Review article: Organ per fusion/permeabilityrelated effects of norepinephrine and vasopressin in sepsis View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2006-09

AUTHORS

Paul Farand, Mélanie Hamel, François Lauzier, Gérard E. Plante, Olivier Lesur

ABSTRACT

PurposeOne invariable hallmark of severe sepsis is generalized tissue “malperfusion” and hyperpermeability secondary to microcirculatory/capillary leakage. This review focuses on direct and/or indirect influences of norepinephrine, as a standard of care, and vasopressin, as an alternative vasoactive drug, on organ and tissue perfusion/permeability in severe sepsis.SourceEnglish and French language articles and books published between 1966 and 2005 were identified through a computerized Medline search using the terms “sepsis, permeability, norepinephrine and vasopressin”. Relevant publications were retrieved and scanned for additional sources.Principal findingsThere are few randomized clinical trials comparing different vasopressors in sepsis; most available literature consists of clinical reports, animal experiments and occasional reviews. Based on the best current evidence from these sources, we describe the status of major organ perfusion/ permeability in sepsis (i.e., the lung, the kidney, the heart, the intestine/gut) in the context of sepsis-induced organ dysfunction/ failure. Potential and differential therapeutic effects of the vasopressors norepinephrine and arginine-vasopressin, in the setting of sepsis, are identified.ConclusionsIn the treatment of sepsis, arginine-vasopressin exhibits organ-specific heterogeneity in vascular responsiveness, compared to norepinephrine. While norepinephrine is a current standard of care in sepsis, arginine-vasopressin shows promise for the treatment of septic shock. More... »

PAGES

934-946

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf03022837

DOI

http://dx.doi.org/10.1007/bf03022837

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1036558622

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/16960272


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