Clinical characteristics of Guillain-Barré syndrome in Shenzhen: a retrospective study.

IF 2.2 3区 医学 Q3 CLINICAL NEUROLOGY BMC Neurology Pub Date : 2025-02-21 DOI:10.1186/s12883-025-04061-3
Feng Guo, Qin-Yuan Yao, Xiao-Hong Wu, Hui-Xia Guo, Xiao-Lin Su, Jin-Fang Zhou, Li-Jie Ren, Yan-Xia Zhou
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Abstract

Background: Guillain-Barré syndrome (GBS) is a group of immune-mediated peripheral neuropathies that causes acute flaccid paralysis. The global incidence of GBS was 0.6-4/100 000, and the incidence in China was 0.698/100 000. Although the diagnosis and treatment of GBS has made rapid progress, approximately 20% of patients with GBS are still unable to walk alone within 6 months after the onset of GBS, and 40% of patients have sequelae, such as weakened strength, limb pain, and numbness, seriously affecting their life and work. We aimed to retrospectively analyze the clinical characteristics of patients with GBS in Shenzhen, China and analyze the factors affecting disease severity to provide a reference for the precise treatment of GBS.

Methods: Clinical data of inpatients diagnosed with GBS in several hospitals in Shenzhen from April 2010 to October 2021 were obtained from an electronic medical record system (HIS system). The clinical characteristics of patients with GBS and the factors affecting disease severity were analyzed.

Results: A total of 146 patients were identified for this study, and 13 were lost during follow-up. During the follow-up period, three patients had acute-onset chronic inflammatory demyelinating polyneuropathy (A-CIDP). One hundred and thirty patients with complete data, comprising 90 males (69.23%) and 40 females (30.77%) with a median age of 39.50 ± 23.75 years, were included in the statistical analyses. Acute inflammatory demyelinating polyneuropathy (AIDP) was the most common electrophysiological variant (106 cases [81.54%]). Miller-Fisher syndrome (MFS), acute motor axonal neuropathy (AMAN), and acute motor-sensory axonal neuropathy (AMSAN) were noted in 21 (16.15%), 2 (1.54%), and 1 (0.77%) patients, respectively. The clinical course of the disease was mainly mild in 95 cases (73.08%), while 35 patients (26.92%) experienced severe disease. Logistic multivariate regression analysis showed that age ≥ 60 years old and having pneumonia may be associated with the severity of the disease.

Conclusions: AIDP is the most common electrophysiological variant of GBS in Shenzhen. Most cases of GBS in our setting are mild, and the long-term prognosis is favorable. Old age (≥ 60 years) and having pneumonia are independent risk factors for severe GBS.

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深圳吉兰-巴罗综合征临床特点的回顾性研究。
背景:格林-巴勒综合征(GBS)是一组引起急性弛缓性麻痹的免疫介导的周围神经病变。GBS全球发病率为0.6-4/10万,中国发病率为0.698/10万。虽然GBS的诊断和治疗取得了快速进展,但约20%的GBS患者在发病后6个月内仍无法独立行走,40%的患者有力量减弱、肢体疼痛、麻木等后遗症,严重影响其生活和工作。我们旨在回顾性分析中国深圳地区GBS患者的临床特点,分析影响病情严重程度的因素,为GBS的精准治疗提供参考。方法:从电子病历系统(HIS)中获取2010年4月至2021年10月深圳多家医院诊断为GBS的住院患者的临床资料。分析GBS患者的临床特点及影响病情严重程度的因素。结果:本研究共确定了146例患者,其中13例在随访期间丢失。随访期间,3例患者出现急性发作性慢性炎症性脱髓鞘性多神经病变(A-CIDP)。纳入资料完整的130例患者,其中男性90例(69.23%),女性40例(30.77%),中位年龄39.50±23.75岁。急性炎症性脱髓鞘性多神经病变(AIDP)是最常见的电生理变异(106例[81.54%])。Miller-Fisher综合征(MFS) 21例(16.15%),急性运动轴索神经病(AMAN) 2例(1.54%),急性运动-感觉轴索神经病(AMSAN) 1例(0.77%)。临床病程以轻症为主95例(73.08%),重症35例(26.92%)。Logistic多因素回归分析显示,年龄≥60岁且患有肺炎可能与疾病严重程度相关。结论:AIDP是深圳地区最常见的GBS电生理变型。在我们的环境中,大多数GBS病例是轻微的,长期预后良好。老年(≥60岁)和肺炎是严重GBS的独立危险因素。
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来源期刊
BMC Neurology
BMC Neurology 医学-临床神经学
CiteScore
4.20
自引率
0.00%
发文量
428
审稿时长
3-8 weeks
期刊介绍: BMC Neurology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of neurological disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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