Evidence map›Paper›PMID 42182834›Full record

ArticleOpen forum infectious diseases2026

Syndromic Multiplex Polymerase Chain Reaction: The Impact on Microbial Yield in Nonventilator Hospital-Acquired Pneumonia.

Jon Anders Feet, Karl Erik Müller, Øyvind Kommedal, Kathrine Brun, Elling Ulvestad, Harleen M S Grewal, Lars Heggelund

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Jon Anders FeetDepartment of Clinical Science, Bergen Integrated Diagnostic Stewardship Cluster, Faculty of Medicine, University of Bergen, Norway.ORCID https://orcid.org/0009-0008-4255-9327
Karl Erik MüllerDepartment of Clinical Science, Bergen Integrated Diagnostic Stewardship Cluster, Faculty of Medicine, University of Bergen, Norway.ORCID https://orcid.org/0000-0003-4020-9733
Øyvind KommedalDepartment of Clinical Science, Bergen Integrated Diagnostic Stewardship Cluster, Faculty of Medicine, University of Bergen, Norway.ORCID https://orcid.org/0000-0002-4390-0370
Kathrine BrunDepartment of Clinical Science, Bergen Integrated Diagnostic Stewardship Cluster, Faculty of Medicine, University of Bergen, Norway.
Elling UlvestadDepartment of Clinical Science, Bergen Integrated Diagnostic Stewardship Cluster, Faculty of Medicine, University of Bergen, Norway.ORCID https://orcid.org/0000-0001-5901-8422
Harleen M S GrewalDepartment of Clinical Science, Bergen Integrated Diagnostic Stewardship Cluster, Faculty of Medicine, University of Bergen, Norway.ORCID https://orcid.org/0000-0002-3380-1117
Lars HeggelundDepartment of Clinical Science, Bergen Integrated Diagnostic Stewardship Cluster, Faculty of Medicine, University of Bergen, Norway.ORCID https://orcid.org/0000-0002-1669-1032

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Nonventilator hospital-acquired pneumonia (NV-HAP) is a leading cause of hospital-acquired infection, associated with substantial morbidity and mortality. Conventional bacterial cultures from lower respiratory tract specimens, as recommended by current guidelines, have limited sensitivity and frequently fail to identify causative pathogens. This study evaluated a rapid, culture-independent molecular diagnostic approach versus standard methods for identifying microbial etiology, assessing antimicrobial prescribing, and determining NV-HAP incidence in a medium-sized Norwegian hospital. We hypothesized that multiplex polymerase chain reaction (mPCR) would shorten time to diagnosis and increase microbial yield. Method: A screening process twice daily was established to prospectively identify NV-HAP patients eligible for inclusion in a single hospital from 11 June 2021 to 26 November 2024. Lower respiratory tract samples were analyzed using a syndromic multiplex PCR assay and compared with conventional culture methods. Results: Eighty-six patients were included, with bacterial pathogens detected in 51.2% of the samples analyzed by mPCR and in 23.5% of cultured samples ( Conclusions: The use of syndromic mPCR provided faster results and a higher detection rate for microbial etiology compared to traditional culture methods.

Indexed as

antimicrobial resistanceantimicrobial therapyclinical coursemultiplex polymerase chain reactionnonventilator hospital-acquired pneumonia

Identifiers

PMID42182834
PMCPMC13195297

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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.