Page 72 - 80 guidelines for the treatment of malaria_opt
P. 72

nd
              Guidelines for the treatment of malaria – 2  edition


            12.  case manaGement in tHe context
                  of malaria elimination




            12.1  use of gametocytocidal drugs to reduce transmission

            Two antimalarial medicines have an effect specifically on gametocytes: primaquine and
            artemisinins. This can be of particular benefit in epidemic control and in programmes
            aiming for malaria elimination.

            Primaquine selectively kills gametocytes. Especially in South-East Asia and South
            America, before the use of ACTs for the treatment of P. falciparum malaria, a single oral
            dose of 0.75 mg base/kg body weight primaquine (45 mg base maximal for adults) was
            added to a fully effective blood schizontocide to eliminate gametocytes and thus reduce
            transmission. Studies on the impact of this strategy are very limited. Where it has been
            used, the single dose of primaquine was well tolerated, and prior testing for G6PD
            deficiency was not required. There is no experience with its use in Africa, where there is
            the highest prevalence of G6PD deficiency in the world.
            ACTs reduce gametocyte carriage. One randomized comparison of ACTs and primaquine
            has reported a greater effect for ACT than primaquine on gametocyte carriage. A
            more recent study compared the added value of primaquine to AS+SP combination in
            the treatment of falciparum malaria in United Republic of Tanzania. It reported that
            primaquine clears gametocytes that persist after treatment with AS+SP, including those
            at a submicroscopic level: this demonstrates an added benefit of combining a single
                                      16
            dose of primaquine with an ACT .  The addition of a single dose of primaquine to ACT
            treatment is, therefore, recommended in programmes aimed at reducing transmission,
            provided the risks of haemolysis in G6PD deficient patients are considered. Primaquine
            should not be given in pregnancy and in children less than 4 years old.



            12.2  mass screening and treatment

            Mass screening for parasitaemia and treating all infected persons in a targeted area or
            population, irrespective of whether they are symptomatic aims to reduce the size of the
            infectious reservoir in the targeted area. Mass screening and treatment may be indicated
            in areas where the parasite reservoir (or parasite gene pool) needs to be quickly and
            selectively reduced. This type of intervention also plays a significant role in reducing
            the infectious reservoir of parasites in a given location and is very useful in the pre-
            elimination and elimination phases of malaria control.  It requires considerable logistics,
                                                       17
            capacity and preparation.
            16  Shekalaghe S et al. Primaquine clears submicroscopic Plasmodium falciparum gametocytes that persist after
              treatment with sulphadoxine-pyrimethamine and artesunate. PLoS ONE, 2007, 2: e1023. doi:10.1371.
    58
   67   68   69   70   71   72   73   74   75   76   77