Congo-Brazzaville has recently adopted
artesunate-
amodiaquine as the first-line
antimalarial drug to replace
chloroquine. Before the implementation of this new strategy, we conducted several clinical studies to assess the therapeutic efficacy of former, classical first-line
antimalarial drugs in the city of Brazzaville, in which reside about 30% of the Congolese population. From 2003 to 2005, non-randomised trials were conducted to evaluate the efficacy of
sulfadoxine-pyrimethamine (SP) (n=97 patients),
amodiaquine (AQ) (n=62 patients), and the combination of
sulfadoxine-pyrimethamine-
amodiaquine (n=54 patients) in children aged between 6 months and 5 years with uncomplicated
malaria using the 2003 WHO guidelines during the 28-day follow-up period. After excluding new
infections by PCR, the proportion of treatment failure on day 28 was 30.2% (95% confidence interval, 19.2-43.0%) for
sulfadoxine-pyrimethamine, 34.8% (95% confidence interval, 21.4-50.2%) for
amodiaquine, and 14.2% (95% confidence interval, 5.9-27.2%) for
sulfadoxine-pyrimethamine+amodiaquine combination. Treatment with
sulfadoxine-pyrimethamine was associated with an increase of gametocyte charge. These results suggest that neither
sulfadoxine-pyrimethamine nor
amodiaquine is efficacious as monotherapy and that their combination may not remain effective in the coming years. Based on our results, the implementation of
artemisinin-based combination
therapy appears to be urgent in the country.