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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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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 |
format | Online Article Text |
id | pubmed-10677455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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