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A Tale of 3 Pandemics: Severe Acute Respiratory Syndrome Coronavirus 2, Hepatitis C Virus, and Human Immunodeficiency Virus in an Urban Emergency Department in Baltimore, Maryland

BACKGROUND: We sought to determine the prevalence and sociodemographic and clinical correlates of acute and convalescent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), hepatitis C virus (HCV), and human immunodeficiency virus (HIV) infections among emergency department (ED) patients i...

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Autores principales: Hsieh, Yu-Hsiang, Rothman, Richard E, Solomon, Sunil S, Anderson, Mark, Stec, Michael, Laeyendecker, Oliver, Lake, Isabel V, Fernandez, Reinaldo E, Dashler, Gaby, Mehta, Radhika, Kickler, Thomas, Kelen, Gabor D, Mehta, Shruti H, Cloherty, Gavin A, Quinn, Thomas C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982772/
https://www.ncbi.nlm.nih.gov/pubmed/35392453
http://dx.doi.org/10.1093/ofid/ofac130
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author Hsieh, Yu-Hsiang
Rothman, Richard E
Solomon, Sunil S
Anderson, Mark
Stec, Michael
Laeyendecker, Oliver
Lake, Isabel V
Fernandez, Reinaldo E
Dashler, Gaby
Mehta, Radhika
Kickler, Thomas
Kelen, Gabor D
Mehta, Shruti H
Cloherty, Gavin A
Quinn, Thomas C
author_facet Hsieh, Yu-Hsiang
Rothman, Richard E
Solomon, Sunil S
Anderson, Mark
Stec, Michael
Laeyendecker, Oliver
Lake, Isabel V
Fernandez, Reinaldo E
Dashler, Gaby
Mehta, Radhika
Kickler, Thomas
Kelen, Gabor D
Mehta, Shruti H
Cloherty, Gavin A
Quinn, Thomas C
author_sort Hsieh, Yu-Hsiang
collection PubMed
description BACKGROUND: We sought to determine the prevalence and sociodemographic and clinical correlates of acute and convalescent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), hepatitis C virus (HCV), and human immunodeficiency virus (HIV) infections among emergency department (ED) patients in Baltimore. METHODS: Remnant blood samples from 7450 unique patients were collected over 4 months in 2020 for SARS-CoV-2 antibody (Ab), HCV Ab, and HIV-1/2 antigen and Ab. Among them, 5012 patients were tested by polymerase chain reaction for SARS-CoV-2 based on clinical suspicion. Sociodemographics, ED clinical presentations, and outcomes associated with coinfections were assessed. RESULTS: Overall, 729 (9.8%) patients had SARS-CoV-2 (acute or convalescent), 934 (12.5%) HCV, 372 (5.0%) HIV infection, and 211 patients (2.8%) had evidence of any coinfection (HCV/HIV, 1.5%; SARS-CoV-2/HCV, 0.7%; SARS-CoV-2/HIV, 0.3%; SARS-CoV-2/HCV/HIV, 0.3%). The prevalence of SARS-CoV-2 (acute or convalescent) was significantly higher in those with HCV or HIV vs those without (13.6% vs 9.1%, P < .001). Key sociodemographic disparities (race, ethnicity, and poverty) and specific ED clinical characteristics were significantly correlated with having any coinfections vs no infection or individual monoinfection. Among those with HCV or HIV, aged 18–34 years, Black race, Hispanic ethnicity, and a cardiovascular-related chief complaint had a significantly higher odds of having SARS-CoV-2 (prevalence ratios: 2.02, 2.37, 5.81, and 2.07, respectively). CONCLUSIONS: The burden of SARS-CoV-2, HCV, and HIV co-pandemics and their associations with specific sociodemographic disparities, clinical presentations, and outcomes suggest that urban EDs should consider implementing integrated screening and linkage-to-care programs for these 3 infections.
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spelling pubmed-89827722022-04-06 A Tale of 3 Pandemics: Severe Acute Respiratory Syndrome Coronavirus 2, Hepatitis C Virus, and Human Immunodeficiency Virus in an Urban Emergency Department in Baltimore, Maryland Hsieh, Yu-Hsiang Rothman, Richard E Solomon, Sunil S Anderson, Mark Stec, Michael Laeyendecker, Oliver Lake, Isabel V Fernandez, Reinaldo E Dashler, Gaby Mehta, Radhika Kickler, Thomas Kelen, Gabor D Mehta, Shruti H Cloherty, Gavin A Quinn, Thomas C Open Forum Infect Dis Major Article BACKGROUND: We sought to determine the prevalence and sociodemographic and clinical correlates of acute and convalescent severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), hepatitis C virus (HCV), and human immunodeficiency virus (HIV) infections among emergency department (ED) patients in Baltimore. METHODS: Remnant blood samples from 7450 unique patients were collected over 4 months in 2020 for SARS-CoV-2 antibody (Ab), HCV Ab, and HIV-1/2 antigen and Ab. Among them, 5012 patients were tested by polymerase chain reaction for SARS-CoV-2 based on clinical suspicion. Sociodemographics, ED clinical presentations, and outcomes associated with coinfections were assessed. RESULTS: Overall, 729 (9.8%) patients had SARS-CoV-2 (acute or convalescent), 934 (12.5%) HCV, 372 (5.0%) HIV infection, and 211 patients (2.8%) had evidence of any coinfection (HCV/HIV, 1.5%; SARS-CoV-2/HCV, 0.7%; SARS-CoV-2/HIV, 0.3%; SARS-CoV-2/HCV/HIV, 0.3%). The prevalence of SARS-CoV-2 (acute or convalescent) was significantly higher in those with HCV or HIV vs those without (13.6% vs 9.1%, P < .001). Key sociodemographic disparities (race, ethnicity, and poverty) and specific ED clinical characteristics were significantly correlated with having any coinfections vs no infection or individual monoinfection. Among those with HCV or HIV, aged 18–34 years, Black race, Hispanic ethnicity, and a cardiovascular-related chief complaint had a significantly higher odds of having SARS-CoV-2 (prevalence ratios: 2.02, 2.37, 5.81, and 2.07, respectively). CONCLUSIONS: The burden of SARS-CoV-2, HCV, and HIV co-pandemics and their associations with specific sociodemographic disparities, clinical presentations, and outcomes suggest that urban EDs should consider implementing integrated screening and linkage-to-care programs for these 3 infections. Oxford University Press 2022-03-16 /pmc/articles/PMC8982772/ /pubmed/35392453 http://dx.doi.org/10.1093/ofid/ofac130 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Hsieh, Yu-Hsiang
Rothman, Richard E
Solomon, Sunil S
Anderson, Mark
Stec, Michael
Laeyendecker, Oliver
Lake, Isabel V
Fernandez, Reinaldo E
Dashler, Gaby
Mehta, Radhika
Kickler, Thomas
Kelen, Gabor D
Mehta, Shruti H
Cloherty, Gavin A
Quinn, Thomas C
A Tale of 3 Pandemics: Severe Acute Respiratory Syndrome Coronavirus 2, Hepatitis C Virus, and Human Immunodeficiency Virus in an Urban Emergency Department in Baltimore, Maryland
title A Tale of 3 Pandemics: Severe Acute Respiratory Syndrome Coronavirus 2, Hepatitis C Virus, and Human Immunodeficiency Virus in an Urban Emergency Department in Baltimore, Maryland
title_full A Tale of 3 Pandemics: Severe Acute Respiratory Syndrome Coronavirus 2, Hepatitis C Virus, and Human Immunodeficiency Virus in an Urban Emergency Department in Baltimore, Maryland
title_fullStr A Tale of 3 Pandemics: Severe Acute Respiratory Syndrome Coronavirus 2, Hepatitis C Virus, and Human Immunodeficiency Virus in an Urban Emergency Department in Baltimore, Maryland
title_full_unstemmed A Tale of 3 Pandemics: Severe Acute Respiratory Syndrome Coronavirus 2, Hepatitis C Virus, and Human Immunodeficiency Virus in an Urban Emergency Department in Baltimore, Maryland
title_short A Tale of 3 Pandemics: Severe Acute Respiratory Syndrome Coronavirus 2, Hepatitis C Virus, and Human Immunodeficiency Virus in an Urban Emergency Department in Baltimore, Maryland
title_sort tale of 3 pandemics: severe acute respiratory syndrome coronavirus 2, hepatitis c virus, and human immunodeficiency virus in an urban emergency department in baltimore, maryland
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982772/
https://www.ncbi.nlm.nih.gov/pubmed/35392453
http://dx.doi.org/10.1093/ofid/ofac130
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