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Analysis of hematologic adverse events reported to a national surveillance system following COVID-19 bivalent booster vaccination
Hematologic complications, including vaccine-induced immune thrombotic thrombocytopenia (VITT), immune thrombocytopenia (ITP), and autoimmune hemolytic anemia (AIHA), have been associated with the original severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines. However, on August 31,...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933824/ https://www.ncbi.nlm.nih.gov/pubmed/36795118 http://dx.doi.org/10.1007/s00277-023-05136-2 |
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author | Jacobs, Jeremy W. Booth, Garrett S. Adkins, Brian D. |
author_facet | Jacobs, Jeremy W. Booth, Garrett S. Adkins, Brian D. |
author_sort | Jacobs, Jeremy W. |
collection | PubMed |
description | Hematologic complications, including vaccine-induced immune thrombotic thrombocytopenia (VITT), immune thrombocytopenia (ITP), and autoimmune hemolytic anemia (AIHA), have been associated with the original severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines. However, on August 31, 2022, new formulations of the Pfizer-BioNTech and Moderna vaccines were approved for use without clinical trial testing. Thus, any potential adverse hematologic effects with these new vaccines remain unknown. We queried the US Centers for Disease Control Vaccine Adverse Event Reporting System (VAERS), a national surveillance database, through February 3, 2023, all reported hematologic adverse events that occurred within 42 days of administration of either the Pfizer-BioNTech or Moderna Bivalent COVID-19 Booster vaccine. We included all patient ages and geographic locations and utilized 71 unique VAERS diagnostic codes pertaining to a hematologic condition as defined in the VAERS database. Fifty-five reports of hematologic events were identified (60.0% Pfizer-BioNTech, 27.3% Moderna, 7.3% Pfizer-BioNTech bivalent booster plus influenza, 5.5% Moderna bivalent booster plus influenza). The median age of patients was 66 years, and 90.9% (50/55) of reports involved a description of cytopenias or thrombosis. Notably, 3 potential cases of ITP and 1 case of VITT were identified. In one of the first safety analyses of the new SARS-CoV-2 booster vaccines, we identified few adverse hematologic events (1.05 per 1,000,000 doses), most of which could not be definitively attributed to vaccination. However, three reports of possible ITP and one report of possible VITT highlight the need for continued safety monitoring of these vaccines as their use expands and new formulations are authorized. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00277-023-05136-2. |
format | Online Article Text |
id | pubmed-9933824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-99338242023-02-17 Analysis of hematologic adverse events reported to a national surveillance system following COVID-19 bivalent booster vaccination Jacobs, Jeremy W. Booth, Garrett S. Adkins, Brian D. Ann Hematol Original Article Hematologic complications, including vaccine-induced immune thrombotic thrombocytopenia (VITT), immune thrombocytopenia (ITP), and autoimmune hemolytic anemia (AIHA), have been associated with the original severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines. However, on August 31, 2022, new formulations of the Pfizer-BioNTech and Moderna vaccines were approved for use without clinical trial testing. Thus, any potential adverse hematologic effects with these new vaccines remain unknown. We queried the US Centers for Disease Control Vaccine Adverse Event Reporting System (VAERS), a national surveillance database, through February 3, 2023, all reported hematologic adverse events that occurred within 42 days of administration of either the Pfizer-BioNTech or Moderna Bivalent COVID-19 Booster vaccine. We included all patient ages and geographic locations and utilized 71 unique VAERS diagnostic codes pertaining to a hematologic condition as defined in the VAERS database. Fifty-five reports of hematologic events were identified (60.0% Pfizer-BioNTech, 27.3% Moderna, 7.3% Pfizer-BioNTech bivalent booster plus influenza, 5.5% Moderna bivalent booster plus influenza). The median age of patients was 66 years, and 90.9% (50/55) of reports involved a description of cytopenias or thrombosis. Notably, 3 potential cases of ITP and 1 case of VITT were identified. In one of the first safety analyses of the new SARS-CoV-2 booster vaccines, we identified few adverse hematologic events (1.05 per 1,000,000 doses), most of which could not be definitively attributed to vaccination. However, three reports of possible ITP and one report of possible VITT highlight the need for continued safety monitoring of these vaccines as their use expands and new formulations are authorized. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00277-023-05136-2. Springer Berlin Heidelberg 2023-02-16 2023 /pmc/articles/PMC9933824/ /pubmed/36795118 http://dx.doi.org/10.1007/s00277-023-05136-2 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Jacobs, Jeremy W. Booth, Garrett S. Adkins, Brian D. Analysis of hematologic adverse events reported to a national surveillance system following COVID-19 bivalent booster vaccination |
title | Analysis of hematologic adverse events reported to a national surveillance system following COVID-19 bivalent booster vaccination |
title_full | Analysis of hematologic adverse events reported to a national surveillance system following COVID-19 bivalent booster vaccination |
title_fullStr | Analysis of hematologic adverse events reported to a national surveillance system following COVID-19 bivalent booster vaccination |
title_full_unstemmed | Analysis of hematologic adverse events reported to a national surveillance system following COVID-19 bivalent booster vaccination |
title_short | Analysis of hematologic adverse events reported to a national surveillance system following COVID-19 bivalent booster vaccination |
title_sort | analysis of hematologic adverse events reported to a national surveillance system following covid-19 bivalent booster vaccination |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933824/ https://www.ncbi.nlm.nih.gov/pubmed/36795118 http://dx.doi.org/10.1007/s00277-023-05136-2 |
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