Single low-dose primaquine for malaria control in Africa: a systematic review of safety, efficacy and implementation barriers

Since 2012, the WHO has recommended a single low dose of primaquine (SLDPQ, 0.25 mg/kg) alongside artemisinin-based combination therapies (ACTs) to block <i>Plasmodium falciparum</i> transmission and combat artemisinin resistance. Despite its proven benefits, SLDPQ adoption in African malaria policies remains limited. We conducted a systematic review of studies published between 2012 and 2023 on the safety, efficacy and implementation of SLDPQ in Africa. Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, we searched 7 databases and screened 819 records. Eligible studies focused on SLDPQ co-administered with ACTs for treating uncomplicated <i>P. falciparum</i> malaria in African contexts. Data were extracted and analysed from 41 studies, including 15 randomised controlled trials (RCTs) and 26 non-trial studies. SLDPQ was found to be safe and well-tolerated, including in glucose-6-phosphate dehydrogenase deficiency individuals and children under 5. Eight RCTs confirmed significant reductions in gametocyte carriage, validating SLDPQ's individual-level efficacy. However, evidence on community-level impact remains limited. Key implementation barriers include persistent misconceptions about primaquine toxicity, absence of paediatric formulations and operational challenges in health systems. Most studies used the WHO-recommended dose (0.25 mg/kg), but higher doses and age-based regimens were also investigated. This review supports SLDPQ as a safe and effective tool for malaria transmission reduction in Africa. Addressing barriers to implementation, through health worker training, community sensitisation and operational research, is essential to accelerate its adoption. The ongoing Implementing Primaquine Single Low Dose in Africa project aims to generate real-world evidence across three countries, with a focus on paediatric use and health system integration. SLDPQ scale-up should be prioritised within malaria elimination strategies across sub-Saharan Africa.

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Journal
BMJ Global Health
Published
2025-08-01
DOI
https://doi.org/10.1136/bmjgh-2025-020264
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
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article

Single low-dose primaquine for malaria control in Africa: a systematic review of safety, efficacy and implementation barriers

Alphonse Ouédraogo, Rianasoambolanoro Rakotosaona, Joseph Nyandwi, Sodiomon B. Sirima et al.
BMJ Global Health
Malaria Research and Control
article

Single low-dose primaquine for malaria control in Africa: a systematic review of safety, efficacy and implementation barriers

Alphonse Ouédraogo, Rianasoambolanoro Rakotosaona, Joseph Nyandwi, Sodiomon B. Sirima, Omega Raobela, T T Ye, Denis Niyomwungere, Didier Ménard, Emmanuelle Caspar, Arsène Ratsimbasoa, Lucas Thiebaut, Pierre-Emeric Strubel
article en

Abstract

Since 2012, the WHO has recommended a single low dose of primaquine (SLDPQ, 0.25 mg/kg) alongside artemisinin-based combination therapies (ACTs) to block <i>Plasmodium falciparum</i> transmission and combat artemisinin resistance. Despite its proven benefits, SLDPQ adoption in African malaria policies remains limited. We conducted a systematic review of studies published between 2012 and 2023 on the safety, efficacy and implementation of SLDPQ in Africa. Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, we searched 7 databases and screened 819 records. Eligible studies focused on SLDPQ co-administered with ACTs for treating uncomplicated <i>P. falciparum</i> malaria in African contexts. Data were extracted and analysed from 41 studies, including 15 randomised controlled trials (RCTs) and 26 non-trial studies. SLDPQ was found to be safe and well-tolerated, including in glucose-6-phosphate dehydrogenase deficiency individuals and children under 5. Eight RCTs confirmed significant reductions in gametocyte carriage, validating SLDPQ's individual-level efficacy. However, evidence on community-level impact remains limited. Key implementation barriers include persistent misconceptions about primaquine toxicity, absence of paediatric formulations and operational challenges in health systems. Most studies used the WHO-recommended dose (0.25 mg/kg), but higher doses and age-based regimens were also investigated. This review supports SLDPQ as a safe and effective tool for malaria transmission reduction in Africa. Addressing barriers to implementation, through health worker training, community sensitisation and operational research, is essential to accelerate its adoption. The ongoing Implementing Primaquine Single Low Dose in Africa project aims to generate real-world evidence across three countries, with a focus on paediatric use and health system integration. SLDPQ scale-up should be prioritised within malaria elimination strategies across sub-Saharan Africa.

BMJ Global HealthVol. 10(8)
University of Antananarivo (MG), Université du Burundi (BI), Ministère de la Santé Publique (BI), Université de Fianarantsoa (MG), Eurométropole de Strasbourg (FR), Groupe de Recherche et d’Action sur le Foncier (BF), Université de Strasbourg (FR)
Openalex Percentile: Top 72%
Malaria Research and Control
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