[用载体疫苗ChAdOx1-S(阿斯利康COVID-19疫苗)免疫SARS-CoV-2后的主观幸福感和工作能力]。

Pub Date : 2022-01-01 Epub Date: 2021-11-07 DOI:10.1007/s40664-021-00448-4
Johannes Kalbhenn, Feline Gabler, Sebastian Heinrich, Daniel Steinmann
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引用次数: 0

摘要

背景:SARS冠状病毒19疫苗ChAdOx1‑S (Vaxzevria, AstraZeneca)已于2021年1月获得德国保罗·埃利希研究所的许可。在几次运动中,保健工作者和医科学生在自愿的基础上获得了这种疫苗。目的:该研究的主要终点是评估首次接种ChAdOx1‑S后丧失工作能力的比率和持续时间。次要终点是不良事件的类型和严重程度以及自我感知的耐受性。材料和方法:所有接种者在接种第一剂ChAdOx1‑S后完成一次匿名在线调查问卷。副作用的严重程度使用数值范围从0到10的有序数值评定量表进行查询。其他关键数据点是年龄、性别和职业组。注射后几天的工作能力也通过自我报告进行评估。结果:对1988名调查对象的数据进行了分析。平均年龄37.13岁(标准差13.7岁)。受访者中女性占69.8%,与患者有接触的治疗和技术专业占48.1%,学生占38%,护理人员占10.6%,医生占4%。只有14.4%的应答者报告耐受无副作用的疫苗接种。最常见的副作用是疲劳,其次是注射部位疼痛。紧随其后的依次是头痛、四肢疼痛和寒战。接种疫苗后,18%的答复者认为能够立即返回工作岗位,51%的答复者必须报告自己在接种疫苗后至少1天不适合工作。副作用在男性和年轻受访者中更为普遍。结论:接种ChAdOx1‑S疫苗经常出现不良反应。这导致37%的受访者报告生病。尽管如此,89.6%的受访者仍会选择再次接种ChAdOx1‑S疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[Subjective well-being and ability to work after SARS-CoV-2 immunization with the vector vaccine ChAdOx1-S (AstraZeneca COVID-19 vaccine)].

[Subjective well-being and ability to work after SARS-CoV-2 immunization with the vector vaccine ChAdOx1-S (AstraZeneca COVID-19 vaccine)].

[Subjective well-being and ability to work after SARS-CoV-2 immunization with the vector vaccine ChAdOx1-S (AstraZeneca COVID-19 vaccine)].

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[Subjective well-being and ability to work after SARS-CoV-2 immunization with the vector vaccine ChAdOx1-S (AstraZeneca COVID-19 vaccine)].

Background: The SARS coronavirus 19 vaccine ChAdOx1‑S (Vaxzevria, AstraZeneca) has been licensed since January 2021 by the Paul Ehrlich Institute for Germany. In several campaigns, healthcare workers and medical students were offered this vaccine on a voluntary basis.

Aim: The primary endpoint of the study was to assess the rate and duration of the incapacity to work as a result of initial immunization with ChAdOx1‑S. Secondary endpoints were type and severity of adverse events and self-perceived tolerability.

Material and methods: Anonymized online questionnaire to be completed once by all vaccinated individuals after receiving the first dose of ChAdOx1‑S. The severity of side effects was queried using an ordinal numerical rating scale with values ranging from 0 to 10. Other key data points were age, sex, and occupational group. Ability to work in the days following the injection was also assessed by self-reporting.

Results: Data from 1988 respondents were analyzed. The mean age was 37.13 years (standard deviation 13.7 years). Of the respondents 69.8% were female, 48.1% belonged to therapeutic and technical professions with patient contact, 38% were students, 10.6% were nursing personnel and 4% were physicians. Only 14.4% of respondents reported having tolerated the vaccination without side effects. The most common side effect was fatigue, followed by pain at the injection site. This was followed in descending frequency by headache, aching limbs, and chills. After vaccination 18% of respondents felt able to return to work immediately, 51% of all respondents had to report themselves unfit for work for at least 1 day after vaccination. Side effects were more prevalent in male and younger respondents.

Conclusion: Vaccination with ChAdOx1‑S frequently resulted in side effects. These resulted in 37% of respondents reporting sick. Nevertheless, 89.6% of all respondents would choose coronavirus vaccination with ChAdOx1‑S again.

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