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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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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 |
format | Online Article Text |
id | pubmed-10676977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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