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ANNEX 9. Treatment of Plasmodium vivax, P. ovale and P. malariae infections



           episodes in this age group as P. falciparum.  Severe vivax malaria presents as wide a range
           of pathologies as is seen in severe P. falciparum malaria ranging from toxic shock and
           cerebral malaria to multiple organ failure (8, 9). During pregnancy, infection with P. vivax,
           as with P. falciparum, reduces birth weight due to chronic anaemia, sequestration and
           pro-inflammatory cytokines in the placenta (10–12), and increases the risk of neonatal
           death. In primegravidae, the reduction is approximately two thirds that associated with
           P. falciparum, but the effect does not appear to decline with successive pregnancies; indeed,
           in the one large series in which this was studied, it increased (12).






           a9.2  diagnosis

           Diagnosis of vivax malaria is based on microscopy. Rapid diagnostic tests based on
           immunochromatographic methods are available for the detection of non-falciparum
           malaria. However, their sensitivities for detecting parasitaemias of ≤ 500/μl are low (13–20).
           The relatively higher cost of P. vivax tests compared to those for P. falciparum is a further
           impediment to their large-scale use in endemic areas. Molecular markers for genotyping
           P. vivax parasites are available for the dihydrofolate reductase (dhfr) gene, and those for
           chloroquine resistance are under development.





           a9.3  treatment

           The objectives of treatment of vivax malaria are twofold: to terminate the acute blood
           infection, to cure the clinical symptoms, and to clear hypnozoites from the liver to prevent
           future relapses. This is known as a radical cure.

           Before 2004, there were relatively few studies on the treatment of P. vivax. Only 11% of the
           435 published antimalarial drug trials have been on P. vivax malaria (21). Thereafter, there
           have been several trials on the efficacy of artemisinin-based combination therapies for the
           treatment of vivax malaria (22–24).


                                                                                       A9
           a9.3.1  standard oral regimen

           Chloroquine monotherapy (25 mg base/kg body weight over 3 days) is recommended as the
           standard treatment for vivax malaria, because the parasite remains sensitive to chloroquine
           in much of the world. Primaquine (0.25 or 0.5 mg base/kg body weight in a single daily
           dose for 14 days) is used as a supplement to the standard treatment for the purpose of
           eradicating dormant parasites in the liver and preventing relapses. Although shorter 5-day

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