was read the article
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=> array:5 [ "identificador" => "fig0020" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => false "mostrarDisplay" => true "figura" => array:1 [ 0 => array:4 [ "imagen" => "fx1.jpeg" "Alto" => 886 "Ancho" => 1575 "Tamanyo" => 191639 ] ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Maria Sorribas, Anna Casajoana, Lucía Sobrino, Víctor Admella, Javier Osorio, Jordi Pujol-Gebellí" "autores" => array:6 [ 0 => array:2 [ "nombre" => "Maria" "apellidos" => "Sorribas" ] 1 => array:2 [ "nombre" => "Anna" "apellidos" => "Casajoana" ] 2 => array:2 [ "nombre" => "Lucía" "apellidos" => "Sobrino" ] 3 => array:2 [ "nombre" => "Víctor" "apellidos" => "Admella" ] 4 => array:2 [ "nombre" => "Javier" "apellidos" => "Osorio" ] 5 => array:2 [ "nombre" => "Jordi" "apellidos" => "Pujol-Gebellí" ] ] ] ] "resumen" => array:1 [ 0 => array:3 [ "titulo" => "Graphical abstract" "clase" => "graphical" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0045" 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membrane of abdominopelvic and thoracic cavities of rats" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "209" "paginaFinal" => "214" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "Francisco Rivas, Rosa-María Penin, Iván Macía, Anna Ureña, Carlos Déniz, Álvaro Gimeno, Ignacio Escobar, Ricard Ramos" "autores" => array:8 [ 0 => array:4 [ "nombre" => "Francisco" "apellidos" => "Rivas" "email" => array:1 [ 0 => "frivas@bellvitgehospital.cat" ] "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0005" ] ] ] 1 => array:3 [ "nombre" => "Rosa-María" "apellidos" => "Penin" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 2 => array:3 [ "nombre" => "Iván" "apellidos" => "Macía" "referencia" => 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"<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] ] ] ] "afiliaciones" => array:4 [ 0 => array:3 [ "entidad" => "Department of Thoracic Surgery, Hospital Universitari de Bellvitge, Medical School, University of Barcelona, L’Hospitalet de Llobregat, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Department of Pathology, Hospital Universitari de Bellvitge, Medical School, University of Barcelona, L’Hospitalet de Llobregat, Spain" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Department of Thoracic Surgery, Hospital Universitari de Bellvitge and Unit of Human Anatomy and Embryology, Medical School, University of Barcelona, L’Hospitalet de Llobregat, Spain" "etiqueta" => "c" "identificador" => "aff0015" ] 3 => array:3 [ "entidad" => "Animal Laboratory, Campus Ciències de la Salut de Bellvitge, Universitat de Barcelona, L’Hospitalet de Llobregat, Spain" "etiqueta" => "d" "identificador" => "aff0020" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "<span class="elsevierStyleItalic">Corresponding author</span>." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Eficacia de la pleurodesis por hipertermia: un estudio experimental comparativo sobre la membrana serosa de las cavidades abdominopélvica y torácica de ratas" ] ] "resumenGrafico" => array:2 [ "original" => 1 "multimedia" => array:5 [ "identificador" => "fig0025" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => false "mostrarDisplay" => true "figura" => array:1 [ 0 => array:4 [ "imagen" => "fx1.jpeg" "Alto" => 740 "Ancho" => 1333 "Tamanyo" => 98506 ] ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Pleurodesis is the main treatment choice to prevent the accumulation of air or liquid in the pleural space caused by pneumothorax or pleural effusion. There are different pleurodesis procedures: chemical pleurodesis, mechanical pleurodesis or a combination of both. There are different chemical agents such as talc, polidocanol, tetracyclines, autologous blood, iodopovidone or hyperthermic saline solution with a greater or lesser effectiveness.<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">1–7</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Few studies have shown the efficacy of hyperthermia without chemotherapy as a sclerosing agent to treat malignant pleural effusion.<a class="elsevierStyleCrossRefs" href="#bib0170"><span class="elsevierStyleSup">7–9</span></a> Pneumothorax is defined as the collection of air in the pleural space between the lung and the chest wall. Primary pneumothoraces can arise in otherwise healthy people without any lung disease. In a recent epidemiological study, primary spontaneous pneumothorax (PSP) occurred in 7.4–18 cases (age-adjusted incidence) per 100,000 population each year in males, and 1.2–6 cases per 100,000 population each year in females. The exact pathogenesis of PSP is unknown.<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">10</span></a> Secondary spontaneous pneumothorax has its origin on various diseases, including infectious processes, interstitial lung disease, connective tissue disease, and chronic obstructive pulmonary disease (COPD). Among the associated conditions, cystic fibrosis and COPD are the most commonly reported.<a class="elsevierStyleCrossRefs" href="#bib0190"><span class="elsevierStyleSup">11–13</span></a> Pleural effusion is a common complication of advanced cancers that may affect the performance status of patients. Pleural effusion can also exacerbate symptoms such as dyspnea and chest pain, which can be distressing for patients. These patients may undergo repeated interventions in search of relief from their symptoms.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">14</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">The aim of this paper is to study the changes in the pleural and/or peritoneal cavity after hyperthermia-induced pleurodesis (hyperthermic saline solution or filtrate hot air), testing the comparative capability of acute hyperthermia for producing pleurodesis in rats.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Materials and methods</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Animal groups</span><p id="par0020" class="elsevierStylePara elsevierViewall">Our study included 35 male and female rats (<span class="elsevierStyleItalic">Sprague-Dawley</span>) that were 6–9 months old and weighed 400–900<span class="elsevierStyleHsp" style=""></span>g. The Ethics Committee of our home institution (Universitat de Barcelona) approved the experimental procedures before. All animals were maintained in adequate cages and fed according to protocol. The animal laboratory at the Barcelona University housed the rat cages and was also the place where the operations took place. Our study was performed in the peritoneal cavity of the test-rats, instead of the pleural cavity, to avoid the risk of severe pneumothorax and mediastinal complications that are associated with the intrapleural administration of saline solution or hot air. However, talc was instilled in five animals to confirm the same lesions in both serous membranes. Although temperatures above 43° have been proved to be ineffective or only as effective as lower temperatures,<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">15</span></a> we decided a hyperthermic treatment at 45° and 50<span class="elsevierStyleHsp" style=""></span>°C because of the higher basal temperature of rats relative to humans.</p><p id="par0025" class="elsevierStylePara elsevierViewall">The test-rats were assigned to the following groups:</p><p id="par0030" class="elsevierStylePara elsevierViewall">Group A: composed of 10 animals that received an intraperitoneal administration of 20<span class="elsevierStyleHsp" style=""></span>mg of talc- (Mg<span class="elsevierStyleInf">3</span>Si<span class="elsevierStyleInf">4</span>O<span class="elsevierStyleInf">10</span>(OH)<span class="elsevierStyleInf">2</span>) (Steritalc, Novatech, La Ciotat, France) in 1<span class="elsevierStyleHsp" style=""></span>ml normal saline (extrapolated from the usual dose of 3–5<span class="elsevierStyleHsp" style=""></span>g for a 70<span class="elsevierStyleHsp" style=""></span>kg adult man). Five of these rats received also intrapleural dose at the same time, in order to confirm that intrapleural and intraperitoneal effects show no differences.</p><p id="par0035" class="elsevierStylePara elsevierViewall">Group B: composed of 5 control animals that received an intraperitoneal administration of 100<span class="elsevierStyleHsp" style=""></span>ml of 0.9% normal saline solution at 25° for 15<span class="elsevierStyleHsp" style=""></span>min.</p><p id="par0040" class="elsevierStylePara elsevierViewall">Group C: composed of 10 animals that received an intraperitoneal administration of 100<span class="elsevierStyleHsp" style=""></span>ml of 0.9% normal saline solution at 45° for 15<span class="elsevierStyleHsp" style=""></span>min.</p><p id="par0045" class="elsevierStylePara elsevierViewall">Group D: composed of 10 animals that received an intraperitoneal administration of filtrate air at 50° for 15<span class="elsevierStyleHsp" style=""></span>min, with 10<span class="elsevierStyleHsp" style=""></span>ml instillations of normal saline every 5<span class="elsevierStyleHsp" style=""></span>min.</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Experimental protocol</span><p id="par0050" class="elsevierStylePara elsevierViewall">All animals were anesthetized by isoflurane inhalation. Following the preparation of the operative field with povidone–iodine, five rats of group A received a 4-mm upper midline laparotomy (subxiphoid incision). Then, we administered 20<span class="elsevierStyleHsp" style=""></span>mg of talc in 1<span class="elsevierStyleHsp" style=""></span>ml of normal saline through a 16-gauge intravenous catheter, which was instilled in the left pleural cavity and in the peritoneal cavity. The remaining five rats underwent the same procedure but only in the peritoneal cavity.</p><p id="par0055" class="elsevierStylePara elsevierViewall">The same procedure (B, 100<span class="elsevierStyleHsp" style=""></span>ml of 0.9% normal saline solution; C, hyperthermic 0.9% normal saline solution; and D, filtrate hot air) was given for the other treatments groups. Body temperature was recorded in animals belonging to groups C and D using a rectal control. We rotated the animals with the purpose of distributing correctly the agents to the whole peritoneal space. Muscles and skin were sutured with a routine 2-layer continuous pattern using 2-0 Vicryl (Ethicon, Inc., Somerville, New Jersey). All animals received a subcutaneous dose of 0.2–0.3<span class="elsevierStyleHsp" style=""></span>ml buprenorphine for three days. No surgery-related deaths or complications were recorded.</p><p id="par0060" class="elsevierStylePara elsevierViewall">On the 21st day after the procedure all animals were euthanized by CO<span class="elsevierStyleInf">2</span> inhalation. We evaluated both the thoracic and abdominal cavities in five rats of group A. However, only the abdominal cavity was evaluated in the remaining rats. Macroscopic examinations of the pleural and peritoneal cavities were scored as 0 for <span class="elsevierStyleItalic">no adhesions</span> and 1 for <span class="elsevierStyleItalic">adhesions present</span>.</p><p id="par0065" class="elsevierStylePara elsevierViewall">We collected representative tissue sections of the parietal pleura, parietal peritoneum, lung (visceral pleura), liver, brain and spleen for the microscopic analysis. The specimens were formalin-fixed and embedded in paraffin blocs. Using the standard methodology, we cut sections of 4–5<span class="elsevierStyleHsp" style=""></span>μm thickness, staining the samples with hematoxylin-eosin (HE) and Masson's trichrome (MT), that stain green the fibrosis and collagen. Tissues were graded as 0 for the <span class="elsevierStyleItalic">absence</span> or 1 for the <span class="elsevierStyleItalic">presence</span> of inflammation and fibrosis.</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Statistical analysis</span><p id="par0070" class="elsevierStylePara elsevierViewall">We used SPSS v. 17.0 software package (SPSS Chicago, IL, USA) for the statistical analysis. We performed a descriptive univariate analysis, with the quantitative variables expressed as the means<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>standard deviations. The means of the continuous variables were then compared using a Kruskal–Wallis rank test. <span class="elsevierStyleItalic">p</span> values under 0.05 were considered statistically significant.</p></span></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Results</span><p id="par0075" class="elsevierStylePara elsevierViewall">The intrapleural administration of talc, saline solution or a filtrate hot air did not cause distress or other complications in any of the animals. We did not record significant differences in the mean weights among the four groups of animals (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0.05).</p><p id="par0080" class="elsevierStylePara elsevierViewall">Four of the five rats (80%) of group A that received intraperitoneal and intrapleural administrations of talc showed few adhesions on the injection side between the pleural layers and also between the peritoneal layers. The microscopic study of these rats showed histological injuries in both the pleural and peritoneal mesothelium. There was a dense foreign body giant cell reaction with of granulomas that contained abundant birefringence talc crystals engulfed by giant cells. We also detected the presence of histiocites and some lymphocytes, as well as fibrosis of the submesothelial tissue. The microscopic results comparing pleural and peritoneal mesothelia showed similar effects and no significant differences (<a class="elsevierStyleCrossRefs" href="#fig0005">Figs. 1 and 2</a>). No systemic distribution of talc was observed in the brain, spleen or liver (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>).</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0085" class="elsevierStylePara elsevierViewall">No adhesions (score: 0<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0) were recorded in groups B, C, and D. Microscopically, we observed chronic lymphocytic inflammation in one rat of group C, without fibrosis or mesothelial proliferation.</p><p id="par0090" class="elsevierStylePara elsevierViewall">There was no evidence of inflammatory response in groups D and B (<a class="elsevierStyleCrossRef" href="#fig0020">Fig. 4</a>, <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>).</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0095" class="elsevierStylePara elsevierViewall">The mean weights of group C were 548.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>174 and 638.7<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>185, before and after the intraperitoneal administration of the hyperthermic saline solution respectively. The rectal temperature increased by an average of 0.6 degrees (presurgery: 37.9<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.5; postsurgery: 38.3<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.5). Similarly, the temperature also increased after the filtrate hot air was administered to rats of group D (presurgery: 37.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.7; postsurgery: 38.5<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.4).</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Discussion</span><p id="par0100" class="elsevierStylePara elsevierViewall">Our results indicate that acute hyperthermia does not induce macroscopic or microscopic lesions such as inflammation, fibrosis or proliferation in peritoneal space. However, Giovanella et al.<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">22</span></a> suggested that hyperthermia is tumoricidal and induces high levels of proinflammatory proteins and cytokines, such as MIP-2, KC, RANTES and MCP-5. Also, hyperthermia may be chemo-attractant for polymorphonuclear leukocytes, monocytes and macrophages.<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">16</span></a> Hyperthermia probably produces these changes acutely rather than chronically. Kimura et al.<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">7</span></a> reported good results with hyper thermotherapy to treat malignant pleural effusion. More recently, Moon et al.<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">8</span></a> studied the effect of hyperthermia by thoracoscopy to treat malignant pleural effusion with good results. In patients with malignant pleural effusion, the intrapleural administration of chemotherapeutic drugs seems to improve the survival rate.<a class="elsevierStyleCrossRefs" href="#bib0220"><span class="elsevierStyleSup">17,18</span></a> A combination of hyperthermia and chemotherapy has also produced good results in terms of survival rate and quality of life by reducing pleural effusion.<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">19,20</span></a></p><p id="par0105" class="elsevierStylePara elsevierViewall">Li et al.<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">9</span></a> through an experimental study have confirmed that the therapeutic effect of hyperthermia without chemotherapy depends on time, temperature and depth. They observed that the response is greater in parietal pleural malignancies than in visceral malignancies. In our study the animals received normal saline solution at 45° for 15<span class="elsevierStyleHsp" style=""></span>min, our opinion is that the perfusion time is an important factor to show pleural inflammation.</p><p id="par0110" class="elsevierStylePara elsevierViewall">No clear surgical technique has emerged as a preferred treatment of choice after the long debate of choosing the ideal method for the management of recurrent pneumothorax and pleural effusion. Pleurodesis is the primary aim of the treatment. However, alternatives involve pleural abrasion and/or the intrapleural instillation of sclerosing agents in the pneumothorax, and also intrapleural instillation of sclerosing agents in pleural effusion. Several chemical agents have been used as sclerosing agents, including tetracycline, iodopovidone, silver nitrate, doxycycline, interleukins, chemotherapeutic drugs and talc.<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">6</span></a> Both the British Thoracic Society and the American College of Chest Physicians have developed guidelines for treating pleural disease, but these guidelines are not uniformly followed because treatment protocols vary among institutions.<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">21</span></a> Antunes et al.<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">22</span></a> concluded that an ideal sclerosing agent should possess several essential qualities, including high molecular weight and chemical polarity, low regional clearance, rapid systemic clearance, and a steep dose-response curve. Also, the sclerosing agent needs to be well tolerated and produce minimal to no side effects. Among the known sclerosing agents, talc currently presents the best results,<a class="elsevierStyleCrossRefs" href="#bib0250"><span class="elsevierStyleSup">23,24</span></a> being the systemic dispersion of talc dependent on its type.<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">5</span></a> The good results of talc pleurodesis were first described more than 20 years ago.<a class="elsevierStyleCrossRefs" href="#bib0260"><span class="elsevierStyleSup">25,26</span></a> However, the benefits of the procedure were later questioned due to possible side effects, although Shaw and Agarwal<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">27</span></a> described talc as the most effective agent for pleurodesis, with thoracoscopic pleurodesis as their technique of choice.</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Conclusions</span><p id="par0115" class="elsevierStylePara elsevierViewall">Through this experimental study, we can conclude that acute hyperthermia apparently does not induce fibrosis, proliferation or inflammation in the mesothelium, thus not producing the macroscopic and microscopic lesions that are requisite for pleurodesis. Because of that, it should not be considered to perform pleurodesis. However, talc is an excellent method for producing pleuro-peritoneal inflammatory lesions.</p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Authors’ contributions</span><p id="par0120" class="elsevierStylePara elsevierViewall">RR generated the hypothesis. IE, CD, AU, AG, FR and RR designed the study. RP performed the pathological study. FR and RR wrote the manuscript.</p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Conflict of interest</span><p id="par0125" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflict of interest.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:14 [ 0 => array:3 [ "identificador" => "xres1704745" "titulo" => "Graphical abstract" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0005" ] ] ] 1 => array:3 [ "identificador" => "xres1704744" "titulo" => "Abstract" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "abst0010" "titulo" => "Background" ] 1 => array:2 [ "identificador" => "abst0015" "titulo" => "Objectives" ] 2 => array:2 [ "identificador" => "abst0020" "titulo" => "Methods" ] 3 => array:2 [ "identificador" => "abst0025" "titulo" => "Results" ] 4 => array:2 [ "identificador" => "abst0030" "titulo" => "Conclusions" ] ] ] 2 => array:2 [ "identificador" => "xpalclavsec1509082" "titulo" => "Keywords" ] 3 => array:3 [ "identificador" => "xres1704743" "titulo" => "Resumen" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "abst0035" "titulo" => "Introducción" ] 1 => array:2 [ "identificador" => "abst0040" "titulo" => "Objetivo" ] 2 => array:2 [ "identificador" => "abst0045" "titulo" => "Métodos" ] 3 => array:2 [ "identificador" => "abst0050" "titulo" => "Resultados" ] 4 => array:2 [ "identificador" => "abst0055" "titulo" => "Conclusión" ] ] ] 4 => array:2 [ "identificador" => "xpalclavsec1509081" "titulo" => "Palabras clave" ] 5 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 6 => array:3 [ "identificador" => "sec0010" "titulo" => "Materials and methods" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0015" "titulo" => "Animal groups" ] 1 => array:2 [ "identificador" => "sec0020" "titulo" => "Experimental protocol" ] 2 => array:2 [ "identificador" => "sec0025" "titulo" => "Statistical analysis" ] ] ] 7 => array:2 [ "identificador" => "sec0030" "titulo" => "Results" ] 8 => array:2 [ "identificador" => "sec0035" "titulo" => "Discussion" ] 9 => array:2 [ "identificador" => "sec0040" "titulo" => "Conclusions" ] 10 => array:2 [ "identificador" => "sec0045" "titulo" => "Authors’ contributions" ] 11 => array:2 [ "identificador" => "sec0050" "titulo" => "Conflict of interest" ] 12 => array:2 [ "identificador" => "xack601030" "titulo" => "Acknowledgments" ] 13 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2020-04-29" "fechaAceptado" => "2021-01-07" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec1509082" "palabras" => array:5 [ 0 => "Hyperthermia" 1 => "Pleurodesis" 2 => "Pleural effusion" 3 => "Pneumothorax" 4 => "Talc" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec1509081" "palabras" => array:5 [ 0 => "Hipertermia" 1 => "Pleurodesis" 2 => "Derrame pleural" 3 => "Neumotórax" 4 => "Talco" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:3 [ "titulo" => "Abstract" "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Background</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Pleurodesis is a common technique for treating the accumulation of air or liquid in the pleural space caused by pneumothorax or pleural effusion, it is based on the bounding of pleural layers through induced inflammatory lesions. There are several pleurodesis procedures.</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Objectives</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">To test and describe the inflammatory effect of hyperthermia on the pleural and peritoneal mesothelia of rats, with the aim of testing the effectiveness of this process for inducing pleurodesis.</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Methods</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">35 <span class="elsevierStyleItalic">Sprague-Dawley</span> (male/female) rats were randomized into four treatment groups: Group A (Talc, 10 individuals); group B (control, 5 individuals); group C (hyperthermic isotonic saline, 10 individuals); and group D (filtrate air at 50°, 10 individuals). Inflammatory effect of hyperthermia was the primary outcome parameter.</p></span> <span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Results</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">In the talc group, minimal adhesions between both pleural and peritoneal layers were observed in seven rats. Talc produced peritoneal mesothelium inflammation and fibrosis associated to foreign body giant cells in 80% (8/10) of the sample. Furthermore, clear evidence of a granulomatous foreign-body reaction was detected. No macroscopic and/or microscopic damage was registered in the remaining three groups (control, hyperthermic, and filtrate air).</p></span> <span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conclusions</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Talc is an excellent method for producing pleuro-peritoneal inflammatory lesions. On the contrary, hyperthermia apparently does not induce the macroscopic and microscopic damage that is required for efficient pleurodesis. Therefore, hyperthermia should not be used for pleurodesis procedures.</p></span>" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "abst0010" "titulo" => "Background" ] 1 => array:2 [ "identificador" => "abst0015" "titulo" => "Objectives" ] 2 => array:2 [ "identificador" => "abst0020" "titulo" => "Methods" ] 3 => array:2 [ "identificador" => "abst0025" "titulo" => "Results" ] 4 => array:2 [ "identificador" => "abst0030" "titulo" => "Conclusions" ] ] ] "es" => array:3 [ "titulo" => "Resumen" "resumen" => "<span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Introducción</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">La pleurodesis es una técnica común como tratamiento de la patología pleural, ya sea en el neumotórax o el derrame pleural; se basa en la delimitación de las capas pleurales mediante lesiones inflamatorias inducidas. Existen múltiples procedimientos para conseguir una sínfisis pleural.</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Objetivo</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Estudiar y describir el efecto inflamatorio de la hipertermia sobre el mesotelio pleural y peritoneal de ratas con el objetivo de valorar si presenta un efecto sinfisiante y por tanto útil para conseguir la pleurodesis.</p></span> <span id="abst0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Métodos</span><p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Treinta y cinco ratas <span class="elsevierStyleItalic">Sprague-Dawley</span> (hembras/machos) fueron aleatorizadas en 4 grupos de tratamiento: grupo<span class="elsevierStyleHsp" style=""></span>A (talco, 10 animales); grupo<span class="elsevierStyleHsp" style=""></span>B (control, 5 animales); grupo<span class="elsevierStyleHsp" style=""></span>C (suero salino hipertérmico: 10 animales), y grupo<span class="elsevierStyleHsp" style=""></span>D (aire filtrado a 50°, 10 animales).</p></span> <span id="abst0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Resultados</span><p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">En el grupo de talco se evidenciaron adherencias entre las dos membranas pleurales y peritoneales en 7 animales. Se observó inflamación, fibrosis asociada a células gigantes de cuerpos extraño en el 80% (8/10) del mesotelio peritoneal. Paralelamente, se observó reacción granulomatosa a cuerpo extraño. No se registraron lesiones macroscópicas ni microscópicas en el resto de grupos estudiados (control, hipertermia y aire filtrado).</p></span> <span id="abst0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Conclusión</span><p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">El talco es un excelente método para producir inflamación a nivel del mesotelio pleural y peritoneal. Por el contrario, la hipertermia no parece inducir lesiones macroscópicas ni microscópicas requeridas para conseguir una pleurodesis eficaz.</p></span>" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "abst0035" "titulo" => "Introducción" ] 1 => array:2 [ "identificador" => "abst0040" "titulo" => "Objetivo" ] 2 => array:2 [ "identificador" => "abst0045" "titulo" => "Métodos" ] 3 => array:2 [ "identificador" => "abst0050" "titulo" => "Resultados" ] 4 => array:2 [ "identificador" => "abst0055" "titulo" => "Conclusión" ] ] ] ] "multimedia" => array:6 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1311 "Ancho" => 1740 "Tamanyo" => 487646 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Microscopic findings on the parietal pleura and parietal peritoneum exposed to talc. Group A and B: parietal pleura and hematoxylin and eosin 100× and 200×. Group C and D: parietal peritoneum and hematoxylin and eosin 100× 200×. Signs of injuries, namely inflammation with foreign body granulomatous reaction (talc crystals), mesothelial proliferation and fibrosis, were observed in the pleural and peritoneal mesothelium.</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" => 627 "Ancho" => 1674 "Tamanyo" => 242270 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">Microscopic findings on the parietal pleura and parietal peritoneum after being exposed to talc. Group A: parietal pleura and hematoxylin and eosin × 400; Group B: parietal peritoneum and Masson's trichrome × 400. Multinucleated foreign body giant cells containing birefringent talc crystals with granulomas formation were observed in the submesothelium.</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" => 415 "Ancho" => 1674 "Tamanyo" => 189240 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">Microscopic findings on the brain, liver and spleen (A–C). Hematoxylin and eosin 200×. Systemic distribution of talc was not assessed.</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" => 433 "Ancho" => 1674 "Tamanyo" => 109711 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Microscopic findings on the parietal peritoneum. A (control group-B): Hematoxylin and eosin 400×; B (hyperthermic group-C): hematoxylin and eosin 200×; C (hot air group-D): hematoxylin and eosin 200×. Lesions were not observed in the peritoneal mesothelium.</p>" ] ] 4 => array:8 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at1" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:3 [ "leyenda" => "<p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">SD: Standard deviation. Microscopic lesions*: inflammation and fibrosis.</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="" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black"> \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="center" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Group A(<span class="elsevierStyleItalic">n</span>: 10) \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="center" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Group B(<span class="elsevierStyleItalic">n</span>: 5) \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="center" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Group C(<span class="elsevierStyleItalic">n</span>: 10) \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="center" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Group D(<span class="elsevierStyleItalic">n</span>: 10) \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="center" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">p</span>-Value \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-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Mean weight (SD) \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">489.8<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>78.4 \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">621.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>134.7 \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">548.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>174 \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">478<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>39.15 \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">>0.05 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Adhesions presentMean<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>SD \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">7/100.77<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.44 \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">0/50<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>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">0/100<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>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">0/100<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>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"><0.005 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Microscopic lesions<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a>Mean<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>SD \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">8/100.8<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.42 \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">0/50<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>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">1/100.1<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.3 \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">0/100<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>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">>0.05 \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab2897108.png" ] ] ] "notaPie" => array:1 [ 0 => array:3 [ "identificador" => "tblfn0005" "etiqueta" => "a" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">The <span class="elsevierStyleItalic">p</span>-value was obtained with a Kruskal–Wallis rank test.</p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">Microscopic and macroscopic scores.</p>" ] ] 5 => array:5 [ "identificador" => "fig0025" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => false "mostrarDisplay" => true "figura" => array:1 [ 0 => array:4 [ "imagen" => "fx1.jpeg" "Alto" => 740 "Ancho" => 1333 "Tamanyo" => 98506 ] ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0015" "bibliografiaReferencia" => array:27 [ 0 => array:3 [ "identificador" => "bib0140" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "The evidence on the effectiveness of management for malignant pleural effusion: a systematic review" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:5 [ 0 => "C. 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2024 June | 30 | 2 | 32 |
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