Evidence map›Paper›PMID 42199547›Full record

ArticleFrontiers in microbiology2026

Comparison of targeted next-generation sequencing and conventional tests for pathogen detection in community-acquired and severe community-acquired pneumonia: a retrospective cohort study.

Feng Wang, Axiang Han, Wanting Hong, Ying Mao, Weijie Sun, Yixuan Hu, Lingling Lu

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Feng Wang *Department of Clinical Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Axiang Han *Department of Clinical Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Wanting HongInfection Technology Platform, Dian Diagnostics Group Co., Ltd., Hangzhou, China.
Ying MaoInfection Technology Platform, Dian Diagnostics Group Co., Ltd., Hangzhou, China.
Weijie SunDepartment of Clinical Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Yixuan HuInfection Technology Platform, Dian Diagnostics Group Co., Ltd., Hangzhou, China.
Lingling LuInfection Technology Platform, Dian Diagnostics Group Co., Ltd., Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Community-acquired pneumonia (CAP) and severe community-acquired pneumonia (sCAP) impose a significant burden on the healthcare system. As a more severe form of CAP, sCAP is associated with a higher mortality rate, and patients frequently require intensive care. Identifying clinical biomarkers to distinguish CAP from sCAP is expected to improve pneumonia management and patient outcomes. Targeted next-generation sequencing (tNGS) has considerable potential for pathogen detection and distinguishing microbial profile differences between CAP and sCAP. Methods: In this retrospective cohort study, we analyzed 380 bronchoalveolar lavage fluid (BALF) samples from patients diagnosed with CAP or sCAP who underwent both conventional tests (CTs) and tNGS to identify and compare the pathogen species and clinical consistency. Results: The results were as follows: tNGS demonstrated a significantly higher clinical consistency rate with the final diagnosis (83.02%) than CTs (38.37%), with a statistically significant difference ( Conclusion: Targeted next-generation sequencing demonstrated superior performance as a sensitive auxiliary diagnostic tool, which resulted in an increased pathogen identification rate and higher clinical diagnostic consistency. Although tNGS provides more comprehensive detection of etiological agents, clinical interpretation, diagnosis, and prediction require careful integration with conventional tests. The distinct clinical features, pathogen profiles, and pathogen composition between patients with CAP and those with sCAP highlight the need for a comprehensive diagnostic approach in pneumonia management.

Indexed as

clinical diagnostic consistencycommunity-acquired pneumoniaconventional testssevere community-acquired pneumoniatargeted next-generation sequencing

Identifiers

PMID42199547
PMCPMC13200559

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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.