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Should we consider the infusion of lipid emulsion in the resuscitation of poisoned patients?

The use of intravenous lipid emulsions (ILEs) as antidote in local anaesthetic systemic toxicity has gained widespread support following convincing data from animal models, and successful case reports in humans. Proposed beneficial mechanisms of action for ILEs include intravascular sequestration of...

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Detalles Bibliográficos
Autores principales: Cave, Grant, Harvey, Martyn G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331416/
https://www.ncbi.nlm.nih.gov/pubmed/25673255
http://dx.doi.org/10.1186/s13054-014-0457-5
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author Cave, Grant
Harvey, Martyn G
author_facet Cave, Grant
Harvey, Martyn G
author_sort Cave, Grant
collection PubMed
description The use of intravenous lipid emulsions (ILEs) as antidote in local anaesthetic systemic toxicity has gained widespread support following convincing data from animal models, and successful case reports in humans. Proposed beneficial mechanisms of action for ILEs include intravascular sequestration of intoxicant and subsequent enhanced redistribution to biologically inert tissues, augmentation of fatty acid utilisation for ATP synthesis in the context of metabolic poisoning, and direct cardiotonic and ion channel effects. The evidence base for use of ILEs in acute drug intoxication is evolving. The present evidence supports use of ILEs only in local anaesthetic systemic toxicity and in lipophilic cardiotoxin intoxication when there is an immediate threat to life, and other therapies have proven ineffective.
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spelling pubmed-43314162015-02-19 Should we consider the infusion of lipid emulsion in the resuscitation of poisoned patients? Cave, Grant Harvey, Martyn G Crit Care Review The use of intravenous lipid emulsions (ILEs) as antidote in local anaesthetic systemic toxicity has gained widespread support following convincing data from animal models, and successful case reports in humans. Proposed beneficial mechanisms of action for ILEs include intravascular sequestration of intoxicant and subsequent enhanced redistribution to biologically inert tissues, augmentation of fatty acid utilisation for ATP synthesis in the context of metabolic poisoning, and direct cardiotonic and ion channel effects. The evidence base for use of ILEs in acute drug intoxication is evolving. The present evidence supports use of ILEs only in local anaesthetic systemic toxicity and in lipophilic cardiotoxin intoxication when there is an immediate threat to life, and other therapies have proven ineffective. BioMed Central 2014-07-30 2014 /pmc/articles/PMC4331416/ /pubmed/25673255 http://dx.doi.org/10.1186/s13054-014-0457-5 Text en © Cave and Harvey; licensee BioMed Central Ltd. 2014 The licensee has exclusive rights to distribute this article, in any medium, for 12 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Cave, Grant
Harvey, Martyn G
Should we consider the infusion of lipid emulsion in the resuscitation of poisoned patients?
title Should we consider the infusion of lipid emulsion in the resuscitation of poisoned patients?
title_full Should we consider the infusion of lipid emulsion in the resuscitation of poisoned patients?
title_fullStr Should we consider the infusion of lipid emulsion in the resuscitation of poisoned patients?
title_full_unstemmed Should we consider the infusion of lipid emulsion in the resuscitation of poisoned patients?
title_short Should we consider the infusion of lipid emulsion in the resuscitation of poisoned patients?
title_sort should we consider the infusion of lipid emulsion in the resuscitation of poisoned patients?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331416/
https://www.ncbi.nlm.nih.gov/pubmed/25673255
http://dx.doi.org/10.1186/s13054-014-0457-5
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