Synergy of antithrombin III concentrate and antivenom in preventing coagulopathy in a rat model of Malayan pit viper envenoming

The effects of unrefined equine antivenom and antithrombin III (AT-III) concentrate on the coagulopathy induced by systemic envenomation by Malayan pit viper (Calloselasma rhodostoma; MPV) venom were investigated in a rat model. 37 rats received an intramuscular injection of MPV venom and serial blo...

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Main Authors: S. Pukrittayakamee, V. Desakorn, R. Clemens, A. Nontprasert, H. L. Bock, N. J. White, D. Bunnag
Other Authors: Mahidol University
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/15969
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spelling th-mahidol.159692018-06-14T16:25:55Z Synergy of antithrombin III concentrate and antivenom in preventing coagulopathy in a rat model of Malayan pit viper envenoming S. Pukrittayakamee V. Desakorn R. Clemens A. Nontprasert H. L. Bock N. J. White D. Bunnag Mahidol University Behringwerke AG Nuffield Department of Clinical Medicine Immunology and Microbiology Medicine The effects of unrefined equine antivenom and antithrombin III (AT-III) concentrate on the coagulopathy induced by systemic envenomation by Malayan pit viper (Calloselasma rhodostoma; MPV) venom were investigated in a rat model. 37 rats received an intramuscular injection of MPV venom and serial blood samples were taken from the femoral vein for simple whole blood clotting tests and measurement of AT-III activity. 30 min after venom injection, treatment (antivenom, AT-III or both) was given intravenously. 6 rats were untreated and all developed uncoagulable blood and AT-III depletion 90-210 (median 180) mm after venom injection. A combination of high dose AT-III concentrate (0.5 units/g) and antivenom (20 μg/g) prevented abnormal clotting (P < ;0.001), whereas AT-III alone, antivenom alone, or a combination of low dose AT-III (0.25 units/g) and antivenom did not (P < 0.05). These results suggest that the coagulation abnormality in MPV envenomation is secondary to activation of the coagulation cascade at several levels, and that treatment with antivenom alone may not be sufficient to reverse or prevent this phenomenon. © 1990, Oxford University Press. All rights reserved. 2018-06-14T09:21:35Z 2018-06-14T09:21:35Z 1990-01-01 Article Transactions of the Royal Society of Tropical Medicine and Hygiene. Vol.84, No.6 (1990), 880-884 10.1016/0035-9203(90)90113-S 18783503 00359203 2-s2.0-0025690432 https://repository.li.mahidol.ac.th/handle/123456789/15969 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0025690432&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Immunology and Microbiology
Medicine
spellingShingle Immunology and Microbiology
Medicine
S. Pukrittayakamee
V. Desakorn
R. Clemens
A. Nontprasert
H. L. Bock
N. J. White
D. Bunnag
Synergy of antithrombin III concentrate and antivenom in preventing coagulopathy in a rat model of Malayan pit viper envenoming
description The effects of unrefined equine antivenom and antithrombin III (AT-III) concentrate on the coagulopathy induced by systemic envenomation by Malayan pit viper (Calloselasma rhodostoma; MPV) venom were investigated in a rat model. 37 rats received an intramuscular injection of MPV venom and serial blood samples were taken from the femoral vein for simple whole blood clotting tests and measurement of AT-III activity. 30 min after venom injection, treatment (antivenom, AT-III or both) was given intravenously. 6 rats were untreated and all developed uncoagulable blood and AT-III depletion 90-210 (median 180) mm after venom injection. A combination of high dose AT-III concentrate (0.5 units/g) and antivenom (20 μg/g) prevented abnormal clotting (P < ;0.001), whereas AT-III alone, antivenom alone, or a combination of low dose AT-III (0.25 units/g) and antivenom did not (P < 0.05). These results suggest that the coagulation abnormality in MPV envenomation is secondary to activation of the coagulation cascade at several levels, and that treatment with antivenom alone may not be sufficient to reverse or prevent this phenomenon. © 1990, Oxford University Press. All rights reserved.
author2 Mahidol University
author_facet Mahidol University
S. Pukrittayakamee
V. Desakorn
R. Clemens
A. Nontprasert
H. L. Bock
N. J. White
D. Bunnag
format Article
author S. Pukrittayakamee
V. Desakorn
R. Clemens
A. Nontprasert
H. L. Bock
N. J. White
D. Bunnag
author_sort S. Pukrittayakamee
title Synergy of antithrombin III concentrate and antivenom in preventing coagulopathy in a rat model of Malayan pit viper envenoming
title_short Synergy of antithrombin III concentrate and antivenom in preventing coagulopathy in a rat model of Malayan pit viper envenoming
title_full Synergy of antithrombin III concentrate and antivenom in preventing coagulopathy in a rat model of Malayan pit viper envenoming
title_fullStr Synergy of antithrombin III concentrate and antivenom in preventing coagulopathy in a rat model of Malayan pit viper envenoming
title_full_unstemmed Synergy of antithrombin III concentrate and antivenom in preventing coagulopathy in a rat model of Malayan pit viper envenoming
title_sort synergy of antithrombin iii concentrate and antivenom in preventing coagulopathy in a rat model of malayan pit viper envenoming
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/15969
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