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沙特阿拉伯与 COVID-19 疫苗相关的不良事件自我报告模式:一项全国性研究。

Pattern of self-reported adverse events related to COVID-19 vaccines in Saudi Arabia: A nationwide study.

机构信息

College of Medicine, King Saud University, Riyadh, Saudi Arabia.

The Saudi Ministry of Health, Riyadh, Saudi Arabia.

出版信息

Front Public Health. 2023 Feb 23;11:1043696. doi: 10.3389/fpubh.2023.1043696. eCollection 2023.

Abstract

BACKGROUND

Vaccination against coronavirus disease 2019 (COVID-19) is the most effective way to end the pandemic. Any development of adverse events (AEs) from various vaccines should be reported. We therefore aimed to explore major and minor AEs among vaccinated individuals in Saudi Arabia.

METHODS

This is a nationwide report based on the Saudi Arabian Ministry of Health (MOH) registry. It included those who received COVID-19 vaccines from 17th December 2020 to 31st December 2021. The study included spontaneous self-reported adverse effects to COVID-19 vaccines where the study participants used a governmental mobile app (Sehhaty) to report their AEs following vaccination using a checklist option that included a selection of side-effects. The primary outcome was to determine AEs reported within 14 days of vaccination which included injection site itching, pain, reaction, redness, swelling, anxiety, dizziness, fever, headache, hoarseness, itchiness, loss of consciousness, nausea, heartburn, sleep disruption, fatigue, seizures, anaphylaxis, shortness of breath, wheezing, swelling of lips, face, and throat, loss of consciousness, and admissions into the intensive care unit (ICU).

RESULTS

The study included a total number of 28,031 individuals who reported 71,480 adverse events (AEs); which were further classified into minor and major adverse events including ICU admissions post vaccination. Of the reported AEs, 38,309 (53. 6%) side-effects were reported following Pfizer-BioNTech, 32,223 (45%) following Oxford-AstraZeneca, and 948 (1.3%) following Moderna. The following reported AEs were statistically significant between the different vaccine types: shortness of breath\difficulty of breathing, dizziness, fever above 39°C, headache, hoarseness, injection site reactions, itchiness, nausea, sleep disruption, fatigue, wheezing, swelling of lips/face and\or throat, and loss of consciousness (-value < 0.05). Fever and seizure were the only statistically significant AEs amongst the number of vaccine doses received (-value < 0.05). Ten ICU admissions were reported in the 14 days observation period post-COVID-19 vaccination with the following diagnoses: acute myocardial infarction, pneumonia, atherosclerosis, acute respiratory failure, intracranial hemorrhage, grand mal seizure, Guillain-Barré syndrome, abnormal blood gas levels, and septic shock.

CONCLUSION

This study demonstrated that the most prevalent SARS-CoV-2 vaccine side-effects among adults in Saudi Arabia were mild in nature. This information will help reduce vaccine hesitancy and encourage further mass vaccination to combat the COVID-19 pandemic, especially as booster doses are now available. Further studies are warranted to obtain a better understanding of the association between risk factors and the experiencing of side-effects post vaccination.

摘要

背景

接种针对 2019 年冠状病毒病(COVID-19)的疫苗是结束大流行的最有效方法。应报告各种疫苗引起的任何不良事件(AE)。因此,我们旨在探讨沙特阿拉伯接种者中的主要和次要 AE。

方法

这是一项基于沙特阿拉伯卫生部(MOH)登记处的全国性报告。它包括自 2020 年 12 月 17 日至 2021 年 12 月 31 日期间接种 COVID-19 疫苗的人。该研究包括对 COVID-19 疫苗的自发自我报告的不良影响,研究参与者使用政府移动应用程序(Sehhaty)通过使用包括副作用选择的清单选项报告接种疫苗后的 AE。主要结果是确定接种疫苗后 14 天内报告的 AE,包括注射部位瘙痒、疼痛、反应、发红、肿胀、焦虑、头晕、发热、头痛、声音嘶哑、瘙痒、意识丧失、恶心、胃灼热、睡眠障碍、疲劳、癫痫发作、过敏反应、呼吸急促、喘息、嘴唇、面部和喉咙肿胀、意识丧失和入住重症监护病房(ICU)。

结果

该研究共纳入 28031 人,报告了 71480 例不良事件(AE);其中进一步分为轻微和严重不良事件,包括接种疫苗后的 ICU 入院。在报告的 AE 中,38309 例(53.6%)为辉瑞-生物技术公司,32223 例(45%)为牛津-阿斯利康公司,948 例(1.3%)为莫德纳公司。以下报告的 AE 在不同疫苗类型之间具有统计学意义:呼吸急促/呼吸困难、头晕、体温高于 39°C、头痛、声音嘶哑、注射部位反应、瘙痒、恶心、睡眠障碍、疲劳、喘息、嘴唇/面部和/或喉咙肿胀以及意识丧失(P 值<0.05)。发热和癫痫发作是接种疫苗次数中唯一具有统计学意义的 AE(P 值<0.05)。在 COVID-19 疫苗接种后 14 天观察期内报告了 10 例 ICU 入院,诊断为:急性心肌梗死、肺炎、动脉粥样硬化、急性呼吸衰竭、颅内出血、大发作性癫痫、格林-巴利综合征、血气水平异常和败血症性休克。

结论

本研究表明,沙特阿拉伯成年人中最常见的 SARS-CoV-2 疫苗副作用性质轻微。这些信息将有助于减少疫苗犹豫,并鼓励进一步大规模接种疫苗以应对 COVID-19 大流行,特别是现在可以提供加强针。需要进一步研究以更好地了解接种疫苗后与风险因素相关的副作用经历之间的关联。

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