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Cost-effectiveness Analysis of Combination Therapies for Visceral Leishmaniasis in the Indian Subcontinent

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Date 2010 Sep 15
PMID 20838649
Citations 46
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Abstract

Background: Visceral leishmaniasis is a systemic parasitic disease that is fatal unless treated. We assessed the cost and cost-effectiveness of alternative strategies for the treatment of visceral leishmaniasis in the Indian subcontinent. In particular we examined whether combination therapies are a cost-effective alternative compared to monotherapies.

Methods And Findings: We assessed the cost-effectiveness of all possible mono- and combination therapies for the treatment of visceral leishmaniasis in the Indian subcontinent (India, Nepal and Bangladesh) from a societal perspective using a decision analytical model based on a decision tree. Primary data collected in each country was combined with data from the literature and an expert poll (Delphi method). The cost per patient treated and average and incremental cost-effectiveness ratios expressed as cost per death averted were calculated. Extensive sensitivity analysis was done to evaluate the robustness of our estimations and conclusions. With a cost of US$92 per death averted, the combination miltefosine-paromomycin was the most cost-effective treatment strategy. The next best alternative was a combination of liposomal amphotericin B with paromomycin with an incremental cost-effectiveness of $652 per death averted. All other strategies were dominated with the exception of a single dose of 10mg per kg of liposomal amphotericin B. While strategies based on liposomal amphotericin B (AmBisome) were found to be the most effective, its current drug cost of US$20 per vial resulted in a higher average cost-effectiveness. Sensitivity analysis showed the conclusion to be robust to variations in the input parameters over their plausible range.

Conclusions: Combination treatments are a cost-effective alternative to current monotherapy for VL. Given their expected impact on the emergence of drug resistance, a switch to combination therapy should be considered once final results from clinical trials are available.

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References
1.
Seifert K, Matu S, Perez-Victoria F, Castanys S, Gamarro F, Croft S . Characterisation of Leishmania donovani promastigotes resistant to hexadecylphosphocholine (miltefosine). Int J Antimicrob Agents. 2003; 22(4):380-7. DOI: 10.1016/s0924-8579(03)00125-0. View

2.
Sundar S, Agrawal N, Arora R, Agarwal D, Rai M, Chakravarty J . Short-course paromomycin treatment of visceral leishmaniasis in India: 14-day vs 21-day treatment. Clin Infect Dis. 2009; 49(6):914-8. DOI: 10.1086/605438. View

3.
Sundar S, Agrawal G, Rai M, Makharia M, Murray H . Treatment of Indian visceral leishmaniasis with single or daily infusions of low dose liposomal amphotericin B: randomised trial. BMJ. 2001; 323(7310):419-22. PMC: 37549. DOI: 10.1136/bmj.323.7310.419. View

4.
Sundar S, Makharia A, More D, Agrawal G, Voss A, Fischer C . Short-course of oral miltefosine for treatment of visceral leishmaniasis. Clin Infect Dis. 2000; 31(4):1110-3. DOI: 10.1086/318122. View

5.
Jha T, Olliaro P, Thakur C, Kanyok T, Singhania B, Singh I . Randomised controlled trial of aminosidine (paromomycin) v sodium stibogluconate for treating visceral leishmaniasis in North Bihar, India. BMJ. 1998; 316(7139):1200-5. PMC: 28521. DOI: 10.1136/bmj.316.7139.1200. View