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Bench-to-bedside review: Sepsis is a disease of the microcirculation

Microcirculatory perfusion is disturbed in sepsis. Recent research has shown that maintaining systemic blood pressure is associated with inadequate perfusion of the microcirculation in sepsis. Microcirculatory perfusion is regulated by an intricate interplay of many neuroendocrine and paracrine path...

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Detalles Bibliográficos
Autores principales: Spronk, Peter E, Zandstra, Durk F, Ince, Can
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1065042/
https://www.ncbi.nlm.nih.gov/pubmed/15566617
http://dx.doi.org/10.1186/cc2894
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author Spronk, Peter E
Zandstra, Durk F
Ince, Can
author_facet Spronk, Peter E
Zandstra, Durk F
Ince, Can
author_sort Spronk, Peter E
collection PubMed
description Microcirculatory perfusion is disturbed in sepsis. Recent research has shown that maintaining systemic blood pressure is associated with inadequate perfusion of the microcirculation in sepsis. Microcirculatory perfusion is regulated by an intricate interplay of many neuroendocrine and paracrine pathways, which makes blood flow though this microvascular network a heterogeneous process. Owing to an increased microcirculatory resistance, a maldistribution of blood flow occurs with a decreased systemic vascular resistance due to shunting phenomena. Therapy in shock is aimed at the optimization of cardiac function, arterial hemoglobin saturation and tissue perfusion. This will mean the correction of hypovolemia and the restoration of an evenly distributed microcirculatory flow and adequate oxygen transport. A practical clinical score for the definition of shock is proposed and a novel technique for bedside visualization of the capillary network is discussed, including its possible implications for the treatment of septic shock patients with vasodilators to open the microcirculation.
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spelling pubmed-10650422005-03-16 Bench-to-bedside review: Sepsis is a disease of the microcirculation Spronk, Peter E Zandstra, Durk F Ince, Can Crit Care Review Microcirculatory perfusion is disturbed in sepsis. Recent research has shown that maintaining systemic blood pressure is associated with inadequate perfusion of the microcirculation in sepsis. Microcirculatory perfusion is regulated by an intricate interplay of many neuroendocrine and paracrine pathways, which makes blood flow though this microvascular network a heterogeneous process. Owing to an increased microcirculatory resistance, a maldistribution of blood flow occurs with a decreased systemic vascular resistance due to shunting phenomena. Therapy in shock is aimed at the optimization of cardiac function, arterial hemoglobin saturation and tissue perfusion. This will mean the correction of hypovolemia and the restoration of an evenly distributed microcirculatory flow and adequate oxygen transport. A practical clinical score for the definition of shock is proposed and a novel technique for bedside visualization of the capillary network is discussed, including its possible implications for the treatment of septic shock patients with vasodilators to open the microcirculation. BioMed Central 2004 2004-06-16 /pmc/articles/PMC1065042/ /pubmed/15566617 http://dx.doi.org/10.1186/cc2894 Text en Copyright © 2004 BioMed Central Ltd
spellingShingle Review
Spronk, Peter E
Zandstra, Durk F
Ince, Can
Bench-to-bedside review: Sepsis is a disease of the microcirculation
title Bench-to-bedside review: Sepsis is a disease of the microcirculation
title_full Bench-to-bedside review: Sepsis is a disease of the microcirculation
title_fullStr Bench-to-bedside review: Sepsis is a disease of the microcirculation
title_full_unstemmed Bench-to-bedside review: Sepsis is a disease of the microcirculation
title_short Bench-to-bedside review: Sepsis is a disease of the microcirculation
title_sort bench-to-bedside review: sepsis is a disease of the microcirculation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1065042/
https://www.ncbi.nlm.nih.gov/pubmed/15566617
http://dx.doi.org/10.1186/cc2894
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