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Post-acute sequelae of SARS-CoV-2 with clinical condition definitions and comparison in a matched cohort
Disease characterization of Post-Acute Sequelae of SARS-CoV-2 (PASC) does not account for pre-existing conditions and time course of incidence. We utilized longitudinal data and matching to a COVID PCR-negative population to discriminate PASC conditions over time within our patient population during...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9556630/ https://www.ncbi.nlm.nih.gov/pubmed/36224218 http://dx.doi.org/10.1038/s41467-022-33573-6 |
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author | Horberg, Michael A. Watson, Eric Bhatia, Mamta Jefferson, Celeena Certa, Julia M. Kim, Seohyun Fathi, Lily Althoff, Keri N. Williams, Carolyn Moore, Richard |
author_facet | Horberg, Michael A. Watson, Eric Bhatia, Mamta Jefferson, Celeena Certa, Julia M. Kim, Seohyun Fathi, Lily Althoff, Keri N. Williams, Carolyn Moore, Richard |
author_sort | Horberg, Michael A. |
collection | PubMed |
description | Disease characterization of Post-Acute Sequelae of SARS-CoV-2 (PASC) does not account for pre-existing conditions and time course of incidence. We utilized longitudinal data and matching to a COVID PCR-negative population to discriminate PASC conditions over time within our patient population during 2020. Clinical Classification Software was used to identify PASC condition groupings. Conditions were specified acute and persistent (occurring 0-30 days post COVID PCR and persisted 30–120 days post-test) or late (occurring initially 30-120 days post-test). We matched 3:1 COVID PCR-negative COVIDPCR-positive by age, sex, testing month and service area, controlling for pre-existing conditions up to four years prior; 28,118 PCR-positive to 70,293 PCR-negative patients resulted. We estimated PASC risk from the matched cohort. Risk of any PASC condition was 12% greater for PCR-positive patients in the late period with a significantly higher risk of anosmia, cardiac dysrhythmia, diabetes, genitourinary disorders, malaise, and nonspecific chest pain. Our findings contribute to a more refined PASC definition which can enhance clinical care. |
format | Online Article Text |
id | pubmed-9556630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95566302022-10-14 Post-acute sequelae of SARS-CoV-2 with clinical condition definitions and comparison in a matched cohort Horberg, Michael A. Watson, Eric Bhatia, Mamta Jefferson, Celeena Certa, Julia M. Kim, Seohyun Fathi, Lily Althoff, Keri N. Williams, Carolyn Moore, Richard Nat Commun Article Disease characterization of Post-Acute Sequelae of SARS-CoV-2 (PASC) does not account for pre-existing conditions and time course of incidence. We utilized longitudinal data and matching to a COVID PCR-negative population to discriminate PASC conditions over time within our patient population during 2020. Clinical Classification Software was used to identify PASC condition groupings. Conditions were specified acute and persistent (occurring 0-30 days post COVID PCR and persisted 30–120 days post-test) or late (occurring initially 30-120 days post-test). We matched 3:1 COVID PCR-negative COVIDPCR-positive by age, sex, testing month and service area, controlling for pre-existing conditions up to four years prior; 28,118 PCR-positive to 70,293 PCR-negative patients resulted. We estimated PASC risk from the matched cohort. Risk of any PASC condition was 12% greater for PCR-positive patients in the late period with a significantly higher risk of anosmia, cardiac dysrhythmia, diabetes, genitourinary disorders, malaise, and nonspecific chest pain. Our findings contribute to a more refined PASC definition which can enhance clinical care. Nature Publishing Group UK 2022-10-12 /pmc/articles/PMC9556630/ /pubmed/36224218 http://dx.doi.org/10.1038/s41467-022-33573-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Horberg, Michael A. Watson, Eric Bhatia, Mamta Jefferson, Celeena Certa, Julia M. Kim, Seohyun Fathi, Lily Althoff, Keri N. Williams, Carolyn Moore, Richard Post-acute sequelae of SARS-CoV-2 with clinical condition definitions and comparison in a matched cohort |
title | Post-acute sequelae of SARS-CoV-2 with clinical condition definitions and comparison in a matched cohort |
title_full | Post-acute sequelae of SARS-CoV-2 with clinical condition definitions and comparison in a matched cohort |
title_fullStr | Post-acute sequelae of SARS-CoV-2 with clinical condition definitions and comparison in a matched cohort |
title_full_unstemmed | Post-acute sequelae of SARS-CoV-2 with clinical condition definitions and comparison in a matched cohort |
title_short | Post-acute sequelae of SARS-CoV-2 with clinical condition definitions and comparison in a matched cohort |
title_sort | post-acute sequelae of sars-cov-2 with clinical condition definitions and comparison in a matched cohort |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9556630/ https://www.ncbi.nlm.nih.gov/pubmed/36224218 http://dx.doi.org/10.1038/s41467-022-33573-6 |
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