<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0003-3170</journal-id>
<journal-title><![CDATA[Angiología]]></journal-title>
<abbrev-journal-title><![CDATA[Angiología]]></abbrev-journal-title>
<issn>0003-3170</issn>
<publisher>
<publisher-name><![CDATA[Arán Ediciones S.L.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0003-31702023000400004</article-id>
<article-id pub-id-type="doi">10.20960/angiologia.00483</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Modelo animal para la evaluación del sellado de colaterales venosas con dispositivos liberadores de energía en cirugía de revascularización]]></article-title>
<article-title xml:lang="en"><![CDATA[Animal model to assess collateral vein sealing with energy-based devices in revascularization surgery]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Falcón-Espínola]]></surname>
<given-names><![CDATA[Moisés]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Plana-Andani]]></surname>
<given-names><![CDATA[Emma]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bisbal-Velasco]]></surname>
<given-names><![CDATA[Viviana]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Clarà-Velasco]]></surname>
<given-names><![CDATA[Albert]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Miralles-Hernández]]></surname>
<given-names><![CDATA[Manuel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="A a"/>
<xref ref-type="aff" rid="A4b"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital de Manises Servicio de Angiología, Cirugía Vascular y Endovascular ]]></institution>
<addr-line><![CDATA[Manises Valencia]]></addr-line>
<country>España</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Instituto de Investigación Sanitaria La Fe  ]]></institution>
<addr-line><![CDATA[Valencia ]]></addr-line>
<country>España</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Hospital del Mar Servicio de Angiología, Cirugía Vascular y Endovascular ]]></institution>
<addr-line><![CDATA[Barcelona ]]></addr-line>
<country>España</country>
</aff>
<aff id="A4a">
<institution><![CDATA[,Hospital Universitari i Politècnic La Fe Servicio de Angiología, Cirugía Vascular y Endovascular ]]></institution>
<addr-line><![CDATA[Valencia ]]></addr-line>
<country>España</country>
</aff>
<aff id="A4b">
<institution><![CDATA[,Universidad de Valencia Facultad de Medicina Departamento de Cirugía]]></institution>
<addr-line><![CDATA[Valencia ]]></addr-line>
<country>España</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2023</year>
</pub-date>
<volume>75</volume>
<numero>4</numero>
<fpage>218</fpage>
<lpage>227</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_arttext&amp;pid=S0003-31702023000400004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_abstract&amp;pid=S0003-31702023000400004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_pdf&amp;pid=S0003-31702023000400004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Introducción: los dispositivos liberadores de energía permiten la hemostasia de los vasos mediante generación de calor y la coagulación de las proteínas de la pared. Sin embargo, se desconoce su comportamiento a medio plazo en la cirugía arterial con injertos venosos.  Objetivos: desarrollar un modelo animal que permita evaluar la eficacia y la seguridad del sellado a medio plazo tras el proceso de cicatrización. Comparar y evaluar qué modelo in vivo presenta menor morbilidad y mayor supervivencia a las 4 semanas.  Material y métodos: estudio experimental animal de 16 conejos New Zealand a los que se interpuso un fragmento de vena safena humana (VS) con una colateral. Se desarrollaron dos modelos arteriales: bypass término-terminal de VS en aorta infrarrenal (n = 5) y plastia de aorta con parche de VS (n = 11). La colateral venosa fue sellada, previa aleatorización, con electrocoagulación bipolar controlada por temperatura (EB) o bisturí armónico (BA). Todos los animales recibieron inmunosupresión y profilaxis antitrombótica. Se registró la tasa de paraplejia, de infección, de hemorragia y de supervivencia.  Resultados: la supervivencia a los 7 días fue del 50 % (2/4) en el modelo de injerto de interposición. Sin embargo, ningún animal sobrevivió a las 4 semanas de seguimiento en este modelo. En el grupo de plastia de aorta, la supervivencia a los 7 días fue del 55,56 % (5/9) y del 44,44 % (4/9) a las 4 semanas (p = 0,5). La tasa de paraplejia en el grupo de interposición fue del 100 % e inferior en el modelo de plastia de aorta (25 %) (p = 0,03). El tiempo medio de isquemia en el modelo de plastia de aorta (37,11 ± 8,1 min) fue inferior al del grupo del bypass (42 ± 10,61 min) (p = 0,414). En ningún caso se objetivó hemorragia intraabdominal ni reacción adversa a la inmunosupresión.  Conclusiones: el modelo arterial de plastia de aorta con parche de VS presentó menor tasa de paraplejia, así como menor mortalidad posoperatoria a los 7 días. Tanto en el modelo arterial de bypass como el de plastia de aorta, demostraron eficacia en la hemostasia del sellado, pero solo el modelo de plastia de aorta presentó supervivientes a las 4 semanas.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Introduction: energy sealing devices achieve hemostasis of the vessels through the heat generated and coagulation of the vascular wall proteins. However, the mid-term efficacy peofile for venous graft sealing in arterial bypass surgery remains unknown.  Objectives: to create an animal model to compare the mid-term efficacy and safety profile at the sealing area after the healing process. To compare and assess which in vivo arterial models show lower morbidity and higher survival rates after 4 weeks.  Material and methods: this was an in vivo experimental study of 16 New Zealand rabbits. In each rabbit a human saphenous vein (SV) with, at least, 1 venous collateral was implanted. Two arterial models were developed: infrarrenal aorta bypass with SV (n = 5) and aortoplasty with SV patch (n = 11). In both models the collateral was randomized and sealed with either 1 these 2 energy sealing devices: electrothermal Bipolar Vessel Sealing (EBVS) or Harmonic scalpel (HS). Every animal was treated with antithrombotic prophylaxis and immunosuppressive medication. The rates of intraoperative mortality, paraplegia, infection, bleeding, and survival were all studied.  Results: two animals (50 %) survive 7 days after surgery in the bypass model. However, no animal survived 4 days after surgery in this model. In the aortoplasty group, the 7-day survival rate was 55.56 % (5/9) while the 4-week survival rate was 44.44 % (4/9) (p = 0.05). The rte of paraplegia was 100 % for the bypass model and much lower for the patch group (25 %) (p = 0.03). The mean ischemic time was lower for the aortoplasty model (37.11 min ± 8.1 min) compared to the bypass group (42 min ± 10.61 min) (p = 0.414). No animal showed intrabdominal hemorrhages or adverse drug reactions associated with the immunosuppressive medication.  Conclusion: aortoplasty with the SV patch model showed lower rates of paraplegia and 7-day mortality in the animal model. Both the bypass and the path model models proved effective at the sealing area. However, only in the aortoplasty model 4 animals survived after 4 weeks.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Electrocoagulación bipolar controlada por temperatura]]></kwd>
<kwd lng="es"><![CDATA[Bisturí armónico]]></kwd>
<kwd lng="es"><![CDATA[Modelo animal]]></kwd>
<kwd lng="es"><![CDATA[Cirugía de revascularización]]></kwd>
<kwd lng="en"><![CDATA[Electrothermal bipolar vessel sealing]]></kwd>
<kwd lng="en"><![CDATA[Harmonic scalpel]]></kwd>
<kwd lng="en"><![CDATA[Animal model]]></kwd>
<kwd lng="en"><![CDATA[Revascularization surgery]]></kwd>
</kwd-group>
</article-meta>
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