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1.
J Infect Dev Ctries ; 7(12): 975-82, 2013 Dec 15.
Article in English | MEDLINE | ID: mdl-24334945

ABSTRACT

INTRODUCTION: The development and spread of Plasmodium falciparum resistance to most commonly used antimalarials remain a major challenge in the control of malaria. Constant monitoring of drug efficacy is an important tool in establishing rational antimalarial drug policies. METHODOLOGY: A randomized comparative study was conducted at the Wesley Guild Hospital, Ilesa, Nigeria between February 2010 and September 2011 comparing the efficacy and safety of artemether-lumefantrine (Coartem) and fixed dose of artesunate plus amodiaquine (Larimal) in the treatment of uncomplicated P. falciparum malaria in children betweem 6 and 144 months of age. P. falciparum malaria parasitemia was assessed by microscopy and rapid diagnostic test. Drugs were administered according to age for three days under supervision. The primary efficacy endpoint was a day 28 PCR-corrected parasitological cure. RESULTS: A total of 182 patients were enrolled in the two treatment groups, Coartem (n = 101) and Larimal (n = 81), and tested after 28 days. In the intention-to-treat population, Coartem (n = 101) and Larimal (n = 81) had a PCR-corrected cure rate of 98% and 100% respectively, while in the per-protocol population, Coartem (n = 89) and Larimal (n = 71) both had a PCR-corrected cure rate of 100% at day 28. Although parasite and fever clearance time was faster in the Larimal group, no significant difference was observed between the two drugs. No serious adverse effects  were reported. CONCLUSION: Five years after being introduced in Nigeria, both Coartem and Larimal have been shown to be safe and highly effective in the treatment of uncomplicated P. falciparum malaria in children.


Subject(s)
Amodiaquine/therapeutic use , Antimalarials/therapeutic use , Artemisinins/therapeutic use , Ethanolamines/therapeutic use , Fluorenes/therapeutic use , Malaria, Falciparum/drug therapy , Amodiaquine/adverse effects , Antimalarials/adverse effects , Artemether, Lumefantrine Drug Combination , Artemisinins/adverse effects , Child , Child, Preschool , Drug Combinations , Drug Therapy, Combination/methods , Ethanolamines/adverse effects , Female , Fluorenes/adverse effects , Humans , Infant , Male , Nigeria , Parasite Load , Parasitemia/parasitology , Polymerase Chain Reaction , Treatment Outcome
2.
J. infect. dev. ctries ; 7(12): 1-8, 2013.
Article in English | AIM (Africa) | ID: biblio-1263633

ABSTRACT

Introduction: The development and spread of Plasmodium falciparum resistance to most commonly used antimalarials remain a major challenge in the control of malaria. Constant monitoring of drug efficacy is an important tool in establishing rational antimalarial drug policies.Methodology: A randomized comparative study was conducted at the Wesley Guild Hospital; Ilesa; Nigeria between February 2010 and September 2011 comparing the efficacy and safety of artemether-lumefantrine (Coartem) and fixed dose of artesunate plus amodiaquine (Larimal) in the treatment of uncomplicated P. falciparum malaria in children betweem 6 and 144 months of age. P. falciparum malaria parasitemia was assessed by microscopy and rapid diagnostic test. Drugs were administered according to age for three days under supervision. The primary efficacy endpoint was a day 28 PCR-corrected parasitological cure. Results: A total of 182 patients were enrolled in the two treatment groups; Coartem (n = 101) and Larimal (n = 81); and tested after 28 days. In the intention-to-treat population; Coartem (n= 101) and Larimal (n= 81) had a PCR-corrected cure rate of 98 and 100 respectively; while in the per-protocol population; Coartem (n = 89) and Larimal (n = 71) both had a PCR-corrected cure rate of 100 at day 28. Although parasite and fever clearance time was faster in the Larimal group; no significant difference was observed between the two drugs. No serious adverse effects were reported. Conclusion: Five years after being introduced in Nigeria; both Coartem and Larimal have been shown to be safe and highly effective in the treatment of uncomplicated P. falciparum malaria in children


Subject(s)
Child , Drug Resistance , Drug Therapy , Malaria
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