Evidence map›Paper›PMID 40264936›Full record

ArticleFrontiers in cellular and infection microbiology2025

A retrospective analysis comparing metagenomic next-generation sequencing with conventional microbiology testing for the identification of pathogens in patients with severe infections.

Fei Hou, Yanting Qiao, Yuanyuan Qiao, Ya Shi, Mingrui Chen, Min Kong, Xiaohang Hu, Liqing Jiang, Xiaowei Liu

Abstract readComparative Study
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

9 authors.

Fei HouMedical Laboratory of Jining Medical University, Jining Medical University, Jining, Shandong, China.
Yanting QiaoDepartment of Critical Care Medicine, The Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Yuanyuan QiaoDepartment of Critical Care Medicine, The Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Ya ShiDepartment of Critical Care Medicine, The Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Mingrui ChenDepartment of Critical Care Medicine, The Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Min KongMedical Laboratory of Jining Medical University, Jining Medical University, Jining, Shandong, China.
Xiaohang HuDepartment of Clinical Laboratory, The Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Liqing JiangDepartment of Clinical Laboratory, The Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Xiaowei LiuDepartment of Critical Care Medicine, The Affiliated Hospital of Jining Medical University, Jining, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The application value of metagenomic next-generation sequencing (mNGS) in detecting pathogenic bacteria was evaluated to promote the rational and accurate use of antibiotics. A total of 180 patients with severe infections were included in this study. Methods: Based on their different symptoms, bronchoalveolar lavage fluid (BALF) or blood samples were collected for conventional microbiological testing (CMT) and mNGS. Results: The results indicated that the etiological diagnosis rate of mNGS (78.89%) was significantly higher than that of CMT (20%) (p<0.001). Notably, mNGS exhibited greater sensitivity towards rare pathogens such as Chlamydia pneumoniae, Mycobacterium tuberculosis complex, and Legionella pneumophila, which were undetectable by CMT. Additionally, 64 cases underwent blood culture, BALF culture, and mNGS testing. Analysis revealed that the positive rate of blood culture (3.1%) was lower than that of BALF (25%), and the positive rate of CMT from both types was significantly lower than that of mNGS (89.1%) (p<0.001). In this study, 168 mNGS results were accepted, and 116 patients had their antibiotic therapy adjustment based on mNGS. Paired analysis indicated that white blood cell count (WBC), procalcitonin (PCT), C-reactive protein (CRP), and neutrophil (NEU) percentage provided valuable therapeutic guidance. The survival rate of patients was 55.36%, influenced by patient physical condition and age. Discussion: Our data indicated that mNGS had significant auxiliary value in the clinical diagnosis and treatment for critically ill patients, especially for those with negative CMT results and clinically undefined infections. mNGS could broaden the detection scope, especially for special pathogens, and improve the detection rate, providing powerful assistance for early clinical diagnosis and treatment.

Indexed as

BacteriaBacterial InfectionsHigh-Throughput Nucleotide SequencingMetagenomicsAdultAgedAged, 80 and overAnti-Bacterial AgentsBronchoalveolar Lavage FluidFemaleHumansMaleMiddle AgedRetrospective StudiesYoung AdultAnti-Bacterial Agentsbloodbronchial alveolar lavage fluidconventional microbiological testingdetection of pathogensmetagenomic next-generation sequencingsevere infections

Identifiers

PMID40264936
PMCPMC12011730

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.