Evidence map›Paper›PMID 30589853›Full record

ArticlePloS one2018

The use of Fionet technology for external quality control of malaria rapid diagnostic tests and monitoring health workers' performance in rural military health facilities in Tanzania.

Akili K Kalinga, Deus S Ishengoma, Reginald Kavishe, Lucky Temu, Christopher Mswanya, Charles Mwanziva, Erick J Mgina, Sarah Chiduo, Lucas Mahikwano, Saidi Mgata and 10 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 10 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

20 authors at 3 institutions in 2 countries.

Akili K KalingaNational Institute for Medical Research, Tukuyu Centre, Tukuyu, Tanzania.ORCID 0000-0003-1884-3869
Deus S IshengomaNational Institute for Medical Research, Tanga Centre, Tanga, Tanzania.
Reginald KavisheKilimanjaro Christian Medical University College, Moshi, Tanzania.
Lucky TemuHenry Jackson Foundation Medical Research International, Dar es Salaam, Tanzania.
Christopher MswanyaTanzania Peoples Defense Forces, Dar es Salaam, Tanzania.
Charles MwanzivaTanzania Peoples Defense Forces, Dar es Salaam, Tanzania.
Erick J MginaNational Institute for Medical Research, Tukuyu Centre, Tukuyu, Tanzania.ORCID 0000-0002-3940-9458
Sarah ChiduoHenry Jackson Foundation Medical Research International, Dar es Salaam, Tanzania.
Lucas MahikwanoHenry Jackson Foundation Medical Research International, Dar es Salaam, Tanzania.
Saidi MgataHenry Jackson Foundation Medical Research International, Dar es Salaam, Tanzania.
Lalaine AnovaWalter Reed Army Institute of Research, MD, Washington DC, United States of America.
George AmooFORGYN Health Systems Consultants LLc, Washington DC, United States of America.
Eyako WurapaWalter Reed Army Institute of Research, MD, Washington DC, United States of America.
Brian VeselyWalter Reed Army Institute of Research, MD, Washington DC, United States of America.
Edwin KamauWalter Reed Army Institute of Research, MD, Washington DC, United States of America.
Mark HickmanWalter Reed Army Institute of Research, MD, Washington DC, United States of America.
Norman WatersWalter Reed Army Institute of Research, MD, Washington DC, United States of America.
Mara Kreishman-DeitrickWalter Reed Army Institute of Research, MD, Washington DC, United States of America.
Robert ParisWalter Reed Army Institute of Research, MD, Washington DC, United States of America.
Colin OhrtWalter Reed Army Institute of Research, MD, Washington DC, United States of America.
Walter Reed Army Institute of Research · USKilimanjaro Christian Medical Centre · TZNational Institute for Medical Research · TZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionInternal and external quality control (QC) of rapid diagnostic tests (RDTs) is important to increase reliability of RDTs currently used to diagnose malaria. However, cross-checking of used RDTs as part of quality assurance can rarely be done by off-site personnel because there is no guarantee of retaining visible test lines after manufacturers' recommended reading time. Therefore, this study examined the potential of using Fionet™ technology for remote RDT quality monitoring at seven clinics, identifying reasons for making RDT processing and interpretation errors, and taking corrective actions for improvement of diagnosis and consequently improved management of febrile patients.

methodsThe study was conducted at seven military health facilities in Mainland Tanzania and utilized RDTs capable of detecting Plasmodium falciparum specific Histidine-rich protein 2 (Pf-HRP2) and the genus specific Plasmodium lactate dehydrogenase (pLDH) for other species of plasmodium (P. vivax, P. malariae or P. ovale; pan-pLDH). Patients' data and images of processed RDTs from seven clinics were uploaded on a Fionet web portal and reviewed regularly to monitor preparation procedures and visual interpretation of test results compared to automated analysis using the Deki reader of RDT. Problems detected were rapidly communicated to remote laboratory personnel at the clinic for corrective action and follow-up of patients who were falsely diagnosed as negative and missed treatment. Factors contributing to making errors in visual interpretation of RDT results were analyzed during visits to the health facilities.

resultsA total of 1,367 (1.6%) out of 83,294 RDT test images uploaded to the Fionet portal had discordant test results of which 822 (60.1%) and 545 (39.9%) were falsely reported as negative and positive, respectively. False negative and false positive test results were common for a single test line in 515 (62.7%) and 741 (54.2%) tests, respectively. Out of 1,367 RDT images assessed, 98 (7.2%) had quality problems related to preparation procedures of which 95(96.9%) errors were due to putting too much blood on the sample well or insufficient buffer in the respective wells. The reasons for discrepant results included, false reporting of none existent lines in 526 (38.5%) tests, missing a faint positive line in 493 (36.1%), missing a strong positive line in 248(18.1%) and errors caused by poorly processed RDTs in 96 (7.2%) tests. Among the false negative tests (n = 822), 669 (48.9%) patients were eligible for follow-up and only 339 (48.5%) were reached and 291 (85.8%) received appropriate anti-malaria therapy.

conclusionFionet technology enabled remote monitoring of RDT quality issues, identifying reasons contributing to laboratory personnel making errors and provided a rapid method to implement corrective actions at remote sites to improve malaria diagnosis and consequently improved health care management of febrile patients infected with malaria.

Indexed as

Diagnostic Tests, RoutineHealth PersonnelTask Performance and AnalysisAdolescentAdultAntigens, ProtozoanChildChild, PreschoolDiagnostic ErrorsFemaleHealth FacilitiesHumansInfantInfant, NewbornL-Lactate DehydrogenaseMalariaAntigens, ProtozoanHRP-2 antigen, Plasmodium falciparumL-Lactate DehydrogenaseProtozoan Proteins

Identifiers

PMID30589853
PMCPMC6307929
OpenAlexW2908074322

What OpenQuestion holds

Textmetadata
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.