Evidence map›Paper›PMID 33239779›Full record

ArticleScientific reports2020

Supporting elimination of lymphatic filariasis in Samoa by predicting locations of residual infection using machine learning and geostatistics.

Helen J Mayfield, Hugh Sturrock, Benjamin F Arnold, Ricardo Andrade-Pacheco, Therese Kearns, Patricia Graves, Take Naseri, Robert Thomsen, Katherine Gass, Colleen L Lau

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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.

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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Progression of lymphatic filariasis antigenaemia and microfilaraemia over 4.5 years in antigen-positive individuals, Samoa 2019-2023.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Artificial intelligence and lymphedema: State of the art.Journal of clinical and translational research · 2022
    Review
  8. Article
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

10 authors.

Helen J MayfieldResearch School of Population Health, Australian National University, Canberra, Australia. Helen.mayfield@anu.edu.au.
Hugh SturrockGlobal Health Group, University of California, San Francisco, San Francisco, USA.
Benjamin F ArnoldProctor Foundation, University of California, San Francisco, San Francisco, USA.
Ricardo Andrade-PachecoGlobal Health Group, University of California, San Francisco, San Francisco, USA.
Therese KearnsMenzies School of Health Research, Charles Darwin University, Brisbane, Australia.
Patricia GravesCollege of Public Health, Medical and Veterinary Sciences, James Cook University, Cairns, QLD, Australia.
Take NaseriMinistry of Health, Apia, Samoa.
Robert ThomsenMinistry of Health, Apia, Samoa.
Katherine GassNeglected Tropical Diseases Support Center, Task Force for Global Heath, Decatur, GA, USA.
Colleen L LauResearch School of Population Health, Australian National University, Canberra, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The global elimination of lymphatic filariasis (LF) is a major focus of the World Health Organization. One key challenge is locating residual infections that can perpetuate the transmission cycle. We show how a targeted sampling strategy using predictions from a geospatial model, combining random forests and geostatistics, can improve the sampling efficiency for identifying locations with high infection prevalence. Predictions were made based on the household locations of infected persons identified from previous surveys, and environmental variables relevant to mosquito density. Results show that targeting sampling using model predictions would have allowed 52% of infections to be identified by sampling just 17.7% of households. The odds ratio for identifying an infected individual in a household at a predicted high risk compared to a predicted low risk location was 10.2 (95% CI 4.2-22.8). This study provides evidence that a 'one size fits all' approach is unlikely to yield optimal results when making programmatic decisions based on model predictions. Instead, model assumptions and definitions should be tailored to each situation based on the objective of the surveillance program. When predictions are used in the context of the program objectives, they can result in a dramatic improvement in the efficiency of locating infected individuals.

Indexed as

AedesAnimalsAntibodies, HelminthAntigens, HelminthBrugia malayiDisease ReservoirsElephantiasis, FilarialEpidemiological MonitoringFamily CharacteristicsHumansInsect VectorsMachine LearningPrevalenceSamoaWuchereria bancroftiAntibodies, HelminthAntigens, Helminth

Identifiers

PMID33239779
PMCPMC7689447

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.