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Primary and booster vaccination in reducing severe clinical outcomes associated with Omicron Naïve infection
BACKGROUND: Little is known about long-term effectiveness of COVID-19 vaccine in reducing severity and deaths associated with Omicron VOC not perturbed by prior infection and independent of oral anti-viral therapy and non-pharmaceutical (NPI). METHODS: A retrospective observational cohort study was...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for Health Sciences.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708104/ https://www.ncbi.nlm.nih.gov/pubmed/36470007 http://dx.doi.org/10.1016/j.jiph.2022.11.028 |
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author | Hsu, Chen-Yang Chang, Jung-Chen Chen, Sam Li-Shen Chang, Hao-Hsiang Lin, Abbie Ting-Yu Yen, Amy Ming-Feng Chen, Hsiu-Hsi |
author_facet | Hsu, Chen-Yang Chang, Jung-Chen Chen, Sam Li-Shen Chang, Hao-Hsiang Lin, Abbie Ting-Yu Yen, Amy Ming-Feng Chen, Hsiu-Hsi |
author_sort | Hsu, Chen-Yang |
collection | PubMed |
description | BACKGROUND: Little is known about long-term effectiveness of COVID-19 vaccine in reducing severity and deaths associated with Omicron VOC not perturbed by prior infection and independent of oral anti-viral therapy and non-pharmaceutical (NPI). METHODS: A retrospective observational cohort study was applied to Taiwan community during the unprecedent large-scale outbreaks of Omicron BA.2 between April and August, 2022. Primary vaccination since March, 2021 and booster vaccination since January, 2022 were offered on population level. Oral Anti-viral therapy was also offered as of mid-May 2022. The population-based effectiveness of vaccination in reducing the risk of moderate and severe cases of and death from Omicron BA.2 with the consideration of NPI and oral anti-viral therapy were assessed by using Bayesian hierarchical models. RESULTS: The risks of three clinical outcomes associated with Omicron VOC infection were lowest for booster vaccination, followed by primary vaccination, and highest for incomplete vaccination with the consistent trends of being at increased risk for three outcomes from the young people aged 12 years or below until the elderly people aged 75 years or older with 7 age groups. Before the period using oral anti-viral therapy, complete primary vaccination with the duration more than 9 months before outbreaks conferred the statistically significant 47 % (23–64 %) reduction of death, 48 % (30–61 %) of severe disease, and 46 % (95 % CI: 37–54 %) of moderate disease after adjusting for 10–20 % independent effect of NPI. The benefits of booster vaccination within three months were further enhanced to 76 % (95 % CI: 67–86 %), 74 % (95 % CI: 67–80 %), and 61 % (95 % CI: 56–65 %) for three corresponding outcomes. The additional effectiveness of oral anti-viral therapy in reducing moderate disease was 13 % for the booster group and 5.8 % for primary vaccination. CONCLUSIONS: We corroborated population effectiveness of primary vaccination and its booster vaccination, independent of oral anti-viral therapy and NPI, in reducing severe clinical outcomes associated with Omicron BA.2 naïve infection population. |
format | Online Article Text |
id | pubmed-9708104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Authors. Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for Health Sciences. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97081042022-11-30 Primary and booster vaccination in reducing severe clinical outcomes associated with Omicron Naïve infection Hsu, Chen-Yang Chang, Jung-Chen Chen, Sam Li-Shen Chang, Hao-Hsiang Lin, Abbie Ting-Yu Yen, Amy Ming-Feng Chen, Hsiu-Hsi J Infect Public Health Original Article BACKGROUND: Little is known about long-term effectiveness of COVID-19 vaccine in reducing severity and deaths associated with Omicron VOC not perturbed by prior infection and independent of oral anti-viral therapy and non-pharmaceutical (NPI). METHODS: A retrospective observational cohort study was applied to Taiwan community during the unprecedent large-scale outbreaks of Omicron BA.2 between April and August, 2022. Primary vaccination since March, 2021 and booster vaccination since January, 2022 were offered on population level. Oral Anti-viral therapy was also offered as of mid-May 2022. The population-based effectiveness of vaccination in reducing the risk of moderate and severe cases of and death from Omicron BA.2 with the consideration of NPI and oral anti-viral therapy were assessed by using Bayesian hierarchical models. RESULTS: The risks of three clinical outcomes associated with Omicron VOC infection were lowest for booster vaccination, followed by primary vaccination, and highest for incomplete vaccination with the consistent trends of being at increased risk for three outcomes from the young people aged 12 years or below until the elderly people aged 75 years or older with 7 age groups. Before the period using oral anti-viral therapy, complete primary vaccination with the duration more than 9 months before outbreaks conferred the statistically significant 47 % (23–64 %) reduction of death, 48 % (30–61 %) of severe disease, and 46 % (95 % CI: 37–54 %) of moderate disease after adjusting for 10–20 % independent effect of NPI. The benefits of booster vaccination within three months were further enhanced to 76 % (95 % CI: 67–86 %), 74 % (95 % CI: 67–80 %), and 61 % (95 % CI: 56–65 %) for three corresponding outcomes. The additional effectiveness of oral anti-viral therapy in reducing moderate disease was 13 % for the booster group and 5.8 % for primary vaccination. CONCLUSIONS: We corroborated population effectiveness of primary vaccination and its booster vaccination, independent of oral anti-viral therapy and NPI, in reducing severe clinical outcomes associated with Omicron BA.2 naïve infection population. The Authors. Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for Health Sciences. 2023-01 2022-11-30 /pmc/articles/PMC9708104/ /pubmed/36470007 http://dx.doi.org/10.1016/j.jiph.2022.11.028 Text en © 2022 The Authors 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 | Original Article Hsu, Chen-Yang Chang, Jung-Chen Chen, Sam Li-Shen Chang, Hao-Hsiang Lin, Abbie Ting-Yu Yen, Amy Ming-Feng Chen, Hsiu-Hsi Primary and booster vaccination in reducing severe clinical outcomes associated with Omicron Naïve infection |
title | Primary and booster vaccination in reducing severe clinical outcomes associated with Omicron Naïve infection |
title_full | Primary and booster vaccination in reducing severe clinical outcomes associated with Omicron Naïve infection |
title_fullStr | Primary and booster vaccination in reducing severe clinical outcomes associated with Omicron Naïve infection |
title_full_unstemmed | Primary and booster vaccination in reducing severe clinical outcomes associated with Omicron Naïve infection |
title_short | Primary and booster vaccination in reducing severe clinical outcomes associated with Omicron Naïve infection |
title_sort | primary and booster vaccination in reducing severe clinical outcomes associated with omicron naïve infection |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708104/ https://www.ncbi.nlm.nih.gov/pubmed/36470007 http://dx.doi.org/10.1016/j.jiph.2022.11.028 |
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