Evidence map›Paper›PMID 32618245›Full record

Trial reportThe American journal of tropical medicine and hygiene2020

A Longitudinal Cohort to Monitor Malaria Infection Incidence during Mass Drug Administration in Southern Province, Zambia.

Adam Bennett, Travis R Porter, Mulenga C Mwenda, Joshua O Yukich, Timothy P Finn, Chris Lungu, Kafula Silumbe, Brenda Mambwe, Sandra Chishimba, Conceptor Mulube and 6 more

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

Trial report in The American journal of tropical medicine and hygiene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02329301 (Assessing the Effectiveness of Mass Drug Administration), which is not on this map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% 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.

NCT02329301 nacompletednot on this map

Assessing the Effectiveness of Mass Drug Administration (MDA) With Dihydroartemisinin + Piperaquine for Reducing Malaria Parasite Infection Prevalence and Incidence in Southern Province Zambia

TypeinterventionalSponsorPATHRan2014 to 2020Enrolled2,430ConditionsMalaria, Malaria, FalciparumArmsMDA with DHAp (Eurartesim), Focal MDA with DHAp (Eurartesim)
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Mass drug administration for malaria.The Cochrane database of systematic reviews · 2021
    Pooled it
  2. Efficacy, Safety and Tolerability of Pyronaridine-artesunate in Asymptomatic Malaria-infected Individuals: a Randomized Controlled Trial.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Trial
  3. Trial
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  5. Prevalence ofThe American journal of tropical medicine and hygiene · 2020
    Trial
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  7. Review
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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

16 authors at 5 institutions in 2 countries.

Adam Bennett1Malaria Elimination Initiative, Global Health Group, University of California San Francisco, San Francisco, California.
Travis R Porter2Department of Tropical Medicine, Center for Applied Malaria Research and Evaluation, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
Mulenga C Mwenda3PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia.
Joshua O Yukich2Department of Tropical Medicine, Center for Applied Malaria Research and Evaluation, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
Timothy P Finn2Department of Tropical Medicine, Center for Applied Malaria Research and Evaluation, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
Chris Lungu3PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia.
Kafula Silumbe3PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia.
Brenda Mambwe3PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia.
Sandra Chishimba3PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia.
Conceptor Mulube3PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia.
Daniel J Bridges3PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia.
Busiku Hamainza4National Malaria Elimination Centre, Zambia Ministry of Health, Lusaka, Zambia.
Laurence Slutsker5PATH MACEPA, Seattle, Washington.
Richard W Steketee5PATH MACEPA, Seattle, Washington.
John M Miller3PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia.
Thomas P Eisele2Department of Tropical Medicine, Center for Applied Malaria Research and Evaluation, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
National HIV/AIDS/STI/TB Council · ZMTulane University · USProgram for Appropriate Technology in Health · USMinistry of Health · ZMUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rigorous evidence of effectiveness is needed to determine where and when to apply mass drug administration (MDA) or focal MDA (fMDA) as part of a malaria elimination strategy. The Zambia National Malaria Elimination Centre recently completed a community-randomized controlled trial in Southern Province to evaluate MDA and fMDA for transmission reduction. To assess the role of MDA and fMDA on infection incidence, we enrolled a longitudinal cohort for an 18-month period of data collection including monthly malaria parasite infection detection based on polymerase chain reaction and compared time to first infection and cumulative infection incidence outcomes across study arms using Cox proportional hazards and negative binomial models. A total of 2,026 individuals from 733 households were enrolled and completed sufficient follow-up for inclusion in analysis. Infection incidence declined dramatically across all study arms during the period of study, and MDA was associated with reduced risk of first infection (hazards ratio: 0.36; 95% CI: 0.16-0.80) and cumulative infection incidence during the first rainy season (first 5 months of follow-up) (incidence rate ratio: 0.34; 95% CI: 0.12-0.95). No significant effect was found for fMDA or for either arm over the full study period. Polymerase chain reaction infection status at baseline was strongly associated with follow-up infection. The short-term effects of MDA suggest it may be an impactful accelerator of transmission reduction in areas with high coverage of case management and vector control and should be considered as part of a malaria elimination strategy.

Indexed as

Mass Drug AdministrationAdolescentAntimalarialsArtemisininsChildChild, PreschoolDisease EradicationDrug Therapy, CombinationFamily CharacteristicsFemaleHumansIncidenceLongitudinal StudiesMalaria, FalciparumMalePiperazinesAntimalarialsArtemisininsartenimolpiperaquinePiperazinesQuinolines

Identifiers

PMID32618245
PMCPMC7416973
OpenAlexW3039276265

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.