Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral

Detalhes bibliográficos
Autor(a) principal: Melo, Edson Carvalho de [UNESP]
Data de Publicação: 2013
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/108511
Resumo: American Visceral Leishmaniasis (AVL) is a disease that causes significant mortality. Since the past two decades it is disseminating widely in Brazil. Its etiologic agent is Leishmania infantum chagasi, a vector-borne parasite. Traditionally, AVL was regarded as an endemic disease in Northern and Northeastern States, but it has emerged in urban areas and in Southeastern States. In São Paulo State, autochtonous cases occur since 1999. Therapeutic options for AVL are scarce, and all leishmanicidal drugs are associated with failures, relapses and serious adverse events. Meglumine antominiate has been the first-line therapy in Brazil for many decades. Lately, amphotericin B deoxycholate or in liposomal formulation have been recommended for more severe cases. However, those data are extrapolated from studies conducted in India, Africa and Europe. The study was designed to fulfill this gap. It was a multicenter, randomized, open-label study that compare the efficacy and safety of three therapeutic options: meglumine antimoniate, amphotericin B deoxycholate and liposomal amphotericin B. Patients with parasitological confirmation of AVL were included. Those that were coinfected with HIV or who had immune-supressing conditions or pregnancy were excluded. We also excluded those for whom governmental guidelines recommended the use of amphotericin B. Patients were followed with physical examination and laboratory tests on days 0, 3 , 14, 30, 90 and 180. We included 59 subjects, 33 of whom completed follow-up (11 in each arm). Clinical response was similar for all groups. However, those receiving amphotericin were more likely to have early recovery of hemoglobin dosage and white cell counts, as well as serum albumin. There was a discrete tendency of better response with liposomal amphotericin. Nephrotoxicity was striking among those receiving amphotericin deoxycholate (42%), an incidence significantly higher than that observed with the other ...
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spelling Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceralLeishmaniose visceral - TratamentoMedicamentos - UtilizaçãoAnfotericina BKala-azarAmerican Visceral Leishmaniasis (AVL) is a disease that causes significant mortality. Since the past two decades it is disseminating widely in Brazil. Its etiologic agent is Leishmania infantum chagasi, a vector-borne parasite. Traditionally, AVL was regarded as an endemic disease in Northern and Northeastern States, but it has emerged in urban areas and in Southeastern States. In São Paulo State, autochtonous cases occur since 1999. Therapeutic options for AVL are scarce, and all leishmanicidal drugs are associated with failures, relapses and serious adverse events. Meglumine antominiate has been the first-line therapy in Brazil for many decades. Lately, amphotericin B deoxycholate or in liposomal formulation have been recommended for more severe cases. However, those data are extrapolated from studies conducted in India, Africa and Europe. The study was designed to fulfill this gap. It was a multicenter, randomized, open-label study that compare the efficacy and safety of three therapeutic options: meglumine antimoniate, amphotericin B deoxycholate and liposomal amphotericin B. Patients with parasitological confirmation of AVL were included. Those that were coinfected with HIV or who had immune-supressing conditions or pregnancy were excluded. We also excluded those for whom governmental guidelines recommended the use of amphotericin B. Patients were followed with physical examination and laboratory tests on days 0, 3 , 14, 30, 90 and 180. We included 59 subjects, 33 of whom completed follow-up (11 in each arm). Clinical response was similar for all groups. However, those receiving amphotericin were more likely to have early recovery of hemoglobin dosage and white cell counts, as well as serum albumin. There was a discrete tendency of better response with liposomal amphotericin. Nephrotoxicity was striking among those receiving amphotericin deoxycholate (42%), an incidence significantly higher than that observed with the other ...A Leishmaniose Visceral Americana (LVA) é uma doença de letalidade significativa e em disseminação no território brasileiro. É causada pela Leishmania infantum chagasi, parasita transmitido por artrópodes (Lutzomyia longipalpis) e tem como reservatórios cães e animais silvestres. Embora endêmica em zonas rurais das Regiões Nordeste, Norte e Centro-Oeste do País há várias décadas, a LVA tem emergido como doença urbana (muitas vezes epidêmica), em áreas anteriormente não afetadas. Nestas últimas, está o Estado de São Paulo, onde os primeiros casos autóctones foram detectados em 1999. As opções terapêuticas para LVA são escassas, e associadas a frequentes recidivas e eventos adversos. Há grande tradição em seu tratamento com antimoniais pentavalentes (mais especificamente o antimoniato de N-metil glucamina). Mais recentemente, as formulações de anfotericina B (deoxicolato e lipossomal), tem sido indicadas para quadros mais severos. No entanto, faltam ensaios clínicos que embasem essa superioridade no tratamento de LVA, e muitas das indicações são feitas por analogia com pesquisa realizada na Índia, África ou Europa. O estudo foi planejado para preencher esse hiato na pesquisa clínica relativa à LVA. Tratou-se de ensaio clínico aberto, multicêntrico, envolvendo instituições nos Estados do Pará, Maranhão e São Paulo. Foram incluídos pacientes com diagnóstico parasitológico de LVA que manifestaram aceite em participar por meio de Termo de Consentimento Livre e Esclarecido (TCLE) aplicado aos próprios sujeitos ou aos seus representantes legais. Foram excluídos pacientes co-infectados pelo vírus da imunodeficiência humana (HIV), portadores de neoplasia, usuários de imunossupressores, gestantes e aqueles para os quais os guias terapêuticos do Ministério da Saúde (MS), ou das Secretarias Estaduais da Saúde recomendavam o uso da anfotericina B – definição que abrangia aqueles sujeitos com ...Universidade Estadual Paulista (Unesp)Fortaleza, Carlos Magno Castelo Branco [UNESP]Universidade Estadual Paulista (Unesp)Melo, Edson Carvalho de [UNESP]2014-08-13T14:50:42Z2014-08-13T14:50:42Z2013-06-18info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesis109 f.application/pdfMELO, Edson Carvalho de. Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral. 2013. 109 f. Tese (doutorado) - Universidade Estadual Paulista Júlio de Mesquita Filho, Faculdade de Medicina de Botucatu, 2013.http://hdl.handle.net/11449/108511000749624000749624.pdf33004064065P4Alephreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporinfo:eu-repo/semantics/openAccess2023-10-14T06:08:20Zoai:repositorio.unesp.br:11449/108511Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-10-14T06:08:20Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral
title Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral
spellingShingle Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral
Melo, Edson Carvalho de [UNESP]
Leishmaniose visceral - Tratamento
Medicamentos - Utilização
Anfotericina B
Kala-azar
title_short Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral
title_full Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral
title_fullStr Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral
title_full_unstemmed Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral
title_sort Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral
author Melo, Edson Carvalho de [UNESP]
author_facet Melo, Edson Carvalho de [UNESP]
author_role author
dc.contributor.none.fl_str_mv Fortaleza, Carlos Magno Castelo Branco [UNESP]
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Melo, Edson Carvalho de [UNESP]
dc.subject.por.fl_str_mv Leishmaniose visceral - Tratamento
Medicamentos - Utilização
Anfotericina B
Kala-azar
topic Leishmaniose visceral - Tratamento
Medicamentos - Utilização
Anfotericina B
Kala-azar
description American Visceral Leishmaniasis (AVL) is a disease that causes significant mortality. Since the past two decades it is disseminating widely in Brazil. Its etiologic agent is Leishmania infantum chagasi, a vector-borne parasite. Traditionally, AVL was regarded as an endemic disease in Northern and Northeastern States, but it has emerged in urban areas and in Southeastern States. In São Paulo State, autochtonous cases occur since 1999. Therapeutic options for AVL are scarce, and all leishmanicidal drugs are associated with failures, relapses and serious adverse events. Meglumine antominiate has been the first-line therapy in Brazil for many decades. Lately, amphotericin B deoxycholate or in liposomal formulation have been recommended for more severe cases. However, those data are extrapolated from studies conducted in India, Africa and Europe. The study was designed to fulfill this gap. It was a multicenter, randomized, open-label study that compare the efficacy and safety of three therapeutic options: meglumine antimoniate, amphotericin B deoxycholate and liposomal amphotericin B. Patients with parasitological confirmation of AVL were included. Those that were coinfected with HIV or who had immune-supressing conditions or pregnancy were excluded. We also excluded those for whom governmental guidelines recommended the use of amphotericin B. Patients were followed with physical examination and laboratory tests on days 0, 3 , 14, 30, 90 and 180. We included 59 subjects, 33 of whom completed follow-up (11 in each arm). Clinical response was similar for all groups. However, those receiving amphotericin were more likely to have early recovery of hemoglobin dosage and white cell counts, as well as serum albumin. There was a discrete tendency of better response with liposomal amphotericin. Nephrotoxicity was striking among those receiving amphotericin deoxycholate (42%), an incidence significantly higher than that observed with the other ...
publishDate 2013
dc.date.none.fl_str_mv 2013-06-18
2014-08-13T14:50:42Z
2014-08-13T14:50:42Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv MELO, Edson Carvalho de. Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral. 2013. 109 f. Tese (doutorado) - Universidade Estadual Paulista Júlio de Mesquita Filho, Faculdade de Medicina de Botucatu, 2013.
http://hdl.handle.net/11449/108511
000749624
000749624.pdf
33004064065P4
identifier_str_mv MELO, Edson Carvalho de. Avaliação da eficácia e segurança da farmacoterapia da leishmaniose visceral. 2013. 109 f. Tese (doutorado) - Universidade Estadual Paulista Júlio de Mesquita Filho, Faculdade de Medicina de Botucatu, 2013.
000749624
000749624.pdf
33004064065P4
url http://hdl.handle.net/11449/108511
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dc.format.none.fl_str_mv 109 f.
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dc.publisher.none.fl_str_mv Universidade Estadual Paulista (Unesp)
publisher.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.source.none.fl_str_mv Aleph
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
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instname_str Universidade Estadual Paulista (UNESP)
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