Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina

Detalhes bibliográficos
Autor(a) principal: Silveira, Lindon Johoson Diniz [UNIFESP]
Data de Publicação: 2010
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/10075
Resumo: Introduction: Visceral Leishmaniasis (VL) is an endemic disease found in Brazil mainly in Northeast region. These protozoosis is an infection, systemic, chronic disease characterized by fever, hepatosplenomegaly and increase of lymph nods, pancytopenia, hypergamaglobulinemia, edema and progressive state of weakness, taking the patient to obit if not treated. The first line drug for this treatment is meglumine antimonite (Glucantime®). Objective: Check the general characteristic of VL patients, the criteria used for diagnosis, possible side effects to meglumine antimonite (Glucantime®) and blood pressure before and after the treatment. Method: Observational transversal descriptive study with evaluation of 89 patients treated with meglumine antimonite (Glucantime®) in HEHA/Maceio/Brazil, in the period of May/2006 to December/2009. For these, we collected data concerning to age, gender, place of origin, diagnostic method, side effects to meglumine antimonite (Glucantime®), hospitalization period and length of treatment and cumulative dose until side effects. Data were analyzed by SPSS Program. Results: the results showed a predominance of males, children of country origin and main diagnostic method by medullar aspiration. From the patients that were treated with meglumine antimonite, 3 (3.37%) died, 12 (13.48%) showed side effects and 74 (83.14%) were healed. The clinical symptoms that led to the substitution of pentavalent antimony were persistent fever, ictericia, exanthema, bleeding and cyanosis. The patients that recovering from illness (83.14%) were hospitalized for a mean of 19.6 days, the period of treatment varied from 21 to 40 days and the given dose varied from 4123 to 44640 (accumulated dose by weigth).The blood pressure before and after treatment did not have any change. Conclusion: During the study were analized 89 patients hospitalized for LV: 74 were healed, 12 were replaced by amphotericin B treatment and 03 died. Most of them were under 5 years old, male and came from the country. The marrow aspirate was the most frequently diagnosis used and little is used the serological diagnosis. The dosage and duration of treatment with meglumine antimoniate (Glucantime ®) were consistent with what advocates the Ministry of Health. Persistence of fever, jaundice, rash, cyanosis and bleeding were the reactions that led the physician to modify treatment. No change was observed in blood pressure before and after treatment.
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spelling Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de megluminaSeries of patients with visceral Leishmaniasis treated with meglumine antimoniteAdverse reactionsMeglumine antimoniteTreatmentVisceral leishmaniasisAntimoniato de megluminaReações adversasTratamentoLeishmaniose visceralEfeitos colaterais e reações adversas relacionados a medicamentosMegluminaTerapêuticaIntroduction: Visceral Leishmaniasis (VL) is an endemic disease found in Brazil mainly in Northeast region. These protozoosis is an infection, systemic, chronic disease characterized by fever, hepatosplenomegaly and increase of lymph nods, pancytopenia, hypergamaglobulinemia, edema and progressive state of weakness, taking the patient to obit if not treated. The first line drug for this treatment is meglumine antimonite (Glucantime®). Objective: Check the general characteristic of VL patients, the criteria used for diagnosis, possible side effects to meglumine antimonite (Glucantime®) and blood pressure before and after the treatment. Method: Observational transversal descriptive study with evaluation of 89 patients treated with meglumine antimonite (Glucantime®) in HEHA/Maceio/Brazil, in the period of May/2006 to December/2009. For these, we collected data concerning to age, gender, place of origin, diagnostic method, side effects to meglumine antimonite (Glucantime®), hospitalization period and length of treatment and cumulative dose until side effects. Data were analyzed by SPSS Program. Results: the results showed a predominance of males, children of country origin and main diagnostic method by medullar aspiration. From the patients that were treated with meglumine antimonite, 3 (3.37%) died, 12 (13.48%) showed side effects and 74 (83.14%) were healed. The clinical symptoms that led to the substitution of pentavalent antimony were persistent fever, ictericia, exanthema, bleeding and cyanosis. The patients that recovering from illness (83.14%) were hospitalized for a mean of 19.6 days, the period of treatment varied from 21 to 40 days and the given dose varied from 4123 to 44640 (accumulated dose by weigth).The blood pressure before and after treatment did not have any change. Conclusion: During the study were analized 89 patients hospitalized for LV: 74 were healed, 12 were replaced by amphotericin B treatment and 03 died. Most of them were under 5 years old, male and came from the country. The marrow aspirate was the most frequently diagnosis used and little is used the serological diagnosis. The dosage and duration of treatment with meglumine antimoniate (Glucantime ®) were consistent with what advocates the Ministry of Health. Persistence of fever, jaundice, rash, cyanosis and bleeding were the reactions that led the physician to modify treatment. No change was observed in blood pressure before and after treatment.Contexto: A leishmaniose visceral (LV) é uma doença endêmica encontrada no Brasil, principalmente na Região Nordeste. Essa protozoose é uma enfermidade infecciosa, sistêmica, crônica, caracterizada por febre, hepatoesplenomegalia, linfadenopatia, pancitopenia, hipergamaglobulinemia, edema e estado de debilidade progressivo, podendo levar o paciente ao óbito se não for tratada. O fármaco de primeira escolha para o tratamento é o antimoniato de meglumina (Glucantime®). Objetivo: Verificar a característica geral dos pacientes com leishmaniose visceral, o critério usado para o diagnóstico, possíveis reações ao antimoniato de meglumina (Glucantime®) e medida da pressão arterial antes e após o tratamento. Método: Estudo observacional, transversal, descritivo, com avaliação de 89 pacientes diagnosticados com leishmaniose visceral tratados com antimoniato de meglumina (Glucantime®) no HEHA/Maceió-AL no período de maio/2006 a dezembro/2009. Para estes, foram coletados dados referentes a idade, sexo, procedência, método de diagnóstico, efeitos adversos ao antimoniato de meglumina (Glucantime®), duração do internamento, duração do tratamento e dose administrada até o aparecimento dos efeitos adversos. Os dados foram tabulados e analisados por meio do programa SPSS® (Microsoft Corporation). Resultados: Foi observado predomínio de pacientes do sexo masculino, crianças, provenientes do interior, o método diagnóstico foi o aspirado de punção medular. Dos pacientes que foram tratados com o antimoniato de meglumina (Glucantime®), 3 (3,37%) evoluíram para óbito, 12 (13,48%) apresentaram alterações que conduziram o médico a mudar o tratamento e 74 (83,14%) foram curados. As manifestações clínicas que levaram a substituição do antimoniato de meglumina (Glucantime®) foram persistência da febre, icterícia, exantema, sangramento e cianose. Os pacientes curados da leishmaniose visceral (83,14%) permaneceram internados em média 19,6 dias, a duração do tratamento variou de 21 a 40 dias e a dose administrada variou de 4123 a 44640 (dose acumulada mg/kg). A verificação da pressão arterial antes e após o tratamento não apresentou alteração significativa e esteve dentro da faixa de normalidade. Conclusão: Durante a pesquisa foram estudados 89 pacientes internados por LV: 74 evoluíram para cura, 12 tiveram tratamento substituído por anfotericina B e 03 vieram a falecer. Na sua maioria eram menores de 5 anos, sexo masculino e procedentes do interior. O aspirado medular foi o diagnóstico mais utilizado e pouco se utilizou o diagnóstico sorológico. A dose e o tempo de tratamento com antimoniato de meglumina (Glucantime®) foram compatíveis com o que preconiza o Ministério da Saúde. Persistência da febre, icterícia, exantema, cianose e sangramento foram as reações que motivaram o médico a modificar o tratamento. Não se observou alteração na pressão arterial antes e depois do tratamento.TEDEBV UNIFESP: Teses e dissertaçõesUniversidade Federal de São Paulo (UNIFESP)Ribeiro, Sandra Aparecida [UNIFESP]Universidade Federal de São Paulo (UNIFESP)Silveira, Lindon Johoson Diniz [UNIFESP]2015-07-22T20:50:48Z2015-07-22T20:50:48Z2010-11-24info:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/publishedVersion77 f.application/pdfSILVEIRA, Lindon Johoson Diniz. Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina. 2010. 77 f. Dissertação (Mestrado) - Universidade Federal de São Paulo (UNIFESP), São Paulo, 2010.Publico-404.pdfhttp://repositorio.unifesp.br/handle/11600/10075porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-06T05:57:09Zoai:repositorio.unifesp.br/:11600/10075Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-06T05:57:09Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina
Series of patients with visceral Leishmaniasis treated with meglumine antimonite
title Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina
spellingShingle Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina
Silveira, Lindon Johoson Diniz [UNIFESP]
Adverse reactions
Meglumine antimonite
Treatment
Visceral leishmaniasis
Antimoniato de meglumina
Reações adversas
Tratamento
Leishmaniose visceral
Efeitos colaterais e reações adversas relacionados a medicamentos
Meglumina
Terapêutica
title_short Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina
title_full Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina
title_fullStr Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina
title_full_unstemmed Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina
title_sort Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina
author Silveira, Lindon Johoson Diniz [UNIFESP]
author_facet Silveira, Lindon Johoson Diniz [UNIFESP]
author_role author
dc.contributor.none.fl_str_mv Ribeiro, Sandra Aparecida [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Silveira, Lindon Johoson Diniz [UNIFESP]
dc.subject.por.fl_str_mv Adverse reactions
Meglumine antimonite
Treatment
Visceral leishmaniasis
Antimoniato de meglumina
Reações adversas
Tratamento
Leishmaniose visceral
Efeitos colaterais e reações adversas relacionados a medicamentos
Meglumina
Terapêutica
topic Adverse reactions
Meglumine antimonite
Treatment
Visceral leishmaniasis
Antimoniato de meglumina
Reações adversas
Tratamento
Leishmaniose visceral
Efeitos colaterais e reações adversas relacionados a medicamentos
Meglumina
Terapêutica
description Introduction: Visceral Leishmaniasis (VL) is an endemic disease found in Brazil mainly in Northeast region. These protozoosis is an infection, systemic, chronic disease characterized by fever, hepatosplenomegaly and increase of lymph nods, pancytopenia, hypergamaglobulinemia, edema and progressive state of weakness, taking the patient to obit if not treated. The first line drug for this treatment is meglumine antimonite (Glucantime®). Objective: Check the general characteristic of VL patients, the criteria used for diagnosis, possible side effects to meglumine antimonite (Glucantime®) and blood pressure before and after the treatment. Method: Observational transversal descriptive study with evaluation of 89 patients treated with meglumine antimonite (Glucantime®) in HEHA/Maceio/Brazil, in the period of May/2006 to December/2009. For these, we collected data concerning to age, gender, place of origin, diagnostic method, side effects to meglumine antimonite (Glucantime®), hospitalization period and length of treatment and cumulative dose until side effects. Data were analyzed by SPSS Program. Results: the results showed a predominance of males, children of country origin and main diagnostic method by medullar aspiration. From the patients that were treated with meglumine antimonite, 3 (3.37%) died, 12 (13.48%) showed side effects and 74 (83.14%) were healed. The clinical symptoms that led to the substitution of pentavalent antimony were persistent fever, ictericia, exanthema, bleeding and cyanosis. The patients that recovering from illness (83.14%) were hospitalized for a mean of 19.6 days, the period of treatment varied from 21 to 40 days and the given dose varied from 4123 to 44640 (accumulated dose by weigth).The blood pressure before and after treatment did not have any change. Conclusion: During the study were analized 89 patients hospitalized for LV: 74 were healed, 12 were replaced by amphotericin B treatment and 03 died. Most of them were under 5 years old, male and came from the country. The marrow aspirate was the most frequently diagnosis used and little is used the serological diagnosis. The dosage and duration of treatment with meglumine antimoniate (Glucantime ®) were consistent with what advocates the Ministry of Health. Persistence of fever, jaundice, rash, cyanosis and bleeding were the reactions that led the physician to modify treatment. No change was observed in blood pressure before and after treatment.
publishDate 2010
dc.date.none.fl_str_mv 2010-11-24
2015-07-22T20:50:48Z
2015-07-22T20:50:48Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv SILVEIRA, Lindon Johoson Diniz. Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina. 2010. 77 f. Dissertação (Mestrado) - Universidade Federal de São Paulo (UNIFESP), São Paulo, 2010.
Publico-404.pdf
http://repositorio.unifesp.br/handle/11600/10075
identifier_str_mv SILVEIRA, Lindon Johoson Diniz. Série histórica de pacientes com Leishmaniose visceral tratados com antimoniato de meglumina. 2010. 77 f. Dissertação (Mestrado) - Universidade Federal de São Paulo (UNIFESP), São Paulo, 2010.
Publico-404.pdf
url http://repositorio.unifesp.br/handle/11600/10075
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 77 f.
application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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