Treatment of Disseminated Leishmaniasis With Liposomal Amphotericin B
Author(s) -
Paulo Roberto Lima Machado,
Maria Elisa A. Rosa,
Luís Henrique Rocha Guimarães,
Fernanda V. O. Prates,
Adriano Queiroz,
Albert Schriefer,
Edgar M. Carvalho
Publication year - 2015
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1093/cid/civ416
Subject(s) - medicine , amphotericin b , context (archaeology) , adverse effect , leishmaniasis , cure rate , meglumine antimoniate , cutaneous leishmaniasis , surgery , gastroenterology , dermatology , antifungal , immunology , paleontology , biology
Disseminated leishmaniasis (DL) is a severe and emerging form of American tegumentary leishmaniasis, associated primarily with infection by Leishmania brasiliensis. DL is defined by the presence of ≥10 mixed-type lesions such as inflammatory papules and ulcers, located in ≥2 body parts. Most patients have hundreds of lesions all over the body, and mucosal involvement is detected in up to 44% of cases. DL is a difficult to cure disease and pentavalent antimony (Sb(v)) is used as standard treatment, its highest dosage being 20 mg/kg/day, for 30 days. However, less than 25% of DL cases will be cured after standard therapy, and the majority of cases will require more than one course of Sb(v) for a cure. In this context, new therapies are needed that offer a higher cure rate and a better safety profile, with convenience in drug administration.
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