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nd
              Guidelines for the treatment of malaria – 2  edition


            are found only in areas where malaria is or has been endemic. There are a large number
            of different genotypes, each with different levels of deficiency. Primaquine is an oxidant
            and causes variable haemolysis in G6PD-deficient individuals. Primaquine also causes
            methemoglobinaemia. The severity of haemolytic anaemia is related to primaquine
            dosing and the variant of the G6PD enzyme. Fortunately, primaquine is eliminated
            rapidly and so haemolysis is self-limiting provided no further drug is taken. Screening
            for G6PD deficiency is not generally available outside hospitals, although rapid tests
            are under development. Many patients are, therefore, unaware of their G6PD status. If
            a patient is known to be severely G6PD deficient, then primaquine should not be given.
            For the majority of patients with mild variants of the deficiency, primaquine should be
            given in a dose of 0.75 mg base/kg body weight once a week for eight weeks. If significant
            haemolysis occurs on treatment, then primaquine should be stopped.
            Primaquine is contraindicated in pregnant women and children less than four years of
            age. There is no reliable data on the excretion of primaquine in breast milk to warrant
            it being contraindicated in women who are breast feeding, however, it is recommended
            that primaquine use in this group of patients should be medically supervised.


            box 9.3
            Summary of recommendations on the treatment of uncomplicated vivax malaria

             chloroquine 25 mg base/kg body weight divided over 3 days, combined with primaquine 0.25 mg
               base/kg body weight, taken with food once daily for 14 days is the treatment of choice for
               chloroquine-sensitive infections. in oceania and south-east asia, the dose of primaquine should
               be 0.5 mg/kg body weight.
             acts combined with primaquine for chloroquine-resistant vivax malaria.

             in mild-to-moderate G6pd deficiency, primaquine 0.75 mg base/kg body weight should be given
               once a week for 8 weeks. in severe G6pd deficiency, primaquine is contraindicated and should
               not be used.

             Where act (exception as+sp) has been adopted as the first-line treatment for P. falciparum
               malaria, it may also be used for P. vivax malaria in combination with primaquine for radical cure.
               artesunate plus sulfadoxine-pyrimethamine is not effective against P. vivax in many places.




            9.4  treatment of severe P. vivax malaria


            Although P. vivax malaria is considered to be benign malaria, with a very low case-fatality
            ratio, it may still cause a severe and debilitating febrile illness. It can also occasionally
            result in severe disease, as in P. falciparum malaria. Severe P. vivax malaria manifestations

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