Antimalarials for children with Plasmodium vivax infection: Current status, challenges, and research priorities

Sze-Ann Woon1, Laurens Manning2, Brioni R Moore3

  • 1Medical School, University of Western Australia, Perth, Western Australia, Australia.

Parasitology International
|November 17, 2021
PubMed

Insights

Treating Plasmodium vivax malaria in children requires optimized dosing and formulations. Early clinical trials and accessible G6PD testing are crucial for effective pediatric antimalarial therapies.

Area of Science:

  • Tropical Medicine
  • Pediatric Pharmacology
  • Malaria Research

Background:

  • Plasmodium vivax malaria disproportionately affects children, posing a significant public health challenge.
  • Relapse due to dormant liver-stage hypnozoites complicates P. vivax treatment and elimination strategies.
  • Current pediatric dosing regimens are often extrapolated from adult data, risking suboptimal treatment.

Purpose of the Study:

  • To review efficacy and pharmacokinetic data for Plasmodium vivax treatments in children.
  • To highlight the critical need for evidence-based pediatric dosing and formulations for P. vivax.
  • To emphasize the importance of early phase clinical trials for antimalarial drugs in pediatric populations.

Main Methods:

  • This narrative review synthesizes existing literature on P. vivax efficacy and pharmacokinetics in children.
  • It examines challenges in pediatric malaria treatment, including hypnozoite relapse and physiological differences.
  • The review discusses the implications of adult-extrapolated dosing for pediatric efficacy.

Main Results:

  • Paediatric pharmacology is influenced by childhood developmental changes, necessitating specific dosing evaluations.
  • Suboptimal dosing in children can occur when regimens are based solely on adult data.
  • Development of pediatric formulations and widespread G6PD testing are identified as key priorities.

Conclusions:

  • There is an urgent need to evaluate antimalarial dosing in children through early phase clinical trials.
  • Prioritizing affordable pediatric formulations and G6PD testing will improve treatment acceptability and efficacy.
  • Ensuring safe, effective, and correctly dosed antimalarial therapies for children is essential for malaria elimination efforts.

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