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1330. Clinical Associations and Trajectory of “Long COVID”

BACKGROUND: Persistent symptoms after acute COVID-19 are being increasingly reported. To date, little is known about the cause, clinical associations, and trajectory of “Long COVID”. METHODS: Participants of an outpatient clinical trial of Peginterferon-Lambda as treatment for uncomplicated SARS-CoV...

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Autores principales: Jacobson, Karen, Balasubramanian, Vidhya, Bonilla, Hector F, Madrigal, Martina, Hack, Isabelle, Purington, Natasha, Singh, Upinder, Hedlin, Haley, Jagannathan, Prasanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8643748/
http://dx.doi.org/10.1093/ofid/ofab466.1522
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author Jacobson, Karen
Balasubramanian, Vidhya
Bonilla, Hector F
Madrigal, Martina
Hack, Isabelle
Purington, Natasha
Singh, Upinder
Hedlin, Haley
Jagannathan, Prasanna
author_facet Jacobson, Karen
Balasubramanian, Vidhya
Bonilla, Hector F
Madrigal, Martina
Hack, Isabelle
Purington, Natasha
Singh, Upinder
Hedlin, Haley
Jagannathan, Prasanna
author_sort Jacobson, Karen
collection PubMed
description BACKGROUND: Persistent symptoms after acute COVID-19 are being increasingly reported. To date, little is known about the cause, clinical associations, and trajectory of “Long COVID”. METHODS: Participants of an outpatient clinical trial of Peginterferon-Lambda as treatment for uncomplicated SARS-CoV-2 infection were invited to long term follow-up visits 4, 7, and 10 months after initial COVID-19 diagnosis. Ongoing symptoms and functional impairment measures (work productivity and activity index (WPAI), NIH toolbox smell test, 6-minute walk test) were assessed and blood samples obtained. “Long COVID” was defined as presence of 2 or more typical symptoms (fatigue, hyposmia/hypogeusia, dyspnea, cough, palpitations, memory problems, joint pain) at follow up. Associations between baseline characteristics, initial COVID-19 clinical course, and presence of “Long COVID” during follow-up were assessed using generalized estimating equations accounting for repeated measurements within individuals. RESULTS: Eighty-seven participants returned for at least one follow-up visit. At four months, 29 (34.1%) had “Long COVID”; 19 (24.7%) met criteria at 7 months and 18 (23.4%) at 10 months (Figure 1). Presence of “Long COVID” symptoms did not correlate significantly with functional impairment measures. Female gender (OR 3.01, 95% CI 1.37-6.61) and having gastrointestinal symptoms during acute COVID-19 illness (OR 5.37, 95% CI 1.02-28.18) were associated with “Long COVID” during follow-up (Figure 2). No significant associations with baseline immunologic signatures were observed. [Image: see text] Figure 1. Alluvial plot of long term follow-up participants showing outcomes of symptoms at each visit. [Image: see text] Figure 2. Generalized Estimating Equations Model showing associations with “Long COVID” (presence of 2+ symptoms) at month 4, 7, and 10 following acute infection using unstructured correlation matrix. CONCLUSION: “Long COVID” was prevalent in this outpatient trial cohort and had low rates of resolution over 10 months of follow up. Female sex and gastrointestinal symptoms during acute illness were associated with “Long COVID”. Identifying modifiable risk factors associated with the development of persistent symptoms following SARS-CoV-2 infection remains a critical need. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-86437482021-12-06 1330. Clinical Associations and Trajectory of “Long COVID” Jacobson, Karen Balasubramanian, Vidhya Bonilla, Hector F Madrigal, Martina Hack, Isabelle Purington, Natasha Singh, Upinder Hedlin, Haley Jagannathan, Prasanna Open Forum Infect Dis Poster Abstracts BACKGROUND: Persistent symptoms after acute COVID-19 are being increasingly reported. To date, little is known about the cause, clinical associations, and trajectory of “Long COVID”. METHODS: Participants of an outpatient clinical trial of Peginterferon-Lambda as treatment for uncomplicated SARS-CoV-2 infection were invited to long term follow-up visits 4, 7, and 10 months after initial COVID-19 diagnosis. Ongoing symptoms and functional impairment measures (work productivity and activity index (WPAI), NIH toolbox smell test, 6-minute walk test) were assessed and blood samples obtained. “Long COVID” was defined as presence of 2 or more typical symptoms (fatigue, hyposmia/hypogeusia, dyspnea, cough, palpitations, memory problems, joint pain) at follow up. Associations between baseline characteristics, initial COVID-19 clinical course, and presence of “Long COVID” during follow-up were assessed using generalized estimating equations accounting for repeated measurements within individuals. RESULTS: Eighty-seven participants returned for at least one follow-up visit. At four months, 29 (34.1%) had “Long COVID”; 19 (24.7%) met criteria at 7 months and 18 (23.4%) at 10 months (Figure 1). Presence of “Long COVID” symptoms did not correlate significantly with functional impairment measures. Female gender (OR 3.01, 95% CI 1.37-6.61) and having gastrointestinal symptoms during acute COVID-19 illness (OR 5.37, 95% CI 1.02-28.18) were associated with “Long COVID” during follow-up (Figure 2). No significant associations with baseline immunologic signatures were observed. [Image: see text] Figure 1. Alluvial plot of long term follow-up participants showing outcomes of symptoms at each visit. [Image: see text] Figure 2. Generalized Estimating Equations Model showing associations with “Long COVID” (presence of 2+ symptoms) at month 4, 7, and 10 following acute infection using unstructured correlation matrix. CONCLUSION: “Long COVID” was prevalent in this outpatient trial cohort and had low rates of resolution over 10 months of follow up. Female sex and gastrointestinal symptoms during acute illness were associated with “Long COVID”. Identifying modifiable risk factors associated with the development of persistent symptoms following SARS-CoV-2 infection remains a critical need. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2021-12-04 /pmc/articles/PMC8643748/ http://dx.doi.org/10.1093/ofid/ofab466.1522 Text en © The Author(s) 2021. 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 Poster Abstracts
Jacobson, Karen
Balasubramanian, Vidhya
Bonilla, Hector F
Madrigal, Martina
Hack, Isabelle
Purington, Natasha
Singh, Upinder
Hedlin, Haley
Jagannathan, Prasanna
1330. Clinical Associations and Trajectory of “Long COVID”
title 1330. Clinical Associations and Trajectory of “Long COVID”
title_full 1330. Clinical Associations and Trajectory of “Long COVID”
title_fullStr 1330. Clinical Associations and Trajectory of “Long COVID”
title_full_unstemmed 1330. Clinical Associations and Trajectory of “Long COVID”
title_short 1330. Clinical Associations and Trajectory of “Long COVID”
title_sort 1330. clinical associations and trajectory of “long covid”
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8643748/
http://dx.doi.org/10.1093/ofid/ofab466.1522
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