Incidence and management of the main serious adverse events reported after COVID-19 vaccination.

IF 2.9 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Teresa Padilla-Flores, Alicia Sampieri, Luis Vaca
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Abstract

Coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2n first appeared in Wuhan, China in 2019. Soon after, it was declared a pandemic by the World Health Organization. The health crisis imposed by a new virus and its rapid spread worldwide prompted the fast development of vaccines. For the first time in human history, two vaccines based on recombinant genetic material technology were approved for human use. These mRNA vaccines were applied in massive immunization programs around the world, followed by other vaccines based on more traditional approaches. Even though all vaccines were tested in clinical trials prior to their general administration, serious adverse events, usually of very low incidence, were mostly identified after application of millions of doses. Establishing a direct correlation (the cause-effect paradigm) between vaccination and the appearance of adverse effects has proven challenging. This review focuses on the main adverse effects observed after vaccination, including anaphylaxis, myocarditis, vaccine-induced thrombotic thrombocytopenia, Guillain-Barré syndrome, and transverse myelitis reported in the context of COVID-19 vaccination. We highlight the symptoms, laboratory tests required for an adequate diagnosis, and briefly outline the recommended treatments for these adverse effects. The aim of this work is to increase awareness among healthcare personnel about the serious adverse events that may arise post-vaccination. Regardless of the ongoing discussion about the safety of COVID-19 vaccination, these adverse effects must be identified promptly and treated effectively to reduce the risk of complications.

接种 COVID-19 疫苗后报告的主要严重不良事件的发生率和处理情况。
由严重急性呼吸系统综合征冠状病毒 2n 引起的 2019 年冠状病毒病(COVID-19)于 2019 年首次在中国武汉出现。不久后,世界卫生组织宣布其为大流行病。新病毒带来的健康危机及其在全球范围内的迅速传播促使疫苗的快速发展。人类历史上首次批准了两种基于基因重组材料技术的疫苗供人类使用。这些 mRNA 疫苗被应用于世界各地的大规模免疫计划中,随后其他疫苗也采用了更传统的方法。尽管所有疫苗在普遍使用前都经过了临床试验,但严重不良事件(通常发生率很低)大多是在使用数百万剂疫苗后发现的。事实证明,建立疫苗接种与不良反应出现之间的直接相关性(因果范式)具有挑战性。本综述重点关注接种疫苗后观察到的主要不良反应,包括过敏性休克、心肌炎、疫苗诱发的血栓性血小板减少症、格林-巴利综合征和横贯性脊髓炎,这些不良反应是在接种 COVID-19 疫苗的背景下报告的。我们重点介绍了这些不良反应的症状、适当诊断所需的实验室检查,并简要概述了针对这些不良反应的建议治疗方法。这项工作旨在提高医护人员对接种疫苗后可能出现的严重不良反应的认识。无论目前关于 COVID-19 疫苗接种安全性的讨论如何,这些不良反应都必须得到及时发现和有效治疗,以降低并发症的风险。
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来源期刊
Pharmacology Research & Perspectives
Pharmacology Research & Perspectives Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
5.30
自引率
3.80%
发文量
120
审稿时长
20 weeks
期刊介绍: PR&P is jointly published by the American Society for Pharmacology and Experimental Therapeutics (ASPET), the British Pharmacological Society (BPS), and Wiley. PR&P is a bi-monthly open access journal that publishes a range of article types, including: target validation (preclinical papers that show a hypothesis is incorrect or papers on drugs that have failed in early clinical development); drug discovery reviews (strategy, hypotheses, and data resulting in a successful therapeutic drug); frontiers in translational medicine (drug and target validation for an unmet therapeutic need); pharmacological hypotheses (reviews that are oriented to inform a novel hypothesis); and replication studies (work that refutes key findings [failed replication] and work that validates key findings). PR&P publishes papers submitted directly to the journal and those referred from the journals of ASPET and the BPS
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