Page 65 - 80 guidelines for the treatment of malaria_opt
P. 65

9. Treatment of malaria caused by P. vivax, P. ovale or P. malariae



           14-day regimen is significantly better at reducing relapses (6 trials, 1072 participants; OR
           0.24, 95% CI 0.12–0.45). The usual adult oral dose is 15 mg base (0.25 mg/kg body weight
           per day), but in South-East Asia, particularly Indonesia, and in Oceania, higher doses
           (0.5 mg base/kg body weight per day) are required. Primaquine causes abdominal
           discomfort when taken on an empty stomach; it should always be taken with food.

           There has been debate as to whether primaquine should be given in endemic areas.
           Repeated vivax malaria relapses are debilitating at any age, and so they must be prevented.
           However, in situations where transmission is intense with a high rate of re-infection,
           simply preventing relapses is unlikely to lower the incidence of infection or disease.
           Therefore, in areas of sustained high transmission, the benefits of the widespread
           deployment of primaquine are not considered to outweigh the risks associated with this
           medication. In low-transmission areas, on the other hand, the benefits of primaquine
           in preventing relapses will exceed its risks and its routine use to prevent relapses is
           recommended in patients who are not G6PD-deficient.



           box 9.2

           recommendation: primaquine for the radical treatment of vivax malaria
            at least a 14-day course of primaquine is required for the radical treatment of P. vivax
             Strong recommendation, very low quality evidence

             GraDE evaluation (see Annex 9, table A9.7.1)
             A 14-day course of primaquine significantly reduces the relapse rate of P. vivax compared to a 5-day
             course (2 trials, 186 participants; RR 0.1, 95% CI 0.03–0.35; low quality evidence).

             Other considerations
             In addition, in clinical trials, CQ plus 14 days of primaquine has been shown to be superior to CQ alone in
             reducing relapses (6 trials, 1071 participants; OR 0.24, 95% CI 0.12– 0.45). No difference has been shown
             between CQ plus 5 days of primaquine and CQ alone (3 trials, 2104 participants).


           Formulation. If available, administer scored tablets containing 7.5 mg or 15 mg of
           primaquine. When there are no scored tablets available, 5 mg tablets can be used.
           Therapeutic dose. Dose range between 0.25 and 0.5mg/kg/day primaquine once a day
           for 14 days (see Annex 3, Section A3.8).



                 9.3.2.1 Primaquine and glucose-6-phosphate dehydrogenase deficiency

           The inherited sex-linked deficiency, G6PD deficiency, is associated with some protection
           against P. falciparum malaria, but there is increased susceptibility to oxidant haemolysis.
           The prevalence of G6PD deficiency varies, but it can be as high as 30%; high frequencies

                                                                                      51
   60   61   62   63   64   65   66   67   68   69   70