Chimiorésistance de P. falciparum en milieu urbain à Yaoundé, Cameroun. Part 1: S urveillance in vitro et in vivo de la résistance de Plasmodium falciparumà la chloroquine entre 1994 et 1999 à Yaoundé, Cameroun

作者: P. Ringwald , A. Ekobo , A. Keundjian , D. Mangamba , L. K. Basco

DOI: 10.1046/J.1365-3156.2000.00613.X

关键词:

摘要: Resume La chloroquine reste le medicament de premiere intention dans la plupart des pays africains pour traitement l'acces palustre simple. Cependant, l'extension resistance Plasmodium falciparuma ce necessite une surveillance reguliere. Nous avons evalue 1994 a 1999, l'evolution chloroquino-resistance chez adultes (> 15 ans) et enfants (5–15 par tests d'efficacite therapeutique in vitro. Le test vivo ete effectue sur 14 jours les resultats ont exprimes selon nouveaux criteres l'Organisation Mondiale Sante. Les du semi-microtest microtest en concentration inhibitrice 50% (CI50) seuil est fixea CI50 > 100 nm. Sur l'ensemble l'etude, pourcentage d'echecs cliniques parasitologiques 39,7% (31,3% – 48,1%) 48,8% (40,2% – 57,4%), respectivement. Parallelement, vitro atteint 52,5% (48,1% – 56,9%) moyenne geometrique CI50 variait au cours suivi 84,6 nm 149,8 nm. sont concordants avec (coefficient kappa = 0,69). Ces etudes completees dosages chloroquinemie plasmas sujets J0, J3, J7 J14. permis mettre evidence variations inter-individuelles importantes concentrations moyennes superieures rapport aux demontre que certains acces palustres pouvaient etre lies insuffisantes chloroquine. confirment niveau eleve Yaounde suggerent l'utilisation d'un autre antipaludique simple. Summary Chloroquine is indicated for the first-line treatment of uncomplicated malaria most African countries. However, spread chloroquine-resistant falciparum requires periodic monitoring. Between and we studied evolution adults (aged > 15 years) children aged 5–15 years by using therapeutic efficacy assays. Responses to 14-day were classified according new criteria established World Health Organization. The results expressed as inhibitory (IC50), threshold level was set at IC50 > 100 nM. overall percentages clinical parasitological failures 39.7% (31.3% – 48.1%) 48.8% (40.2% – 57.4%), respectively. Similarly, percentage isolates that resistant 52.5%. During study, IC50 geometric mean varied between 84,6 nM 149,8 nM. assays agreed with those (kappa coefficient 0.69). patients' plasma levels measured on day 0, 3, 7, 14. Drug measurement showed wide inter-individual higher than children. Some cases failure associated inadequate Our confirm high suggest use an alternative antimalarial drug warranted.

参考文章(21)
C. M. Kihamia, U. Hellgren, A. Björkman, O. Eriksson, L. Rombo, L. F. Mahikwano, Response of Plasmodium falciparum to chloroquine treatment: relation to whole blood concentrations of chloroquine and desethylchloroquine. Bulletin of The World Health Organization. ,vol. 67, pp. 197- 202 ,(1989)
Kathryn Maitland, Thomas N Williams, Barbara M Kotecka, Michael D Edstein, Karl H Rieckmann, Plasma chloroquine concentrations in young and older malaria patients treated with chloroquine Acta Tropica. ,vol. 66, pp. 155- 161 ,(1997) , 10.1016/S0001-706X(97)00046-6
Eric Pussard, Francoise Verdier, Marie-Claude Blayo, Simultaneous determination of chloroquine, amodiaquine and their metabolites in human plasma, red blood cells, whole blood and urine by column liquid chromatography Journal of Chromatography B: Biomedical Sciences and Applications. ,vol. 374, pp. 111- 118 ,(1986) , 10.1016/S0378-4347(00)83258-2
U. Hellgren, G. Alv�n, M. Jerling, On the question of interindividual variations in chloroquine concentrations European Journal of Clinical Pharmacology. ,vol. 45, pp. 383- 385 ,(1993) , 10.1007/BF00265960
SA Adelusi, AH Dawodu, LA Salako, Kinetics of the uptake and elimination of chloroquine in children with malaria. British Journal of Clinical Pharmacology. ,vol. 14, pp. 483- 487 ,(1982) , 10.1111/J.1365-2125.1982.TB02016.X
Leonardo K Basco, Pascal Ringwald, Auguste Bilongo Manéné, Jacques Chandenier, False chloroquine resistance in Africa. The Lancet. ,vol. 350, pp. 224- 224 ,(1997) , 10.1016/S0140-6736(05)62397-5
B Carme, F Gay, J Chandenier, M Ndounga, L Ciceron, B Ebikili, J.L Schmit, M Gentilini, Unexpected trend in chemosensitivity of Plasmodium falciparum in Brazzaville, Congo. The Lancet. ,vol. 338, pp. 582- 583 ,(1991) , 10.1016/0140-6736(91)91158-Q
Marianne Faehlmann, Lars Rombo, Per Hedman, Serum concentrations of chloroquine in a patient with a late recrudescence of Kenyan Plasmodium falciparum malaria Transactions of The Royal Society of Tropical Medicine and Hygiene. ,vol. 75, pp. 362- 364 ,(1981) , 10.1016/0035-9203(81)90093-6
J.P. Louis, F.J. Louis, A. Trebucq, R. Migliani, M. Cot, C. Hengy, Chemoresistance of Plasmodium falciparum in central Africa The Lancet. ,vol. 340, pp. 610- 611 ,(1992) , 10.1016/0140-6736(92)92144-5
Jean Bickii, Leonardo K. Basco, Pascal Ringwald, Assessment of three in vitro tests and an in vivo test for chloroquine resistance in Plasmodium falciparum clinical isolates. Journal of Clinical Microbiology. ,vol. 36, pp. 243- 247 ,(1998) , 10.1128/JCM.36.1.243-247.1998