Parés-Badell Oleguer, Zules-Oña Ricardo, Armadans Lluís, Pinós Laia, Borrás-Bermejo Blanca, Otero Susana, Rodrigo-Pendás José Ángel, Vivet-Escalé Martí, Cossio-Gil Yolima, Agustí Antònia, Aguilera Cristina, Campins Magda, Martínez-Gómez Xavier
Servei de Medicina Preventiva i Epidemiologia, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035 Barcelona, Spain.
Grup de recerca de Epidemiologia i Salut Pública, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035 Barcelona, Spain.
Vaccines (Basel). 2022 Jul 29;10(8):1217. doi: 10.3390/vaccines10081217.
The objective of this study was to assess the local and systemic adverse reactions after the administration of a COVID-19 mRNA-1273 booster between December 2021 and February 2022 by comparing the type of mRNA vaccine used as primary series (mRNA-1273 or BNT162b2) and homologous versus heterologous booster in health care workers (HCW). A cross-sectional study was performed in HCW at a tertiary hospital in Barcelona, Spain. A total of 17% of booster recipients responded to the questionnaire. The frequency of reactogenicity after the mRNA-1273 booster (88.5%) was similar to the mRNA-1273 primary doses (85.8%), and higher than the BNT162b2 primary doses (71.1%). The reactogenicity was similar after receiving a heterologous booster compared to a homologous booster (88.0% vs. 90.2%, = 0.3), and no statistically significant differences were identified in any local or systemic reactions. A higher frequency of medical leave was identified in the homologous booster dose group vs. the heterologous booster dose group (AOR 1.45; 95% CI: 1.00-2.07; = 0.045). Our findings could be helpful in improving vaccine confidence toward heterologous combinations in the general population and in health care workers.
本研究的目的是通过比较医疗工作者(HCW)中用作初始系列的mRNA疫苗类型(mRNA-1273或BNT162b2)以及同源与异源加强针,评估2021年12月至2022年2月期间接种COVID-19 mRNA-1273加强针后的局部和全身不良反应。在西班牙巴塞罗那一家三级医院的医疗工作者中进行了一项横断面研究。共有17%的加强针接种者回复了问卷。mRNA-1273加强针后的反应原性频率(88.5%)与mRNA-1273初始剂量(85.8%)相似,且高于BNT162b2初始剂量(71.1%)。与同源加强针相比,接种异源加强针后的反应原性相似(88.0%对90.2%,P = 0.3),在任何局部或全身反应中均未发现统计学上的显著差异。与异源加强针剂量组相比,同源加强针剂量组的病假频率更高(调整后的比值比1.45;95%置信区间:1.00 - 2.07;P = 0.045)。我们的研究结果可能有助于提高普通人群和医疗工作者对异源组合疫苗的信心。