Clinical Features of Post-Vaccination Guillain-Barré Syndrome (GBS) in Korea.
10.3346/jkms.2017.32.7.1154
- Author:
Yong Shik PARK
1
;
Keon Joo LEE
;
Seung Woo KIM
;
Kyung Min KIM
;
Bum Chun SUH
Author Information
1. Department of Neurology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.
- Publication Type:Original Article
- Keywords:
Guillain-Barré Syndrome;
Vaccination;
Adverse Events;
Brighton Criteria;
Korea
- MeSH:
Adult;
Advisory Committees;
Axons;
Cerebrospinal Fluid;
Compensation and Redress;
Follow-Up Studies;
Guillain-Barre Syndrome*;
Humans;
Immunization;
Influenza, Human;
Korea*;
Neural Conduction;
Polyradiculoneuropathy;
Quadriplegia;
Vaccination
- From:Journal of Korean Medical Science
2017;32(7):1154-1159
- CountryRepublic of Korea
- Language:English
-
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.
