Evidence map›Paper›PMID 34022958›Full record

ArticleInfectious diseases of poverty2021

Comparison of conventional and non-invasive diagnostic tools for detecting Plasmodium falciparum infection in southwestern Cameroon: a cross-sectional study.

Tobias O Apinjoh, Veronica N Ntasin, Phil Collins C Tataw, Vincent N Ntui, Dieudonne L Njimoh, Fidelis Cho-Ngwa, Eric A Achidi

Open access · goldAbstract readComparative Study
In one paragraph

Article in Infectious diseases of poverty, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Diagnostic accuracy ofExperimental biology and medicine (Maywood, N.J.) · 2025
    Article
  3. Urine and Saliva: Relevant Specimens for Malaria Diagnosis?Diagnostics (Basel, Switzerland) · 2022
    Review
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

7 authors at 1 institution in 1 country.

Tobias O ApinjohDepartment of Biochemistry and Molecular Biology, University of Buea, Buea, Cameroon. apinjoh.tobias@ubuea.cm.ORCID http://orcid.org/0000-0001-9889-7271
Veronica N NtasinDepartment of Biochemistry and Molecular Biology, University of Buea, Buea, Cameroon.
Phil Collins C TatawDepartment of Biochemistry and Molecular Biology, University of Buea, Buea, Cameroon.
Vincent N NtuiDepartment of Biochemistry and Molecular Biology, University of Buea, Buea, Cameroon.
Dieudonne L NjimohDepartment of Biochemistry and Molecular Biology, University of Buea, Buea, Cameroon.
Fidelis Cho-NgwaDepartment of Biochemistry and Molecular Biology, University of Buea, Buea, Cameroon.
Eric A AchidiDepartment of Biochemistry and Molecular Biology, University of Buea, Buea, Cameroon.
University of Buea · CM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMalaria remains a significant health challenge in sub-Saharan Africa, with early diagnosis critical to reducing its morbidity and mortality. Despite the increasing Plasmodium spp. diagnostic capabilities, access to testing is limited in some cases by the almost absolute requirement for blood from potentially infected subjects as the only sample source for all conventional methods. A rapid test on non-invasive specimen with comparable performance to microscopy for the screening or diagnosis of all participants is invaluable. This study sought to compare conventional and non-invasive diagnostic tools for detecting Plasmodium falciparum.

methodsThis was a cross-sectional study, carried out between March and August 2019 to evaluate and compare the diagnostic performance of a PfHRP2/pLDH-based malaria rapid diagnostic test (mRDT) on patients' blood, saliva and urine relative to conventional light microscopy and nested PCR at outpatient clinics in the Buea and Tiko health districts of Southwestern Cameroon. The significance of differences in proportions was explored using the Pearson's χ

resultsA total of 359 individuals of both sexes, aged 1-92 years, were enrolled into the study. Of the 301 individuals tested by light microscopy and mRDTs on blood, saliva and urine, 84 (27.9%), 81 (26.9%), 87 (28.9%) and 107 (35.5%) respectively were positive. However, only 34.3%, 90.5%, 91.4%, 83.9% and 65.4% febrile, light microscopy and mRDT positives on blood, saliva and urine respectively had P. falciparum infection as confirmed by PCR. The sensitivity and specificity of presumptive diagnosis, light microscopy and mRDT on blood, saliva and urine were 86.9% and 19.7%, 77.8% and 96.1%, 75.8% and 96.6%, 74.5% and 93.1%, and 70.7% and 81.8%, respectively. The agreement between mRDT on saliva (k = 0.696) and microscopy (k = 0.766) compared to PCR was good.

conclusionThe study highlighted the low performance of presumptive diagnosis, reinforcing the need for parasitological tests prior to antimalarial therapy. The higher PfHRP2/pLDH mRDT parasite detection rates and sensitivity in saliva compared to urine suggests that the former is a practical adjunct to or alternative worth optimising for the routine diagnosis of malaria. Flow chart for diagnosis of P. falciparum infection by light microscopy, rapid diagnostic tests and nested PCR.

Indexed as

AdolescentAdultAgedAged, 80 and overAntigens, ProtozoanCameroonChildChild, PreschoolCross-Sectional StudiesEarly DiagnosisFemaleHumansInfantMalaria, FalciparumMaleMicroscopyAntigens, ProtozoanHRP-2 antigen, Plasmodium falciparumProtozoan ProteinsBloodMicroscopyNested PCRPlasmodium falciparumRapid diagnostic testSalivaUrine

Identifiers

PMID34022958
PMCPMC8140564
OpenAlexW3164716502

What OpenQuestion holds

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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.