Abuawwad Mohammad T, Taha Mohammad J J, Taha Ahmad J, Kozaa Yasmeena Abdelall, Falah Obaida, Abuawwad Ibrahim T, Hammad Elsayed Mohamed, Mahmoud Ayman A, Aladawi Mohammad, Serhan Hashem Abu
Department of Clinical Medicine, Kasr Alainy Faculty of Medicine, Cairo University, Cairo, Egypt.
Mansoura Manchester Programme For Medical Education, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Clin Neurol Neurosurg. 2024 Mar;238:108183. doi: 10.1016/j.clineuro.2024.108183. Epub 2024 Feb 20.
Cases of Guillain-Barré Syndrome (GBS) have been believed to be associated with the novel COVID-19 infection, and also with the following vaccines developed against the infection. Our work aims to investigate the incidence of GBS after COVID-19 vaccination, and describe its clinical characteristics and potential confounders.
An electronic search was conducted through four databases: PubMed, Scopus, medRxiv, and Google Scholar for all case reports and case series describing after COVID-19 vaccine administration. All published articles from inception until November 1st, 2022 were included. Differences between groups were assessed using Pearson chi-square test. Modified Erasmus GBS Outcome Score (mEGOS) for the ability to walk after GBS was calculated for all cases with sufficient clinical data, and Kaplan-Meier survival analysis was performed to study the effect of vaccine type on the relationship between vaccination time and complication of GBS.
About 103 studies describing 175 cases of GBS following COVID-19 vaccination were included. The Acute Inflammatory Demyelinating Polyradiculoneuropathy subtype was the most reported subtype with 74 cases (42.29%). The affected age group averaged around 53.59 ±18.83 years, with AMSAN occurring in a rather older group (63.88 ±20.87 years, p=0.049). The AstraZeneca vaccine was associated with AIDP (n=38, 21.71%) more than other vaccines, p=0.02. The bilateral facial palsy subtype was mostly linked to adenoviral vector vaccinations, accounting for an average of 72% of the total BFP cases. Dysesthesias was the most reported sensory complication (60%, p=0.349). Most GBS patients survived (96%, p=0.036), however, most patients had low mEGOS scores (4 ±3.57, p<0.01). On average, patients developed GBS at 13.43 ±11.45 days from vaccination (p=0.73), and survival analysis for complication of GBS into mechanical ventilation or walking impairment yielded a severely increased probability of complication after 25 days (p<0.01). Intravenous immunoglobulins (p=0.03) along with rehabilitation (p=0.19) were the most commonly used treatment.
This work investigates the incidence of Guillain-Barré Syndrome after COVID-19 vaccination. Most cases occurred after receiving the AstraZeneca or Pfizer vaccines, and despite low mortality rates, ambulation was compromised in most patients. A higher risk of GBS complication is associated with an onset later than 12-13 days, particularly with Pfizer, AstraZeneca, and Moderna vaccines. No specific predisposing or prognostic factor was identified, and the relation between the COVID-19 vaccines and GBS remain unclear.
格林-巴利综合征(GBS)病例被认为与新型冠状病毒肺炎(COVID-19)感染有关,也与随后研发的针对该感染的疫苗有关。我们的研究旨在调查COVID-19疫苗接种后GBS的发病率,并描述其临床特征和潜在混杂因素。
通过四个数据库进行电子检索:PubMed、Scopus、medRxiv和谷歌学术搜索,查找所有描述COVID-19疫苗接种后情况的病例报告和病例系列。纳入自数据库建立至2022年11月1日发表的所有文章。使用Pearson卡方检验评估组间差异。对所有有足够临床数据的病例计算GBS后行走能力的改良伊拉斯谟GBS结局评分(mEGOS),并进行Kaplan-Meier生存分析,以研究疫苗类型对接种时间与GBS并发症关系的影响。
纳入了约103项描述175例COVID-19疫苗接种后GBS病例的研究。急性炎症性脱髓鞘性多发性神经根神经病亚型是报告最多的亚型,有74例(42.29%)。受影响年龄组平均约为53.59±18.83岁,急性运动轴索性神经病(AMSAN)多见于年龄较大的组(63.88±20.87岁,p=0.049)。与其他疫苗相比,阿斯利康疫苗与急性炎症性脱髓鞘性多发性神经根神经病(AIDP)的关联更强(n=38,21.71%),p=0.02。双侧面瘫亚型大多与腺病毒载体疫苗接种有关,平均占双侧面瘫病例总数的72%。感觉异常是报告最多的感觉并发症(60%,p=0.349)。大多数GBS患者存活(96%,p=0.036),然而,大多数患者的mEGOS评分较低(4±3.57,p<0.01)。平均而言,患者在接种疫苗后13.43±11.45天发生GBS(p=0.73),对GBS并发机械通气或行走障碍的生存分析显示,25天后并发症发生概率大幅增加(p<0.01)。静脉注射免疫球蛋白(p=0.03)和康复治疗(p=0.19)是最常用的治疗方法。
本研究调查了COVID-19疫苗接种后格林-巴利综合征的发病率。大多数病例发生在接种阿斯利康或辉瑞疫苗后,尽管死亡率较低,但大多数患者的行走能力受到影响。GBS并发症风险较高与发病时间晚于12 - 13天有关,尤其是辉瑞、阿斯利康和莫德纳疫苗。未发现特定的易感或预后因素,COVID-19疫苗与GBS之间的关系仍不清楚。