Drug policy for visceral leishmaniasis: a cost-effectiveness analysis

被引:42
|
作者
Vanlerberghe, V.
Diap, G.
Guerin, P. J.
Meheus, F.
Gerstl, S.
Van der Stuyft, P.
Boelaert, M.
机构
[1] Inst Trop Med Prince Leopold, Epidemiol & Dis Unit, B-2000 Antwerp, Belgium
[2] Medecins Sans Frontieres, Campaign Access Essential Med, Geneva, Switzerland
[3] EPICTR, Paris, France
[4] Royal Trop Inst, NL-1105 AZ Amsterdam, Netherlands
关键词
visceral leishmaniasis; drug policy; cost-effectiveness analysis;
D O I
10.1111/j.1365-3156.2006.01782.x
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objectives To facilitate the choice of the best visceral leishmaniasis (VL) treatment strategy for first-line health services in (VL)-endemic areas, we compared in a formal decision analysis the cost and the cost-effectiveness of the different available options. Method We selected four drug regimens for VL on the basis of frequency of use, feasibility and reported efficacy studies. The point estimates and the range of plausible values of effectiveness and cost were retrieved from a literature review. A decision tree was constructed and the strategy minimizing the cost per death averted was selected. Results Treatment with amphotericin B deoxycholate was the most effective approach in the baseline analysis and averted 87.2% of all deaths attributable to VL. The least expensive and the most cost-effective treatment was the miltefosine regimen, and the most expensive and the least cost-effective was AmBisome((R)) treatment. The cost of drug and medical care are the main determinants of the cost-effectiveness ranking of the alternative schemes. Sensitivity analysis showed that antimonial was competitive with miltefosine in the low-resistance regions. Conclusions In areas with > 94% response rates to antimonials, generic sodium stibogluconate remains the most cost-effective option for VL treatment, mainly due to low drug cost. In other regions, miltefosine is the most cost-effective option of treatment, but its use as a first-line drug is limited by its teratogenicity and rapid resistance development. AmBisome in mono- or combination therapy is too expensive to compete in cost-effectiveness with the other regimens.
引用
收藏
页码:274 / 283
页数:10
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