Evidence map›Paper›PMID 40205516›Full record

ArticleMalaria journal2025

Performance of rapid diagnostic tests, microscopy, and qPCR for detection of Plasmodium parasites among community members with or without symptoms of malaria in villages located in North-western Tanzania.

Rule Budodo, Salehe S Mandai, Catherine Bakari, Misago D Seth, Filbert Francis, Gervas A Chacha, Angelina J Kisambale, Daniel P Challe, Daniel A Petro, Dativa Pereus and 11 more

Abstract read
In one paragraph

Article in Malaria journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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

8 citing papers in PubMed.

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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

21 authors.

Rule BudodoNational Institute for Medical Research, Dar es Salaam, Tanzania.
Salehe S MandaiNational Institute for Medical Research, Dar es Salaam, Tanzania.
Catherine BakariNational Institute for Medical Research, Dar es Salaam, Tanzania.
Misago D SethNational Institute for Medical Research, Dar es Salaam, Tanzania.
Filbert FrancisNational Institute for Medical Research, Tanga Research Centre, Tanga, Tanzania.
Gervas A ChachaNational Institute for Medical Research, Dar es Salaam, Tanzania.
Angelina J KisambaleNational Institute for Medical Research, Dar es Salaam, Tanzania.
Daniel P ChalleNational Institute for Medical Research, Tanga Research Centre, Tanga, Tanzania.
Daniel A PetroUniversity of Dar es Salaam, Dar es Salaam, Tanzania.
Dativa PereusNational Institute for Medical Research, Dar es Salaam, Tanzania.
Rashid A MadebeNational Institute for Medical Research, Dar es Salaam, Tanzania.
Ruth B MbwamboNational Institute for Medical Research, Dar es Salaam, Tanzania.
Ramadhan MoshiNational Institute for Medical Research, Dar es Salaam, Tanzania.
Sijenunu AaronNational Malaria Control Programme, Dodoma, Tanzania.
Daniel MbwamboNational Malaria Control Programme, Dodoma, Tanzania.
Abdallah LusasiNational Malaria Control Programme, Dodoma, Tanzania.
Stella KajangePresident's Office, Regional Administration and Local Government, Dodoma, Tanzania.
Samwel LazaroNational Malaria Control Programme, Dodoma, Tanzania.
Ntuli KapologweDirectorate of Preventive Services, Ministry of Health, Dodoma, Tanzania.
Celine I MandaraNational Institute for Medical Research, Dar es Salaam, Tanzania.
Deus S IshengomaNational Institute for Medical Research, Dar es Salaam, Tanzania. deusishe@yahoo.com.

Funding

Bill and Melinda Gates Foundation Grant number 002202
6 · The paper itself

Abstract

backgroundDespite the implementation of different control interventions, Plasmodium parasite infections in the communities (among asymptomatic and symptomatic individuals) still play a crucial role in sustaining malaria transmission. This study evaluated the performance of rapid diagnostic tests (RDTs), microscopy, and quantitative PCR (qPCR) in detecting Plasmodium parasites among community members in five villages of Kyerwa district, Kagera region in north-western Tanzania.

methodsThe study used samples and data collected during a community cross-sectional survey of asymptomatic and symptomatic participants (n = 4454) aged ≥ 6 months which was conducted in July and August 2023. Plasmodium parasites were detected using RDTs, microscopy, and qPCR (targeting 18S rRNA gene). The performance of RDTs and microscopy was assessed by sensitivity, specificity, and predictive values, using qPCR as the reference method. Factors affecting the accuracy of these methods were determined using a multivariate logistic regression model.

resultsThe prevalence of Plasmodium parasite infections among 4454 participants was 44.4%, 32.1%, and 39.8% by RDTs, microscopy, and qPCR, respectively. The prevalence of Plasmodium falciparum, Plasmodium malariae and Plasmodium ovale mono-infection by microscopy was 28.7%, 0.2%, and 0.3%, while by qPCR it was 35.3%, 0.4% and 0.5%, respectively. The geometric mean parasite densities (GMPDs) by microscopy were 642 (95% confidence intervals (CI) = 570-723), 126 (95% CI = 98-162), and 124 (95% CI = 82-160) asexual parasites/µL for P. falciparum, P. ovale spp., and P. malariae, respectively. By qPCR, the GMPDs were 1180 (95% CI = 1032-1349) parasites/µL for P. falciparum, 44 (95% CI = 32-61) for P. ovale spp., and 50 (95% CI = 29-89) for P. malariae. The sensitivity and specificity of RDTs were 94.0% (95% CI = 92.8-95.1%) and 87.5% (95% CI = 86.2-88.7%), respectively, whereas those of microscopy were 74.6% (95% CI = 72.5-76.6%) and 95.2% (95% CI = 94.3-96.0%), respectively. The sensitivity of RDTs, and microscopy was low at very low parasitaemia (< 100 parasites/μL) but increased significantly with increasing parasitaemia, reaching ≥ 99.6% at > 10,000 parasites/μL (p < 0.001).

conclusionHigh prevalence of Plasmodium parasites was detected, and the performance of RDTs and qPCR was comparable, but microscopy had lower performance. Higher sensitivity of RDTs compared to microscopy indicates that RDTs are effective for detection of infections caused by Plasmodium parasites in routine case management and surveillance in this area with confirmed artemisinin partial resistance (ART-R) and can be utilized in the ongoing plans to develop a response to ART-R.

Indexed as

Diagnostic Tests, RoutineMalariaMicroscopyPlasmodiumReal-Time Polymerase Chain ReactionAdolescentAdultAgedChildChild, PreschoolCross-Sectional StudiesFemaleHumansInfantMaleMiddle AgedArtemisinin partial resistancemalariaMicroscopyNorthwestern TanzaniaqPCRRapid diagnostic tests

Identifiers

PMID40205516
PMCPMC11984112

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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.