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[接种载体疫苗ChAdOx1-S(阿斯利康新冠疫苗)后感染严重急性呼吸综合征冠状病毒2的主观幸福感和工作能力]

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

作者信息

Kalbhenn Johannes, Gabler Feline, Heinrich Sebastian, Steinmann Daniel

机构信息

Klinik für Anästhesiologie und Intensivmedizin, Universitätsklinikum Freiburg, Hugstetter Straße 55, 79106 Freiburg im Breisgau, Deutschland.

Betriebsärztlicher Dienst, Universitätsklinikum Freiburg, Freiburg, Deutschland.

出版信息

Zentralbl Arbeitsmed Arbeitsschutz Ergon. 2022;72(2):51-57. doi: 10.1007/s40664-021-00448-4. Epub 2021 Nov 7.

Abstract

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.

摘要

背景

严重急性呼吸综合征冠状病毒2疫苗ChAdOx1-S(阿斯利康公司的Vaxzevria)自2021年1月起已获德国保罗·埃利希研究所批准。在几次接种活动中,医护人员和医学生可自愿接种这种疫苗。

目的

该研究的主要终点是评估初次接种ChAdOx1-S后无法工作的发生率和持续时间。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。

材料与方法

所有接种者在接种第一剂ChAdOx1-S后通过匿名在线问卷一次性完成调查。使用从0到10的有序数字评分量表询问副作用的严重程度。其他关键数据点包括年龄、性别和职业群体。还通过自我报告评估注射后几天内的工作能力。

结果

对1988名受访者的数据进行了分析。平均年龄为37.13岁(标准差13.7岁)。在受访者中,69.8%为女性,48.1%属于与患者有接触的治疗和技术职业,38%为学生,10.6%为护理人员,4%为医生。只有14.4%的受访者报告接种疫苗后无副作用。最常见的副作用是疲劳,其次是注射部位疼痛。接下来按频率从高到低依次是头痛、四肢酸痛和发冷。接种疫苗后,18%的受访者感觉能够立即返回工作岗位,所有受访者中有51%在接种疫苗后至少有1天不得不报告自己无法工作。副作用在男性和年轻受访者中更为普遍。

结论

接种ChAdOx1-S疫苗经常会导致副作用。这些副作用导致37%的受访者报告生病。尽管如此,所有受访者中有89.6%会再次选择接种ChAdOx1-S冠状病毒疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea50/8572530/107e38328c01/40664_2021_448_Fig1_HTML.jpg

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