Evidence map›Paper›PMID 38358148›Full record

ArticleAnnals of African medicine

SD-Bioline malaria rapid diagnostic test performance and time to become negative after treatment of malaria infection in Southwest Nigerian Children.

Adebola Emmanuel Orimadegun, Hannah O Dada-Adegbola, Obaro S Michael, Akinlolu Adedayo Adepoju, Roland Ibenipere Funwei, Fiyinfoluwa Ibukun Olusola, IkeOluwapo O Ajayi, Oluwatoyin O Ogunkunle, Olusegun George Ademowo, Ayodele Samuel Jegede and 5 more

Open access · greenAbstract read
In one paragraph

Article in Annals of African medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

15 authors at 5 institutions in 3 countries.

Adebola Emmanuel OrimadegunInstitute of Child Health, College of Medicine, University of Ibadan, Ibadan, Nigeria.
Hannah O Dada-AdegbolaDepartments of Medical Microbiology, College of Medicine, University of Ibadan, Ibadan, Nigeria.
Obaro S MichaelDepartment of Pharmacology and Therapeutics, College of Medicine, University of Ibadan, Ibadan, Nigeria.
Akinlolu Adedayo AdepojuDepartment of Paediatrics College of Medicine, University of Ibadan, Ibadan, Nigeria.
Roland Ibenipere FunweiDepartment of Pharmacology, Babcock University, Ogun State, Nigeria.
Fiyinfoluwa Ibukun OlusolaDepartment of Pharmacology and Therapeutics, College of Medicine, University of Ibadan, Ibadan, Nigeria.
IkeOluwapo O Ajayiepartment of Epidemiology and Biostatistics, College of Medicine, University of Ibadan, Ibadan, Nigeria.
Oluwatoyin O OgunkunleDepartment of Paediatrics College of Medicine, University of Ibadan, Ibadan, Nigeria.
Olusegun George AdemowoDepartment of Pharmacology and Therapeutics, College of Medicine, University of Ibadan; Institute for Advanced Medical Research and Training, College of Medicine, Ibadan, Nigeria.
Ayodele Samuel JegedeDepartment of Sociology, Faculty of the Social Sciences, University of Ibadan, Ibadan, Nigeria.
Ebenezer BabaMalaria Consortium Regional Office for Africa, Kampala, Uganda.
Prudence HamadeMalaria Consortium, London, United Kingdom.
Jayne WebsterLondon School of Tropical Medicine and Hygiene, London, United Kingdom.
Daniel ChandramohanLondon School of Tropical Medicine and Hygiene, London, United Kingdom.
Catherine Olufunke FaladeDepartment of Pharmacology and Therapeutics, College of Medicine, University of Ibadan; Institute for Advanced Medical Research and Training, College of Medicine, Ibadan, Nigeria.
University of Ibadan · NGLondon School of Hygiene & Tropical Medicine · GBBabcock University · NGMalaria Consortium · UGMalaria Consortium · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Context and Aim: Given the challenges of microscopy, we compared its performance with SD-Bioline malaria rapid diagnostic test (MRDT) and polymerase chain reaction (PCR) and evaluated the time it took for positive results to become negative after treatment of children with acute uncomplicated malaria. Subjects and Methods: We present the report of 485 participants with complete MRDT, microscopy, and PCR data out of 511 febrile children aged 3-59 months who participated in a cohort study over a 12-month period in rural and urban areas of Ibadan, Nigeria. MRDT-positive children received antimalaria and tested at every visit over 28 days. Speciation was also carried out by PCR. Results: With microscopy as the gold standard, SD-Bioline™ had 95.2% sensitivity, 66.4% specificity, 67.5% positive predictive value (PPV), and 94.9 negative predictive value (NPV), while with PCR the findings were 84.3% sensitivity, 66.5% specificity, 72.7% PPV, and 80.1% NPV. PCR speciation of malaria parasites revealed 91.6% Plasmodium falciparum, 18.9% Plasmodium malariae, and 4.4% Plasmodium ovale. Among the 47 children with P. malariae infections, 66.0% were coinfected with P. falciparum, while 54.6% cases of P. ovale occurred as coinfections with P. falciparum. The median time to a negative MRDT was 23.2 days, while the median time to a negative malaria microscopy was 3.8 days. The two survival curves were significantly different. Conclusions: The SD-Bioline

Indexed as

MalariaMalaria, FalciparumChildCohort StudiesHumansNigeriaPlasmodium falciparumRapid Diagnostic TestsSensitivity and SpecificityMalariamicroscopyNigeriapolymerase chain reactionrapid diagnostic testspeciation

Identifiers

PMID38358148
PMCPMC10775936
OpenAlexW4385060878

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.