Department of Neurology, Wuhan University, Renmin Hospital, Wuhan, China.
Department of Neurology, Wuhan University, Renmin Hospital, Wuhan, China,
Eur Neurol. 2019;81(5-6):231-238. doi: 10.1159/000503101. Epub 2019 Oct 1.
To analyze the clinical phenotypes and features of Guillain-Barré syndrome (GBS) in our hospital and explore the diagnostic value of the Brighton criteria.
We retrospectively analyzed the clinical data of GBS patients hospitalized in our hospital from January 1, 2013, to September 30, 2016. The patients were affirmatively graded according to the Brighton criteria (highest: level 1, lowest: level 4).
(1) We enrolled 72 patients with GBS, including 7 with cranial nerve variants, 4 with Miler-Fisher syndrome, and 61 with classic GBS that mainly presented as limb weakness. (2) A total of 56.94% of the included patients had preceding events, of which respiratory tract infections accounted for 63.41%; there was a significant difference in the incidence of GBS across the spring, summer, autumn, and winter. Weakness was the first symptom in 75% of patients, all patients reached peaked within 4 weeks, and 94.44% of the patients presented with decreased or absent deep tendon reflexes. Among the patients who completed a lumbar puncture cerebrospinal fluid (CSF) examination, 73.24% showed proteins dissociated from CSF cells. Demyelinating GBS was found in 54%, and axonal GBS was found in 22% of the patients who completed an electrophysiological examination. All patients with classic GBS were graded according to the Brighton diagnostic criteria as level 1 (60.66%, 37/61), level 2 (34.42%, 21/61), level 3 (4.92%, 3/61), or level 4 (0%).
In our hospital, the clinical features of patients with GBS were similar to those described in previous studies, but demyelinating GBS was the most important subtype. Most preceding events were upper respiratory tract infections. The Brighton criteria were highly sensitive, and perfect clinical data improved diagnostic grading. In areas where medical resources are relatively scarce, a detailed medical history and physical examination can help improve diagnostic accuracy.
分析我院吉兰-巴雷综合征(GBS)的临床表型和特征,并探讨 Brighton 标准的诊断价值。
回顾性分析 2013 年 1 月 1 日至 2016 年 9 月 30 日我院收治的 GBS 患者的临床资料。患者根据 Brighton 标准进行分级(最高:1 级,最低:4 级)。
(1)共纳入 72 例 GBS 患者,其中颅神经变异型 7 例,Miler-Fisher 综合征 4 例,经典 GBS 61 例,主要表现为四肢无力。(2)63.41%的患者有前驱事件,总的前驱感染发生率为 56.94%;GBS 的发病率在春夏秋冬各季有显著差异。75%的患者首发症状为无力,所有患者在 4 周内达到高峰,94.44%的患者深腱反射减弱或消失。完成腰椎穿刺脑脊液(CSF)检查的患者中,73.24%的蛋白与 CSF 细胞分离。电生理学检查发现脱髓鞘型 GBS 占 54%,轴索性 GBS 占 22%。所有经典 GBS 患者均根据 Brighton 诊断标准分级为 1 级(60.66%,37/61)、2 级(34.42%,21/61)、3 级(4.92%,3/61)或 4 级(0%)。
我院 GBS 患者的临床特征与以往研究相似,但脱髓鞘型 GBS 是最重要的亚型。大多数前驱事件为上呼吸道感染。Brighton 标准具有较高的敏感性,完善的临床资料可提高诊断分级的准确性。在医疗资源相对匮乏的地区,详细的病史和体格检查有助于提高诊断准确性。