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Metagenomic next-generation sequencing diagnosis of peripheral pulmonary infectious lesions through virtual navigation, radial EBUS, ultrathin bronchoscopy, and ROSE

OBJECTIVE: To evaluate the efficacy of combined rapid on-site evaluation of cytology (ROSE), ultrathin bronchoscopy, virtual bronchoscopic navigation, radial endobronchial ultrasound (EBUS), and metagenomic next-generation sequencing (mNGS) for diagnosis of peripheral pulmonary infectious lesions. M...

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Autores principales: Liu, Nana, Kan, Jianying, Cao, Wenbin, Cao, Jie, Jiang, Erlie, Zhou, Yang, Zhao, Mingfeng, Feng, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833387/
https://www.ncbi.nlm.nih.gov/pubmed/31436107
http://dx.doi.org/10.1177/0300060519866953
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author Liu, Nana
Kan, Jianying
Cao, Wenbin
Cao, Jie
Jiang, Erlie
Zhou, Yang
Zhao, Mingfeng
Feng, Jing
author_facet Liu, Nana
Kan, Jianying
Cao, Wenbin
Cao, Jie
Jiang, Erlie
Zhou, Yang
Zhao, Mingfeng
Feng, Jing
author_sort Liu, Nana
collection PubMed
description OBJECTIVE: To evaluate the efficacy of combined rapid on-site evaluation of cytology (ROSE), ultrathin bronchoscopy, virtual bronchoscopic navigation, radial endobronchial ultrasound (EBUS), and metagenomic next-generation sequencing (mNGS) for diagnosis of peripheral pulmonary infectious lesions. METHODS: Specimens from patients with peripheral lung infection were obtained by transbronchial lung biopsy (TBLB) and bronchoalveolar lavage (BAL), and mNGS was used to detect pathogenic microorganisms. The sensitivity and specificity of mNGS were compared between TBLB tissue and BAL fluid. RESULTS: The most common pathogens of pulmonary infectious lesions in this study were Pseudomonas aeruginosa, Klebsiella pneumoniae, and Acinetobacter baumannii. The specificity of mNGS was higher in TBLB tissue than in BAL fluid, but mNGS of BAL fluid had higher sensitivity. CONCLUSIONS: The combination of ROSE, ultrathin bronchoscopy, virtual bronchoscopic navigation, radial EBUS, and mNGS technology yielded high efficacy for the diagnosis of peripheral pulmonary infectious lesions. TBLB and BAL specimens have respective advantages in specificity and sensitivity for mNGS analysis.
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spelling pubmed-68333872019-11-13 Metagenomic next-generation sequencing diagnosis of peripheral pulmonary infectious lesions through virtual navigation, radial EBUS, ultrathin bronchoscopy, and ROSE Liu, Nana Kan, Jianying Cao, Wenbin Cao, Jie Jiang, Erlie Zhou, Yang Zhao, Mingfeng Feng, Jing J Int Med Res Clinical Research Reports OBJECTIVE: To evaluate the efficacy of combined rapid on-site evaluation of cytology (ROSE), ultrathin bronchoscopy, virtual bronchoscopic navigation, radial endobronchial ultrasound (EBUS), and metagenomic next-generation sequencing (mNGS) for diagnosis of peripheral pulmonary infectious lesions. METHODS: Specimens from patients with peripheral lung infection were obtained by transbronchial lung biopsy (TBLB) and bronchoalveolar lavage (BAL), and mNGS was used to detect pathogenic microorganisms. The sensitivity and specificity of mNGS were compared between TBLB tissue and BAL fluid. RESULTS: The most common pathogens of pulmonary infectious lesions in this study were Pseudomonas aeruginosa, Klebsiella pneumoniae, and Acinetobacter baumannii. The specificity of mNGS was higher in TBLB tissue than in BAL fluid, but mNGS of BAL fluid had higher sensitivity. CONCLUSIONS: The combination of ROSE, ultrathin bronchoscopy, virtual bronchoscopic navigation, radial EBUS, and mNGS technology yielded high efficacy for the diagnosis of peripheral pulmonary infectious lesions. TBLB and BAL specimens have respective advantages in specificity and sensitivity for mNGS analysis. SAGE Publications 2019-08-22 2019-10 /pmc/articles/PMC6833387/ /pubmed/31436107 http://dx.doi.org/10.1177/0300060519866953 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Clinical Research Reports
Liu, Nana
Kan, Jianying
Cao, Wenbin
Cao, Jie
Jiang, Erlie
Zhou, Yang
Zhao, Mingfeng
Feng, Jing
Metagenomic next-generation sequencing diagnosis of peripheral pulmonary infectious lesions through virtual navigation, radial EBUS, ultrathin bronchoscopy, and ROSE
title Metagenomic next-generation sequencing diagnosis of peripheral pulmonary infectious lesions through virtual navigation, radial EBUS, ultrathin bronchoscopy, and ROSE
title_full Metagenomic next-generation sequencing diagnosis of peripheral pulmonary infectious lesions through virtual navigation, radial EBUS, ultrathin bronchoscopy, and ROSE
title_fullStr Metagenomic next-generation sequencing diagnosis of peripheral pulmonary infectious lesions through virtual navigation, radial EBUS, ultrathin bronchoscopy, and ROSE
title_full_unstemmed Metagenomic next-generation sequencing diagnosis of peripheral pulmonary infectious lesions through virtual navigation, radial EBUS, ultrathin bronchoscopy, and ROSE
title_short Metagenomic next-generation sequencing diagnosis of peripheral pulmonary infectious lesions through virtual navigation, radial EBUS, ultrathin bronchoscopy, and ROSE
title_sort metagenomic next-generation sequencing diagnosis of peripheral pulmonary infectious lesions through virtual navigation, radial ebus, ultrathin bronchoscopy, and rose
topic Clinical Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833387/
https://www.ncbi.nlm.nih.gov/pubmed/31436107
http://dx.doi.org/10.1177/0300060519866953
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