Evidence map›Paper›PMID 30819624›Full record

ArticleDiagnostic microbiology and infectious disease2019

Community-acquired pneumonia in children: cell-free plasma sequencing for diagnosis and management.

Lauge Farnaes, Julianne Wilke, Kathleen Ryan Loker, John S Bradley, Christopher R Cannavino, David K Hong, Alice Pong, Jennifer Foley, Nicole G Coufal

Open access · hybridAbstract read
In one paragraph

Article in Diagnostic microbiology and infectious disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
6.1field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 75 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Impact of direct from clinical sample sequencing assays for infectious diseases diagnostics: A single-centre retrospective cohort study.Journal of the Association of Medical Microbiology and Infectious Disease Canada = Journal officiel de l'Association pour la microbiologie medicale et l'infectiologie Canada · 2026
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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

9 authors at 1 institution in 1 country.

Lauge FarnaesUniversity of California San Diego, Department of Pediatrics, Division of Infectious Disease; Rady Children's Institute of Genomic Medicine. Electronic address: lfarnaes@rchsd.org.
Julianne WilkeUniversity of California San Diego, Department of Pediatrics, Division of Critical Care.
Kathleen Ryan LokerUniversity of California San Diego, Department of Pediatrics, Division of Infectious Disease.
John S BradleyUniversity of California San Diego, Department of Pediatrics, Division of Infectious Disease.
Christopher R CannavinoUniversity of California San Diego, Department of Pediatrics, Division of Infectious Disease.
David K HongKarius Inc. Redwood City, CA.
Alice PongUniversity of California San Diego, Department of Pediatrics, Division of Infectious Disease.
Jennifer FoleyUniversity of California San Diego, Department of Pediatrics, Division of Critical Care.
Nicole G CoufalUniversity of California San Diego, Department of Pediatrics, Division of Critical Care.
University of California, San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Community-acquired pneumonia (CAP) is a common cause of pediatric hospital admission. Empiric antibiotic therapy for hospitalized children with serious CAP now targets the most likely pathogen(s), including those that may demonstrate significant antibiotic resistance. Cell-free plasma next-generation sequencing (CFPNGS) was first made available for Pediatric Infectious Diseases physicians in June 1, 2017, to supplement standard-of-care diagnostic techniques. A retrospective chart review was performed for children hospitalized with CAP between June 1, 2017, and January 22, 2018, to evaluate the impact of CFPNGS. We identified 15 hospitalized children with CAP without other underlying medical conditions for whom CFPNGS was performed. CFPNGS identified a pathogen in 13 of 15 (86%) children compared with 47% for those using standard culture and PCR-based methods alone. Changes in antibiotic management were made in 7 of 15 (47%) of children as a result of CFPNGS.

Indexed as

Anti-Bacterial AgentsBacteriaChildChild, PreschoolCommunity-Acquired InfectionsDisease ManagementDNA, BacterialFemaleHigh-Throughput Nucleotide SequencingHumansInfantMaleMolecular Diagnostic TechniquesPlasmaPneumonia, BacterialRetrospective StudiesAnti-Bacterial AgentsDNA, BacterialCell-free plasma sequencingInfectious diseaseNGSPediatricPneumoniaPrecision medicine

Identifiers

PMID30819624
PMCPMC7125591
OpenAlexW2911464243

What OpenQuestion holds

Textmetadata
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.