医学
2019年冠状病毒病(COVID-19)
冠状病毒
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
倍他科诺病毒
2019-20冠状病毒爆发
大流行
冠状病毒感染
重症监护医学
肺炎
疾病
呼吸系统
内科学
急诊医学
病毒学
免疫学
传染病(医学专业)
爆发
作者
Liang En Wee,Deanette Pang,Calvin J Chiew,Tan Jian-cheng,Vernon Lee,Benjamin Ong,David Chien Lye,Kelvin Bryan Tan
摘要
Abstract Background Literature on long-term real-world vaccine effectiveness of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) booster vaccines (up to and beyond 360 days) is scarce. We report estimates of protection against symptomatic infection, emergency department (ED) attendances and hospitalizations up to and beyond 360 days post-receipt of booster messenger RNA (mRNA) vaccines among Singaporeans aged ≥60 years during an Omicron XBB wave. Methods We conducted a population-based cohort study including all Singaporeans aged ≥60 years with no documented prior SARS-CoV-2 infection who had previously received ≥3 doses of mRNA vaccines (BNT162b2/mRNA-1273), over a 4-month period during transmission of Omicron XBB. We reported the adjusted incidence-rate-ratio (IRR) for symptomatic infections, ED attendances and hospitalizations at different time-intervals from both first and second boosters, using Poisson regression; with the reference group being those who received their first booster 90 to 179 days prior. Results In total, 506 856 boosted adults were included, contributing 55 846 165 person-days of observation. Protection against symptomatic infections among those who received a third vaccine dose (first booster) waned after 180 days with increasing adjusted IRRs; however, protection against ED attendances and hospitalizations held up, with comparable adjusted IRRs with increasing time from third vaccine doses (≥360 days from third dose: adjusted IRR [ED attendances] = 0.73, 95% confidence interval [CI] = .62–.85; adjusted IRR [hospitalization] = 0.58, 95% CI = .49–.70). Conclusions Our results highlight the benefit of a booster dose in reducing ED attendances and hospitalizations amongst older adults aged ≥60 years with no documented prior SARS-CoV-2 infection, during an Omicron XBB wave; up to and beyond 360 days post-booster. A second booster provided further reduction.
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