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The effects of QuikClot Combat Gauze on hemorrhage control in the presence of hemodilution and hypothermia
Hemorrhage is the leading cause of death from trauma. Intravenous (IV) fluid resuscitation in these patients may cause hemodilution and secondary hemorrhage. In addition, hypothermia may interfere with coagulation. The purposes of this study were to compare the effectiveness QuikClot Combat Gauze (Q...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268478/ https://www.ncbi.nlm.nih.gov/pubmed/25568780 http://dx.doi.org/10.1016/j.amsu.2014.03.001 |
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author | Johnson, Don Bates, Sheri Nukalo, Sofiya Staub, Amy Hines, Aaron Leishman, Taylor Michel, Jennifer Sikes, Dusti Gegel, Brian Burgert, James |
author_facet | Johnson, Don Bates, Sheri Nukalo, Sofiya Staub, Amy Hines, Aaron Leishman, Taylor Michel, Jennifer Sikes, Dusti Gegel, Brian Burgert, James |
author_sort | Johnson, Don |
collection | PubMed |
description | Hemorrhage is the leading cause of death from trauma. Intravenous (IV) fluid resuscitation in these patients may cause hemodilution and secondary hemorrhage. In addition, hypothermia may interfere with coagulation. The purposes of this study were to compare the effectiveness QuikClot Combat Gauze (QCG) to a control group on hemorrhage in a hemodiluted, hypothermic model, and to determine the effects of IV volume resuscitation on rebleeding. This was a prospective, between subjects, experimental design. Yorkshire swine were randomly assigned to two groups: QCG (n = 13) or control (n = 13). The subjects were anesthetized. Hypothermia (temperature of ≤34.0 °C) was induced; 30% of their blood volume was exsanguinated. A 3:1 replacement of Lactated Ringer's was administered to dilute the remaining blood. The femoral artery and vein were transected. After 1 min of uncontrolled hemorrhage, QCG was placed into the wound followed by standard wound packing. The control group underwent the same procedures without QCG. After 5 min of manual pressure, a pressure dressing was applied. Following 30 min, the dressings were removed, and blood loss was calculated. For subjects achieving hemostasis, up to 5 L of IV fluid was administered or until bleeding occurred, which was defined as >2% total blood volume. The QCG had significantly less hemorrhage than the control (QCG = 30 ± 99 mL; control = 404 ± 406 mL) (p = .004). Further, the QCG group was able to tolerate more resuscitation fluid before hemorrhage (QCG = 4615 ± 1386 mL; control = 846 ± 1836) (p = .000). |
format | Online Article Text |
id | pubmed-4268478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-42684782015-01-07 The effects of QuikClot Combat Gauze on hemorrhage control in the presence of hemodilution and hypothermia Johnson, Don Bates, Sheri Nukalo, Sofiya Staub, Amy Hines, Aaron Leishman, Taylor Michel, Jennifer Sikes, Dusti Gegel, Brian Burgert, James Ann Med Surg (Lond) Article Hemorrhage is the leading cause of death from trauma. Intravenous (IV) fluid resuscitation in these patients may cause hemodilution and secondary hemorrhage. In addition, hypothermia may interfere with coagulation. The purposes of this study were to compare the effectiveness QuikClot Combat Gauze (QCG) to a control group on hemorrhage in a hemodiluted, hypothermic model, and to determine the effects of IV volume resuscitation on rebleeding. This was a prospective, between subjects, experimental design. Yorkshire swine were randomly assigned to two groups: QCG (n = 13) or control (n = 13). The subjects were anesthetized. Hypothermia (temperature of ≤34.0 °C) was induced; 30% of their blood volume was exsanguinated. A 3:1 replacement of Lactated Ringer's was administered to dilute the remaining blood. The femoral artery and vein were transected. After 1 min of uncontrolled hemorrhage, QCG was placed into the wound followed by standard wound packing. The control group underwent the same procedures without QCG. After 5 min of manual pressure, a pressure dressing was applied. Following 30 min, the dressings were removed, and blood loss was calculated. For subjects achieving hemostasis, up to 5 L of IV fluid was administered or until bleeding occurred, which was defined as >2% total blood volume. The QCG had significantly less hemorrhage than the control (QCG = 30 ± 99 mL; control = 404 ± 406 mL) (p = .004). Further, the QCG group was able to tolerate more resuscitation fluid before hemorrhage (QCG = 4615 ± 1386 mL; control = 846 ± 1836) (p = .000). Elsevier 2014-03-26 /pmc/articles/PMC4268478/ /pubmed/25568780 http://dx.doi.org/10.1016/j.amsu.2014.03.001 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Article Johnson, Don Bates, Sheri Nukalo, Sofiya Staub, Amy Hines, Aaron Leishman, Taylor Michel, Jennifer Sikes, Dusti Gegel, Brian Burgert, James The effects of QuikClot Combat Gauze on hemorrhage control in the presence of hemodilution and hypothermia |
title | The effects of QuikClot Combat Gauze on hemorrhage control in the presence of hemodilution and hypothermia |
title_full | The effects of QuikClot Combat Gauze on hemorrhage control in the presence of hemodilution and hypothermia |
title_fullStr | The effects of QuikClot Combat Gauze on hemorrhage control in the presence of hemodilution and hypothermia |
title_full_unstemmed | The effects of QuikClot Combat Gauze on hemorrhage control in the presence of hemodilution and hypothermia |
title_short | The effects of QuikClot Combat Gauze on hemorrhage control in the presence of hemodilution and hypothermia |
title_sort | effects of quikclot combat gauze on hemorrhage control in the presence of hemodilution and hypothermia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268478/ https://www.ncbi.nlm.nih.gov/pubmed/25568780 http://dx.doi.org/10.1016/j.amsu.2014.03.001 |
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