Evidence map›Paper›PMID 37249984›Full record

ArticleFrontiers in cellular and infection microbiology2023

Time-series prediction and detection of potential pathogens in bloodstream infection using mcfDNA sequencing.

Yinghao Cao, Tingting Jiang, Yanfeng Lin, Xiaofeng Fang, Peipei Ding, Hongbin Song, Peng Li, Yanjun Li

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 35% of its field
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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Observational
  2. Review
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

8 authors at 4 institutions in 1 country.

Yinghao CaoDepartment of Clinical Laboratory Medicine, School of Medicine, South China University of Technology, Guangzhou, China.
Tingting JiangDepartment of Epidemiology and Biostatistics, School of Public Health, An Hui Medical University, Hefei, China.
Yanfeng LinBiosecurity Department, Chinese People's Liberation Army (PLA) Center for Disease Control and Prevention, Beijing, China.
Xiaofeng FangDepartment of Clinical Laboratory Medicine, School of Medicine, South China University of Technology, Guangzhou, China.
Peipei DingDepartment of Clinical Laboratory Medicine, The Sixth Medical Center of People's Liberation Army (PLA) General Hospital of Beijing, Beijing, China.
Hongbin SongDepartment of Epidemiology and Biostatistics, School of Public Health, An Hui Medical University, Hefei, China.
Peng LiBiosecurity Department, Chinese People's Liberation Army (PLA) Center for Disease Control and Prevention, Beijing, China.
Yanjun LiDepartment of Clinical Laboratory Medicine, School of Medicine, South China University of Technology, Guangzhou, China.
South China University of Technology · CNChinese Center For Disease Control and Prevention · CNAnhui Medical University · CNChinese People's Liberation Army · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Next-generation sequencing of microbial cell free DNA (mcfDNA-seq) has emerged as a promising diagnostic method for blood stream infection (BSI) and offers the potential to detect pathogens before blood culture. However, its application is limited by a lack of clinical validation. Methods: We conducted sequential mcfDNA-seq on blood samples from ICU participants at high risk of BSI due to pneumonia, or intravascular catheterization; and explored whether mcfDNA-seq could diagnose and detect pathogens in advance of blood culture positivity. Blood culture results were used as evaluation criteria. Results: A total of 111 blood samples were collected during the seven days preceding and on the day of onset of 16 BSI episodes from 13 participants. The diagnostic and total predictive sensitivity of mcfDNA-seq were 90% and 87.5%, respectively. The proportion of pathogenic bacteria was relatively high in terms of both diagnosis and prediction. The reads per million of etiologic agents trended upwards in the days approaching the onset of BSI. Discussion: Our work found that mcfDNA-seq has high diagnostic sensitivity and could be used to identify pathogens before the onset of BSI, which could help expand the clinical application of mcfDNA-seq.

Indexed as

Cell-Free Nucleic AcidsSepsisBacteriaHigh-Throughput Nucleotide SequencingHumansTime FactorsCell-Free Nucleic Acidsblood stream infectionmicrobial cell free DNAmicrobiologynext-generation sequencingpathogens

Identifiers

PMID37249984
PMCPMC10213887
OpenAlexW4376279238

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.