Paediatric visceral leishmaniasis: experience of a paediatric referral center 1990-2009.

Detalhes bibliográficos
Autor(a) principal: Dionísio, Maria Teresa
Data de Publicação: 2011
Outros Autores: Dias, Andrea, Rodrigues, Fernanda, Félix, Miguel, Estêvão, Maria Helena
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/466
Resumo: Visceral Leishmaniasis (VL) is a systemic infection, endemic in many parts of the world, including Portugal. The aim is to review all cases of VL admitted to our hospital.Retrospective analysis of all cases of VL admitted to a Level III Paediatric Hospital, between January 1990 and December 2009 (20 years). Demographic, epidemiological, clinical, laboratorial, therapeutic and follow-up data were analysed.During the study period, 54 children were admitted with VL, three of which were excluded from the study due to incomplete clinical records. The mean age was 27 months (seven months - twelve years) and 53% were female. Two thirds of the cases were diagnosed during Spring and Summer. The mean time for diagnosis was 31 days (2-188 days). The most common clinical findings were splenomegaly (100%), fever (96%), pallor (90%) and hepatomegaly (82%). Bone marrow aspiration was performed in all children, with amastigotes identified in 73% of the cases. Indirect immunofluorescence was performed in 30 cases, being positive in 29 (97%). All were treated with meglumine antimoniate. Three children relapsed during the first year after the initial episode. A 17 months-old child died due to cardiac failure.The early diagnosis of VL is essential to carry out prompt management and prevent potential fatal complications. In our analysis, the management with meglumine antimoniate resulted in an overall favourable outcome.
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spelling Paediatric visceral leishmaniasis: experience of a paediatric referral center 1990-2009.Leishmaniose visceral: experiência de um centro pediátrico de referência 1990-2009.Visceral Leishmaniasis (VL) is a systemic infection, endemic in many parts of the world, including Portugal. The aim is to review all cases of VL admitted to our hospital.Retrospective analysis of all cases of VL admitted to a Level III Paediatric Hospital, between January 1990 and December 2009 (20 years). Demographic, epidemiological, clinical, laboratorial, therapeutic and follow-up data were analysed.During the study period, 54 children were admitted with VL, three of which were excluded from the study due to incomplete clinical records. The mean age was 27 months (seven months - twelve years) and 53% were female. Two thirds of the cases were diagnosed during Spring and Summer. The mean time for diagnosis was 31 days (2-188 days). The most common clinical findings were splenomegaly (100%), fever (96%), pallor (90%) and hepatomegaly (82%). Bone marrow aspiration was performed in all children, with amastigotes identified in 73% of the cases. Indirect immunofluorescence was performed in 30 cases, being positive in 29 (97%). All were treated with meglumine antimoniate. Three children relapsed during the first year after the initial episode. A 17 months-old child died due to cardiac failure.The early diagnosis of VL is essential to carry out prompt management and prevent potential fatal complications. In our analysis, the management with meglumine antimoniate resulted in an overall favourable outcome.Visceral Leishmaniasis (VL) is a systemic infection, endemic in many parts of the world, including Portugal. The aim is to review all cases of VL admitted to our hospital.Retrospective analysis of all cases of VL admitted to a Level III Paediatric Hospital, between January 1990 and December 2009 (20 years). Demographic, epidemiological, clinical, laboratorial, therapeutic and follow-up data were analysed.During the study period, 54 children were admitted with VL, three of which were excluded from the study due to incomplete clinical records. The mean age was 27 months (seven months - twelve years) and 53% were female. Two thirds of the cases were diagnosed during Spring and Summer. The mean time for diagnosis was 31 days (2-188 days). The most common clinical findings were splenomegaly (100%), fever (96%), pallor (90%) and hepatomegaly (82%). Bone marrow aspiration was performed in all children, with amastigotes identified in 73% of the cases. Indirect immunofluorescence was performed in 30 cases, being positive in 29 (97%). All were treated with meglumine antimoniate. Three children relapsed during the first year after the initial episode. A 17 months-old child died due to cardiac failure.The early diagnosis of VL is essential to carry out prompt management and prevent potential fatal complications. In our analysis, the management with meglumine antimoniate resulted in an overall favourable outcome.Ordem dos Médicos2011-08-12info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/466oai:ojs.www.actamedicaportuguesa.com:article/466Acta Médica Portuguesa; Vol. 24 No. 3 (2011): Maio-Junho; 399-404Acta Médica Portuguesa; Vol. 24 N.º 3 (2011): Maio-Junho; 399-4041646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/466https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/466/174Dionísio, Maria TeresaDias, AndreaRodrigues, FernandaFélix, MiguelEstêvão, Maria Helenainfo:eu-repo/semantics/openAccess2022-12-20T10:56:16Zoai:ojs.www.actamedicaportuguesa.com:article/466Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:16:30.648943Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Paediatric visceral leishmaniasis: experience of a paediatric referral center 1990-2009.
Leishmaniose visceral: experiência de um centro pediátrico de referência 1990-2009.
title Paediatric visceral leishmaniasis: experience of a paediatric referral center 1990-2009.
spellingShingle Paediatric visceral leishmaniasis: experience of a paediatric referral center 1990-2009.
Dionísio, Maria Teresa
title_short Paediatric visceral leishmaniasis: experience of a paediatric referral center 1990-2009.
title_full Paediatric visceral leishmaniasis: experience of a paediatric referral center 1990-2009.
title_fullStr Paediatric visceral leishmaniasis: experience of a paediatric referral center 1990-2009.
title_full_unstemmed Paediatric visceral leishmaniasis: experience of a paediatric referral center 1990-2009.
title_sort Paediatric visceral leishmaniasis: experience of a paediatric referral center 1990-2009.
author Dionísio, Maria Teresa
author_facet Dionísio, Maria Teresa
Dias, Andrea
Rodrigues, Fernanda
Félix, Miguel
Estêvão, Maria Helena
author_role author
author2 Dias, Andrea
Rodrigues, Fernanda
Félix, Miguel
Estêvão, Maria Helena
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Dionísio, Maria Teresa
Dias, Andrea
Rodrigues, Fernanda
Félix, Miguel
Estêvão, Maria Helena
description Visceral Leishmaniasis (VL) is a systemic infection, endemic in many parts of the world, including Portugal. The aim is to review all cases of VL admitted to our hospital.Retrospective analysis of all cases of VL admitted to a Level III Paediatric Hospital, between January 1990 and December 2009 (20 years). Demographic, epidemiological, clinical, laboratorial, therapeutic and follow-up data were analysed.During the study period, 54 children were admitted with VL, three of which were excluded from the study due to incomplete clinical records. The mean age was 27 months (seven months - twelve years) and 53% were female. Two thirds of the cases were diagnosed during Spring and Summer. The mean time for diagnosis was 31 days (2-188 days). The most common clinical findings were splenomegaly (100%), fever (96%), pallor (90%) and hepatomegaly (82%). Bone marrow aspiration was performed in all children, with amastigotes identified in 73% of the cases. Indirect immunofluorescence was performed in 30 cases, being positive in 29 (97%). All were treated with meglumine antimoniate. Three children relapsed during the first year after the initial episode. A 17 months-old child died due to cardiac failure.The early diagnosis of VL is essential to carry out prompt management and prevent potential fatal complications. In our analysis, the management with meglumine antimoniate resulted in an overall favourable outcome.
publishDate 2011
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publisher.none.fl_str_mv Ordem dos Médicos
dc.source.none.fl_str_mv Acta Médica Portuguesa; Vol. 24 No. 3 (2011): Maio-Junho; 399-404
Acta Médica Portuguesa; Vol. 24 N.º 3 (2011): Maio-Junho; 399-404
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