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韩国接种疫苗后吉兰-巴雷综合征(GBS)的临床特征

Clinical Features of Post-Vaccination Guillain-Barré Syndrome (GBS) in Korea.

作者信息

Park Yong Shik, Lee Keon Joo, Kim Seung Woo, Kim Kyung Min, Suh Bum Chun

机构信息

Department of Neurology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.

Division of Epidemic Intelligence Service, Korea Centers for Disease Control and Prevention, Cheongju, Korea.

出版信息

J Korean Med Sci. 2017 Jul;32(7):1154-1159. doi: 10.3346/jkms.2017.32.7.1154.

Abstract

Guillain-Barré syndrome (GBS) is the most common immune-mediated polyradiculoneuropathy and it is also the most commonly reported severe adverse event following immunization in adults. To evaluate the results of clinical and laboratory features of GBS after vaccination in Korea, we analyzed the claims-based data from 2002 to 2014 using materials collected for the Advisory Committee Vaccination Injury Compensation (ACVIC) meeting including, clinical features, nerve conduction studies (NCSs), cerebrospinal fluid (CSF) profiles, treatment, and outcomes. Forty-eight compensated GBS cases (median age, 15 years; interquartile range [IQR], 13-51; male:female ratio, 1:1) of 68 suspected GBS were found following immunization and all of them with influenza immunizations with either monovalent (n = 35) or trivalent (n = 13). Among them, 30 cases fulfilled the Brighton criteria level 1-3 (62.5%). The median duration between the onset of symptoms to nadir, duration of the nadir, and total admission period were 3 (IQR, 2-7 days), 2 (IQR, 1-5 days), and 14 (IQR, 6-33 days) days, respectively. The most frequently reported symptom was quadriparesis which was present in 36 cases (75%) at nadir. CSF examination revealed albuminocytologic dissociation in 25.0% and NCS was abnormal in 61.8%. After treatment, most of them showed improvement. Clinical features were similar to typical post-infectious GBS and there were both demyelinating and axonal forms suggesting heterogeneous pathogenic mechanism. In order to improve the diagnostic certainty of post-vaccination GBS, careful documentation of clinical features and timely diagnostic work-up with follow-up studies are needed.

摘要

吉兰-巴雷综合征(GBS)是最常见的免疫介导性多发性神经根神经病,也是成人免疫接种后最常报告的严重不良事件。为评估韩国疫苗接种后GBS的临床和实验室特征结果,我们使用为疫苗接种损伤咨询委员会(ACVIC)会议收集的材料,分析了2002年至2014年基于索赔的数据,包括临床特征、神经传导研究(NCS)、脑脊液(CSF)检查结果、治疗及转归。在免疫接种后发现68例疑似GBS病例中有48例获得赔偿(中位年龄15岁;四分位间距[IQR],13 - 51岁;男女比例1:1),所有病例均接种了单价(n = 35)或三价(n = 13)流感疫苗。其中,30例符合布莱顿标准1 - 3级(62.5%)。症状出现至最低点的中位持续时间、最低点持续时间及总住院时间分别为3天(IQR,2 - 7天)、2天(IQR,1 - 5天)和14天(IQR,6 - 33天)。最常报告的症状是四肢瘫,最低点时36例(75%)出现该症状。脑脊液检查显示25.0%存在蛋白细胞分离,NCS异常率为61.8%。治疗后,大多数患者病情改善。临床特征与典型感染后GBS相似,存在脱髓鞘和轴索性两种类型,提示致病机制具有异质性。为提高疫苗接种后GBS的诊断确定性,需要仔细记录临床特征并及时进行诊断检查及随访研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4402/5461320/cb108dafc7b6/jkms-32-1154-g001.jpg

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