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CoolClot, a novel hemostatic agent for controlling life-threatening arterial bleeding

BACKGROUND: Uncontrolled bleeding is the first leading cause of preventable death in the battlefield and the 2nd cause of mortality in civil accidents. Incompressible hemorrhage control is among the interventions that drastically increase the survival rate in wound individuals. We have previously sh...

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Autores principales: Mortazavi, SMJ, Tavasoli, A, Atefi, M, Tanide, N, Radpey, N, Roshan-shomal, P, Moradi, H, Taeb, S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Second Affiliated Hospital of Zhejiang University School of Medicine 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129838/
https://www.ncbi.nlm.nih.gov/pubmed/25215105
http://dx.doi.org/10.5847/wjem.j.issn.1920-8642.2013.02.007
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author Mortazavi, SMJ
Tavasoli, A
Atefi, M
Tanide, N
Radpey, N
Roshan-shomal, P
Moradi, H
Taeb, S
author_facet Mortazavi, SMJ
Tavasoli, A
Atefi, M
Tanide, N
Radpey, N
Roshan-shomal, P
Moradi, H
Taeb, S
author_sort Mortazavi, SMJ
collection PubMed
description BACKGROUND: Uncontrolled bleeding is the first leading cause of preventable death in the battlefield and the 2nd cause of mortality in civil accidents. Incompressible hemorrhage control is among the interventions that drastically increase the survival rate in wound individuals. We have previously shown that a certain mixture of bentonite and zeolite minerals can significantly decrease the bleeding in rats. METHODS: In this study, nine healthy hybrid dogs were selected and after induction of anesthesia with ether, either arterial puncture by a needle or arteriotomy was performed on both groin regions of the dogs. For control arteries (either the right or left femoral artery), only pressure by sterilized gauze was performed, while for the femoral arteries of the opposite side, our invented hemostatic agent, namely CoolClot, was topically used before applying the pressure. In the second stage of the study, to assess the coagulation time, blood samples were collected from 10 volunteer students. RESULTS: CoolClot significantly decreased the bleeding time in animals whose femoral arteries were cut or punctured. In the human phase of the study, the mean coagulation time in control blood samples was 253.4±44.1 seconds, whereas it was 149.5±50.0, 162.3±74.6 and 143.4±114.6 seconds, respectively in blood samples treated with bentonite, zeolite and CoolClot (P<0.05). CONCLUSIONS: As controlling bleeding after a life-threatening arterial damage is critical for increasing the chance of survival, the results obtained in this study indicate the significant efficacy of CoolClot in shortening the bleeding time. Our experiments also indicate that CoolClot can significantly reduce the clotting time in human blood samples.
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spelling pubmed-41298382014-09-11 CoolClot, a novel hemostatic agent for controlling life-threatening arterial bleeding Mortazavi, SMJ Tavasoli, A Atefi, M Tanide, N Radpey, N Roshan-shomal, P Moradi, H Taeb, S World J Emerg Med Original Article BACKGROUND: Uncontrolled bleeding is the first leading cause of preventable death in the battlefield and the 2nd cause of mortality in civil accidents. Incompressible hemorrhage control is among the interventions that drastically increase the survival rate in wound individuals. We have previously shown that a certain mixture of bentonite and zeolite minerals can significantly decrease the bleeding in rats. METHODS: In this study, nine healthy hybrid dogs were selected and after induction of anesthesia with ether, either arterial puncture by a needle or arteriotomy was performed on both groin regions of the dogs. For control arteries (either the right or left femoral artery), only pressure by sterilized gauze was performed, while for the femoral arteries of the opposite side, our invented hemostatic agent, namely CoolClot, was topically used before applying the pressure. In the second stage of the study, to assess the coagulation time, blood samples were collected from 10 volunteer students. RESULTS: CoolClot significantly decreased the bleeding time in animals whose femoral arteries were cut or punctured. In the human phase of the study, the mean coagulation time in control blood samples was 253.4±44.1 seconds, whereas it was 149.5±50.0, 162.3±74.6 and 143.4±114.6 seconds, respectively in blood samples treated with bentonite, zeolite and CoolClot (P<0.05). CONCLUSIONS: As controlling bleeding after a life-threatening arterial damage is critical for increasing the chance of survival, the results obtained in this study indicate the significant efficacy of CoolClot in shortening the bleeding time. Our experiments also indicate that CoolClot can significantly reduce the clotting time in human blood samples. Second Affiliated Hospital of Zhejiang University School of Medicine 2013 /pmc/articles/PMC4129838/ /pubmed/25215105 http://dx.doi.org/10.5847/wjem.j.issn.1920-8642.2013.02.007 Text en Copyright: © World Journal of Emergency Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mortazavi, SMJ
Tavasoli, A
Atefi, M
Tanide, N
Radpey, N
Roshan-shomal, P
Moradi, H
Taeb, S
CoolClot, a novel hemostatic agent for controlling life-threatening arterial bleeding
title CoolClot, a novel hemostatic agent for controlling life-threatening arterial bleeding
title_full CoolClot, a novel hemostatic agent for controlling life-threatening arterial bleeding
title_fullStr CoolClot, a novel hemostatic agent for controlling life-threatening arterial bleeding
title_full_unstemmed CoolClot, a novel hemostatic agent for controlling life-threatening arterial bleeding
title_short CoolClot, a novel hemostatic agent for controlling life-threatening arterial bleeding
title_sort coolclot, a novel hemostatic agent for controlling life-threatening arterial bleeding
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129838/
https://www.ncbi.nlm.nih.gov/pubmed/25215105
http://dx.doi.org/10.5847/wjem.j.issn.1920-8642.2013.02.007
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