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ANNEX 4. Antimalarials and malaria transmission



           ANNEX 4
           antimalarials and malaria transmission







           a4.1  principles of malaria transmission

           Malaria is spread among people by a mosquito belonging to the genus Anopheles. The
           female mosquito is infected by gametocytes, the sexual stages of the parasite when it
           takes a blood meal from an infected person. Gametocytes undergo further development
           in the insect for a period of 6–12 days, after which transformed parasites as sporozoites
           can infect a human through the bite of the infected mosquito.
                                                                                       A4
           The intensity of malaria transmission in an area is the rate at which people are inoculated
           with malaria parasites by infected mosquitoes. It is expressed as the annual entomological
           inoculation rate or EIR, which is the number of infectious mosquito bites received by an
           individual in one year. The EIR determines to a large extent the epidemiology of malaria
           and the pattern of clinical disease in an area. The high end of the malaria transmission
           range is found in a few parts of tropical Africa, where EIRs of 500–1000 can be reached
           (1). At the low end of the range are EIRs of 0.01 or below, as found in the temperate
           climates of the Caucasus and Central Asia where malaria transmission is only barely
           sustained. Between these extremes are situations of unstable seasonal malaria, such as
           in much of Asia and Latin America, where EIRs lie below 10, and often around 1–2, and
           situations of stable but seasonal malaria, as in much of West Africa, where the EIR is in
           the range 10–100.
           The proportion of infected mosquitoes in a locality is related to the number of infected
           and infectious humans in the area; therefore, lowering the infectivity of infected persons
           to mosquito vectors will contribute to reducing malaria transmission and to eventually
           reducing the incidence and prevalence of the disease. However, the relationship between
           EIR and the prevalence of malaria is complex, and it is affected by the extent of immunity
           to malaria, the pattern of its acquisition and loss, and to whether or not there is effective
           drug treatment in the area. The hypothetical relationship represented in figure A4.1
           assumes no drug treatment. In areas of low transmission where EIRs are below 1 or 2, a
           reduction in the inoculation rate will result in an almost proportionate reduction in the
           prevalence (and incidence rate) of malaria. In EIRs in excess of 10, where there is great
           redundancy in the infectious reservoir, larger reductions in transmission are needed to
           make a significant impact on malaria prevalence. The experience with major interventions,
           such as the use of insecticide-treated nets and artemisinin-based combination therapies,
           suggests, however, that effective transmission-reducing interventions will be beneficial
           with respect to mortality and even morbidity in most situations (2,3).
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