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格林-巴利综合征的自主神经功能紊乱:患病率、临床谱及结局。

Dysautonomia in Guillain-Barré Syndrome: Prevalence, Clinical Spectrum, and Outcomes.

机构信息

Mayo Clinic Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Department of Neurology, The University of Chicago, Chicago, IL, USA.

出版信息

Neurocrit Care. 2020 Feb;32(1):113-120. doi: 10.1007/s12028-019-00781-w.

Abstract

BACKGROUND

Guillain-Barré syndrome (GBS), when severe, involves the autonomic nervous system; our objective was to assess the spectrum and predictors of dysautonomia, and how it may impact functional outcomes.

METHODS

A retrospective review of patients admitted to the Mayo Clinic in Rochester, MN between January 1, 2000, and December 31, 2017, with GBS and dysautonomia was performed. Demographics, comorbidities, parameters of dysautonomia, clinical course, GBS disability score, and Erasmus GBS Outcome Score (EGOS) at discharge were recorded.

RESULTS

One hundred eighty seven patients were included with 71 (38%) noted to have at least one manifestation of dysautonomia. There are 72% of patients with a demyelinating form of GBS and 36% of patients with demyelination had dysautonomia. Ileus (42%), hypertension (39%), hypotension (37%), fever (29%), tachycardia or bradycardia (27%), and urinary retention (24%) were the most common features. Quadriparesis, bulbar and neck flexor weakness, and mechanical ventilation were associated with autonomic dysfunction. Patients with dysautonomia more commonly had cardiogenic complications, syndrome of inappropriate antidiuretic hormone, posterior reversible encephalopathy syndrome, and higher GBS disability score and EGOS. Mortality was 6% in patients with dysautonomia versus 2% in the entire cohort (P = 0.02).

CONCLUSIONS

Dysautonomia in GBS is a manifestation of more severe involvement of the peripheral nervous system. Accordingly, mortality and functional outcomes are worse. There is a need to investigate if more aggressive treatment is warranted in this category of GBS.

摘要

背景

格林-巴利综合征(GBS)严重时会累及自主神经系统;我们的目的是评估自主神经功能障碍的类型和预测因素,以及它如何影响功能结局。

方法

对 2000 年 1 月 1 日至 2017 年 12 月 31 日期间在明尼苏达州罗切斯特市 Mayo 诊所住院的 GBS 合并自主神经功能障碍患者进行回顾性分析。记录患者的人口统计学、合并症、自主神经功能障碍参数、临床病程、GBS 残疾评分和出院时的 Erasmus GBS 结局评分(EGOS)。

结果

共纳入 187 例患者,其中 71 例(38%)至少有 1 种自主神经功能障碍表现。脱髓鞘型 GBS 患者占 72%,脱髓鞘型患者中有 36%出现自主神经功能障碍。最常见的表现为肠麻痹(42%)、高血压(39%)、低血压(37%)、发热(29%)、心动过速或心动过缓(27%)和尿潴留(24%)。四肢瘫痪、球麻痹和颈屈肌无力与自主神经功能障碍相关。自主神经功能障碍患者更常发生心源性并发症、抗利尿激素不适当分泌综合征、可逆性后部脑病综合征,且 GBS 残疾评分和 EGOS 更高。自主神经功能障碍患者的死亡率为 6%,而整个队列的死亡率为 2%(P=0.02)。

结论

GBS 中的自主神经功能障碍是更严重的周围神经系统受累的表现。因此,死亡率和功能结局更差。需要研究在这一类型的 GBS 中是否需要更积极的治疗。

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