2021
DOI: 10.1016/j.imu.2021.100795
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Assessing the impact of vaccination in a COVID-19 compartmental model

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Cited by 9 publications
(10 citation statements)
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“…Antonini et al [12] used a mean duration of vaccinal and infection immunity of 240 days to predict short-term outcomes in Italy. For the first wave of COVID-19, Esteban & Almodovar-Abreu [14] used a sevencompartment vaccination model, which assumed no waning of efficacy, to forecast and compare deaths at 180 days into the first wave for assumed unvaccinated and vaccinated populations under an assumed 95% vaccine efficacy. Steyn et al [15] developed a vaccination model for New Zealand, assuming no waning of efficacy, with an assumed basic reproduction number of 6 for the delta variant.…”
Section: Vaccine Models Reviewedmentioning
confidence: 99%
“…Antonini et al [12] used a mean duration of vaccinal and infection immunity of 240 days to predict short-term outcomes in Italy. For the first wave of COVID-19, Esteban & Almodovar-Abreu [14] used a sevencompartment vaccination model, which assumed no waning of efficacy, to forecast and compare deaths at 180 days into the first wave for assumed unvaccinated and vaccinated populations under an assumed 95% vaccine efficacy. Steyn et al [15] developed a vaccination model for New Zealand, assuming no waning of efficacy, with an assumed basic reproduction number of 6 for the delta variant.…”
Section: Vaccine Models Reviewedmentioning
confidence: 99%
“…Antonini, Calandrini, and Bianconi, 2021 use a mean duration of vaccinal and infection immunity of 240 days to predict short-term outcomes in Italy. For the first wave of Covid-19, Esteban and Almodovar-Abreu, 2021 use a 7 compartment vaccination model, which assumes no waning of efficacy, to forecast and compare deaths at 180 days into the first wave for assumed un-vaccinated and vaccinated populations under an assumed 95% vaccine efficacy. Steyn et al, 2022 develop a vaccination model for New Zealand, assuming no waning of efficacy, with an assumed basic reproduction number of 6 for the delta variant.…”
Section: Vaccine Models Reviewedmentioning
confidence: 99%
“…Recently, Kanj et al ( 20 ), Hasan and Saeed ( 21 ), and Jeta et al ( 22 ) reviewed nineteen diseases, of which nine employed compartments compartmental (deterministic) models to analyze the transmission dynamics of the Mpox virus in populations comprising both humans and non-humans. These studies explored variations of the classical SIR (Susceptible-Infected-Recovered) vector-borne models ( 23 25 ) within the context of human and non-human interaction and utilized them to study Mpox disease transmission. Incorporating vaccination classes ( 26 ) is essential for the disease’s accurate representation of progression and incubation.…”
Section: Introductionmentioning
confidence: 99%