Clinical Infectious Diseases · 2003 · 132 citations · 18 references
Veterinary MedicineInfectious DiseasesPharmacologyAntimicrobial PharmacotherapyChemotherapyInfectious Disease PharmacotherapyAntifungal PharmacotherapyLiposomal FormulationsParasitic DiseasesParasitic InfectionsProtozoal InfectionsTreatmentAntileishmanial ChemotherapyAntileishmanial TreatmentCure TimeSafety Factor ProfileSafety Profile CharacterizationSerious Adverse EventsTreatment Of LeishmaniasisVisceral Leishmaniasis
Widespread antimony resistance renders conventional amphotericin B the only option for the treatment of visceral leishmaniasis (VL) in North Bihar, India. Because of its excellent safety profile, a large dose (7.5 mg/kg) of liposomal amphotericin B (L-AmB) was given to each of 203 patients with VL at 4 treatment centers, and the patients were discharged the next day. At initial clinical and parasitological follow-up, performed on day 30 after treatment, evidence of a cure was seen in 195 (96%) of 203 patients (95% CI, 92-98); 4 patients experienced treatment failure. Two patients were lost to follow-up, 2 died (one due to progressive disease and another, 5 months after treatment, due to an unrelated illness), and 12 experienced relapses during follow-up. Thus, 183 patients (90%; 95% CI, 85-94) had obtained final cure 6 months after treatment. Very few adverse events (fever with rigor, in 9.8% of patients) were seen. Single-dose L-AmB (7.5 mg/kg) treatment is safe and effective, and it may be used for the mass treatment of VL in India.
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Oral Miltefosine for Indian Visceral Leishmaniasis
Shyam Sundar, T. K. Jha, C.P. Thakur et al. · New England Journal of Medicine · 2002 · 774 citations · Full text
ICH Harmonised Tripartite Guideline: Guideline for Good Clinical Practice.
P. S. Bhuiyan, N. N. Rege · PubMed · 2002 · 531 citations · Full text
Miltefosine, an Oral Agent, for the Treatment of Indian Visceral Leishmaniasis
T. K. Jha, Shyam Sundar, C.P. Thakur et al. · New England Journal of Medicine · 1999 · 462 citations · Full text