Cargando…

Clinical application of cell-free next-generation sequencing for infectious diseases at a tertiary children’s hospital

BACKGROUND: Children affected by infectious diseases may not always have a detectable infectious etiology. Diagnostic uncertainty can lead to prolonged hospitalizations, inappropriately broad or extended courses of antibiotics, invasive diagnostic procedures, and difficulty predicting the clinical c...

Descripción completa

Detalles Bibliográficos
Autores principales: Wilke, Julianne, Ramchandar, Nanda, Cannavino, Christopher, Pong, Alice, Tremoulet, Adriana, Padua, Leidy Tovar, Harvey, Helen, Foley, Jennifer, Farnaes, Lauge, Coufal, Nicole G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192220/
https://www.ncbi.nlm.nih.gov/pubmed/34112116
http://dx.doi.org/10.1186/s12879-021-06292-4
_version_ 1783706014022893568
author Wilke, Julianne
Ramchandar, Nanda
Cannavino, Christopher
Pong, Alice
Tremoulet, Adriana
Padua, Leidy Tovar
Harvey, Helen
Foley, Jennifer
Farnaes, Lauge
Coufal, Nicole G.
author_facet Wilke, Julianne
Ramchandar, Nanda
Cannavino, Christopher
Pong, Alice
Tremoulet, Adriana
Padua, Leidy Tovar
Harvey, Helen
Foley, Jennifer
Farnaes, Lauge
Coufal, Nicole G.
author_sort Wilke, Julianne
collection PubMed
description BACKGROUND: Children affected by infectious diseases may not always have a detectable infectious etiology. Diagnostic uncertainty can lead to prolonged hospitalizations, inappropriately broad or extended courses of antibiotics, invasive diagnostic procedures, and difficulty predicting the clinical course and outcome. Cell-free plasma next-generation sequencing (cfNGS) can identify viral, bacterial, and fungal infections by detecting pathogen DNA in peripheral blood. This testing modality offers the ability to test for many organisms at once in a shotgun metagenomic approach with a rapid turnaround time. We sought to compare the results of cfNGS to conventional diagnostic test results and describe the impact of cfNGS on clinical care in a diverse pediatric population at a large academic children’s hospital. METHODS: We performed a retrospective chart review of hospitalized subjects at a tertiary pediatric hospital to determine the diagnostic yield of cfNGS and its impact on clinical care. RESULTS: We describe the clinical application of results from 142 cfNGS tests in the management of 110 subjects over an 8-month study period. In comparison to conventional testing as a reference standard, cfNGS was found to have a positive percent agreement of 89.6% and negative percent agreement of 52.3%. Furthermore, 32.4% of cfNGS results were directly applied to make a clinical change in management. CONCLUSIONS: We demonstrate the clinically utility of cfNGS in the management of acutely ill children. Future studies, both retrospective and prospective, are needed to clarify the optimal indications for testing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-021-06292-4.
format Online
Article
Text
id pubmed-8192220
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-81922202021-06-11 Clinical application of cell-free next-generation sequencing for infectious diseases at a tertiary children’s hospital Wilke, Julianne Ramchandar, Nanda Cannavino, Christopher Pong, Alice Tremoulet, Adriana Padua, Leidy Tovar Harvey, Helen Foley, Jennifer Farnaes, Lauge Coufal, Nicole G. BMC Infect Dis Research BACKGROUND: Children affected by infectious diseases may not always have a detectable infectious etiology. Diagnostic uncertainty can lead to prolonged hospitalizations, inappropriately broad or extended courses of antibiotics, invasive diagnostic procedures, and difficulty predicting the clinical course and outcome. Cell-free plasma next-generation sequencing (cfNGS) can identify viral, bacterial, and fungal infections by detecting pathogen DNA in peripheral blood. This testing modality offers the ability to test for many organisms at once in a shotgun metagenomic approach with a rapid turnaround time. We sought to compare the results of cfNGS to conventional diagnostic test results and describe the impact of cfNGS on clinical care in a diverse pediatric population at a large academic children’s hospital. METHODS: We performed a retrospective chart review of hospitalized subjects at a tertiary pediatric hospital to determine the diagnostic yield of cfNGS and its impact on clinical care. RESULTS: We describe the clinical application of results from 142 cfNGS tests in the management of 110 subjects over an 8-month study period. In comparison to conventional testing as a reference standard, cfNGS was found to have a positive percent agreement of 89.6% and negative percent agreement of 52.3%. Furthermore, 32.4% of cfNGS results were directly applied to make a clinical change in management. CONCLUSIONS: We demonstrate the clinically utility of cfNGS in the management of acutely ill children. Future studies, both retrospective and prospective, are needed to clarify the optimal indications for testing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-021-06292-4. BioMed Central 2021-06-11 /pmc/articles/PMC8192220/ /pubmed/34112116 http://dx.doi.org/10.1186/s12879-021-06292-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wilke, Julianne
Ramchandar, Nanda
Cannavino, Christopher
Pong, Alice
Tremoulet, Adriana
Padua, Leidy Tovar
Harvey, Helen
Foley, Jennifer
Farnaes, Lauge
Coufal, Nicole G.
Clinical application of cell-free next-generation sequencing for infectious diseases at a tertiary children’s hospital
title Clinical application of cell-free next-generation sequencing for infectious diseases at a tertiary children’s hospital
title_full Clinical application of cell-free next-generation sequencing for infectious diseases at a tertiary children’s hospital
title_fullStr Clinical application of cell-free next-generation sequencing for infectious diseases at a tertiary children’s hospital
title_full_unstemmed Clinical application of cell-free next-generation sequencing for infectious diseases at a tertiary children’s hospital
title_short Clinical application of cell-free next-generation sequencing for infectious diseases at a tertiary children’s hospital
title_sort clinical application of cell-free next-generation sequencing for infectious diseases at a tertiary children’s hospital
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192220/
https://www.ncbi.nlm.nih.gov/pubmed/34112116
http://dx.doi.org/10.1186/s12879-021-06292-4
work_keys_str_mv AT wilkejulianne clinicalapplicationofcellfreenextgenerationsequencingforinfectiousdiseasesatatertiarychildrenshospital
AT ramchandarnanda clinicalapplicationofcellfreenextgenerationsequencingforinfectiousdiseasesatatertiarychildrenshospital
AT cannavinochristopher clinicalapplicationofcellfreenextgenerationsequencingforinfectiousdiseasesatatertiarychildrenshospital
AT pongalice clinicalapplicationofcellfreenextgenerationsequencingforinfectiousdiseasesatatertiarychildrenshospital
AT tremouletadriana clinicalapplicationofcellfreenextgenerationsequencingforinfectiousdiseasesatatertiarychildrenshospital
AT padualeidytovar clinicalapplicationofcellfreenextgenerationsequencingforinfectiousdiseasesatatertiarychildrenshospital
AT harveyhelen clinicalapplicationofcellfreenextgenerationsequencingforinfectiousdiseasesatatertiarychildrenshospital
AT foleyjennifer clinicalapplicationofcellfreenextgenerationsequencingforinfectiousdiseasesatatertiarychildrenshospital
AT farnaeslauge clinicalapplicationofcellfreenextgenerationsequencingforinfectiousdiseasesatatertiarychildrenshospital
AT coufalnicoleg clinicalapplicationofcellfreenextgenerationsequencingforinfectiousdiseasesatatertiarychildrenshospital