Evidence map›Paper›PMID 40181528›Full record

ArticleClinical and translational medicine2025

Clinical implement of Probe-Capture Metagenomics in sepsis patients: A multicentre and prospective study.

Qin Sun, Ran Teng, Qiankun Shi, Yun Liu, Xing Cai, Bin Yang, Quan Cao, Chang Shu, Xu Mei, Weiqi Zeng and 4 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in Clinical and translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03760315 (Department of Critical Care Medicine, Nanjing Zhong-Da Hospital, Southeast University School of Medicine,China;), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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.

NCT03760315 unknown statusnot on this map

Department of Critical Care Medicine, Nanjing Zhong-Da Hospital, Southeast University School of Medicine,China;

TypeobservationalSponsorSoutheast University, ChinaRan2022 to 2022Enrolled210ConditionsSepsisArmsblood mNGS (IDSeqTM Ultra), blood Culture
3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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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

14 authors.

Qin Sun *Jiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Ran Teng *Jiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Qiankun Shi *Department of Intensive Care Unit, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Yun Liu *Department of Critical Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Xing Cai *Department of Critical Care Medicine, Northern Jiangsu People's Hospital, Clinical Medical College, Yangzhou University, Yangzhou, China.
Bin Yang *Center for Infectious Diseases, Vision Medicals Co., Ltd, Guangzhou, China.
Quan CaoDepartment of Critical Care Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Chang ShuDepartment of Intensive Care Unit, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Xu MeiCenter for Infectious Diseases, Vision Medicals Co., Ltd, Guangzhou, China.
Weiqi ZengCenter for Infectious Diseases, Vision Medicals Co., Ltd, Guangzhou, China.
Bingxue HuCenter for Infectious Diseases, Vision Medicals Co., Ltd, Guangzhou, China.ORCID 0000-0001-9116-6249
Junyi ZhangJiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Haibo QiuJiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Ling LiuJiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.

Funding

Hongmian Plan' Project of Guangzhou HMJH-2020-0005Jiangsu Provincial Medical Key Laboratory ZDXYS202205National Key Research and Development Program of China 2022YFC2504405National Natural Science Foundation of China 81930058National Natural Science Foundation of China 82270083National Natural Science Foundation of China 82341032Second Level Talents of the '333 High Level Talents Training Project' in the sixth phase in Jiangsu LGY2022025
6 · The paper itself

Abstract

backgroundAccurate pathogen identification is critical for managing sepsis. However, traditional microbiological methods are time-consuming and exhibit limited sensitivity, particularly with blood samples. Metagenomic sequencing of plasma or whole blood was highly affected by the proportion of host nucleic acid.

methodsWe developed a Probe-Capture Metagenomic assay and established a multicentre prospective cohort to assess its clinical utility. In this study, 184 blood samples from patients suspected of sepsis were sent for blood culture and Probe-Capture Metagenomic sequencing before using antibiotics. The pathogen-positive rate and auxiliary abilities in diagnosis were compared among Probe-Capture Metagenomics, blood culture and real-time PCR (RT-PCR). Antibiotic therapy adjustments were based on the identification of pathogens, and changes in the Sequential Organ Failure Assessment (SOFA) score were monitored on days 0, 3 and 7 of admission.

resultsA total of 184 sepsis patients were enrolled, with a mean age of 66 years (range 56-74). The Probe-Capture Metagenomics method, confirmed by RT-PCR, demonstrated a significantly higher pathogen detection rate than blood culture alone (51.6% vs. 17.4%, p < .001). When combining the results of blood culture and RT-PCR, Probe-Capture Metagenomics achieved a concordance rate of 91.8% (169/184), with a sensitivity of 100% and specificity of 87.1%. In terms of clinical impact, antibiotic therapy was adjusted for 64 patients (34.8%) based on the results from Probe-Capture Metagenomics, and 41 patients (22.3%) showed a > 2-point decrease in SOFA score following antibiotic adjustments.

conclusionProbe-Capture Metagenomics significantly enhances the ability of pathogen detection compared with traditional metagenomics. Compared to blood culture and RT-PCR in sepsis patients, it leads to improved antibiotic treatment and better patient outcomes. This study, for the first time, evaluates the clinical impact of metagenomic sequencing by integrating antibiotic adjustments and SOFA score changes, indicating that approximately one-fifth of sepsis patients benefit from this advanced diagnostic approach.

trial registrationThis study has been registered in clinical trials (clinicaltrials.gov) on 30 November 2018, and the registration number is NCT03760315. KEY POINTS: Probe-Capture Metagenome had a significantly higher positive rate than blood culture (51.6% vs. 17.4%, p < .001). Combining blood culture and RT-PCR results, Probe-Capture Metagenome achieved a consistency rate of 91.8%. Antibiotics were adjusted in 34.8% of patients based on Probe-Capture Metagenome results, and 22.3% of patients experienced a more than 2-point decrease in SOFA score.

Indexed as

MetagenomicsSepsisAgedBlood CultureFemaleHumansMaleMiddle AgedProspective Studiesantibiotics adjustmentclinical impactdiagnosismetagenomicssepsis

Identifiers

PMID40181528
PMCPMC11968419

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Registered trials

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.