1. Identification of high risk individuals |
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Proportion of adolescent ANC attendees |
>80% of adolescents attending ANC |
Health facility assessments |
Strategies for delaying pregnancies |
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Proportion of primigravidae with late ANC attendance |
<10% attendees |
Health facility assessment |
Reasons for late attendance |
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Distance indicators of household residence from main health facility |
Identification of high risk areas |
Household surveys |
Community SP-IPTp distribution |
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Antenatal HIV infection |
Prevalence reduction |
Mother to child HIV transmission assessments |
Implementation of HIV prevention strategies |
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2. Antimalarial drug efficacy estimates |
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Antimalarial therapeutic efficacy |
Agreed surveillance interval (2–5 years) |
Antimalarial in vivo sensitivity tests |
Comparative drug evaluations |
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Proportional reduction in parasitaemia between first antenatal visit and delivery |
New indicator |
Health facility prevalence estimate |
Comparison with birthweight or anaemia outcomes |
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Proportion of women with placental infection who have received two SP-IPTp doses |
Assessment in sentinel health facilities |
Case-coverage methodology for determining SP-ITPp efficacy |
Comparison of case-coverage efficacy estimates method with in vivo tests |
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Antimalarial post-treatment prophylaxis |
Agreed surveillance interval (2–5 years) |
Antimalarial prophylactic efficacy tests |
Evaluation in aparasitaemic women on IPTp |
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3. Safety indicators |
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Inadvertent antimalarial drug exposure in first trimester |
No exposures in asymptomatic women |
Cross-sectional household/health facility surveys |
Prevalence estimates and associated pregnancy outcomes |
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Assessment of safety indicators via national and international antimalarial exposure registry |
Establishing functional registry |
Standardized protocol under development by WHO |
Demonstration sites; new methods for drug exposure, ascertainment, congenital anomaly detection |