Islam Mohammad B, Islam Zhahirul, Farzana Kaniz S, Sarker Sumit K, Endtz Hubert P, Mohammad Quazi D, Jacobs Bart C
Emerging Diseases and Immunobiology Research Group, Laboratory Sciences and Services Division, International Centre for Diarrhoeal Disease Research, (icddr,b), Dhaka, Bangladesh.
Department of Medical Microbiology and Infectious Diseases, Erasmus University Medical Centre, Rotterdam, The Netherlands.
J Peripher Nerv Syst. 2016 Dec;21(4):345-351. doi: 10.1111/jns.12189.
Guillain-Barré syndrome has a diverse clinical phenotype related to geographical origin. To date, the majority of large-scale studies on Guillain-Barré syndrome (GBS) have been conducted in developed countries. We aimed to evaluate the key diagnostic features and assess the suitability of the Brighton criteria in 344 adult GBS patients from Bangladesh. All patients fulfilled the National Institute of Neurological Diseases and Stroke (NINDS) diagnostic criteria. Standardized data on demographic characteristics and clinical features, cerebrospinal fluid (CSF) analysis, and nerve conduction study (NCS) results were elaborated to measure the sensitivity of Brighton criteria. Most patients (88%) were admitted to hospital after the nadir weakness. Symmetrical weakness and reduced reflexes were found in 98% of patients. CSF albuminocytologic dissociation was detected in 238/269 (89%) cases and abnormal nerve physiology in 258/259 (>99%) cases. Only 27 (8%) patients received either intravenous immunoglobulin (IVIg) or plasmapheresis. In total, 200 (58%) patients met level 1 of the Brighton criteria; 97 (28%) patients met level 2; 42 (12%) patients met level 3; and 5 (2%) patients met level 4. This analysis showed that despite the heterogeneity of GBS in Bangladesh, the Brighton criteria showed a high sensitivity in the diagnosis of GBS.
吉兰-巴雷综合征具有与地理起源相关的多样临床表型。迄今为止,大多数关于吉兰-巴雷综合征(GBS)的大规模研究是在发达国家进行的。我们旨在评估344例来自孟加拉国的成年GBS患者的关键诊断特征,并评估布莱顿标准的适用性。所有患者均符合美国国立神经疾病和中风研究所(NINDS)的诊断标准。详细阐述了关于人口统计学特征和临床特征、脑脊液(CSF)分析以及神经传导研究(NCS)结果的标准化数据,以测量布莱顿标准的敏感性。大多数患者(88%)在肌无力最低点后入院。98%的患者出现对称性肌无力和反射减弱。238/269(89%)例检测到脑脊液蛋白细胞分离,258/259(>99%)例出现神经生理学异常。只有27例(8%)患者接受了静脉注射免疫球蛋白(IVIg)或血浆置换。总共200例(58%)患者符合布莱顿标准1级;97例(28%)患者符合2级;42例(12%)患者符合3级;5例(2%)患者符合4级。该分析表明,尽管孟加拉国的GBS存在异质性,但布莱顿标准在GBS诊断中显示出高敏感性。