Abstract |
Mefloquine (MQ) single dose 20 mg/kg treatment of falciparum malaria was evaluated in 186 children of 6-24 months of age in northern Ghana. There were 15 RII/RIII-type parasitologic failures, all with Day 2 MQ blood levels significantly lower than children whose parasitemias cleared before Day 7 and remained clear through 28 days. Predictors of RII/RIII parasitologic response were vomiting after MQ dosing, Day 2 MQ levels < 500 ng/mL, and undetectable Day 2 levels of the carboxymefloquine metabolite. There were 50 cases of delayed RI parasitologic failure, but 71% of these cases had undetectable Day 28 blood levels of MQ and drug levels in the remaining 29% ranged below the 620 ng/mL level that suppresses MQ sensitive strains of P. falciparum. Drug levels among infants that tolerated MQ well were not associated with age, weight, hemoglobin, parasitemia, and pre-existing symptoms of vomiting or diarrhea. An observed recurrent parasitemia of 34,400 trophozoites/microL against a MQ blood concentration of 550 ng/mL was taken as indication of tolerance to suppressive levels of the drug at this location.
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Authors | David J Fryauff, Seth Owusu-Agyei, Gregory Utz, J Kevin Baird, Kwadwo A Koram, Fred Binka, Francis Nkrumah, Stephen L Hoffman |
Journal | The American journal of tropical medicine and hygiene
(Am J Trop Med Hyg)
Vol. 76
Issue 2
Pg. 224-31
(Feb 2007)
ISSN: 0002-9637 [Print] United States |
PMID | 17297028
(Publication Type: Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
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Chemical References |
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Topics |
- Animals
- Antimalarials
(adverse effects, blood, therapeutic use)
- Child, Preschool
- Cohort Studies
- Diarrhea
(chemically induced)
- Female
- Ghana
- Humans
- Infant
- Linear Models
- Malaria, Falciparum
(blood, drug therapy, parasitology)
- Male
- Mefloquine
(adverse effects, blood, therapeutic use)
- Parasitemia
(drug therapy)
- Plasmodium falciparum
(growth & development)
- Prospective Studies
- Vomiting
(chemically induced)
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