A phase IV, prospective, observational study of the clinical safety of snake antivenoms
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Revista do Instituto de Medicina Tropical de São Paulo |
Texto Completo: | https://www.revistas.usp.br/rimtsp/article/view/193266 |
Resumo: | Snake envenoming is a neglected tropical disease that affects more than 2.7 million people worldwide. The treatment is based on the administration of antivenom composed of heterologous immunoglobulins, species-specific therapy involving the possibility of adverse reactions due to activation of the immune system. Considering the scarcity of prospective studies evaluating the safety of snake antivenoms, this study aimed to describe and characterize adverse events after antivenom infusion in an observational, prospective, single-centre investigation conducted in a referral centre in Brazil. A total of 47 victims of snake envenoming were included in the study, who were mostly men (75%), with ages ranging from 2 to 83 years. Twenty-two participants (47%) presented manifestations compatible with infusion-related reactions (IRRs) during or up to two hours after F(ab’)2 heterologous immunoglobulin infusion. The most common clinical manifestation related to the infusion was a diffuse cutaneous rash (82%), followed by respiratory manifestations (46%) and facial swelling (23%). In four cases (9%), IRR were considered serious adverse events (SAE), characterized by haemodynamic instability, airway obstruction or hypoxia. Only one patient developed symptoms compatible with serum sickness. Although almost half of the patients treated with antivenom sera experienced IRRs, the SAE rate was 9%; in all cases, the adverse reaction was reversible by using supportive treatment, and there were no deaths. The results have shown that there is much to improve in the antivenom production process to obtain a more purified and specific product. Even so, a timely antivenom serum administration managed by well-trained health teams is safe and prevents complications after snake-related accidents. |
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A phase IV, prospective, observational study of the clinical safety of snake antivenomsAntivenomsSnakebitesSnake envenomingSafetySnake envenoming is a neglected tropical disease that affects more than 2.7 million people worldwide. The treatment is based on the administration of antivenom composed of heterologous immunoglobulins, species-specific therapy involving the possibility of adverse reactions due to activation of the immune system. Considering the scarcity of prospective studies evaluating the safety of snake antivenoms, this study aimed to describe and characterize adverse events after antivenom infusion in an observational, prospective, single-centre investigation conducted in a referral centre in Brazil. A total of 47 victims of snake envenoming were included in the study, who were mostly men (75%), with ages ranging from 2 to 83 years. Twenty-two participants (47%) presented manifestations compatible with infusion-related reactions (IRRs) during or up to two hours after F(ab’)2 heterologous immunoglobulin infusion. The most common clinical manifestation related to the infusion was a diffuse cutaneous rash (82%), followed by respiratory manifestations (46%) and facial swelling (23%). In four cases (9%), IRR were considered serious adverse events (SAE), characterized by haemodynamic instability, airway obstruction or hypoxia. Only one patient developed symptoms compatible with serum sickness. Although almost half of the patients treated with antivenom sera experienced IRRs, the SAE rate was 9%; in all cases, the adverse reaction was reversible by using supportive treatment, and there were no deaths. The results have shown that there is much to improve in the antivenom production process to obtain a more purified and specific product. Even so, a timely antivenom serum administration managed by well-trained health teams is safe and prevents complications after snake-related accidents.Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo2021-12-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/rimtsp/article/view/19326610.1590/S1678-9946202163079 Revista do Instituto de Medicina Tropical de São Paulo; Vol. 63 (2021); e79Revista do Instituto de Medicina Tropical de São Paulo; Vol. 63 (2021); e79Revista do Instituto de Medicina Tropical de São Paulo; v. 63 (2021); e791678-99460036-4665reponame:Revista do Instituto de Medicina Tropical de São Pauloinstname:Instituto de Medicina Tropical (IMT)instacron:IMTenghttps://www.revistas.usp.br/rimtsp/article/view/193266/178128Copyright (c) 2021 Denise Christie Souto Nogueira, Iara Pinheiro Calil, Roberta Márcia Marques dos Santos, Adebal de Andrade Filho, Gláucia Cotahttps://creativecommons.org/licenses/by-nc/4.0info:eu-repo/semantics/openAccessNogueira, Denise Christie Souto Calil, Iara Pinheiro Santos, Roberta Márcia Marques dos Andrade Filho, Adebal de Cota, Gláucia 2022-05-16T13:44:35Zoai:revistas.usp.br:article/193266Revistahttp://www.revistas.usp.br/rimtsp/indexPUBhttps://www.revistas.usp.br/rimtsp/oai||revimtsp@usp.br1678-99460036-4665opendoar:2022-12-13T16:53:00.329113Revista do Instituto de Medicina Tropical de São Paulo - Instituto de Medicina Tropical (IMT)true |
dc.title.none.fl_str_mv |
A phase IV, prospective, observational study of the clinical safety of snake antivenoms |
title |
A phase IV, prospective, observational study of the clinical safety of snake antivenoms |
spellingShingle |
A phase IV, prospective, observational study of the clinical safety of snake antivenoms Nogueira, Denise Christie Souto Antivenoms Snakebites Snake envenoming Safety |
title_short |
A phase IV, prospective, observational study of the clinical safety of snake antivenoms |
title_full |
A phase IV, prospective, observational study of the clinical safety of snake antivenoms |
title_fullStr |
A phase IV, prospective, observational study of the clinical safety of snake antivenoms |
title_full_unstemmed |
A phase IV, prospective, observational study of the clinical safety of snake antivenoms |
title_sort |
A phase IV, prospective, observational study of the clinical safety of snake antivenoms |
author |
Nogueira, Denise Christie Souto |
author_facet |
Nogueira, Denise Christie Souto Calil, Iara Pinheiro Santos, Roberta Márcia Marques dos Andrade Filho, Adebal de Cota, Gláucia |
author_role |
author |
author2 |
Calil, Iara Pinheiro Santos, Roberta Márcia Marques dos Andrade Filho, Adebal de Cota, Gláucia |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Nogueira, Denise Christie Souto Calil, Iara Pinheiro Santos, Roberta Márcia Marques dos Andrade Filho, Adebal de Cota, Gláucia |
dc.subject.por.fl_str_mv |
Antivenoms Snakebites Snake envenoming Safety |
topic |
Antivenoms Snakebites Snake envenoming Safety |
description |
Snake envenoming is a neglected tropical disease that affects more than 2.7 million people worldwide. The treatment is based on the administration of antivenom composed of heterologous immunoglobulins, species-specific therapy involving the possibility of adverse reactions due to activation of the immune system. Considering the scarcity of prospective studies evaluating the safety of snake antivenoms, this study aimed to describe and characterize adverse events after antivenom infusion in an observational, prospective, single-centre investigation conducted in a referral centre in Brazil. A total of 47 victims of snake envenoming were included in the study, who were mostly men (75%), with ages ranging from 2 to 83 years. Twenty-two participants (47%) presented manifestations compatible with infusion-related reactions (IRRs) during or up to two hours after F(ab’)2 heterologous immunoglobulin infusion. The most common clinical manifestation related to the infusion was a diffuse cutaneous rash (82%), followed by respiratory manifestations (46%) and facial swelling (23%). In four cases (9%), IRR were considered serious adverse events (SAE), characterized by haemodynamic instability, airway obstruction or hypoxia. Only one patient developed symptoms compatible with serum sickness. Although almost half of the patients treated with antivenom sera experienced IRRs, the SAE rate was 9%; in all cases, the adverse reaction was reversible by using supportive treatment, and there were no deaths. The results have shown that there is much to improve in the antivenom production process to obtain a more purified and specific product. Even so, a timely antivenom serum administration managed by well-trained health teams is safe and prevents complications after snake-related accidents. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-12-09 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/rimtsp/article/view/193266 10.1590/S1678-9946202163079 |
url |
https://www.revistas.usp.br/rimtsp/article/view/193266 |
identifier_str_mv |
10.1590/S1678-9946202163079 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/rimtsp/article/view/193266/178128 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by-nc/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo |
publisher.none.fl_str_mv |
Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo |
dc.source.none.fl_str_mv |
Revista do Instituto de Medicina Tropical de São Paulo; Vol. 63 (2021); e79 Revista do Instituto de Medicina Tropical de São Paulo; Vol. 63 (2021); e79 Revista do Instituto de Medicina Tropical de São Paulo; v. 63 (2021); e79 1678-9946 0036-4665 reponame:Revista do Instituto de Medicina Tropical de São Paulo instname:Instituto de Medicina Tropical (IMT) instacron:IMT |
instname_str |
Instituto de Medicina Tropical (IMT) |
instacron_str |
IMT |
institution |
IMT |
reponame_str |
Revista do Instituto de Medicina Tropical de São Paulo |
collection |
Revista do Instituto de Medicina Tropical de São Paulo |
repository.name.fl_str_mv |
Revista do Instituto de Medicina Tropical de São Paulo - Instituto de Medicina Tropical (IMT) |
repository.mail.fl_str_mv |
||revimtsp@usp.br |
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1798951653740642304 |