Evidence map›Paper›PMID 36085071›Full record

ArticleMalaria journal2022

Evaluation of HRP2 and pLDH-based rapid diagnostic tests for malaria and prevalence of pfhrp2/3 deletions in Aweil, South Sudan.

Emily Lynch, Tomas O Jensen, Bachir Assao, Menard Chihana, Thadeous Turuho, Dan Nyehangane, John B Manyok, Harriet Pasquale, Nimol Khim, Benoit Witkowski and 1 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 12 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

11 authors at 6 institutions in 6 countries.

Emily Lynch *Epicentre, 14-34 Avenue Jean Jaurès, Paris, France. Emily.Lynch@newyork.msf.org.
Tomas O Jensen *Médecins Sans Frontières, 14-34 Avenue Jean Jaurès, Paris, France.
Bachir AssaoEpicentre, Maradi, Niger.
Menard ChihanaEpicentre, Cape Town, South Africa.
Thadeous TuruhoEpicentre, Mbarara, Uganda.
Dan NyehanganeEpicentre, Mbarara, Uganda.
John B ManyokMédecins Sans Frontières - France, Aweil, South Sudan.
Harriet PasqualeNational Ministry of Health, Juba, South Sudan.
Nimol KhimMalaria Molecular Epidemiology Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Benoit WitkowskiMalaria Molecular Epidemiology Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Matthew E ColdironEpicentre, 14-34 Avenue Jean Jaurès, Paris, France.
Epicentre Uganda · UGInstitut Pasteur du Cambodge · KHCentre of Excellence for Health, Immunity and Infections · DKEpicentre (South Africa) · ZAMédecins Sans Frontières · FRUnited Nations Children's Fund Niger · NE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRapid diagnostic tests (RDT) for malaria are the primary tool for malaria diagnosis in sub-Saharan Africa but the utility of the most commonly used histidine-rich protein 2 (HRP2) antigen-based tests is limited in high transmission settings due to the long duration of positivity after successful malaria treatment. HRP2 tests are also threatened by the emergence of Plasmodium that do not carry pfhrp2 or pfhrp 3 genes. Plasmodium lactate dehydrogenase (pLDH)-based tests are promising alternatives, but less available. This study assessed the performances of HRP2 and pLDH(pan) tests under field conditions.

methodsThe study performed a prospective facility-based diagnostic evaluation of two malaria RDTs in Aweil, South Sudan, during the high transmission season. Capillary blood by fingerprick was collected from 800 children under 15 years of age with fever and no signs of severity. SD Bioline HRP2 and CareStart pLDH(pan) RDTs were performed in parallel, thick and thin smears for microscopy were examined, and dried blood was used for PCR testing.

resultsUsing microscopy as the gold standard, the sensitivity of both tests was estimated at  > 99%, but the specificity of each was lower: 55.0% for the pLDH test and 61.7% for the HRP2 test. When using PCR as the gold standard, the sensitivity of both tests was lower than the values assessed using microscopy (97.0% for pLDH and 96.5% for HRP2), but the specificity increased (65.1% for pLDH and 72.9% for HRP2). Performance was similar across different production lots, sex, and age. Specificity of both the pLDH and HRP2 tests was significantly lower in children who reported taking a therapeutic course of anti-malarials in the 2 months prior to enrollment. The prevalence of pfhrp2/3 deletions in the study population was 0.6%.

conclusionsThe low specificity of the pLDH RDT in this setting confirms previous results and suggests a problem with this specific test. The prevalence of pfhrp2/3 deletions in the study area warrants continued monitoring and underscores the relevance of assessing deletion prevalence nationally. Improved malaria RDTs for high-transmission environments are needed.

Indexed as

MalariaPlasmodiumChildDiagnostic Tests, RoutineHistidineHumansL-Lactate DehydrogenasePrevalenceProspective StudiesSouth SudanHistidineL-Lactate DehydrogenaseHistidine-rich protein 2MalariaPlasmodium lactate dehydrogenaseRapid diagnostic testSouth Sudan

Identifiers

PMID36085071
PMCPMC9461093
OpenAlexW4295494349

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.