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Snakebite Associated Thrombotic Microangiopathy and Recommendations for Clinical Practice
Snakebite is a significant and under-resourced global public health issue. Snake venoms cause a variety of potentially fatal clinical toxin syndromes, including venom-induced consumption coagulopathy (VICC) which is associated with major haemorrhage. A subset of patients with VICC develop a thrombot...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778654/ https://www.ncbi.nlm.nih.gov/pubmed/35051033 http://dx.doi.org/10.3390/toxins14010057 |
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author | Noutsos, Tina Currie, Bart J. Wijewickrama, Eranga S. Isbister, Geoffrey K. |
author_facet | Noutsos, Tina Currie, Bart J. Wijewickrama, Eranga S. Isbister, Geoffrey K. |
author_sort | Noutsos, Tina |
collection | PubMed |
description | Snakebite is a significant and under-resourced global public health issue. Snake venoms cause a variety of potentially fatal clinical toxin syndromes, including venom-induced consumption coagulopathy (VICC) which is associated with major haemorrhage. A subset of patients with VICC develop a thrombotic microangiopathy (TMA). This article reviews recent evidence regarding snakebite-associated TMA and its epidemiology, diagnosis, outcomes, and effectiveness of interventions including antivenom and therapeutic plasma-exchange. Snakebite-associated TMA presents with microangiopathic haemolytic anaemia (evidenced by schistocytes on the blood film), thrombocytopenia in almost all cases, and a spectrum of acute kidney injury (AKI). A proportion of patients require dialysis, most survive and achieve dialysis free survival. There is no evidence that antivenom prevents TMA specifically, but early antivenom remains the mainstay of treatment for snake envenoming. There is no evidence for therapeutic plasma-exchange being effective. We propose diagnostic criteria for snakebite-associated TMA as anaemia with >1.0% schistocytes on blood film examination, together with absolute thrombocytopenia (<150 × 10(9)/L) or a relative decrease in platelet count of >25% from baseline. Patients are at risk of long-term chronic kidney disease and long term follow up is recommended. |
format | Online Article Text |
id | pubmed-8778654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87786542022-01-22 Snakebite Associated Thrombotic Microangiopathy and Recommendations for Clinical Practice Noutsos, Tina Currie, Bart J. Wijewickrama, Eranga S. Isbister, Geoffrey K. Toxins (Basel) Review Snakebite is a significant and under-resourced global public health issue. Snake venoms cause a variety of potentially fatal clinical toxin syndromes, including venom-induced consumption coagulopathy (VICC) which is associated with major haemorrhage. A subset of patients with VICC develop a thrombotic microangiopathy (TMA). This article reviews recent evidence regarding snakebite-associated TMA and its epidemiology, diagnosis, outcomes, and effectiveness of interventions including antivenom and therapeutic plasma-exchange. Snakebite-associated TMA presents with microangiopathic haemolytic anaemia (evidenced by schistocytes on the blood film), thrombocytopenia in almost all cases, and a spectrum of acute kidney injury (AKI). A proportion of patients require dialysis, most survive and achieve dialysis free survival. There is no evidence that antivenom prevents TMA specifically, but early antivenom remains the mainstay of treatment for snake envenoming. There is no evidence for therapeutic plasma-exchange being effective. We propose diagnostic criteria for snakebite-associated TMA as anaemia with >1.0% schistocytes on blood film examination, together with absolute thrombocytopenia (<150 × 10(9)/L) or a relative decrease in platelet count of >25% from baseline. Patients are at risk of long-term chronic kidney disease and long term follow up is recommended. MDPI 2022-01-14 /pmc/articles/PMC8778654/ /pubmed/35051033 http://dx.doi.org/10.3390/toxins14010057 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Noutsos, Tina Currie, Bart J. Wijewickrama, Eranga S. Isbister, Geoffrey K. Snakebite Associated Thrombotic Microangiopathy and Recommendations for Clinical Practice |
title | Snakebite Associated Thrombotic Microangiopathy and Recommendations for Clinical Practice |
title_full | Snakebite Associated Thrombotic Microangiopathy and Recommendations for Clinical Practice |
title_fullStr | Snakebite Associated Thrombotic Microangiopathy and Recommendations for Clinical Practice |
title_full_unstemmed | Snakebite Associated Thrombotic Microangiopathy and Recommendations for Clinical Practice |
title_short | Snakebite Associated Thrombotic Microangiopathy and Recommendations for Clinical Practice |
title_sort | snakebite associated thrombotic microangiopathy and recommendations for clinical practice |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778654/ https://www.ncbi.nlm.nih.gov/pubmed/35051033 http://dx.doi.org/10.3390/toxins14010057 |
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