Tn. Trung et al., Treatment of falciparum malaria in Vietnamese children: the need for combination therapy and optimized dosage regimens, ANN TROP PA, 21(4), 2001, pp. 307-312
To assess the in vivo sensitivity of Plasmodium falciparum to mefloquine an
d artesunate in a hyperendemic area of southern Viet Nam, we studied 41 chi
ldren and 21 adults from a remote commune who had uncomplicated falciparum
malaria without previous treatment. Patients were randomly allocated to art
esunate (4 mg/kg on day 0 and 2 mg/kg on days 1-4) or mefloquine (10 mg/kg
followed by 5 mg/kg at 6 h). Serial assessments were performed over 28 days
. Of 31 patients allocated artesunate, nine (29%) redeveloped parasitaemia
during follow-up compared with 23% (seven of 30) who received mefloquine. O
f the 41 children, 15 (37%) had recrudescence/re-infection compared with on
ly one of 20 adults (5%; p < 0.001). Significantly more children than adult
s failed on mefloquine treatment (37% vs 0%; p = 0.021) and one case showed
RIII resistance. There was no significant difference in the case of artesu
nate. In regression analysis, parasitaemia was an independent predictor of
recrudescence/re-infection after mefloquine (p = 0.02). These data support
the use of combination therapy such as artesunate plus mefloquine for falci
parum malaria in a hyperendemic area of Viet Nam. Primarily because of thei
r greater parasite densities, children should be given higher doses of mefl
oquine (e.g. 25 mg/kg).