Evidence map›Paper›PMID 34112116›Full record

ArticleBMC infectious diseases2021

Clinical application of cell-free next-generation sequencing for infectious diseases at a tertiary children's hospital.

Julianne Wilke, Nanda Ramchandar, Christopher Cannavino, Alice Pong, Adriana Tremoulet, Leidy Tovar Padua, Helen Harvey, Jennifer Foley, Lauge Farnaes, Nicole G Coufal

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

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  13. Which trial do we need? Plasma metagenomic next-generation sequencing to diagnose infections in patients with haematological malignancies and febrile neutropenia: proposal for a randomized-controlled trial.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2023
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  19. Molecular Methodologies for Improved Polymicrobial Sepsis Diagnosis.International journal of molecular sciences · 2022
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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

10 authors at 1 institution in 1 country.

Julianne Wilke *Department of Pediatrics, University of California, 3020 Children's Way, San Diego, CA, 92123, USA.
Nanda Ramchandar *Department of Pediatrics, University of California, 3020 Children's Way, San Diego, CA, 92123, USA.
Christopher CannavinoDepartment of Pediatrics, University of California, 3020 Children's Way, San Diego, CA, 92123, USA.
Alice PongDepartment of Pediatrics, University of California, 3020 Children's Way, San Diego, CA, 92123, USA.
Adriana TremouletDepartment of Pediatrics, University of California, 3020 Children's Way, San Diego, CA, 92123, USA.
Leidy Tovar PaduaDepartment of Pediatrics, University of California, 3020 Children's Way, San Diego, CA, 92123, USA.
Helen HarveyDepartment of Pediatrics, University of California, 3020 Children's Way, San Diego, CA, 92123, USA.
Jennifer FoleyDepartment of Pediatrics, Rady Children's Hospital of San Diego, San Diego, USA.
Lauge Farnaes *Department of Pediatrics, Rady Children's Hospital of San Diego, San Diego, USA.
Nicole G Coufal *Department of Pediatrics, University of California, 3020 Children's Way, San Diego, CA, 92123, USA. ncoufal@health.ucsd.edu.
Rady Children's Hospital-San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChildren affected by infectious diseases may not always have a detectable infectious etiology. Diagnostic uncertainty can lead to prolonged hospitalizations, inappropriately broad or extended courses of antibiotics, invasive diagnostic procedures, and difficulty predicting the clinical course and outcome. Cell-free plasma next-generation sequencing (cfNGS) can identify viral, bacterial, and fungal infections by detecting pathogen DNA in peripheral blood. This testing modality offers the ability to test for many organisms at once in a shotgun metagenomic approach with a rapid turnaround time. We sought to compare the results of cfNGS to conventional diagnostic test results and describe the impact of cfNGS on clinical care in a diverse pediatric population at a large academic children's hospital.

methodsWe performed a retrospective chart review of hospitalized subjects at a tertiary pediatric hospital to determine the diagnostic yield of cfNGS and its impact on clinical care.

resultsWe describe the clinical application of results from 142 cfNGS tests in the management of 110 subjects over an 8-month study period. In comparison to conventional testing as a reference standard, cfNGS was found to have a positive percent agreement of 89.6% and negative percent agreement of 52.3%. Furthermore, 32.4% of cfNGS results were directly applied to make a clinical change in management.

conclusionsWe demonstrate the clinically utility of cfNGS in the management of acutely ill children. Future studies, both retrospective and prospective, are needed to clarify the optimal indications for testing.

Indexed as

High-Throughput Nucleotide SequencingHospitals, PediatricAdolescentCell-Free Nucleic AcidsChildChild, PreschoolCommunicable DiseasesDiagnostic Tests, RoutineFemaleHumansMaleMetagenomeMetagenomicsRetrospective StudiesCell-Free Nucleic AcidsCell-free plasmaChildrenMetagenomicsNext-generation sequencing

Identifiers

PMID34112116
PMCPMC8192220
OpenAlexW3169665067

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.