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1例可能与新型冠状病毒病加强疫苗相关的横纹肌溶解症和急性肾损伤病例

A Possible Case of COVID-19 Booster Vaccine-Associated Rhabdomyolysis and Acute Kidney Injury.

作者信息

Unger Kendra, Ponte Charles D, Anderson Dylan

机构信息

Department of Family Medicine, West Virginia University School of Medicine, Morgantown, WV, USA.

Department of Clinical Pharmacy, School of Pharmacy, West Virginia University, Morgantown, WV, USA.

出版信息

J Pharm Technol. 2022 Aug;38(4):247-250. doi: 10.1177/87551225221093944. Epub 2022 May 3.

Abstract

Nearly 10 billion doses of the various messenger ribonucleic acid (mRNA) and viral vector vaccines against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) have been administered worldwide. Adverse drug reactions (ADRs) have been overwhelmingly mild to moderate in nature. Rare side effects have included myocarditis/pericarditis, , Guillain-Barré Syndrome (GBS), and death. However, vaccine-related ADR data are still being collected using a variety of reporting systems. We will describe a case of suspected mRNA coronavirus disease 2019 (COVID-19) booster-related rhabdomyolysis in a woman who developed signs and symptoms 10 days after administration of the vaccine dose. With a Naranjo ADR probability score of 4, the vaccine was deemed to be a possible cause of our patient's rhabdomyolysis. A search of the VAERS (Vaccine Adverse Event Reporting System) mined in November 2021 revealed 386 reported cases of COVID-19 vaccine-related rhabdomyolysis. However, system limitations make the utility of the information problematic. It is vitally important that clinicians, scientists, and patients are aware of rhabdomyolysis as a potential side effect of vaccination. Suspected vaccine-related ADRs should be promptly and accurately reported via VAERS or other surveillance systems to support the ongoing effort to ensure vaccine safety.

摘要

全球已接种了近100亿剂针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的各种信使核糖核酸(mRNA)和病毒载体疫苗。药物不良反应(ADR)在本质上绝大多数为轻度至中度。罕见的副作用包括心肌炎/心包炎、吉兰-巴雷综合征(GBS)和死亡。然而,仍在使用各种报告系统收集与疫苗相关的ADR数据。我们将描述一例疑似mRNA冠状病毒病2019(COVID-19)加强针相关横纹肌溶解症的病例,该病例发生在一名女性身上,她在接种疫苗剂量10天后出现了相关症状和体征。根据Naranjo药物不良反应概率评分4分,该疫苗被认为可能是我们患者横纹肌溶解症的病因。对2021年11月挖掘的疫苗不良事件报告系统(VAERS)进行搜索后发现,有386例报告的与COVID-19疫苗相关的横纹肌溶解症病例。然而,系统的局限性使得这些信息的实用性存在问题。临床医生、科学家和患者必须意识到横纹肌溶解症是疫苗接种的一种潜在副作用。疑似与疫苗相关的ADR应通过VAERS或其他监测系统及时、准确地报告,以支持正在进行的确保疫苗安全的工作。

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