<?xml version="1.0" encoding="UTF-8"?>
<collection>
<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.25107/2474-1647</dc:identifier><dc:language>eng</dc:language><dc:creator>Pañella, C.</dc:creator><dc:creator>Moll, X.</dc:creator><dc:creator>Quesada, R.</dc:creator><dc:creator>Villanueva, A.</dc:creator><dc:creator>Iglesias, M.</dc:creator><dc:creator>Andaluz, A.</dc:creator><dc:creator>Lucía, O.</dc:creator><dc:creator>Sánchez-Velázquez, P.</dc:creator><dc:creator>Grande, L.</dc:creator><dc:creator>Burdío, F.</dc:creator><dc:title>Hypersaline infusion protocol through the portal vein may focus electroporation on tumor tissue, but is it really safe? Ppreliminary results</dc:title><dc:identifier>ART-2019-111136</dc:identifier><dc:description>Introduction: irreversible Electroporation (IRE) is highly dependent on the electrical conductivity of the tissue and the high conductivity of tumor tissue, which leads to a lower field than that in the surrounding healthy tissue. Hypersaline Infusion (HI) through the portal vein focuses IRE on scattered liver tumors, by creating a differential conductivity between the different types of tissue. The aim of this study is to determine the effects of the HI protocol on the hepatic and histological biochemical results. Methods: Ten male Sprague Dawley rats were used for HI protocol. Blood samples were collected at pre-, immediately post-, 24-hrs, 72-hrs, 1- week and 3-weeks post-HI. All the animals were sacrificed after a one-month follow-up in order to collect histological samples. Results: The mortality rate in this procedure reached 30% (3/10). Only the pH and transaminases at 24-hrs were significantly and directly linked to mortality (p=0.036 and p=0.004, respectively). The three non-surviving animals had a four-time higher AST level at 24-hrs. Natremianormalized at 24-hrs post-HI. Statistically significant differences were found in hepatic necrosis between the non-surviving (n=3) and surviving rats (n=7) (30.67 ± 10.97 vs. 2.86 ± 7.56% respectively, p=0.01). Discussion: HI through the portal system involves a significant risk of possibly lethal cytolysis and acidosis. Therefore, compensatory measures and a reduced saline overload are warranted to improve the survival rates.</dc:description><dc:date>2019</dc:date><dc:source>http://zaguan.unizar.es/record/78930</dc:source><dc:doi>10.25107/2474-1647</dc:doi><dc:identifier>http://zaguan.unizar.es/record/78930</dc:identifier><dc:identifier>oai:zaguan.unizar.es:78930</dc:identifier><dc:identifier.citation>Clinics in Surgery 4, 1 (2019), 2335 [5 pp.]</dc:identifier.citation><dc:rights>by-nc</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

</collection>