Springer eBooks, Journal Year: 2023, Volume and Issue: unknown, P. 1 - 20
Published: Jan. 1, 2023
Language: Английский
Springer eBooks, Journal Year: 2023, Volume and Issue: unknown, P. 1 - 20
Published: Jan. 1, 2023
Language: Английский
Malaria Journal, Journal Year: 2024, Volume and Issue: 23(1)
Published: Oct. 10, 2024
The RTS,S malaria vaccine has been prequalified for use in endemic settings prioritizing areas with moderate to high disease transmission. impact of a at the population level may differ from observations during clinical trial due programmatic, and individual-related factors, among others. objective this study was assess on uncomplicated children aged 12-59 months Phase IV districts, Upper East Region, Ghana.
Language: Английский
Citations
0Vaccine, Journal Year: 2024, Volume and Issue: 42(26), P. 126490 - 126490
Published: Nov. 1, 2024
Following the successful pilot of RTS,S malaria vaccine, it has been recommended by WHO for prevention Plasmodium falciparum in children living endemic areas. Despite proven benefits uptake especially fourth dose, remains relatively low. We assessed complete vaccine among 24-59 months and associated factors Sunyani Municipality Ghana.
Language: Английский
Citations
0medRxiv (Cold Spring Harbor Laboratory), Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 12, 2024
Abstract New malaria vaccine development builds on groundbreaking recommendations and roll-out of two approved pre-erythrocytic vaccines (PEVs); RTS,S/AS01 R21/MM. Whilst these are effective in reducing childhood within yearly routine immunization programs or seasonal vaccination, there is little evidence how different PEV efficacies, durations protection, spacing between doses influence the potential to avert uncomplicated severe malaria. Mainly, lacking understanding required properties delivery strategies that lead an with multi-year protection. We used individual-based model transmission informed by trial data quantify trade-offs performance impact across endemicities, deployment schedules, coverage levels. found deploying a 90% initial efficacy, six 12-month half-life duration co-administered blood-stage drug, followed boosters, results 60-80% incidence reduction, consistent RTS,S R21 trials. Halting vaccination after five years, leads sustained protection at least 35% reduction children <six years 12 months following cessation settings where Pf PR 2-10 <30%. Increasing -18 reaching more provides same health lower efficacy. Without booster (fourth dose), high efficacy (>90%) longer (>12 months) sustain beyond primary averting up half preceding year’s burden. The contribution each property overall varies setting clinical endpoint, indicating public goals should dictate key criteria. Overall, our findings support need for well-defined target product profiles long linking priority use cases where, how, whom deploy new vaccines, maximize impact.
Language: Английский
Citations
0Research Square (Research Square), Journal Year: 2024, Volume and Issue: unknown
Published: Dec. 1, 2024
Language: Английский
Citations
0Springer eBooks, Journal Year: 2023, Volume and Issue: unknown, P. 1 - 20
Published: Jan. 1, 2023
Language: Английский
Citations
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