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Clinical, electrophysiological findings and evaluation of prognosis of patients with Guillain-Barre syndrome

机译:临床,电生理调查结果与灭菌术患者预后的评价

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Guillain-Barre syndrome (GBS) is an acute inflammatory polyneuropathy characterized by frequent rapid progressive, ascending, symmetric weakness and areflexia. We aimed to evaluate the etiology, clinical and electrophysiological findings with treatment and prognosis of the patients with GBS in our clinic. Patients who were diagnosed with GBS in our clinic between 2009 and 2017 were evaluated retrospectively. The study included 20 female and 25 male patients. The most frequent symptom was the absence of walking (95.5%). All of the patients had muscle weakness on examination; in addition to that hyperesthesia (31%), autonomic symptoms (13.3%), sensory loss (11.1%), ataxia (11.1%), bilateral facial nerve palsy (6.6%), oculomotor nerve palsy (2.2%), and multiple cranial nerve involvement (2.2%) were the other detected findings. Ventilation support was required in 6 cases (13.3%). Acute motor axonal neuropathy (AMAN) was found in 20 patients (44.5%), acute inflammatory demyelinating polyradiculoneuropathy (AIDP) was found in 24 patients (53.3%), and acute motor and sensory axonal neuropathy (AMSAN) was only present in 1 patient (2.2%). Intravenous immunoglobulin (IVIG) was administered to 33 of the patients (73.3%). The mean hospital stay was 8.4±3.5 (2-17 days), and the relationship between the duration of hospital stay and the treatment given was statistically significant (p = 0.001). Complete remission was observed in 37 patients (82.3%) and the remaining 5 children (11.1%) experienced incomplete recovery. Three patients (6.7%) died of treatment-resistant hypotension, arrhythmia and severe pulmonary infection. The short duration of neurological deficit following infection, clinical stage of application, need for mechanical ventilation, dysautonomia, cranial nerve involvement, and current subtype were the negative prognostic factors. Although GBS is a self-limiting disease, early diagnosis and treatment are very important to reduce hospital stay with morbidity and mortality. Patients expected to be at high risk should be monitored closely.
机译:格林-巴利综合征(GBS)是一种急性炎症性多发性神经病,其特征是频繁的快速进行性、上升性、对称性虚弱和无反射。我们的目的是评估GBS患者的病因、临床和电生理表现、治疗和预后。对2009年至2017年间在我们诊所诊断为GBS的患者进行回顾性评估。这项研究包括20名女性和25名男性患者。最常见的症状是缺乏行走(95.5%)。所有患者检查时均出现肌无力;除此之外,还有感觉过敏(31%)、自主神经症状(13.3%)、感觉丧失(11.1%)、共济失调(11.1%)、双侧面神经麻痹(6.6%)、动眼神经麻痹(2.2%)和多发性颅神经受累(2.2%)。6例(13.3%)需要通气支持。急性运动轴索神经病(AMAN)20例(44.5%),急性炎性脱髓鞘多神经根神经病(AIDP)24例(53.3%),急性运动和感觉轴索神经病(AMSAN)仅1例(2.2%)。33例(73.3%)患者接受了静脉注射免疫球蛋白(IVIG)。平均住院时间为8.4±3.5(2-17天),住院时间与治疗之间的关系具有统计学意义(p=0.001)。37名患者(82.3%)完全缓解,其余5名儿童(11.1%)未完全康复。3例(6.7%)死于难治性低血压、心律失常和严重肺部感染。感染后短暂的神经功能缺损、应用的临床阶段、机械通气的需要、自主神经障碍、颅神经受累和当前亚型是负面预后因素。虽然GBS是一种自限性疾病,但早期诊断和治疗对于减少住院时间、降低发病率和死亡率非常重要。应密切监测预计处于高危状态的患者。

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