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878. Clinical impact of plasma cell-free metagenomic next-generation sequencing: A retrospective cohort study 

BACKGROUND: Plasma cell-free metagenomic next-generation sequencing (cf-mNGS) offers potential for rapid, noninvasive diagnosis of complex infections, though clinical impact remains incompletely characterized. Here, we describe impacts on diagnosis and antimicrobial management among patients evaluat...

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Autores principales: Vasishta, Shilpa, Vo, Christopher, Neogi, Sushrita, Alahmdi, Bayan, Sullivan, Timothy, Gitman, Melissa R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676977/
http://dx.doi.org/10.1093/ofid/ofad500.923
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author Vasishta, Shilpa
Vo, Christopher
Neogi, Sushrita
Alahmdi, Bayan
Sullivan, Timothy
Gitman, Melissa R
author_facet Vasishta, Shilpa
Vo, Christopher
Neogi, Sushrita
Alahmdi, Bayan
Sullivan, Timothy
Gitman, Melissa R
author_sort Vasishta, Shilpa
collection PubMed
description BACKGROUND: Plasma cell-free metagenomic next-generation sequencing (cf-mNGS) offers potential for rapid, noninvasive diagnosis of complex infections, though clinical impact remains incompletely characterized. Here, we describe impacts on diagnosis and antimicrobial management among patients evaluated with plasma cf-mNGS. METHODS: Patients evaluated with plasma cf-mNGS (Karius®) in the Mount Sinai Health System from January 1, 2019 to December 23, 2022 were included. Cases were each reviewed independently in the medical record by two investigators using a standardized data collection form with discrepancies adjudicated collectively. Data were analyzed descriptively. RESULTS: Plasma cf-mNGS was sent for 37 patients of whom 29 (78%) were immunocompromised. 26 (70%) had prior invasive diagnostics. Median time from admission to NGS was 15 days. NGS was positive in 24 cases (65%), with results reflecting 20 bacterial infections, 9 viral, and 4 fungal (14 monomicrobial, 10 polymicrobial). Results were deemed clinically relevant in 18 cases (49%) including 12 positive and 6 negative tests. Testing led to antimicrobial changes in 11 cases (30%), discontinuation in 3 cases (8%), and no change in 23 cases (62%). After plasma cf-mNGS (compared with prior), fewer patients received 3 or 4 antimicrobials, while more received 0, 1, or 2 antimicrobials (Fig. 1A); fewer patients received combined antibiotic/antifungal therapy, while more received no antimicrobials or antifungal therapy alone; there was no change in use of antibiotic therapy alone (Fig. 1B). Final diagnoses included 15 bacterial infections (41%), 9 fungal (24%), 0 viral, and 7 noninfectious conditions (19%). Final diagnoses were attributed to NGS in 6 cases (16%), other diagnostics in 9 cases (24%), and both NGS and other diagnostics in 6 cases (16%); in the latter group, NGS provided a diagnosis prior to another study in 3 cases by intervals of 13, 19, and 72 days, respectively. [Figure: see text] A. Changes in number of antimicrobials, B. Changes in classes of antimicrobials CONCLUSION: Plasma cf-mNGS, as an adjunct to traditional methods, may provide unique or expedited diagnosis of bacterial or fungal infections, accelerate diagnosis of noninfectious conditions, or inform changes in broad-spectrum antimicrobial regimens. Continued study is warranted to delineate clinical impact and optimal use of plasma cf-mNGS. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106769772023-11-27 878. Clinical impact of plasma cell-free metagenomic next-generation sequencing: A retrospective cohort study  Vasishta, Shilpa Vo, Christopher Neogi, Sushrita Alahmdi, Bayan Sullivan, Timothy Gitman, Melissa R Open Forum Infect Dis Abstract BACKGROUND: Plasma cell-free metagenomic next-generation sequencing (cf-mNGS) offers potential for rapid, noninvasive diagnosis of complex infections, though clinical impact remains incompletely characterized. Here, we describe impacts on diagnosis and antimicrobial management among patients evaluated with plasma cf-mNGS. METHODS: Patients evaluated with plasma cf-mNGS (Karius®) in the Mount Sinai Health System from January 1, 2019 to December 23, 2022 were included. Cases were each reviewed independently in the medical record by two investigators using a standardized data collection form with discrepancies adjudicated collectively. Data were analyzed descriptively. RESULTS: Plasma cf-mNGS was sent for 37 patients of whom 29 (78%) were immunocompromised. 26 (70%) had prior invasive diagnostics. Median time from admission to NGS was 15 days. NGS was positive in 24 cases (65%), with results reflecting 20 bacterial infections, 9 viral, and 4 fungal (14 monomicrobial, 10 polymicrobial). Results were deemed clinically relevant in 18 cases (49%) including 12 positive and 6 negative tests. Testing led to antimicrobial changes in 11 cases (30%), discontinuation in 3 cases (8%), and no change in 23 cases (62%). After plasma cf-mNGS (compared with prior), fewer patients received 3 or 4 antimicrobials, while more received 0, 1, or 2 antimicrobials (Fig. 1A); fewer patients received combined antibiotic/antifungal therapy, while more received no antimicrobials or antifungal therapy alone; there was no change in use of antibiotic therapy alone (Fig. 1B). Final diagnoses included 15 bacterial infections (41%), 9 fungal (24%), 0 viral, and 7 noninfectious conditions (19%). Final diagnoses were attributed to NGS in 6 cases (16%), other diagnostics in 9 cases (24%), and both NGS and other diagnostics in 6 cases (16%); in the latter group, NGS provided a diagnosis prior to another study in 3 cases by intervals of 13, 19, and 72 days, respectively. [Figure: see text] A. Changes in number of antimicrobials, B. Changes in classes of antimicrobials CONCLUSION: Plasma cf-mNGS, as an adjunct to traditional methods, may provide unique or expedited diagnosis of bacterial or fungal infections, accelerate diagnosis of noninfectious conditions, or inform changes in broad-spectrum antimicrobial regimens. Continued study is warranted to delineate clinical impact and optimal use of plasma cf-mNGS. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10676977/ http://dx.doi.org/10.1093/ofid/ofad500.923 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Vasishta, Shilpa
Vo, Christopher
Neogi, Sushrita
Alahmdi, Bayan
Sullivan, Timothy
Gitman, Melissa R
878. Clinical impact of plasma cell-free metagenomic next-generation sequencing: A retrospective cohort study 
title 878. Clinical impact of plasma cell-free metagenomic next-generation sequencing: A retrospective cohort study 
title_full 878. Clinical impact of plasma cell-free metagenomic next-generation sequencing: A retrospective cohort study 
title_fullStr 878. Clinical impact of plasma cell-free metagenomic next-generation sequencing: A retrospective cohort study 
title_full_unstemmed 878. Clinical impact of plasma cell-free metagenomic next-generation sequencing: A retrospective cohort study 
title_short 878. Clinical impact of plasma cell-free metagenomic next-generation sequencing: A retrospective cohort study 
title_sort 878. clinical impact of plasma cell-free metagenomic next-generation sequencing: a retrospective cohort study 
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676977/
http://dx.doi.org/10.1093/ofid/ofad500.923
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