Reviewing anti-malarial usage and resistance patterns and its effects on World Health Organisation Programs.

2015 
AbstractThe two most signifi cant strains of human malaria parasites responsible for morbidity and mortality are Plasmodium falciparum and P. vivax. One issue, which further compounds treatment of these pathogens, is one of drug resistance. Drug resistance often emerges from key mutations selected for by inadequate treatment regimes and has shown to be able to spread globally, further compounding the development of newer and more effective drug treatment programs, such as those from the World Health Organisation (WHO). Here we review the historical usage of anti-malarial drugs, the development of resistance in Africa and Asia, mechanisms of drug action and resistance, and the effects of resistance on WHO policy.Keywords: malaria, drug-resistance, Plasmodium , World Health Organisation, drug policy.IntroductionDrug resistant Plasmodium falciparum and P. vivax can be considered emerging infectious diseases because of the development of resistance mechanisms that decreases the amenability of the microorganisms to treatment, in addition to an increasing geographic range where these parasites are found [1].This complicates the treatment of malaria as well as threatening current World Health Organization (WHO) programs to eliminate malaria globally. Whilst fi ve
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