# Improving malaria chemoprevention coverage in pregnancy: Surveying stakeholder preferences for new product profiles and community-delivery approaches across five African countries

**Authors:** Céline Audibert, Isabelle Borghini-Fuhrer, Myriam El Gaaloul, Hanu Ramachandruni, André-Marie Tchouatieu, Maud Majeres Lugand

PMC · DOI: 10.1371/journal.pgph.0005607 · PLOS Global Public Health · 2026-03-13

## TL;DR

The study explores stakeholder preferences for new malaria chemoprevention products during pregnancy to improve coverage and adherence in five African countries.

## Contribution

The study identifies stakeholder preferences for next-generation IPTp products and community-delivery approaches to improve malaria prevention in pregnancy.

## Key findings

- Safety in all trimesters was the most important attribute for stakeholders.
- Long-acting injectable formulations were preferred for adherence.
- Delivery by CHWs was seen as a way to expand IPTp uptake.

## Abstract

Sulfadoxine-pyrimethamine (SP) is the only WHO-recommended option for the intermittent preventive treatment of malaria in pregnancy (IPTp). However, coverage is suboptimal, efficacy is limited in areas of high resistance and SP is contraindicated in the first trimester and women living with HIV receiving cotrimoxazole. This study investigated stakeholder perspectives on next-generation IPTp product characteristics and their potential impact on uptake, adherence and community deployment. Surveys were conducted in five malaria endemic countries, including pregnant women (n = 75), nurses/community health workers (CHWs) (n = 53), clinicians (n = 75) and policymakers (n = 51). Surveys included quantitative elements and open-ended questions to examine stakeholder perceptions of chemoprevention product characteristics influencing uptake, adherence and implementation. Additionally, a discrete choice experiment (DCE) conducted among clinicians and policymakers compared next-generation IPTp oral product profiles against SP. Across stakeholders the most important attribute was safety in all trimesters, followed by short duration of therapy, few tablets per day, food requirements and impact on birthweight was the least influential. Clinicians and policymakers also believed resistance markers to be important. All stakeholder groups indicated that a long-acting injectable with at least three months’ coverage would enhance adherence. For oral medication, pregnant women believed being able to take food with treatment was the most important attribute to enhance adherence, while a four-tablet daily dosing would decrease adherence. Clinicians and policymakers felt that delivery by CHWs would increase adherence and expand IPTp uptake in currently unreached women. However, three-quarters of pregnant women preferred ante-natal clinic delivery of a new medicine. The DCE favored products without food restrictions most strongly. This study offers important insights for the development and deployment of next-generation IPTp products. Minimizing food-related restrictions and addressing resistance concerns are key priorities, together with safety and tolerability. Long-acting injectable formulations and hybrid delivery models could play a substantial role in improving adherence and uptake.

## Linked entities

- **Chemicals:** Sulfadoxine-pyrimethamine (PubChem CID 65404), cotrimoxazole (PubChem CID 358641)
- **Diseases:** malaria (MONDO:0005136)

## Full-text entities

- **Diseases:** premature delivery (MESH:C536271), intrauterine growth restriction (MESH:D005317), appetite loss (MESH:D001068), allergies (MESH:D004342), vomiting (MESH:D014839), gestational diabetes (MESH:D016640), stillbirth (MESH:D050497), dizziness (MESH:D004244), HIV (MESH:D015658), infected (MESH:D007239), nausea (MESH:D009325), deaths (MESH:D003643), tuberculosis (MESH:D014376), maternal (MESH:D000079262), Malaria (MESH:D008288), phobia (MESH:D010698), anemia (MESH:D000740), nausea/vomiting (MESH:D020250), miscarriage (MESH:D000022), weakness (MESH:D018908), placental damage (MESH:D010922)
- **Chemicals:** sulfonamide (MESH:D013449), artemisinin (MESH:C031327), SP (MESH:C001205), piperaquine (MESH:C034759), PYN (MESH:C027871), Cotrimoxazole (MESH:D015662), ASPY (MESH:C000712628), IPT3 (-)
- **Species:** Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Lys540Glu

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12987456/full.md

## References

65 references — full list in the complete paper: https://tomesphere.com/paper/PMC12987456/full.md

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Source: https://tomesphere.com/paper/PMC12987456