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Epidermal wound healing in severe sepsis and septic shock in humans

INTRODUCTION: The effect of sepsis on epidermal wound healing has not been previously studied. It was hypothesised that epidermal wound healing is disturbed in severe sepsis. METHODS: Blister wounds were induced in 35 patients with severe sepsis and in 15 healthy controls. The healing of the wounds...

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Autores principales: Koskela, Marjo, Gäddnäs, Fiia, Ala-Kokko, Tero I, Laurila, Jouko J, Saarnio, Juha, Oikarinen, Aarne, Koivukangas, Vesa
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2717472/
https://www.ncbi.nlm.nih.gov/pubmed/19552820
http://dx.doi.org/10.1186/cc7932
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author Koskela, Marjo
Gäddnäs, Fiia
Ala-Kokko, Tero I
Laurila, Jouko J
Saarnio, Juha
Oikarinen, Aarne
Koivukangas, Vesa
author_facet Koskela, Marjo
Gäddnäs, Fiia
Ala-Kokko, Tero I
Laurila, Jouko J
Saarnio, Juha
Oikarinen, Aarne
Koivukangas, Vesa
author_sort Koskela, Marjo
collection PubMed
description INTRODUCTION: The effect of sepsis on epidermal wound healing has not been previously studied. It was hypothesised that epidermal wound healing is disturbed in severe sepsis. METHODS: Blister wounds were induced in 35 patients with severe sepsis and in 15 healthy controls. The healing of the wounds was followed up by measuring transepidermal water loss and blood flow in the wound, reflecting the restoration of the epidermal barrier function and inflammation, respectively. The first set of suction blisters (early wound) was made within 48 hours of the first sepsis-induced organ failure and the second set (late wound) four days after the first wound. In addition, measurements were made on the intact skin. RESULTS: The average age of the whole study population was 62 years (standard deviation [SD] 12). The mean Acute Physiology and Chronic Health Evaluation II (APACHE II) score on admission was 25 (SD 8). The two most common causes of infections were peritonitis and pneumonia. Sixty-six percent of the patients developed multiple organ failure. The decrease in water evaporation from the wound during the first four days was lower in septic patients than in the control subjects (56 g/m(2 )per hour versus 124 g/m(2 )per hour, P = 0.004). On the fourth day, septic patients had significantly higher blood flow in the wound compared with the control subjects (septic patients 110 units versus control subjects 47 units, P = 0.001). No difference in transepidermal water loss from the intact skin was found between septic patients and controls. Septic patients had higher blood flow in the intact skin on the fourth and on the eighth day of study compared with the controls. CONCLUSIONS: The restoration of the epidermal barrier function is delayed and wound blood flow is increased in patients with severe sepsis.
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spelling pubmed-27174722009-07-29 Epidermal wound healing in severe sepsis and septic shock in humans Koskela, Marjo Gäddnäs, Fiia Ala-Kokko, Tero I Laurila, Jouko J Saarnio, Juha Oikarinen, Aarne Koivukangas, Vesa Crit Care Research INTRODUCTION: The effect of sepsis on epidermal wound healing has not been previously studied. It was hypothesised that epidermal wound healing is disturbed in severe sepsis. METHODS: Blister wounds were induced in 35 patients with severe sepsis and in 15 healthy controls. The healing of the wounds was followed up by measuring transepidermal water loss and blood flow in the wound, reflecting the restoration of the epidermal barrier function and inflammation, respectively. The first set of suction blisters (early wound) was made within 48 hours of the first sepsis-induced organ failure and the second set (late wound) four days after the first wound. In addition, measurements were made on the intact skin. RESULTS: The average age of the whole study population was 62 years (standard deviation [SD] 12). The mean Acute Physiology and Chronic Health Evaluation II (APACHE II) score on admission was 25 (SD 8). The two most common causes of infections were peritonitis and pneumonia. Sixty-six percent of the patients developed multiple organ failure. The decrease in water evaporation from the wound during the first four days was lower in septic patients than in the control subjects (56 g/m(2 )per hour versus 124 g/m(2 )per hour, P = 0.004). On the fourth day, septic patients had significantly higher blood flow in the wound compared with the control subjects (septic patients 110 units versus control subjects 47 units, P = 0.001). No difference in transepidermal water loss from the intact skin was found between septic patients and controls. Septic patients had higher blood flow in the intact skin on the fourth and on the eighth day of study compared with the controls. CONCLUSIONS: The restoration of the epidermal barrier function is delayed and wound blood flow is increased in patients with severe sepsis. BioMed Central 2009 2009-06-24 /pmc/articles/PMC2717472/ /pubmed/19552820 http://dx.doi.org/10.1186/cc7932 Text en Copyright © 2009 Koskela et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Koskela, Marjo
Gäddnäs, Fiia
Ala-Kokko, Tero I
Laurila, Jouko J
Saarnio, Juha
Oikarinen, Aarne
Koivukangas, Vesa
Epidermal wound healing in severe sepsis and septic shock in humans
title Epidermal wound healing in severe sepsis and septic shock in humans
title_full Epidermal wound healing in severe sepsis and septic shock in humans
title_fullStr Epidermal wound healing in severe sepsis and septic shock in humans
title_full_unstemmed Epidermal wound healing in severe sepsis and septic shock in humans
title_short Epidermal wound healing in severe sepsis and septic shock in humans
title_sort epidermal wound healing in severe sepsis and septic shock in humans
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2717472/
https://www.ncbi.nlm.nih.gov/pubmed/19552820
http://dx.doi.org/10.1186/cc7932
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