Plasmodium falciparum antimalarial drug susceptibility on the north-western border of Thailand during five years of extensive use of artesunate-mefloquine - PubMed (original) (raw)

Plasmodium falciparum antimalarial drug susceptibility on the north-western border of Thailand during five years of extensive use of artesunate-mefloquine

A Brockman et al. Trans R Soc Trop Med Hyg. 2000 Sep-Oct.

Abstract

Following a marked decline in the efficacy in vivo of mefloquine between 1990 and 1994, a combination of artesunate (4 mg/kg/d for 3 d) and mefloquine (25 mg/kg) has been used as first line treatment of uncomplicated falciparum malaria in camps for displaced persons located along the north-western border of Thailand. Antimalarial drug susceptibility of fresh isolates of Plasmodium falciparum from this population was evaluated using a radioisotope microdilution assay between 1995 and 1999. In total, 268 isolates were collected, of which 189 were from primary infections and 79 from recrudescent infections. The geometric mean 50% inhibitory concentration (IC50) values from primary infections were: dihydroartemisinin 1.2 ng/mL, artesunate 1.6 ng/mL, artemether 4.8 ng/mL, atovaquone 0.4 ng/mL, lumefantrine 32 ng/mL, chloroquine 149 ng/mL, quinine 354 ng/mL, mefloquine 27 ng/mL and halofantrine 4.1 ng/mL. A significant positive correlation was found between the susceptibility in vitro to artesunate and quinine (r = 0.43, P < 0.001), mefloquine (r = 0.46, P < 0.001), and halofantrine (r = 0.51, P < 0.001). These levels of resistance in vitro are among the highest reported and confirm continuing high level multidrug resistance in this area. Despite intensive use of the combination between 1995 and 1999 there has been a significant improvement in mefloquine sensitivity (P < 0.001) and artesunate sensitivity (P < 0.001). This supports observations in vivo that the combination of artesunate and mefloquine has reversed the previous decline in mefloquine sensitivity.

PubMed Disclaimer

Figures

Fig. 1

Fig. 1

Scatter plots of the relationship between the 50% inhibitory concentrations (IC50) against Plasmodium falciparum in vitro of artesunate and those of quinine, mefloquine, and halofantrine.

Fig. 2

Fig. 2

Trend of drug susceptibilities in vitro of isolates at Plasmodium falciparum from primary infections over time. Values are geometric mean 50% inhibitory concentrations (IC50) and 95% confidence intervals.

Fig. 3

Fig. 3

Trend of drug of susceptibilities in vitro of isolates of Plasmodium falciparum from recrudescent infections over time. Values are geometric mean 50% inhibitory concentrations (IC50) and 95% confidence intervals.

Similar articles

Cited by

References

    1. Basco LK, Le Bras J. In vitro activity of artemisinin derivatives against African isolates and clones of Plasmodium falciparum. American Journal of Tropical Medicine and Hygiene. 1993;49:301–307. - PubMed
    1. Basco LK, Le Bras J. In vitro susceptibility of Cambodian isolates of Plasmodium falciparum to halofantrine, pyronaridine and artemisinin derivatives. Annals of Tropical Medicine and Parasitology. 1994;88:137, 144. - PubMed
    1. Gay F, Ciceron L, Litaudon M, Bustos MD, Astagneau P, Diquet B, Danis M, Gentilini M. In vitro resistance of Plasmodium falciparum to qinghaosu derivatives in West Africa. Lancet. 1997;343:850–851. - PubMed
    1. Heppner DG, Ballou WR. Malaria in 1998: recent advances in diagnosis, drugs and vaccine development. Current Opinion in Infectious Diseases. 1998;11:519–530. - PubMed
    1. Inselburg J. Induction and isolation of artemisinine-resistant mutants of Plasmodium falciparum. American Journal of Tropical Medicine and Hygiene. 1985;34:417–418. - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources