Evidence map›Paper›PMID 39552715›Full record

ArticleEClinicalMedicine2024

The performance of a point-of-care test for the diagnosis of Neurocysticercosis in a resource-poor community setting in Zambia - a diagnostic accuracy study.

Gideon Zulu, Dominik Stelzle, Kabemba E Mwape, Inge Van Damme, Chiara Trevisan, Chishimba Mubanga, Veronika Schmidt, Isaac K Phiri, Richard Mambo, Mwelwa Chembensofu and 10 more

Abstract read
In one paragraph

Article in EClinicalMedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. 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

20 authors.

Gideon ZuluMinistry of Health, Lusaka, Zambia.
Dominik StelzleDepartment of Neurology, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Kabemba E MwapeDepartment of Clinical Studies, School of Veterinary Medicine, University of Zambia, Lusaka, Zambia.
Inge Van DammeDepartment of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, Belgium.
Chiara TrevisanDepartment of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, Belgium.
Chishimba MubangaDepartment of Clinical Studies, School of Veterinary Medicine, University of Zambia, Lusaka, Zambia.
Veronika SchmidtDepartment of Neurology, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Isaac K PhiriDepartment of Clinical Studies, School of Veterinary Medicine, University of Zambia, Lusaka, Zambia.
Richard MamboMinistry of Health, Lusaka, Zambia.
Mwelwa ChembensofuDepartment of Clinical Studies, School of Veterinary Medicine, University of Zambia, Lusaka, Zambia.
Maxwell MasukuDepartment of Clinical Studies, School of Veterinary Medicine, University of Zambia, Lusaka, Zambia.
Charlotte RuetherDepartment of Neurology, School of Medicine and Health, Technical University of Munich, Munich, Germany.
John NohDivision of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, United States.
Sukwan HandaliDivision of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, United States.
Emmanuel BottieauDepartment of Clinical Sciences, Institute of Tropical Medicine, 2000, Antwerp, Belgium.
Pascal MagnussenDepartment of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Pierre DornyDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Agnes FleuryInstituto de Investigaciones Biomédicas-UNAM/Instituto Nacional de Neurología y Neurocirugía/Facultad de Medicina-UNAM, Ciudad de México, Mexico.
Andrea S WinklerDepartment of Neurology, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Sarah GabriëlDepartment of Translational Physiology, Infectiology and Public Health, Faculty of Veterinary Medicine, Ghent University, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Neurocysticercosis (NCC) is the main cause of epilepsy in Methods: A diagnostic accuracy study with prospective data collection, using a two-stage design was conducted in Sinda district of the Eastern province of Zambia between December 2017 and June 2019. Eligible participants were tested with the TS POC test. Thereafter, participants with a TS POC CC+ result and a subset of participants with a TS POC CC- result were subjected to serological testing for reference assays, and cerebral computed tomography (CT) for the reference diagnosis of NCC. Findings: A total of 1249 participants were tested with the TS POC of which 177 (14%) were positive. Of the 151 TS POC CC+ and 82 TS POC CC- participants with cerebral CT examination, 35 TS POC CC+ and 10 TS POC CC-, respectively, had NCC. The sensitivity of the TS POC CC strip was 26% (uncertainty interval [UI] 15-41) for any type of NCC, which was similar to that estimated for the rT24H-EITB (23%, UI 8-48) and the serum antigen ELISA (30%, UI 11-58). The specificity was 88% (UI 85-90) for the TS POC, 89% (UI 79-94) for the rT24H-EITB, and 82% (UI 71-89) for the antigen ELISA. For NCC with active stage lesions, sensitivity was >99% (UI 58->99) for the TS POC, 76% (UI 40-94) for the rT24H-EITB and 76% (UI 39-94) for the antigen ELISA. Interpretation: The TS POC CC had a promising sensitivity for diagnosis of participants with active NCC lesions within a community-based setting. Accuracy for NCC at any stage was limited for all tests (TS POC, rT24H-EITB and antigen ELISA). With further development the TS POC CC may enable a better detection and faster referral of NCC patients who may benefit from antiparasitic treatment. Funding: European and Developing Countries Clinical Trials Partnership (EDCTP) and the German Federal Ministry of Education and Research (BMBF).

Indexed as

Antigen ELISADiagnosisNeurocysticercosisPoint-of-care testrT24H-EITBTaenia solium

Identifiers

PMID39552715
PMCPMC11567943

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.