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Recent evolution of renal replacement therapy in the critically ill patient

The epidemiology of severe acute renal failure has dramatically changed in the past decade. Its leading cause is sepsis and the syndrome develops mostly in the intensive care unit as part of multiple organ dysfunction syndrome. After the significant improvements obtained from the mid 1970s to the mi...

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Detalles Bibliográficos
Autor principal: Ronco, Claudio
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550862/
https://www.ncbi.nlm.nih.gov/pubmed/16542480
http://dx.doi.org/10.1186/cc4843
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author Ronco, Claudio
author_facet Ronco, Claudio
author_sort Ronco, Claudio
collection PubMed
description The epidemiology of severe acute renal failure has dramatically changed in the past decade. Its leading cause is sepsis and the syndrome develops mostly in the intensive care unit as part of multiple organ dysfunction syndrome. After the significant improvements obtained from the mid 1970s to the mid 1990s, the past decade has seen a dramatic evolution in technology leading to new machines and new techniques for renal and multiple organ support. Extracorporeal therapies are now performed using adequate treatment doses, which have resulted in improved survival in the general population. At the same time, patients with sepsis seem to benefit from the use of increased doses, as in the case of high-volume hemofiltration or of increased membrane permeability and sorbents as in the case of continuous plasmafiltration adsorption. The humoral theory of sepsis and the peak concentration hypothesis have spurred a significant interest in the use of such extracorporeal therapies for renal support and possibly for the therapy of sepsis. Ongoing research and prospective studies will further elucidate the role of such therapies in this setting.
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spelling pubmed-15508622006-08-22 Recent evolution of renal replacement therapy in the critically ill patient Ronco, Claudio Crit Care Commentary The epidemiology of severe acute renal failure has dramatically changed in the past decade. Its leading cause is sepsis and the syndrome develops mostly in the intensive care unit as part of multiple organ dysfunction syndrome. After the significant improvements obtained from the mid 1970s to the mid 1990s, the past decade has seen a dramatic evolution in technology leading to new machines and new techniques for renal and multiple organ support. Extracorporeal therapies are now performed using adequate treatment doses, which have resulted in improved survival in the general population. At the same time, patients with sepsis seem to benefit from the use of increased doses, as in the case of high-volume hemofiltration or of increased membrane permeability and sorbents as in the case of continuous plasmafiltration adsorption. The humoral theory of sepsis and the peak concentration hypothesis have spurred a significant interest in the use of such extracorporeal therapies for renal support and possibly for the therapy of sepsis. Ongoing research and prospective studies will further elucidate the role of such therapies in this setting. BioMed Central 2006 2006-02-17 /pmc/articles/PMC1550862/ /pubmed/16542480 http://dx.doi.org/10.1186/cc4843 Text en Copyright © 2006 BioMed Central Ltd
spellingShingle Commentary
Ronco, Claudio
Recent evolution of renal replacement therapy in the critically ill patient
title Recent evolution of renal replacement therapy in the critically ill patient
title_full Recent evolution of renal replacement therapy in the critically ill patient
title_fullStr Recent evolution of renal replacement therapy in the critically ill patient
title_full_unstemmed Recent evolution of renal replacement therapy in the critically ill patient
title_short Recent evolution of renal replacement therapy in the critically ill patient
title_sort recent evolution of renal replacement therapy in the critically ill patient
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550862/
https://www.ncbi.nlm.nih.gov/pubmed/16542480
http://dx.doi.org/10.1186/cc4843
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