Evidence map›Paper›PMID 34098984›Full record

Trial reportMalaria journal2021

Reactive, self-administered malaria treatment against asymptomatic malaria infection: results of a cluster randomized controlled trial in The Gambia.

Joseph Okebe, Edgard Dabira, Fatou Jaiteh, Nuredin Mohammed, John Bradley, Ndey-Fatou Drammeh, Amadou Bah, Yoriko Masunaga, Jane Achan, Joan Muela Ribera and 4 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Malaria journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02878200 (Reactive Household-based Self-administered Treatment Against Residual Malaria Transmission), which is not on this map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 11% of its field
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.

NCT02878200 nacompletednot on this map

Reactive Household-based Self-administered Treatment Against Residual Malaria Transmission: a Cluster Randomized Trial

TypeinterventionalSponsorLondon School of Hygiene and Tropical MedicineRan2016 to 2020Enrolled2,236ConditionsMalariaArmsdihydroartemisinin-piperaquine
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Observational
  7. Review
  8. Article
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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

14 authors at 6 institutions in 4 countries.

Joseph OkebeMedical Research Council Unit The Gambia At the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Edgard DabiraMedical Research Council Unit The Gambia At the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Fatou JaitehMedical Anthropology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Nuredin MohammedMedical Research Council Unit The Gambia At the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
John BradleyMRC International Statistics and Epidemiology Group, London School of Hygiene and Tropical Medicine, London, UK.
Ndey-Fatou DrammehMedical Research Council Unit The Gambia At the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Amadou BahMedical Research Council Unit The Gambia At the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Yoriko MasunagaMedical Anthropology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Jane AchanMedical Research Council Unit The Gambia At the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
Joan Muela RiberaPASS Suisse, Neuchâtel, Switzerland.
Shunmay YeungClinical Research Department, London School of Hygiene and Tropical Medicine, London, UK.
Julie BalenSchool of Health and Related Research, The University of Sheffield, Sheffield, UK.
Koen Peeters GrietensMedical Anthropology Unit, Institute of Tropical Medicine, Antwerp, Belgium.
Umberto D'AlessandroMedical Research Council Unit The Gambia At the London School of Hygiene and Tropical Medicine, Fajara, The Gambia. Umberto.Dalessandro@lshtm.ac.uk.
MRC Unit the Gambia · GMInstituut voor Tropische Geneeskunde · BELondon School of Hygiene & Tropical Medicine · GBMalaria Consortium · GBObservatoire Cantonal de Neuchâtel · CHUniversity of Sheffield · GB

Funding

Medical Research Council MC-EX_MR/N006100/1Medical Research Council MC_EX_MR/N006100/1Medical Research Council MR/R010161/1
6 · The paper itself

Abstract

backgroundSelectively targeting and treating malaria-infected individuals may further decrease parasite carriage in low-burden settings. Using a trans-disciplinary approach, a reactive treatment strategy to reduce Plasmodium falciparum prevalence in participating communities was co-developed and tested.

methodsThis is a 2-arm, open-label, cluster-randomized trial involving villages in Central Gambia during the 2017 and 2018 malaria transmission season. Villages were randomized in a 1:1 ratio using a minimizing algorithm. In the intervention arm, trained village health workers delivered a full course of pre-packed dihydroartemisinin-piperaquine to all residents of compounds where clinical cases were reported while in the control arm, compound residents were screened for infection at the time of the index case reporting. All index cases were treated following national guidelines. The primary endpoint was malaria prevalence, determined by molecular methods, at the end of the intervention period.

resultsThe trial was carried out in 50 villages: 34 in 2017 and 16 additional villages in 2018. At the end of the 2018 transmission season, malaria prevalence was 0.8% (16/1924, range 0-4%) and 1.1% (20/1814, range 0-17%) in the intervention and control arms, respectively. The odds of malaria infection were 29% lower in the intervention than in the control arm after adjustment for age (OR 0.71, 95% CI 0.27-1.84, p = 0.48). Adherence to treatment was high, with 98% (964/979) of those treated completing the 3-day treatment. Over the course of the study, only 37 villages, 20 in the intervention and 17 in the control arm, reported at least one clinical case. The distribution of clinical cases by month in both transmission seasons was similar and the odds of new clinical malaria cases during the trial period did not vary between arms (OR 1.04, 95% CI 0.57-1.91, p = 0.893). All adverse events were classified as mild to moderate and resolved completely.

conclusionThe systematic and timely administration of an anti-malarial treatment to residents of compounds with confirmed malaria cases did not significantly decrease malaria prevalence and incidence in communities where malaria prevalence was already low. Treatment coverage and adherence was very high. Results were strongly influenced by the lower-than-expected malaria prevalence, and by no clinical cases in villages with asymptomatic malaria-infected individuals.

trial registrationThis study is registered with ClinicalTrials.gov, NCT02878200. Registered 25 August 2016. https://clinicaltrials.gov/ct2/show/NCT02878200 .

Indexed as

AdolescentAdultAgedAged, 80 and overAntimalarialsArtemisininsAsymptomatic InfectionsChildChild, PreschoolCluster AnalysisDrug CombinationsFemaleGambiaHumansIncidenceInfantAntimalarialsArtemisininsartenimolDrug CombinationspiperaquinePiperazinesQuinolinesAsymptomatic infectionMalaria prevalenceReactive treatmentVillage health worker

Identifiers

PMID34098984
PMCPMC8186162
OpenAlexW3170762588

What OpenQuestion holds

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LicenceCC BY
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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.