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Arginine vasopressin versus norepinephrine: will the stronger one win the race?

In the current issue of Critical Care, Friesenecker and colleagues present a well-designed comparative study on the microvascular effects of arginine vasopressin (AVP) and norepinephrine (NE) in a physiological, unanesthetized hamster model. The authors clearly demonstrate that AVP, but not NE, has...

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Detalles Bibliográficos
Autores principales: Ertmer, Christian, Bone, Hans-Georg, Westphal, Martin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550944/
https://www.ncbi.nlm.nih.gov/pubmed/16732898
http://dx.doi.org/10.1186/cc4942
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author Ertmer, Christian
Bone, Hans-Georg
Westphal, Martin
author_facet Ertmer, Christian
Bone, Hans-Georg
Westphal, Martin
author_sort Ertmer, Christian
collection PubMed
description In the current issue of Critical Care, Friesenecker and colleagues present a well-designed comparative study on the microvascular effects of arginine vasopressin (AVP) and norepinephrine (NE) in a physiological, unanesthetized hamster model. The authors clearly demonstrate that AVP, but not NE, has marked vasoconstrictive effects on large arterioles, whereas the impact on small arterioles is comparable for both vasopressors. However, it remains unclear if these results, per se, reflect a stronger vasopressive potential of AVP versus NE, as macrohemodynamic variables were not different between study groups. Since the authors did not investigate the effects of AVP and NE in vasodilatory shock states, the microcirculatory response in sepsis or systemic inflammatory response syndrome remains inconclusive. The same authors previously reported that AVP infusion in patients suffering from vasodilatory shock carries the risk for ischemic skin lesions. This in turn raises the question whether the quality of vasopressors should be judged by their potency.
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spelling pubmed-15509442006-08-22 Arginine vasopressin versus norepinephrine: will the stronger one win the race? Ertmer, Christian Bone, Hans-Georg Westphal, Martin Crit Care Commentary In the current issue of Critical Care, Friesenecker and colleagues present a well-designed comparative study on the microvascular effects of arginine vasopressin (AVP) and norepinephrine (NE) in a physiological, unanesthetized hamster model. The authors clearly demonstrate that AVP, but not NE, has marked vasoconstrictive effects on large arterioles, whereas the impact on small arterioles is comparable for both vasopressors. However, it remains unclear if these results, per se, reflect a stronger vasopressive potential of AVP versus NE, as macrohemodynamic variables were not different between study groups. Since the authors did not investigate the effects of AVP and NE in vasodilatory shock states, the microcirculatory response in sepsis or systemic inflammatory response syndrome remains inconclusive. The same authors previously reported that AVP infusion in patients suffering from vasodilatory shock carries the risk for ischemic skin lesions. This in turn raises the question whether the quality of vasopressors should be judged by their potency. BioMed Central 2006 2006-05-25 /pmc/articles/PMC1550944/ /pubmed/16732898 http://dx.doi.org/10.1186/cc4942 Text en Copyright © 2006 BioMed Central Ltd
spellingShingle Commentary
Ertmer, Christian
Bone, Hans-Georg
Westphal, Martin
Arginine vasopressin versus norepinephrine: will the stronger one win the race?
title Arginine vasopressin versus norepinephrine: will the stronger one win the race?
title_full Arginine vasopressin versus norepinephrine: will the stronger one win the race?
title_fullStr Arginine vasopressin versus norepinephrine: will the stronger one win the race?
title_full_unstemmed Arginine vasopressin versus norepinephrine: will the stronger one win the race?
title_short Arginine vasopressin versus norepinephrine: will the stronger one win the race?
title_sort arginine vasopressin versus norepinephrine: will the stronger one win the race?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550944/
https://www.ncbi.nlm.nih.gov/pubmed/16732898
http://dx.doi.org/10.1186/cc4942
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