Efficacy and safety of artesunate plus amodiaquine in routine use for the treatment of uncomplicated malaria in Casamance, southern Senegal

被引:34
作者
Brasseur, Philippe [2 ]
Agnamey, Patrice [3 ]
Gaye, Oumar [4 ]
Vaillant, Michel [1 ,5 ]
Taylor, Walter R. J. [6 ,7 ]
Olliaro, Piero L. [1 ,7 ]
机构
[1] Univ Victor Segalen Bordeaux 2, U3677, Bordeaux, France
[2] IRD, UR077, Dakar, Senegal
[3] Mycol CHU Amiens, Parasitol Lab, Amiens, France
[4] Univ Cheikh Anta Diop, Dakar, Senegal
[5] CRP Sante, Ctr Hlth Studies, Clin Epidemiol & Publ Hlth Unit, Luxembourg, Luxembourg
[6] Univ Hosp Geneva, Travel & Migrat Med Unit, Geneva, Switzerland
[7] UNICEF UNDP WB, WHO, Special Programme Res & Training Trop Dis TDR, CH-1211 Geneva 27, Switzerland
关键词
D O I
10.1186/1475-2875-6-150
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: There are no data on the long term use of an artemisinin combination treatment in moderate or high transmission areas of Africa. Methods and findings: Artesunate plus amodiaquine (AS+AQ) was used to treat slide-proven Plasmodium falciparum-infected patients of all ages in the Oussouye district, Casamance, Senegal, over a period of six years (2000 to 2005). Efficacy, by Kaplan Meier survival analysis (n = 966), and safety (adverse event rates, n = 752) were determined over 28 days. A weight-based dosing regimen was used for the loose tablets during 2000-2003 (n = 731) and a commercially available co-blister was used during 2004-2005 (n = 235). Annual crude (non PCR corrected) rates remained stable over the study period [range 88.5-96.7%; overall 94.6 (95% CI 92.9-95.9)]. Nine co-blister treated patients (0.9%) withdrew because of drug-related adverse events; seven had gastrointestinal complaints of whom two were hospitalized for vomiting. By Day 28, the mean total bilirubin (n = 72), AST (n = 94) and ALT (n = 95) values decreased. Three patients had Day 28 AST/ALT values > 40 < 200 IU/L. Changes in white cell counts were unremarkable (n = 87). Conclusion: AS+AQ in combination was highly efficacious and well-tolerated in this area and justifies the decision to use it as first line treatment. Long-term monitoring of safety and efficacy should continue.
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