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Broad spectrum vasopressors: a new approach to the initial management of septic shock?

The mainstay of hemodynamic treatment of septic shock is fluid resuscitation followed by vasopressors where fluids alone are insufficient to achieve target blood pressure. Norepinephrine, a catecholamine, is the first-line vasopressor used worldwide but given that all routinely used catecholamines t...

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Autores principales: Chawla, Lakhmir S., Ostermann, Marlies, Forni, Lui, Tidmarsh, George F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469125/
https://www.ncbi.nlm.nih.gov/pubmed/30992045
http://dx.doi.org/10.1186/s13054-019-2420-y
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author Chawla, Lakhmir S.
Ostermann, Marlies
Forni, Lui
Tidmarsh, George F.
author_facet Chawla, Lakhmir S.
Ostermann, Marlies
Forni, Lui
Tidmarsh, George F.
author_sort Chawla, Lakhmir S.
collection PubMed
description The mainstay of hemodynamic treatment of septic shock is fluid resuscitation followed by vasopressors where fluids alone are insufficient to achieve target blood pressure. Norepinephrine, a catecholamine, is the first-line vasopressor used worldwide but given that all routinely used catecholamines target the same adrenergic receptors, many clinicians may add a non-catecholamine vasopressor where refractory hypotension due to septic shock is present. However, the timing of this additional intervention is variable. This decision is based on three key factors: availability, familiarity, and safety profile. In our opinion, further consideration should be potential vasopressor response because following appropriate volume resuscitation, the response to different vasopressor classes is neither uniform nor predictable. Critically ill patients who are non-responders to high-dose catecholamines have a dismal outcome. Similarly, patients have a variable response to non-catecholamine agents including vasopressin and angiotensin II: but where patients exhibit a blood pressure response the outcomes are improved over non-responders. This variable responsiveness to vasopressors is similar to the clinical approach of anti-microbial sensitivity. In this commentary, the authors propose the concept of “broad spectrum vasopressors” wherein patients with septic shock are started on multiple vasopressors with a different mechanism of action simultaneously while the vasopressor sensitivity is assessed. Once the vasopressor sensitivities are assessed, then the vasopressors are ‘de-escalated’ accordingly. We believe that this concept may offer a new approach to the treatment of septic shock.
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spelling pubmed-64691252019-04-23 Broad spectrum vasopressors: a new approach to the initial management of septic shock? Chawla, Lakhmir S. Ostermann, Marlies Forni, Lui Tidmarsh, George F. Crit Care Commentary The mainstay of hemodynamic treatment of septic shock is fluid resuscitation followed by vasopressors where fluids alone are insufficient to achieve target blood pressure. Norepinephrine, a catecholamine, is the first-line vasopressor used worldwide but given that all routinely used catecholamines target the same adrenergic receptors, many clinicians may add a non-catecholamine vasopressor where refractory hypotension due to septic shock is present. However, the timing of this additional intervention is variable. This decision is based on three key factors: availability, familiarity, and safety profile. In our opinion, further consideration should be potential vasopressor response because following appropriate volume resuscitation, the response to different vasopressor classes is neither uniform nor predictable. Critically ill patients who are non-responders to high-dose catecholamines have a dismal outcome. Similarly, patients have a variable response to non-catecholamine agents including vasopressin and angiotensin II: but where patients exhibit a blood pressure response the outcomes are improved over non-responders. This variable responsiveness to vasopressors is similar to the clinical approach of anti-microbial sensitivity. In this commentary, the authors propose the concept of “broad spectrum vasopressors” wherein patients with septic shock are started on multiple vasopressors with a different mechanism of action simultaneously while the vasopressor sensitivity is assessed. Once the vasopressor sensitivities are assessed, then the vasopressors are ‘de-escalated’ accordingly. We believe that this concept may offer a new approach to the treatment of septic shock. BioMed Central 2019-04-16 /pmc/articles/PMC6469125/ /pubmed/30992045 http://dx.doi.org/10.1186/s13054-019-2420-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Commentary
Chawla, Lakhmir S.
Ostermann, Marlies
Forni, Lui
Tidmarsh, George F.
Broad spectrum vasopressors: a new approach to the initial management of septic shock?
title Broad spectrum vasopressors: a new approach to the initial management of septic shock?
title_full Broad spectrum vasopressors: a new approach to the initial management of septic shock?
title_fullStr Broad spectrum vasopressors: a new approach to the initial management of septic shock?
title_full_unstemmed Broad spectrum vasopressors: a new approach to the initial management of septic shock?
title_short Broad spectrum vasopressors: a new approach to the initial management of septic shock?
title_sort broad spectrum vasopressors: a new approach to the initial management of septic shock?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469125/
https://www.ncbi.nlm.nih.gov/pubmed/30992045
http://dx.doi.org/10.1186/s13054-019-2420-y
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