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Low-dose heparin as treatment for early disseminated intravascular coagulation during sepsis: A prospective clinical study
The present study aimed to investigate whether low-dose heparin improves the condition of patients suffering from early disseminated intravascular coagulation (pre-DIC) during sepsis. In total, 37 patients were randomly divided into low-dose heparin intervention and control groups. The heparin group...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919907/ https://www.ncbi.nlm.nih.gov/pubmed/24520253 http://dx.doi.org/10.3892/etm.2013.1466 |
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author | LIU, XIAO-LI WANG, XIAO-ZHI LIU, XIU-XIANG HAO, DONG JALADAT, YASAMAN LU, FENG SUN, TING LV, CHANG-JUN |
author_facet | LIU, XIAO-LI WANG, XIAO-ZHI LIU, XIU-XIANG HAO, DONG JALADAT, YASAMAN LU, FENG SUN, TING LV, CHANG-JUN |
author_sort | LIU, XIAO-LI |
collection | PubMed |
description | The present study aimed to investigate whether low-dose heparin improves the condition of patients suffering from early disseminated intravascular coagulation (pre-DIC) during sepsis. In total, 37 patients were randomly divided into low-dose heparin intervention and control groups. The heparin group received a low-dose of heparin for 5–7 days, while the other group received only saline. The two groups were treated for sepsis. Blood samples were collected at various times and acute physiology and chronic health evaluation (APACHE)-II scores were recorded at day 1 and 7. In addition, the number of days applying mechanical ventilation and in the intensive care unit (ICU) were recorded, as well as the 28-day mortality rate. APACHE-II scores in the two groups decreased following treatment, however, scores in the heparin group decreased more significantly. Prothrombin fragment and thrombin-antithrombin complex levels in the heparin group were significantly decreased. In addition, the number of days applying a ventilator was fewer and the total stay in ICU was significantly shorter compared with the control group. Significantly fewer complications were observed in the heparin group, however, there was no significant difference in the 28-day mortality rate. In conclusion, low-dose heparin improves the hypercoagulable state of sepsis, which subsequently reduces the incidence of DIC or multiple organ dysfunction syndrome, decreasing the number of days of mechanical ventilation and hospitalization. |
format | Online Article Text |
id | pubmed-3919907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-39199072014-02-11 Low-dose heparin as treatment for early disseminated intravascular coagulation during sepsis: A prospective clinical study LIU, XIAO-LI WANG, XIAO-ZHI LIU, XIU-XIANG HAO, DONG JALADAT, YASAMAN LU, FENG SUN, TING LV, CHANG-JUN Exp Ther Med Articles The present study aimed to investigate whether low-dose heparin improves the condition of patients suffering from early disseminated intravascular coagulation (pre-DIC) during sepsis. In total, 37 patients were randomly divided into low-dose heparin intervention and control groups. The heparin group received a low-dose of heparin for 5–7 days, while the other group received only saline. The two groups were treated for sepsis. Blood samples were collected at various times and acute physiology and chronic health evaluation (APACHE)-II scores were recorded at day 1 and 7. In addition, the number of days applying mechanical ventilation and in the intensive care unit (ICU) were recorded, as well as the 28-day mortality rate. APACHE-II scores in the two groups decreased following treatment, however, scores in the heparin group decreased more significantly. Prothrombin fragment and thrombin-antithrombin complex levels in the heparin group were significantly decreased. In addition, the number of days applying a ventilator was fewer and the total stay in ICU was significantly shorter compared with the control group. Significantly fewer complications were observed in the heparin group, however, there was no significant difference in the 28-day mortality rate. In conclusion, low-dose heparin improves the hypercoagulable state of sepsis, which subsequently reduces the incidence of DIC or multiple organ dysfunction syndrome, decreasing the number of days of mechanical ventilation and hospitalization. D.A. Spandidos 2014-03 2013-12-31 /pmc/articles/PMC3919907/ /pubmed/24520253 http://dx.doi.org/10.3892/etm.2013.1466 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles LIU, XIAO-LI WANG, XIAO-ZHI LIU, XIU-XIANG HAO, DONG JALADAT, YASAMAN LU, FENG SUN, TING LV, CHANG-JUN Low-dose heparin as treatment for early disseminated intravascular coagulation during sepsis: A prospective clinical study |
title | Low-dose heparin as treatment for early disseminated intravascular coagulation during sepsis: A prospective clinical study |
title_full | Low-dose heparin as treatment for early disseminated intravascular coagulation during sepsis: A prospective clinical study |
title_fullStr | Low-dose heparin as treatment for early disseminated intravascular coagulation during sepsis: A prospective clinical study |
title_full_unstemmed | Low-dose heparin as treatment for early disseminated intravascular coagulation during sepsis: A prospective clinical study |
title_short | Low-dose heparin as treatment for early disseminated intravascular coagulation during sepsis: A prospective clinical study |
title_sort | low-dose heparin as treatment for early disseminated intravascular coagulation during sepsis: a prospective clinical study |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919907/ https://www.ncbi.nlm.nih.gov/pubmed/24520253 http://dx.doi.org/10.3892/etm.2013.1466 |
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