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926. COVID-19 Infections After SARS-CoV-2 Vaccination in Solid Organ Transplant Recipients

BACKGROUND: Solid organ transplant recipients (SOTR) have lower humoral responses following SARS-CoV-2 vaccination. Whether this equates to reduced vaccine effectiveness in SOTR or impacts disease severity is not yet known. We used the IDSA Emerging Infections Network (EIN) to identify SARS-CoV-2 ca...

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Autores principales: Saharia, Kapil, Streit, Judy, Beekmann, Susan E, Polgreen, Philip M, Kuehnert, Matthew, Segev, Dorry, Baddley, John W, Miller, Rachel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8644968/
http://dx.doi.org/10.1093/ofid/ofab466.1121
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author Saharia, Kapil
Streit, Judy
Beekmann, Susan E
Polgreen, Philip M
Kuehnert, Matthew
Segev, Dorry
Baddley, John W
Miller, Rachel
author_facet Saharia, Kapil
Streit, Judy
Beekmann, Susan E
Polgreen, Philip M
Kuehnert, Matthew
Segev, Dorry
Baddley, John W
Miller, Rachel
author_sort Saharia, Kapil
collection PubMed
description BACKGROUND: Solid organ transplant recipients (SOTR) have lower humoral responses following SARS-CoV-2 vaccination. Whether this equates to reduced vaccine effectiveness in SOTR or impacts disease severity is not yet known. We used the IDSA Emerging Infections Network (EIN) to identify SARS-CoV-2 cases in vaccinated SOTR. We describe their clinical characteristics and outcomes. METHODS: On 4/7/21, we requested case reports via the EIN listserv of COVID-19 infection following SARS-CoV-2 vaccination in immunocompromised individuals. Case reports were collected until June 7(th). Online data collection included patient demographics, dates of SARS-CoV-2 vaccine administration and clinical data related to COVID-19 infection. We performed a descriptive analysis of these patient factors and compared differences between early onset (< / = 21 days after completing vaccine series) and late onset infection ( > 21 days after completing vaccine series). RESULTS: As of 6/7/21, 34 cases of COVID-19 infection after vaccination in SOTR were submitted. Most cases (79%) occurred in individuals who were fully vaccinated. Only 3 cases (8.5%) occurred in SOTR within their first year after transplantation. Clinical characteristics are listed in Table 1. The vaccine administration date was known for 26 SOTR among whom symptoms occurred a median of 26.5 days (IQR 21.75 days, range 5-79 days) after completing the COVID-19 vaccine series. Twenty-three SOTR (68%) required hospitalization of which 12 had critical illness. Outcome data was available for 29 individuals of whom 20 (69%) demonstrated improvement. When comparing SOTR with early versus late onset COVID-19 infection in relation to vaccination timing, there were no differences in disease severity (80% vs 75% with severe or critical disease, p=NS) or outcome (30% vs 31% died or deteriorating, p=NS). Table 1: Characteristics of Solid Organ Transplant Recipients with COVID-19 Infection Following SARS-CoV-2 Vaccination [Image: see text] CONCLUSION: SARS-CoV-2 infections after vaccination are occurring in SOTR, including cases of critical illness, suggesting reduced vaccine effectiveness within this vulnerable population. We did not appreciate any correlation between time from vaccination and COVID-19 disease severity or outcome. Further studies evaluating the true incidence of and risk factors for breakthrough infections among vaccinated SOTR are needed. DISCLOSURES: Matthew Kuehnert, M.D., American Association of Tissue Banks (Board Member)ICCBBA (Board Member)Musculoskeletal Transplant Foundation (Employee) John W. Baddley, M.D., Eli Lilly (Consultant)Pfizer (Consultant)R-Pharm (Consultant)Viela Bio (Consultant)
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spelling pubmed-86449682021-12-06 926. COVID-19 Infections After SARS-CoV-2 Vaccination in Solid Organ Transplant Recipients Saharia, Kapil Streit, Judy Beekmann, Susan E Polgreen, Philip M Kuehnert, Matthew Segev, Dorry Baddley, John W Miller, Rachel Open Forum Infect Dis Poster Abstracts BACKGROUND: Solid organ transplant recipients (SOTR) have lower humoral responses following SARS-CoV-2 vaccination. Whether this equates to reduced vaccine effectiveness in SOTR or impacts disease severity is not yet known. We used the IDSA Emerging Infections Network (EIN) to identify SARS-CoV-2 cases in vaccinated SOTR. We describe their clinical characteristics and outcomes. METHODS: On 4/7/21, we requested case reports via the EIN listserv of COVID-19 infection following SARS-CoV-2 vaccination in immunocompromised individuals. Case reports were collected until June 7(th). Online data collection included patient demographics, dates of SARS-CoV-2 vaccine administration and clinical data related to COVID-19 infection. We performed a descriptive analysis of these patient factors and compared differences between early onset (< / = 21 days after completing vaccine series) and late onset infection ( > 21 days after completing vaccine series). RESULTS: As of 6/7/21, 34 cases of COVID-19 infection after vaccination in SOTR were submitted. Most cases (79%) occurred in individuals who were fully vaccinated. Only 3 cases (8.5%) occurred in SOTR within their first year after transplantation. Clinical characteristics are listed in Table 1. The vaccine administration date was known for 26 SOTR among whom symptoms occurred a median of 26.5 days (IQR 21.75 days, range 5-79 days) after completing the COVID-19 vaccine series. Twenty-three SOTR (68%) required hospitalization of which 12 had critical illness. Outcome data was available for 29 individuals of whom 20 (69%) demonstrated improvement. When comparing SOTR with early versus late onset COVID-19 infection in relation to vaccination timing, there were no differences in disease severity (80% vs 75% with severe or critical disease, p=NS) or outcome (30% vs 31% died or deteriorating, p=NS). Table 1: Characteristics of Solid Organ Transplant Recipients with COVID-19 Infection Following SARS-CoV-2 Vaccination [Image: see text] CONCLUSION: SARS-CoV-2 infections after vaccination are occurring in SOTR, including cases of critical illness, suggesting reduced vaccine effectiveness within this vulnerable population. We did not appreciate any correlation between time from vaccination and COVID-19 disease severity or outcome. Further studies evaluating the true incidence of and risk factors for breakthrough infections among vaccinated SOTR are needed. DISCLOSURES: Matthew Kuehnert, M.D., American Association of Tissue Banks (Board Member)ICCBBA (Board Member)Musculoskeletal Transplant Foundation (Employee) John W. Baddley, M.D., Eli Lilly (Consultant)Pfizer (Consultant)R-Pharm (Consultant)Viela Bio (Consultant) Oxford University Press 2021-12-04 /pmc/articles/PMC8644968/ http://dx.doi.org/10.1093/ofid/ofab466.1121 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
Saharia, Kapil
Streit, Judy
Beekmann, Susan E
Polgreen, Philip M
Kuehnert, Matthew
Segev, Dorry
Baddley, John W
Miller, Rachel
926. COVID-19 Infections After SARS-CoV-2 Vaccination in Solid Organ Transplant Recipients
title 926. COVID-19 Infections After SARS-CoV-2 Vaccination in Solid Organ Transplant Recipients
title_full 926. COVID-19 Infections After SARS-CoV-2 Vaccination in Solid Organ Transplant Recipients
title_fullStr 926. COVID-19 Infections After SARS-CoV-2 Vaccination in Solid Organ Transplant Recipients
title_full_unstemmed 926. COVID-19 Infections After SARS-CoV-2 Vaccination in Solid Organ Transplant Recipients
title_short 926. COVID-19 Infections After SARS-CoV-2 Vaccination in Solid Organ Transplant Recipients
title_sort 926. covid-19 infections after sars-cov-2 vaccination in solid organ transplant recipients
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8644968/
http://dx.doi.org/10.1093/ofid/ofab466.1121
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