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array:24 [ "pii" => "S1665268119304387" "issn" => "16652681" "doi" => "10.5604/01.3001.0010.2789" "estado" => "S300" "fechaPublicacion" => "2017-09-01" "aid" => "70260" "copyright" => "Fundación Clínica Médica Sur, A.C." "copyrightAnyo" => "2017" "documento" => "article" "crossmark" => 0 "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "fla" "cita" => "Ann Hepatol. 2017;16:780-7" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 178 "formatos" => array:3 [ "EPUB" => 18 "HTML" => 104 "PDF" => 56 ] ] "itemSiguiente" => array:19 [ "pii" => "S1665268119304399" "issn" => "16652681" "doi" => "10.5604/01.3001.0010.2797" "estado" => "S300" "fechaPublicacion" => "2017-09-01" "aid" => "70261" "copyright" => "Fundación Clínica Médica Sur, A.C." "documento" => "article" "crossmark" => 0 "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "fla" "cita" => "Ann Hepatol. 2017;16:788-96" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 211 "formatos" => array:3 [ "EPUB" => 12 "HTML" => 144 "PDF" => 55 ] ] "en" => array:11 [ "idiomaDefecto" => true "titulo" => "Algorithm for Screening of Adrenal Function in Stable Patients with Cirrhosis" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => "en" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "788" "paginaFinal" => "796" ] ] "contieneResumen" => array:1 [ "en" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "f0025" "etiqueta" => "Figure 4" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr4.jpeg" "Alto" => 1098 "Ancho" => 1000 "Tamanyo" => 107063 ] ] "descripcion" => array:1 [ "en" => "<p id="sp0025" class="elsevierStyleSimplePara elsevierViewall">Proposed algorithm for the assessment of adrenal function in stable patients with cirrhosis. BTC: basal total cortisol. Sen: sensitivity. Spe: Specificity. PPV: positive predictive value. NPV: negative predictive value. CP: Child-Pugh. MELD: Model for End-stage Liver Disease. PTC: peak total cortisol. AI: adrenal insufficiency. NAF: normal adrenal function.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Jonathan Paz-Delgadillo, Roberto Monreal-Robles, Jesús Z. Villarreal-Pérez, Fernando J. Lavalle-González, Héctor J. Maldonado-Garza, Francisco J. Bosques-Padilla" "autores" => array:6 [ 0 => array:2 [ "nombre" => "Jonathan" "apellidos" => "Paz-Delgadillo" ] 1 => array:2 [ "nombre" => "Roberto" "apellidos" => "Monreal-Robles" ] 2 => array:2 [ "nombre" => "Jesús Z." "apellidos" => "Villarreal-Pérez" ] 3 => array:2 [ "nombre" => "Fernando J." "apellidos" => "Lavalle-González" ] 4 => array:2 [ "nombre" => "Héctor J." "apellidos" => "Maldonado-Garza" ] 5 => array:2 [ "nombre" => "Francisco J." "apellidos" => "Bosques-Padilla" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1665268119304399?idApp=UINPBA00004N" "url" => "/16652681/0000001600000005/v1_201905301208/S1665268119304399/v1_201905301208/en/main.assets" ] "itemAnterior" => array:19 [ "pii" => "S1665268119304375" "issn" => "16652681" "doi" => "10.5604/01.3001.0010.2787" "estado" => "S300" "fechaPublicacion" => "2017-09-01" "aid" => "70259" "copyright" => "Fundación Clínica Médica Sur, A.C." "documento" => "article" "crossmark" => 0 "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "fla" "cita" => "Ann Hepatol. 2017;16:772-9" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 134 "formatos" => array:3 [ "EPUB" => 10 "HTML" => 78 "PDF" => 46 ] ] "en" => array:11 [ "idiomaDefecto" => true "titulo" => "Validation of the Simplified Criteria for the Diagnosis of Autoimmune Hepatitis in Chilean-Hispanic Patients" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => "en" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "772" "paginaFinal" => "779" ] ] "contieneResumen" => array:1 [ "en" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "f0010" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 815 "Ancho" => 985 "Tamanyo" => 75921 ] ] "descripcion" => array:1 [ "en" => "<p id="sp0010" class="elsevierStyleSimplePara elsevierViewall">Distribution of patients according to the score obtained with the simplified criteria for the diagnosis of AIH. AIH: autoimmune hepatitis. n: amount of patients.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Roberto Candia, Blanca Norero, Carlos Agüero, Luis Díaz, Juan Pablo Ortega, Rodrigo Wolff, Cristian Hernández-Rocha, Ignacio Duarte, Alejandro Soza, Carlos Benítez, Marco Arrese" "autores" => array:11 [ 0 => array:2 [ "nombre" => "Roberto" "apellidos" => "Candia" ] 1 => array:2 [ "nombre" => "Blanca" "apellidos" => "Norero" ] 2 => array:2 [ "nombre" => "Carlos" "apellidos" => "Agüero" ] 3 => array:2 [ "nombre" => "Luis" "apellidos" => "Díaz" ] 4 => array:2 [ "nombre" => "Juan Pablo" "apellidos" => "Ortega" ] 5 => array:2 [ "nombre" => "Rodrigo" "apellidos" => "Wolff" ] 6 => array:2 [ "nombre" => "Cristian" "apellidos" => "Hernández-Rocha" ] 7 => array:2 [ "nombre" => "Ignacio" "apellidos" => "Duarte" ] 8 => array:2 [ "nombre" => "Alejandro" "apellidos" => "Soza" ] 9 => array:2 [ "nombre" => "Carlos" "apellidos" => "Benítez" ] 10 => array:2 [ "nombre" => "Marco" "apellidos" => "Arrese" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1665268119304375?idApp=UINPBA00004N" "url" => "/16652681/0000001600000005/v1_201905301208/S1665268119304375/v1_201905301208/en/main.assets" ] "en" => array:17 [ "idiomaDefecto" => true "titulo" => "Circulating levels of pentraxin-3 (PTX3) in patients with liver cirrhosis" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "780" "paginaFinal" => "787" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "Jéssica G. Pereira, Telma Erotides Silva, Emília T.O. Bansho, Edelton F. Morato, José T. Pinheiro, Letícia Muraro-Wildner, Maria Luiza Bazzo, Esther Buzaglo Dantas-Corrêa, Leonardo L. Schiavon, Janaína L. Narciso-Schiavon" "autores" => array:10 [ 0 => array:3 [ "nombre" => "Jéssica G." "apellidos" => "Pereira" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "aff1" ] ] ] 1 => array:3 [ "nombre" => "Telma" "apellidos" => "Erotides Silva" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">†</span>" "identificador" => "aff2" ] ] ] 2 => array:3 [ "nombre" => "Emília T.O." "apellidos" => "Bansho" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "aff1" ] ] ] 3 => array:3 [ "nombre" => "Edelton F." "apellidos" => "Morato" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">‡</span>" "identificador" => "aff3" ] ] ] 4 => array:3 [ "nombre" => "José T." "apellidos" => "Pinheiro" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">‡</span>" "identificador" => "aff3" ] ] ] 5 => array:3 [ "nombre" => "Letícia" "apellidos" => "Muraro-Wildner" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">§</span>" "identificador" => "aff4" ] ] ] 6 => array:3 [ "nombre" => "Maria" "apellidos" => "Luiza Bazzo" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">§</span>" "identificador" => "aff4" ] ] ] 7 => array:3 [ "nombre" => "Esther" "apellidos" => "Buzaglo Dantas-Corrêa" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "aff1" ] ] ] 8 => array:3 [ "nombre" => "Leonardo L." "apellidos" => "Schiavon" "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "aff1" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">†</span>" "identificador" => "aff2" ] ] ] 9 => array:4 [ "nombre" => "Janaína L." "apellidos" => "Narciso-Schiavon" "email" => array:1 [ 0 => "janaina.narciso@uol.com.br" ] "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "aff1" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor1" ] ] ] ] "afiliaciones" => array:4 [ 0 => array:3 [ "entidad" => "Núcleo de Estudos em Gastroenterologia e Hepatologia, Department of Internal Medicine, Federal University of Santa Catarina, Florianópolis, Santa Catarina, Brazil" "etiqueta" => "*" "identificador" => "aff1" ] 1 => array:3 [ "entidad" => "Postgraduate Program in Medical Sciences, Health Sciences Center, Federal University of Santa Catarina, Florianópolis, Santa Catarina,Brazil" "etiqueta" => "†" "identificador" => "aff2" ] 2 => array:3 [ "entidad" => "Center for Assessment of Allergic Type Reactions to Drugs, University Hospital Polydoro Ernani de São Thiago - Federal University of Santa Catarina, Florianópolis, Santa Catarina, Brazil" "etiqueta" => "‡" "identificador" => "aff3" ] 3 => array:3 [ "entidad" => "Clinical Analysis Laboratory, University Hospital Polydoro Ernani de São Thiago - Federal University of Santa Catarina, Florianópolis, Santa Catarina, Brazil" "etiqueta" => "§" "identificador" => "aff4" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor1" "etiqueta" => "*" "correspondencia" => "Correspondence and reprint request:" ] ] ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "f0010" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 669 "Ancho" => 957 "Tamanyo" => 38406 ] ] "descripcion" => array:1 [ "en" => "<p id="sp0010" class="elsevierStyleSimplePara elsevierViewall">Pentraxin 3 levels according to patient group.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="s0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0040">Introduction</span><p id="p0010" class="elsevierStylePara elsevierViewall">Liver cirrhosis is the most advanced stage of chronic liver disease. It is characterized histologically by the presence of regenerative nodules. Its prevalence is estimated at 0.27% in the United States,<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">1</span></a> and it is associated with multiple etiologies, most commonly ethanol consumption, chronic viral hepatitis B and C and diabetes mellitus.<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">1,2</span></a> In-hospital mortality for disease decompensation is 9.1% in South Korea<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">3</span></a> and is 25.0% after 30 days of admission in Brazil.<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">4</span></a> Identifying patients with worse prognosis would facilitate early management of potentially severe cases. Several prognostic markers have been studied to identify mortality associated with decompensated cirrhosis, including the Model for End-Stage Liver Disease (MELD) score and its derivatives, Acute-on-Chronic Liver Failure (ACLF) score, Interleukins 2, 6 and 8 (IL-2, IL-6 and IL-8, respectively), C-reactive protein (CRP) and even total leukocyte count.</p><p id="p0015" class="elsevierStylePara elsevierViewall">Pentraxins are proteins formed by 5 monomers that form a ring in radial symmetry. They are a class of pattern recognition receptors. Among pentraxins, the main ones are pentraxin-3, CRP and serum amyloid P component. PTX3 is a long-chain pentraxin considered an acute phase marker produced mainly by endothelial and vascular smooth muscle cells at the site of inflammation. It is also produced by macrophages, fibroblasts, neutrophils, epithelial cells, dendritic cells and other cell types both near and far from the inflammation site,<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">5,6</span></a> Pentraxin production is influenced by certain inflammatory stimuli such as interleukin 1 beta (IL-1β) and tumor necrosis factor alfa (TNF-α).<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">7</span></a> It differs considerably from CRP in terms of expression patterns by affected organs. In particular, this is a short pentraxin mainly produced in the liver in response to IL-6.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">8</span></a></p><p id="p0020" class="elsevierStylePara elsevierViewall">PTX3 has been recognized as an independent marker of inflammation associated with various disorders<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">8,9</span></a> such as atherosclerosis, cancer, respiratory diseases and central nervous system diseases in which increased levels are related to the risk of the disease or its progression.<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">10</span></a> However, according to our knowledge there are no studies that analyze its role in liver cirrhosis.</p><p id="p0025" class="elsevierStylePara elsevierViewall">The aim of this study is to describe PTX3 levels in ambulatory patients and hospitalized patients with liver cirrhosis and their association with disease prognosis.</p></span><span id="s0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0045">Material and Methods</span><span id="s0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0050">Sample</span><p id="p0030" class="elsevierStylePara elsevierViewall">This is a prospective cohort study with consecutive inclusion of patients with liver cirrhosis treated at the hepa-tology ambulatory department and admitted to the emergency service of a tertiary hospital in southern Brazil between January 2011 and January 2014 because of disease decompensation. Patients were excluded from the study because of insufficient clinical and laboratory data in the medical records, hepatocellular carcinoma that did not meet Milan criteria and refusal to participate in the study.</p><p id="p0035" class="elsevierStylePara elsevierViewall">During routine outpatient or emergency admission, subjects were asked to participate and sign the free and informed consent form. A family member or guardian would authorize data collection if the patient had encepha-lopathy grades III or IV. Clinical and laboratory variables were collected from interviews and from the medical records. The following clinical variables were studied: age, sex, skin color, etiology of cirrhosis and presence of ascites. Laboratory variables collected on admission included serum creatinine, MELD, Child-Pugh and Chronic Liver Failure - Sequential Organ Failure Assessment (CLIF-SOFA) scores, total leukocyte count, serum sodium, platelet count, international normalized ratio (INR), albumin, CRP and total bilirubin.</p><p id="p0040" class="elsevierStylePara elsevierViewall">The diagnosis of cirrhosis was established either histo-logically when liver biopsy was available or by a combination of clinical, imaging and laboratory data in patients with evidence of portal hypertension.</p><p id="p0045" class="elsevierStylePara elsevierViewall">PTX3 assays were performed by Enzyme-Linked Im-munosorbent Assay with serum samples collected on admission or at an outpatient visit and stored in a freezer at -80 °C (ELISA; R&D Systems - Minneapolis, MN).</p></span><span id="s0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0055">Methods</span><p id="p0050" class="elsevierStylePara elsevierViewall">Patients were followed during hospitalization and 90-day mortality was assessed by telephone in case of discharge. The 90-day mortality rates did not include patients who underwent liver transplantation (because they were excluded from the study).</p><p id="p0055" class="elsevierStylePara elsevierViewall">Individuals with suspected bacterial infection at admission underwent clinical examination to confirm the diagnosis and establish the primary source of infection. The diagnosis of infection was performed according to the criteria of the Center for Disease Control.<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">11</span></a> Diagnostic paracentesis was performed for all patients with ascites present at admission. Hepatic encephalopathy was graded according to the criteria of West-Haven.<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">12</span></a> If present, the precipitating factor was investigated and lactulose was administered with dose adjustment as needed.</p><p id="p0060" class="elsevierStylePara elsevierViewall">The severity of liver disease was estimated by Child-Pugh<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">13</span></a> and MELD scores<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">14</span></a> calculated based on laboratory tests performed on admission. ACLF and CLIF-SOFA were defined as proposed by the European Association for the Study of the Liver-Chronic Liver Failure (EASL-CLIF).<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">15</span></a></p></span><span id="s0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0060">Statistical analysis</span><p id="p0065" class="elsevierStylePara elsevierViewall">Numerical variables with normal distribution were expressed as the mean and standard deviation (SD) and were compared using Student's t test. Numerical variables with non-normal distribution were expressed as medians and compared using the Mann-Whitney test. The normality of variable distribution was determined by the Kolmorogov-Smirnov test. Qualitative variables were represented by frequency (%) and chi-square test or Fisher's exact test were used when needed for analysis. Bivariate analyses were performed to compare cirrhotic individuals from outpatient visits with hospitalized patients. Bivariate analysis was performed to compare the mean levels of PTX3 in terms of the presence of cirrhosis complications at time of admission. Spearman correlation analysis was performed to compare the values of serum PTX3 to the laboratory variables and prognostic markers MELD, Child-Pugh and CLIF-SOFA. A cutoff point for the PTX3 was determined by Receiver Operating Characteristic (ROC) curve. Survival probability was calculated using Kaplan-Meier method and differences in survival between groups were compared using the log-rank test.</p><p id="p0070" class="elsevierStylePara elsevierViewall">All tests were performed using the Statistical Package for the Social Sciences, version 22.0 (IBM SPSS statistics, Chicago, Illinois, USA). P values lower than 0.05 were considered statistically significant.</p><p id="p0075" class="elsevierStylePara elsevierViewall">The study protocol was in accordance with the ethical principles of the Declaration of Helsinki and was approved by the local research ethics committee under the number 252709.</p></span></span><span id="s0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0065">RESULTS</span><span id="s0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0070">Casuistry analysis</span><p id="p0080" class="elsevierStylePara elsevierViewall">Between January 2011 and January 2014, studied patients included 32 healthy controls, 29 subjects with liver cirrhosis treated at the hepatology ambulatory department and 130 cirrhotic patients admitted to the hospital for disease decompensation. <a class="elsevierStyleCrossRef" href="#t0010">Table 1</a> shows the demographic and epi-demiological characteristics of patients included in the study. The mean age of the controls was 41.8 ± 15.4 years and 78.0% were male. Individuals with cirrhosis had a mean age of 54.1 ± 11.7 years, 73.8% were male, 35.6% were Child-Pugh class C and the mean MELD score was 15.0 ± 6.2. Only seven patients underwent needle biopsy of the liver to diagnose cirrhosis. The etiology of cirrhosis was related to alcohol in 35.0%, alcohol and hepatitis C virus (HCV) in 22.5% and HCV only in 16.9%.</p><elsevierMultimedia ident="t0010"></elsevierMultimedia></span><span id="s0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0075">Comparative analysis of outpatient and hospitalized patients with liver cirrhosis</span><p id="p0085" class="elsevierStylePara elsevierViewall">Outpatients and hospitalized patients with liver cirrhosis had similar clinical characteristics except for skin color, in which there was a higher proportion of individuals with white skin color among outpatients (50.0% <span class="elsevierStyleItalic">vs.</span> 71.3%; p = 0.025). These characteristics are shown in <a class="elsevierStyleCrossRef" href="#t0010">table 1</a>. When comparing PTX3 levels between groups, it was observed that the cirrhotic outpatients had higher means compared to healthy controls (2.6 <span class="elsevierStyleItalic">vs.</span> 1.1 ng/mL; p < 0.001). Hospitalized cirrhotic patients had higher means compared both to healthy controls (3.8 <span class="elsevierStyleItalic">vs.</span> 1.1 ng/mL; p < 0.001) and to cirrhotic outpatients (3.8 <span class="elsevierStyleItalic">vs.</span> 2.6 ng/mL; p < 0.001) as can be seen in <a class="elsevierStyleCrossRef" href="#f0010">figure 1</a>.</p><elsevierMultimedia ident="f0010"></elsevierMultimedia></span><span id="s0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0080">Correlation analysis of PTX3 with variables of interest</span><p id="p0090" class="elsevierStylePara elsevierViewall">There was a positive correlation between serum levels of PTX3 and creatinine (r = 0.220; p = 0.012), MELD (r = 0.279; p = 0.001), Child-Pugh score (r = 0.224; p = 0.010) and CLIF-SOFA score (r = 0.225; p = 0.010). There was no correlation between PTX3 levels and total leukocyte count, serum sodium, platelet count, INR, albumin, CRP and total bilirubin.</p></span><span id="s0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0085">Comparative analysis of serum PTX3 levels according to complications on admission</span><p id="p0095" class="elsevierStylePara elsevierViewall">When comparing PTX3 levels in terms of the presence or absence of ACLF (<a class="elsevierStyleCrossRef" href="#f0015">Figure 2</a>), it was observed that patients with ACLF showed higher PTX3 medians than those without ACLF (8.0 <span class="elsevierStyleItalic">vs.</span> 3.1 ng/mL; p < 0.001). When comparing PTX3 levels according to MELD score (<a class="elsevierStyleCrossRef" href="#f0020">Figure 3</a>), it was observed that patients with MELD higher than 20 had higher median PTX3 levels compared to others (6.7 <span class="elsevierStyleItalic">vs.</span> 3.4 ng/mL; p = 0.002).</p><elsevierMultimedia ident="f0015"></elsevierMultimedia><elsevierMultimedia ident="f0020"></elsevierMultimedia><p id="p0100" class="elsevierStylePara elsevierViewall">When comparing PTX3 levels according to Child classification, it was observed that individuals in Child class C had similar levels of PTX3 to the others (3.9 <span class="elsevierStyleItalic">vs.</span> 3.6 ng/mL; p = 0.559). When comparing PTX3 levels in terms of the presence of complications of cirrhosis, similar levels of PTX3 were observed in subjects presenting decompensation in infection (4.5 <span class="elsevierStyleItalic">vs.</span> 3.5 ng/mL; p = 0.197), ascites (4.0 <span class="elsevierStyleItalic">vs.</span> 3.6 ng/mL; p = 0.384) and grades III or IV encephalopa-thy (4.2 <span class="elsevierStyleItalic">vs.</span> 3.0 ng/mL; p = 0.247).</p><p id="p0105" class="elsevierStylePara elsevierViewall">It was observed that the number of organ failures was associated with higher mean serum levels of PTX3 (<a class="elsevierStyleCrossRef" href="#f0025">Figure 4</a>) as follows: none = 3.2 ng/mL; one = 4.7 ng/mL; two or more failures = 8.0 ng/mL (p = 0.006).</p><elsevierMultimedia ident="f0025"></elsevierMultimedia></span><span id="s0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0090">Survival analysis according to serum levels of PTX3</span><p id="p0110" class="elsevierStylePara elsevierViewall">Forty patients died within 90 days (30.8%). It was observed that patients who died within 90 days had higher serum levels of PTX3 on admission compared to those who survived (5.3 <span class="elsevierStyleItalic">vs.</span> 3.4 ng/mL; p = 0.009). <a class="elsevierStyleCrossRef" href="#f0030">Figure 5</a> shows the Kaplan-Meier curves associated with serum PTX3 levels. The probability of survival of patients with serum levels of PTX3 higher than or equal to 5.4 ng/mL was 54.0%, while those with serum levels lower than 5.4 ng/mL showed a 90-day survival rate of higher than 77.0% (p = 0.002).</p><elsevierMultimedia ident="f0030"></elsevierMultimedia></span></span><span id="s0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0095">Discussion</span><p id="p0115" class="elsevierStylePara elsevierViewall">This study has identified unprecedentedly higher PTX3 levels in cirrhotic outpatients compared to healthy controls as well as higher levels in cirrhotic patients hospitalized for disease decompensation compared to cirrhotic outpatients. The higher PTX3 levels in patients with acute decompensation in comparison to cirrhotic outpatients and healthy controls is consistent with the results of studies that showed elevated PTX3 levels in diseases with an inflammatory component that affect other organs such as acute myocardial infarction,<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">16</span></a> chronic kidney disease,<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">17</span></a> acute respiratory distress syndrome (ARDS)<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">18</span></a> and severe infectious diseases affecting patients in intensive care.<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">19</span></a> Serum levels are positively correlated with disease severity.</p><p id="p0120" class="elsevierStylePara elsevierViewall">This finding is corroborated by the positive correlation between serum PTX3 levels and the scores associated with severity of liver cirrhosis (MELD, Child-Pugh and CLIF-SOFA). In patients in intensive care with systemic inflammatory response syndrome (SIRS), sepsis, severe sepsis and septic shock, there was also a positive correlation between serum PTX3 levels and the clinical severity scores APACHE II (Acute Physiology and Chronic Health Evaluation) and SAPS II (Simplified Acute Physiology Score).<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">19</span></a> PTX3 expression was evaluated serially in studies in patients with ARDS<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">18</span></a> and in patients with SIRS, sepsis, severe sepsis and septic shock.<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">19</span></a> In both studies it was observed that PTX3 was the first plasma protein to rise, with a peak at approximately 7.5 h in patients with SIRS or infections in the clinical spectrum of sepsis. Levels declined in patients with ARDS after 24 h of intu-bation.<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">18</span></a> CRP, a commonly used inflammation marker, had a later serum peak at approximately 24 h19 and remained elevated longer.<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">18</span></a> Mauri, et al. performed a preliminary retrospective study if patients with ARDS that also showed a positive correlation between PTX3 levels and the number of organ failures,<a class="elsevierStyleCrossRef" href="#bib0105"><span class="elsevierStyleSup">20</span></a> consistent with the results of this study.</p><p id="p0125" class="elsevierStylePara elsevierViewall">In this study a positive correlation was also observed between serum PTX3 levels and 90-day mortality, consistent with the results of other groups that evaluated mortality in patients with chronic kidney disease, acute myocardial infarction and ARDS. In these studies, PTX3 proved to be an important and early predictor of mortali-ty.<a class="elsevierStyleCrossRefs" href="#bib0090"><span class="elsevierStyleSup">17,18</span></a> In patients with SIRS, sepsis, severe sepsis or septic shock, both PTX3 and IL-6 showed significant positive correlations with mortality.<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">19</span></a> IL-6 was not assessed in this study. However, our group showed that IL-6 levels were positively associated with 90-day mortality (OR 1.002; 95% CI 1.000 - 1.004; p = 0.029).<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">21</span></a></p><p id="p0130" class="elsevierStylePara elsevierViewall">Many studies have compared the efficacy of PTX3 to CRP as a predictor of severity and mortality, given the widespread use of CRP for this purpose. The results as mentioned above show positive correlation when serum levels are compared without time reference. However, no correlation was apparent when considering the time to peak of each of these markers. In liver cirrhosis, however, CRP production is affected because it is synthesized almost entirely in the liver. This may compromise its utility as an inflammation biomarker in these patients.<a class="elsevierStyleCrossRefs" href="#bib0115"><span class="elsevierStyleSup">22,23</span></a> This might explain the absence of correlation between CRP and PTX3 in this study. However, Bota, <span class="elsevierStyleItalic">et al</span>. have not found statistically significant differences in CRP levels between intensive care patients with or without liver cirrhosis.<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">24</span></a> Lazzarotto, et al. demonstrated that CRP levels are sensitive for diagnosis of infection and as predictors of 90-day mortality in patients with cirrhosis.<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">25</span></a> Importantly, there is, to a lesser extent, production of CRP in inflamed tis-sues.<a class="elsevierStyleCrossRefs" href="#bib0135"><span class="elsevierStyleSup">26,27</span></a> This synthesis may be responsible for incomplete suppression of CRP levels even in patients with severe hepatic impairment.</p><p id="p0135" class="elsevierStylePara elsevierViewall">There was also a positive correlation between serum levels of PTX3 and creatinine. Due to its high molecular weight (40.6 KD) and multimeric structure, PTX3 levels appear to increase as the glomerular filtration rate (GFR) decreases secondary to reduced clearance.<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">17</span></a> The same phenomenon occurs with creatinine, it is therefore used as a marker of renal function. Numerous pathological conditions that lead to reduced GFR -such as sepsis, which generates numerous shunts in circulation and redistribution of blood volume; major bleeding, by an absolute reduction in blood volume; ascites, by third space volume retention and reduction of effective circulating volume-tend to increase serum creatinine. The complications of cirrhosis involve the above hemodynamic dysfunctions. One could imagine that this would be the reason for the positive correlation between serum levels of PTX3 and creatinine. However, more hemodynamic studies are needed to confirm this hypothesis.</p><p id="p0140" class="elsevierStylePara elsevierViewall">Although recently published studies present PTX3 as a marker of severity and/or mortality, little is known about its role <span class="elsevierStyleItalic">in vivo</span> in humans. Garlanda, et al. demonstrated in mice deficient in PTX3 that it has many functions including regulation of innate immunity against various microorganisms, discrimination of self- from non-self molecular patterns and tissue repair.<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">27</span></a> Other studies showed that the initial function of PTX3 is protective.<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">28</span></a> It participates in the recognition of harmful stimuli, migration of neutrophils to sites of infection and promotion of phagocytosis of bacteria by neutrophils,<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">29</span></a> enhancement of nitric oxide production<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">30</span></a> and increased expression of tissue factor.<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">31</span></a> However, the prolonged persistence of stimuli can lead to overexpression of PTX3 and amplification of these inflammatory pathways,<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">28</span></a> with resulting damage to the organism. Thus far, there are no known specific antagonists to the action of PTX3. Therefore, there are no data regarding blocking of this pathway and its repercussions.</p><p id="p0145" class="elsevierStylePara elsevierViewall">Finally, the relevance of this study relies on the current difficulty in early determination of the severity of cirrhotic patients. Hemodynamic disturbances hinder the use of SIRS criteria;<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">32</span></a> because the hyperdynamic circulatory state leads to tachycardia, beta-blocker use by many of these patients reduces the heart rate and can mask SIRS, hepatic encephalopathy can lead to tachyp-nea and hypersplenism caused by congestion of the portal system can lead to reductions in the number of circulating leukocytes.<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">33</span></a> Added to these factors are the immunological changes associated with advanced liver disease, probably related to deficiencies in the complement system, which impair the elimination of op-sonized bacteria and increased bacterial translocation.<a class="elsevierStyleCrossRefs" href="#bib0175"><span class="elsevierStyleSup">34-36</span></a> This in turn predisposes patients with liver cirrhosis to infections. Furthermore, cultures of micro-organisms knowingly take at least 24 to 48 h to present results, which hampers their utility for diagnosing infectious complications. Therefore, it is important to find early markers of severity and mortality to guide appropriate treatment.</p></span><span id="s0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0100">Conclusions</span><p id="p0150" class="elsevierStylePara elsevierViewall">Circulating levels of PTX3 are increased in patients with liver cirrhosis, particularly those with acute decompensation. Serum PTX3 is related to the severity of the disease, the presence of ACLF and 90-day mortality. These results are promising and indicate a potential use for PTX3 as an inflammatory and prognostic biomarker for patients with liver cirrhosis.</p></span><span id="s0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0105">Author Contributions</span><p id="p0155" class="elsevierStylePara elsevierViewall">Schiavon LL designed the study. Bansho ETO and Silva TE were responsible for data collection. Morato EF, Pinheiro JT, Pereira JG, Wildner LM and Bazzo ML performed the pentraxin-3 sample processing. Schiavon LL, Narciso-Schiavon JL and Pereira JG analyzed the data and are responsible for the article as a whole. Narciso-Schia-von JL and Pereira JG wrote the paper and Dantas-Correa EB and Schiavon LL revised the manuscript.</p></span><span id="s0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0110">Supportive Foundations</span><p id="p0160" class="elsevierStylePara elsevierViewall">This study was financed by Conselho Nacional de Desenvolvimento Científico e Técnológico (CNPq).</p><span id="s0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0115">Institutional review board statement</span><p id="p0165" class="elsevierStylePara elsevierViewall">The study was reviewed and approved by the Federal University of Santa Catarina Institutional Review Board under the number 252709.</p></span></span><span id="s0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0120">Informed Consent Statement</span><p id="p0170" class="elsevierStylePara elsevierViewall">All study participants or their respective legal guardians provided written informed consent prior to study enrollment.</p></span><span id="s0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0125">Conflicts of Interest</span><p id="p0175" class="elsevierStylePara elsevierViewall">The authors declare no conflicts of interest.</p></span><span id="s0100" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0130">Data Sharing Statement</span><p id="p0180" class="elsevierStylePara elsevierViewall">No additional data are available.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:13 [ 0 => array:3 [ "identificador" => "xres1197558" "titulo" => "Abstract" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abs0010" "titulo" => "Background" ] 1 => array:2 [ "identificador" => "abs0015" "titulo" => "Material and methods" ] 2 => array:2 [ "identificador" => "abs0020" "titulo" => "Results" ] 3 => array:2 [ "identificador" => "abs0025" "titulo" => "Conclusion" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec1116244" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "s0010" "titulo" => "Introduction" ] 3 => array:3 [ "identificador" => "s0015" "titulo" => "Material and Methods" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "s0020" "titulo" => "Sample" ] 1 => array:2 [ "identificador" => "s0025" "titulo" => "Methods" ] 2 => array:2 [ "identificador" => "s0030" "titulo" => "Statistical analysis" ] ] ] 4 => array:3 [ "identificador" => "s0035" "titulo" => "RESULTS" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "s0040" "titulo" => "Casuistry analysis" ] 1 => array:2 [ "identificador" => "s0045" "titulo" => "Comparative analysis of outpatient and hospitalized patients with liver cirrhosis" ] 2 => array:2 [ "identificador" => "s0050" "titulo" => "Correlation analysis of PTX3 with variables of interest" ] 3 => array:2 [ "identificador" => "s0055" "titulo" => "Comparative analysis of serum PTX3 levels according to complications on admission" ] 4 => array:2 [ "identificador" => "s0060" "titulo" => "Survival analysis according to serum levels of PTX3" ] ] ] 5 => array:2 [ "identificador" => "s0065" "titulo" => "Discussion" ] 6 => array:2 [ "identificador" => "s0070" "titulo" => "Conclusions" ] 7 => array:2 [ "identificador" => "s0075" "titulo" => "Author Contributions" ] 8 => array:3 [ "identificador" => "s0080" "titulo" => "Supportive Foundations" "secciones" => array:1 [ 0 => array:2 [ "identificador" => "s0085" "titulo" => "Institutional review board statement" ] ] ] 9 => array:2 [ "identificador" => "s0090" "titulo" => "Informed Consent Statement" ] 10 => array:2 [ "identificador" => "s0095" "titulo" => "Conflicts of Interest" ] 11 => array:2 [ "identificador" => "s0100" "titulo" => "Data Sharing Statement" ] 12 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2016-10-27" "fechaAceptado" => "2017-03-20" "PalabrasClave" => array:1 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec1116244" "palabras" => array:7 [ 0 => "Liver cirrhosis" 1 => "Inflammation" 2 => "Biomarkers" 3 => "PTX3 protein" 4 => "Prognosis" 5 => "Acute-On-Chronic Liver Failure" 6 => "Mortality" ] ] ] ] "tieneResumen" => true "resumen" => array:1 [ "en" => array:3 [ "titulo" => "Abstract" "resumen" => "<span id="abs0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0015"><span class="elsevierStyleBold">Background</span></span><p id="sp0045" class="elsevierStyleSimplePara elsevierViewall">Despite the circulating levels of PTX3 were related to the severity of various diseases, there are no studies investigating its role in patients with liver cirrhosis. We aimed to study PTX3 levels in patients with liver cirrhosis.</p></span> <span id="abs0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0020"><span class="elsevierStyleBold">Material and methods</span></span><p id="sp0050" class="elsevierStyleSimplePara elsevierViewall">A prospective cohort study included 130 patients hospitalized for acute decompensation of liver cirrhosis, 29 stable cirrhotic outpatients and 32 healthy controls evaluated in a tertiary hospital in Southern Brasil.</p></span> <span id="abs0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0025"><span class="elsevierStyleBold">Results</span></span><p id="sp0055" class="elsevierStyleSimplePara elsevierViewall">The median PTX3 level was significantly higher in stable cirrhotic patients compared to controls (2.6 <span class="elsevierStyleItalic">vs</span>. 1.1 ng/mL; p < 0.001), hospitalized cirrhotic patients compared to controls (3.8 <span class="elsevierStyleItalic">vs</span>. 1.1 ng/mL; p < 0.001), and hospitalized cirrhotic patients compared to stable cirrhotic patients (3.8 <span class="elsevierStyleItalic">vs</span>. 2.6 ng/ mL; p = 0.001). A positive correlation was found between PTX3 and serum creatinine (r = 0.220; p = 0.012), Chronic Liver Failure -Sequential Organ Failure Assessment score (CLIF-SOFA) (r = 0.220; p = 0.010), MELD (r = 0.279; p = 0.001) and Child-Pugh score (r = 0.224; p = 0.010). Significantly higher levels of PTX3 were observed in patients on admission with ACLF (8.9 <span class="elsevierStyleItalic">vs</span>. 3.1 ng/mL; p < 0.001) and MELD score ≥ 20 (6.6 <span class="elsevierStyleItalic">vs</span>. 3.4 ng/mL; p = 0.002). Death within 90 days occurred in 30.8% of patients and was associated with higher levels of PTX3 (5.3 <span class="elsevierStyleItalic">vs</span>. 3.4 ng/mL; p = 0.009). The probability of Kaplan-Meier survival was 77.0% in patients with PTX-3 < 5.3 ng mL (upper tercile) and 53.5% in those with PTX3 ≥ 5.3 ng/mL (p = 0.002).</p></span> <span id="abs0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0030"><span class="elsevierStyleBold">Conclusion</span></span><p id="sp0060" class="elsevierStyleSimplePara elsevierViewall">These results indicate the potential for use of PTX3 as an inflammatory biomarker for the prognosis of patients with hepatic cirrhosis.</p></span>" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abs0010" "titulo" => "Background" ] 1 => array:2 [ "identificador" => "abs0015" "titulo" => "Material and methods" ] 2 => array:2 [ "identificador" => "abs0020" "titulo" => "Results" ] 3 => array:2 [ "identificador" => "abs0025" "titulo" => "Conclusion" ] ] ] ] "multimedia" => array:6 [ 0 => array:7 [ "identificador" => "f0010" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 669 "Ancho" => 957 "Tamanyo" => 38406 ] ] "descripcion" => array:1 [ "en" => "<p id="sp0010" class="elsevierStyleSimplePara elsevierViewall">Pentraxin 3 levels according to patient group.</p>" ] ] 1 => array:7 [ "identificador" => "f0015" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 675 "Ancho" => 946 "Tamanyo" => 28047 ] ] "descripcion" => array:1 [ "en" => "<p id="sp0015" class="elsevierStyleSimplePara elsevierViewall">Pentraxin 3 levels according to the presence or absence of Acute-on-Chronic Liver Failure (ACLF).</p>" ] ] 2 => array:7 [ "identificador" => "f0020" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 713 "Ancho" => 961 "Tamanyo" => 30805 ] ] "descripcion" => array:1 [ "en" => "<p id="sp0020" class="elsevierStyleSimplePara elsevierViewall">Pentraxin 3 levels according to Model for End-Stage Liver Disease (MELD) score.</p>" ] ] 3 => array:7 [ "identificador" => "f0025" "etiqueta" => "Figure 4" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr4.jpeg" "Alto" => 725 "Ancho" => 969 "Tamanyo" => 31856 ] ] "descripcion" => array:1 [ "en" => "<p id="sp0025" class="elsevierStyleSimplePara elsevierViewall">Pentraxin 3 levels according to the number of organ failures.</p>" ] ] 4 => array:7 [ "identificador" => "f0030" "etiqueta" => "Figure 5" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr5.jpeg" "Alto" => 846 "Ancho" => 2078 "Tamanyo" => 93206 ] ] "descripcion" => array:1 [ "en" => "<p id="sp0030" class="elsevierStyleSimplePara elsevierViewall">Ninety days survival according to pentraxin 3 levels</p>" ] ] 5 => array:7 [ "identificador" => "t0010" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="sp0040" class="elsevierStyleSimplePara elsevierViewall">χ: Chi-square test. f: Fisher's exact test. t: Student's t test.</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"><th 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" scope="col" style="border-bottom: 2px solid black">Characteristic \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th 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" scope="col" style="border-bottom: 2px solid black">Outpatients \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th 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" scope="col" style="border-bottom: 2px solid black">Emergency \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th 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" scope="col" style="border-bottom: 2px solid black">p \t\t\t\t\t\t\n \t\t\t\t\t\t</th></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">Male \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">86.7% \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">70.8% \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">0.074 <span class="elsevierStyleItalic">χ</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">White skin color \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">50.0% \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">71.3% \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">0.025 <span class="elsevierStyleItalic">χ</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">Diabetes mellitus \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">23.3% \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">23.4% \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">0.990 <span class="elsevierStyleItalic">χ</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">Systemic arterial hypertension \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">30.0% \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">21.7% \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">0.333 <span class="elsevierStyleItalic">χ</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">Human immunodeficiency virus \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">3.3% \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">3.1% \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">1.000 <span class="elsevierStyleItalic">f</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">Previous alcoholism \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">76.7% \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">69.0% \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">0.411 <span class="elsevierStyleItalic">t</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">Current alcoholism \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">36.7% \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">36.9% \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">0.979 <span class="elsevierStyleItalic">t</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">Previous decompensation \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">50.0% \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">64.3% \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">0.148 <span class="elsevierStyleItalic">χ</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">Child-Pugh A \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">10.0% \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">15.4% \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">0.572 <span class="elsevierStyleItalic">f</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">Child-Pugh B \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">63.3% \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">46.9% \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">0.105 <span class="elsevierStyleItalic">χ</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">Child-Pugh C \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">26.7% \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">37.7% \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">0.256 <span class="elsevierStyleItalic">χ</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">Model for End-Stage Liver Disease \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">10.8 ± 2.4 \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">15.9 ± 6.4 \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"><0.001 <span class="elsevierStyleItalic">t</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">Etiology = hepatitis B virus \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">13.3% \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">19.2% \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">0.450 <span class="elsevierStyleItalic">χ</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">Etiology = hepatitis C virus \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">36.7% \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">40.0% \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">0.736 <span class="elsevierStyleItalic">χ</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">Etiology = alcoholism \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">66.7% \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">56.5% \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">0.328 <span class="elsevierStyleItalic">χ</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab2045118.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="sp0035" class="elsevierStyleSimplePara elsevierViewall">Demographic and epidemiological characteristics of the sample, according to the origin of the patients.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bs0010" "bibliografiaReferencia" => array:36 [ 0 => array:3 [ "identificador" => "bib0010" "etiqueta" => "1." 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Year/Month | Html | Total | |
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2024 November | 5 | 1 | 6 |
2024 October | 22 | 8 | 30 |
2024 September | 31 | 9 | 40 |
2024 August | 39 | 7 | 46 |
2024 July | 31 | 7 | 38 |
2024 June | 22 | 8 | 30 |
2024 May | 20 | 10 | 30 |
2024 April | 38 | 6 | 44 |
2024 March | 30 | 4 | 34 |
2024 February | 23 | 4 | 27 |
2024 January | 13 | 3 | 16 |
2023 December | 4 | 4 | 8 |
2023 November | 13 | 4 | 17 |
2023 October | 22 | 7 | 29 |
2023 September | 10 | 3 | 13 |
2023 August | 24 | 3 | 27 |
2023 July | 20 | 6 | 26 |
2023 June | 19 | 2 | 21 |
2023 May | 48 | 0 | 48 |
2023 April | 55 | 2 | 57 |
2023 March | 36 | 4 | 40 |
2023 February | 25 | 0 | 25 |
2023 January | 18 | 6 | 24 |
2022 December | 38 | 7 | 45 |
2022 November | 28 | 8 | 36 |
2022 October | 63 | 10 | 73 |
2022 September | 35 | 7 | 42 |
2022 August | 38 | 13 | 51 |
2022 July | 35 | 6 | 41 |
2022 June | 29 | 11 | 40 |
2022 May | 56 | 10 | 66 |
2022 April | 72 | 12 | 84 |
2022 March | 124 | 12 | 136 |
2022 February | 126 | 7 | 133 |
2022 January | 106 | 18 | 124 |
2021 December | 112 | 14 | 126 |
2021 November | 77 | 9 | 86 |
2021 October | 59 | 12 | 71 |
2021 September | 31 | 12 | 43 |
2021 August | 59 | 6 | 65 |
2021 July | 38 | 12 | 50 |
2021 June | 25 | 5 | 30 |
2021 May | 27 | 15 | 42 |
2021 April | 89 | 27 | 116 |
2021 March | 79 | 28 | 107 |
2021 February | 44 | 8 | 52 |
2021 January | 30 | 10 | 40 |
2020 December | 30 | 8 | 38 |
2020 November | 53 | 17 | 70 |
2020 October | 31 | 5 | 36 |
2020 September | 32 | 9 | 41 |
2020 August | 21 | 7 | 28 |
2020 July | 32 | 11 | 43 |
2020 June | 25 | 6 | 31 |
2020 May | 23 | 9 | 32 |
2020 April | 22 | 2 | 24 |
2020 March | 31 | 6 | 37 |
2020 February | 21 | 5 | 26 |
2020 January | 19 | 7 | 26 |
2019 December | 23 | 5 | 28 |
2019 November | 12 | 6 | 18 |
2019 October | 17 | 7 | 24 |
2019 September | 8 | 6 | 14 |
2019 August | 1 | 3 | 4 |
2019 July | 3 | 7 | 10 |
2019 June | 9 | 9 | 18 |
2019 May | 2 | 5 | 7 |