The efficacy of two antivenoms against the venom of North American snakes
Mortality due to snake envenomation is not a major problem in the United States with approximately 8–12 deaths per year, but envenomation is a serious problem that can result in functional disability, loss of extremities, and a costly recovery. Physicians encounter different clinical situations with...
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Veröffentlicht in: | Toxicon (Oxford) 2003-03, Vol.41 (3), p.357-365 |
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description | Mortality due to snake envenomation is not a major problem in the United States with approximately 8–12 deaths per year, but envenomation is a serious problem that can result in functional disability, loss of extremities, and a costly recovery. Physicians encounter different clinical situations with each new snakebite victim because of the geographical variations in snake venoms. The best and most acceptable form of treatment is the use of antivenom; however, it must be administered as soon as possible since it is not so effective at reducing local signs of envenomation such as necrosis. The antivenom in the United States is in short supply, expensive and may not even be the most effective for neutralizing all North American snake venoms. In this study, we tested two antivenoms. The first was a Crotalidae Polyvalent Fab fragment with Ovine origin (FabO) manufactured in London, and the second was Antivipmyn, a Mexican manufactured antivenom that is F(ab′)
2 fragment produced in horse (Fab
2H). The efficacy of the two antivenoms was tested with 15 different snake venoms found in North America. Three different assays were used to test the efficacy of the antivenoms, the in vivo serum protection test (ED
50), antihemorrhagic and anticoagulant. The Fab
2H antivenom was most effective in neutralizing the hemorrhagic activity of 78% of the hemorrhagic venoms used in this study. In the ED
50 assay, the Fab
2H antivenom was effective in neutralizing all venoms used in this study, while FabO neutralized all but
C. m. molossus venom. However, in most cases, FabO required less antivenom than Fab
2H antivenom to neutralize three LD
50. |
doi_str_mv | 10.1016/S0041-0101(02)00330-6 |
format | Article |
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2 fragment produced in horse (Fab
2H). The efficacy of the two antivenoms was tested with 15 different snake venoms found in North America. Three different assays were used to test the efficacy of the antivenoms, the in vivo serum protection test (ED
50), antihemorrhagic and anticoagulant. The Fab
2H antivenom was most effective in neutralizing the hemorrhagic activity of 78% of the hemorrhagic venoms used in this study. In the ED
50 assay, the Fab
2H antivenom was effective in neutralizing all venoms used in this study, while FabO neutralized all but
C. m. molossus venom. However, in most cases, FabO required less antivenom than Fab
2H antivenom to neutralize three LD
50.</description><identifier>ISSN: 0041-0101</identifier><identifier>EISSN: 1879-3150</identifier><identifier>DOI: 10.1016/S0041-0101(02)00330-6</identifier><identifier>PMID: 12565759</identifier><identifier>CODEN: TOXIA6</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Agkistrodon ; Animal poisons toxicology. Antivenoms ; Animals ; Antihemorrhagic ; Antivenins - immunology ; Antivenins - therapeutic use ; Antivenom ; Antivipmyn ; Biological and medical sciences ; Biological Assay ; Blood Coagulation - drug effects ; Coagulopathy ; Crotalid Venoms - antagonists & inhibitors ; Crotalid Venoms - immunology ; Crotalid Venoms - toxicity ; Crotalidae polyvalent immune fab (ovine) ; Crotalus ; ED 50 ; Fibrinogen - immunology ; Fibrinogen - metabolism ; Hemorrhage - chemically induced ; Hemorrhage - prevention & control ; Hemorrhagic ; Horses ; Immunoglobulin Fab Fragments - therapeutic use ; LD 50 ; Lethal Dose 50 ; Medical sciences ; Neutralization Tests ; North America ; Rabbits ; Sheep ; Sistrurus ; Species Specificity ; Thrombosis - chemically induced ; Thrombosis - prevention & control ; Toxicology</subject><ispartof>Toxicon (Oxford), 2003-03, Vol.41 (3), p.357-365</ispartof><rights>2003</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-fe40e34df66926329008dd37afcfd3fd60fd8f83144bd220730997a7fdc60c203</citedby><cites>FETCH-LOGICAL-c422t-fe40e34df66926329008dd37afcfd3fd60fd8f83144bd220730997a7fdc60c203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0041010102003306$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14545378$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12565759$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sánchez, Elda E</creatorcontrib><creatorcontrib>Galán, Jacob A</creatorcontrib><creatorcontrib>Perez, John C</creatorcontrib><creatorcontrib>Rodrı́guez-Acosta, Alexis</creatorcontrib><creatorcontrib>Chase, Peter B</creatorcontrib><creatorcontrib>Pérez, John C</creatorcontrib><title>The efficacy of two antivenoms against the venom of North American snakes</title><title>Toxicon (Oxford)</title><addtitle>Toxicon</addtitle><description>Mortality due to snake envenomation is not a major problem in the United States with approximately 8–12 deaths per year, but envenomation is a serious problem that can result in functional disability, loss of extremities, and a costly recovery. Physicians encounter different clinical situations with each new snakebite victim because of the geographical variations in snake venoms. The best and most acceptable form of treatment is the use of antivenom; however, it must be administered as soon as possible since it is not so effective at reducing local signs of envenomation such as necrosis. The antivenom in the United States is in short supply, expensive and may not even be the most effective for neutralizing all North American snake venoms. In this study, we tested two antivenoms. The first was a Crotalidae Polyvalent Fab fragment with Ovine origin (FabO) manufactured in London, and the second was Antivipmyn, a Mexican manufactured antivenom that is F(ab′)
2 fragment produced in horse (Fab
2H). The efficacy of the two antivenoms was tested with 15 different snake venoms found in North America. Three different assays were used to test the efficacy of the antivenoms, the in vivo serum protection test (ED
50), antihemorrhagic and anticoagulant. The Fab
2H antivenom was most effective in neutralizing the hemorrhagic activity of 78% of the hemorrhagic venoms used in this study. In the ED
50 assay, the Fab
2H antivenom was effective in neutralizing all venoms used in this study, while FabO neutralized all but
C. m. molossus venom. However, in most cases, FabO required less antivenom than Fab
2H antivenom to neutralize three LD
50.</description><subject>Agkistrodon</subject><subject>Animal poisons toxicology. Antivenoms</subject><subject>Animals</subject><subject>Antihemorrhagic</subject><subject>Antivenins - immunology</subject><subject>Antivenins - therapeutic use</subject><subject>Antivenom</subject><subject>Antivipmyn</subject><subject>Biological and medical sciences</subject><subject>Biological Assay</subject><subject>Blood Coagulation - drug effects</subject><subject>Coagulopathy</subject><subject>Crotalid Venoms - antagonists & inhibitors</subject><subject>Crotalid Venoms - immunology</subject><subject>Crotalid Venoms - toxicity</subject><subject>Crotalidae polyvalent immune fab (ovine)</subject><subject>Crotalus</subject><subject>ED 50</subject><subject>Fibrinogen - immunology</subject><subject>Fibrinogen - metabolism</subject><subject>Hemorrhage - chemically induced</subject><subject>Hemorrhage - prevention & control</subject><subject>Hemorrhagic</subject><subject>Horses</subject><subject>Immunoglobulin Fab Fragments - therapeutic use</subject><subject>LD 50</subject><subject>Lethal Dose 50</subject><subject>Medical sciences</subject><subject>Neutralization Tests</subject><subject>North America</subject><subject>Rabbits</subject><subject>Sheep</subject><subject>Sistrurus</subject><subject>Species Specificity</subject><subject>Thrombosis - chemically induced</subject><subject>Thrombosis - prevention & control</subject><subject>Toxicology</subject><issn>0041-0101</issn><issn>1879-3150</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0MtOxCAUgGFiNDqOPoKmG40uqodLabsyk4mXSYwu1DVh4KDotFXoaHx7mUt06QpCvgPkJ-SAwhkFKs8fAATNIe1PgJ0CcA653CADWpV1zmkBm2TwS3bIboyvkFRVy22yQ1khi7KoB2Ty-IIZOueNNt9Z57L-q8t02_tPbLsmZvpZ-zb2WZ_Y8mhh7rrQv2SjBkMaa7PY6jeMe2TL6VnE_fU6JE9Xl4_jm_z2_noyHt3mRjDW5w4FIBfWSVkzyVkNUFnLS-2Ms9xZCc5WruJUiKllDEoOdV3q0lkjwTDgQ3K8uvc9dB9zjL1qfDQ4m-kWu3lUtAQBRUUTLFbQhC7GgE69B9_o8K0oqEVDtWyoFoEUMLVsqGSaO1w_MJ82aP-m1tESOFoDHY2euaBb4-OfE4UoeFkld7FymHJ8egwqGo-tQesDml7Zzv_zlR-XzYyh</recordid><startdate>20030301</startdate><enddate>20030301</enddate><creator>Sánchez, Elda E</creator><creator>Galán, Jacob A</creator><creator>Perez, John C</creator><creator>Rodrı́guez-Acosta, Alexis</creator><creator>Chase, Peter B</creator><creator>Pérez, John C</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20030301</creationdate><title>The efficacy of two antivenoms against the venom of North American snakes</title><author>Sánchez, Elda E ; Galán, Jacob A ; Perez, John C ; Rodrı́guez-Acosta, Alexis ; Chase, Peter B ; Pérez, John C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-fe40e34df66926329008dd37afcfd3fd60fd8f83144bd220730997a7fdc60c203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Agkistrodon</topic><topic>Animal poisons toxicology. Antivenoms</topic><topic>Animals</topic><topic>Antihemorrhagic</topic><topic>Antivenins - immunology</topic><topic>Antivenins - therapeutic use</topic><topic>Antivenom</topic><topic>Antivipmyn</topic><topic>Biological and medical sciences</topic><topic>Biological Assay</topic><topic>Blood Coagulation - drug effects</topic><topic>Coagulopathy</topic><topic>Crotalid Venoms - antagonists & inhibitors</topic><topic>Crotalid Venoms - immunology</topic><topic>Crotalid Venoms - toxicity</topic><topic>Crotalidae polyvalent immune fab (ovine)</topic><topic>Crotalus</topic><topic>ED 50</topic><topic>Fibrinogen - immunology</topic><topic>Fibrinogen - metabolism</topic><topic>Hemorrhage - chemically induced</topic><topic>Hemorrhage - prevention & control</topic><topic>Hemorrhagic</topic><topic>Horses</topic><topic>Immunoglobulin Fab Fragments - therapeutic use</topic><topic>LD 50</topic><topic>Lethal Dose 50</topic><topic>Medical sciences</topic><topic>Neutralization Tests</topic><topic>North America</topic><topic>Rabbits</topic><topic>Sheep</topic><topic>Sistrurus</topic><topic>Species Specificity</topic><topic>Thrombosis - chemically induced</topic><topic>Thrombosis - prevention & control</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sánchez, Elda E</creatorcontrib><creatorcontrib>Galán, Jacob A</creatorcontrib><creatorcontrib>Perez, John C</creatorcontrib><creatorcontrib>Rodrı́guez-Acosta, Alexis</creatorcontrib><creatorcontrib>Chase, Peter B</creatorcontrib><creatorcontrib>Pérez, John C</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicon (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sánchez, Elda E</au><au>Galán, Jacob A</au><au>Perez, John C</au><au>Rodrı́guez-Acosta, Alexis</au><au>Chase, Peter B</au><au>Pérez, John C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The efficacy of two antivenoms against the venom of North American snakes</atitle><jtitle>Toxicon (Oxford)</jtitle><addtitle>Toxicon</addtitle><date>2003-03-01</date><risdate>2003</risdate><volume>41</volume><issue>3</issue><spage>357</spage><epage>365</epage><pages>357-365</pages><issn>0041-0101</issn><eissn>1879-3150</eissn><coden>TOXIA6</coden><abstract>Mortality due to snake envenomation is not a major problem in the United States with approximately 8–12 deaths per year, but envenomation is a serious problem that can result in functional disability, loss of extremities, and a costly recovery. Physicians encounter different clinical situations with each new snakebite victim because of the geographical variations in snake venoms. The best and most acceptable form of treatment is the use of antivenom; however, it must be administered as soon as possible since it is not so effective at reducing local signs of envenomation such as necrosis. The antivenom in the United States is in short supply, expensive and may not even be the most effective for neutralizing all North American snake venoms. In this study, we tested two antivenoms. The first was a Crotalidae Polyvalent Fab fragment with Ovine origin (FabO) manufactured in London, and the second was Antivipmyn, a Mexican manufactured antivenom that is F(ab′)
2 fragment produced in horse (Fab
2H). The efficacy of the two antivenoms was tested with 15 different snake venoms found in North America. Three different assays were used to test the efficacy of the antivenoms, the in vivo serum protection test (ED
50), antihemorrhagic and anticoagulant. The Fab
2H antivenom was most effective in neutralizing the hemorrhagic activity of 78% of the hemorrhagic venoms used in this study. In the ED
50 assay, the Fab
2H antivenom was effective in neutralizing all venoms used in this study, while FabO neutralized all but
C. m. molossus venom. However, in most cases, FabO required less antivenom than Fab
2H antivenom to neutralize three LD
50.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>12565759</pmid><doi>10.1016/S0041-0101(02)00330-6</doi><tpages>9</tpages></addata></record> |
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subjects | Agkistrodon Animal poisons toxicology. Antivenoms Animals Antihemorrhagic Antivenins - immunology Antivenins - therapeutic use Antivenom Antivipmyn Biological and medical sciences Biological Assay Blood Coagulation - drug effects Coagulopathy Crotalid Venoms - antagonists & inhibitors Crotalid Venoms - immunology Crotalid Venoms - toxicity Crotalidae polyvalent immune fab (ovine) Crotalus ED 50 Fibrinogen - immunology Fibrinogen - metabolism Hemorrhage - chemically induced Hemorrhage - prevention & control Hemorrhagic Horses Immunoglobulin Fab Fragments - therapeutic use LD 50 Lethal Dose 50 Medical sciences Neutralization Tests North America Rabbits Sheep Sistrurus Species Specificity Thrombosis - chemically induced Thrombosis - prevention & control Toxicology |
title | The efficacy of two antivenoms against the venom of North American snakes |
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