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Intralesional meglumine antimoniate for the treatment of localised cutaneous leishmaniasis: a retrospective review of a Brazilian referral centre
Although intralesional meglumine antimoniate (MA) infiltration is considered an option for cutaneous leishmaniasis (CL) therapy and is widely used in the Old World, there have been few studies supporting this therapeutic approach in the Americas. This study aims to describe outcomes and adverse even...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Instituto Oswaldo Cruz, Ministério da Saúde
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981119/ https://www.ncbi.nlm.nih.gov/pubmed/27508321 http://dx.doi.org/10.1590/0074-02760160183 |
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author | da Silva, Rosiana Estéfane Toledo, Antonio Senna, Maria Camilo Rabello, Ana Cota, Gláucia |
author_facet | da Silva, Rosiana Estéfane Toledo, Antonio Senna, Maria Camilo Rabello, Ana Cota, Gláucia |
author_sort | da Silva, Rosiana Estéfane |
collection | PubMed |
description | Although intralesional meglumine antimoniate (MA) infiltration is considered an option for cutaneous leishmaniasis (CL) therapy and is widely used in the Old World, there have been few studies supporting this therapeutic approach in the Americas. This study aims to describe outcomes and adverse events associated with intralesional therapy for CL. This retrospective study reviewed the experience of a Brazilian leishmaniasis reference centre using intralesional MA to treat 31 patients over five years (2008 and 2013). The median age was 63 years (22-86) and the median duration time of the lesions up to treatment was 16 weeks. In 22 patients (71%), intralesional therapy was indicated due to the presence of contraindications or previous serious adverse events with systemic MA. Other indications were failure of systemic therapy or ease of administration. Intralesional treatment consisted of one-six infiltrations (median three) for a period of up to 12 weeks. The initial (three months) and definitive (six months) cure rates were 70.9% and 67.7%, respectively. Most patients reported mild discomfort during infiltration and no serious adverse events were observed. In conclusion, these results show that the intralesional MA efficacy rate was very similar to that of systemic MA treatment, and reinforce the need for further studies with adequate design to establish the efficacy and safety of this therapeutic approach. |
format | Online Article Text |
id | pubmed-4981119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Instituto Oswaldo Cruz, Ministério da Saúde |
record_format | MEDLINE/PubMed |
spelling | pubmed-49811192016-08-12 Intralesional meglumine antimoniate for the treatment of localised cutaneous leishmaniasis: a retrospective review of a Brazilian referral centre da Silva, Rosiana Estéfane Toledo, Antonio Senna, Maria Camilo Rabello, Ana Cota, Gláucia Mem Inst Oswaldo Cruz Articles Although intralesional meglumine antimoniate (MA) infiltration is considered an option for cutaneous leishmaniasis (CL) therapy and is widely used in the Old World, there have been few studies supporting this therapeutic approach in the Americas. This study aims to describe outcomes and adverse events associated with intralesional therapy for CL. This retrospective study reviewed the experience of a Brazilian leishmaniasis reference centre using intralesional MA to treat 31 patients over five years (2008 and 2013). The median age was 63 years (22-86) and the median duration time of the lesions up to treatment was 16 weeks. In 22 patients (71%), intralesional therapy was indicated due to the presence of contraindications or previous serious adverse events with systemic MA. Other indications were failure of systemic therapy or ease of administration. Intralesional treatment consisted of one-six infiltrations (median three) for a period of up to 12 weeks. The initial (three months) and definitive (six months) cure rates were 70.9% and 67.7%, respectively. Most patients reported mild discomfort during infiltration and no serious adverse events were observed. In conclusion, these results show that the intralesional MA efficacy rate was very similar to that of systemic MA treatment, and reinforce the need for further studies with adequate design to establish the efficacy and safety of this therapeutic approach. Instituto Oswaldo Cruz, Ministério da Saúde 2016-08 /pmc/articles/PMC4981119/ /pubmed/27508321 http://dx.doi.org/10.1590/0074-02760160183 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles da Silva, Rosiana Estéfane Toledo, Antonio Senna, Maria Camilo Rabello, Ana Cota, Gláucia Intralesional meglumine antimoniate for the treatment of localised cutaneous leishmaniasis: a retrospective review of a Brazilian referral centre |
title | Intralesional meglumine antimoniate for the treatment of localised
cutaneous leishmaniasis: a retrospective review of a Brazilian referral
centre |
title_full | Intralesional meglumine antimoniate for the treatment of localised
cutaneous leishmaniasis: a retrospective review of a Brazilian referral
centre |
title_fullStr | Intralesional meglumine antimoniate for the treatment of localised
cutaneous leishmaniasis: a retrospective review of a Brazilian referral
centre |
title_full_unstemmed | Intralesional meglumine antimoniate for the treatment of localised
cutaneous leishmaniasis: a retrospective review of a Brazilian referral
centre |
title_short | Intralesional meglumine antimoniate for the treatment of localised
cutaneous leishmaniasis: a retrospective review of a Brazilian referral
centre |
title_sort | intralesional meglumine antimoniate for the treatment of localised
cutaneous leishmaniasis: a retrospective review of a brazilian referral
centre |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981119/ https://www.ncbi.nlm.nih.gov/pubmed/27508321 http://dx.doi.org/10.1590/0074-02760160183 |
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