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dc.contributor.authorGil Antón, Javier
dc.contributor.authorMielgo, Victoria
dc.contributor.authorRey Santano, María Carmen
dc.contributor.authorGalbarriatu, Lara
dc.contributor.authorSantos, Carlos
dc.contributor.authorUnceta Suárez, María
dc.contributor.authorLópez Fernández, Yolanda
dc.contributor.authorRedondo, Silvia
dc.contributor.authorMorteruel, Elvira
dc.date.accessioned2020-11-26T13:32:49Z
dc.date.available2020-11-26T13:32:49Z
dc.date.issued2020-07-02
dc.identifier.citationPlos One 15(7) : (2019) // Article ID e0235084es_ES
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10810/48610
dc.description.abstractHemorrhagic shock is one of the leading causes of mortality and morbidity in pediatric trauma. Current treatment based on volume resuscitation is associated to adverse effects, and it has been proposed that vasopressors may be used in the pharmacological management of trauma. Terlipressin has demonstrated its usefulness in other pediatric critical care scenarios and its long half-life allows its use as a bolus in an outpatient critical settings. The aim of this study was to analyze whether the addition of a dose of terlipressin to the initial volume expansion produces an improvement in hemodynamic and cerebral perfusion at early stages of hemorrhagic shock in an infant animal model. We conducted an experimental randomized animal study with 1-month old pigs. After 30 minutes of hypotension (mean arterial blood pressure [MAP]<45 mmHg) induced by the withdrawal of blood over 30 min, animals were randomized to receive either normal saline (NS) 30 mL/kg (n = 8) or a bolus of 20 mcg/kg of terlipressin plus 30 mL/kg of normal saline (TP) (n = 8). Global hemodynamic and cerebral monitoring parameters, brain damage markers and histology samples were compared. After controlled bleeding, significant decreases were observed in MAP, cardiac index (CI), central venous pressure, global end-diastolic volume index (GEDI), left cardiac output index, SvO(2), intracranial pressure, carotid blood flow, bispectral index (BIS), cerebral perfusion pressure (CPP) and increases in systemic vascular resistance index, heart rate and lactate. After treatment, MAP, GEDI, CI, CPP and BIS remained significantly higher in the TP group. The addition of a dose of terlipressin to initial fluid resuscitation was associated with hemodynamic improvement, intracranial pressure maintenance and better cerebral perfusion, which would mean protection from ischemic injury. Brain monitoring through BIS was able to detect changes caused by hemorrhagic shock and treatment.es_ES
dc.description.sponsorshipThis work was partially supported by Basque Government Grant (GIU19/026) to VEM and Spanish Society of pediatric critical care (Ruza Grant 2017) to JG.es_ES
dc.language.isoenges_ES
dc.publisherPublic Library Sciencees_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectbrain-damagees_ES
dc.subjectvasopressines_ES
dc.subjectpressurees_ES
dc.titleAddition of terlipressin to initial volume resuscitation in a pediatric model of hemorrhagic shock improves hemodynamics and cerebral perfusiones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder2020 Gil-Anton et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0235084es_ES
dc.identifier.doi10.1371/journal.pone.0235084
dc.departamentoesPediatríaes_ES
dc.departamentoeuPediatriaes_ES


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2020 Gil-Anton et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Except where otherwise noted, this item's license is described as 2020 Gil-Anton et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.