basic complementary tests (chest X-ray, electrocardiogram and arterial blood gases) rule out other differential diagnoses. <a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a> lists some of the usual radiological and electrocardiographic findings in PE. Standardized testing using clinical prediction rules classifies patients into categories with different PE prevalence (approximately 10% for low probability, 25% for intermediate probability and >60% for high probability) and facilitates the interpretation of other diagnostic tests. The Wells and Geneva scores (<a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a>) have been the most extensively validated.<ul class="elsevierStyleList" id="lis0010"><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0045" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">The use of adequately validated clinical scales (Wells or Geneva) is recommended as a first step in the diagnostic approach to the hemodynamically stable patient with suspected PE.</span></p></li></ul></p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><elsevierMultimedia ident="tbl0015"></elsevierMultimedia></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">D-Dimer</span><p id="par0050" class="elsevierStylePara elsevierViewall">D-dimer is a fibrin degradation product present in the thrombus, generated when the clot undergoes proteolysis by plasmin. It is a highly sensitive test, but has low specificity, because the finding of high levels may also be associated with other clinical situations such as advanced age, infection, cancer, pregnancy or hospital admission.</p><p id="par0055" class="elsevierStylePara elsevierViewall">In normotensive patients with a low or intermediate probability of PE, a negative high sensitivity (≥95%) D-dimer (<500<span class="elsevierStyleHsp" style=""></span>ng/ml) excludes the diagnosis of PE. In patients who do not receive anticoagulant therapy, the incidence of VTE in the following 3 months is 0.14% (95% confidence interval [CI], 0.05–0.41).<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> Low or moderate sensitivity methods for determination of D-dimer (<95%) (<a class="elsevierStyleCrossRef" href="#tbl0020">Table 4</a>) only exclude the disease in the group of patients with low clinical probability (or with PE unlikely according to the dichotomized Wells score).<ul class="elsevierStyleList" id="lis0015"><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0060" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">It is recommended that the sensitivity of the D-dimer method used in each setting is known.</span></p></li><li class="elsevierStyleListItem" id="lsti0020"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0065" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">A negative high sensitivity D-dimer excludes PE in patients with low or intermediate clinical probability.</span></p></li><li class="elsevierStyleListItem" id="lsti0025"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0070" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">A negative moderate or low sensitivity D-dimer excludes PE in patients with low clinical probability (or PE unlikely).</span></p></li><li class="elsevierStyleListItem" id="lsti0030"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0075" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">It is recommended not to measure D-dimer in patients with a high probability of PE.</span></p></li></ul></p><elsevierMultimedia ident="tbl0020"></elsevierMultimedia></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Imaging Tests</span><p id="par0080" class="elsevierStylePara elsevierViewall">The most commonly used imaging tests are multidetector chest computed tomography angiography (angio-CT), ventilation/perfusion (V/Q) lung scan and venous ultrasound of the LE, with or without Doppler (DU).</p><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Multidetector Computed Tomography Angiography</span><p id="par0085" class="elsevierStylePara elsevierViewall">Multidetector angio-CT is currently the imaging test of choice for the diagnosis of PE. In a systematic review and meta-analysis<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> that included 2020 patients from 3 studies, the thromboembolic risk in patients who did not receive anticoagulant treatment based on a negative angio-CT was 1.2% (95% CI, 0.8–1.8), with a risk of fatal PE of 0.6%.</p><p id="par0090" class="elsevierStylePara elsevierViewall">PIOPED II<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> was a multicenter study that evaluated the diagnostic usefulness of 4, 8 or 16 detector angio-CT in patients with suspected PE. The overall sensitivity was 83% (95% CI, 76–92) and the specificity was 96% (95% CI, 93–97). In this study, the negative predictive value (NPV) of multidetector angio-CT increased marginally when venography was added in the same examination. It should be noted that the NPV of multidetector angio-CT was only 60% in patients with a high clinical probability of PE.</p><p id="par0095" class="elsevierStylePara elsevierViewall">Multidetector angio-CT provides an effective dose of radiation of 7<span class="elsevierStyleHsp" style=""></span>milliSievert, equivalent to 2 years of natural background radiation, which translates into a low additional lifetime risk of fatal cancer.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> Existing equipment enables the test to be performed with a reduced radiation dose. Nevertheless, the indication in fertile women must be justified in terms of the risk-benefit balance. In pregnant women, it is advisable to perform a perfusion scan before multidetector angio-CT, due to the lower radiation, provided that the chest X-ray is normal.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> If multidetector angio-CT is done, breast protection is recommended. It is not known if it has any effect on breast milk during breastfeeding. In patients with renal failure, angio-CT may be performed following local protocols for prevention of contrast-induced nephropathy.<ul class="elsevierStyleList" id="lis0020"><li class="elsevierStyleListItem" id="lsti0035"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0100" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">A negative multidetector angio-CT (technically adequate) rules out PE, except in patients with a high clinical probability of the disease.</span></p></li><li class="elsevierStyleListItem" id="lsti0040"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0105" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">It is recommended that additional diagnostic tests be carried out in patients with suspected PE and inconclusive multidetector angio-CT.</span></p></li><li class="elsevierStyleListItem" id="lsti0045"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0110" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">It is suggested that additional diagnostic tests be carried out in patients with a high suspicion of PE and negative multidetector angio-CT.</span></p></li><li class="elsevierStyleListItem" id="lsti0050"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0115" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">It is recommended not to perform CT venography routinely to increase the diagnostic yield of multidetector angio-CT.</span></p></li></ul></p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Lung Scintigraphy</span><p id="par0120" class="elsevierStylePara elsevierViewall">The V/Q scan has been replaced by multidetector angio-CT as the diagnostic test of choice. At present, it is generally reserved for patients with iodinated contrast allergy, some cases with renal failure or for pregnant women with suspected PE in which the DU of the LE was negative, providing that the chest x-ray was normal.</p><p id="par0125" class="elsevierStylePara elsevierViewall">In the PIOPED I study,<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> the NPV of a normal scan was 97% and the positive predictive value (PPV) of a high-probability scan was 85%–90%. However, the scan was diagnostic (normal or high probability) in only 30%–50% of patients. In the remaining patients, the V/Q scan was inconclusive (low, intermediate or indeterminate probability).<ul class="elsevierStyleList" id="lis0025"><li class="elsevierStyleListItem" id="lsti0055"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0130" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">A normal V/Q scan rules out clinically significant PE.</span></p></li><li class="elsevierStyleListItem" id="lsti0060"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0135" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">A high-probability V/Q scan confirms PE in patients with an intermediate or high probability of the disease.</span></p></li><li class="elsevierStyleListItem" id="lsti0065"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0140" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">It is recommended that additional diagnostic tests be carried out in patients with suspected PE and inconclusive V/Q scan.</span></p></li></ul></p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Lower Extremity Venous Ultrasound</span><p id="par0145" class="elsevierStylePara elsevierViewall">DU is the method of choice for the detection of concomitant DVT in patients with PE. The main diagnostic criterion is lack of compressibility of the venous lumen. It is particularly sensitive and specific in patients with DVT symptoms and in the femoropopliteal territory, but its yield decreases when the DVT is asymptomatic or located in the sural territory. Approximately 50% of patients with acute symptomatic PE have concomitant DVT at the time of diagnosis, only half of whom are symptomatic. It is presently reserved for use in patients with discrepancy between the clinical probability and the result of the thoracic imaging tests, for patients with inconclusive thoracic tests, and for pregnant patients as a first examination in the diagnostic algorithm.<ul class="elsevierStyleList" id="lis0030"><li class="elsevierStyleListItem" id="lsti0070"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0150" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">DU is recommended as a first examination in pregnant patients with suspected PE.</span></p></li></ul></p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Pulmonary Magnetic Resonance Angiography</span><p id="par0155" class="elsevierStylePara elsevierViewall">A priori, this test does not differ from multidetector angio-CT in obtaining images of the pulmonary arterial tree. It has the advantage that it uses gadolinium (which does not contain iodine) as a contrast and does not radiate patients. In the PIOPED III study, its sensitivity was 78% and specificity was 99%.<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">11</span></a> On extending the study with magnetic resonance venography, the sensitivity increased to 92% with a specificity of 96%. The examination was technically inadequate in 25% of patients, which is its major limitation. It may be reserved for patients with iodinated contrast allergy. In the case of severe renal failure (creatinine clearance <30<span class="elsevierStyleHsp" style=""></span>ml/min), it is contraindicated due to the toxicity of gadolinium. It should be avoided in pregnancy and breastfeeding, although there is no clear evidence of teratogenic effects.<ul class="elsevierStyleList" id="lis0035"><li class="elsevierStyleListItem" id="lsti0075"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0160" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">It is recommended not to perform pulmonary magnetic resonance angiography routinely for the diagnosis of patients with suspected PE.</span></p></li></ul></p></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Transthoracic Echocardiography</span><p id="par0165" class="elsevierStylePara elsevierViewall">In general, transthoracic echocardiography is not useful in the diagnostic algorithm of patients with suspected PE. Although multidetector angio-CT is also the diagnostic test of choice in hemodynamically unstable patients with suspected PE, bedside echocardiography may provide very valuable diagnostic information in centers in which multidetector angio-CT is not available, or in cases in which the patient's instability prevents their transfer to the radiology department. In critically ill patients, the absence of echocardiography signs of right-sided heart dysfunction or overload rules out PE as a cause of hemodynamic compromise.<ul class="elsevierStyleList" id="lis0040"><li class="elsevierStyleListItem" id="lsti0080"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0170" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">It is recommended not to perform transthoracic echocardiography routinely for the diagnosis of stable patients with suspected PE.</span></p></li></ul></p></span></span></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Prognostic Stratification of Patients With Pulmonary Embolism</span><p id="par0175" class="elsevierStylePara elsevierViewall">PE is a disease with a wide spectrum of clinical manifestations, with different prognoses and treatment. The most important prognostic factor is the patient's hemodynamic status at the time of diagnosis.<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">12</span></a><span class="elsevierStyleItalic">High-risk</span> PE (previously known as massive PE), which is characterized by hypotension or shock, accounts for around 5% of cases and is associated with early mortality in at least 15%. Thrombolytic treatment is usually recommended for these patients.</p><p id="par0180" class="elsevierStylePara elsevierViewall">However, most patients with PE present with few symptoms. Early mortality in hemodynamically stable patients diagnosed with PE varies between 2% and 10%. Risk stratification of normotensive patients with PE should be used to identify a subgroup of patients with a <span class="elsevierStyleItalic">low risk</span> of all-cause mortality, who may benefit from early discharge or even outpatient treatment of their disease, and a subgroup of patients with a higher risk of complications associated with the PE itself (<span class="elsevierStyleItalic">intermediate-risk</span> PE, previously sub-massive PE), who may benefit from aggressive treatments for their disease (intensive monitoring, fibrinolysis).<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a></p><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Prognostic Factors</span><p id="par0185" class="elsevierStylePara elsevierViewall">The most commonly used prognostic factors in normotensive patients with PE are summarized in <a class="elsevierStyleCrossRef" href="#tbl0025">Table 5</a>. In general, these tools assess the patient's clinical condition and general health status, right ventricular dysfunction, the thrombotic burden and myocardial damage.</p><elsevierMultimedia ident="tbl0025"></elsevierMultimedia></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Identification of Patients With Low-Risk Pulmonary Embolism</span><p id="par0190" class="elsevierStylePara elsevierViewall">The most useful tools for classifying low risk patients with acute symptomatic PE are the prognostic clinical scores. The combination of a set of variables that takes into account the age, comorbidity and cardiovascular repercussion of PE reliably identifies a subgroup of patients (approximately 30%) with a less than 2% risk of early mortality. The Pulmonary Embolism Severity Index (PESI) and simplified PESI (sPESI) clinical scores (<a class="elsevierStyleCrossRef" href="#tbl0030">Table 6</a>) have been extensively validated as excellent tools for the identification of these low risk patients.<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">14,15</span></a> The sPESI score is easier to use than the original, while retaining its prognostic ability.</p><elsevierMultimedia ident="tbl0030"></elsevierMultimedia><p id="par0195" class="elsevierStylePara elsevierViewall">The value of combining the clinical scores and some biochemical markers (particularly brain natriuretic peptide [BNP] or high sensitivity troponin [hsTnT]) or imaging tests (transthoracic echocardiogram or DU) for the identification of this group of low risk patients has not been completely clarified.<ul class="elsevierStyleList" id="lis0045"><li class="elsevierStyleListItem" id="lsti0085"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0200" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">It is recommended to use well validated prognostic clinical scores (PESI or simplified PESI) as a first step for the identification of patients with low-risk PE.</span></p></li></ul></p></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Identification of Patients With Intermediate-Risk Pulmonary Embolism</span><p id="par0205" class="elsevierStylePara elsevierViewall">The most widely used method in clinical practice for evaluating right ventricular function is transthoracic echocardiography. Various quantitative parameters (right ventricular end-diastolic diameter in the parasternal long axis view, ventricular end-diastolic diameter ratio in the apical 4C projection, tricuspid regurgitation peak velocity, diameter of the inferior vena cava, pulmonary artery acceleration time or TAPSE [Tricuspid Annular Plane Systolic Excursion]) have been used to estimate the degree of ventricular dysfunction. Its use for the identification of patients with intermediate-risk PE is limited by its operator-dependence, cost and lack of continuous availability in many centers. Furthermore, there is no echocardiographic pattern of right ventricular dysfunction that is sufficiently reliable as to justify, on its own, the use of fibrinolytic treatment.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a></p><p id="par0210" class="elsevierStylePara elsevierViewall">The images generated by angio-CT not only enable the diagnosis of PE to be confirmed or discarded, but they can also assess the extension of the arterial obstruction and the presence or not of right ventricular dilatation.<a class="elsevierStyleCrossRefs" href="#bib0085"><span class="elsevierStyleSup">17,18</span></a> Although ventricular size volumetric reconstruction studies may offer a more accurate prognostic assessment, more recent studies use the ratio between the ventricular diameters as a parameter of ventricular dysfunction (with different cut-off points). Its isolated use for identifying patients with intermediate-risk PE who could benefit from fibrinolytic treatment is not recommended.</p><p id="par0215" class="elsevierStylePara elsevierViewall">Various meta-analyses have demonstrated the prognostic value of myocardial ischemia (identified by elevated troponin I or T levels) in hemodynamically stable patients with PE, although the power of the association is not sufficiently robust as to justify therapeutic escalation.<a class="elsevierStyleCrossRefs" href="#bib0095"><span class="elsevierStyleSup">19,20</span></a> Cardiomyocyte stress causes release of natriuretic peptides into the circulation (BNP and NT-pro-BNP).<a class="elsevierStyleCrossRefs" href="#bib0105"><span class="elsevierStyleSup">21,22</span></a> Several studies and meta-analyses suggest that they are useful for identifying patients with intermediate-risk PE. However, the sensitivity of these cardiac biomarkers for death due to PE is insufficient to establish the indication for thrombolytic treatment.</p><p id="par0220" class="elsevierStylePara elsevierViewall">An association has been shown between the persistence of thrombotic material in the lower extremity deep vein system and short- and mid-term mortality of patients with PE.<a class="elsevierStyleCrossRef" href="#bib0115"><span class="elsevierStyleSup">23</span></a> The presence of concomitant DVT, together with other imaging tests and cardiac biomarkers, may serve to identify a patient profile with a particularly high risk of complications associated with the PE itself.<ul class="elsevierStyleList" id="lis0050"><li class="elsevierStyleListItem" id="lsti0090"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0225" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">A combination of prognostic tests (which identify right ventricular dysfunction, myocardial ischemia, cardiomyocyte stress or thrombotic burden) is suggested for identifying patients with intermediate risk PE.</span></p></li></ul></p></span></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Treatment of Pulmonary Embolism in the Initial Phase (Acute Phase And up to 3–6 Months)</span><p id="par0230" class="elsevierStylePara elsevierViewall">The initial treatment of PE is aimed at medical stabilization of the patient and symptom relief, resolution of the vascular obstruction and prevention of recurrence. The priority in achieving these objectives depends on the severity of the patient. On most occasions, all the objectives are reached with conventional anticoagulant treatment, which prevents progression of the clot while the endogenous fibrinolytic system resolves the vascular obstruction and collateral circulation develops. A minority of patients, usually those with hemodynamic instability (high-risk PE) or contraindication for anticoagulation, require other pharmacological treatments (thrombolytics) or mechanical measures (vena caval filters) to accelerate lysis of the clot or prevent its embolization to the lungs<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>). <a class="elsevierStyleCrossRef" href="#tbl0035">Table 7</a> lists the administration guidelines for drugs approved for treatment of the acute phase of PE.</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><elsevierMultimedia ident="tbl0035"></elsevierMultimedia><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Anticoagulation With Unfractionated Heparin, Low Molecular Weight Heparins or Fondaparinux</span><p id="par0235" class="elsevierStylePara elsevierViewall">For decades, unfractionated heparin (UFH) has been the drug of choice for the treatment of PE. It exerts its anticoagulant action by binding to antithrombin and potentiating its effect in the inactivation of a series of activated coagulation factors, mainly thrombin (IIa). It is usually administered intravenously (iv) as a continuous infusion, but it is also safe and effective using the subcutaneous route (sc). It requires monitoring using the activated partial thromboplastin time (APTT), which should be 1.5–2.5 times the control value, so an initial infusion rate of 18<span class="elsevierStyleHsp" style=""></span>U/kg/h is used. As well as continuous infusion, an 80<span class="elsevierStyleHsp" style=""></span>U/kg bolus is usually administered to achieve a more rapid anticoagulant effect. Patients who are treated with lower doses and who do not reach a therapeutic APTT in the first few days of treatment have an increased risk of recurrent VTE. It is not known if there is a relationship between sub-therapeutic APTT levels and recurrence in patients who are treated initially with the recommended doses. UFH is currently reserved for patients in whom the use of fibrinolytic treatment is considered (intermediate- or high-risk PE), and for patients at a high risk of bleeding who are to receive anticoagulant therapy. For patients with severe renal failure (creatinine clearance <30<span class="elsevierStyleHsp" style=""></span>ml/min), some indirect evidence suggests that low molecular weight heparins (LMWH) (at the doses recommended in the Summary of Product Characteristics) could be safer and more effective than UFH.<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">24</span></a></p><p id="par0240" class="elsevierStylePara elsevierViewall">LMWH are prepared from the fractionation of UFH by chemical or enzymatic methods. They have potent antiXa action (greater than that of UFH). Most studies suggest that LMWH and UFH are equivalent in terms of efficacy (recurrent VTE) and safety (major bleeding) for treatment of the acute phase of VTE. In a meta-analysis that included 1951 patients from 12 studies comparing LMWH with UFH, LMWH were associated with fewer recurrent VTE (odds ratio [OR] 0.63; 95% CI, 0.33–1.18) and fewer major bleeding events (OR 0.67; 95% CI, 0.36–1.27), with no differences in mortality (OR 1.20; 95% CI, 0.59–2.45).<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a></p><p id="par0245" class="elsevierStylePara elsevierViewall">Fondaparinux is a synthetic pentasaccharide that selectively inhibits factor Xa without inactivating thrombin. It is administered subcutaneously once daily at weight-adjusted doses and does not require monitoring. The Matisse investigators evaluated its efficacy and safety in the treatment of acute DVT and PE.<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a> Compared with UFH, they did not observe any differences in the rate of recurrent thromboembolic events (1.3% vs 1.7% in the acute phase), major bleeds (1.3% vs 1.1%) or mortality in the first 3 months of follow-up. A potential advantage of this drug is that it is not associated with heparin-induced thrombocytopenia (HIT).<ul class="elsevierStyleList" id="lis0055"><li class="elsevierStyleListItem" id="lsti0095"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0250" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">The use of LMWH or fondaparinux instead of UFH is suggested in hemodynamically stable patients with acute PE.</span></p></li><li class="elsevierStyleListItem" id="lsti0100"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0255" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">The use of LMWH at doses adjusted to the UFH is suggested in patients with acute PE and severe renal failure.</span></p></li></ul></p></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Beginning Oral Anticoagulation</span><p id="par0260" class="elsevierStylePara elsevierViewall">Studies demonstrating that heparin treatment for 5 days instead of 10 is a safe, effective practice also showed that oral anticoagulants could be started on the first day of anticoagulation, without losing efficacy. Two clinical trials with warfarin have shown that: (1) loading doses (which may cause hemorrhages) should be avoided without this incurring a delay in reaching therapeutic INR levels; (2) commencing vitamin K antagonists (VKA) at lower doses avoids excessive falls in protein C levels, which would theoretically induce a state of hypercoagulability.<ul class="elsevierStyleList" id="lis0060"><li class="elsevierStyleListItem" id="lsti0105"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0265" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In hemodynamically stable patients with PE, it is recommended that parenteral anticoagulation be maintained for at least 5 days, and until the INR is >2.0 for 24<span class="elsevierStyleHsp" style=""></span>h.</span></p></li></ul></p></span><span id="sec0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">New Oral Anticoagulants</span><p id="par0270" class="elsevierStylePara elsevierViewall">New oral anticoagulants have recently been introduced that act differently to the VKA, among which are dabigatran (direct thrombin inhibitor), rivaroxaban and apixaban (factor Xa inhibitors). Rivaroxaban is a direct selective factor Xa inhibitor. In the joint analysis of two clinical trials (for DVT and PE), rivaroxaban was associated with an efficacy similar to that of standard treatment (hazard ratio [HR] 0.87; 95% CI, 0.66–1.19) while major bleeding was reduced to half (HR 0.54, 95% CI, 0.37–0.79).<a class="elsevierStyleCrossRefs" href="#bib0135"><span class="elsevierStyleSup">27,28</span></a> Its oral administration, at a dose of 15<span class="elsevierStyleHsp" style=""></span>mg twice daily for 3 weeks followed by 20<span class="elsevierStyleHsp" style=""></span>mg once daily, could provide a simple, single-drug approach to the acute and long-term treatment of PE.</p><p id="par0275" class="elsevierStylePara elsevierViewall">Apixaban has been evaluated in a clinical trial for the treatment of patients with DVT or PE (34%) for the first 6 months after a thrombotic event.<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">29</span></a> Compared with standard treatment, apixaban showed similar efficacy (relative risk [RR] 0.84; 95% CI, 0.60–1.18) and a statistically significant reduction in major bleeding (RR 0.31; IC 95%, 0.17–0.55) and clinically relevant non-major bleeding (RR 0.48; 95% CI, 0.38–0.60). It was administered orally, at a dose of 10<span class="elsevierStyleHsp" style=""></span>mg twice daily for the first 7 days followed by 5<span class="elsevierStyleHsp" style=""></span>mg twice daily.</p><p id="par0280" class="elsevierStylePara elsevierViewall">The efficacy and safety of dabigatran has not been evaluated during the first 10 days (on average) of treatment of acute symptomatic PE.<ul class="elsevierStyleList" id="lis0065"><li class="elsevierStyleListItem" id="lsti0110"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0285" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Treatment with rivaroxaban as monotherapy is suggested in hemodynamically stable patients with PE.</span></p></li></ul></p></span><span id="sec0100" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Early vs Standard Discharge in Pulmonary Embolism Patients</span><p id="par0290" class="elsevierStylePara elsevierViewall">The results of a clinical trial and some cohort studies suggest that, compared with hospitalization, outpatient treatment in low risk patients is equally effective and safe in terms of recurrent VTE, bleeding events and mortality.<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">30</span></a> Outpatient treatment can be considered in patients with PE who meet the following requirements: (1) clinically stable with good cardiopulmonary reserve, and a low risk validated clinical score (e.g. PESI or sPESI), (2) good social support with rapid access to medical care and (3) expected treatment compliance.<ul class="elsevierStyleList" id="lis0070"><li class="elsevierStyleListItem" id="lsti0115"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0295" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In patients with low-risk PE and adequate home conditions, early discharge is suggested instead of standard discharge (more than 5 days admission).</span></p></li></ul></p></span><span id="sec0105" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Early Mobilization vs Rest in Acute Pulmonary Embolism</span><p id="par0300" class="elsevierStylePara elsevierViewall">Several meta-analyses have shown that early mobilization is a safe practice in patients with proximal DVT.<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">31</span></a> The evidence is less consistent for patients with symptomatic PE. The presence of concomitant DVT worsens the prognosis in patients with PE, particularly when associated with right ventricular dysfunction and myocardial ischemia.<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">32</span></a><ul class="elsevierStyleList" id="lis0075"><li class="elsevierStyleListItem" id="lsti0120"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0305" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Early mobilization is suggested in patients with low-risk PE.</span></p></li><li class="elsevierStyleListItem" id="lsti0125"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0310" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Rest is suggested for the first few days of treatment in patients with intermediate-risk PE.</span></p></li></ul></p></span><span id="sec0110" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Fibrinolytic Treatment</span><p id="par0315" class="elsevierStylePara elsevierViewall">Thrombolytic treatment accelerates clot lysis and hemodynamic improvement occurs more rapidly than with UFH treatment, although there are no differences in the residual thrombosis after 5–7 days. Analysis of a subgroup of patients in the Urokinase Pulmonary Embolism Trial (UPET), which compared urokinase followed by UFH or UFH alone, showed that fibrinolytic treatment reduces mortality in patients with shock secondary to massive PE.<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a> Based on these findings, and in the absence of a high risk of bleeding, thrombolytic treatment is indicated in patients with acute symptomatic PE and hemodynamic instability (defined as cardiogenic shock or sustained systolic blood pressure <90<span class="elsevierStyleHsp" style=""></span>mmHg, not due to hypovolemia, sepsis or cardiac arrhythmias).<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">34</span></a> Hemodynamic instability is rare, but up to half of patients with PE without hemodynamic instability have clinical and echocardiographic signs of right ventricular dysfunction (intermediate-risk PE). Although not routinely recommended,<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a> and pending publication of the results of the Pulmonary Embolism Thrombolysis Study (PEITHO),<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">36</span></a> the decision to use thrombolytic treatment in a very selected group of patients will depend on their risk of bleeding and the severity of the clinical symptoms.</p><p id="par0320" class="elsevierStylePara elsevierViewall">Thrombolytic treatment administered for 2<span class="elsevierStyleHsp" style=""></span>h is safer and more effective than 12–24-h regimens. Streptokinase and recombinant tissue plasminogen activator (rt-PA) are equally effective with this short administration regimen. It should be administered via a peripheral route. Administration through a central line is not more effective and increases the risk of bleeding at the venous access insertion site.<ul class="elsevierStyleList" id="lis0080"><li class="elsevierStyleListItem" id="lsti0130"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0325" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">The administration of systemic fibrinolytic treatment is recommended in patients with PE and cardiogenic shock.</span></p></li><li class="elsevierStyleListItem" id="lsti0135"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0330" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">The administration of systemic fibrinolytic treatment is suggested in patients with PE and hypotension without a high risk of bleeding.</span></p></li><li class="elsevierStyleListItem" id="lsti0140"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0335" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">It is recommended not to administer fibrinolytic treatment in most hemodynamically stable patients with PE.</span></p></li><li class="elsevierStyleListItem" id="lsti0145"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0340" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In hemodynamically stable patients with intermediate-risk PE and a low risk of bleeding, particularly in the under 75<span class="elsevierStyleHsp" style=""></span>s, it is suggested that the administration of fibrinolytic treatment be assessed.</span></p></li></ul></p></span><span id="sec0115" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Vena Caval Filters</span><p id="par0345" class="elsevierStylePara elsevierViewall">Vena caval filters are indicated in PE patients with a contraindication for anticoagulation therapy. Decousus et al. published a clinical trial evaluating the usefulness of vena caval filters, as a complement to conventional anticoagulation, in patients with DVT and high-risk PE.<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">37</span></a> The filters reduced the frequency of PE during the first 12 days of treatment, and a tendency toward a lower number of fatal episodes was detected. After 2 years, there were no differences between the two groups in terms of mortality or recurrent VTE, due to an increase in the frequency of DVT in the group treated with filters. These findings indirectly support the use of vena caval filters in patients in whom anticoagulation is contraindicated in the acute phase. A recoverable filter should be inserted when possible, and should be removed as soon as anticoagulation can be commenced.<ul class="elsevierStyleList" id="lis0085"><li class="elsevierStyleListItem" id="lsti0150"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0350" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Placement of an inferior vena caval filter is recommended in hemodynamically stable patients with PE and a contraindication for anticoagulation.</span></p></li></ul></p></span><span id="sec0120" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Other Treatments</span><p id="par0355" class="elsevierStylePara elsevierViewall">In experienced centers, mechanical thrombus fragmentation is performed in patients with high-risk PE and a contraindication for the use of fibrinolytics. Pulmonary embolectomy is another method of treatment for high-risk PE. It is indicated in cases of right-sided heart thrombi, high risk of paradoxical arterial embolism or in patients with high-risk PE in whom fibrinolysis has not been effective.<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a> The results improve if patients undergo the procedure before developing cardiogenic shock.<ul class="elsevierStyleList" id="lis0090"><li class="elsevierStyleListItem" id="lsti0155"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0360" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In patients with high-risk PE and who (i) have a contraindication for fibrinolysis, (ii) fibrinolysis has failed, or (iii) the shock is likely to cause death of the patient before the fibrinolysis is effective, the use of interventionist catheterization techniques or pulmonary embolectomy is suggested if the necessary resources and expertise are available.</span></p></li></ul></p></span><span id="sec0125" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Support Treatment</span><p id="par0365" class="elsevierStylePara elsevierViewall">Patients with acute symptomatic PE should receive supplementary oxygen to obtain saturations higher than 92%. Oxygen therapy, especially in patients with right-sided heart overload, acts as a vasodilator and may contribute to the decrease in pressure in the pulmonary arteries.</p><p id="par0370" class="elsevierStylePara elsevierViewall">Pleuritic chest pain is a common symptom in patients with PE. It can be relieved on most occasions by administering non-steroidal anti-inflammatory agents within 24–48<span class="elsevierStyleHsp" style=""></span>h. The administration of these drugs does not increase the risk of bleeding in acute PE.</p><p id="par0375" class="elsevierStylePara elsevierViewall">The administration of fluids (<500<span class="elsevierStyleHsp" style=""></span>ml) may be beneficial for increasing the cardiac output in patients with PE, low output and sustained systemic pressures. Dopamine or dobutamine can be used in patients with low output and sustained systemic pressures. For hypotensive patients with PE, adrenaline combines the beneficial effects of noradrenaline and dobutamine.</p></span><span id="sec0130" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Treatment of Isolated Subsegmental Pulmonary Embolism</span><p id="par0380" class="elsevierStylePara elsevierViewall">A meta-analysis of studies that performed chest angio-CT for suspected PE found that the incidence of subsegmental PE was 4.7% (95% CI, 2.5–7.6) and 9.4% (95% CI, 5.5–14.2) in patients undergoing single- and multidetector CT. respectively.<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">39</span></a> There were no differences between the two groups in the incidence of thrombotic events during the first 3 months of follow-up when the patients did not receive anticoagulant therapy based on a negative angio-CT.</p></span><span id="sec0135" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Treatment of Incidental Pulmonary Embolism</span><p id="par0385" class="elsevierStylePara elsevierViewall">Incidental PE (unsuspected) is detected in approximately 2% of patients (most with cancer) in whom a chest CT is performed for reasons other than suspected PE. Some indirect evidence suggests that incidental PE worsens the prognosis in these patients.<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">40</span></a> The recommendation for indicating anticoagulant therapy is more consistent when the incidental PE is associated with concomitant PE, the PE is lobar or in the main arteries and the risk of bleeding is not high.<ul class="elsevierStyleList" id="lis0095"><li class="elsevierStyleListItem" id="lsti0160"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0390" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Anticoagulant therapy is suggested in patients with incidental PE in a segmental, lobar or main location.</span></p></li></ul></p></span><span id="sec0140" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Treatment of Right-Sided Heart Thrombi</span><p id="par0395" class="elsevierStylePara elsevierViewall">The presence of right-sided heart thrombi, particularly when they are mobile, significantly worsens the prognosis in patients with PE. Some indirect evidence suggests that fibrinolysis or surgical embolectomy is more effective than conventional anticoagulant therapy in these patients.</p></span></span><span id="sec0145" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0145">Long-term Treatment of Pulmonary Thromboembolism (After the First 3–6 Months)</span><span id="sec0150" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0150">Duration of Treatment</span><p id="par0400" class="elsevierStylePara elsevierViewall">The appropriate duration of anticoagulant treatment requires a balance between the risk of recurrent VTE and the risk of bleeding complications.</p></span><span id="sec0155" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0155">Risk of Recurrence</span><p id="par0405" class="elsevierStylePara elsevierViewall">The risk of recurrent VTE depends on (1) the efficacy of treatment of the acute episode, (2) a minimum duration of long-term treatment, (3) the possibility of the patient having an intrinsic risk factor for suffering a new VTE episode.</p><p id="par0410" class="elsevierStylePara elsevierViewall">In a meta-analysis that included 2925 patients who had suffered a first episode of VTE not secondary to cancer, and who had received treatment of different durations, the risk of recurrence increased significantly for treatment durations less than 3 months (HR 1.52; 95% CI, 1.14–2.02).<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a> There were no differences in the risk of recurrence for treatment durations of 3 months compared to durations of 6 or more months (HR 1.19; 95% CI, 0.86–1.85). Based on this evidence, it is agreed that long-term treatment of patients with PE should have a minimum duration of 3 months.</p><p id="par0415" class="elsevierStylePara elsevierViewall">In the aforementioned meta-analysis,<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a> the risk of recurrence was significantly lower for events caused by a temporary risk factor than for unprovoked events (HR 0.55; 95% CI, 0.41–0.74). In a systematic review<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">42</span></a> that included 15 clinical trials, the risk of recurrent VTE during follow-up for patients with unprovoked VTE was 2.3–2.5 times higher than that of patients with provoked VTE, 7.9–10.6 times higher than patients with VTE provoked by a surgical risk factor, and 1.4–1.8 times higher than that of patients with VTE provoked by a non-surgical risk factor.</p><p id="par0420" class="elsevierStylePara elsevierViewall">Although the literature is not consistent, for the purpose of decision-making on treatment duration, these guidelines stratify PE as provoked by a major risk factor, provoked by a minor risk factor, unprovoked or secondary to cancer (<a class="elsevierStyleCrossRef" href="#fig0020">Fig. 4</a>).</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia><span id="sec0160" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0160">Bleeding Risk</span><p id="par0425" class="elsevierStylePara elsevierViewall">There are no bleeding risk scales that have been sufficiently validated in patients on anticoagulant therapy for an episode of VTE. The RIETE registry<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">43</span></a> derived a score for predicting the risk of bleeding in the first 3 months of anticoagulant therapy from 19<span class="elsevierStyleHsp" style=""></span>274 patients diagnosed with DVT or PE (<a class="elsevierStyleCrossRef" href="#tbl0040">Table 8</a>). Based on the weight of each of the variables on the scale, patients were classified into three risk groups: low, intermediate and high. The incidence of major bleeding in the internal validation cohort was 0.1%, 2.8% and 6.2%, respectively.</p><elsevierMultimedia ident="tbl0040"></elsevierMultimedia><p id="par0430" class="elsevierStylePara elsevierViewall">After the third month of anticoagulant therapy, the evidence is more limited. The 9th edition of the ACCP<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> proposes a scale for risk of bleeding from a series of variables that have been associated with bleeding events in the literature (<a class="elsevierStyleCrossRef" href="#tbl0045">Table 9</a>). According to this model, the risk of a major bleed is low (0.3%) in the absence of any risk factor, moderate (0.6%) in the presence of one risk factor, and high (≥2.5%) if there are two or more risk factors. This model has not been validated in an external cohort of patients with VTE.</p><elsevierMultimedia ident="tbl0045"></elsevierMultimedia></span><span id="sec0165" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0165">Decision Strategies</span><p id="par0435" class="elsevierStylePara elsevierViewall">Two decision strategies have been developed on the duration of long-term anticoagulation in patients with PE: a population strategy and an individualized strategy. The first of these only considers provoked PE, unprovoked PE or PE secondary to cancer for making set recommendations on the duration of anticoagulant treatment. The second takes into account the clinical characteristics of each patient (age, sex, comorbidity, presentation of the event) and some other additional factor (D-dimer) to suggest individualized plans for duration of anticoagulant treatment. The authors of these guidelines suggest a mixed approach for decision-making.<ul class="elsevierStyleList" id="lis0100"><li class="elsevierStyleListItem" id="lsti0165"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0440" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In patients with PE provoked by surgical transient risk factors, 3 months of anticoagulant treatment is recommended.</span></p></li><li class="elsevierStyleListItem" id="lsti0170"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0445" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In patients with PE provoked by non-surgical transient risk factors, 3 months anticoagulant treatment is suggested.</span></p></li><li class="elsevierStyleListItem" id="lsti0175"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0450" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In patients with unprovoked PE, a minimum of 3–6 months anticoagulant treatment is recommended, and it is suggested that indefinite treatment be assessed according to the balance between the risk of recurrence and the risk of bleeding.</span></p></li><li class="elsevierStyleListItem" id="lsti0180"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0455" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In patients with cancer, at least 3–6 months anticoagulant treatment is recommended, and it is suggested that the treatment be prolonged while the cancer is active.</span></p></li><li class="elsevierStyleListItem" id="lsti0185"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0460" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Indefinite anticoagulant treatment is recommended in patients with a second episode of unprovoked PE.</span></p></li><li class="elsevierStyleListItem" id="lsti0190"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0465" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In patients with an indication for indefinite anticoagulation, periodical reevaluation of this indication is recommended.</span></p></li></ul></p></span><span id="sec0170" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0170">Individual Markers for Risk of Recurrence in Unprovoked Pulmonary Embolism</span><p id="par0470" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Event presentation</span>. In a meta-analysis that included 2554 patients with PE or DVT who were followed-up for 5 years, the initial presentation of the thrombotic event as PE tripled the risk that the recurrent VTE was again a PE (vs DVT) (HR 3.1, 95% CI, 1.9–5.1).<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">44</span></a> These results highlight the importance of presentation of the event, since the mortality of PE is significantly higher than that of DVT.</p><p id="par0475" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">D-dimer</span>. In the PROLONG<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">45</span></a> trial, D-dimer was measured 1 month after discontinuing anticoagulant therapy in patients with a first episode of unprovoked VTE who had received at least 3 months VKA treatment. Patients with negative D-dimer did not receive anticoagulant therapy, while those with positive D-dimer were randomized to restart or discontinue anticoagulant therapy definitively. The rate of recurrent VTE during follow-up was 15% in the group with positive D-dimer who stopped anticoagulant treatment, 6.2% in the group with negative D-dimer, and 2.6% in the group with positive D-dimer who received anticoagulant treatment. These results have been confirmed in subsequent systematic reviews and meta-analyses.</p><p id="par0480" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Residual deep vein thrombosis</span>. Residual DVT is defined as persistence of the organized thrombus adhered to the vein wall over time. In a systematic review and meta-analysis of 9 cohort studies and 5 randomized trials,<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">46</span></a> it was concluded that residual DVT was modestly associated with an increase in the risk of recurrence for all patients with DVT (both provoked and unprovoked) (OR 1.5; 95%, CI 1.1–2.0), but the effect disappeared when only the subgroup of patients with unprovoked DVT was considered (OR 1.2; 95% CI, 0.9–1.7). Its limitation is that the evaluation is operator-dependent and interobserver variability is high.</p><p id="par0485" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">First vs second episode of PE</span>. After a second episode of VTE, the risk of recurrence is approximately 1.5 times higher than after the first episode.<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">47</span></a> The risk of recurrence is particularly high when the second episode occurs shortly after discontinuing anticoagulant therapy.</p><p id="par0490" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Hereditary and acquired thrombophilia</span>. In a meta-analysis, the risk of recurrent VTE was 1.6 (95% CI, 1.1–2.1) for patients heterozygous for factor V Leiden (1.2; 95% CI, 0.6–2.2, for the subgroup of patients with unprovoked VTE), 2.6 (95% CI, 1.2–6.0) for homozygous patients, and 1.4 (95% CI, 1.0–2.2) for patients heterozygous for the prothrombin G20210A gene.<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">48</span></a> Given that the association between hereditary thrombophilia and the risk of recurrence is weak (if it exists), its measurement to determine the duration of anticoagulant treatment is not recommended.</p><p id="par0495" class="elsevierStylePara elsevierViewall">Studies that have evaluated the association between the presence of antiphospholipid antibodies (APA) and the risk of recurrent VTE do not provide consistent data for deciding the duration of anticoagulation if they are detected.</p><p id="par0500" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Other risk factors of recurrence</span>. Advanced age, male gender, obesity, post-thrombotic syndrome secondary to DVT concomitant with PE, some anti-psychotic drugs and certain chronic diseases such as inflammatory bowel disease have been associated with an increased risk of recurrence when anticoagulant treatment is discontinued.</p></span><span id="sec0175" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0175">Predictive Models of Recurrence for Patients With Unprovoked Pulmonary Embolism</span><p id="par0505" class="elsevierStylePara elsevierViewall">Various predictive models have been developed that could identify patients with unprovoked PE and low risk of recurrence. However, none have been prospectively validated. The most widely used models are the DASH (D-Dimer, Age, Sex, Hormonal treatment) score,<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">49</span></a> Vienna nomogram,<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">50</span></a> developed with 3 variables associated independently with the risk of recurrence: female sex, proximal DVT vs PE and D-dimer value determined after discontinuation of anticoagulant treatment, and the Canadian model,<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">51</span></a> valid for women, which includes the following variables: age, body mass index, D-dimer determined after discontinuing anticoagulant treatment and presence of post-thrombotic symptoms or signs in the LE.</p></span></span><span id="sec0180" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0180">Drugs For Long-Term Treatment</span><p id="par0510" class="elsevierStylePara elsevierViewall">These guidelines only make recommendations or suggestions for drugs approved in Spain for this indication.</p><span id="sec0185" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0185">Vitamin K Antagonists</span><p id="par0515" class="elsevierStylePara elsevierViewall">Acenocumarol and warfarin are the two dicumarol derivatives available in Spain. They interfere competitively in the metabolism of vitamin K and inhibit the production of coagulation proteins dependent on this vitamin (factors II, VII, IX and X and proteins C, S and Z). Acenocumarol has a shorter half-life and faster metabolic clearance than warfarin. Control of the therapeutic action requires monitoring expressed as the international normalized ratio (INR). An INR range between 2.0 and 3.0 has the best balance between efficacy and safety,<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">52</span></a> and reduces the risk of recurrence by 80%. After having completed a minimum of 6 months with a range between 2.0 and 3.0, a clinical trial found that the administration of VKA with a lower range, between 1.5 and 1.9, reduced the risk of recurrence by 64% (HR 0.36; 95% CI, 0.19–0.67) without increasing the risk of major bleeding (HR 2.53; 95% CI, 0.49–13.03).<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a> In another clinical trial, when this regimen (range between 1.5 and 1.9) was compared with the conventional regimen (range between 2.0 and 3.0), the risk of recurrence was significantly higher (HR 2.8; 95% CI, 1.1–7.0), with no differences in the risk of major bleeding (HR 1.2; 95% CI, 0.4–3.0).<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">52</span></a></p><p id="par0520" class="elsevierStylePara elsevierViewall">In patients with difficulty in regular monitoring or maintaining a stable INR with VKA (more than 50% of measurements within range over a 6-month period), the balance between efficacy and safety of VKA is not guaranteed.</p></span><span id="sec0190" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0190">Low Molecular Weight Heparins</span><p id="par0525" class="elsevierStylePara elsevierViewall">These are indicated for at least the first 3 months of treatment of VTE in patients with active cancer, where they have been shown to be more effective than VKAs. However, as the doses for long-term treatment are not well established and their administration is parenteral, their use is not recommended as first choice in patients with VTE not secondary to cancer, although they could be an alternative for patients with difficulty in properly controlling VKA levels or unstable INR.</p></span><span id="sec0195" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0195">New Oral Anticoagulants</span><p id="par0530" class="elsevierStylePara elsevierViewall">At the time of writing of this consensus, the European Medicines Agency (EMA) has only approved rivaroxaban for the secondary prevention of VTE after a first episode of DVT or PE. Other anticoagulants, such as dabigatran or apixaban, already marketed for other indications, are pending approval.</p><p id="par0535" class="elsevierStylePara elsevierViewall">The Einstein-Extension study<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a> randomly assigned 1197 patients who had completed 6–12 months of anticoagulation (with VKA or rivaroxaban) to receive rivaroxaban at doses of 20<span class="elsevierStyleHsp" style=""></span>mg/day or placebo. During the study period, rivaroxaban significantly reduced the risk of recurrent VTE (HR 0.18; 95% CI, 0.09–0.39). There were no significant differences in the incidence of major bleeding, but rivaroxaban increased the risk of major or clinically relevant non-major bleeding (HR 5.19; IC 95%, 2.3–11.7).</p><p id="par0540" class="elsevierStylePara elsevierViewall">In the AMPLIFY-EXT trial,<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">54</span></a> two doses of apixaben (2.5 and 5<span class="elsevierStyleHsp" style=""></span>mg, twice daily) were compared with placebo in patients with VTE who had completed 6–12 months of anticoagulant treatment (with VKA or apixaban). During the study period, apixaban significantly reduced the risk of recurrent VTE (relative risk [RR] 0.19; 95% CI, 0.11–0.33 for the 2.5<span class="elsevierStyleHsp" style=""></span>mg dose; RR 0.20; 95% CI, 0.11–0.34 for the 5<span class="elsevierStyleHsp" style=""></span>mg dose), with no differences in the incidence of major or clinically relevant non-major bleeding (RR 1.20; 95% CI, 0.69–2.10 for the 2.5<span class="elsevierStyleHsp" style=""></span>mg dose; RR 1.62; 95% CI, 0.96–2.73 for the 5<span class="elsevierStyleHsp" style=""></span>mg dose).</p><p id="par0545" class="elsevierStylePara elsevierViewall">In two clinical trials, RE-MEDY and RE-SONATE,<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">55</span></a> dabigatran at a dose of 150<span class="elsevierStyleHsp" style=""></span>mg twice daily was compared with VKA and placebo (respectively) in patients with VTE who had completed at least 3 months of anticoagulation (with VKA or dabigatran). During the study period, dabigatran was equally as effective as the VKAs (HR 1.44; 95% CI, 0.78–2.64) and more effective than placebo (HR 0.08; 95% CI, 0.02–0.25) in reducing recurrent VTE. Dabigatran reduced the total incidence of major or clinically relevant non-major bleeding when compared with VKA (HR 0.54; 95% CI, 0.41–0.71), but these increased when compared with placebo (HR 2.92; 95% CI, 1.52–5.60).</p></span><span id="sec0200" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0200">Aspirin</span><p id="par0550" class="elsevierStylePara elsevierViewall">Two clinical trials were published in 2012, WARFASA<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">56</span></a> and ASPIRE,<a class="elsevierStyleCrossRef" href="#bib0285"><span class="elsevierStyleSup">57</span></a> which evaluated the efficacy and safety of aspirin compared to placebo in the secondary prevention of VTE in patients with a first unprovoked episode of PE or DVT. In the WARFASA study, aspirin was compared to placebo in patients with VTE who had completed a 6–18-month period of treatment with VKA (DVT 63%; PE 37%). During the 2 years of follow-up, aspirin significantly reduced the risk of recurrent VTE (HR 0.55; 95% CI, 0.33–0.92), without increasing bleeding episodes (HR 0.98; 95% CI, 0.24–3.96). In the ASPIRE study, aspirin was compared to placebo in patients with VTE who had completed a 6-week to 24-month period of treatment with VKA. No differences were observed in the rate of recurrent VTE (HR 0.74; 95% CI, 0.52–1.09), although there was an overall clinical benefit in the reduction of the composite of cardiovascular episodes, bleeding, and death from any cause (HR 0.67; 95% CI, 0.49–0.91).<ul class="elsevierStyleList" id="lis0105"><li class="elsevierStyleListItem" id="lsti0195"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0555" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">The use of VKA is recommended for most patients with PE, with a target INR of 2.5 (range 2.0–3.0), for long-term anticoagulant treatment.</span></p></li><li class="elsevierStyleListItem" id="lsti0200"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0560" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">It is suggested not to use VKA with a target INR of 1.5–1.9 for long-term anticoagulant treatment.</span></p></li><li class="elsevierStyleListItem" id="lsti0205"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0565" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">The use of LMWH is recommended for patients with PE secondary to cancer throughout treatment.</span></p></li><li class="elsevierStyleListItem" id="lsti0210"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0570" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">The use of rivaroxaban for long-term anticoagulant treatment is suggested in patients with difficulty in regular monitoring or maintaining a stable INR with VKA.</span></p></li><li class="elsevierStyleListItem" id="lsti0215"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0575" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In patients with unprovoked PE in whom oral anticoagulation has been discontinued, it is suggested to assess the use of aspirin, at a dose of 100<span class="elsevierStyleHsp" style=""></span>mg/day, once the minimum treatment duration (3 months) has been completed.</span></p></li></ul></p></span></span><span id="sec0205" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0205">Residual Thrombosis and Chronic Thromboembolic Pulmonary Hypertension</span><p id="par0580" class="elsevierStylePara elsevierViewall">In a review of 4 studies in which serial imaging tests were carried out, the percentage of patients with residual PE was 87% at 8 days, 68% at 6 weeks, 65% at 3 months, 57% at 6 months and 52% at 11 months.<a class="elsevierStyleCrossRef" href="#bib0290"><span class="elsevierStyleSup">58</span></a> However, in a study of 673 patients from a single center who were followed-up for 3 months, the rate of symptomatic recurrent VTE was only 3%.<a class="elsevierStyleCrossRef" href="#bib0295"><span class="elsevierStyleSup">59</span></a> Therefore, there is disagreement between the percentage of patients with residual thrombosis and the percentage of patients with recurrent VTE.</p><p id="par0585" class="elsevierStylePara elsevierViewall">The incidence of symptomatic chronic thromboembolic pulmonary hypertension (CTEPH) in patients who have had an episode of PE varies according to the series and follow-up period, and has reached up to 3.8%.<a class="elsevierStyleCrossRef" href="#bib0300"><span class="elsevierStyleSup">60</span></a> Some characteristics of the initial PE episode (age >70 years, young age, female gender, pulmonary systolic pressure >50<span class="elsevierStyleHsp" style=""></span>mmHg, massive or sub-massive PE, recurrent or idiopathic PE) increase the risk of developing CTEPH.<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">61</span></a><ul class="elsevierStyleList" id="lis0110"><li class="elsevierStyleListItem" id="lsti0220"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0590" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In patients with a history of PE, it is recommended not to use thoracic imaging tests to evaluate the persistence of residual thrombosis or reperfusion of the initial defects.</span></p></li><li class="elsevierStyleListItem" id="lsti0225"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0595" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In patients with a history of PE and signs or symptoms suggestive of CTEPH, it is recommended to perform a follow-up transthoracic echocardiogram.</span></p></li></ul></p></span><span id="sec0210" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0210">Search for Occult Neoplasm in Unprovoked Pulmonary Embolism</span><p id="par0600" class="elsevierStylePara elsevierViewall">VTE is associated with an occult neoplasm in approximately 10% of patients. The Trousseau study<a class="elsevierStyleCrossRef" href="#bib0310"><span class="elsevierStyleSup">62</span></a> compared the utility of extensive screening for cancer by thoracoabdominal CT and mammography (in women) with limited screening. The results did not show any differences in the incidence of cancer or mortality between the two patient groups. Extensive screening significantly increased the healthcare costs due to the additional diagnostic process associated with false positive results.<ul class="elsevierStyleList" id="lis0115"><li class="elsevierStyleListItem" id="lsti0230"><span class="elsevierStyleLabel"><span class="elsevierStyleItalic">•</span></span><p id="par0605" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">In patients with an episode of unprovoked PE, it is suggested not to perform specific tests searching for neoplasia if there are no clinical symptoms or basic complementary examinations that suggest the presence of this disease.</span></p></li></ul></p></span></span><span id="sec0215" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0215">Conflicts of Interest</span><p id="par0610" class="elsevierStylePara elsevierViewall">Fernando Uresandi has received funding for giving lectures at educational events and/or scientific advice and/or research from Bayer HealthCare Pharmaceuticals.</p><p id="par0615" class="elsevierStylePara elsevierViewall">Manuel Monreal has received funding for giving lectures at educational events and/or scientific advice and/or research from Bayer HealthCare Pharmaceuticals; Boehringer Ingelheim Pharmaceuticals, Inc.; Daiichi Sankyo, Inc; Pfizer; ROVI; Sanofi-Aventis.</p><p id="par0620" class="elsevierStylePara elsevierViewall">Ferrán García-Bragado has received funding for giving lectures at educational events and/or scientific advice and/or research from Bayer HealthCare Pharmaceuticals; Boehringer Ingelheim Pharmaceuticals, Inc.; Bristol-Myers Squibb Company; Daiichi Sankyo, Inc; ROVI; Sanofi-Aventis.</p><p id="par0625" class="elsevierStylePara elsevierViewall">Ramón Lecumberri has received funding for giving lectures at educational events and/or scientific advice and/or research from Bayer HealthCare Pharmaceuticals; Boehringer Ingelheim Pharmaceuticals, Inc.; Bristol-Myers Squibb Company; Leo Pharma; ROVI; Sanofi-Aventis.</p><p id="par0630" class="elsevierStylePara elsevierViewall">Sonia Jiménez has received funding for giving lectures at educational events and/or scientific advice and/or research from Bayer HealthCare Pharmaceuticals; Boehringer Ingelheim Pharmaceuticals, Inc.; ROVI; Sanofi-Aventis.</p><p id="par0635" class="elsevierStylePara elsevierViewall">Pedro Ruiz-Artacho has received funding for giving lectures at educational events and/or scientific advice and/or research from Bayer HealthCare Pharmaceuticals; LeoPharma; Sanofi-Aventis.</p><p id="par0640" class="elsevierStylePara elsevierViewall">Francisco Lozano has received funding for giving lectures at educational events and/or scientific advice and/or research from Bayer HealthCare Pharmaceuticals; Bristol-Myers Squibb Company; Leo Pharma; ROVI; Sanofi-Aventis.</p><p id="par0645" class="elsevierStylePara elsevierViewall">Antonio Romera has received funding for giving lectures at educational events and/or scientific advice and/or research from Bayer HealthCare Pharmaceuticals; Leo Pharma; ROVI; Sanofi-Aventis.</p><p id="par0650" class="elsevierStylePara elsevierViewall">David Jiménez has received funding for giving lectures at educational events and/or scientific advice and/or research from Bayer HealthCare Pharmaceuticals; Boehringer Ingelheim Pharmaceuticals, Inc.; Bristol-Myers Squibb Company; Daiichi Sankyo, Inc; Leo Pharma; ROVI; Sanofi-Aventis.</p><p id="par0655" class="elsevierStylePara elsevierViewall">Pere Domenech has received funding for giving lectures at educational events and/or scientific advice and/or research from Bayer HealthCare Pharmaceuticals; Boehringer Ingelheim Pharmaceuticals, Inc.; Bristol-Myers Squibb Company; Leo Pharma; ROVI; Sanofi-Aventis.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:8 [ 0 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 1 => array:2 [ "identificador" => "sec0010" "titulo" => "Concept, Pathogenesis, Risk Factors and Epidemiology" ] 2 => array:3 [ "identificador" => "sec0015" "titulo" => "Diagnosis" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0225" "titulo" => "Clinical Suspicion" ] 1 => array:2 [ "identificador" => "sec0025" "titulo" => "D-Dimer" ] 2 => array:3 [ "identificador" => "sec0030" "titulo" => "Imaging Tests" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "sec0035" "titulo" => "Multidetector Computed Tomography Angiography" ] 1 => array:2 [ "identificador" => "sec0040" "titulo" => "Lung Scintigraphy" ] 2 => array:2 [ "identificador" => "sec0045" "titulo" => "Lower Extremity Venous Ultrasound" ] 3 => array:2 [ "identificador" => "sec0050" "titulo" => "Pulmonary Magnetic Resonance Angiography" ] 4 => array:2 [ "identificador" => "sec0055" "titulo" => "Transthoracic Echocardiography" ] ] ] ] ] 3 => array:3 [ "identificador" => "sec0060" "titulo" => "Prognostic Stratification of Patients With Pulmonary Embolism" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0065" "titulo" => "Prognostic Factors" ] 1 => array:2 [ "identificador" => "sec0070" "titulo" => "Identification of Patients With Low-Risk Pulmonary Embolism" ] 2 => array:2 [ "identificador" => "sec0075" "titulo" => "Identification of Patients With Intermediate-Risk Pulmonary Embolism" ] ] ] 4 => array:3 [ "identificador" => "sec0080" "titulo" => "Treatment of Pulmonary Embolism in the Initial Phase (Acute Phase And up to 3–6 Months)" "secciones" => array:12 [ 0 => array:2 [ "identificador" => "sec0085" "titulo" => "Anticoagulation With Unfractionated Heparin, Low Molecular Weight Heparins or Fondaparinux" ] 1 => array:2 [ "identificador" => "sec0090" "titulo" => "Beginning Oral Anticoagulation" ] 2 => array:2 [ "identificador" => "sec0095" "titulo" => "New Oral Anticoagulants" ] 3 => array:2 [ "identificador" => "sec0100" "titulo" => "Early vs Standard Discharge in Pulmonary Embolism Patients" ] 4 => array:2 [ "identificador" => "sec0105" "titulo" => "Early Mobilization vs Rest in Acute Pulmonary Embolism" ] 5 => array:2 [ "identificador" => "sec0110" "titulo" => "Fibrinolytic Treatment" ] 6 => array:2 [ "identificador" => "sec0115" "titulo" => "Vena Caval Filters" ] 7 => array:2 [ "identificador" => "sec0120" "titulo" => "Other Treatments" ] 8 => array:2 [ "identificador" => "sec0125" "titulo" => "Support Treatment" ] 9 => array:2 [ "identificador" => "sec0130" "titulo" => "Treatment of Isolated Subsegmental Pulmonary Embolism" ] 10 => array:2 [ "identificador" => "sec0135" "titulo" => "Treatment of Incidental Pulmonary Embolism" ] 11 => array:2 [ "identificador" => "sec0140" "titulo" => "Treatment of Right-Sided Heart Thrombi" ] ] ] 5 => array:3 [ "identificador" => "sec0145" "titulo" => "Long-term Treatment of Pulmonary Thromboembolism (After the First 3–6 Months)" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "sec0150" "titulo" => "Duration of Treatment" ] 1 => array:3 [ "identificador" => "sec0155" "titulo" => "Risk of Recurrence" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "sec0160" "titulo" => "Bleeding Risk" ] 1 => array:2 [ "identificador" => "sec0165" "titulo" => "Decision Strategies" ] 2 => array:2 [ "identificador" => "sec0170" "titulo" => "Individual Markers for Risk of Recurrence in Unprovoked Pulmonary Embolism" ] 3 => array:2 [ "identificador" => "sec0175" "titulo" => "Predictive Models of Recurrence for Patients With Unprovoked Pulmonary Embolism" ] ] ] 2 => array:3 [ "identificador" => "sec0180" "titulo" => "Drugs For Long-Term Treatment" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "sec0185" "titulo" => "Vitamin K Antagonists" ] 1 => array:2 [ "identificador" => "sec0190" "titulo" => "Low Molecular Weight Heparins" ] 2 => array:2 [ "identificador" => "sec0195" "titulo" => "New Oral Anticoagulants" ] 3 => array:2 [ "identificador" => "sec0200" "titulo" => "Aspirin" ] ] ] 3 => array:2 [ "identificador" => "sec0205" "titulo" => "Residual Thrombosis and Chronic Thromboembolic Pulmonary Hypertension" ] 4 => array:2 [ "identificador" => "sec0210" "titulo" => "Search for Occult Neoplasm in Unprovoked Pulmonary Embolism" ] ] ] 6 => array:2 [ "identificador" => "sec0215" "titulo" => "Conflicts of Interest" ] 7 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2013-05-11" "fechaAceptado" => "2013-07-19" "NotaPie" => array:4 [ 0 => array:3 [ "etiqueta" => "1" "nota" => "<p class="elsevierStyleNotepara" id="npar0035">General Coordinators: Fernando Uresandi and David Jimenez.</p>" "identificador" => "fn1" ] 1 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0025">Please cite this article as: Uresandi F, Monreal M, García-Bragado F, Domenech P, Lecumberri R, Escribano P, et al. Consenso nacional sobre el diagnóstico, estratificación de riesgo y tratamiento de los pacientes con tromboembolia pulmonar. Arch Bronconeumol. 2013;49:534–547.</p>" ] 2 => array:2 [ "etiqueta" => "☆☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0030">In this consensus document have participated the following scientific societies: Spanish Society of Pneumology and Thoracic Surgery (SEPAR); Society Española Internal Medicine (SEMI); Spanish Society of Thrombosis and Haemostasis (SETH); Spanish Society of Cardiology (ESC); Spanish Society of Medicine Accident and Emergency (SEMES); Spanish Society of Angiology and Surgery Vascular (SEACV).</p>" ] 3 => array:3 [ "etiqueta" => "2" "nota" => "<p class="elsevierStyleNotepara" id="npar0040">A complete list of participating authors is available in the appendix.</p>" "identificador" => "fn2" ] ] "apendice" => array:1 [ 0 => array:1 [ "seccion" => array:1 [ 0 => array:4 [ "apendice" => "<p id="par0660" class="elsevierStylePara elsevierViewall">SEACV: Sergi Bellmunt, Jorge Cuenca, Álvaro Fernández, Fidel Fernández, Vicente Ibáñez, Francisco Lozano, José Ramón March, Antonio Romera; SEC: Luis Almenar, Antonio Castro, Pilar Escribano, María Lázaro, José Luis Zamorano; SEMES: José Ramón Alonso, José Ramón Casal, José Miguel Franco, Sonia Jiménez, Marta Merlo, Ramón Perales, Pascual Piñera, Pedro Ruiz-Artacho; Coral Suero; SEMI: Raquel Barba, Carmen Fernández-Capitán, Ferrán García-Bragado, Vicente Gómez, Manuel Monreal, José Antonio Nieto, Antoni Riera-Mestre, Carmen Suárez, Javier Trujillo-Santos; SEPAR: Francisco Conget, Luis Jara, David Jiménez, José Luis Lobo, Javier de Miguel, Dolores Nauffal, Mikel Oribe, Remedios Otero, Fernando Uresandi; SETH: Pere Domenech, José Ramón González-Porras, Ramón Lecumberri, Pilar Llamas, Eva Mingot, Elena Pina, Javier Rodríguez-Martorell.</p>" "etiqueta" => "Appendix I" "titulo" => "Participating authors (alphabetical order)" "identificador" => "sec0220" ] ] ] ] "multimedia" => array:13 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 4041 "Ancho" => 2253 "Tamanyo" => 312359 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Diagnostic algorithm for the hemodynamically stable outpatient. (A) Angio-CT, computed tomography angiography. <span class="elsevierStyleSup">1</span>Refers to high sensitivity D-dimer. In the case of less sensitive D-dimer, PE can only be ruled out in patients with low clinical probability or PE unlikely. <span class="elsevierStyleSup">2</span>In case of high clinical probability and negative multidetector angio-CT, additional diagnostic tests are suggested (V/Q scan and/or Doppler ultrasound of lower extremities). (B) DVT, deep vein thrombosis. <span class="elsevierStyleSup">1</span>Refers to low or intermediate probability V/Q scans. <span class="elsevierStyleSup">2</span>In case of high clinical probability, inconclusive perfusion scan, and negative ultrasound of lower extremities, the need for multidetector angio-CT should be assessed with the appropriate specialist.</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Fig. 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 1862 "Ancho" => 2503 "Tamanyo" => 187810 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Diagnostic algorithm for the hemodynamically unstable patient with suspected pulmonary embolism. Angio-CT, computed tomography angiography; PE, pulmonary embolism; RV, right ventricle.</p>" ] ] 2 => array:7 [ "identificador" => "fig0015" "etiqueta" => "Fig. 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 2263 "Ancho" => 3137 "Tamanyo" => 354485 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Prognostic stratification and treatment of acute pulmonary embolism. *Cardiogenic shock or sustained systolic blood pressure <90<span class="elsevierStyleHsp" style=""></span>mmHg, not due to hypovolemia, sepsis or cardiac arrhythmias. The broken line indicates absence of definitive evidence (fibrinolysis) or extensive clinical experience (rivaroxaban). For situations not considered in the algorithm, hospitalization and conventional anticoagulant therapy is recommended. BNP, brain natriuretic peptide; DVT, deep vein thrombosis; Fx, fondaparinux; HFABP, heart fatty acid binding protein; hsTnT, high sensitivity troponin T; ICU, intensive care unit; LMWH, low molecular weight heparin; PE, pulmonary embolism; PESI, Pulmonary Embolism Severity Index; RVD, right ventricular dysfunction; sPESI, simplified PESI; UFH, unfractionated heparin.</p>" ] ] 3 => array:7 [ "identificador" => "fig0020" "etiqueta" => "Fig. 4" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr4.jpeg" "Alto" => 840 "Ancho" => 1621 "Tamanyo" => 66548 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Risk of recurrence according to the pulmonary embolism precipitating factor.</p>" ] ] 4 => array:7 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">DVT, deep vein thrombosis; LE, lower extremities; PE, pulmonary embolism.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">High risk</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Hip or knee prosthesis or fracture \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Major surgery \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Multiple trauma \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Spinal damage \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Moderate risk</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Plaster cast immobilization of LE \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Stroke with paralysis of LE \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Puerperium \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Previous PE or DVT \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Estrogenic drugs or devices \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Thrombophilia \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Cancer \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Chemotherapy \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Anti-psychotic drugs \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Inflammatory bowel disease \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Knee arthroscopy \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Central venous catheters or devices \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Low risk</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Advanced age \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Laparoscopic surgery \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Bed rest >3 days \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Long trips of >6–8<span class="elsevierStyleHsp" style=""></span>h \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Morbid obesity \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Varicose veins \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Pregnancy \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab431814.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Risk Factors for Venous Thromboembolism.</p>" ] ] 5 => array:7 [ "identificador" => "tbl0010" "etiqueta" => "Table 2" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Chest X-ray \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Electrocardiogram \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Normal ≈50% \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Normal ≈50% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Small pleural effusion \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Sinus tachycardia \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Opacities (areas of pulmonary infarction) \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Right precordial T-wave inversion \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Hampton's hump \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Right bundle branch block \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Linear atelectasis \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">S1Q3T3 pattern \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Local oligaemia \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Cardiac arrhythmias \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Slight elevation of the hemidiaphragm \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="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Increase in pulmonary arteries \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="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Cardiomegaly \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="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab431812.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Chest X-ray and Electrocardiogram in Acute Symptomatic Pulmonary Embolism.</p>" ] ] 6 => array:7 [ "identificador" => "tbl0015" "etiqueta" => "Table 3" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0105" class="elsevierStyleSimplePara elsevierViewall">DVT, deep vein thrombosis; LE, lower extremities; PE, pulmonary embolism.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Score \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Wells Score</span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Alternative diagnosis less likely than PE</span> \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 \t\t\t\t\ttop\n \t\t\t\t">3.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Signs or symptoms of DVT</span> \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 \t\t\t\t\ttop\n \t\t\t\t">3.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">History of PE or DVT</span> \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 \t\t\t\t\ttop\n \t\t\t\t">1.5 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Immobilization for at least 3 days or surgery in the previous month</span> \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 \t\t\t\t\ttop\n \t\t\t\t">1.5 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Heart rate >100 beats/min</span> \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 \t\t\t\t\ttop\n \t\t\t\t">1.5 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Hemoptysis</span> \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 \t\t\t\t\ttop\n \t\t\t\t">1.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Active cancer (treatment ongoing, within previous 6 months or palliative)</span> \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 \t\t\t\t\ttop\n \t\t\t\t">1.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">For high sensitivity D-dimer:</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Low probability: <2 points<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Intermediate probability: 2–6 points<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>High probability: ≥6 points<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">For lower sensitivity D-dimer:</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>PE unlikely: ≤4 points<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>PE likely: >4 points \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="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Geneva Score</span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Age >65 years</span> \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 \t\t\t\t\ttop\n \t\t\t\t">1.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Previous DVT or PE</span> \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 \t\t\t\t\ttop\n \t\t\t\t">3.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Surgery under general anesthesia or fracture ≤1 month</span> \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 \t\t\t\t\ttop\n \t\t\t\t">2.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Active cancer, solid or hematologic, or considered cured ≤1 year</span> \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 \t\t\t\t\ttop\n \t\t\t\t">2.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Unilateral lower limb pain</span> \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 \t\t\t\t\ttop\n \t\t\t\t">3.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Hemoptysis</span> \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 \t\t\t\t\ttop\n \t\t\t\t">2.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Heart rate 75–94 beats/min</span> \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 \t\t\t\t\ttop\n \t\t\t\t">3.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Heart rate ≥95 beats/min</span> \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 \t\t\t\t\ttop\n \t\t\t\t">5.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Pain on LE palpation and unilateral edema</span> \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 \t\t\t\t\ttop\n \t\t\t\t">4.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Low probability: 0–3 points</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Intermediate probability: 4–10 points</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">High probability: ≥11 points</span> \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="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab431811.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Scoring Scales for Grading the Clinical Likelihood of Acute Symptomatic Pulmonary Embolism.</p>" ] ] 7 => array:7 [ "identificador" => "tbl0020" "etiqueta" => "Table 4" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:3 [ "leyenda" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">ELFA, enzyme-linked fluorescence assay; ELISA, enzyme-linked immunosorbent assay.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Sensitivity \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Method \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Laboratory Test<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">*</span></a> \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">High \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">ELISA (gold standard) \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Asserachrom<span class="elsevierStyleSup">®</span> (Diagnostica Stago)Dimertest Gold EIA<span class="elsevierStyleSup">®</span> (Agen Biomedical) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">ELFA \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">VIDAS<span class="elsevierStyleSup">®</span> (BioMerieux) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Latex-enhanced immunoturbidimetry \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IL test<span class="elsevierStyleSup">®</span> (Instrumentation Laboratory, SpA)Liatest<span class="elsevierStyleSup">®</span> (Diagnostica Stago)Auto Dimertest (Agen Biomedical) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Moderate \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Whole blood immunoassay (red cell agglutination) \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">SimpliRED<span class="elsevierStyleSup">®</span> (Agen Biomedical) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Low \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Latex immunoagglutination \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Dimertest<span class="elsevierStyleSup">®</span> (Agen Biomedical)D-Dimer test<span class="elsevierStyleSup">®</span> (Diagnostica Stago) \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab431817.png" ] ] ] "notaPie" => array:1 [ 0 => array:3 [ "identificador" => "tblfn0005" "etiqueta" => "*" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Laboratory test generally used in Spain.</p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">D-Dimer Measurement Techniques for Acute Symptomatic Pulmonary Thromboembolism.</p>" ] ] 8 => array:7 [ "identificador" => "tbl0025" "etiqueta" => "Table 5" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:3 [ "leyenda" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">Angio-CT, computed tomography angiography; BNP, brain natriuretic peptide; cTnI, cardiac troponin I; cTnT, cardiac troponin T; DVT, deep vein thrombosis; HFABP, heart fatty acid binding protein; hsTnT, high sensitivity troponin T; PESI, Pulmonary Embolism Severity Index.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Clinical markers \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">PESI ScoreSimplified PESI Score \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Markers of right ventricular dysfunction \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Transthoracic echocardiographyAngio-CTBNP or NT-proBNP<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">*</span></a> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Markers of thrombotic burden \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Residual DVTD-Dimer<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">*</span></a> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Markers of tissue damage \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Lactate<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">*</span></a> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Markers of myocardial damage \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">cTnI or cTnT<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">*</span></a>hsTnT<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">*</span></a>HFABP<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">*</span></a> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab431818.png" ] ] ] "notaPie" => array:1 [ 0 => array:3 [ "identificador" => "tblfn0010" "etiqueta" => "*" "nota" => "<p class="elsevierStyleNotepara" id="npar0010">Measurement methods and cut-off points according to local practices.</p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Prognostic Tools for Hemodynamically Stable Patients With Acute Symptomatic Pulmonary Embolism.</p>" ] ] 9 => array:7 [ "identificador" => "tbl0030" "etiqueta" => "Table 6" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Variable \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Points \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">PESI Score (Pulmonary Embolism Severity Index)</span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Age</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1/year \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Male gender</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">10 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Cancer</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">30 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Heart failure</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">10 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Chronic lung disease</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">10 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Heart rate ≥110 beats/min</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">20 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Systolic blood pressure <100</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">mmHg</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">30 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Respiratory rate ≥30 breaths/min</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">20 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Temperature <36</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">°C</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">20 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Altered mental status</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">60 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">O</span><span class="elsevierStyleInf"><span class="elsevierStyleItalic">2</span></span><span class="elsevierStyleItalic">saturation <90%</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">20 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Risk stratification:</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Class I (very low risk): <65 points<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Class II (low risk): 66–85 points<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Class III (intermediate risk): 86–105 points<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Class IV (high risk): 106–125 points<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Class V (very high risk): >125 points \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="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Simplified PESI Score</span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Age >80 years</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Cancer</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Chronic cardiopulmonary disease</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Heart rate ≥110 beats/min</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Systolic blood pressure <100</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">mmHg</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">O</span><span class="elsevierStyleInf"><span class="elsevierStyleItalic">2</span></span><span class="elsevierStyleItalic">saturation <90%</span> \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Risk stratification:</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Low risk: 0 points<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>High risk: ≥1 point(s) \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="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab431813.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">Prognostic Scores in Patients With Acute Symptomatic Pulmonary Embolism.</p>" ] ] 10 => array:7 [ "identificador" => "tbl0035" "etiqueta" => "Table 7" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:3 [ "leyenda" => "<p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">IU, international units; rt-P, recombinant tissue plasminogen activator.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Active substance \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Dose \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Interval \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Bemiparin \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">115<span class="elsevierStyleHsp" style=""></span>IU/kg \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Every 24<span class="elsevierStyleHsp" style=""></span>h \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Dalteparin \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">100<span class="elsevierStyleHsp" style=""></span>IU/kg200<span class="elsevierStyleHsp" style=""></span>IU/kg \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Every 12<span class="elsevierStyleHsp" style=""></span>hEvery 24<span class="elsevierStyleHsp" style=""></span>h \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Enoxaparin \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1.0<span class="elsevierStyleHsp" style=""></span>mg/kg1.5<span class="elsevierStyleHsp" style=""></span>mg/kg \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Every 12<span class="elsevierStyleHsp" style=""></span>hEvery 24<span class="elsevierStyleHsp" style=""></span>h \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Nadroparin \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">85.5<span class="elsevierStyleHsp" style=""></span>IU/kg171<span class="elsevierStyleHsp" style=""></span>IU/kg \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Every 12<span class="elsevierStyleHsp" style=""></span>hEvery 24<span class="elsevierStyleHsp" style=""></span>h \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Tinzaparin \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">175<span class="elsevierStyleHsp" style=""></span>IU/kg \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Every 24<span class="elsevierStyleHsp" style=""></span>h \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Fondaparinux \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">5.0<span class="elsevierStyleHsp" style=""></span>mg (<50<span class="elsevierStyleHsp" style=""></span>kg)7.5<span class="elsevierStyleHsp" style=""></span>mg (50–100<span class="elsevierStyleHsp" style=""></span>kg)10<span class="elsevierStyleHsp" style=""></span>mg (>100<span class="elsevierStyleHsp" style=""></span>kg) \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Every 24<span class="elsevierStyleHsp" style=""></span>h \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Rivaroxaban \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">15<span class="elsevierStyleHsp" style=""></span>mg (days 1–21)20<span class="elsevierStyleHsp" style=""></span>mg (starting from day 22) \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Every 12<span class="elsevierStyleHsp" style=""></span>hEvery 24<span class="elsevierStyleHsp" style=""></span>h \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Unfractionated heparin \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">18<span class="elsevierStyleHsp" style=""></span>U/kg/h \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Perfusion \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">rt-PA \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">100<span class="elsevierStyleHsp" style=""></span>mg0.6<span class="elsevierStyleHsp" style=""></span>mg/kg \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">In 2<span class="elsevierStyleHsp" style=""></span>hIn 15<span class="elsevierStyleHsp" style=""></span>min \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Urokinase \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">3 million IU \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">In 2<span class="elsevierStyleHsp" style=""></span>h \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Streptokinase \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1.5 million IU \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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">In 2<span class="elsevierStyleHsp" style=""></span>h \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab431810.png" ] ] ] "notaPie" => array:1 [ 0 => array:3 [ "identificador" => "tblfn0015" "etiqueta" => "*" "nota" => "<p class="elsevierStyleNotepara" id="npar0015">Only drugs with approval for this indication are included.</p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Treatment Guidelines for the Acute Phase of Pulmonary Embolism.<a class="elsevierStyleCrossRef" href="#tblfn0015"><span class="elsevierStyleSup">*</span></a></p>" ] ] 11 => array:7 [ "identificador" => "tbl0040" "etiqueta" => "Table 8" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0090" class="elsevierStyleSimplePara elsevierViewall">DVT, deep vein thrombosis; PE, pulmonary embolism; RIETE, Computerized Registry of Patients with Venous Thromboembolism.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">RIETE Score \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Score \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Recent major bleed (1 month) \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 \t\t\t\t\ttop\n \t\t\t\t">2.0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Creatinine >1.2<span class="elsevierStyleHsp" style=""></span>mg/dl \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 \t\t\t\t\ttop\n \t\t\t\t">1.5 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Anemia \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 \t\t\t\t\ttop\n \t\t\t\t">1.5 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Cancer \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 \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Clinical presentation as PE (vs DVT) \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 \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Age >75 years \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 \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Low risk: 0–3 points<span class="elsevierStyleHsp" style=""></span>Intermediate risk: 1–4 points<span class="elsevierStyleHsp" style=""></span>High risk: >4 points \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="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab431816.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">RIETE Score for Bleeding Risk in Patients With Venous Thromboembolism During the First 3 Months of Anticoagulant Treatment.</p>" ] ] 12 => array:7 [ "identificador" => "tbl0045" "etiqueta" => "Table 9" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:3 [ "leyenda" => "<p id="spar0100" class="elsevierStyleSimplePara elsevierViewall">ACCP, American College of Chest Physicians.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Variable \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Age >65 years \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Age >75 years \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Previous bleed \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Cancer \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Cancer with metastasis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Renal failure \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Liver failure \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Thrombocytopenia \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Previous stroke \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Diabetes \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Anemia \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Anti-platelet therapy \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Poorly controlled anticoagulation \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Comorbidity and reduced functional capacity \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Recent surgery \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Frequent falls \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Alcohol abuse \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Low risk: 0 risk factors<span class="elsevierStyleHsp" style=""></span>Moderate risk: 1 risk factor<span class="elsevierStyleHsp" style=""></span>High risk: ≥2 risk factors \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab431815.png" ] ] ] "notaPie" => array:1 [ 0 => array:3 [ "identificador" => "tblfn0020" "etiqueta" => "*" "nota" => "<p class="elsevierStyleNotepara" id="npar0020">Adapted from Ref.<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a></p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0095" class="elsevierStyleSimplePara elsevierViewall">ACCP Score for Bleeding Risk in Patients on Anticoagulant Therapy for More Than 3 Months Due to Venous Thromboembolic Disease.<a class="elsevierStyleCrossRef" href="#tblfn0020"><span class="elsevierStyleSup">*</span></a></p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:62 [ 0 => array:3 [ "identificador" => 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Year/Month | Html | Total | |
---|---|---|---|
2024 November | 7 | 4 | 11 |
2024 October | 73 | 35 | 108 |
2024 September | 64 | 30 | 94 |
2024 August | 86 | 62 | 148 |
2024 July | 69 | 25 | 94 |
2024 June | 81 | 29 | 110 |
2024 May | 152 | 53 | 205 |
2024 April | 69 | 48 | 117 |
2024 March | 62 | 26 | 88 |
2024 February | 47 | 43 | 90 |
2023 November | 1 | 0 | 1 |
2023 October | 1 | 2 | 3 |
2023 July | 13 | 0 | 13 |
2023 March | 18 | 3 | 21 |
2023 February | 103 | 20 | 123 |
2023 January | 65 | 51 | 116 |
2022 December | 121 | 35 | 156 |
2022 November | 122 | 39 | 161 |
2022 October | 71 | 36 | 107 |
2022 September | 65 | 40 | 105 |
2022 August | 85 | 40 | 125 |
2022 July | 65 | 54 | 119 |
2022 June | 85 | 47 | 132 |
2022 May | 103 | 33 | 136 |
2022 April | 93 | 40 | 133 |
2022 March | 107 | 57 | 164 |
2022 February | 122 | 31 | 153 |
2022 January | 150 | 44 | 194 |
2021 December | 167 | 39 | 206 |
2021 November | 152 | 48 | 200 |
2021 October | 137 | 50 | 187 |
2021 September | 110 | 51 | 161 |
2021 August | 122 | 53 | 175 |
2021 July | 140 | 36 | 176 |
2021 June | 123 | 41 | 164 |
2021 May | 119 | 62 | 181 |
2021 April | 304 | 80 | 384 |
2021 March | 249 | 40 | 289 |
2021 February | 137 | 38 | 175 |
2021 January | 128 | 21 | 149 |
2020 December | 94 | 32 | 126 |
2020 November | 109 | 18 | 127 |
2020 October | 101 | 15 | 116 |
2020 September | 74 | 20 | 94 |
2020 August | 75 | 13 | 88 |
2020 July | 100 | 33 | 133 |
2020 June | 86 | 15 | 101 |
2020 May | 103 | 27 | 130 |
2020 April | 114 | 19 | 133 |
2020 March | 97 | 29 | 126 |
2020 February | 97 | 17 | 114 |
2020 January | 133 | 25 | 158 |
2019 December | 169 | 37 | 206 |
2019 November | 132 | 28 | 160 |
2019 October | 63 | 24 | 87 |
2019 September | 84 | 28 | 112 |
2019 August | 86 | 21 | 107 |
2019 July | 72 | 25 | 97 |
2019 June | 82 | 15 | 97 |
2019 May | 180 | 20 | 200 |
2019 April | 122 | 24 | 146 |
2019 March | 97 | 23 | 120 |
2019 February | 96 | 35 | 131 |
2019 January | 64 | 28 | 92 |
2018 December | 73 | 25 | 98 |
2018 November | 126 | 42 | 168 |
2018 October | 106 | 58 | 164 |
2018 September | 74 | 21 | 95 |
2018 May | 107 | 0 | 107 |
2018 April | 148 | 5 | 153 |
2018 March | 116 | 10 | 126 |
2018 February | 103 | 9 | 112 |
2018 January | 136 | 7 | 143 |
2017 December | 120 | 7 | 127 |
2017 November | 80 | 16 | 96 |
2017 October | 82 | 9 | 91 |
2017 September | 107 | 67 | 174 |
2017 August | 107 | 54 | 161 |
2017 July | 101 | 41 | 142 |
2017 June | 131 | 41 | 172 |
2017 May | 139 | 47 | 186 |
2017 April | 128 | 63 | 191 |
2017 March | 121 | 104 | 225 |
2017 February | 93 | 54 | 147 |
2017 January | 84 | 51 | 135 |
2016 December | 129 | 55 | 184 |
2016 November | 220 | 68 | 288 |
2016 October | 220 | 57 | 277 |
2016 September | 291 | 46 | 337 |
2016 August | 246 | 25 | 271 |
2016 July | 112 | 34 | 146 |
2016 June | 1 | 0 | 1 |
2016 March | 3 | 0 | 3 |
2016 February | 1 | 0 | 1 |
2016 January | 2 | 0 | 2 |
2015 December | 4 | 0 | 4 |
2015 October | 149 | 4 | 153 |
2015 September | 162 | 41 | 203 |
2015 August | 145 | 27 | 172 |
2015 July | 199 | 26 | 225 |
2015 June | 174 | 33 | 207 |
2015 May | 146 | 43 | 189 |
2015 April | 148 | 35 | 183 |
2015 March | 211 | 32 | 243 |
2015 February | 179 | 27 | 206 |
2015 January | 88 | 38 | 126 |
2014 December | 98 | 46 | 144 |
2014 November | 116 | 24 | 140 |
2014 October | 134 | 40 | 174 |
2014 September | 122 | 50 | 172 |
2014 August | 85 | 13 | 98 |
2014 July | 92 | 21 | 113 |
2014 June | 99 | 24 | 123 |
2014 May | 113 | 24 | 137 |
2014 April | 116 | 32 | 148 |
2014 March | 84 | 42 | 126 |
2014 February | 3 | 0 | 3 |
2014 January | 5 | 9 | 14 |
2013 December | 8 | 5 | 13 |