Evidence map›Paper›PMID 28369085›Full record

ArticlePLoS neglected tropical diseases2017

Defining the next generation of Plasmodium vivax diagnostic tests for control and elimination: Target product profiles.

Xavier C Ding, Maria Paz Ade, J Kevin Baird, Qin Cheng, Jane Cunningham, Mehul Dhorda, Chris Drakeley, Ingrid Felger, Dionicia Gamboa, Matthias Harbers and 9 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 5 pooled it
4.0field-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.

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

24 citing papers in PubMed, 5 syntheses or guidelines pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Article
  7. Spatiotemporal Epidemiology of Malaria in India from 2007 to 2022.The American journal of tropical medicine and hygiene · 2024
    Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Proteomic Analysis of Urine from Patients withTropical medicine and infectious disease · 2022
    Article
  13. Article
  14. Ultrasensitive CRISPR-based diagnostic for field-applicable detection ofProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Observational
  20. The American journal of tropical medicine and hygiene · 2019
    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

19 authors at 15 institutions in 12 countries.

Xavier C DingFIND, Geneva, Switzerland.ORCID 0000-0001-8409-3678
Maria Paz AdeDepartment of Communicable Diseases and Health Analysis, Pan American Health Organization/World Health Organization, Washington, DC, Unites States of America.
J Kevin BairdEijkman-Oxford Clinical Research Unit, Jakarta, Indonesia.
Qin ChengAustralian Army Malaria Institute, Brisbane, Australia.
Jane CunninghamGlobal Malaria Programme, World Health Organization, Geneva, Switzerland.
Mehul DhordaCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Chris DrakeleyDepartment of Immunology and Infection, London School of Hygiene & Tropical Medicine, London, United Kingdom.
Ingrid FelgerUniversity of Basel, Basel, Switzerland.
Dionicia GamboaInstitute of Tropical Medicine Alexander von Humboldt, Universidad Peruana Cayetano Heredia, Lima, Peru.
Matthias HarbersRIKEN Center for Life Science Technologies, Division of Genomic Technologies, Yokohama, Japan.
Socrates HerreraCaucaseco Scientific Research Center, Cali, Colombia.
Naomi LucchiMalaria Branch, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Alfredo MayorISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital Clínic-Universitat de Barcelona, Barcelona, Spain.
Ivo MuellerPopulation Health and Immunity Division, Walter and Eliza Hall Institute, Parkville, Australia.
Jetsumon SattabongkotMahidol Vivax Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Arsène RatsimbasonProgramme National de Lutte contre le Paludisme, Antananarivo, Madagascar.
Jack RichardsCentre for Biomedical Research, Burnet Institute, Melbourne, Victoria, Australia.
Marcel TannerUniversity of Basel, Basel, Switzerland.
Iveth J GonzálezFIND, Geneva, Switzerland.
FIND · CHSwiss Tropical and Public Health Institute · CHBurnet Institute · AUCaucaseco Scientific Research Center · COCenters for Disease Control and Prevention · USChurchill Hospital · GBEijkman Institute for Molecular Biology · IDInstitut Pasteur · FRLondon School of Hygiene & Tropical Medicine · GBMahidol University · THManhiça Health Research Centre · MZUniversidad Peruana Cayetano Heredia · PEUniversity of Antananarivo · MGWorld Health Organization · CHWorld Health Organization Regional Office for the Americas · US

Funding

Vector Biology Research and Integrated Vector Management For Malaria ControlU19AI089702 · NIAID · CAUCASECO SCIENTIFIC RESEARCH CENTER · PI HERRERA VALENCIA, SOCRATES · 2010 to 2016
$11.5M
NIAID NIH HHS U19 AI089702World Health Organization 001
6 · The paper itself

Abstract

The global prevalence of malaria has decreased over the past fifteen years, but similar gains have not been realized against Plasmodium vivax because this species is less responsive to conventional malaria control interventions aimed principally at P. falciparum. Approximately half of all malaria cases outside of Africa are caused by P. vivax. This species places dormant forms in human liver that cause repeated clinical attacks without involving another mosquito bite. The diagnosis of acute patent P. vivax malaria relies primarily on light microscopy. Specific rapid diagnostic tests exist but typically perform relatively poorly compared to those for P. falciparum. Better diagnostic tests are needed for P. vivax. To guide their development, FIND, in collaboration with P. vivax experts, identified the specific diagnostic needs associated with this species and defined a series of three distinct target product profiles, each aimed at a particular diagnostic application: (i) point-of-care of acutely ill patients for clinical care purposes; (ii) point-of-care asymptomatic and otherwise sub-patent residents for public health purposes, e.g., mass screen and treat campaigns; and (iii) ultra-sensitive not point-of-care diagnosis for epidemiological research/surveillance purposes. This report presents and discusses the rationale for these P. vivax-specific diagnostic target product profiles. These contribute to the rational development of fit-for-purpose diagnostic tests suitable for the clinical management, control and elimination of P. vivax malaria.

Indexed as

Point-of-Care SystemsDiagnostic Tests, RoutineHumansMalaria, FalciparumMalaria, VivaxPlasmodium falciparumPlasmodium vivaxSpecies Specificity

Identifiers

PMID28369085
PMCPMC5391123
OpenAlexW2604418387

What OpenQuestion holds

Textmetadata
LicenceCC0
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.