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447. Clinical Features, Risk Factors, and Outcomes of COVID-19 in Immunocompromised Adults Hospitalized with Acute Respiratory Infection

BACKGROUND: Individuals with immunocompromising conditions are at high risk of severe disease from COVID-19. The objectives of this study were to describe the clinical features, risk factors, and outcomes of COVID-19 in immunocompromised (IC) adults hospitalized with acute respiratory infection (ARI...

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Autores principales: Taylor, Elizabeth G, Tippett, Ashley, Salazar, Luis W, Hussaini, Laila, Choi, Chris, De Castro, Khalel, Reese, Olivia, Momin, Humerazehra, Lew, Ashley, Ciric, Caroline R, Banerjee, Amrita, Keane, Amy E, Puzniak, Laura A, Hubler, Robin, Valluri, Srinivas, Wiemken, Timothy L, Lopman, Benjamin, Rouphael, Nadine, Kamidani, Satoshi, Anderson, Evan J, Rostad, Christina A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677455/
http://dx.doi.org/10.1093/ofid/ofad500.517
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author Taylor, Elizabeth G
Tippett, Ashley
Salazar, Luis W
Hussaini, Laila
Choi, Chris
De Castro, Khalel
Reese, Olivia
Momin, Humerazehra
Lew, Ashley
Ciric, Caroline R
Banerjee, Amrita
Keane, Amy E
Puzniak, Laura A
Hubler, Robin
Valluri, Srinivas
Wiemken, Timothy L
Lopman, Benjamin
Rouphael, Nadine
Kamidani, Satoshi
Anderson, Evan J
Rostad, Christina A
author_facet Taylor, Elizabeth G
Tippett, Ashley
Salazar, Luis W
Hussaini, Laila
Choi, Chris
De Castro, Khalel
Reese, Olivia
Momin, Humerazehra
Lew, Ashley
Ciric, Caroline R
Banerjee, Amrita
Keane, Amy E
Puzniak, Laura A
Hubler, Robin
Valluri, Srinivas
Wiemken, Timothy L
Lopman, Benjamin
Rouphael, Nadine
Kamidani, Satoshi
Anderson, Evan J
Rostad, Christina A
author_sort Taylor, Elizabeth G
collection PubMed
description BACKGROUND: Individuals with immunocompromising conditions are at high risk of severe disease from COVID-19. The objectives of this study were to describe the clinical features, risk factors, and outcomes of COVID-19 in immunocompromised (IC) adults hospitalized with acute respiratory infection (ARI). METHODS: We enrolled patients ≥ 18 years of age hospitalized with ARI at two Emory University hospitals from May 2021 – Aug 2022. Patient interviews and medical abstractions were completed. Nasopharyngeal and oropharyngeal swabs were tested for SARS-CoV-2 using BioFire Respiratory Panel, and results of standard-of-care testing were recorded. IC was defined using comorbidities from the medical chart (cancer, HIV, organ/stem cell/bone marrow transplant, long-term steroid use, other immunosuppressive conditions). Primary vaccination consisted of 3 mRNA or 1 J&J + 1 other dose for IC patients, and 2 mRNA or 1 J&J for non-IC patients. Vaccine effectiveness (VE) was calculated using a test-negative case-control design. Multivariable logistic regression with stepwise selection yielded a final model controlling for employment, past COVID-19, and blood disorders using SAS v9.4. RESULTS: Of 1677 enrolled participants, 1653 had SARS-CoV-2 testing, of whom 850 (50.7%) were positive and 231 (27.2% of 850) were IC. Compared to non-IC patients with SARS-CoV-2, IC patients were significantly older (median 58, IQR [44-67)), male (57.1%), and had underlying comorbidities, including blood disorders (13.9%) and chronic kidney disease (36.8%). IC patients were more commonly infected with the Omicron variant, while non-IC patients were more commonly infected with Alpha or Delta. Compared to non-IC, IC patients had longer hospitalization duration (median 4.7, IQR [2.9-9.5]), required positive-pressure ventilation (CPAP/BiPAP) (13.9%), and died (6.5%). IC patients had less commonly received a full COVID-19 vaccine series (19.9% vs. 25.8%) and adjusted VE of primary COVID-19 vaccine series against hospitalization for ARI was lower in the IC (48.7 (17.9, 68.0)) vs. non-IC patients (76.0 (68.4, 81.7)). [Figure: see text] CONCLUSION: Compared to non-IC hospitalized adults, COVID-19 VE against hospitalization for ARI was lower in IC patients, who were more likely to experience severe outcomes and death. DISCLOSURES: Laura A. Puzniak, PhD. MPH, Pfizer, Inc.: Employee|Pfizer, Inc.: Stocks/Bonds Robin Hubler, MS, Pfizer, Inc.: Employee|Pfizer, Inc.: Stocks/Bonds Srinivas Valluri, PhD, Pfizer Inc: Pfizer Employee and hold Pfizer stocks/options|Pfizer Inc: Ownership Interest|Pfizer Inc: Stocks/Bonds Timothy L. Wiemken, PhD, Pfizer Inc: Employee|Pfizer Inc: Stocks/Bonds Benjamin Lopman, PhD, Epidemiological Research and Methods, LLC: Advisor/Consultant|Hillevax, Inc: Advisor/Consultant Nadine Rouphael, MD, Icon, EMMES, Sanofi, Seqirus, Moderna: Advisor/Consultant Satoshi Kamidani, MD, CDC: Grant/Research Support|Emergent BioSolutions: Grant/Research Support|NIH: Grant/Research Support|Pfizer Inc: Grant/Research Support Evan J. Anderson, MD, GSK: Advisor/Consultant|GSK: Grant/Research Support|Janssen: Advisor/Consultant|Janssen: Grant/Research Support|Kentucky Bioprocessing, Inc.: Safety Monitoring Board|Moderna: Advisor/Consultant|Moderna: Grant/Research Support|Moderna: Currently an employee|Moderna: Stocks/Bonds|Pfizer: Advisor/Consultant|Pfizer: Grant/Research Support|Sanofi Pasteur: Advisor/Consultant|Sanofi Pasteur: Grant/Research Support|Sanofi Pasteur: Safety Monitoring Board|WCG/ACI Clinical: Data Adjudication Board Christina A. Rostad, MD, BioFire Inc.: Grant/Research Support|GlaxoSmithKline Biologicals: Grant/Research Support|Janssen: Grant/Research Support|MedImmune LLC: Grant/Research Support|Meissa Vaccines, Inc.: RSV vaccine technology|Merck & Co., Inc.: Grant/Research Support|Micron Technology, Inc.: Grant/Research Support|Moderna, Inc.: Grant/Research Support|Novavax: Grant/Research Support|PaxVax: Grant/Research Support|Pfizer, Inc.: Grant/Research Support|Regeneron: Grant/Research Support|Sanofi Pasteur: Grant/Research Support
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spelling pubmed-106774552023-11-27 447. Clinical Features, Risk Factors, and Outcomes of COVID-19 in Immunocompromised Adults Hospitalized with Acute Respiratory Infection Taylor, Elizabeth G Tippett, Ashley Salazar, Luis W Hussaini, Laila Choi, Chris De Castro, Khalel Reese, Olivia Momin, Humerazehra Lew, Ashley Ciric, Caroline R Banerjee, Amrita Keane, Amy E Puzniak, Laura A Hubler, Robin Valluri, Srinivas Wiemken, Timothy L Lopman, Benjamin Rouphael, Nadine Kamidani, Satoshi Anderson, Evan J Rostad, Christina A Open Forum Infect Dis Abstract BACKGROUND: Individuals with immunocompromising conditions are at high risk of severe disease from COVID-19. The objectives of this study were to describe the clinical features, risk factors, and outcomes of COVID-19 in immunocompromised (IC) adults hospitalized with acute respiratory infection (ARI). METHODS: We enrolled patients ≥ 18 years of age hospitalized with ARI at two Emory University hospitals from May 2021 – Aug 2022. Patient interviews and medical abstractions were completed. Nasopharyngeal and oropharyngeal swabs were tested for SARS-CoV-2 using BioFire Respiratory Panel, and results of standard-of-care testing were recorded. IC was defined using comorbidities from the medical chart (cancer, HIV, organ/stem cell/bone marrow transplant, long-term steroid use, other immunosuppressive conditions). Primary vaccination consisted of 3 mRNA or 1 J&J + 1 other dose for IC patients, and 2 mRNA or 1 J&J for non-IC patients. Vaccine effectiveness (VE) was calculated using a test-negative case-control design. Multivariable logistic regression with stepwise selection yielded a final model controlling for employment, past COVID-19, and blood disorders using SAS v9.4. RESULTS: Of 1677 enrolled participants, 1653 had SARS-CoV-2 testing, of whom 850 (50.7%) were positive and 231 (27.2% of 850) were IC. Compared to non-IC patients with SARS-CoV-2, IC patients were significantly older (median 58, IQR [44-67)), male (57.1%), and had underlying comorbidities, including blood disorders (13.9%) and chronic kidney disease (36.8%). IC patients were more commonly infected with the Omicron variant, while non-IC patients were more commonly infected with Alpha or Delta. Compared to non-IC, IC patients had longer hospitalization duration (median 4.7, IQR [2.9-9.5]), required positive-pressure ventilation (CPAP/BiPAP) (13.9%), and died (6.5%). IC patients had less commonly received a full COVID-19 vaccine series (19.9% vs. 25.8%) and adjusted VE of primary COVID-19 vaccine series against hospitalization for ARI was lower in the IC (48.7 (17.9, 68.0)) vs. non-IC patients (76.0 (68.4, 81.7)). [Figure: see text] CONCLUSION: Compared to non-IC hospitalized adults, COVID-19 VE against hospitalization for ARI was lower in IC patients, who were more likely to experience severe outcomes and death. DISCLOSURES: Laura A. Puzniak, PhD. MPH, Pfizer, Inc.: Employee|Pfizer, Inc.: Stocks/Bonds Robin Hubler, MS, Pfizer, Inc.: Employee|Pfizer, Inc.: Stocks/Bonds Srinivas Valluri, PhD, Pfizer Inc: Pfizer Employee and hold Pfizer stocks/options|Pfizer Inc: Ownership Interest|Pfizer Inc: Stocks/Bonds Timothy L. Wiemken, PhD, Pfizer Inc: Employee|Pfizer Inc: Stocks/Bonds Benjamin Lopman, PhD, Epidemiological Research and Methods, LLC: Advisor/Consultant|Hillevax, Inc: Advisor/Consultant Nadine Rouphael, MD, Icon, EMMES, Sanofi, Seqirus, Moderna: Advisor/Consultant Satoshi Kamidani, MD, CDC: Grant/Research Support|Emergent BioSolutions: Grant/Research Support|NIH: Grant/Research Support|Pfizer Inc: Grant/Research Support Evan J. Anderson, MD, GSK: Advisor/Consultant|GSK: Grant/Research Support|Janssen: Advisor/Consultant|Janssen: Grant/Research Support|Kentucky Bioprocessing, Inc.: Safety Monitoring Board|Moderna: Advisor/Consultant|Moderna: Grant/Research Support|Moderna: Currently an employee|Moderna: Stocks/Bonds|Pfizer: Advisor/Consultant|Pfizer: Grant/Research Support|Sanofi Pasteur: Advisor/Consultant|Sanofi Pasteur: Grant/Research Support|Sanofi Pasteur: Safety Monitoring Board|WCG/ACI Clinical: Data Adjudication Board Christina A. Rostad, MD, BioFire Inc.: Grant/Research Support|GlaxoSmithKline Biologicals: Grant/Research Support|Janssen: Grant/Research Support|MedImmune LLC: Grant/Research Support|Meissa Vaccines, Inc.: RSV vaccine technology|Merck & Co., Inc.: Grant/Research Support|Micron Technology, Inc.: Grant/Research Support|Moderna, Inc.: Grant/Research Support|Novavax: Grant/Research Support|PaxVax: Grant/Research Support|Pfizer, Inc.: Grant/Research Support|Regeneron: Grant/Research Support|Sanofi Pasteur: Grant/Research Support Oxford University Press 2023-11-27 /pmc/articles/PMC10677455/ http://dx.doi.org/10.1093/ofid/ofad500.517 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
Taylor, Elizabeth G
Tippett, Ashley
Salazar, Luis W
Hussaini, Laila
Choi, Chris
De Castro, Khalel
Reese, Olivia
Momin, Humerazehra
Lew, Ashley
Ciric, Caroline R
Banerjee, Amrita
Keane, Amy E
Puzniak, Laura A
Hubler, Robin
Valluri, Srinivas
Wiemken, Timothy L
Lopman, Benjamin
Rouphael, Nadine
Kamidani, Satoshi
Anderson, Evan J
Rostad, Christina A
447. Clinical Features, Risk Factors, and Outcomes of COVID-19 in Immunocompromised Adults Hospitalized with Acute Respiratory Infection
title 447. Clinical Features, Risk Factors, and Outcomes of COVID-19 in Immunocompromised Adults Hospitalized with Acute Respiratory Infection
title_full 447. Clinical Features, Risk Factors, and Outcomes of COVID-19 in Immunocompromised Adults Hospitalized with Acute Respiratory Infection
title_fullStr 447. Clinical Features, Risk Factors, and Outcomes of COVID-19 in Immunocompromised Adults Hospitalized with Acute Respiratory Infection
title_full_unstemmed 447. Clinical Features, Risk Factors, and Outcomes of COVID-19 in Immunocompromised Adults Hospitalized with Acute Respiratory Infection
title_short 447. Clinical Features, Risk Factors, and Outcomes of COVID-19 in Immunocompromised Adults Hospitalized with Acute Respiratory Infection
title_sort 447. clinical features, risk factors, and outcomes of covid-19 in immunocompromised adults hospitalized with acute respiratory infection
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677455/
http://dx.doi.org/10.1093/ofid/ofad500.517
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