Results from phase one of a hybrid effectiveness-implementation study to assess the feasibility, acceptability and effectiveness of implementing seasonal malaria chemoprevention in Nampula province, Mozambique

Author:

Baker Kevin1,Tarquino Ivan Alejandro Pulido1,Aide Pedro2,Bonnington Craig1,Rassi Christian1,Richardson Sol3,Nnaji Chuks1,Roca-Feltrer Arantxa4,Rodrigues Maria1,Sitoe Mercia1,Enosse Sonia1,McGugan Caitlin5,Saute Francisco2,Matambisso Gloria2,Candrinho Baltazar6

Affiliation:

1. Malaria Consortium

2. Manhiça Health Research Centre

3. Tsinghua University

4. PATH

5. GiveWell

6. Ministry of Health

Abstract

Abstract Introduction Seasonal malaria chemoprevention (SMC) is a highly effective intervention for malaria prevention in high burden areas with seasonal transmission, historically implemented in the Sahel. Mozambique contributes to 4% of global malaria cases, malaria being one of four major causes of mortality nationally. The mid-term review of the Malaria Strategic Plan 2017–2022 recommended SMC in Mozambique. Malaria Consortium, in partnership with the National Malaria Control Program, conducted a two-year phased SMC study in Nampula province using sulfadoxine-pyrimethamine (SP) plus amodiaquine (AQ), or SPAQ, in children under five. Phase one investigated acceptability, feasibility, and protective effect of SMC; while phase two, researched the effectiveness of SMC, chemoprevention efficacy and changes in resistance markers prevalence. The following references phase one results.Methods A pragmatic type II hybrid effectiveness-implementation study design was adopted, using mixed methods. The study was conducted in three districts, utilising: (1) non-randomised controlled trial; (2) drug resistance molecular marker study; (3) coverage and quality assessment; and (4) acceptability and feasibility assessment with stakeholders.Results Children who received SMC had 86% (hazard ratio 0.14, 95% CI: 0.09–0.24) lower hazards of developing clinical malaria during the peak transmission season compared with children in the comparison district. Prevalence of SP molecular markers associated with resistance was high at baseline (K540E 66.1%). However, a non-statistically significant trend of increasing prevalence was observed. SMC achieved high coverage of eligible children over four cycles (87.7%, 95% CI: 83.9%-90.8%). Qualitative results indicate SMC was positively accepted by the targeted community, with few negative opinions reported.Conclusions Results suggest that SMC was effective at preventing clinical malaria, did not significantly impact resistance profile, and was feasible and acceptable in the context. Phase two will assess SMC impact in reducing malaria incidence and if chemoprevention efficacy of SPAQ is impacted by drug resistance and drug concentrations.

Publisher

Research Square Platform LLC

Reference35 articles.

1. World Health Organization. WHO Guidelines for malaria, 14 March 2023. Geneva: World Health Organization, Global Malaria Programme. ; 2023. Report No.: WHO/UCN/GMP/2023.01, https://apps.who.int/iris/handle/10665/366432.

2. World Health Organization. WHO policy recommendation: seasonal malaria chemoprevention (SMC) for plasmodium falciparum malaria control in highly seasonal transmission areas of the Sahel sub-region in Africa. Geneva: World Health Organization. ; 2012 2012. Contract No.: WHO/HTM/GMP/2012.02, https://apps.who.int/iris/handle/10665/337978.

3. Plasmodium falciparum resistance to sulfadoxine-pyrimethamine in Africa: a systematic analysis of national trends;Amimo F;BMJ Glob Health,2020

4. Intermittent preventive treatment for malaria in children living in areas with seasonal transmission;Meremikwu MM;Cochrane Database Syst Rev,2012

5. Effectiveness of seasonal malaria chemoprevention (SMC) treatments when SMC is implemented at scale: Case-control studies in 5 countries;Cairns M;PLoS Med,2021

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