CV8, a new combination of dihydroartemisinin, piperaquine, trimethoprim and primaquine, compared with atovaquone-proguanil against falciparum malaria in Vietnam

被引:35
作者
Giao, PT
de Vries, PJ
Hung, LQ
Binh, TQ
Nam, NV
Kager, PA
机构
[1] Univ Amsterdam, Acad Med Ctr, Div Infect Dis Trop Med & AIDS, NL-1105 AZ Amsterdam, Netherlands
[2] Cho Ray Hosp, Trop Dis Clin Res Ctr, Ho Chi Minh City, Vietnam
[3] Binh Thuan Prov Malaria Stn, Phan Thiet, Binh Thuan Prov, Vietnam
关键词
Plasmodium falciparum; combination therapy; dihydroartemisinin; piperaquine; trimethoprim; primaquine; proguanil; atovaquone; Vietnam;
D O I
10.1046/j.1365-3156.2003.01180.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 study a new combination, based on dihydroartemisinin and piperaquine (CV8) and atovaquone/proguanil (Malarone) for treatment of uncomplicated falciparum malaria in Vietnam. METHODS Vietnamese adults with falciparum malaria were allocated randomly to treatment with dihydroartemisinin/piperaquine/trimethoprim/primaquine 256/2560/720/40 mg (CV8, n = 84) or Malarone 3000/1200 mg (n = 81), both over 3 days. Patients were followed-up for 28 days. RESULTS All patients recovered rapidly. The mean (95% CI) parasite elimination half-life of CV8 was 6.8 h (6.2-7.4) and of Malarone 6.5 h (6.1-6.9) (P = 0.4). Complete parasite clearance time was 35 (31-39) and 34 h (31-38) (P = 0.9). The 28-day cure rate was 94% and 95%, respectively (odds ratio 0.84, 95% CI 0.18-3.81). No significant side-effects were found. CONCLUSION CV8 and Malarone are effective combinations against multi-drug resistant falciparum malaria. CV8 has the advantage of a low price.
引用
收藏
页码:209 / 216
页数:8
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