Short-course, cost-effective treatment with amphotericin B-fat emulsion cures visceral leishmaniasis.
- 1 March 2000
- journal article
- clinical trial
- Published by Oxford University Press (OUP) in Transactions of the Royal Society of Tropical Medicine and Hygiene
- Vol. 94 (2) , 200-204
- https://doi.org/10.1016/s0035-9203(00)90277-3
Abstract
Although short-course therapy with new lipid formulations of amphotericin B represents an advance over lengthy traditional treatments in visceral leishmaniasis (kala-azar), high cost has rendered these agents largely irrelevant in developing countries where the disease is endemic. Therefore, we tested standard amphotericin B deoxycholate mixed with a commercial fat emulsion as short-course treatment for Indian visceral leishmaniasis in Bihar in 1997/98. Seventy children and adults with splenic aspirate-documented infection, 23 of whom had failed prior antimony (Sb) therapy, received 5 alternate-day infusions of 2 mg/kg. Apparent cure, which required a parasite-free splenic aspirate smear, was assessed 20 days after treatment (day 30); definitive cure was determined at 6 months. Other than anticipated infusion-related fever and/or chills, treatment was safe and well tolerated. One patient required dose modification because of mild, reversible renal insufficiency. Sixty-nine patients (98.6%, CI 92.3-100%) had apparent cures; during follow-up, there were 4 treatment failures (relapses, 3; unrelated death, 1), yielding definitive cures in 65 of 70 patients (92.9%, CI 84.1-97.6%). Including retreatment costs for patients in Bihar (who now often fail initial Sb therapy), the final per patient cost of the tested regimen (US $260) was 59% and 43% less than treatment with Sb or conventional amphotericin B alone, respectively. Short-course treatment with amphotericin B-fat emulsion is active, cost-effective treatment for patients with visceral leishmaniasis including those with Sb-unresponsive infection.Keywords
This publication has 19 references indexed in Scilit:
- Treatment of antimony-unresponsive Indian visceral leishmaniasis with ultra-short courses of amphotericin B-lipid complexPathogens and Global Health, 1998
- Do the diminishing efficacy and increasing toxicity of sodium stibogluconate in the treatment of visceral leishmaniasis in Bihar, India, justify its continued use as a first line drug? An observational study of 80 casesPathogens and Global Health, 1998
- Response to Interferon‐γ plus Pentavalent Antimony in Indian Visceral LeishmaniasisThe Journal of Infectious Diseases, 1997
- Safety and efficacy of Intralipid emulsions of amphotericin BJournal of Antimicrobial Chemotherapy, 1996
- Short-Course Treatment of Visceral Leishmaniasis with Liposomal Amphotericin B (AmBisome)Clinical Infectious Diseases, 1996
- Cure of Antimony-Unresponsive Indian Visceral Leishmaniasis with Amphotericin B Lipid ComplexThe Journal of Infectious Diseases, 1996
- Liposomal Amphotericin B (AmBisome) in the Treatment of Complicated Kala-Azar Under Field ConditionsClinical Infectious Diseases, 1995
- Amphotericin versus sodium stibogluconate in first-line treatment of Indian kala-azarThe Lancet, 1994
- Amphotericin versus pentamidine in antimony-unresponsive kala-azarThe Lancet, 1992
- Trial of glucose versus fat emulsion in preparation of amphotericin for use in HIV infected patients with candidiasis.BMJ, 1992