Evidence map›Paper›PMID 41410682›Full record

ArticleJournal of clinical microbiology2026

Development of a dual-target measles virus PCR assay and testing trends at a national reference laboratory.

Cole Anderson, Megha Rawal, Weston Hymas, Patricia Slev, Benjamin T Bradley

Abstract readValidation Study
In one paragraph

Article in Journal of clinical microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

5 authors.

Cole AndersonDepartment of Pathology, University of Utah, Salt Lake City, Utah, USA.
Megha RawalARUP Laboratories, Salt Lake City, Utah, USA.
Weston HymasARUP Laboratories, Salt Lake City, Utah, USA.
Patricia SlevDepartment of Pathology, University of Utah, Salt Lake City, Utah, USA.
Benjamin T BradleyDepartment of Pathology, University of Utah, Salt Lake City, Utah, USA.ORCID 0000-0002-8064-9314

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In 2025, measles cases in the United States have reached their highest level since the disease was officially declared eliminated in 2000. Molecular assays may assist in the early diagnosis of measles and improve contact tracing efforts. In this manuscript, we describe the validation of a real-time PCR assay on the Hologic Panther Fusion Open Access system for the detection of measles virus (MeV) and differentiation between wild-type and vaccine strains. After implementation, we examined 3 months of clinical testing data to understand testing trends and utilization. Over the study period, a total of 525 tests from 491 patients were performed. MeV was detected in 16 specimens with 6 wild-type and 10 vaccine strain identifications. Children less than 10 years old constituted the largest proportion of tested individuals (54.3%) and vaccine strain detections (9/10, median age 1.2 years), while wild-type infections were observed in individuals aged 20-50 (6/6, median age 32.6 years). Those with vaccine strain detected had significantly higher Ct values for the pan-measles target versus wild-type infections (33.6 vs 28.3;

Indexed as

MeaslesMeasles virusMolecular Diagnostic TechniquesReal-Time Polymerase Chain ReactionAdolescentAdultChildChild, PreschoolFemaleHumansInfantMaleMeasles VaccineMiddle AgedUnited StatesYoung AdultMeasles Vaccineassay developmentgenotype AmeaslesPCRvaccine strain

Identifiers

PMID41410682
PMCPMC12802152

What OpenQuestion holds

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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.