Department of Neurology, Shifa Tameer-e-Millat University, Islamabad, Pakistan.
Department of Neurology, Shifa International Hospital, Islamabad, Pakistan.
J Coll Physicians Surg Pak. 2022 Mar;32(3):364-368. doi: 10.29271/jcpsp.2022.03.364.
To determine electrophysiological pattern and predictors of functional outcomes of patients with Gullain Barre Syndrome (GBS) at a tertiary care hospital.
Observational study.
Shifa International Hospital, Islamabad, Pakistan from January 2016 to July 2020.
A total of 62 patients with GBS of all age groups, gender, locations and those with no other primary diagnosis such as poliomyelitis, botulism, hysterical paralysis, toxin neuropathy and diabetic neuropathy were included. Functional outcome using modified Rankin Scale (mRS) and HUGHES score were recorded at presentation, on discharge and 6-month follow-up. Results of this study were analyzed using SPSS version 20.
There were 69% males with mean age of 31 ± 21years. The frequency of different GBS variants were 53% acute inflammatory demyelinating polyneuropathy (AIDP), 29% acute motor axonal neuropathy (AMAN), 11% acute motor and sensory axonal neuropathy (AMSAN) and pure sensory and atypical GBS were 2% each. The frequency of various antecedent events was recorded in 33 patients, including respiratory tract infection in 9 (14%) and diarrhea/vomiting in 13 (21%) patients. AIDP and AMSAN had a good prognosis where 31 (77%) patients out of the 40 fully recovered with HUGHES score 0-2 after 6 months. AMAN had poor prognosis as 2 (12%) patients died in the Hospital. Majority (n=32, 52%) of the patients were treated with plasmapheresis.
In this study population, AIDP was the most common variant with good prognosis and AMAN variant had the worst prognosis. Key Words: Guillain Barre syndrome (GBS), Acute inflammatory demyelinating polyneuropathy (AIDP), Acute motor axonal neuropathy (AMAN), Peripheral neuropathy, Lower limb weakness, Acute motor and sensory axonal neuropathy (AMSAN), Sensory neuropathy, Autoimmune disease.
在一家三级保健医院确定吉兰-巴雷综合征(GBS)患者的电生理模式和功能预后的预测因素。
观察性研究。
巴基斯坦伊斯兰堡 Shifa 国际医院,2016 年 1 月至 2020 年 7 月。
共纳入 62 例年龄、性别、位置各不相同的 GBS 患者,以及无其他原发性诊断(如脊髓灰质炎、肉毒中毒、癔病性瘫痪、毒素神经病和糖尿病性神经病)的患者。使用改良 Rankin 量表(mRS)和 Hughes 评分在入院时、出院时和 6 个月随访时记录功能预后。本研究结果使用 SPSS 20 版进行分析。
男性占 69%,平均年龄为 31 ± 21 岁。不同 GBS 变异型的频率分别为:急性炎症性脱髓鞘性多发性神经病(AIDP)53%、急性运动轴索性神经病(AMAN)29%、急性运动感觉轴索性神经病(AMSAN)11%、单纯感觉型和非典型 GBS 各占 2%。33 例患者记录了各种前驱事件的发生频率,其中呼吸道感染 9 例(14%),腹泻/呕吐 13 例(21%)。AIDP 和 AMSAN 的预后较好,40 例完全恢复的患者中有 31 例(77%)在 6 个月后 Hughes 评分 0-2。AMAN 预后较差,2 例(12%)患者在医院死亡。大多数(n=32,52%)患者接受了血浆置换治疗。
在本研究人群中,AIDP 是最常见的变异型,预后良好,AMAN 变异型预后最差。关键词:吉兰-巴雷综合征(GBS)、急性炎症性脱髓鞘性多发性神经病(AIDP)、急性运动轴索性神经病(AMAN)、周围神经病、下肢无力、急性运动感觉轴索性神经病(AMSAN)、感觉神经病、自身免疫性疾病。