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A global epidemiological analysis of COVID-19 vaccine types and clinical outcomes

OBJECTIVES: To compare messenger RNA (mRNA)–based and adenovirus-vectored vaccines (ADVVs) with inactivated virus vaccines (IVVs) using real-world aggregate data. METHODS: We performed longitudinal analyses of publicly accessible epidemiological, clinical, virological, vaccine-related, and other pub...

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Autores principales: Alhinai, Zaid, Park, Sangshin, Choe, Young-June, Michelow, Ian C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499984/
https://www.ncbi.nlm.nih.gov/pubmed/36155824
http://dx.doi.org/10.1016/j.ijid.2022.09.014
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author Alhinai, Zaid
Park, Sangshin
Choe, Young-June
Michelow, Ian C.
author_facet Alhinai, Zaid
Park, Sangshin
Choe, Young-June
Michelow, Ian C.
author_sort Alhinai, Zaid
collection PubMed
description OBJECTIVES: To compare messenger RNA (mRNA)–based and adenovirus-vectored vaccines (ADVVs) with inactivated virus vaccines (IVVs) using real-world aggregate data. METHODS: We performed longitudinal analyses of publicly accessible epidemiological, clinical, virological, vaccine-related, and other public health data from 41 eligible countries during the first half of 2021. The relationships between vaccination coverage and clinical outcomes were analyzed using repeated measures correlation analyses and mixed-effects modeling to adjust for potential mediating and confounding factors. RESULTS: Countries that used mRNA and/or ADVV (n = 31) vs IVV, among other vaccine types (n = 10), had different distributions of age (42.4 vs 33.9 years, respectively; P-value = 0.0006), gross domestic product per capita ($ 38,606 vs $ 20,422, respectively; P <0.0001), and population sizes (8,655,541 vs 5,139,162, respectively; P-value = 0.36). After adjustment for country differences, the stringency of nonpharmaceutical interventions, and dominant SARS-CoV-2 variant types, populations that received mRNA and/or ADVV had significantly lower rates of cases and deaths over time (P <0.001 for each analysis). Populations vaccinated with IVV, among others, had significantly higher rates of cases and deaths over time (P <0.05 for each analysis). CONCLUSION: The real-world effectiveness of IVV may be inferior to mRNA and/or ADVV, and prospective comparative studies are needed to critically evaluate the role of IVV in the context of contemporary SARS-CoV-2 variants.
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spelling pubmed-94999842022-09-23 A global epidemiological analysis of COVID-19 vaccine types and clinical outcomes Alhinai, Zaid Park, Sangshin Choe, Young-June Michelow, Ian C. Int J Infect Dis Article OBJECTIVES: To compare messenger RNA (mRNA)–based and adenovirus-vectored vaccines (ADVVs) with inactivated virus vaccines (IVVs) using real-world aggregate data. METHODS: We performed longitudinal analyses of publicly accessible epidemiological, clinical, virological, vaccine-related, and other public health data from 41 eligible countries during the first half of 2021. The relationships between vaccination coverage and clinical outcomes were analyzed using repeated measures correlation analyses and mixed-effects modeling to adjust for potential mediating and confounding factors. RESULTS: Countries that used mRNA and/or ADVV (n = 31) vs IVV, among other vaccine types (n = 10), had different distributions of age (42.4 vs 33.9 years, respectively; P-value = 0.0006), gross domestic product per capita ($ 38,606 vs $ 20,422, respectively; P <0.0001), and population sizes (8,655,541 vs 5,139,162, respectively; P-value = 0.36). After adjustment for country differences, the stringency of nonpharmaceutical interventions, and dominant SARS-CoV-2 variant types, populations that received mRNA and/or ADVV had significantly lower rates of cases and deaths over time (P <0.001 for each analysis). Populations vaccinated with IVV, among others, had significantly higher rates of cases and deaths over time (P <0.05 for each analysis). CONCLUSION: The real-world effectiveness of IVV may be inferior to mRNA and/or ADVV, and prospective comparative studies are needed to critically evaluate the role of IVV in the context of contemporary SARS-CoV-2 variants. The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. 2022-11 2022-09-23 /pmc/articles/PMC9499984/ /pubmed/36155824 http://dx.doi.org/10.1016/j.ijid.2022.09.014 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 Article
Alhinai, Zaid
Park, Sangshin
Choe, Young-June
Michelow, Ian C.
A global epidemiological analysis of COVID-19 vaccine types and clinical outcomes
title A global epidemiological analysis of COVID-19 vaccine types and clinical outcomes
title_full A global epidemiological analysis of COVID-19 vaccine types and clinical outcomes
title_fullStr A global epidemiological analysis of COVID-19 vaccine types and clinical outcomes
title_full_unstemmed A global epidemiological analysis of COVID-19 vaccine types and clinical outcomes
title_short A global epidemiological analysis of COVID-19 vaccine types and clinical outcomes
title_sort global epidemiological analysis of covid-19 vaccine types and clinical outcomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499984/
https://www.ncbi.nlm.nih.gov/pubmed/36155824
http://dx.doi.org/10.1016/j.ijid.2022.09.014
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