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Antimalarial drug response of Plasmodium falciparum from Zaria, Nigeria

1995; Oxford University Press; Volume: 89; Issue: 4 Linguagem: Inglês

10.1016/0035-9203(95)90037-3

1878-3503

I. S. Adagu, D. C. Warhurst, W. N. Ogala, I. Abdu‐Aguye, L.I. Audu, F.O. Bamgbola, U B Ovwigho,

Drug-Induced Hepatotoxicity and Protection

The sensitivity of Zaria strains of Plasmodium falciparum to chloroquine, mefloquine, quinine and sulphadoxine/pyrimethamine was investigated 5 years after the appearance of in vivo/in vitro chloroquine resistance in urban Zaria. Infections in 36/43 children (83·7%) treated with chloroquine were sensitive while those in 7 (16·3%) were resistant. 8/13 isolates cultured (61·5%) were sensitive in vitro to chloroquine and 5 (38·5%) were resistant. Of the cultured isolates, 13/13 (100%), 12/13 (92·3%) and 5/7 (71·4%) showed mefloquine, quinine and sulphadoxine/pyrimethamine sensitivity, respectively. The results confirmed chloroquine and sulphadoxine/pyrimethamine resistance in urban Zaria and revealed emerging quinine resistance. Resistance to chloroquine and sulphadoxine/pyrimethamine is at RI level and chloroquine should continue to be the first-line drug for the treatment and prevention of P. falciparum infection in the Zaria area of northern Nigeria. We suggest that, while quinine serves as second-line drug, mefloquine should be reserved for infections resistant to chloroquine, quinine and sulphadoxine/pyrimethamine.