Efficacy of a 3-day oral regimen of a quinine-quinidine-cinchonine association (Quinimax) for treatment of falciparum malaria in Madagascar

Trans R Soc Trop Med Hyg. 1989 Nov-Dec;83(6):751-4. doi: 10.1016/0035-9203(89)90317-9.

Abstract

In the search for an effective, safe and field-adapted alternative to chloroquine for therapy of chloroquine-resistant Plasmodium falciparum infections in Africa, a 3-d oral regimen of Quinimax (an association of quinine, quinidine and cinchonine) was evaluated in 35 individuals with P. falciparum in Madagascar, an area with chloroquine resistance. 63% of the parasite strains isolated were resistant in vitro to chloroquine, and 59% of the infections were present despite previous chloroquine intake. Three daily oral doses of 10 mg/kg Quinimax for 3 d cleared parasitaemia and improved clinical status in all subjects. Mean parasite and fever clearance times were 51.7 and 37.4 h, respectively. All patients were aparasitaemic at the end of the 7-d follow-up. When formulating therapy guidelines, the 3-d Quinimax regimen should be considered as a valuable alternative to chloroquine for treating falciparum malaria in African areas with clinical resistance to chloroquine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chloroquine / administration & dosage
  • Drug Administration Schedule
  • Drug Combinations
  • Female
  • Humans
  • Madagascar
  • Malaria / drug therapy*
  • Male
  • Plasmodium falciparum / drug effects
  • Plasmodium falciparum / isolation & purification
  • Quinine / administration & dosage
  • Quinine / therapeutic use*

Substances

  • Drug Combinations
  • Chloroquine
  • Quinine