dc.contributor.author | Miranda-Verastegui, Cesar | |
dc.contributor.author | Tulliano, GianFranco | |
dc.contributor.author | Gyorkos, Theresa W. | |
dc.contributor.author | Calderon, Wessmark | |
dc.contributor.author | Rahme, Elham | |
dc.contributor.author | Ward, Brian | |
dc.contributor.author | Cruz, Maria | |
dc.contributor.author | Llanos Cuentas, Alejandro | |
dc.contributor.author | Matlashewski, Greg | |
dc.date.accessioned | 2019-04-24T13:44:03Z | |
dc.date.available | 2019-04-24T13:44:03Z | |
dc.date.issued | 2009 | |
dc.identifier.citation | PLOS Neglected Tropical Diseases. 2009;3(7). | es_PE |
dc.identifier.uri | https://hdl.handle.net/20.500.12959/403 | |
dc.description.abstract | Se evaluó si el antimonio pentavalente (un fármaco antiparasitario) combinado con imiquimod (un inmunomodulador) sería más eficaz que el antimonio pentavalente solo en pacientes con leishmaniasis cutánea que no habían sido tratados previamente. Se realizó un estudio clínico doble ciego randomizado con 80 pacientes con leishmaniasis cutánea. Los pacientes de estudio fueron seleccionados en Lima y Cusco, 20 experimentales y 20 sujetos de control en cada lugar. Se concluye que el tratamiento combinado de imiquimod con antimonio pentavalente fue más efectivo que el placebo con antimonio pentavalente, pero la diferencia no fue significativa estadísticamente. | es_PE |
dc.description.abstract | Background: Current therapies for cutaneous leishmaniasis are limited by poor efficacy, long-term course of treatment, and the development of resistance. We evaluated if pentavalent antimony (an anti-parasitic drug) combined with imiquimod (an immunomodulator) was more effective than pentavalent antimony alone in patients who had not previously been treated. Methods: A randomized double-blind clinical trial involving 80 cutaneous leishmaniasis patients was conducted in Peru. The study subjects were recruited in Lima and Cusco (20 experimental and 20 control subjects at each site). Experimental arm: Standard dose of pentavalent antimony plus 5% imiquimod cream applied to each lesion three times per week for 20 days. Control arm: Standard dose of pentavalent antimony plus placebo (vehicle cream) applied as above. The primary outcome was cure defined as complete re-epithelization with no inflammation assessed during the 12 months post-treatment period. Results: Of the 80 subjects enrolled, 75 completed the study. The overall cure rate at the 12-month follow-up for the intention-to-treat analysis was 75% (30/40) in the experimental arm and 58% (23/40) in the control arm (p = 0.098). Subgroup analyses suggested that combination treatment benefits were most often observed at the Cusco site, where L. braziliensis is the prevalent species. Over the study period, only one adverse event (rash) was recorded, in the experimental arm. Conclusion: The combination treatment of imiquimod plus pentavalent antimony performed better than placebo plus pentavalent antimony, but the difference was not statistically significant. | |
dc.format | application/pdf | es_PE |
dc.language.iso | eng | es_PE |
dc.publisher | Marleen Boelaert, Institute of Tropical Medicine, Belgium | es_PE |
dc.relation.uri | https://journals.plos.org/plosntds/article?id=10.1371/journal.pntd.0000491#abstract1 | |
dc.rights | info:eu-repo/semantics/openAccess | es_PE |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | es_PE |
dc.source | Seguro Social de Salud (EsSalud) | es_PE |
dc.source | Repositorio Institucional EsSalud | es_PE |
dc.subject | Enfermedades Infecciosas | es_PE |
dc.subject | Leishmaniasis Cutánea | es_PE |
dc.subject | Acciones Farmacológicas | es_PE |
dc.subject | Factores Inmunológicos | es_PE |
dc.title | First-line therapy for human cutaneous leishmaniasis in Peru using the TLR7 agonist imiquimod in combination with pentavalent antimony | es_PE |
dc.type | info:eu-repo/semantics/article | es_PE |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.05.00 | es_PE |
dc.publisher.country | PE | es_PE |
dc.identifier.doi | https://doi.org/10.1371/journal.pntd.0000491 | |