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Risk factor, monitoring, and treatment for snakebite induced coagulopathy: a multicenter retrospective study
BACKGROUND: Snakebite can cause various complications, including coagulopathy. The clinical features of snakebite-associated coagulopathy differ from those of disseminated intravascular coagulation (DIC) caused by other diseases and its treatment is controversial. METHODS: We retrospectively reviewe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Critical Care Medicine
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895465/ https://www.ncbi.nlm.nih.gov/pubmed/31743633 http://dx.doi.org/10.4266/acc.2019.00591 |
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author | Jeon, Yong Jun Kim, Jong Wan Park, SungGil Shin, Dong Woo |
author_facet | Jeon, Yong Jun Kim, Jong Wan Park, SungGil Shin, Dong Woo |
author_sort | Jeon, Yong Jun |
collection | PubMed |
description | BACKGROUND: Snakebite can cause various complications, including coagulopathy. The clinical features of snakebite-associated coagulopathy differ from those of disseminated intravascular coagulation (DIC) caused by other diseases and its treatment is controversial. METHODS: We retrospectively reviewed the medical records of patients hospitalized for snakebite between January 2006 and September 2018. RESULTS: A total of 226 patients were hospitalized due to snakebite. Their median hospital stay was 4.0 days (interquartile range, 2.0 to 7.0 days). Five patients arrived at hospital with shock and one patient died. Twenty-one patients had overt DIC according to the International Society of Thrombosis and Hemostasis scoring system. Two patients developed major bleeding complications. Initial lower cholesterol level at presentation was associated with the development of overt DIC. International normalization ratio (INR) exceeding the laboratory’s measurement limit was recorded as late as 4 to 5 days after the bite. Higher antivenom doses (≥18,000 units) and transfusion of fresh frozen plasma (FFP) or cryoprecipitate did not affect prolonged INR duration or hospital stay in the overt DIC patients without bleeding. CONCLUSIONS: Initial lower cholesterol level may be a risk factor for overt DIC following snakebite. Although patients lack apparent symptoms, the risk of coagulopathy should be assessed for at least 4 to 5 days following snakebite. Higher antivenom doses and transfusion of FFP or cryoprecipitate may be unbeneficial for coagulopathic patients without bleeding. |
format | Online Article Text |
id | pubmed-6895465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society of Critical Care Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-68954652019-12-30 Risk factor, monitoring, and treatment for snakebite induced coagulopathy: a multicenter retrospective study Jeon, Yong Jun Kim, Jong Wan Park, SungGil Shin, Dong Woo Acute Crit Care Original Article BACKGROUND: Snakebite can cause various complications, including coagulopathy. The clinical features of snakebite-associated coagulopathy differ from those of disseminated intravascular coagulation (DIC) caused by other diseases and its treatment is controversial. METHODS: We retrospectively reviewed the medical records of patients hospitalized for snakebite between January 2006 and September 2018. RESULTS: A total of 226 patients were hospitalized due to snakebite. Their median hospital stay was 4.0 days (interquartile range, 2.0 to 7.0 days). Five patients arrived at hospital with shock and one patient died. Twenty-one patients had overt DIC according to the International Society of Thrombosis and Hemostasis scoring system. Two patients developed major bleeding complications. Initial lower cholesterol level at presentation was associated with the development of overt DIC. International normalization ratio (INR) exceeding the laboratory’s measurement limit was recorded as late as 4 to 5 days after the bite. Higher antivenom doses (≥18,000 units) and transfusion of fresh frozen plasma (FFP) or cryoprecipitate did not affect prolonged INR duration or hospital stay in the overt DIC patients without bleeding. CONCLUSIONS: Initial lower cholesterol level may be a risk factor for overt DIC following snakebite. Although patients lack apparent symptoms, the risk of coagulopathy should be assessed for at least 4 to 5 days following snakebite. Higher antivenom doses and transfusion of FFP or cryoprecipitate may be unbeneficial for coagulopathic patients without bleeding. Korean Society of Critical Care Medicine 2019-11 2019-11-18 /pmc/articles/PMC6895465/ /pubmed/31743633 http://dx.doi.org/10.4266/acc.2019.00591 Text en Copyright © 2019 The Korean Society of Critical Care Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jeon, Yong Jun Kim, Jong Wan Park, SungGil Shin, Dong Woo Risk factor, monitoring, and treatment for snakebite induced coagulopathy: a multicenter retrospective study |
title | Risk factor, monitoring, and treatment for snakebite induced coagulopathy: a multicenter retrospective study |
title_full | Risk factor, monitoring, and treatment for snakebite induced coagulopathy: a multicenter retrospective study |
title_fullStr | Risk factor, monitoring, and treatment for snakebite induced coagulopathy: a multicenter retrospective study |
title_full_unstemmed | Risk factor, monitoring, and treatment for snakebite induced coagulopathy: a multicenter retrospective study |
title_short | Risk factor, monitoring, and treatment for snakebite induced coagulopathy: a multicenter retrospective study |
title_sort | risk factor, monitoring, and treatment for snakebite induced coagulopathy: a multicenter retrospective study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895465/ https://www.ncbi.nlm.nih.gov/pubmed/31743633 http://dx.doi.org/10.4266/acc.2019.00591 |
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