Evidence map›Paper›PMID 32691047›Full record

ArticleThe Journal of infectious diseases2022

Evaluating the Impact of Programmatic Mass Drug Administration for Malaria in Zambia Using Routine Incidence Data.

Maya Fraser, John M Miller, Kafula Silumbe, Michael Hainsworth, Mutinta Mudenda, Busiku Hamainza, Hawela Moonga, Elizabeth Chizema Kawesha, Laina D Mercer, Adam Bennett and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the 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
1.3field-weighted citation impact, top 18% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 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
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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 5 institutions in 3 countries.

Maya FraserPATH Malaria Control and Elimination Partnership in Africa (MACEPA), Seattle, Washington, USA.
John M MillerPATH MACEPA, Lusaka, Zambia.
Kafula SilumbePATH MACEPA, Lusaka, Zambia.
Michael HainsworthPATH Malaria Control and Elimination Partnership in Africa (MACEPA), Seattle, Washington, USA.
Mutinta MudendaNational Malaria Elimination Centre, Zambia Ministry of Health, Lusaka, Zambia.
Busiku HamainzaNational Malaria Elimination Centre, Zambia Ministry of Health, Lusaka, Zambia.
Hawela MoongaNational Malaria Elimination Centre, Zambia Ministry of Health, Lusaka, Zambia.
Elizabeth Chizema KaweshaNational Malaria Elimination Centre, Zambia Ministry of Health, Lusaka, Zambia.
Laina D MercerPATH Malaria Control and Elimination Partnership in Africa (MACEPA), Seattle, Washington, USA.
Adam BennettPATH Malaria Control and Elimination Partnership in Africa (MACEPA), Seattle, Washington, USA.
Kammerle SchneiderPATH Malaria Control and Elimination Partnership in Africa (MACEPA), Seattle, Washington, USA.
Hannah C SlaterPATH Malaria Control and Elimination Partnership in Africa (MACEPA), Seattle, Washington, USA.
Thomas P EiseleCenter for Applied Malaria Research and Evaluation, Department of Tropical Medicine, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana, USA.
Caterina GuinovartPATH Malaria Control and Elimination Partnership in Africa (MACEPA), Seattle, Washington, USA.
Program for Appropriate Technology in Health · USMinistry of Health · ZMNational HIV/AIDS/STI/TB Council · ZMTulane University · USUniversitat de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn 2016, the Zambian National Malaria Elimination Centre started programmatic mass drug administration (pMDA) campaigns with dihydroartemisinin-piperaquine as a malaria elimination tool in Southern Province. Two rounds were administered, 2 months apart (coverage 70% and 57%, respectively). We evaluated the impact of 1 year of pMDA on malaria incidence using routine data.

methodsWe conducted an interrupted time series with comparison group analysis on monthly incidence data collected at the health facility catchment area (HFCA) level, with a negative binomial model using generalized estimating equations. Programmatic mass drug administration was conducted in HFCAs with greater than 50 cases/1000 people per year. Ten HFCAs with incidence rates marginally above this threshold (pMDA group) were compared with 20 HFCAs marginally below (comparison group).

resultsThe pMDA HFCAs saw a 46% greater decrease in incidence at the time of intervention than the comparison areas (incidence rate ratio = 0.536; confidence interval = 0.337-0.852); however, incidence increased toward the end of the season. No HFCAs saw a transmission interruption.

conclusionsProgrammatic mass drug administration, implemented during 1 year with imperfect coverage in low transmission areas with suboptimal vector control coverage, significantly reduced incidence. However, elimination will require additional tools. Routine data are important resources for programmatic impact evaluations and should be considered for future analyses.

Indexed as

AntimalarialsMalariaHumansIncidenceMass Drug AdministrationZambiaAntimalarialsimpact evaluationmalariamass drug administrationroutine data

Identifiers

PMID32691047
PMCPMC9016426
OpenAlexW3044964366

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.