Evidence map›Paper›PMID 35755839›Full record

ArticleFrontiers in cellular and infection microbiology2022

Simultaneous Detection of Pathogens and Tumors in Patients With Suspected Infections by Next-Generation Sequencing.

Jiachun Su, Xu Han, Xiaogang Xu, Wenchao Ding, Ming Li, Weiqin Wang, Mi Tian, Xiyuan Chen, Binbin Xu, Zhongqing Chen and 8 more

Abstract readMulticenter Study
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Observational
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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

18 authors.

Jiachun SuInstitute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.
Xu HanResearch and Development Department, MatriDx Biotechnology Co., Ltd, Hangzhou, China.
Xiaogang XuInstitute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.
Wenchao DingResearch and Development Department, MatriDx Biotechnology Co., Ltd, Hangzhou, China.
Ming LiDepartment of Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Weiqin WangDepartment of Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Mi TianDepartment of Critical Care Medicine, Huashan Hospital, Fudan University, Shanghai, China.
Xiyuan ChenDepartment of Critical Care Medicine, Jing'an District Centre Hospital, Fudan University, Shanghai, China.
Binbin XuDepartment of Neurosurgery, Putuo District People's Hospital, Tongji University, Shanghai, China.
Zhongqing ChenDepartment of Pathology, Huashan Hospital, Fudan University, Shanghai, China.
Jinyi YuanInstitute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.
Xiaohua QinInstitute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.
Dongfang LinInstitute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.
Ruilan WangDepartment of Critical Care Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Ye GongDepartment of Critical Care Medicine, Huashan Hospital, Fudan University, Shanghai, China.
Liping PanDepartment of Critical Care Medicine, Jing'an District Centre Hospital, Fudan University, Shanghai, China.
Jun WangResearch and Development Department, MatriDx Biotechnology Co., Ltd, Hangzhou, China.
Minggui WangInstitute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Differential diagnosis of patients with suspected infections is particularly difficult, but necessary for prompt diagnosis and rational use of antibiotics. A substantial proportion of these patients have non-infectious diseases that include malignant tumors. This study aimed to explore the clinical value of metagenomic next-generation sequencing (mNGS) for tumor detection in patients with suspected infections. Methods: A multicenter, prospective case study involving patients diagnosed with suspected infections was conducted in four hospitals in Shanghai, China between July 2019 and January 2020. Based upon mNGS technologies and chromosomal copy number variation (CNV) analysis on abundant human genome, a new procedure named Onco-mNGS was established to simultaneously detect pathogens and malignant tumors in all of the collected samples from patients. Results: Of 140 patients screened by Onco-mNGS testing, 115 patients were diagnosed with infections; 17 had obvious abnormal CNV signals indicating malignant tumors that were confirmed clinically. The positive percent agreement and negative percent agreement of mNGS testing compared to clinical diagnosis was 53.0% (61/115) and 60% (15/25), Conclusion: This preliminary study demonstrates the feasibility and clinical value of using Onco-mNGS to simultaneously search for potential pathogens and malignant tumors in patients with suspected infections.

Indexed as

DNA Copy Number VariationsNeoplasmsChinaHigh-Throughput Nucleotide SequencingHumansMetagenomicsSensitivity and Specificitycopy number variationinfectionnext-generation sequencingpathogentumor

Identifiers

PMID35755839
PMCPMC9218804

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Registered trials

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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.