TY - JOUR
T1 - High residual chloroquine blood levels in African children with severe malaria seeking healthcare
AU - Wichmann, Ole
AU - Eggelte, Teunis A.
AU - Gellert, Sabine
AU - Osman, Maha Elhadi
AU - Mylius, Franziska
AU - Ehrhardt, Stephan
AU - Anemana, Sylvester D.
AU - Bienzle, Ulrich
AU - Mockenhaupt, Frank P.
PY - 2007/7
Y1 - 2007/7
N2 - Despite widespread resistance, chloroquine remains widely used in West Africa, particularly in home treatment. We examined chloroquine blood levels on admission to a referral hospital with respect to the manifestation of severe malaria in 290 Ghanaian children. Of the patients, 78% exhibited chloroquine concentrations (subtherapeutic, 35%; therapeutic, 37%; supratherapeutic, 6%) and 11% died. Most parasites (78%) carried the pfcrt-T76 chloroquine resistance mutation. High drug concentrations correlated with reduced parasitaemia but also with selection of resistant parasites, lower respiratory and heart rates, increased plasma lactate levels and impaired consciousness. Geometric mean chloroquine concentrations tended to be higher in children who died than in survivors (1.135 vs. 778 nmol/l; P = 0.09). Supratherapeutic drug levels (>5000 nmol/l) were associated with fatal outcome (odds ratio 8.6; 95% CI 1.4-51.7). Residual chloroquine concentrations were found to be abundant in children with severe malaria and to be associated with alterations in the clinical manifestation of the disease and its case fatality. This may result from toxic effects of the drug and/or reflect preceding overtreatment in children with acute life-threatening disease. In areas of intense chloroquine resistance and frequent pre-treatment, additional administration of chloroquine at hospital admission is not only ineffective but may even further endanger patients.
AB - Despite widespread resistance, chloroquine remains widely used in West Africa, particularly in home treatment. We examined chloroquine blood levels on admission to a referral hospital with respect to the manifestation of severe malaria in 290 Ghanaian children. Of the patients, 78% exhibited chloroquine concentrations (subtherapeutic, 35%; therapeutic, 37%; supratherapeutic, 6%) and 11% died. Most parasites (78%) carried the pfcrt-T76 chloroquine resistance mutation. High drug concentrations correlated with reduced parasitaemia but also with selection of resistant parasites, lower respiratory and heart rates, increased plasma lactate levels and impaired consciousness. Geometric mean chloroquine concentrations tended to be higher in children who died than in survivors (1.135 vs. 778 nmol/l; P = 0.09). Supratherapeutic drug levels (>5000 nmol/l) were associated with fatal outcome (odds ratio 8.6; 95% CI 1.4-51.7). Residual chloroquine concentrations were found to be abundant in children with severe malaria and to be associated with alterations in the clinical manifestation of the disease and its case fatality. This may result from toxic effects of the drug and/or reflect preceding overtreatment in children with acute life-threatening disease. In areas of intense chloroquine resistance and frequent pre-treatment, additional administration of chloroquine at hospital admission is not only ineffective but may even further endanger patients.
KW - Chloroquine
KW - Drug resistance
KW - Ghana
KW - Malaria
KW - Plasmodium falciparum
KW - Toxicity
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U2 - 10.1016/j.trstmh.2007.03.004
DO - 10.1016/j.trstmh.2007.03.004
M3 - Article
C2 - 17467758
AN - SCOPUS:34248174792
SN - 0035-9203
VL - 101
SP - 637
EP - 642
JO - Transactions of the Royal Society of Tropical Medicine and Hygiene
JF - Transactions of the Royal Society of Tropical Medicine and Hygiene
IS - 7
ER -