Evidence map›Paper›PMID 31676244›Full record

Observational studyThe Lancet. Infectious diseases2020

Implications for annual retesting after a test-and-not-treat strategy for onchocerciasis elimination in areas co-endemic with Loa loa infection: an observational cohort study.

Sébastien Ds Pion, Hugues Nana-Djeunga, Yannick Niamsi-Emalio, Cédric B Chesnais, Hugo Deléglise, Charles Mackenzie, Wilma Stolk, Daniel A Fletcher, Amy D Klion, Thomas B Nutman and 2 more

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in The Lancet. Infectious diseases, 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
2.9field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. AI sees an end to filariasis.PLoS neglected tropical diseases · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Feasibility of Onchocerciasis Elimination Using a "Test-and-not-treat" Strategy in Loa loa Co-endemic Areas.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 3 countries.

Sébastien Ds PionFrench Research Institute for Development-Unité Mixte Internationale 233 and French National Institute of Health and Medical Research-Unit 1175, University of Montpellier Montpellier, France. Electronic address: sebastien.pion@ird.fr.
Hugues Nana-DjeungaCentre for Research on Filariasis and other Tropical Diseases, Yaounde, Cameroon.
Yannick Niamsi-EmalioCentre for Research on Filariasis and other Tropical Diseases, Yaounde, Cameroon.
Cédric B ChesnaisFrench Research Institute for Development-Unité Mixte Internationale 233 and French National Institute of Health and Medical Research-Unit 1175, University of Montpellier Montpellier, France.
Hugo DelégliseFrench Research Institute for Development-Unité Mixte Internationale 233 and French National Institute of Health and Medical Research-Unit 1175, University of Montpellier Montpellier, France.
Charles MackenzieDepartment of Pathobiology and Diagnostic Investigation, Michigan State University, East Lansing, MI, USA.
Wilma StolkDepartment of Public Health, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Daniel A FletcherDepartment of Bioengineering and Biophysics Programme, University of California, Berkeley, CA, USA.
Amy D KlionLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Thomas B NutmanLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Michel BoussinesqFrench Research Institute for Development-Unité Mixte Internationale 233 and French National Institute of Health and Medical Research-Unit 1175, University of Montpellier Montpellier, France.
Joseph KamgnoCentre for Research on Filariasis and other Tropical Diseases, Yaounde, Cameroon.
National Institutes of Health · USRecherches Translationnelles sur le VIH et les Maladies InfectieusesAgropolis International · FRErasmus MC · NLInstitut de Recherche pour le Développement · FRMichigan State University · USUniversity of California, Berkeley · US

Funding

Eosinophils and Eosinophil Activation in the Pathogenesis of Human DiseaseZIAAI001130 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KLION, AMY · 2010 to 2025
$22.5M
Clinical And Therapeutic Studies Of Human Filariasis and Related DiseasesZIAAI000439 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI NUTMAN, THOMAS · 2009 to 2025
$14.8M
6 · The paper itself

Abstract

backgroundA test-and-not-treat (TaNT) strategy has been developed to prevent people with high concentrations of circulating Loa loa microfilariae (>20 000 microfilariae per mL) developing serious adverse events after ivermectin treatment during mass drug administration to eliminate onchocerciasis. An important question related to cost and programmatic issues is whether annual retesting is required for everyone. We therefore aimed to investigate changes in L loa microfilarial densities during TaNT campaigns run 18 months apart.

methodsIn this observational cohort study, we assessed the participants of two TaNT campaigns for onchocerciasis. These campaigns, which were run by a research team, together with personnel from the Ministry of Health and community health workers, were done in six health areas (in 89 communities) in Okola health district (Cameroon); the first campaign was run between Aug 10, and Oct 29, 2015, and the second was run between March 7, and May 26, 2017. All individuals aged 5 years and older were invited to be screened for Loa loa microfilaraemia before being offered ivermectin (unless contraindicated). L loa microfilarial density was measured at the point of care using the LoaScope. All those with a L loa microfilarial density of 20 000 microfilariae per mL or less were offered treatment; in the first 2 weeks of the 2015 campaign, a higher exclusion threshold of 26 000 microfilariae per mL or less was used. At both rounds of the intervention, participants were registered with a paper form, in which personal information were collected. In 2017, we also recorded whether each individual reported participation in the 2015 campaign. The primary outcome, assessed in all participants, was whether L loa microfilarial density was above or below the exclusion threshold (ie, the criteria that guided the decision to treat).

findingsIn the 2015 TaNT campaign, 26 415 people were censused versus 29 587 people in the 2017 TaNT campaign. All individuals aged 5 years and older without other contraindications to treatment (22 842 people in 2015 and 25 421 people in 2017) were invited to be screened for L loa microfilaraemia before being offered ivermectin. In 2015, 16 182 individuals were examined with the LoaScope, versus 18 697 individuals in the same communities in 2017. 344 (2·1%) individuals were excluded from ivermectin treatment because of a high L loa microfilarial density in 2015, versus 283 (1·5%) individuals in 2017 (p<0·0001). Records from 2017 could be matched to those from 2015 for 6983 individuals (43·2% of the 2015 participants). In this cohort, in 2017, 6981 (>99·9%) of 6983 individuals treated with ivermectin in 2015 had L loa microfilariae density below the level associated with neurological serious adverse events.

interpretationIndividuals treated with ivermectin do not need to be retested for L loa microfilaraemia before the next treatment, provided that they can be re-identified. This adjusted approach will enable substantial cost savings and facilitate reaching programmatic goals for elimination of onchocerciasis in areas that are co-endemic for loiasis.

fundingBill & Melinda Gates Foundation, Division of Intramural Research (National Institute of Allergy and Infectious Diseases, US National Institutes of Health).

Indexed as

Endemic DiseasesAdolescentAdultAnimalsCameroonChildCohort StudiesFemaleHumansIvermectinLoaLoiasisMaleMass Drug AdministrationMiddle AgedOnchocerciasisIvermectin

Identifiers

PMID31676244
PMCPMC8150319
OpenAlexW2982486238

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.