Evidence map›Paper›PMID 35507552›Full record

ArticlePLoS neglected tropical diseases2022

Combining rapid diagnostic tests to estimate primary and post-primary dengue immune status at the point of care.

Joseph R Biggs, Ava Kristy Sy, James Ashall, Marsha S Santoso, Oliver J Brady, Mary Anne Joy Reyes, Mary Ann Quinones, William Jones-Warner, Amadou O Tandoc, Nemia L Sucaldito and 23 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

5 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

33 authors at 11 institutions in 7 countries.

Joseph R BiggsDepartment of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0001-7273-874X
Ava Kristy SyDepartment of Virology, Research Institute for Tropical Medicine, Manila, Philippines.
James AshallDepartment of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Marsha S SantosoDengue Research Unit, Eijkman Institute for Molecular Biology, National Agency for Research and Innovation of the Republic of Indonesia, Jakarta, Indonesia.
Oliver J BradyDepartment of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Mary Anne Joy ReyesDepartment of Virology, Research Institute for Tropical Medicine, Manila, Philippines.
Mary Ann QuinonesDepartment of Virology, Research Institute for Tropical Medicine, Manila, Philippines.
William Jones-WarnerDepartment of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Amadou O TandocDepartment of Virology, Research Institute for Tropical Medicine, Manila, Philippines.
Nemia L SucalditoPhilippine Epidemiology Bureau, Department of Health, Manila, Philippines.
Huynh Kim MaiPasteur Institute of Nha Trang, Nha Trang, Vietnam.
Le Thuy LienPasteur Institute of Nha Trang, Nha Trang, Vietnam.
Hung Do ThaiPasteur Institute of Nha Trang, Nha Trang, Vietnam.
Hien Anh Thi NguyenNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Dang Duc AnhNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Chihiro IwasakiPaediatric Infectious Diseases Department, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Noriko KitamuraPaediatric Infectious Diseases Department, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Marnix Van LoockJanssen Global Public Health, Janssen Pharmaceutica NV, Beerse, Belgium.
Guillermo Herrera-TaracenaJanssen Global Public Health, Janssen Research & Development, Horsham, Pennsylvania, United States of America.
Joris MentenQuantitative Sciences, Janssen Pharmaceutica NV, Beerse, Belgium.
Freya RasschaertJanssen Global Public Health, Janssen Pharmaceutica NV, Beerse, Belgium.
Liesbeth Van WesenbeeckJanssen Global Public Health, Janssen Pharmaceutica NV, Beerse, Belgium.
Sri MasyeniDepartment of Internal Medicine, Faculty of Medicine and Health Sciences, Universitas Warmadewa, Denpasar, Bali, Indonesia.
Sotianingsih HaryantoRaden Mattaher Hospital, Jambi, Indonesia.
Benediktus YohanDengue Research Unit, Eijkman Institute for Molecular Biology, National Agency for Research and Innovation of the Republic of Indonesia, Jakarta, Indonesia.
Eva Cutiongco-de la PazInstitute of Human Genetics, University of the Philippines, Manila, Philippines.
Lay-Myint YoshidaPaediatric Infectious Diseases Department, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Stephane HueDepartment of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Maria Rosario Z CapedingDengue Study Group, Research Institute for Tropical Medicine, Manila, Philippines.
Carmencita D PadillaInstitute of Human Genetics, University of the Philippines, Manila, Philippines.
R Tedjo SasmonoDengue Research Unit, Eijkman Institute for Molecular Biology, National Agency for Research and Innovation of the Republic of Indonesia, Jakarta, Indonesia.
Julius Clemence R HafallaDepartment of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Martin L HibberdDepartment of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
London School of Hygiene & Tropical Medicine · GBResearch Institute for Tropical Medicine · PHJanssen (Belgium) · BEEijkman Institute for Molecular Biology · IDInstitute of Vaccine and Medical Biologicals · VNNagasaki University · JPNational Institute Of Hygiene And Epidemiology · VNUniversity of the Philippines Manila · PHDepartment of Health · PHJanssen (United States) · USWarmadewa University · ID

Funding

Medical Research Council MR/V031112/1Wellcome Trust 206471/Z/17/Z
6 · The paper itself

Abstract

backgroundCharacterising dengue virus (DENV) infection history at the point of care is challenging as it relies on intensive laboratory techniques. We investigated how combining different rapid diagnostic tests (RDTs) can be used to accurately determine the primary and post-primary DENV immune status of reporting patients during diagnosis. METHODS AND

findingsSerum from cross-sectional surveys of acute suspected dengue patients in Indonesia (N:200) and Vietnam (N: 1,217) were assayed using dengue laboratory assays and RDTs. Using logistic regression modelling, we determined the probability of being DENV NS1, IgM and IgG RDT positive according to corresponding laboratory viremia, IgM and IgG ELISA metrics. Laboratory test thresholds for RDT positivity/negativity were calculated using Youden's J index and were utilized to estimate the RDT outcomes in patients from the Philippines, where only data for viremia, IgM and IgG were available (N:28,326). Lastly, the probabilities of being primary or post-primary according to every outcome using all RDTs, by day of fever, were calculated. Combining NS1, IgM and IgG RDTs captured 94.6% (52/55) and 95.4% (104/109) of laboratory-confirmed primary and post-primary DENV cases, respectively, during the first 5 days of fever. Laboratory test predicted, and actual, RDT outcomes had high agreement (79.5% (159/200)). Among patients from the Philippines, different combinations of estimated RDT outcomes were indicative of post-primary and primary immune status. Overall, IgG RDT positive results were confirmatory of post-primary infections. In contrast, IgG RDT negative results were suggestive of both primary and post-primary infections on days 1-2 of fever, yet were confirmatory of primary infections on days 3-5 of fever.

conclusionWe demonstrate how the primary and post-primary DENV immune status of reporting patients can be estimated at the point of care by combining NS1, IgM and IgG RDTs and considering the days since symptoms onset. This framework has the potential to strengthen surveillance operations and dengue prognosis, particularly in low resource settings.

Indexed as

DengueDengue VirusAntibodies, ViralCross-Sectional StudiesDiagnostic Tests, RoutineFeverHumansImmunoglobulin GImmunoglobulin MPoint-of-Care SystemsSensitivity and SpecificityViral Nonstructural ProteinsViremiaAntibodies, ViralImmunoglobulin GImmunoglobulin MViral Nonstructural Proteins

Identifiers

PMID35507552
PMCPMC9067681
OpenAlexW4229038149

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.