To evaluate the efficacy of a short course of a lipid formulation of amphotericin B (L-AmB) for the treatment of Mediterranean visceral leishmaniasis (VL), an open prospective study was conducted. Forty-one children with parasitologically confirmed leishmaniasis received L-AmB, 10 mg/kg daily for 2 days. The comparison groups were 30 children who, in a previous study, were treated with L-AmB, 4 mg/kg daily for 5 days, and 52 children who were treated with meglumine antimoniate. At 6 months after completion of treatment, overall treatment success was noted for 40 of 41 children treated with 2 doses of L-AmB, 27 of 30 children treated with 5 doses of L-AmB, and 47 of 52 children treated with meglumine antimoniate. Abatement of fever, reductio...
Background: India is home to 60 % of the total global visceral leishmaniasis (VL) population. Use of...
Widespread antimony resistance renders conventional amphotericin B the only option for the treatment...
High cost is the principal drawback of treating visceral leishmaniasis (VL; kala-azar) with any of t...
We used liposomal amphotericin B as first-choice treatment of visceral leishmaniasis in 106 immunoco...
We evaluated liposomal amphotericin B (AmBisome; Vestar, San Dimas, CA) administered to 88 immunocom...
Although short-course therapy with new lipid formulations of amphotericin B represents an advance ov...
Liposomal amphotericin B has been used with increasing frequency to treat visceral leishmaniasis (VL...
India is home to 60% of the total global visceral leishmaniasis (VL) population. Use of long-term or...
Objectives: To evaluate in a retrospective analysis the efficacy and safety of a 6 day course of lip...
In Bihar, India, where visceral leishmaniasis is hyperendemic, amphotericin B deoxycholate is now fi...
The rapidity and efficacy of a short course of liposomal amphotericin B was evaluated in 29 children...
Background: Visceral leishmaniasis (kala-azar) is a world-wide, disseminated intracellular protozoal...
Amphotericin B (AB) deoxycholate is highly effective in antimony refractory cases for the treatment ...
Liposomal amphotericin B (LAmB) is the drug of choice in Bangladesh to eliminate the burden of visce...
Background: In Bihar, India, where visceral leishmaniasis (VL) is hyperendemic and refractory to ant...
Background: India is home to 60 % of the total global visceral leishmaniasis (VL) population. Use of...
Widespread antimony resistance renders conventional amphotericin B the only option for the treatment...
High cost is the principal drawback of treating visceral leishmaniasis (VL; kala-azar) with any of t...
We used liposomal amphotericin B as first-choice treatment of visceral leishmaniasis in 106 immunoco...
We evaluated liposomal amphotericin B (AmBisome; Vestar, San Dimas, CA) administered to 88 immunocom...
Although short-course therapy with new lipid formulations of amphotericin B represents an advance ov...
Liposomal amphotericin B has been used with increasing frequency to treat visceral leishmaniasis (VL...
India is home to 60% of the total global visceral leishmaniasis (VL) population. Use of long-term or...
Objectives: To evaluate in a retrospective analysis the efficacy and safety of a 6 day course of lip...
In Bihar, India, where visceral leishmaniasis is hyperendemic, amphotericin B deoxycholate is now fi...
The rapidity and efficacy of a short course of liposomal amphotericin B was evaluated in 29 children...
Background: Visceral leishmaniasis (kala-azar) is a world-wide, disseminated intracellular protozoal...
Amphotericin B (AB) deoxycholate is highly effective in antimony refractory cases for the treatment ...
Liposomal amphotericin B (LAmB) is the drug of choice in Bangladesh to eliminate the burden of visce...
Background: In Bihar, India, where visceral leishmaniasis (VL) is hyperendemic and refractory to ant...
Background: India is home to 60 % of the total global visceral leishmaniasis (VL) population. Use of...
Widespread antimony resistance renders conventional amphotericin B the only option for the treatment...
High cost is the principal drawback of treating visceral leishmaniasis (VL; kala-azar) with any of t...