Evidence map›Paper›PMID 34259557›Full record

ArticlemSphere2021

Diagnostic Accuracy of Dried Blood Spots Collected on HemaSpot HF Devices Compared to Venous Blood Specimens To Estimate Measles and Rubella Seroprevalence.

Christine Prosperi, Ojas Kaduskar, Vaishali Bhatt, Alvira Z Hasan, Jeromie W Vivian Thangaraj, Muthusamy S Kumar, R Sabarinathan, Saravana Kumar, Augustine Duraiswamy, Gururaj Rao Deshpande and 14 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in mSphere, 2021. 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
0.9field-weighted citation impact, top 26% 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, 11 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

24 authors at 7 institutions in 2 countries.

Christine Prosperi *Department of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Ojas Kaduskar *Diagnostic Virology Group, ICMR-National Institute of Virology, Pune, Maharashtra, India.
Vaishali BhattDiagnostic Virology Group, ICMR-National Institute of Virology, Pune, Maharashtra, India.
Alvira Z HasanDepartment of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Jeromie W Vivian ThangarajIndian Council of Medical Researchgrid.19096.37 (ICMR)-National Institute of Epidemiology, Chennai, India.
Muthusamy S KumarIndian Council of Medical Researchgrid.19096.37 (ICMR)-National Institute of Epidemiology, Chennai, India.
R SabarinathanIndian Council of Medical Researchgrid.19096.37 (ICMR)-National Institute of Epidemiology, Chennai, India.
Saravana KumarIndian Council of Medical Researchgrid.19096.37 (ICMR)-National Institute of Epidemiology, Chennai, India.
Augustine DuraiswamyIndian Council of Medical Researchgrid.19096.37 (ICMR)-National Institute of Epidemiology, Chennai, India.
Gururaj Rao DeshpandeDiagnostic Virology Group, ICMR-National Institute of Virology, Pune, Maharashtra, India.
Ullas Padinjaremattathil ThankappanDiagnostic Virology Group, ICMR-National Institute of Virology, Pune, Maharashtra, India.
Sanjay L ChauhanDepartment of Operational Research, Indian Council of Medical Researchgrid.19096.37 (ICMR)-National Institute for Research in Reproductive Health (NIRRH), Mumbai, Maharashtra, India.
Ragini N KulkarniDepartment of Operational Research, Indian Council of Medical Researchgrid.19096.37 (ICMR)-National Institute for Research in Reproductive Health (NIRRH), Mumbai, Maharashtra, India.
Avi Kumar BansalDivision of Epidemiology, ICMR-National JALMA Institute for Leprosy & Other Mycobacterial Diseases, Agra, India.
Itta K ChaaithanyaDepartment of Operational Research, Indian Council of Medical Researchgrid.19096.37 (ICMR)-National Institute for Research in Reproductive Health (NIRRH), Mumbai, Maharashtra, India.
Neha R SalviDepartment of Health Research, Model Rural Health Research Unit Dahanu, Sub District Hospital Compound, Dahanu, Maharashtra, India.
Sandeep SharmaDivision of Epidemiology, ICMR-National JALMA Institute for Leprosy & Other Mycobacterial Diseases, Agra, India.
William J MossDepartment of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Lucky SangalWorld Health Organization, Southeast Asia Region Office, New Delhi, India.
Nivedita GuptaDivision of Epidemiology & Communicable Diseases, Indian Council of Medical Researchgrid.19096.37, New Delhi, India.
Manoj V MurherkarIndian Council of Medical Researchgrid.19096.37 (ICMR)-National Institute of Epidemiology, Chennai, India.
Sanjay M MehendaleDivision of Epidemiology & Communicable Diseases, Indian Council of Medical Researchgrid.19096.37, New Delhi, India.
Gajanan N Sapkal *Diagnostic Virology Group, ICMR-National Institute of Virology, Pune, Maharashtra, India.
Kyla Hayford *Department of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Indian Council of Medical Research · INICMR-National Institute of Virology · INJohns Hopkins University · USNational Institute for Research in Reproductive Health · INNational JALMA Institute for Leprosy & Other Mycobacterial Diseases · INDepartment of Health ResearchWorld Health Organization Regional Office for South-East Asia · IN

Funding

World Health Organization 001
6 · The paper itself

Abstract

Fingerprick blood spotted onto filter paper offers an alternative to venous blood for use in population-based surveillance because it is comparatively inexpensive, acceptable, and easy to manage in the field. Prior studies have shown excellent agreement for immunoglobulin G (IgG) antibody detection from dried blood spots (DBS) and venous blood samples. However, much of this evidence is from high-income settings or laboratories where the samples were unlikely to be exposed to extreme temperatures and humidity, factors known to degrade DBS. We report the diagnostic accuracy of DBS collected using HemaSpot HF devices against venous sera in measuring measles- and rubella-specific IgG antibodies in a household serosurvey conducted in two districts in India. Paired serum and DBS samples collected by fingerprick were collected from women aged 15 to 50 years enrolled in a serosurvey in Palghar District of Maharashtra and Kanpur Nagar District of Uttar Pradesh in India. Specimen quality and volume were assessed in the laboratory. Samples were tested for antimeasles and antirubella IgG antibodies by an enzyme-linked immunosorbent assay (ELISA) (Euroimmun). Sensitivity of antibody detection by DBS was greater than 98%, and specificity was 90% and 98%, for measles and rubella IgG, respectively. Antibody concentrations were strongly correlated between paired specimens with adequate volume (measles

Indexed as

AdolescentAdultAntibodies, ViralBlood Specimen CollectionDried Blood Spot TestingEnzyme-Linked Immunosorbent AssayFemaleHumansImmunoglobulin GImmunoglobulin MIndiaMeaslesMiddle AgedReproducibility of ResultsRubellaSeroepidemiologic StudiesAntibodies, ViralImmunoglobulin GImmunoglobulin Mrubella antibodiesdiagnostic accuracydried blood spotsELISAIndiameaslesrubellaserology

Identifiers

PMID34259557
PMCPMC8386429
OpenAlexW3178835630

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.