Abstract:Severe global malnutrition and cerebral malaria have a similar effect on quinine pharmacokinetics in children. Moderate malnutrition does not potentiate cerebral malaria-mediated modifications of quinine disposition. These results suggest that current parenteral quinine regimens can be used, unmodified, to treat children with both malaria and malnutrition.
“…In human, Pussard and al observed that malaria and malnutrition increased plasma concentrations of quinine and reduced both the volume of distribution and the total plasma clearance [26]. Measuring the response to an acute uncomplicated Plasmodium falciparum malaria treatment with CQ, Olanrewaju WI and Johnson AW [27] observed that the proportion of children with persistence or recrudescence of parasitemia on days 4-7 and no significant reduction of parasitemia was higher among malnourished children compared to children with satisfactory nutritional status.…”
Background: Recent published studies on efficacy and safety of antimalarial treatment in children with Severe Acute Malnutrition (SAM) suffering from uncomplicated malaria are not available.
“…In human, Pussard and al observed that malaria and malnutrition increased plasma concentrations of quinine and reduced both the volume of distribution and the total plasma clearance [26]. Measuring the response to an acute uncomplicated Plasmodium falciparum malaria treatment with CQ, Olanrewaju WI and Johnson AW [27] observed that the proportion of children with persistence or recrudescence of parasitemia on days 4-7 and no significant reduction of parasitemia was higher among malnourished children compared to children with satisfactory nutritional status.…”
Background: Recent published studies on efficacy and safety of antimalarial treatment in children with Severe Acute Malnutrition (SAM) suffering from uncomplicated malaria are not available.
“…In the case of streptomycin, children with kwashiorkor exhibited an increased Vd [48] whereas children with marasmus or underweight had a decreased Vd [48]. A decreased Vd for quinine in children with undefined PEM in one study [51] was in contrast to a separate study involving children with marasmus and marasmic-kwashiorkor where the Vd was unaffected [21]. Table 4 shows the effect of PEM on the total clearance and half-life of seven drugs that are primarily metabolised in the liver.…”
Section: Protein Binding and Distributionmentioning
“…The scaled estimate of CL for a 15-kg child (OE) was 0.37 liter/h/kg. By comparison, the mean adult CL is 0.17 liter/h/kg (Table 3), the estimated CL based on a fixed exponent of 3/4 is 0.25 liter/h/kg, and the CL from one clinical study in children (15 kg) was 0.24 liter/h/kg (118). child doses will decrease for children with higher body weights and will also decrease as the exponent approaches unity.…”
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.