03049nas a2200469 4500000000100000008004100001260001200042653002400054653001500078653002100093653001700114653001500131100001500146700002300161700001900184700001100203700001500214700001200229700001300241700001000254700001500264700001200279700001800291700001400309700001600323700002000339700002100359700001700380700001900397700001200416700001400428700002200442700001000464700002000474700001200494245008700506856007600593300001400669490000800683520187400691022001402565 2026 d c09/202610aFeasibility Studies10apaediatric10aSchistosomiasis 10aPraziquantel10aMadagascar1 aMarchese V1 aAndrianarimanana D1 aRatefiarisoa S1 aGuth A1 aLassmann M1 aFranz F1 aRemkes A1 aHey J1 aSchramke L1 aBrito A1 aRasamoelina T1 aRausche P1 aTotofotsy O1 aZafinimampera A1 aRandrianarisoa T1 aRambeloson H1 aRatiaharison E1 aGarba A1 aKislaya I1 aRasoamanamihaja C1 aMay J1 aRakotoarivelo R1 aFusco D00aFeasibility of paediatric schistosomiasis prevention with praziquantel, Madagascar uhttps://pmc.ncbi.nlm.nih.gov/articles/PMC13527690/pdf/BLT.25.295521.pdf a601 - 6120 v1043 a
OBJECTIVE:
To assess the feasibility of fixed-dose, praziquantel preventive chemotherapy against schistosomiasis in young children in rural Madagascar, focusing on treatment uptake and sustainability.
METHODS:
We used the Consolidated Framework for Implementation Research to guide the study. Between November 2022 and December 2023, children aged 9 to 24 months at various venues were offered 300 mg of praziquantel as a crushed half tablet mixed with water and sugar. We conducted a cross-sectional survey among caregivers to assess treatment uptake and acceptability, children's compliance with drug administration, anxiety about adverse events, and praziquantel's tolerability and safety. Factors associated with uptake and acceptability were identified using Poisson regression.
FINDINGS:
The study analysis included 5142 child-caregiver pairs. The praziquantel uptake rate was 86.2% (95% confidence interval, CI: 85.3-87.1) and 80.2% (95% CI: 79.1-81.3) of caregivers regarded repeated preventive chemotherapy acceptable. Clear anxiety, and uncertainty, about adverse events were the most significant factors associated with refusal of both initial and repeated treatment. No children experienced serious adverse events or choking. Of the 4434 children who received praziquantel, 152 (3.4%) swallowed a partial dose, whereas 2467 (55.6%) cried and 1833 (41.3%) initially resisted treatment, but ultimately received it.
CONCLUSION:
Fixed-dose praziquantel preventive chemotherapy using a crushed half tablet with water and sugar was feasible in preschool-aged children and was potentially sustainable. This approach has a strong potential for scaling up in areas where schistosomiasis is highly endemic.
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