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Clinical Features of Post-Vaccination Guillain-Barré Syndrome (GBS) in Korea
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 clai...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Academy of Medical Sciences
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461320/ https://www.ncbi.nlm.nih.gov/pubmed/28581273 http://dx.doi.org/10.3346/jkms.2017.32.7.1154 |
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author | Park, Yong-Shik Lee, Keon-Joo Kim, Seung Woo Kim, Kyung Min Suh, Bum Chun |
author_facet | Park, Yong-Shik Lee, Keon-Joo Kim, Seung Woo Kim, Kyung Min Suh, Bum Chun |
author_sort | Park, Yong-Shik |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5461320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-54613202017-07-01 Clinical Features of Post-Vaccination Guillain-Barré Syndrome (GBS) in Korea Park, Yong-Shik Lee, Keon-Joo Kim, Seung Woo Kim, Kyung Min Suh, Bum Chun J Korean Med Sci Original Article 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. The Korean Academy of Medical Sciences 2017-07 2016-05-19 /pmc/articles/PMC5461320/ /pubmed/28581273 http://dx.doi.org/10.3346/jkms.2017.32.7.1154 Text en © 2017 The Korean Academy of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Park, Yong-Shik Lee, Keon-Joo Kim, Seung Woo Kim, Kyung Min Suh, Bum Chun Clinical Features of Post-Vaccination Guillain-Barré Syndrome (GBS) in Korea |
title | Clinical Features of Post-Vaccination Guillain-Barré Syndrome (GBS) in Korea |
title_full | Clinical Features of Post-Vaccination Guillain-Barré Syndrome (GBS) in Korea |
title_fullStr | Clinical Features of Post-Vaccination Guillain-Barré Syndrome (GBS) in Korea |
title_full_unstemmed | Clinical Features of Post-Vaccination Guillain-Barré Syndrome (GBS) in Korea |
title_short | Clinical Features of Post-Vaccination Guillain-Barré Syndrome (GBS) in Korea |
title_sort | clinical features of post-vaccination guillain-barré syndrome (gbs) in korea |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461320/ https://www.ncbi.nlm.nih.gov/pubmed/28581273 http://dx.doi.org/10.3346/jkms.2017.32.7.1154 |
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