Early Adverse Reactions to Snake Antivenom: Poison Center Data Analysis

Antivenom is an essential treatment for snake envenomation; however, early adverse reactions (EARs) are major limitations to its use. We performed a retrospective cross-sectional study using Ramathibodi Poison Center data (January 2016 to December 2017) to clarify the incidence and severity of EARs...

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Main Authors: Charuwan Sriapha, Panee Rittilert, Taksa Vasaruchapong, Sahaphume Srisuma, Winai Wananukul, Satariya Trakulsrichai
Format: Article
Language:English
Published: MDPI AG 2022-10-01
Series:Toxins
Subjects:
Online Access:https://www.mdpi.com/2072-6651/14/10/694
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author Charuwan Sriapha
Panee Rittilert
Taksa Vasaruchapong
Sahaphume Srisuma
Winai Wananukul
Satariya Trakulsrichai
author_facet Charuwan Sriapha
Panee Rittilert
Taksa Vasaruchapong
Sahaphume Srisuma
Winai Wananukul
Satariya Trakulsrichai
author_sort Charuwan Sriapha
collection DOAJ
description Antivenom is an essential treatment for snake envenomation; however, early adverse reactions (EARs) are major limitations to its use. We performed a retrospective cross-sectional study using Ramathibodi Poison Center data (January 2016 to December 2017) to clarify the incidence and severity of EARs following different F(ab’)<sub>2</sub> antivenoms. Among 1006 envenomed patients, 684 (68%) received antivenom therapy with a total of 1157 doses, mostly green pit viper antivenom. The overall EAR incidence and rate were 22. 5% (154/684) and 15% (173/1157), respectively. The EAR rate following each type of antivenom was >10%, except for Russell’s viper antivenom (2.9%); the severe reaction rate was 2.6% (30/1157). Malayan pit viper bites caused a high incidence of EARs (37.8%) and the highest EAR rate (22.3%). Fifty-two cases developed anaphylaxis. All EARs occurred within 2 h after treatment initiation. No deaths were attributed to EARs. The duration of administration was significantly different between doses of antivenom that induced EARs and those that did not. In conclusion, all types and every dose of antivenom should be infused for 30–60 min. Preparation of resuscitation equipment and continuous clinical observation are crucial for at least 2 h after administration, and prompt treatment should be provided when EARs occur.
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spelling doaj.art-c581d784a0974167a48cbb3d38fd71ae2023-11-24T02:59:15ZengMDPI AGToxins2072-66512022-10-01141069410.3390/toxins14100694Early Adverse Reactions to Snake Antivenom: Poison Center Data AnalysisCharuwan Sriapha0Panee Rittilert1Taksa Vasaruchapong2Sahaphume Srisuma3Winai Wananukul4Satariya Trakulsrichai5Ramathibodi Poison Center, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, ThailandRamathibodi Poison Center, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, ThailandSnake Farm, Queen Saovabha Memorial Institute, The Thai Red Cross Society, Bangkok 10330, ThailandRamathibodi Poison Center, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, ThailandRamathibodi Poison Center, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, ThailandRamathibodi Poison Center, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, ThailandAntivenom is an essential treatment for snake envenomation; however, early adverse reactions (EARs) are major limitations to its use. We performed a retrospective cross-sectional study using Ramathibodi Poison Center data (January 2016 to December 2017) to clarify the incidence and severity of EARs following different F(ab’)<sub>2</sub> antivenoms. Among 1006 envenomed patients, 684 (68%) received antivenom therapy with a total of 1157 doses, mostly green pit viper antivenom. The overall EAR incidence and rate were 22. 5% (154/684) and 15% (173/1157), respectively. The EAR rate following each type of antivenom was >10%, except for Russell’s viper antivenom (2.9%); the severe reaction rate was 2.6% (30/1157). Malayan pit viper bites caused a high incidence of EARs (37.8%) and the highest EAR rate (22.3%). Fifty-two cases developed anaphylaxis. All EARs occurred within 2 h after treatment initiation. No deaths were attributed to EARs. The duration of administration was significantly different between doses of antivenom that induced EARs and those that did not. In conclusion, all types and every dose of antivenom should be infused for 30–60 min. Preparation of resuscitation equipment and continuous clinical observation are crucial for at least 2 h after administration, and prompt treatment should be provided when EARs occur.https://www.mdpi.com/2072-6651/14/10/694incidence of early adverse reactionsearly adverse reaction ratesnake antiveninadverse reactionsanaphylactic reactionssnakebite
spellingShingle Charuwan Sriapha
Panee Rittilert
Taksa Vasaruchapong
Sahaphume Srisuma
Winai Wananukul
Satariya Trakulsrichai
Early Adverse Reactions to Snake Antivenom: Poison Center Data Analysis
Toxins
incidence of early adverse reactions
early adverse reaction rate
snake antivenin
adverse reactions
anaphylactic reactions
snakebite
title Early Adverse Reactions to Snake Antivenom: Poison Center Data Analysis
title_full Early Adverse Reactions to Snake Antivenom: Poison Center Data Analysis
title_fullStr Early Adverse Reactions to Snake Antivenom: Poison Center Data Analysis
title_full_unstemmed Early Adverse Reactions to Snake Antivenom: Poison Center Data Analysis
title_short Early Adverse Reactions to Snake Antivenom: Poison Center Data Analysis
title_sort early adverse reactions to snake antivenom poison center data analysis
topic incidence of early adverse reactions
early adverse reaction rate
snake antivenin
adverse reactions
anaphylactic reactions
snakebite
url https://www.mdpi.com/2072-6651/14/10/694
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AT sahaphumesrisuma earlyadversereactionstosnakeantivenompoisoncenterdataanalysis
AT winaiwananukul earlyadversereactionstosnakeantivenompoisoncenterdataanalysis
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