4.5 Article

Short Report: Increased Risk of Early Vomiting among Infants and Young Children Treated with Dihydroartemisinin-Piperaquine Compared with Artemether-Lumefantrine for Uncomplicated Malaria

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AMER SOC TROP MED & HYGIENE
DOI: 10.4269/ajtmh.2010.10-0158

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  1. U.S. President's Emergency Plan for AIDS Relief
  2. Department of Health and Human Services/Centers for Disease Control and Prevention, National Center for HIV, Viral Hepatitis, Si]) [U62P024421]
  3. TB Prevention, Global AIDS Program
  4. Doris Duke Charitable Foundation
  5. Puget Sound Partners in Global Health
  6. National Institutes of Health/National Institute of Allergy and Infectious Disease [K23-AI082553]

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Artemether-lumefantrine (AL) and dihydroartemisinin-piperaquine (DP) are highly efficacious antimalarial therapies in Africa. However, there are limited data regarding the tolerability of these drugs in young children. We used data from a randomized control trial in rural Uganda to compare the risk of early vomiting (within one hour of dosing) for children 6-24 months of age randomized to receive DP (n = 240) or AL (n = 228) for treatment of uncomplicated malaria. Overall, DP was associated with a higher risk of early vomiting than AL (15.1% versus 7.1%; P = 0.007). The increased risk of early vomiting with DP was only present among breastfeeding children (relative risk [RR] = 3.35, P = 0.001) compared with children who were not breastfeeding (RR = 1.03, P = 0.94). Age less than 18 months was a risk factor for early vomiting independent of treatment (RR = 3.27, P = 0.02). Our findings indicate that AL may be better tolerated than DP among young breastfeeding children treated for uncomplicated malaria.

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