The path towards herd immunity: Predicting COVID-19 vaccination uptake through results from a stated choice study across six continents
Fecha
2022-04Autor
Hess, Stephane
Lancsar, Emily
Meyerhoff, Jürgen
Song, Fangqing
Van den Broek-Altenburg, Eline
Alaba, Olufunke A.
Amaris, Gloria
Arellana, Julián
Basso, Leonardo J.
Benson, Jamie
Bravo-Moncayo, Luis
Chanel, Olivier
Choi, Syngjoo
Crastes dit Sourd, Romain
Bettella Cybis, Helena
Dorner, Zack
Falco, Paolo
Garzón-Pérez, Luis
Glass, Kathryn
Guzman, Luis A.
Huang, Zhiran
Huynh, Elisabeth
Kim, Bongseop
Konstantinus, Abisai
Konstantinus, Iyaloo
Larranaga, Ana Margarita
Longo, Alberto
Loo, Becky P.Y.
Oehlmann, Malte
O ’ Neill, Vikki
Ortúzar, Juan de Dios
Sanz Sánchez, María José
Sarmiento, Olga L.
Moyo, Hazvinei Tamuka
Tucker, Steven
Wang, Yacan
Wang, Yu
Webb, Edward J.D.
Zhang, Junyi
Zuidgeest, Mark H.P.
Metadatos
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Social Sciences & Medicine 298 : (2022) // Article ID 114800
Resumen
Despite unprecedented progress in developing COVID-19 vaccines, global vaccination levels needed to reach herd immunity remain a distant target, while new variants keep emerging. Obtaining near universal vaccine uptake relies on understanding and addressing vaccine resistance. Simple questions about vaccine acceptance however ignore that the vaccines being offered vary across countries and even population subgroups, and differ in terms of efficacy and side effects. By using advanced discrete choice models estimated on stated choice data collected in 18 countries/territories across six continents, we show a substantial influence of vaccine characteristics. Uptake increases if more efficacious vaccines (95% vs 60%) are offered (mean across study areas=3.9%, range of 0.6%-8.1%) or if vaccines offer at least 12 months of protection (mean across study areas=2.4%, range of 0.2%-5.8%), while an increase in severe side effects (from 0.001% to 0.01%) leads to reduced uptake (mean=-1.3%, range of -0.2% to -3.9%). Additionally, a large share of individuals (mean=55.2%, range of 28%-75.8%) would delay vaccination by 3 months to obtain a more efficacious (95% vs 60%) vaccine, where this increases further if the low efficacy vaccine has a higher risk (0.01% instead of 0.001%) of severe side effects (mean=65.9%, range of 41.4%-86.5%). Our work highlights that careful consideration of which vaccines to offer can be beneficial. In support of this, we provide an interactive tool to predict uptake in a country as a function of the vaccines being deployed, and also depending on the levels of infectiousness and severity of circulating variants of COVID-19.