Department of Neurology, Texas Tech University Health Sciences Center El Paso, Paul L. Foster School of Medicine, El Paso, TX 79905, USA.
Department of Internal Medicine, Hospitalist Sovah Health, Martinsville, VA 24112, USA.
Medicina (Kaunas). 2019 Jul 15;55(7):375. doi: 10.3390/medicina55070375.
Myasthenia gravis (MG) and Guillain-Barré Syndrome (GBS) are autoimmune neuromuscular disorders that may present as neuromuscular emergencies requiring mechanical ventilation and critical care. Comparative outcomes of these disease processes, once severe enough to require mechanical ventilation, are not known. In this study, we compared the patients requiring mechanical ventilation in terms of in-hospital complications, length of stay, disability, and mortality between these two disease entities at a national level. Mechanically ventilated patients with primary diagnosis of MG (n = 6684) and GBS (n = 5834) were identified through retrospective analysis of Nationwide Inpatient Sample (NIS) database for the years 2006 to 2014. Even though mechanically ventilated MG patients were older (61.0 ± 19.1 versus 54.9 ± 20.1 years) and presented with more medical comorbidities, they had lower disease severity on admission, as well as lower in-hospital complications sepsis, pneumonia, and urinary tract infections as compared with GBS patients. In the multivariate analysis, after adjusting for confounders including treatment, GBS patients had significantly higher disability (odds ratio (OR) 15.6, 95% confidence interval (CI) 10.9-22.2) and a longer length of stay (OR 3.48, 95% CI 2.22-5.48). There was no significant difference in mortality between the groups (8.45% MG vs. 10.0% GBS, = 0.16). Mechanically ventilated GBS patients have higher disease severity at admission along with more in-hospital complications, length of stay, and disability compared with MG patients. Potential explanations for these findings include delay in the diagnosis, poor response to immunotherapy particularly in patients with axonal GBS variant, or longer recovery time after nerve damage.
重症肌无力(MG)和格林-巴利综合征(GBS)是自身免疫性神经肌肉疾病,可能表现为需要机械通气和重症监护的神经肌肉急症。一旦这些疾病过程严重到需要机械通气,它们的治疗结果尚不清楚。在这项研究中,我们比较了这两种疾病在全国范围内需要机械通气的患者的住院并发症、住院时间、残疾和死亡率。通过对 2006 年至 2014 年全国住院患者样本(NIS)数据库的回顾性分析,确定了原发性诊断为 MG(n=6684)和 GBS(n=5834)的机械通气患者。尽管机械通气的 MG 患者年龄较大(61.0±19.1 岁比 54.9±20.1 岁),并伴有更多的合并症,但与 GBS 患者相比,他们入院时疾病严重程度较低,住院并发症(如败血症、肺炎和尿路感染)也较少。在多变量分析中,调整了包括治疗在内的混杂因素后,GBS 患者的残疾程度显著更高(比值比(OR)15.6,95%置信区间(CI)10.9-22.2),住院时间也更长(OR 3.48,95%CI 2.22-5.48)。两组之间的死亡率无显著差异(8.45%MG 与 10.0%GBS,=0.16)。与 MG 患者相比,机械通气的 GBS 患者入院时疾病严重程度更高,且住院并发症、住院时间和残疾程度也更高。这些发现的潜在解释包括诊断延迟、免疫治疗反应不佳(特别是在轴索性 GBS 变异型患者中)或神经损伤后的恢复时间较长。