Evaluating the impact of extended dosing intervals on mRNA COVID-19 vaccine effectiveness in adolescents.

Tim K Tsang, Sheena G Sullivan, Yu Meng, Francisco Tsz Tsun Lai, Min Fan, Xiaotong Huang, Yun Lin, Liping Peng, Chengyao Zhang, Bingyi Yang, Kylie E C Ainslie, Benjamin J Cowling
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Abstract

Extending the dosing interval of a primary series of mRNA COVID-19 vaccination has been employed to reduce myocarditis risk in adolescents, but previous evaluation of impact on vaccine effectiveness (VE) is limited to risk after second dose. Here, we quantified the impact of the dosing interval based on case notifications and vaccination uptake in Hong Kong from January to April 2022. We estimated that the hazard ratio (HR) and odds ratio (OR) of infections after the second dose for extended (28 days or more) versus regular (21-27 days) dosing intervals ranged from 0.86 to 0.99 from calendar-time proportional hazards models, and from 0.85 to 0.87 from matching approaches, respectively. Adolescents in the extended dosing groups (including those who did not receive a second dose in the study period) had a higher hazard of infection than those with a regular dosing interval during the intra-dose period (HR: 1.66; 95% CI: 1.07, 2.59; p = 0.02) after the first dose. Implementing an extended dosing interval should consider multiple factors including the degree of myocarditis risk, the degree of protection afforded by each dose, and the extra protection achievable using an extended dosing interval.

评估延长给药间隔对青少年 mRNA COVID-19 疫苗有效性的影响。
延长mRNA COVID-19疫苗初次接种的间隔时间可降低青少年患心肌炎的风险,但以往对疫苗有效性(VE)影响的评估仅限于第二次接种后的风险。在此,我们根据2022年1月至4月香港的病例通报和疫苗接种率,量化了剂量间隔的影响。根据历时比例危险模型,我们估计延长服药间隔(28 天或以上)与常规服药间隔(21-27 天)的第二次服药后感染的危险比 (HR) 和几率比 (OR) 分别为 0.86 至 0.99,而匹配方法的危险比和几率比分别为 0.85 至 0.87。延长给药间隔组的青少年(包括在研究期间未接受第二次给药的青少年)在第一次给药后的给药间隔期内的感染风险高于正常给药间隔组(HR:1.66;95% CI:1.07,2.59;P = 0.02)。延长给药间隔应考虑多种因素,包括心肌炎风险程度、每次给药所提供的保护程度以及延长给药间隔可获得的额外保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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