Very early Guillain-Barre syndrome: A clinical-electrophysiological and ultrasonographic study

被引:24
作者
Berciano, Jose [1 ]
Orizaola, Pedro [2 ]
Gallardo, Elena [3 ]
Pelayo-Negro, Ana L. [1 ]
Sanchez-Juan, Pascual [1 ]
Infante, Jon [1 ]
Sedano, Maria J. [1 ]
机构
[1] Univ Cantabria, Univ Hosp Marques Valdecilla IDIVAL, Ctr Invest Biomed Red Enfermedades Neurodegenerat, Serv Neurol, Santander, Spain
[2] Univ Hosp Marques Valdecilla IDIVAL, Serv Clin Neurophysiol, Santander, Spain
[3] Univ Cantabria, Ctr Invest Biomed Red Enfermedades Neurodegenerat, Univ Hosp Marques Valdecilla IDIVAL, Serv Radiol, Santander, Spain
来源
CLINICAL NEUROPHYSIOLOGY PRACTICE | 2020年 / 5卷
关键词
Axonal degeneration; Demyelination; Endoneurial inflammatory oedema; Guillain-Barre syndrome; Ultrasonography; Very early Guillain-Barre syndrome; EARLY ELECTRODIAGNOSTIC FINDINGS; CROSS-SECTIONAL AREA; BLOOD-NERVE BARRIER; SYNDROME SUBTYPES; EARLY-STAGE; ULTRASOUND; NEUROPATHY; DIAGNOSIS; PATHOGENESIS; STIMULATION;
D O I
10.1016/j.cnp.2019.11.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Objectives: Using recent optimized electrodiagnostic criteria sets, we primarily aimed at verifying the accuracy of the initial electrophysiological test in very early Guillain-Barre syndrome (VEGBS), <= 4 days of onset, compared with the results of serial electrophysiology. Our secondary objective was to correlate early electrophysiological results with sonographic nerve changes. Methods: This is a retrospective study based on consecutive VEGBS patients admitted to the hospital. Each patient had serial nerve conduction studies (NCS) in at least 4 nerves. Initial NCS were done within 4 days after onset, and serial ones from the second week onwards. Electrophysiological recordings of each case were re-evaluated, GBS subtype being established accordingly. Nerve ultrasonography was almost always performed within 2 weeks after onset. Results: Fifteen adult VEGBS patients were identified with a mean age of 57.8 years. At first NCS, VEGBS sub-typing was only possible in 3 (20%) cases that showed an axonal pattern, the remaining patterns being mixed (combining axonal and demyelinating features) in 6 (40%), equivocal in 5 (33.3%), and normal in 1 (6.7%). Upon serial NCS, 7 (46.7%) cases were categorized as acute demyelinating polyneuropathy, 7 (46.7%) as axonal GBS, and 1 (6.6%) as unclassified syndrome. Antiganglioside reactivity was detected in 5 out of the 7 axonal cases. Nerve US showed that lesions mainly involved the ventral rami of scanned cervical nerves. Conclusions: Serial electrophysiological evaluation is necessary for accurate VEGBS subtype classification. Ultrasonography helps delineate the topography of nerve changes. Significance: We provide new VEGBS pathophysiological insights into nerve conduction alterations within the first 4 days of the clinical course. (C) 2019 International Federation of Clinical Neurophysiology. Published by Elsevier B.V.
引用
收藏
页码:1 / 9
页数:9
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