Abstract

Simple SummaryThe main way to overcome the COVID-19 pandemic is mass vaccination of the public. However, the public’s vaccine hesitancy toward the available vaccines is a big challenge in the fighting against the coronavirus spreading. We aimed in this study to report for the first time the short-term side effects following mRNA-based (Pfizer-BioNTech and Moderna) and viral vector-based (AstraZeneca) COVID-19 vaccines among German healthcare workers. A survey-based study was conducted through an online validated questionnaire. Overall, 88.1% of the German healthcare workers included in this study reported at least one side effect following the COVID-19 vaccination. The mRNA-based vaccines were associated with a higher prevalence of local side effects (e.g., injection site pain), while the viral vector-based vaccine was associated with a higher prevalence of systemic side effects (e.g., headache/fatigue). The vast majority (84.9%) of side effects resolved within 1–3 days after vaccination, which are promising results from a safety point of view for both types of vaccines. This study is one of the few studies that aims to enhance our emerging knowledge about the risk factors of COVID-19 vaccines side effects by inquiring and analyzing the self-reported side effects across various demographic and medical parameters.Background: the increasing number of COVID-19 vaccines available to the public may trigger hesitancy or selectivity towards vaccination. This study aimed to evaluate the post-vaccination side effects of the different vaccines approved in Germany; Methods: a cross-sectional survey-based study was carried out using an online questionnaire validated and tested for a priori reliability. The questionnaire inquired about demographic data, medical and COVID-19-related anamneses, and local, systemic, oral, and skin-related side effects following COVID-19 vaccination; Results: out of the 599 participating healthcare workers, 72.3% were females, and 79.1% received mRNA-based vaccines, while 20.9% received a viral vector-based vaccine. 88.1% of the participants reported at least one side effect. Injection site pain (75.6%) was the most common local side effect, and headache/fatigue (53.6%), muscle pain (33.2%), malaise (25%), chills (23%), and joint pain (21.2%) were the most common systemic side effects. The vast majority (84.9%) of side effects resolved within 1–3 days post-vaccination; Conclusions: the mRNA-based vaccines were associated with a higher prevalence of local side effects (78.3% vs. 70.4%; Sig. = 0.064), while the viral vector-based vaccine was associated with a higher prevalence of systemic side effects (87.2% vs. 61%; Sig. < 0.001). Females and the younger age group were associated with an increased risk of side effects either after mRNA-based or viral vector-based vaccines. The gender- and age-based differences warrant further rigorous investigation and standardized methodology.

Highlights

  • Since the spreading of the COVID-19 pandemic, its influence has become evident worldwide in all disciplines and sectors, e.g., social, financial, and health sectors, etc

  • The vast majority (84.9%) of side effects resolved within 1–3 days post-vaccination; Conclusions: the messenger RNA (mRNA)-based vaccines were associated with a higher prevalence of local side effects (78.3% vs. 70.4%; Sig. = 0.064), while the viral vector-based vaccine was associated with a higher prevalence of systemic side effects (87.2% vs. 61%; Sig. < 0.001)

  • Females and the younger age group were associated with an increased risk of side effects either after mRNA-based or viral vector-based vaccines

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Summary

Introduction

Since the spreading of the COVID-19 pandemic, its influence has become evident worldwide in all disciplines and sectors, e.g., social, financial, and health sectors, etc. The currently available vaccines against SARS-CoV-2 are manufactured by one of the following technologies: (a) mRNA-based vaccines, (b) viral vector-based vaccines, (c) protein subunit vaccines, and (d) whole virus or inactivated virus vaccines [3]. Heretofore, the European Medicines Agency (EMA) has approved vaccines that only belong to the first two technologies (mRNA-based and viral vector-based vaccines), which aim to produce spike protein-specific antibodies [4]. The mRNA-based technology is relatively novel in vaccine industry, and it employs molecular templates of messenger RNA (mRNA) to deliver the genetic information to produce the spike (S) glycoprotein antigen, not to deliver the antigen itself [5]. The viral vector-based vaccines against SARS-CoV-2 use a non-replicating harmless version of adenovirus as a vehicle to deliver the genetic code of the S glycoprotein antigen, eliciting the targeted immune response [6]

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