Evidence map›Paper›PMID 32797101›Full record

Observational studyPLoS medicine2020

A multiphase program for malaria elimination in southern Mozambique (the Magude project): A before-after study.

Beatriz Galatas, Francisco Saúte, Helena Martí-Soler, Caterina Guinovart, Lidia Nhamussua, Wilson Simone, Humberto Munguambe, Camilo Hamido, Júlia Montañà, Olinda Muguande and 11 more

Registry-linked trialAbstract readComparative StudyObservational Study
In one paragraph

Observational study in PLoS medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02914145 (Mass Drug Administration of Monthly DHA-PQP to Accelerate Towards Malaria Elimination in Magude District, Southern Mozambique), which is not on this map. Cited by 43 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02914145 nacompletednot on this map

Mass Drug Administration of Monthly DHA-PQP to Accelerate Towards Malaria Elimination in Magude District, Southern Mozambique

TypeinterventionalSponsorCentro de Investigacao em Saude de ManhicaRan2015 to 2017Enrolled240,502ConditionsMalariaArmsDihydroartemisinin-piperaquine
3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
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  3. Mass drug administration for malaria.The Cochrane database of systematic reviews · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Beatriz GalatasISGlobal, Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0002-9546-6385
Francisco SaúteCentro de Investigação em Saúde de Manhiça, Maputo, Mozambique.
Helena Martí-SolerISGlobal, Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0002-7127-205X
Caterina GuinovartISGlobal, Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0001-8118-2026
Lidia NhamussuaCentro de Investigação em Saúde de Manhiça, Maputo, Mozambique.ORCID 0000-0003-4867-6301
Wilson SimoneCentro de Investigação em Saúde de Manhiça, Maputo, Mozambique.
Humberto MunguambeCentro de Investigação em Saúde de Manhiça, Maputo, Mozambique.
Camilo HamidoCentro de Investigação em Saúde de Manhiça, Maputo, Mozambique.ORCID 0000-0002-2219-5895
Júlia MontañàISGlobal, Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0003-0454-0306
Olinda MuguandeFundação para o Desenvolvimento da Comunidade, Maputo, Mozambique.
Francois MaartensGood Bye Malaria, Johannesburg, South Africa.
Fabião LuisCentro de Investigação em Saúde de Manhiça, Maputo, Mozambique.ORCID 0000-0002-9972-2788
Krijn PaaijmansISGlobal, Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0003-4837-2818
Alfredo MayorISGlobal, Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.
Quique BassatISGlobal, Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0003-0875-7596
Clara MenéndezISGlobal, Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0002-2641-6907
Eusebio MaceteCentro de Investigação em Saúde de Manhiça, Maputo, Mozambique.
Regina RabinovichISGlobal, Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0003-1065-0173
Pedro L AlonsoISGlobal, Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.
Baltazar CandrinhoNational Malaria Control Program, Ministry of Health, Maputo, Mozambique.
Pedro AideCentro de Investigação em Saúde de Manhiça, Maputo, Mozambique.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMalaria eradication remains the long-term vision of the World Health Organization (WHO). However, whether malaria elimination is feasible in areas of stable transmission in sub-Saharan Africa with currently available tools remains a subject of debate. This study aimed to evaluate a multiphased malaria elimination project to interrupt Plasmodium falciparum malaria transmission in a rural district of southern Mozambique. METHODS AND

findingsA before-after study was conducted between 2015 and 2018 in the district of Magude, with 48,448 residents living in 10,965 households. Building on an enhanced surveillance system, two rounds of mass drug administrations (MDAs) per year over two years (phase I, August 2015-2017), followed by one year of reactive focal mass drug administrations (rfMDAs) (phase II, September 2017-June 2018) were deployed with annual indoor residual spraying (IRS), programmatically distributed long-lasting insecticidal nets (LLINs), and standard case management. The four MDA rounds covered 58%-72% of the population, and annual IRS reported coverage was >70%. Yearly parasite surveys and routine surveillance data were used to monitor the primary outcomes of the study-malaria prevalence and incidence-at baseline and annually since the onset of the project. Parasite prevalence by rapid diagnostic test (RDT) declined from 9.1% (95% confidence interval [CI] 7.0-11.8) in May 2015 to 2.6% (95% CI 2.0-3.4), representing a 71.3% (95% CI 71.1-71.4, p < 0.001) reduction after phase I, and to 1.4% (95% CI 0.9-2.2) after phase II. This represented an 84.7% (95% CI 81.4-87.4, p < 0.001) overall reduction in all-age prevalence. Case incidence fell from 195 to 75 cases per 1,000 during phase I (61.5% reduction) and to 67 per 1,000 during phase II (65.6% overall reduction). Interrupted time series (ITS) analysis was used to estimate the level and trend change in malaria cases associated with the set of project interventions and the number of cases averted. Phase I interventions were associated with a significant immediate reduction in cases of 69.1% (95% CI 57.5-77.6, p < 0.001). Phase II interventions were not associated with a level or trend change. An estimated 76.7% of expected cases were averted throughout the project (38,369 cases averted of 50,005 expected). One malaria-associated inpatient death was observed during the study period. There were 277 mild adverse events (AEs) recorded through the passive pharmacovigilance system during the four MDA rounds. One serious adverse event (SAE) that resulted in death was potentially related to the drug. The study was limited by the incomplete coverage of interventions, the quality of the routine and cross-sectional data collected, and the restricted accuracy of ITS analysis with a short pre-intervention period.

conclusionIn this study, we observed that the interventions deployed during the Magude project fell short of interrupting P. falciparum transmission with the coverages achieved. While new tools and strategies may be required to eventually achieve malaria elimination in stable transmission areas of sub-Saharan Africa, this project showed that innovative mixes of interventions can achieve large reductions in disease burden, a necessary step in the pathway towards elimination.

trial registrationClinicalTrials.gov NCT02914145.

Indexed as

AdolescentAdultAntimalarialsChildChild, PreschoolCross-Sectional StudiesFemaleHumansInfection ControlMalaria, FalciparumMaleMiddle AgedMosquito ControlMozambiqueYoung AdultAntimalarials

Identifiers

PMID32797101
PMCPMC7428052

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.