Additional considerations for P. vivax and P. ovale
P. vivax and P. ovale can exist as dormant parasites (hypnozoites) in the liver that can reactivate to cause a relapse of malaria. The treatment regimens for uncomplicated malaria (see above) do not eliminate hypnozoites, so concurrent treatment with primaquine (for P. vivax or P. ovale) or tafenoquine (for P. vivax) is required to eliminate dormant liver parasites.
Primaquine and tafenoquine1 can cause severe haemolysis in patients who are glucose-6-phosphate dehydrogenase (G6PD) deficient—if the patient is G6PD deficient, seek expert advice.
For P. vivax infection, once G6PD deficiency has been excluded, add to the standard treatment regimen for uncomplicated malaria:
primaquine 30 mg (child over 6 months: 0.5 mg/kg up to 30 mg) orally, daily, or if nausea occurs 15 mg (child over 6 months: 0.25 mg/kg up to 15 mg) orally, 12-hourly. Treat for 14 days or, in adults more than 70 kg, until a total cumulative dose of 6 mg/kg is reached2 3. malaria, Plasmodium vivax primaquine
For P. ovale infection, once G6PD deficiency has been excluded, add to the standard treatment regimen for uncomplicated malaria:
primaquine 15 mg (child over 6 months: 0.25 mg/kg up to 15 mg) orally, daily for 14 days3. malaria, Plasmodium ovale primaquine
If a relapse of malaria occurs despite treatment with primaquine or tafenoquine, seek expert advice.