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Background rates of adverse events of special interest for COVID-19 vaccine safety monitoring in the United States, 2019–2020
BACKGROUND: The U.S. Food and Drug Administration (FDA) Biologics Effectiveness and Safety (BEST) Initiative conducts active surveillance of adverse events of special interest (AESI) after COVID-19 vaccination. Historical incidence rates (IRs) of AESI are comparators to evaluate safety. METHODS: We...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640387/ https://www.ncbi.nlm.nih.gov/pubmed/36404170 http://dx.doi.org/10.1016/j.vaccine.2022.11.003 |
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author | Moll, Keran Lufkin, Bradley Fingar, Kathryn R. Ke Zhou, Cindy Tworkoski, Ellen Shi, Chianti Hobbi, Shayan Hu, Mao Sheng, Minya McCarty, Jillian Shangguan, Shanlai Burrell, Timothy Chillarige, Yoganand Beers, Jeff Saunders-Hastings, Patrick Muthuri, Stella Edwards, Kathryn Black, Steven Kelman, Jeff Reich, Christian Amend, Kandace L. Djibo, Djeneba Audrey Beachler, Daniel Ogilvie, Rachel P. Secora, Alex McMahill-Walraven, Cheryl N. Seeger, John D. Lloyd, Patricia Thompson, Deborah Dimova, Rositsa MaCurdy, Thomas Obidi, Joyce Anderson, Steve Forshee, Richard Wong, Hui-Lee Shoaibi, Azadeh |
author_facet | Moll, Keran Lufkin, Bradley Fingar, Kathryn R. Ke Zhou, Cindy Tworkoski, Ellen Shi, Chianti Hobbi, Shayan Hu, Mao Sheng, Minya McCarty, Jillian Shangguan, Shanlai Burrell, Timothy Chillarige, Yoganand Beers, Jeff Saunders-Hastings, Patrick Muthuri, Stella Edwards, Kathryn Black, Steven Kelman, Jeff Reich, Christian Amend, Kandace L. Djibo, Djeneba Audrey Beachler, Daniel Ogilvie, Rachel P. Secora, Alex McMahill-Walraven, Cheryl N. Seeger, John D. Lloyd, Patricia Thompson, Deborah Dimova, Rositsa MaCurdy, Thomas Obidi, Joyce Anderson, Steve Forshee, Richard Wong, Hui-Lee Shoaibi, Azadeh |
author_sort | Moll, Keran |
collection | PubMed |
description | BACKGROUND: The U.S. Food and Drug Administration (FDA) Biologics Effectiveness and Safety (BEST) Initiative conducts active surveillance of adverse events of special interest (AESI) after COVID-19 vaccination. Historical incidence rates (IRs) of AESI are comparators to evaluate safety. METHODS: We estimated IRs of 17 AESI in six administrative claims databases from January 1, 2019, to December 11, 2020: Medicare claims for adults ≥ 65 years and commercial claims (Blue Health Intelligence®, CVS Health, HealthCore Integrated Research Database, IBM® MarketScan® Commercial Database, Optum pre-adjudicated claims) for adults < 65 years. IRs were estimated by sex, age, race/ethnicity (Medicare), and nursing home residency (Medicare) in 2019 and for specific periods in 2020. RESULTS: The study included >100 million enrollees annually. In 2019, rates of most AESI increased with age. However, compared with commercially insured adults, Medicare enrollees had lower IRs of anaphylaxis (11 vs 12–19 per 100,000 person-years), appendicitis (80 vs 117–155), and narcolepsy (38 vs 41–53). Rates were higher in males than females for most AESI across databases and varied by race/ethnicity and nursing home status (Medicare). Acute myocardial infarction (Medicare) and anaphylaxis (all databases) IRs varied by season. IRs of most AESI were lower during March–May 2020 compared with March–May 2019 but returned to pre-pandemic levels after May 2020. However, rates of Bell’s palsy, Guillain-Barré syndrome, narcolepsy, and hemorrhagic/non-hemorrhagic stroke remained lower in multiple databases after May 2020, whereas some AESI (e.g., disseminated intravascular coagulation) exhibited higher rates after May 2020 compared with 2019. CONCLUSION: AESI background rates varied by database and demographics and fluctuated in March–December 2020, but most returned to pre-pandemic levels after May 2020. It is critical to standardize demographics and consider seasonal and other trends when comparing historical rates with post-vaccination AESI rates in the same database to evaluate COVID-19 vaccine safety. |
format | Online Article Text |
id | pubmed-9640387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-96403872022-11-14 Background rates of adverse events of special interest for COVID-19 vaccine safety monitoring in the United States, 2019–2020 Moll, Keran Lufkin, Bradley Fingar, Kathryn R. Ke Zhou, Cindy Tworkoski, Ellen Shi, Chianti Hobbi, Shayan Hu, Mao Sheng, Minya McCarty, Jillian Shangguan, Shanlai Burrell, Timothy Chillarige, Yoganand Beers, Jeff Saunders-Hastings, Patrick Muthuri, Stella Edwards, Kathryn Black, Steven Kelman, Jeff Reich, Christian Amend, Kandace L. Djibo, Djeneba Audrey Beachler, Daniel Ogilvie, Rachel P. Secora, Alex McMahill-Walraven, Cheryl N. Seeger, John D. Lloyd, Patricia Thompson, Deborah Dimova, Rositsa MaCurdy, Thomas Obidi, Joyce Anderson, Steve Forshee, Richard Wong, Hui-Lee Shoaibi, Azadeh Vaccine Article BACKGROUND: The U.S. Food and Drug Administration (FDA) Biologics Effectiveness and Safety (BEST) Initiative conducts active surveillance of adverse events of special interest (AESI) after COVID-19 vaccination. Historical incidence rates (IRs) of AESI are comparators to evaluate safety. METHODS: We estimated IRs of 17 AESI in six administrative claims databases from January 1, 2019, to December 11, 2020: Medicare claims for adults ≥ 65 years and commercial claims (Blue Health Intelligence®, CVS Health, HealthCore Integrated Research Database, IBM® MarketScan® Commercial Database, Optum pre-adjudicated claims) for adults < 65 years. IRs were estimated by sex, age, race/ethnicity (Medicare), and nursing home residency (Medicare) in 2019 and for specific periods in 2020. RESULTS: The study included >100 million enrollees annually. In 2019, rates of most AESI increased with age. However, compared with commercially insured adults, Medicare enrollees had lower IRs of anaphylaxis (11 vs 12–19 per 100,000 person-years), appendicitis (80 vs 117–155), and narcolepsy (38 vs 41–53). Rates were higher in males than females for most AESI across databases and varied by race/ethnicity and nursing home status (Medicare). Acute myocardial infarction (Medicare) and anaphylaxis (all databases) IRs varied by season. IRs of most AESI were lower during March–May 2020 compared with March–May 2019 but returned to pre-pandemic levels after May 2020. However, rates of Bell’s palsy, Guillain-Barré syndrome, narcolepsy, and hemorrhagic/non-hemorrhagic stroke remained lower in multiple databases after May 2020, whereas some AESI (e.g., disseminated intravascular coagulation) exhibited higher rates after May 2020 compared with 2019. CONCLUSION: AESI background rates varied by database and demographics and fluctuated in March–December 2020, but most returned to pre-pandemic levels after May 2020. It is critical to standardize demographics and consider seasonal and other trends when comparing historical rates with post-vaccination AESI rates in the same database to evaluate COVID-19 vaccine safety. Elsevier Science 2023-01-09 2022-11-08 /pmc/articles/PMC9640387/ /pubmed/36404170 http://dx.doi.org/10.1016/j.vaccine.2022.11.003 Text en Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Moll, Keran Lufkin, Bradley Fingar, Kathryn R. Ke Zhou, Cindy Tworkoski, Ellen Shi, Chianti Hobbi, Shayan Hu, Mao Sheng, Minya McCarty, Jillian Shangguan, Shanlai Burrell, Timothy Chillarige, Yoganand Beers, Jeff Saunders-Hastings, Patrick Muthuri, Stella Edwards, Kathryn Black, Steven Kelman, Jeff Reich, Christian Amend, Kandace L. Djibo, Djeneba Audrey Beachler, Daniel Ogilvie, Rachel P. Secora, Alex McMahill-Walraven, Cheryl N. Seeger, John D. Lloyd, Patricia Thompson, Deborah Dimova, Rositsa MaCurdy, Thomas Obidi, Joyce Anderson, Steve Forshee, Richard Wong, Hui-Lee Shoaibi, Azadeh Background rates of adverse events of special interest for COVID-19 vaccine safety monitoring in the United States, 2019–2020 |
title | Background rates of adverse events of special interest for COVID-19 vaccine safety monitoring in the United States, 2019–2020 |
title_full | Background rates of adverse events of special interest for COVID-19 vaccine safety monitoring in the United States, 2019–2020 |
title_fullStr | Background rates of adverse events of special interest for COVID-19 vaccine safety monitoring in the United States, 2019–2020 |
title_full_unstemmed | Background rates of adverse events of special interest for COVID-19 vaccine safety monitoring in the United States, 2019–2020 |
title_short | Background rates of adverse events of special interest for COVID-19 vaccine safety monitoring in the United States, 2019–2020 |
title_sort | background rates of adverse events of special interest for covid-19 vaccine safety monitoring in the united states, 2019–2020 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640387/ https://www.ncbi.nlm.nih.gov/pubmed/36404170 http://dx.doi.org/10.1016/j.vaccine.2022.11.003 |
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