4.4 Article

Reducing the risk of Plasmodium vivax after falciparum infections in co-endemic areas - a randomized controlled trial (PRIMA)

Journal

TRIALS
Volume 23, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13063-022-06364-z

Keywords

Vivax malaria; Falciparum malaria; Radical cure; Universal radical cure; Vivax elimination; Co-endemic; Randomized controlled trial

Funding

  1. Australian Academy of Science, on behalf of the Department of Industry, Innovation and Science
  2. Australian Government under the National Innovation and Science Agenda
  3. Bill & Melinda Gates Foundation [INV-010504]
  4. Australian National Health and Medical Research Council (NHMRC) Program grant [APP1132975]

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This study aims to evaluate the potential benefits of universal radical cure for both Plasmodium vivax and Plasmodium falciparum in different endemic areas. If proven safe and effective, universal radical cure could be a cost-effective approach to eliminate unrecognized P. vivax infections and accelerate P. vivax elimination.
Background: Plasmodium vivax forms dormant liver stages that can reactivate weeks or months following an acute infection. Recurrent infections are often associated with a febrile illness and can cause a cumulative risk of severe anaemia, direct and indirect mortality, and onward transmission of the parasite. There is an increased risk of P. vivax parasitaemia following falciparum malaria suggesting a rationale for universal use of radically curative treatment in patients with P. falciparum malaria even in the absence of detectable P. vivax parasitaemia in areas that are co-endemic for both species. Methods: This is a multicentre, health care facility-based, randomized, controlled, open-label trial in Bangladesh, Indonesia and Ethiopia. Patients with uncomplicated falciparum malaria, G6PD activity of >= 70% of the adjusted male median (AMM) and haemoglobin levels >= 8g/dl are recruited into the study and randomized to either receive standard schizonticidal treatment plus 7-day high dose primaquine (total dose 7mg/kg) or standard care in a 1:1 ratio. Patients are followed up weekly until day 63. The primary endpoint is the incidence risk of any P. vivax parasitemia on day 63. Secondary endpoints include incidence risk on day 63 of symptomatic P. vivax malaria and the risk of any P. falciparum parasitaemia. Secondary safety outcomes include the proportion of adverse events and serious adverse events, the incidence risk of severe anaemia (Hb<5g/dl and <7g/dl) and/or the risk for blood transfusion, the incidence risk of >= 25% fall in haemoglobin with and without haemoglobinuria, and the incidence risk of >= 25% fall in haemoglobin to under 7g/dl with and without haemoglobinuria. Discussion: This study evaluates the potential benefit of a universal radical cure for both P. vivax and P. falciparum in different endemic locations. If found safe and effective universal radical cure could represent a cost-effective approach to clear otherwise unrecognised P vivax infections and hence accelerate P. vivax elimination.

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