Abstract

SummaryBackgroundArtemisinin-based combination therapies (ACTs) are the most effective treatment for uncomplicated Plasmodium falciparum malaria infection. A commonly used indicator for monitoring and assessing progress in coverage of malaria treatment is the proportion of children younger than 5 years with reported fever in the previous 14 days who have received an ACT. We propose an improved indicator that incorporates parasite infection status (as assessed by a rapid diagnostic test [RDT]), which is available in recent household surveys. In this study we estimated the annual proportion of children younger than 5 years with fever and a positive RDT in Africa who received an ACT in 2003–15.MethodsOur modelling study used cross-sectional data on treatment for fever and RDT status for children younger than 5 years compiled from all nationally available representative household surveys (the Malaria Indicator Surveys, Demographic and Health Surveys, and Multiple Indicator Cluster Surveys) across sub-Saharan Africa between 2003 and 2015. Estimates for the proportion of children younger than 5 years with a fever within the previous 14 days and P falciparum infection assessed by RDT who received an ACT were incorporated in a generalised additive mixed model, including data on ACT distributions, to estimate coverage across all countries and time periods. We did random effects meta-analyses to examine individual, household, and community effects associated with ACT coverage.FindingsWe obtained data on 201 704 children younger than 5 years from 103 surveys (22 MIS, 61 DHS, and 20 MICS) across 33 countries. RDT results were available for 40 of these surveys including 40 261 (20%) children, and we predicted RDT status for the remaining 161 443 (80%) children. Our results showed that ACT coverage in children younger than 5 years with a fever and P falciparum infection increased across sub-Saharan Africa in 2003–15, but even in 2015, only 19.7% (95% CI 15.6–24.8) of children younger than 5 years with a fever and P falciparum infection received an ACT. In meta-analyses, children younger than 5 years were more likely to receive an ACT for fever and P falciparum infection if they lived in an urban area (vs rural area; odds ratio [OR] 1.18, 95% CI 1.06–1.31), had household wealth above the national median (vs wealth below the median; OR 1.26, 1.16–1.39), had a caregiver with any education (vs no education; OR 1.31, 1.22–1.41), had a household insecticide-treated net (ITN; vs no ITN; OR 1.21, 1.13–1.29), were older than 2 years (vs ≤2 years; OR 1.09, 1.01–1.17), or lived in an area with a higher mean P falciparum prevalence in children aged 2–10 years (OR 1.12, 1.02–1.23). In the subgroup of children for whom treatment was sought, those who sought treatment in the public sector were more likely to receive an ACT (vs the private sector; OR 3.18, 2.67–3.78).InterpretationDespite progress during the 2003–15 malaria programme, ACT treatment for children with malaria remains unacceptably low. More work is needed at the country level to understand how health-care access, service delivery, and ACT supply might be improved to ensure appropriate treatment for all children with malaria.FundingUS President's Malaria Initiative and Medicines for Malaria Venture.

Highlights

  • Half of the world’s population is at risk of Plasmodium falciparum malaria,[1] the most lethal species of malaria parasite

  • Our results showed that artemisinin-based combination therapies (ACTs) coverage in children younger than 5 years with a fever and P falciparum infection increased across sub-Saharan Africa in 2003–15, but even in 2015, only 19·7% of children younger than 5 years with a fever and P falciparum infection received an ACT

  • National-level and continent-level coverage estimates First, for national surveys without rapid diagnostic tests (RDTs), we modelled the propensity of children with a fever to be RDT positive on the basis of a set of predictive factors

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Summary

Introduction

Half of the world’s population is at risk of Plasmodium falciparum malaria,[1] the most lethal species of malaria parasite. Following the emergence of widespread drug resistance to chloroquine and sulfadoxine–pyrimethamine,[3] artemisinin-based combination therapies (ACTs) were introduced as a highly effective treatment for uncomplicated malaria (both for P falciparum and Plasmodium vivax infections), preventing progression to severe disease and death.[4,5] www.thelancet.com/lancetgh Vol 5 April 2017 e418. Evidence before this study A wealth of nationally representative household survey data has become available over the past 10 years to help malaria programmes monitor and assess their progress in achieving high population coverage of effective interventions, including case management with effective diagnostic tools and treatment with antimalarials, which over the past decade have been artemisinin-based combination therapies (ACTs). We found no studies that examined coverage of ACT treatment at the continental level over time for children with fever, or that examined ACT coverage for children with a Plasmodium falciparum infection from household survey data

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