A retrospective cohort study of the effectiveness and adverse events of intralesional pentavalent antimonials in the treatment of cutaneous leishmaniasis
Autor: | Sofia Sales Martins, Cláudia Porto, Marina Freitas Ferreira, Jorgeth de Oliveira Carneiro da Motta, Carmen Déa Ribeiro de Paula, Ciro Martins Gomes, Bruna Côrtes Rodrigues, Raimunda Nonata Ribeiro Sampaio, Daniel Holanda Barroso |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Male medicine.medical_specialty N-methyl glucamine Meglumine antimoniate 030231 tropical medicine Pentavalent antimonial Antiprotozoal Agents Leishmaniasis Cutaneous Context (language use) Injections Intralesional Article law.invention lcsh:Infectious and parasitic diseases Lesion 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Meglumine Randomized controlled trial law Internal medicine medicine Organometallic Compounds Humans Pharmacology (medical) lcsh:RC109-216 Prospective Studies Adverse effect New world leishmaniasis Retrospective Studies Pharmacology Cutaneous leishmaniasis Intralesional antimonial business.industry Retrospective cohort study 030104 developmental biology Infectious Diseases Treatment Outcome chemistry Intralesional therapy Relative risk Parasitology Female medicine.symptom business medicine.drug |
Zdroj: | International Journal for Parasitology: Drugs and Drug Resistance, Vol 14, Iss, Pp 257-263 (2020) International Journal for Parasitology: Drugs and Drug Resistance |
ISSN: | 2211-3207 |
Popis: | Introduction The standard therapy for American cutaneous leishmaniasis (ACL) is intravenous meglumine antimoniate (IV-MA). However, treatment interruptions due to adverse events (AEs) and non-adherence are frequent. Consequently, intralesional MA (IL-MA) was proposed. Objective This study examined the effectiveness of and AEs associated with IL-MA. Methods We performed a retrospective cohort study of 240 patients with ACL. We excluded patients with mucous lesions and disseminated leishmaniasis and those who received treatment in the previous 6 months. We considered protocol treatments as the main risk factors. IL-MA was performed using a subcutaneous injection of MA in a volume sufficient to elevate the lesion base (approximately 1 mL/cm2 of lesion area) once weekly for 1–8 weeks. IV-MA was performed via intravenous injections of MA at a dosage of 10–20 mg Sb5+/kg/day for 20 days. The primary outcome was defined as a lesion cure 3 months after treatment, and AEs were secondary outcomes. Results Seventy-three patients were included. The IL-MA group consisted of 21 patients, and the IV-MA group consisted of 52 patients. The IL-MA group was older, had more comorbidities and more previous unsuccessful treatment of ACL. The antimonial dose was significantly lower in this group. The cure rate for IL-MA was 66.7%, which was lower than that in the IV-MA group (relative risk (RR) = 0.68, 95% CI: 0.50–0.92, p Graphical abstract Image 1 Highlights • Intralesional antimonials (IL-MA) had a 66.7% lower cure compared to systemic. • IL-MA group was older, had more comorbidities and unsuccessful previous treatment. • IL-MA was useful in this group, where worse clinical responses are expected. • Lesions larger than 3 cm did not have more chance of failure with IL-MA. • There was no mucous recurrence after IL-MA in an area of New World Leishmaniasis. |
Databáze: | OpenAIRE |
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