Evidence map›Paper›PMID 33059646›Full record

ArticleBMC pulmonary medicine2020

Optimal specimen type for accurate diagnosis of infectious peripheral pulmonary lesions by mNGS.

Qing Wang, Bo Wu, Donglin Yang, Chao Yang, Zhixian Jin, Jie Cao, Jing Feng

Open access · goldAbstract read
In one paragraph

Article in BMC pulmonary medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  18. Value of metagenomic next-generation sequencing in children with severe infectious diseases.Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2022
    Article
  19. Metagenomic next-generation sequencing may assist diagnosis of cat-scratch disease.Frontiers in cellular and infection microbiology · 2022
    Article
  20. 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 at 4 institutions in 1 country.

Qing WangDepartment of Respiratory and Critical Care Medicine, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Bo WuTransplantation Center, Nanjing Medical University, Affiliated Wuxi People's Hospital, Wuxi, 214023, China.
Donglin YangHematopoietic Stem Cell Transplantation Center, Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, 300052, China.
Chao YangRespiratory Department of Kunming Municipal First People's Hospital, Kunming, 650000, China.
Zhixian JinRespiratory Department of Kunming Municipal First People's Hospital, Kunming, 650000, China. jzx666999@163.com.
Jie CaoDepartment of Respiratory and Critical Care Medicine, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Jing FengDepartment of Respiratory and Critical Care Medicine, Tianjin Medical University General Hospital, Tianjin, 300052, China. zyyhxkfjing@126.com.
Tianjin Medical University General Hospital · CNThe First Hospital of Kunming · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNWuxi People's Hospital · CN

Funding

National Natural Science Foundation of China 81970083
6 · The paper itself

Abstract

backgroundReports on the application of metagenomic next-generation sequencing (mNGS) to the diagnosis of peripheral pulmonary lesions (PPLs) are scarce. There have been no studies investigating the optimal specimen type for mNGS.

methodsWe used mNGS to detect pathogens in matched transbronchial lung biopsy (TBLB), bronchoalveolar lavage fluid (BALF), and bronchial needle brushing (BB) specimens from 39 patients suspected of having infectious PPLs. We explored differences in microbial composition and diagnostic accuracy of mNGS for the 3 specimen types.

resultsmNGS was more sensitive than conventional culture for detection of bacteria and fungi in TBLB, BALF, and BB specimens, with no difference in the sensitivity of mNGS across the different specimen types. mNGS showed higher sensitivity for fungi or uncategorized pulmonary pathogens in TBLB+BALF+BB compared to TBLB but not BALF or BB specimens. There were no significant differences between the 3 specimen types in the relative abundance of pathogens, or between TBLB and BB specimens in the relative abundance of 6 common lower respiratory tract commensals.

conclusionsmNGS has a higher sensitivity than the conventional culture method for detecting pathogens in TBLB, BALF, or BB specimens. mNGS of BB samples is a less invasive alternative to TBLB for the diagnosis of infectious PPLs.

Indexed as

AdolescentAdultAgedBiopsyBronchoalveolar Lavage FluidBronchoscopyChinaFemaleHigh-Throughput Nucleotide SequencingHumansLungMaleMiddle AgedOutcome and Process Assessment, Health CareRespiratory Tract InfectionsRetrospective StudiesAnd bronchial needle brushingBronchoalveolar lavage fluid (BALF)Infectious peripheral pulmonary lesionsMetagenomic next-generation sequencing (mNGS)Transbronchial lung biopsy (TBLB)

Identifiers

PMID33059646
PMCPMC7566056
OpenAlexW3092874611

What OpenQuestion holds

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LicenceCC BY
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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.